Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2247 |
| ensemblid | ENSG00000138685.18 |
| hgncid | 3676 |
| symbol | FGF2 |
| name | fibroblast growth factor 2 |
| refseq_nuc | NM_001361665.2 |
| refseq_prot | NP_001348594.1 |
| ensembl_nuc | ENST00000644866.2 |
| ensembl_prot | ENSP00000494222.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 122826831 |
| end | 122898236 |
| strand | + |
| ver | v1.2 |
| region | chr4:122826831-122898236 |
| region5000 | chr4:122821831-122903236 |
| regionname0 | FGF2_chr4_122826831_122898236 |
| regionname5000 | FGF2_chr4_122821831_122903236 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 465 | 255 | 89 | 58 | 60 | 10 | 36 | FGF2_chr4_122821831_122903236 | FGF2 | ATGGC others(460): Show |
chr4 | 122821831 | 122903236 | ||
| a0001c0002 | 0/0 | 465 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | ATGGC others(460): Show |
chr4 | 122821831 | 122903236 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6651 | 48 | 1 | 8 | 24 | 4 | 11 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0002 | 0/0 | 6652 | 47 | 4 | 19 | 14 | 4 | 6 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0003 | 1/0 | 6652 | 23 | 7 | 8 | 5 | 0 | 2 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0004 | 0/0 | 6652 | 13 | 8 | 4 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0005 | 0/0 | 6651 | 11 | 1 | 5 | 0 | 2 | 3 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0006 | 0/0 | 6652 | 11 | 0 | 2 | 7 | 0 | 2 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0007 | 0/0 | 6652 | 10 | 10 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0008 | 0/0 | 6652 | 8 | 2 | 1 | 0 | 0 | 5 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0009 | 0/0 | 6651 | 7 | 6 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0010 | 0/0 | 6651 | 7 | 7 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0011 | 0/0 | 6652 | 6 | 6 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0012 | 0/0 | 6652 | 5 | 0 | 0 | 4 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0013 | 0/0 | 6652 | 4 | 3 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0014 | 0/0 | 6652 | 4 | 4 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0015 | 0/0 | 6652 | 4 | 1 | 1 | 1 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0016 | 0/0 | 6651 | 4 | 0 | 0 | 3 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0017 | 0/0 | 6652 | 3 | 2 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0018 | 0/0 | 6652 | 3 | 2 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0019 | 0/0 | 6652 | 3 | 1 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0020 | 0/0 | 6652 | 3 | 3 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0021 | 0/0 | 6651 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0022 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0023 | 0/0 | 6652 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0024 | 0/0 | 6651 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0025 | 0/1 | 6651 | 1 | 0 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0026 | 0/0 | 6651 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0027 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0028 | 0/0 | 6648 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6643): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0029 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0030 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0031 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0032 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0033 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0034 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0035 | 0/0 | 6651 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0036 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0037 | 0/0 | 6651 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0038 | 0/0 | 6652 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0039 | 0/0 | 6651 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0040 | 0/0 | 6652 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0041 | 0/0 | 6648 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6643): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0042 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0043 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0044 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0045 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0046 | 0/0 | 6652 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0047 | 0/0 | 6651 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0048 | 0/0 | 6651 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0001t0049 | 0/0 | 6651 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6646): Show |
chr4 | 122821831 | 122903236 |
| a0001c0002t0022 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | GCCAG others(6647): Show |
chr4 | 122821831 | 122903236 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0005g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0008g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0009g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0009g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0010g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0010g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0011g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0011g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0012g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0012g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0012g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0012g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0012g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0013g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0013g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0013g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0014g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0014g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0015g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0015g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0015g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0015g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0016g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0016g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0016g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0016g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0017g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0017g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0017g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0018g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0018g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0019g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0019g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0019g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0020g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0020g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0021g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0021g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0022g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0023g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0023g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0024g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0025g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0026g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0027g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0028g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0029g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0030g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0031g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0032g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0033g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0034g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0035g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0036g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0037g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0038g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0039g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0040g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0041g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0042g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0043g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0044g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0045g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0046g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0047g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0048g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0001t0049g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| a0001c0002t0022g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0107 | EUR | GBR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00609 | hp1 | a0001 | c0001 | t0015 | g0145 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00639 | hp1 | a0001 | c0001 | t0018 | g0009 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0135 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0132 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01106 | hp1 | a0001 | c0001 | t0049 | g0229 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01109 | hp2 | a0001 | c0001 | t0015 | g0214 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0106 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01192 | hp2 | a0001 | c0001 | t0013 | g0245 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0228 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01255 | hp1 | a0001 | c0001 | t0038 | g0031 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01255 | hp2 | a0001 | c0001 | t0019 | g0023 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0230 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01261 | hp2 | a0001 | c0001 | t0026 | g0108 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01346 | hp2 | a0001 | c0001 | t0019 | g0024 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01361 | hp1 | a0001 | c0001 | t0046 | g0186 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0118 | EUR | IBS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0058 | EUR | IBS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | IBS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0188 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01934 | hp2 | a0001 | c0001 | t0008 | g0117 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01975 | hp2 | a0001 | c0001 | t0017 | g0150 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0037 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02015 | hp1 | a0001 | c0001 | t0012 | g0032 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02055 | hp2 | a0001 | c0001 | t0030 | g0206 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02056 | hp2 | a0001 | c0001 | t0048 | g0020 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02145 | hp1 | a0001 | c0001 | t0017 | g0131 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02145 | hp2 | a0001 | c0001 | t0020 | g0238 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02257 | hp1 | a0001 | c0001 | t0022 | g0235 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02280 | hp1 | a0001 | c0001 | t0019 | g0015 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0244 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0222 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0205 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0060 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0169 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02615 | hp2 | a0001 | c0001 | t0034 | g0216 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0219 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02622 | hp2 | a0001 | c0001 | t0036 | g0199 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0218 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0109 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02698 | hp2 | a0001 | c0001 | t0035 | g0177 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02717 | hp1 | a0001 | c0001 | t0039 | g0197 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0223 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0168 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02735 | hp2 | a0001 | c0001 | t0016 | g0232 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0180 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0201 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0008 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02896 | hp1 | a0001 | c0001 | t0020 | g0010 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0149 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02897 | hp2 | a0001 | c0001 | t0020 | g0010 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02922 | hp1 | a0001 | c0001 | t0018 | g0217 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0148 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02965 | hp1 | a0001 | c0001 | t0023 | g0191 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02965 | hp2 | a0001 | c0001 | t0028 | g0203 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02970 | hp1 | a0001 | c0001 | t0011 | g0185 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0220 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02976 | hp1 | a0001 | c0001 | t0021 | g0234 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03041 | hp2 | a0001 | c0001 | t0027 | g0202 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0204 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0200 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0243 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0221 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03139 | hp2 | a0001 | c0001 | t0032 | g0246 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0144 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03195 | hp2 | a0001 | c0001 | t0029 | g0215 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03209 | hp1 | a0001 | c0001 | t0041 | g0225 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03209 | hp2 | a0001 | c0001 | t0043 | g0014 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03225 | hp1 | a0001 | c0001 | t0047 | g0184 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0224 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03490 | hp1 | a0001 | c0001 | t0015 | g0137 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0006 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0033 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0006 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0153 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0242 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0179 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0008 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03579 | hp2 | a0001 | c0001 | t0033 | g0151 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03654 | hp2 | a0001 | c0001 | t0008 | g0161 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0167 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0231 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0034 | SAS | BEB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | BEB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG04115 | hp2 | a0001 | c0001 | t0012 | g0012 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG04199 | hp1 | a0001 | c0001 | t0040 | g0022 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG04199 | hp2 | a0001 | c0001 | t0024 | g0052 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0110 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG04228 | hp2 | a0001 | c0001 | t0008 | g0159 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18522 | hp1 | a0001 | c0001 | t0014 | g0183 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0124 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18906 | hp1 | a0001 | c0001 | t0023 | g0190 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18906 | hp2 | a0001 | c0001 | t0018 | g0009 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18945 | hp1 | a0001 | c0001 | t0012 | g0013 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18957 | hp2 | a0001 | c0001 | t0016 | g0038 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18961 | hp1 | a0001 | c0001 | t0012 | g0021 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18966 | hp1 | a0001 | c0001 | t0037 | g0102 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18973 | hp1 | a0001 | c0001 | t0016 | g0027 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19003 | hp2 | a0001 | c0001 | t0016 | g0041 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0018 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0170 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19059 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19059 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19060 | hp1 | a0001 | c0001 | t0012 | g0026 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19070 | hp1 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA19240 | hp2 | a0001 | c0001 | t0031 | g0129 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA20129 | hp1 | a0001 | c0001 | t0014 | g0128 | AFR | ASW | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA20129 | hp2 | a0001 | c0001 | t0042 | g0016 | AFR | ASW | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | TSI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0061 | EUR | TSI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0181 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0239 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02559 | hp1 | a0001 | c0002 | t0022 | g0017 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0163 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG03471 | hp2 | a0001 | c0001 | t0021 | g0233 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0171 | AFR | USA | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| HG06807 | hp2 | a0001 | c0001 | t0045 | g0187 | AFR | USA | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA21309 | hp1 | a0001 | c0001 | t0014 | g0158 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| NA21309 | hp2 | a0001 | c0001 | t0044 | g0192 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0025 | g0142 | REF | REF | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0133 | REF | REF | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:122876382 | C | T | 1 | a0001c0002 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.240C>T | p.Asn80Asn | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/3 | 584/6652 | 240/468 | 80/155 | chr4 | 122876382 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:122826931 | C | T | 23 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0011 others(20): Show |
63 | HG00609.hp2 HG01106.hp1 HG01168.hp1 others(60): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-244C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/3 | chr4 | 122826931 | |||||||
| chr4:122892421 | T | C | 1 | a0001c0001t0024 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 25 | chr4 | 122892421 | ||||||
| chr4:122892564 | A | C | 2 | a0001c0001t0037 a0001c0001t0049 |
2 | HG01106.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*168A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 168 | chr4 | 122892564 | ||||||
| chr4:122892878 | A | G | 1 | a0001c0001t0048 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 482 | chr4 | 122892878 | ||||||
| chr4:122892929 | G | T | 1 | a0001c0001t0036 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*533G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 533 | chr4 | 122892929 | ||||||
| chr4:122893080 | T | C | 1 | a0001c0001t0038 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*684T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 684 | chr4 | 122893080 | ||||||
| chr4:122893153 | C | T | 6 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0024 others(3): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*757C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 757 | chr4 | 122893153 | ||||||
| chr4:122893230 | G | T | 6 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0020 others(3): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*834G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 834 | chr4 | 122893230 | ||||||
| chr4:122893344 | A | G | 1 | a0001c0001t0033 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*948A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 948 | chr4 | 122893344 | ||||||
| chr4:122893445 | CT | C | 5 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0021 others(2): Show |
22 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1052delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1052 | INFO_REALIGN_3_PRIME | chr4 | 122893445 | |||||
| chr4:122893745 | G | A | 3 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0038 |
59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1349G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1349 | chr4 | 122893745 | ||||||
| chr4:122893765 | C | T | 1 | a0001c0001t0023 | 2 | HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1369C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1369 | chr4 | 122893765 | ||||||
| chr4:122893863 | A | G | 2 | a0001c0001t0037 a0001c0001t0049 |
2 | HG01106.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1467A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1467 | chr4 | 122893863 | ||||||
| chr4:122893926 | A | G | 6 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0020 others(3): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1530A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1530 | chr4 | 122893926 | ||||||
| chr4:122894147 | C | A | 6 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0020 others(3): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1751C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1751 | chr4 | 122894147 | ||||||
| chr4:122894197 | A | G | 2 | a0001c0001t0036 a0001c0001t0044 |
2 | HG02622.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1801A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1801 | chr4 | 122894197 | ||||||
| chr4:122894207 | T | C | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(42): Show |
216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1811T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1811 | chr4 | 122894207 | ||||||
| chr4:122894208 | G | A | 37 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(34): Show |
143 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*1812G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1812 | chr4 | 122894208 | ||||||
| chr4:122894313 | G | A | 3 | a0001c0001t0013 a0001c0001t0022 a0001c0002t0022 |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1917G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1917 | chr4 | 122894313 | ||||||
| chr4:122894343 | C | A | 6 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0020 others(3): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1947C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1947 | chr4 | 122894343 | ||||||
| chr4:122894480 | G | A | 3 | a0001c0001t0013 a0001c0001t0022 a0001c0002t0022 |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2084G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2084 | chr4 | 122894480 | ||||||
| chr4:122894509 | G | C | 1 | a0001c0001t0043 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2113G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2113 | chr4 | 122894509 | ||||||
| chr4:122894619 | T | TA | 3 | a0001c0001t0013 a0001c0001t0022 a0001c0002t0022 |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2225dupA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2226 | INFO_REALIGN_3_PRIME | chr4 | 122894619 | |||||
| chr4:122894710 | C | G | 2 | a0001c0001t0020 a0001c0001t0034 |
4 | HG02145.hp2 HG02615.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2314C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2314 | chr4 | 122894710 | ||||||
| chr4:122894867 | T | C | 3 | a0001c0001t0008 a0001c0001t0019 a0001c0001t0040 |
12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2471T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2471 | chr4 | 122894867 | ||||||
| chr4:122894941 | C | G | 1 | a0001c0001t0046 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2545C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2545 | chr4 | 122894941 | ||||||
| chr4:122895136 | T | C | 8 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0021 others(5): Show |
25 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2740T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2740 | chr4 | 122895136 | ||||||
| chr4:122895162 | C | G | 1 | a0001c0001t0049 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2766C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2766 | chr4 | 122895162 | ||||||
| chr4:122895433 | G | T | 1 | a0001c0001t0030 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3037G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3037 | chr4 | 122895433 | ||||||
| chr4:122895552 | T | G | 8 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0021 others(5): Show |
25 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3156T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3156 | chr4 | 122895552 | ||||||
| chr4:122895638 | C | T | 3 | a0001c0001t0013 a0001c0001t0022 a0001c0002t0022 |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3242C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3242 | chr4 | 122895638 | ||||||
| chr4:122895737 | ATTC | A | 2 | a0001c0001t0028 a0001c0001t0041 |
2 | HG02965.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3345_*3347delTTC | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3345 | INFO_REALIGN_3_PRIME | chr4 | 122895737 | |||||
| chr4:122896020 | T | C | 2 | a0001c0001t0037 a0001c0001t0049 |
2 | HG01106.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3624T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3624 | chr4 | 122896020 | ||||||
| chr4:122896024 | T | G | 1 | a0001c0001t0045 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3628T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3628 | chr4 | 122896024 | ||||||
| chr4:122896067 | C | T | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(42): Show |
216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*3671C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3671 | chr4 | 122896067 | ||||||
| chr4:122896098 | C | T | 4 | a0001c0001t0013 a0001c0001t0022 a0001c0001t0026 others(1): Show |
7 | HG01192.hp2 HG01261.hp2 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3702C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3702 | chr4 | 122896098 | ||||||
| chr4:122896181 | CT | C | 14 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0013 others(11): Show |
73 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*3798delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3798 | INFO_REALIGN_3_PRIME | chr4 | 122896181 | |||||
| chr4:122896327 | C | G | 1 | a0001c0001t0017 | 3 | HG01975.hp2 HG02145.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3931C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3931 | chr4 | 122896327 | ||||||
| chr4:122896373 | T | C | 32 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(29): Show |
130 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*3977T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3977 | chr4 | 122896373 | ||||||
| chr4:122896411 | C | T | 1 | a0001c0001t0040 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4015C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4015 | chr4 | 122896411 | ||||||
| chr4:122896590 | A | G | 1 | a0001c0001t0026 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4194A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4194 | chr4 | 122896590 | ||||||
| chr4:122896731 | G | A | 2 | a0001c0001t0009 a0001c0001t0039 |
8 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4335G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4335 | chr4 | 122896731 | ||||||
| chr4:122896919 | T | C | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(3): Show |
69 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*4523T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4523 | chr4 | 122896919 | ||||||
| chr4:122896930 | C | G | 3 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0026 |
14 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4534C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4534 | chr4 | 122896930 | ||||||
| chr4:122896975 | G | A | 1 | a0001c0001t0047 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4579G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4579 | chr4 | 122896975 | ||||||
| chr4:122896985 | A | C | 2 | a0001c0001t0037 a0001c0001t0049 |
2 | HG01106.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4589A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4589 | chr4 | 122896985 | ||||||
| chr4:122897092 | A | G | 2 | a0001c0001t0037 a0001c0001t0049 |
2 | HG01106.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4696A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4696 | chr4 | 122897092 | ||||||
| chr4:122897116 | A | T | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(43): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*4720A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4720 | chr4 | 122897116 | ||||||
| chr4:122897117 | C | T | 1 | a0001c0001t0031 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4721C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4721 | chr4 | 122897117 | ||||||
| chr4:122897143 | T | A | 11 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0011 others(8): Show |
39 | HG01255.hp2 HG01346.hp2 HG01361.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*4747T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4747 | chr4 | 122897143 | ||||||
| chr4:122897338 | G | A | 1 | a0001c0001t0035 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4942G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4942 | chr4 | 122897338 | ||||||
| chr4:122897350 | C | G | 1 | a0001c0001t0045 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4954C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4954 | chr4 | 122897350 | ||||||
| chr4:122897356 | A | C | 32 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(29): Show |
130 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*4960A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4960 | chr4 | 122897356 | ||||||
| chr4:122897401 | G | A | 3 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0026 |
14 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5005G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 5005 | chr4 | 122897401 | ||||||
| chr4:122897745 | C | T | 1 | a0001c0001t0027 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5349C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 5349 | chr4 | 122897745 | ||||||
| chr4:122897858 | C | G | 6 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0020 others(3): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5462C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 5462 | chr4 | 122897858 | ||||||
| chr4:122897885 | C | A | 1 | a0001c0001t0032 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5489C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 5489 | chr4 | 122897885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:122827369 | T | C | 31 | a0001c0001t0004g0011 a0001c0001t0004g0029 a0001c0001t0004g0030 others(28): Show |
31 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+17T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827369 | |||||||
| chr4:122827460 | G | T | 5 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(2): Show |
5 | HG01192.hp2 HG02280.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+108G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827460 | |||||||
| chr4:122827461 | C | G | 135 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(132): Show |
140 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.178+109C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827461 | |||||||
| chr4:122827579 | C | T | 31 | a0001c0001t0004g0011 a0001c0001t0004g0029 a0001c0001t0004g0030 others(28): Show |
31 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+227C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827579 | |||||||
| chr4:122827639 | G | C | 21 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(18): Show |
22 | HG01975.hp2 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+287G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827639 | |||||||
| chr4:122827750 | A | T | 2 | a0001c0001t0003g0240 a0001c0001t0003g0241 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.178+398A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827750 | |||||||
| chr4:122828039 | T | A | 31 | a0001c0001t0004g0011 a0001c0001t0004g0029 a0001c0001t0004g0030 others(28): Show |
31 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+687T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828039 | |||||||
| chr4:122828082 | T | C | 21 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(18): Show |
22 | HG01975.hp2 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+730T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828082 | |||||||
| chr4:122828251 | T | C | 6 | a0001c0001t0010g0168 a0001c0001t0013g0242 a0001c0001t0013g0243 others(3): Show |
6 | HG01192.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+899T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828251 | |||||||
| chr4:122828273 | C | T | 3 | a0001c0001t0011g0239 a0001c0001t0020g0010 a0001c0001t0020g0238 |
4 | HG02145.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+921C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828273 | |||||||
| chr4:122828300 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178+948G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828300 | |||||||
| chr4:122828345 | C | T | 1 | a0001c0001t0003g0147 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.178+993C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828345 | |||||||
| chr4:122828397 | C | T | 2 | a0001c0001t0002g0236 a0001c0001t0002g0237 |
2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.178+1045C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828397 | |||||||
| chr4:122828510 | A | T | 21 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(18): Show |
22 | HG01975.hp2 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+1158A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828510 | |||||||
| chr4:122828621 | C | G | 1 | a0001c0001t0022g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.178+1269C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828621 | |||||||
| chr4:122828643 | C | T | 2 | a0001c0001t0021g0233 a0001c0001t0021g0234 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.178+1291C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828643 | |||||||
| chr4:122828796 | G | C | 21 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(18): Show |
22 | HG01975.hp2 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+1444G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828796 | |||||||
| chr4:122828832 | AAC | A | 60 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(57): Show |
61 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(58): Show |
intron_variant | MODIFIER | c.178+1481_178+1482d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828832 | |||||||
| chr4:122828835 | T | G | 60 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(57): Show |
61 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(58): Show |
intron_variant | MODIFIER | c.178+1483T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828835 | |||||||
| chr4:122828836 | C | T | 60 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(57): Show |
61 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(58): Show |
intron_variant | MODIFIER | c.178+1484C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828836 | |||||||
| chr4:122829048 | CT | C | 91 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0001g0157 others(88): Show |
93 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(90): Show |
intron_variant | MODIFIER | c.178+1705delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122829048 | ||||||
| chr4:122829088 | C | G | 4 | a0001c0001t0011g0185 a0001c0001t0045g0187 a0001c0001t0046g0186 others(1): Show |
4 | HG01361.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+1736C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829088 | |||||||
| chr4:122829112 | C | T | 21 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(18): Show |
22 | HG01975.hp2 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+1760C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829112 | |||||||
| chr4:122829417 | A | G | 39 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(36): Show |
41 | HG00741.hp1 HG01074.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.178+2065A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829417 | |||||||
| chr4:122829531 | C | T | 4 | a0001c0001t0004g0231 a0001c0001t0006g0230 a0001c0001t0016g0232 others(1): Show |
4 | HG01106.hp1 HG01261.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+2179C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829531 | |||||||
| chr4:122829554 | T | A | 1 | a0001c0001t0010g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+2202T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829554 | |||||||
| chr4:122829582 | G | A | 14 | a0001c0001t0004g0189 a0001c0001t0004g0193 a0001c0001t0004g0194 others(11): Show |
15 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+2230G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829582 | |||||||
| chr4:122829587 | C | A | 1 | a0001c0001t0003g0044 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.178+2235C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829587 | |||||||
| chr4:122829701 | A | G | 8 | a0001c0001t0001g0164 a0001c0001t0002g0162 a0001c0001t0003g0165 others(5): Show |
9 | HG02258.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+2349A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829701 | |||||||
| chr4:122829909 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.178+2557G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829909 | |||||||
| chr4:122830054 | C | T | 2 | a0001c0001t0009g0224 a0001c0001t0010g0223 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.178+2702C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830054 | |||||||
| chr4:122830101 | A | T | 26 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(23): Show |
27 | HG00741.hp1 HG01074.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.178+2749A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830101 | |||||||
| chr4:122830232 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.178+2880G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830232 | |||||||
| chr4:122830304 | G | A | 3 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0007g0169 |
3 | HG02615.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.178+2952G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830304 | |||||||
| chr4:122830365 | T | C | 2 | a0001c0001t0020g0010 a0001c0001t0020g0238 |
3 | HG02145.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.178+3013T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830365 | |||||||
| chr4:122830406 | T | TGGAAACA | 12 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(9): Show |
12 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.178+3055_178+3056i others(9): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830406 | ||||||
| chr4:122830419 | C | T | 1 | a0001c0001t0045g0187 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.178+3067C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830419 | |||||||
| chr4:122830444 | C | T | 23 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0006g0019 others(20): Show |
23 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.178+3092C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830444 | |||||||
| chr4:122830580 | T | C | 1 | a0001c0001t0036g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.178+3228T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830580 | |||||||
| chr4:122830582 | C | T | 26 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(23): Show |
27 | HG00741.hp1 HG01074.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.178+3230C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830582 | |||||||
| chr4:122830672 | A | G | 1 | a0001c0001t0015g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.178+3320A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830672 | |||||||
| chr4:122830816 | C | CA | 22 | a0001c0001t0001g0123 a0001c0001t0001g0130 a0001c0001t0002g0126 others(19): Show |
23 | HG00639.hp1 HG00642.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.178+3488dupA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | ||||||
| chr4:122830816 | C | CAA | 26 | a0001c0001t0001g0121 a0001c0001t0001g0156 a0001c0001t0001g0157 others(23): Show |
27 | HG01074.hp1 HG01243.hp2 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.178+3487_178+3488d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | ||||||
| chr4:122830816 | C | CAAA | 81 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(78): Show |
86 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.178+3486_178+3488d others(5): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | ||||||
| chr4:122830816 | C | CAAAA | 23 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(20): Show |
24 | HG00642.hp2 HG01071.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.178+3485_178+3488d others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | ||||||
| chr4:122830816 | C | CAAAAA | 5 | a0001c0001t0006g0037 a0001c0001t0006g0039 a0001c0001t0006g0040 others(2): Show |
5 | HG02004.hp1 NA18957.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+3484_178+3488d others(7): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | ||||||
| chr4:122830816 | C | CAAAAAA | 13 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0006g0025 others(10): Show |
13 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+3483_178+3488d others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | ||||||
| chr4:122830816 | C | CAAAAAAA | 7 | a0001c0001t0012g0021 a0001c0001t0019g0015 a0001c0001t0019g0023 others(4): Show |
7 | HG01255.hp2 HG01346.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+3482_178+3488d others(9): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | ||||||
| chr4:122830816 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0004g0011 a0001c0001t0006g0019 a0001c0001t0012g0012 others(3): Show |
6 | HG02056.hp2 HG02129.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+3481_178+3488d others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | ||||||
| chr4:122830816 | CAAAAAA | C | 10 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+3483_178+3488d others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | ||||||
| chr4:122830816 | CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0003g0182 a0001c0001t0009g0007 a0001c0001t0009g0181 others(5): Show |
9 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+3481_178+3488d others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | ||||||
| chr4:122830841 | T | C | 52 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(49): Show |
53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+3489T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830841 | |||||||
| chr4:122830862 | T | G | 108 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(105): Show |
112 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(109): Show |
intron_variant | MODIFIER | c.178+3510T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830862 | |||||||
| chr4:122830873 | G | T | 1 | a0001c0001t0003g0044 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.178+3521G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830873 | |||||||
| chr4:122831120 | G | T | 1 | a0001c0001t0008g0117 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.178+3768G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831120 | |||||||
| chr4:122831180 | T | C | 3 | a0001c0001t0009g0201 a0001c0001t0015g0200 a0001c0001t0027g0202 |
3 | HG02818.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.178+3828T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831180 | |||||||
| chr4:122831192 | A | G | 52 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(49): Show |
53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+3840A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831192 | |||||||
| chr4:122831385 | G | C | 14 | a0001c0001t0004g0189 a0001c0001t0004g0193 a0001c0001t0004g0194 others(11): Show |
15 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+4033G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831385 | |||||||
| chr4:122831438 | T | C | 52 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(49): Show |
53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+4086T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831438 | |||||||
| chr4:122831505 | C | T | 52 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(49): Show |
53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+4153C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831505 | |||||||
| chr4:122831508 | G | A | 52 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(49): Show |
53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+4156G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831508 | |||||||
| chr4:122831537 | G | T | 52 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(49): Show |
53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+4185G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831537 | |||||||
| chr4:122831545 | T | G | 6 | a0001c0001t0010g0168 a0001c0001t0013g0242 a0001c0001t0013g0243 others(3): Show |
6 | HG01192.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+4193T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831545 | |||||||
| chr4:122831585 | G | C | 6 | a0001c0001t0004g0189 a0001c0001t0011g0008 a0001c0001t0011g0188 others(3): Show |
7 | HG01891.hp1 HG02109.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+4233G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831585 | |||||||
| chr4:122831659 | A | G | 1 | a0001c0001t0034g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.178+4307A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831659 | |||||||
| chr4:122831846 | G | A | 1 | a0001c0001t0007g0149 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.178+4494G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831846 | |||||||
| chr4:122831904 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.178+4552A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831904 | |||||||
| chr4:122832102 | CTTG | C | 4 | a0001c0001t0011g0185 a0001c0001t0045g0187 a0001c0001t0046g0186 others(1): Show |
4 | HG01361.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+4753_178+4755d others(5): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122832102 | ||||||
| chr4:122832409 | T | A | 1 | a0001c0001t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178+5057T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122832409 | |||||||
| chr4:122832447 | GAA | G | 126 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(123): Show |
131 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(128): Show |
intron_variant | MODIFIER | c.178+5096_178+5097d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122832447 | |||||||
| chr4:122832609 | T | C | 12 | a0001c0001t0004g0189 a0001c0001t0004g0193 a0001c0001t0004g0194 others(9): Show |
13 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+5257T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122832609 | |||||||
| chr4:122832742 | G | A | 1 | a0001c0001t0005g0058 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.178+5390G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122832742 | |||||||
| chr4:122832960 | C | A | 5 | a0001c0001t0002g0046 a0001c0001t0002g0059 a0001c0001t0002g0061 others(2): Show |
5 | HG01516.hp1 HG01517.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+5608C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122832960 | |||||||
| chr4:122833074 | T | A | 50 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(47): Show |
52 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.178+5722T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122833074 | |||||||
| chr4:122833179 | A | ATG | 3 | a0001c0001t0001g0042 a0001c0001t0001g0116 a0001c0001t0017g0131 |
3 | HG02145.hp1 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.178+5849_178+5850d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | ||||||
| chr4:122833179 | A | ATGTG | 3 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0007g0169 |
3 | HG02615.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.178+5847_178+5850d others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | ||||||
| chr4:122833179 | A | ATGTGTG | 16 | a0001c0001t0003g0182 a0001c0001t0004g0226 a0001c0001t0004g0227 others(13): Show |
17 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.178+5845_178+5850d others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | ||||||
| chr4:122833179 | A | ATGTGTGT others(3): Show |
15 | a0001c0001t0001g0164 a0001c0001t0002g0162 a0001c0001t0003g0165 others(12): Show |
16 | HG00609.hp2 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.178+5841_178+5850d others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | ||||||
| chr4:122833179 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0042g0016 a0001c0002t0022g0017 |
2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.178+5839_178+5850d others(14): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | ||||||
| chr4:122833179 | A | ATGTGTGT others(7): Show |
25 | a0001c0001t0002g0160 a0001c0001t0004g0011 a0001c0001t0004g0029 others(22): Show |
25 | HG01175.hp2 HG01255.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.178+5837_178+5850d others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | ||||||
| chr4:122833179 | A | ATGTGTGT others(9): Show |
2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.178+5835_178+5850d others(18): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | ||||||
| chr4:122833201 | G | A | 4 | a0001c0001t0009g0224 a0001c0001t0010g0223 a0001c0001t0018g0009 others(1): Show |
5 | HG00639.hp1 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+5849G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122833201 | |||||||
| chr4:122833203 | A | G | 8 | a0001c0001t0003g0182 a0001c0001t0009g0007 a0001c0001t0009g0181 others(5): Show |
10 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+5851A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122833203 | |||||||
| chr4:122833444 | TAATTA | T | 14 | a0001c0001t0004g0189 a0001c0001t0004g0193 a0001c0001t0004g0194 others(11): Show |
15 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+6096_178+6100d others(7): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833444 | ||||||
| chr4:122833598 | G | T | 4 | a0001c0001t0008g0204 a0001c0001t0010g0205 a0001c0001t0028g0203 others(1): Show |
4 | HG02055.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+6246G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122833598 | |||||||
| chr4:122833723 | G | C | 102 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(99): Show |
106 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(103): Show |
intron_variant | MODIFIER | c.178+6371G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122833723 | |||||||
| chr4:122834021 | C | T | 12 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(9): Show |
12 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.178+6669C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834021 | |||||||
| chr4:122834274 | C | T | 8 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(5): Show |
8 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+6922C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834274 | |||||||
| chr4:122834346 | C | T | 1 | a0001c0001t0014g0144 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.178+6994C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834346 | |||||||
| chr4:122834775 | G | A | 4 | a0001c0001t0004g0231 a0001c0001t0006g0230 a0001c0001t0016g0232 others(1): Show |
4 | HG01106.hp1 HG01261.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+7423G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834775 | |||||||
| chr4:122834787 | A | G | 2 | a0001c0001t0021g0233 a0001c0001t0021g0234 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.178+7435A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834787 | |||||||
| chr4:122834801 | A | G | 4 | a0001c0001t0003g0182 a0001c0001t0009g0007 a0001c0001t0009g0181 others(1): Show |
5 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+7449A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834801 | |||||||
| chr4:122834825 | G | T | 1 | a0001c0001t0007g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178+7473G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834825 | |||||||
| chr4:122834905 | G | A | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+7553G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834905 | |||||||
| chr4:122835077 | A | G | 1 | a0001c0001t0002g0005 | 2 | NA18984.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.178+7725A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835077 | |||||||
| chr4:122835191 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.178+7839A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835191 | |||||||
| chr4:122835292 | G | A | 4 | a0001c0001t0004g0231 a0001c0001t0006g0230 a0001c0001t0016g0232 others(1): Show |
4 | HG01106.hp1 HG01261.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+7940G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835292 | |||||||
| chr4:122835338 | G | GT | 10 | a0001c0001t0001g0164 a0001c0001t0002g0141 a0001c0001t0002g0162 others(7): Show |
11 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+7996dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122835338 | ||||||
| chr4:122835382 | C | T | 46 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(43): Show |
47 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.178+8030C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835382 | |||||||
| chr4:122835607 | T | C | 1 | a0001c0001t0041g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.178+8255T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835607 | |||||||
| chr4:122835790 | T | A | 1 | a0001c0001t0008g0006 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.178+8438T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835790 | |||||||
| chr4:122835876 | T | C | 11 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(8): Show |
11 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+8524T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835876 | |||||||
| chr4:122835879 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0115 |
2 | HG01257.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.178+8527C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835879 | |||||||
| chr4:122836141 | G | A | 46 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(43): Show |
47 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.178+8789G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836141 | |||||||
| chr4:122836202 | A | C | 6 | a0001c0001t0009g0218 a0001c0001t0010g0219 a0001c0001t0010g0220 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+8850A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836202 | |||||||
| chr4:122836377 | G | A | 50 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(47): Show |
52 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.178+9025G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836377 | |||||||
| chr4:122836537 | G | T | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+9185G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836537 | |||||||
| chr4:122836593 | C | T | 134 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(131): Show |
139 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.178+9241C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836593 | |||||||
| chr4:122836595 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178+9243T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836595 | |||||||
| chr4:122836730 | A | C | 1 | a0001c0001t0043g0014 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.178+9378A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836730 | |||||||
| chr4:122836734 | A | G | 22 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(19): Show |
22 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+9382A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836734 | |||||||
| chr4:122836833 | C | T | 50 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(47): Show |
52 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.178+9481C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836833 | |||||||
| chr4:122836839 | G | A | 1 | a0001c0001t0019g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178+9487G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836839 | |||||||
| chr4:122836978 | A | C | 1 | a0001c0001t0002g0178 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.178+9626A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836978 | |||||||
| chr4:122837066 | T | C | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+9714T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837066 | |||||||
| chr4:122837184 | C | T | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+9832C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837184 | |||||||
| chr4:122837187 | T | A | 1 | a0001c0001t0002g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.178+9835T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837187 | |||||||
| chr4:122837343 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.178+9991G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837343 | |||||||
| chr4:122837378 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.178+10026A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837378 | |||||||
| chr4:122837466 | A | G | 50 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(47): Show |
52 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.178+10114A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837466 | |||||||
| chr4:122837830 | C | T | 1 | a0001c0001t0007g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.178+10478C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837830 | |||||||
| chr4:122837831 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.178+10479G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837831 | |||||||
| chr4:122837983 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.178+10631A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837983 | |||||||
| chr4:122838023 | G | C | 84 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(81): Show |
86 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.178+10671G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838023 | |||||||
| chr4:122838596 | C | T | 50 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(47): Show |
52 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.178+11244C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838596 | |||||||
| chr4:122838643 | A | C | 1 | a0001c0001t0006g0036 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.178+11291A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838643 | |||||||
| chr4:122838701 | A | G | 4 | a0001c0001t0003g0182 a0001c0001t0009g0007 a0001c0001t0009g0181 others(1): Show |
5 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+11349A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838701 | |||||||
| chr4:122838827 | C | G | 6 | a0001c0001t0004g0189 a0001c0001t0011g0008 a0001c0001t0011g0188 others(3): Show |
7 | HG01891.hp1 HG02109.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+11475C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838827 | |||||||
| chr4:122838836 | C | T | 8 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(5): Show |
8 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+11484C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838836 | |||||||
| chr4:122838847 | A | T | 4 | a0001c0001t0011g0239 a0001c0001t0020g0010 a0001c0001t0020g0238 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+11495A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838847 | |||||||
| chr4:122838863 | A | T | 1 | a0001c0001t0008g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.178+11511A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838863 | |||||||
| chr4:122839178 | T | A | 1 | a0001c0001t0002g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.178+11826T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839178 | |||||||
| chr4:122839221 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.178+11869G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839221 | |||||||
| chr4:122839350 | G | C | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+11998G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839350 | |||||||
| chr4:122839372 | A | AAAC | 21 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(18): Show |
21 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.178+12038_178+1204 others(7): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122839372 | ||||||
| chr4:122839534 | G | A | 12 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(9): Show |
12 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.178+12182G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839534 | |||||||
| chr4:122839614 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.178+12262C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839614 | |||||||
| chr4:122839632 | A | G | 53 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(50): Show |
55 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.178+12280A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839632 | |||||||
| chr4:122839647 | T | C | 23 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0006g0019 others(20): Show |
23 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.178+12295T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839647 | |||||||
| chr4:122839731 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.178+12379T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839731 | |||||||
| chr4:122839891 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.178+12539G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839891 | |||||||
| chr4:122840061 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.178+12709T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840061 | |||||||
| chr4:122840098 | T | G | 4 | a0001c0001t0003g0182 a0001c0001t0009g0007 a0001c0001t0009g0181 others(1): Show |
5 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+12746T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840098 | |||||||
| chr4:122840486 | A | C | 5 | a0001c0001t0009g0224 a0001c0001t0010g0223 a0001c0001t0018g0009 others(2): Show |
6 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+13134A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840486 | |||||||
| chr4:122840531 | G | C | 8 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(5): Show |
8 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+13179G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840531 | |||||||
| chr4:122840668 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.178+13316G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840668 | |||||||
| chr4:122840817 | C | T | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178+13465C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840817 | |||||||
| chr4:122840875 | A | G | 14 | a0001c0001t0004g0189 a0001c0001t0004g0193 a0001c0001t0004g0194 others(11): Show |
15 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+13523A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840875 | |||||||
| chr4:122841098 | G | A | 1 | a0001c0001t0021g0234 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178+13746G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841098 | |||||||
| chr4:122841139 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.178+13787T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841139 | |||||||
| chr4:122841366 | A | G | 4 | a0001c0001t0002g0054 a0001c0001t0002g0111 a0001c0001t0002g0112 others(1): Show |
4 | HG01928.hp2 HG01981.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+14014A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841366 | |||||||
| chr4:122841593 | G | C | 5 | a0001c0001t0009g0224 a0001c0001t0010g0223 a0001c0001t0018g0009 others(2): Show |
6 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+14241G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841593 | |||||||
| chr4:122841742 | A | G | 11 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(8): Show |
11 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+14390A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841742 | |||||||
| chr4:122841789 | C | T | 49 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(46): Show |
50 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.178+14437C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841789 | |||||||
| chr4:122841926 | A | G | 1 | a0001c0001t0010g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+14574A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841926 | |||||||
| chr4:122842037 | G | A | 1 | a0001c0001t0008g0171 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.178+14685G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842037 | |||||||
| chr4:122842092 | G | T | 1 | a0001c0001t0043g0014 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.178+14740G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842092 | |||||||
| chr4:122842471 | A | T | 4 | a0001c0001t0004g0231 a0001c0001t0006g0230 a0001c0001t0016g0232 others(1): Show |
4 | HG01106.hp1 HG01261.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+15119A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842471 | |||||||
| chr4:122842564 | C | G | 1 | a0001c0001t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178+15212C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842564 | |||||||
| chr4:122842746 | C | T | 17 | a0001c0001t0001g0053 a0001c0001t0001g0130 a0001c0001t0002g0045 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+15394C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842746 | |||||||
| chr4:122842972 | C | T | 126 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(123): Show |
131 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(128): Show |
intron_variant | MODIFIER | c.178+15620C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842972 | |||||||
| chr4:122843303 | G | T | 49 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(46): Show |
50 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.178+15951G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843303 | |||||||
| chr4:122843353 | A | G | 98 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(95): Show |
101 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(98): Show |
intron_variant | MODIFIER | c.178+16001A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843353 | |||||||
| chr4:122843636 | A | G | 49 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(46): Show |
50 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.178+16284A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843636 | |||||||
| chr4:122843690 | A | G | 102 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(99): Show |
106 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(103): Show |
intron_variant | MODIFIER | c.178+16338A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843690 | |||||||
| chr4:122843758 | T | C | 12 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(9): Show |
12 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+16406T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843758 | |||||||
| chr4:122843823 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.178+16471G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843823 | |||||||
| chr4:122843917 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.178+16565G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843917 | |||||||
| chr4:122844047 | A | G | 4 | a0001c0001t0011g0185 a0001c0001t0045g0187 a0001c0001t0046g0186 others(1): Show |
4 | HG01361.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+16695A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844047 | |||||||
| chr4:122844282 | A | G | 12 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(9): Show |
12 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+16930A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844282 | |||||||
| chr4:122844537 | T | C | 1 | a0001c0001t0005g0058 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.178+17185T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844537 | |||||||
| chr4:122844557 | TTTTCTTT others(11): Show |
T | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+17220_178+1723 others(22): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844557 | ||||||
| chr4:122844565 | CTTTCTT | C | 9 | a0001c0001t0004g0231 a0001c0001t0006g0230 a0001c0001t0007g0148 others(6): Show |
9 | HG01261.hp1 HG02735.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+17221_178+1722 others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844565 | ||||||
| chr4:122844568 | T | C | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.178+17216T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844568 | |||||||
| chr4:122844569 | C | T | 29 | a0001c0001t0004g0011 a0001c0001t0004g0029 a0001c0001t0004g0030 others(26): Show |
29 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.178+17217C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844569 | |||||||
| chr4:122844571 | T | C | 29 | a0001c0001t0004g0011 a0001c0001t0004g0029 a0001c0001t0004g0030 others(26): Show |
29 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.178+17219T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844571 | |||||||
| chr4:122844571 | T | TCCTTCC | 5 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(2): Show |
5 | HG01192.hp2 HG02280.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+17219_178+1722 others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844571 | |||||||
| chr4:122844571 | T | TCCTTCCT others(3): Show |
1 | a0001c0001t0010g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+17219_178+1722 others(14): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844571 | |||||||
| chr4:122844574 | T | C | 10 | a0001c0001t0004g0231 a0001c0001t0006g0230 a0001c0001t0010g0168 others(7): Show |
10 | HG01106.hp1 HG01192.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+17222T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844574 | |||||||
| chr4:122844578 | T | C | 10 | a0001c0001t0004g0231 a0001c0001t0006g0230 a0001c0001t0010g0168 others(7): Show |
10 | HG01106.hp1 HG01192.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+17226T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844578 | |||||||
| chr4:122844582 | T | C | 16 | a0001c0001t0004g0231 a0001c0001t0006g0230 a0001c0001t0007g0148 others(13): Show |
16 | HG01106.hp1 HG01192.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.178+17230T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844582 | |||||||
| chr4:122844582 | T | TCTTC | 13 | a0001c0001t0006g0019 a0001c0001t0006g0033 a0001c0001t0006g0034 others(10): Show |
13 | HG01346.hp2 HG02015.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+17233_178+1723 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | ||||||
| chr4:122844582 | T | TCTTCCTT others(1): Show |
17 | a0001c0001t0004g0011 a0001c0001t0004g0029 a0001c0001t0004g0030 others(14): Show |
17 | HG01175.hp2 HG01255.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+17233_178+1723 others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | ||||||
| chr4:122844582 | T | TCTTCCTT others(5): Show |
3 | a0001c0001t0002g0175 a0001c0001t0003g0176 a0001c0001t0035g0177 |
3 | HG00741.hp1 HG01256.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.178+17233_178+1723 others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | ||||||
| chr4:122844582 | T | TCTTCCTT others(9): Show |
7 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0008g0171 others(4): Show |
7 | HG01257.hp2 HG01258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+17233_178+1723 others(20): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | ||||||
| chr4:122844582 | T | TCTTCCTT others(13): Show |
4 | a0001c0001t0002g0237 a0001c0001t0003g0172 a0001c0001t0018g0009 others(1): Show |
5 | HG00639.hp1 HG01074.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+17233_178+1723 others(24): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | ||||||
| chr4:122844582 | T | TCTTCCTT others(17): Show |
2 | a0001c0001t0002g0236 a0001c0001t0006g0025 |
2 | HG00609.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.178+17233_178+1723 others(28): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | ||||||
| chr4:122844582 | T | TCTTCCTT others(21): Show |
2 | a0001c0001t0002g0178 a0001c0001t0007g0179 |
2 | HG03540.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.178+17233_178+1723 others(32): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | ||||||
| chr4:122844586 | T | C | 68 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(65): Show |
69 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.178+17234T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844586 | |||||||
| chr4:122844586 | T | TCTTC | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0123 others(18): Show |
22 | HG01891.hp1 HG01934.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.178+17262_178+1726 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTCCTT others(1): Show |
8 | a0001c0001t0001g0164 a0001c0001t0002g0160 a0001c0001t0003g0165 others(5): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+17258_178+1726 others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTCCTT others(5): Show |
7 | a0001c0001t0002g0162 a0001c0001t0007g0163 a0001c0001t0008g0161 others(4): Show |
7 | HG01975.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+17254_178+1726 others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTCCTT others(9): Show |
3 | a0001c0001t0008g0006 a0001c0001t0020g0010 a0001c0001t0020g0238 |
5 | HG02145.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+17250_178+1726 others(20): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTCCTT others(13): Show |
6 | a0001c0001t0003g0182 a0001c0001t0009g0007 a0001c0001t0009g0181 others(3): Show |
7 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+17246_178+1726 others(24): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTCCTT others(17): Show |
4 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0004g0198 others(1): Show |
4 | HG01168.hp1 HG02486.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+17242_178+1726 others(28): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTCCTT others(21): Show |
2 | a0001c0001t0004g0193 a0001c0001t0004g0194 |
2 | HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.178+17238_178+1726 others(32): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTCCTT others(25): Show |
1 | a0001c0001t0007g0180 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.178+17265_178+1726 others(36): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTTCTT others(25): Show |
1 | a0001c0001t0047g0184 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.178+17237_178+1723 others(36): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTTCTT others(25): Show |
1 | a0001c0001t0046g0186 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.178+17237_178+1723 others(36): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTTCTT others(29): Show |
1 | a0001c0001t0011g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.178+17237_178+1723 others(40): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | T | TCTTTCTT others(37): Show |
1 | a0001c0001t0045g0187 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.178+17237_178+1723 others(48): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844586 | TCTTCCTT others(5): Show |
T | 17 | a0001c0001t0001g0053 a0001c0001t0001g0130 a0001c0001t0002g0045 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+17254_178+1726 others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | ||||||
| chr4:122844601 | T | C | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+17249T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844601 | |||||||
| chr4:122844618 | T | C | 5 | a0001c0001t0004g0231 a0001c0001t0006g0230 a0001c0001t0011g0239 others(2): Show |
5 | HG01106.hp1 HG01261.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+17266T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844618 | |||||||
| chr4:122844711 | C | A | 4 | a0001c0001t0003g0182 a0001c0001t0009g0007 a0001c0001t0009g0181 others(1): Show |
5 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+17359C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844711 | |||||||
| chr4:122844727 | C | T | 12 | a0001c0001t0004g0189 a0001c0001t0004g0193 a0001c0001t0004g0194 others(9): Show |
13 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+17375C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844727 | |||||||
| chr4:122844829 | G | T | 11 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(8): Show |
11 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+17477G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844829 | |||||||
| chr4:122844892 | T | A | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+17540T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844892 | |||||||
| chr4:122844921 | G | A | 4 | a0001c0001t0004g0231 a0001c0001t0006g0230 a0001c0001t0016g0232 others(1): Show |
4 | HG01106.hp1 HG01261.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+17569G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844921 | |||||||
| chr4:122844944 | G | T | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+17592G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844944 | |||||||
| chr4:122844988 | C | G | 2 | a0001c0001t0020g0010 a0001c0001t0020g0238 |
3 | HG02145.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.178+17636C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844988 | |||||||
| chr4:122845064 | G | A | 55 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(52): Show |
56 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.178+17712G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845064 | |||||||
| chr4:122845281 | G | A | 66 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(63): Show |
68 | HG00609.hp2 HG00639.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.178+17929G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845281 | |||||||
| chr4:122845484 | G | A | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+18132G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845484 | |||||||
| chr4:122845566 | G | A | 4 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(1): Show |
4 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+18214G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845566 | |||||||
| chr4:122845588 | T | G | 119 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(116): Show |
124 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(121): Show |
intron_variant | MODIFIER | c.178+18236T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845588 | |||||||
| chr4:122845654 | C | T | 11 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(8): Show |
11 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+18302C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845654 | |||||||
| chr4:122845751 | G | A | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+18399G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845751 | |||||||
| chr4:122845829 | T | C | 1 | a0001c0001t0010g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.178+18477T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845829 | |||||||
| chr4:122845865 | T | C | 1 | a0001c0001t0019g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.178+18513T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845865 | |||||||
| chr4:122845944 | G | A | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.178+18592G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845944 | |||||||
| chr4:122846085 | G | A | 66 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(63): Show |
68 | HG00609.hp2 HG00639.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.178+18733G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846085 | |||||||
| chr4:122846097 | A | G | 58 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(55): Show |
60 | HG00609.hp2 HG00639.hp1 HG01175.hp2 others(57): Show |
intron_variant | MODIFIER | c.178+18745A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846097 | |||||||
| chr4:122846364 | G | A | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+19012G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846364 | |||||||
| chr4:122846603 | A | G | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+19251A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846603 | |||||||
| chr4:122846669 | A | G | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+19317A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846669 | |||||||
| chr4:122846753 | T | C | 2 | a0001c0001t0002g0236 a0001c0001t0002g0237 |
2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.178+19401T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846753 | |||||||
| chr4:122846788 | G | A | 55 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(52): Show |
56 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.178+19436G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846788 | |||||||
| chr4:122846965 | G | C | 66 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(63): Show |
68 | HG00609.hp2 HG00639.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.178+19613G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846965 | |||||||
| chr4:122847108 | A | G | 122 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(119): Show |
126 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(123): Show |
intron_variant | MODIFIER | c.178+19756A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847108 | |||||||
| chr4:122847182 | A | C | 61 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(58): Show |
62 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(59): Show |
intron_variant | MODIFIER | c.178+19830A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847182 | |||||||
| chr4:122847205 | A | G | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+19853A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847205 | |||||||
| chr4:122847297 | G | A | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+19945G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847297 | |||||||
| chr4:122847471 | C | T | 47 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(44): Show |
48 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.178+20119C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847471 | |||||||
| chr4:122847603 | C | CTCTA | 25 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0053 others(22): Show |
25 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.178+20287_178+2029 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847603 | ||||||
| chr4:122847603 | C | CTCTATCT others(1): Show |
8 | a0001c0001t0001g0115 a0001c0001t0002g0048 a0001c0001t0002g0068 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+20283_178+2029 others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847603 | ||||||
| chr4:122847603 | C | CTCTATCT others(5): Show |
3 | a0001c0001t0001g0066 a0001c0001t0002g0105 a0001c0001t0002g0213 |
3 | HG00438.hp2 HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.178+20279_178+2029 others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847603 | ||||||
| chr4:122847603 | C | CTCTATTA others(4): Show |
1 | a0001c0001t0001g0104 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.178+20256_178+2025 others(15): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847603 | ||||||
| chr4:122847603 | CTCTA | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0064 others(42): Show |
46 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.178+20287_178+2029 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847603 | ||||||
| chr4:122847606 | T | C | 53 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(50): Show |
54 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(51): Show |
intron_variant | MODIFIER | c.178+20254T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847606 | |||||||
| chr4:122847623 | ATCTATCT others(13): Show |
A | 12 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(9): Show |
12 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+20280_178+2029 others(24): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847623 | ||||||
| chr4:122847627 | ATCTATCT others(9): Show |
A | 4 | a0001c0001t0003g0182 a0001c0001t0009g0007 a0001c0001t0009g0181 others(1): Show |
5 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+20284_178+2029 others(20): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847627 | ||||||
| chr4:122847635 | ATCTATCT others(1): Show |
A | 8 | a0001c0001t0008g0171 a0001c0001t0009g0170 a0001c0001t0009g0201 others(5): Show |
8 | HG02717.hp1 HG02818.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+20291_178+2029 others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847635 | ||||||
| chr4:122847638 | TATCTGTC others(6): Show |
T | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178+20291_178+2030 others(17): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847638 | ||||||
| chr4:122847639 | ATCTG | A | 57 | a0001c0001t0001g0116 a0001c0001t0001g0157 a0001c0001t0001g0164 others(54): Show |
58 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.178+20291_178+2029 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847639 | ||||||
| chr4:122847642 | TGTCTATC others(2): Show |
T | 6 | a0001c0001t0010g0168 a0001c0001t0010g0223 a0001c0001t0013g0244 others(3): Show |
7 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+20291_178+2029 others(13): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847642 | |||||||
| chr4:122847643 | G | A | 41 | a0001c0001t0001g0042 a0001c0001t0001g0156 a0001c0001t0002g0178 others(38): Show |
42 | HG01106.hp1 HG01243.hp1 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.178+20291G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847643 | |||||||
| chr4:122847646 | TATCTA | T | 4 | a0001c0001t0009g0224 a0001c0001t0013g0242 a0001c0001t0013g0243 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+20300_178+2030 others(9): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847646 | ||||||
| chr4:122847653 | T | C | 10 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0013g0242 others(7): Show |
11 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+20301T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847653 | |||||||
| chr4:122847657 | T | C | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+20305T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847657 | |||||||
| chr4:122847661 | T | C | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+20309T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847661 | |||||||
| chr4:122847802 | G | T | 1 | a0001c0001t0001g0049 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.178+20450G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847802 | |||||||
| chr4:122847872 | C | T | 4 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0007g0169 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+20520C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847872 | |||||||
| chr4:122847881 | A | G | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+20529A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847881 | |||||||
| chr4:122847898 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.178+20546C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847898 | |||||||
| chr4:122847974 | G | A | 55 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(52): Show |
56 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.178+20622G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847974 | |||||||
| chr4:122848013 | C | T | 11 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0236 others(8): Show |
11 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+20661C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848013 | |||||||
| chr4:122848094 | C | G | 12 | a0001c0001t0004g0189 a0001c0001t0004g0193 a0001c0001t0004g0194 others(9): Show |
13 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+20742C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848094 | |||||||
| chr4:122848103 | G | A | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+20751G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848103 | |||||||
| chr4:122848130 | C | T | 2 | a0001c0001t0010g0221 a0001c0001t0010g0222 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.178+20778C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848130 | |||||||
| chr4:122848228 | T | C | 1 | a0001c0001t0002g0162 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.178+20876T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848228 | |||||||
| chr4:122848291 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.178+20939T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848291 | |||||||
| chr4:122848354 | A | G | 1 | a0001c0001t0031g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.178+21002A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848354 | |||||||
| chr4:122848379 | T | C | 1 | a0001c0001t0003g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.178+21027T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848379 | |||||||
| chr4:122848400 | A | G | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+21048A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848400 | |||||||
| chr4:122848434 | T | A | 122 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(119): Show |
126 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(123): Show |
intron_variant | MODIFIER | c.178+21082T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848434 | |||||||
| chr4:122848661 | A | G | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+21309A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848661 | |||||||
| chr4:122848699 | A | C | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0002g0160 others(1): Show |
4 | HG03669.hp2 HG03834.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+21347A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848699 | |||||||
| chr4:122848793 | G | A | 4 | a0001c0001t0019g0015 a0001c0001t0021g0233 a0001c0001t0021g0234 others(1): Show |
4 | HG02280.hp1 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+21441G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848793 | |||||||
| chr4:122848967 | C | CAG | 5 | a0001c0001t0009g0224 a0001c0001t0010g0223 a0001c0001t0018g0009 others(2): Show |
6 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+21620_178+2162 others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122848967 | ||||||
| chr4:122848983 | T | C | 11 | a0001c0001t0009g0224 a0001c0001t0010g0168 a0001c0001t0010g0223 others(8): Show |
12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+21631T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848983 | |||||||
| chr4:122849027 | C | T | 5 | a0001c0001t0009g0218 a0001c0001t0010g0219 a0001c0001t0010g0220 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+21675C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849027 | |||||||
| chr4:122849455 | G | T | 6 | a0001c0001t0010g0168 a0001c0001t0013g0242 a0001c0001t0013g0243 others(3): Show |
6 | HG01192.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+22103G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849455 | |||||||
| chr4:122849530 | C | T | 8 | a0001c0001t0003g0182 a0001c0001t0009g0007 a0001c0001t0009g0181 others(5): Show |
9 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+22178C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849530 | |||||||
| chr4:122849654 | A | G | 2 | a0001c0001t0019g0015 a0001c0001t0042g0016 |
2 | HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.178+22302A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849654 | |||||||
| chr4:122849880 | T | A | 1 | a0001c0001t0006g0037 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.178+22528T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849880 | |||||||
| chr4:122849987 | C | T | 10 | a0001c0001t0004g0189 a0001c0001t0004g0193 a0001c0001t0004g0194 others(7): Show |
11 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+22635C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849987 | |||||||
| chr4:122849990 | G | A | 7 | a0001c0001t0001g0080 a0001c0001t0010g0168 a0001c0001t0013g0242 others(4): Show |
7 | HG01192.hp2 HG02280.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+22638G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849990 | |||||||
| chr4:122850090 | C | T | 55 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(52): Show |
56 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.178+22738C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850090 | |||||||
| chr4:122850238 | G | T | 54 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0164 others(51): Show |
55 | HG00609.hp2 HG01175.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.178+22886G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850238 | |||||||
| chr4:122850247 | G | A | 5 | a0001c0001t0009g0224 a0001c0001t0010g0223 a0001c0001t0018g0009 others(2): Show |
6 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+22895G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850247 | |||||||
| chr4:122850261 | CA | C | 23 | a0001c0001t0004g0189 a0001c0001t0004g0193 a0001c0001t0004g0194 others(20): Show |
25 | HG00639.hp1 HG01168.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.178+22920delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122850261 | ||||||
| chr4:122850371 | C | T | 1 | a0001c0001t0027g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.178+23019C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850371 | |||||||
| chr4:122850393 | C | T | 5 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(2): Show |
5 | HG01192.hp2 HG02280.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+23041C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850393 | |||||||
| chr4:122850673 | C | T | 80 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0002g0160 others(77): Show |
84 | HG00741.hp1 HG01074.hp2 HG01109.hp1 others(81): Show |
intron_variant | MODIFIER | c.178+23321C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850673 | |||||||
| chr4:122850804 | G | C | 5 | a0001c0001t0007g0148 a0001c0001t0007g0152 a0001c0001t0007g0153 others(2): Show |
5 | HG02809.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+23452G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850804 | |||||||
| chr4:122850863 | C | A | 89 | a0001c0001t0002g0126 a0001c0001t0002g0134 a0001c0001t0002g0136 others(86): Show |
94 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(91): Show |
intron_variant | MODIFIER | c.178+23511C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850863 | |||||||
| chr4:122850999 | C | T | 2 | a0001c0001t0002g0048 a0001c0001t0002g0074 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.178+23647C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850999 | |||||||
| chr4:122851149 | A | G | 18 | a0001c0001t0001g0042 a0001c0001t0001g0116 a0001c0001t0003g0165 others(15): Show |
19 | HG01192.hp2 HG02258.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.178+23797A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851149 | |||||||
| chr4:122851459 | C | G | 94 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0103 others(91): Show |
98 | HG00639.hp1 HG01109.hp1 HG01175.hp2 others(95): Show |
intron_variant | MODIFIER | c.178+24107C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851459 | |||||||
| chr4:122851544 | G | A | 2 | a0001c0001t0019g0015 a0001c0001t0042g0016 |
2 | HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.178+24192G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851544 | |||||||
| chr4:122851732 | C | T | 21 | a0001c0001t0001g0053 a0001c0001t0003g0240 a0001c0001t0003g0241 others(18): Show |
22 | HG01192.hp2 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+24380C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851732 | |||||||
| chr4:122851862 | A | T | 3 | a0001c0001t0011g0185 a0001c0001t0045g0187 a0001c0001t0046g0186 |
3 | HG01361.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.179-24459A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851862 | |||||||
| chr4:122851917 | T | C | 2 | a0001c0001t0004g0189 a0001c0001t0044g0192 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.179-24404T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851917 | |||||||
| chr4:122852029 | ACTGTTAT others(8): Show |
A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0069 |
2 | HG01361.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.179-24290_179-2427 others(19): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122852029 | ||||||
| chr4:122852057 | A | G | 1 | a0001c0001t0024g0052 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.179-24264A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852057 | |||||||
| chr4:122852111 | A | G | 1 | a0001c0001t0003g0211 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.179-24210A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852111 | |||||||
| chr4:122852284 | T | C | 115 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0063 others(112): Show |
121 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(118): Show |
intron_variant | MODIFIER | c.179-24037T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852284 | |||||||
| chr4:122852347 | T | C | 27 | a0001c0001t0003g0182 a0001c0001t0004g0193 a0001c0001t0004g0194 others(24): Show |
29 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.179-23974T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852347 | |||||||
| chr4:122852381 | G | A | 2 | a0001c0001t0018g0009 a0001c0001t0018g0217 |
3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-23940G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852381 | |||||||
| chr4:122852424 | T | G | 26 | a0001c0001t0001g0053 a0001c0001t0004g0193 a0001c0001t0004g0194 others(23): Show |
28 | HG01168.hp1 HG01891.hp1 HG02717.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-23897T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852424 | |||||||
| chr4:122852532 | G | A | 2 | a0001c0001t0018g0009 a0001c0001t0018g0217 |
3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-23789G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852532 | |||||||
| chr4:122852652 | C | G | 7 | a0001c0001t0001g0053 a0001c0001t0005g0125 a0001c0001t0008g0006 others(4): Show |
8 | HG02886.hp1 HG03098.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-23669C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852652 | |||||||
| chr4:122852659 | G | A | 21 | a0001c0001t0007g0149 a0001c0001t0007g0163 a0001c0001t0007g0179 others(18): Show |
22 | HG00639.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.179-23662G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852659 | |||||||
| chr4:122852910 | C | T | 90 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0063 others(87): Show |
96 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(93): Show |
intron_variant | MODIFIER | c.179-23411C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852910 | |||||||
| chr4:122852955 | A | T | 16 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(13): Show |
16 | HG01361.hp1 HG02055.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.179-23366A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852955 | |||||||
| chr4:122853042 | A | T | 1 | a0001c0001t0005g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-23279A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853042 | |||||||
| chr4:122853109 | G | A | 28 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0001c0001t0001g0088 others(25): Show |
30 | HG00741.hp2 HG01070.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.179-23212G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853109 | |||||||
| chr4:122853183 | A | C | 22 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(19): Show |
22 | HG01361.hp1 HG02015.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.179-23138A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853183 | |||||||
| chr4:122853217 | G | A | 7 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(4): Show |
7 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-23104G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853217 | |||||||
| chr4:122853289 | T | A | 2 | a0001c0001t0009g0201 a0001c0001t0027g0202 |
2 | HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.179-23032T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853289 | |||||||
| chr4:122853655 | ACTC | A | 113 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0063 others(110): Show |
119 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(116): Show |
intron_variant | MODIFIER | c.179-22663_179-2266 others(7): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122853655 | ||||||
| chr4:122853677 | G | A | 30 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0001c0001t0001g0088 others(27): Show |
32 | HG00741.hp2 HG01070.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.179-22644G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853677 | |||||||
| chr4:122853726 | G | T | 14 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0008g0171 others(11): Show |
14 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-22595G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853726 | |||||||
| chr4:122853758 | T | A | 137 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0063 others(134): Show |
144 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(141): Show |
intron_variant | MODIFIER | c.179-22563T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853758 | |||||||
| chr4:122853801 | C | A | 33 | a0001c0001t0001g0053 a0001c0001t0003g0240 a0001c0001t0003g0241 others(30): Show |
34 | HG01192.hp2 HG01361.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.179-22520C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853801 | |||||||
| chr4:122853942 | T | C | 8 | a0001c0001t0009g0201 a0001c0001t0010g0168 a0001c0001t0011g0239 others(5): Show |
8 | HG02015.hp1 HG02486.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-22379T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853942 | |||||||
| chr4:122853961 | A | C | 1 | a0001c0001t0005g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-22360A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853961 | |||||||
| chr4:122853984 | G | A | 1 | a0001c0001t0005g0107 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.179-22337G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853984 | |||||||
| chr4:122854129 | C | A | 1 | a0001c0001t0036g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.179-22192C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854129 | |||||||
| chr4:122854186 | ATAAGGAT others(9): Show |
A | 1 | a0001c0001t0019g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.179-22131_179-2211 others(20): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122854186 | ||||||
| chr4:122854222 | A | G | 12 | a0001c0001t0009g0201 a0001c0001t0010g0168 a0001c0001t0010g0205 others(9): Show |
12 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-22099A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854222 | |||||||
| chr4:122854278 | G | A | 66 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0001c0001t0001g0088 others(63): Show |
70 | HG00741.hp2 HG01070.hp2 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.179-22043G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854278 | |||||||
| chr4:122854341 | C | T | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-21980C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854341 | |||||||
| chr4:122854439 | T | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0005g0003 |
4 | HG01256.hp2 HG01258.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-21882T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854439 | |||||||
| chr4:122854494 | T | C | 14 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0008g0171 others(11): Show |
14 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-21827T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854494 | |||||||
| chr4:122854612 | G | A | 33 | a0001c0001t0001g0053 a0001c0001t0003g0240 a0001c0001t0003g0241 others(30): Show |
34 | HG01192.hp2 HG01361.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.179-21709G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854612 | |||||||
| chr4:122854668 | G | A | 1 | a0001c0001t0005g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-21653G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854668 | |||||||
| chr4:122854920 | A | G | 1 | a0001c0001t0005g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-21401A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854920 | |||||||
| chr4:122854985 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.179-21336C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854985 | |||||||
| chr4:122855207 | C | T | 1 | a0001c0001t0007g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.179-21114C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855207 | |||||||
| chr4:122855243 | A | G | 2 | a0001c0001t0018g0009 a0001c0001t0018g0217 |
3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-21078A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855243 | |||||||
| chr4:122855245 | A | G | 10 | a0001c0001t0009g0201 a0001c0001t0010g0168 a0001c0001t0011g0239 others(7): Show |
10 | HG00609.hp1 HG02015.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.179-21076A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855245 | |||||||
| chr4:122855254 | A | G | 1 | a0001c0001t0003g0120 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.179-21067A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855254 | |||||||
| chr4:122855376 | G | A | 26 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0001c0001t0001g0088 others(23): Show |
28 | HG00741.hp2 HG01070.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-20945G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855376 | |||||||
| chr4:122855639 | A | T | 9 | a0001c0001t0003g0182 a0001c0001t0007g0169 a0001c0001t0009g0007 others(6): Show |
10 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.179-20682A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855639 | |||||||
| chr4:122855667 | C | G | 2 | a0001c0001t0011g0185 a0001c0001t0046g0186 |
2 | HG01361.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.179-20654C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855667 | |||||||
| chr4:122855908 | T | C | 28 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0004g0193 others(25): Show |
28 | HG01192.hp2 HG01361.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-20413T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855908 | |||||||
| chr4:122855991 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.179-20330T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855991 | |||||||
| chr4:122856084 | A | T | 6 | a0001c0001t0003g0182 a0001c0001t0009g0007 a0001c0001t0009g0170 others(3): Show |
7 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-20237A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856084 | |||||||
| chr4:122856412 | G | A | 1 | a0001c0001t0006g0230 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.179-19909G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856412 | |||||||
| chr4:122856705 | C | G | 5 | a0001c0001t0010g0219 a0001c0001t0010g0220 a0001c0001t0010g0221 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-19616C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856705 | |||||||
| chr4:122856714 | A | G | 4 | a0001c0001t0005g0003 a0001c0001t0016g0232 a0001c0001t0037g0102 others(1): Show |
5 | HG01106.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-19607A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856714 | |||||||
| chr4:122856812 | C | T | 4 | a0001c0001t0014g0128 a0001c0001t0017g0124 a0001c0001t0017g0131 others(1): Show |
4 | HG01975.hp2 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-19509C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856812 | |||||||
| chr4:122856897 | A | G | 12 | a0001c0001t0002g0212 a0001c0001t0003g0182 a0001c0001t0005g0109 others(9): Show |
13 | HG01109.hp1 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-19424A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856897 | |||||||
| chr4:122857017 | G | C | 13 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0013g0242 others(10): Show |
13 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-19304G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857017 | |||||||
| chr4:122857118 | A | G | 7 | a0001c0001t0010g0168 a0001c0001t0011g0239 a0001c0001t0012g0012 others(4): Show |
7 | HG02015.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-19203A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857118 | |||||||
| chr4:122857219 | C | G | 2 | a0001c0001t0011g0185 a0001c0001t0046g0186 |
2 | HG01361.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.179-19102C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857219 | |||||||
| chr4:122857220 | CT | C | 16 | a0001c0001t0004g0193 a0001c0001t0004g0194 a0001c0001t0004g0195 others(13): Show |
16 | HG01168.hp1 HG02015.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.179-19098delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122857220 | ||||||
| chr4:122857222 | T | C | 16 | a0001c0001t0004g0193 a0001c0001t0004g0194 a0001c0001t0004g0195 others(13): Show |
16 | HG01168.hp1 HG02015.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.179-19099T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857222 | |||||||
| chr4:122857391 | A | G | 5 | a0001c0001t0003g0119 a0001c0001t0004g0011 a0001c0001t0004g0189 others(2): Show |
5 | HG02109.hp2 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-18930A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857391 | |||||||
| chr4:122857917 | C | A | 2 | a0001c0001t0018g0009 a0001c0001t0018g0217 |
3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-18404C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857917 | |||||||
| chr4:122858186 | T | C | 2 | a0001c0001t0005g0125 a0001c0001t0005g0132 |
2 | HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.179-18135T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122858186 | |||||||
| chr4:122858246 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0016g0038 |
2 | HG02132.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.179-18075G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122858246 | |||||||
| chr4:122858429 | G | A | 3 | a0001c0001t0016g0232 a0001c0001t0037g0102 a0001c0001t0049g0229 |
3 | HG01106.hp1 HG02735.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.179-17892G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122858429 | |||||||
| chr4:122858811 | A | C | 5 | a0001c0001t0010g0219 a0001c0001t0010g0220 a0001c0001t0010g0221 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-17510A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122858811 | |||||||
| chr4:122858912 | AT | A | 7 | a0001c0001t0010g0219 a0001c0001t0010g0220 a0001c0001t0010g0221 others(4): Show |
8 | HG00639.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-17405delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122858912 | ||||||
| chr4:122858936 | C | CT | 24 | a0001c0001t0003g0182 a0001c0001t0003g0240 a0001c0001t0003g0241 others(21): Show |
25 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.179-17384dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122858936 | ||||||
| chr4:122858954 | T | TA | 24 | a0001c0001t0003g0182 a0001c0001t0003g0240 a0001c0001t0003g0241 others(21): Show |
25 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.179-17361dupA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122858954 | ||||||
| chr4:122859108 | C | G | 26 | a0001c0001t0003g0182 a0001c0001t0003g0240 a0001c0001t0003g0241 others(23): Show |
27 | HG01071.hp1 HG01109.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.179-17213C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859108 | |||||||
| chr4:122859306 | C | CTGAA | 13 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0013g0242 others(10): Show |
13 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-17005_179-1700 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859306 | ||||||
| chr4:122859398 | AATTT | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0064 a0001c0001t0001g0091 |
3 | HG02040.hp2 HG02129.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.179-16915_179-1691 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859398 | ||||||
| chr4:122859432 | G | A | 1 | a0001c0001t0005g0132 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.179-16889G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859432 | |||||||
| chr4:122859559 | T | C | 3 | a0001c0001t0010g0205 a0001c0001t0029g0215 a0001c0001t0030g0206 |
3 | HG02055.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.179-16762T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859559 | |||||||
| chr4:122859590 | CA | C | 3 | a0001c0001t0016g0232 a0001c0001t0037g0102 a0001c0001t0049g0229 |
3 | HG01106.hp1 HG02735.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.179-16728delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859590 | ||||||
| chr4:122859650 | A | G | 1 | a0001c0001t0013g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.179-16671A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859650 | |||||||
| chr4:122859653 | T | TAC | 12 | a0001c0001t0003g0182 a0001c0001t0005g0109 a0001c0001t0005g0125 others(9): Show |
13 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-16646_179-1664 others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859653 | ||||||
| chr4:122859653 | TAC | T | 172 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(169): Show |
179 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.179-16646_179-1664 others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859653 | ||||||
| chr4:122859653 | TACAC | T | 18 | a0001c0001t0004g0193 a0001c0001t0004g0194 a0001c0001t0004g0195 others(15): Show |
18 | HG01168.hp1 HG02015.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.179-16648_179-1664 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859653 | ||||||
| chr4:122859655 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0164 |
3 | NA18953.hp2 NA18968.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.179-16666C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859655 | |||||||
| chr4:122859660 | A | ACACACAC others(5): Show |
13 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0013g0242 others(10): Show |
13 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-16650_179-1664 others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859660 | ||||||
| chr4:122859677 | A | C | 13 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0013g0242 others(10): Show |
13 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-16644A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859677 | |||||||
| chr4:122859704 | G | T | 2 | a0001c0001t0005g0125 a0001c0001t0005g0132 |
2 | HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.179-16617G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859704 | |||||||
| chr4:122860263 | T | G | 27 | a0001c0001t0003g0182 a0001c0001t0003g0240 a0001c0001t0003g0241 others(24): Show |
28 | HG01071.hp1 HG01109.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-16058T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860263 | |||||||
| chr4:122860447 | C | CT | 23 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0115 others(20): Show |
24 | HG01070.hp2 HG01167.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.179-15849dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122860447 | ||||||
| chr4:122860447 | C | CTT | 107 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(104): Show |
110 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.179-15850_179-1584 others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122860447 | ||||||
| chr4:122860447 | C | CTTT | 16 | a0001c0001t0001g0049 a0001c0001t0001g0079 a0001c0001t0001g0086 others(13): Show |
16 | HG00642.hp2 HG01358.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.179-15851_179-1584 others(7): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122860447 | ||||||
| chr4:122860447 | CT | C | 16 | a0001c0001t0003g0176 a0001c0001t0004g0011 a0001c0001t0004g0189 others(13): Show |
18 | HG00639.hp1 HG01168.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.179-15849delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122860447 | ||||||
| chr4:122860525 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.179-15796G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860525 | |||||||
| chr4:122860544 | C | T | 36 | a0001c0001t0003g0119 a0001c0001t0004g0011 a0001c0001t0004g0030 others(33): Show |
39 | HG01175.hp2 HG01255.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.179-15777C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860544 | |||||||
| chr4:122860583 | G | A | 2 | a0001c0001t0018g0009 a0001c0001t0018g0217 |
3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-15738G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860583 | |||||||
| chr4:122860611 | A | G | 11 | a0001c0001t0003g0182 a0001c0001t0005g0109 a0001c0001t0009g0007 others(8): Show |
12 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-15710A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860611 | |||||||
| chr4:122860662 | G | A | 2 | a0001c0001t0003g0165 a0001c0001t0003g0166 |
2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.179-15659G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860662 | |||||||
| chr4:122860677 | G | A | 2 | a0001c0001t0005g0125 a0001c0001t0005g0132 |
2 | HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.179-15644G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860677 | |||||||
| chr4:122860702 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.179-15619C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860702 | |||||||
| chr4:122860716 | C | T | 3 | a0001c0001t0016g0232 a0001c0001t0037g0102 a0001c0001t0049g0229 |
3 | HG01106.hp1 HG02735.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.179-15605C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860716 | |||||||
| chr4:122860717 | G | A | 52 | a0001c0001t0003g0182 a0001c0001t0003g0240 a0001c0001t0003g0241 others(49): Show |
54 | HG00639.hp1 HG01071.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.179-15604G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860717 | |||||||
| chr4:122860754 | C | T | 11 | a0001c0001t0003g0182 a0001c0001t0005g0109 a0001c0001t0009g0007 others(8): Show |
12 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-15567C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860754 | |||||||
| chr4:122860798 | A | G | 2 | a0001c0001t0016g0232 a0001c0001t0049g0229 |
2 | HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.179-15523A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860798 | |||||||
| chr4:122860851 | C | T | 24 | a0001c0001t0004g0193 a0001c0001t0004g0194 a0001c0001t0004g0195 others(21): Show |
24 | HG01168.hp1 HG02015.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.179-15470C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860851 | |||||||
| chr4:122860890 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.179-15431A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860890 | |||||||
| chr4:122860928 | T | C | 19 | a0001c0001t0004g0193 a0001c0001t0004g0194 a0001c0001t0004g0195 others(16): Show |
19 | HG01168.hp1 HG02015.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.179-15393T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860928 | |||||||
| chr4:122861041 | C | T | 5 | a0001c0001t0004g0193 a0001c0001t0004g0194 a0001c0001t0004g0195 others(2): Show |
5 | HG01168.hp1 HG02818.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-15280C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861041 | |||||||
| chr4:122861186 | C | T | 1 | a0001c0001t0004g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.179-15135C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861186 | |||||||
| chr4:122861289 | T | C | 12 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0013g0242 others(9): Show |
12 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-15032T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861289 | |||||||
| chr4:122861337 | T | C | 1 | a0001c0001t0002g0127 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.179-14984T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861337 | |||||||
| chr4:122861368 | T | C | 4 | a0001c0001t0010g0205 a0001c0001t0029g0215 a0001c0001t0030g0206 others(1): Show |
4 | HG02055.hp2 HG02572.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-14953T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861368 | |||||||
| chr4:122861413 | C | A | 23 | a0001c0001t0003g0182 a0001c0001t0004g0193 a0001c0001t0004g0194 others(20): Show |
24 | HG01071.hp1 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.179-14908C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861413 | |||||||
| chr4:122861540 | A | T | 1 | a0001c0001t0017g0150 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.179-14781A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861540 | |||||||
| chr4:122861631 | GT | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0093 others(31): Show |
35 | HG00408.hp2 HG01074.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.179-14689delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861631 | |||||||
| chr4:122861667 | T | A | 4 | a0001c0001t0009g0170 a0001c0001t0009g0224 a0001c0001t0018g0009 others(1): Show |
5 | HG00639.hp1 HG02922.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-14654T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861667 | |||||||
| chr4:122861671 | A | G | 5 | a0001c0001t0010g0205 a0001c0001t0013g0244 a0001c0001t0013g0245 others(2): Show |
5 | HG01192.hp2 HG02055.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-14650A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861671 | |||||||
| chr4:122861741 | A | T | 186 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0047 others(183): Show |
195 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.179-14580A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861741 | |||||||
| chr4:122861747 | C | G | 5 | a0001c0001t0003g0119 a0001c0001t0004g0011 a0001c0001t0004g0189 others(2): Show |
5 | HG02109.hp2 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-14574C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861747 | |||||||
| chr4:122861821 | G | T | 1 | a0001c0001t0002g0127 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.179-14500G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861821 | |||||||
| chr4:122861876 | G | A | 49 | a0001c0001t0003g0209 a0001c0001t0003g0240 a0001c0001t0003g0241 others(46): Show |
53 | HG00639.hp1 HG01192.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.179-14445G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861876 | |||||||
| chr4:122861950 | G | A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(212): Show |
223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.179-14371G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861950 | |||||||
| chr4:122861989 | A | C | 14 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0013g0242 others(11): Show |
14 | HG01192.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.179-14332A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861989 | |||||||
| chr4:122862039 | T | C | 27 | a0001c0001t0004g0193 a0001c0001t0004g0194 a0001c0001t0004g0195 others(24): Show |
29 | HG00099.hp1 HG01071.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.179-14282T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862039 | |||||||
| chr4:122862061 | G | A | 10 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(7): Show |
11 | HG01346.hp2 HG01934.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.179-14260G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862061 | |||||||
| chr4:122862104 | T | C | 5 | a0001c0001t0003g0119 a0001c0001t0004g0011 a0001c0001t0004g0189 others(2): Show |
5 | HG02109.hp2 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-14217T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862104 | |||||||
| chr4:122862232 | A | G | 57 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(54): Show |
58 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.179-14089A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862232 | |||||||
| chr4:122862240 | A | G | 11 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(8): Show |
12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-14081A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862240 | |||||||
| chr4:122862257 | A | G | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-14064A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862257 | |||||||
| chr4:122862292 | T | C | 1 | a0001c0001t0005g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-14029T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862292 | |||||||
| chr4:122862655 | C | T | 2 | a0001c0001t0002g0090 a0001c0001t0002g0092 |
2 | NA18953.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.179-13666C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862655 | |||||||
| chr4:122862681 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.179-13640A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862681 | |||||||
| chr4:122862849 | G | A | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-13472G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862849 | |||||||
| chr4:122863140 | G | A | 55 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(52): Show |
55 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.179-13181G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863140 | |||||||
| chr4:122863209 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.179-13112C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863209 | |||||||
| chr4:122863248 | G | A | 209 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(206): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.179-13073G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863248 | |||||||
| chr4:122863566 | A | G | 70 | a0001c0001t0001g0004 a0001c0001t0002g0005 a0001c0001t0002g0045 others(67): Show |
72 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.179-12755A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863566 | |||||||
| chr4:122863766 | T | C | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-12555T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863766 | |||||||
| chr4:122863770 | G | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-12551G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863770 | |||||||
| chr4:122863903 | C | A | 3 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 |
3 | HG01243.hp1 HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.179-12418C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863903 | |||||||
| chr4:122863931 | A | G | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-12390A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863931 | |||||||
| chr4:122863948 | GTTCTTTA others(48): Show |
G | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-12363_179-1230 others(59): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122863948 | ||||||
| chr4:122864021 | A | G | 4 | a0001c0001t0014g0128 a0001c0001t0014g0144 a0001c0001t0014g0158 others(1): Show |
4 | HG03195.hp1 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-12300A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864021 | |||||||
| chr4:122864029 | T | C | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.179-12292T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864029 | |||||||
| chr4:122864105 | A | T | 12 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(9): Show |
13 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-12216A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864105 | |||||||
| chr4:122864159 | T | C | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-12162T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864159 | |||||||
| chr4:122864293 | C | T | 86 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(83): Show |
89 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.179-12028C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864293 | |||||||
| chr4:122864297 | T | C | 20 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(17): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.179-12024T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864297 | |||||||
| chr4:122864377 | G | A | 1 | a0001c0001t0029g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.179-11944G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864377 | |||||||
| chr4:122864475 | T | C | 2 | a0001c0001t0018g0009 a0001c0001t0018g0217 |
3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-11846T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864475 | |||||||
| chr4:122864553 | C | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-11768C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864553 | |||||||
| chr4:122864623 | G | A | 2 | a0001c0001t0036g0199 a0001c0001t0044g0192 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.179-11698G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864623 | |||||||
| chr4:122864739 | A | G | 1 | a0001c0001t0029g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.179-11582A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864739 | |||||||
| chr4:122864959 | A | G | 31 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(28): Show |
33 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.179-11362A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864959 | |||||||
| chr4:122865050 | A | G | 4 | a0001c0001t0014g0128 a0001c0001t0014g0144 a0001c0001t0014g0158 others(1): Show |
4 | HG03195.hp1 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-11271A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865050 | |||||||
| chr4:122865125 | A | G | 1 | a0001c0001t0030g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.179-11196A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865125 | |||||||
| chr4:122865160 | G | A | 13 | a0001c0001t0010g0168 a0001c0001t0010g0205 a0001c0001t0010g0219 others(10): Show |
13 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-11161G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865160 | |||||||
| chr4:122865269 | C | T | 72 | a0001c0001t0001g0004 a0001c0001t0002g0005 a0001c0001t0002g0045 others(69): Show |
75 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.179-11052C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865269 | |||||||
| chr4:122865277 | T | G | 88 | a0001c0001t0001g0004 a0001c0001t0002g0005 a0001c0001t0002g0045 others(85): Show |
92 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.179-11044T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865277 | |||||||
| chr4:122865277 | TTTTG | T | 54 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(51): Show |
54 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.179-11028_179-1102 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122865277 | ||||||
| chr4:122865376 | C | T | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-10945C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865376 | |||||||
| chr4:122865475 | A | G | 3 | a0001c0001t0017g0124 a0001c0001t0017g0131 a0001c0001t0017g0150 |
3 | HG01975.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.179-10846A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865475 | |||||||
| chr4:122865552 | T | C | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-10769T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865552 | |||||||
| chr4:122865677 | A | G | 209 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(206): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.179-10644A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865677 | |||||||
| chr4:122865706 | T | C | 1 | a0001c0001t0045g0187 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-10615T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865706 | |||||||
| chr4:122865742 | C | A | 1 | a0001c0001t0002g0075 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.179-10579C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865742 | |||||||
| chr4:122865862 | C | G | 1 | a0001c0001t0002g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.179-10459C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865862 | |||||||
| chr4:122865879 | T | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.179-10442T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865879 | |||||||
| chr4:122865924 | G | A | 121 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(118): Show |
126 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.179-10397G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865924 | |||||||
| chr4:122865972 | T | A | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.179-10349T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865972 | |||||||
| chr4:122866096 | G | A | 1 | a0001c0001t0011g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.179-10225G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866096 | |||||||
| chr4:122866165 | C | G | 1 | a0001c0001t0034g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-10156C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866165 | |||||||
| chr4:122866165 | C | T | 50 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(47): Show |
50 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.179-10156C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866165 | |||||||
| chr4:122866186 | A | G | 209 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(206): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.179-10135A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866186 | |||||||
| chr4:122866249 | T | C | 1 | a0001c0001t0044g0192 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.179-10072T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866249 | |||||||
| chr4:122866294 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0016g0038 |
2 | HG02132.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.179-10027G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866294 | |||||||
| chr4:122866299 | C | T | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-10022C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866299 | |||||||
| chr4:122866325 | G | A | 1 | a0001c0001t0030g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.179-9996G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866325 | |||||||
| chr4:122866363 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.179-9958G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866363 | |||||||
| chr4:122866367 | C | CA | 105 | a0001c0001t0001g0004 a0001c0001t0002g0005 a0001c0001t0002g0045 others(102): Show |
109 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.179-9940dupA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122866367 | ||||||
| chr4:122866378 | A | AT | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(72): Show |
76 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.179-9943_179-9942i others(3): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866378 | |||||||
| chr4:122866378 | A | T | 3 | a0001c0001t0004g0196 a0001c0001t0028g0203 a0001c0001t0041g0225 |
3 | HG02897.hp1 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.179-9943A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866378 | |||||||
| chr4:122866392 | T | A | 85 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(82): Show |
87 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.179-9929T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866392 | |||||||
| chr4:122866502 | A | G | 4 | a0001c0001t0002g0077 a0001c0001t0002g0082 a0001c0001t0002g0083 others(1): Show |
4 | HG00438.hp1 HG01884.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-9819A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866502 | |||||||
| chr4:122866537 | G | T | 31 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(28): Show |
33 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.179-9784G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866537 | |||||||
| chr4:122866572 | A | G | 206 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(203): Show |
213 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.179-9749A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866572 | |||||||
| chr4:122866600 | C | A | 1 | a0001c0001t0002g0134 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.179-9721C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866600 | |||||||
| chr4:122866855 | A | G | 13 | a0001c0001t0010g0168 a0001c0001t0010g0205 a0001c0001t0010g0219 others(10): Show |
13 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-9466A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866855 | |||||||
| chr4:122866872 | T | C | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-9449T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866872 | |||||||
| chr4:122867220 | C | A | 209 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(206): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.179-9101C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867220 | |||||||
| chr4:122867223 | A | G | 1 | a0001c0001t0006g0033 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.179-9098A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867223 | |||||||
| chr4:122867340 | T | C | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-8981T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867340 | |||||||
| chr4:122867387 | A | G | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-8934A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867387 | |||||||
| chr4:122867486 | G | T | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-8835G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867486 | |||||||
| chr4:122867513 | A | T | 1 | a0001c0001t0015g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.179-8808A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867513 | |||||||
| chr4:122867536 | G | C | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-8785G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867536 | |||||||
| chr4:122867586 | C | G | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-8735C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867586 | |||||||
| chr4:122867793 | T | C | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-8528T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867793 | |||||||
| chr4:122867870 | C | G | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-8451C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867870 | |||||||
| chr4:122867938 | G | C | 4 | a0001c0001t0014g0128 a0001c0001t0014g0144 a0001c0001t0014g0158 others(1): Show |
4 | HG03195.hp1 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-8383G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867938 | |||||||
| chr4:122867956 | T | G | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-8365T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867956 | |||||||
| chr4:122868083 | G | A | 16 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(13): Show |
17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-8238G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868083 | |||||||
| chr4:122868214 | C | T | 16 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(13): Show |
17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-8107C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868214 | |||||||
| chr4:122868252 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.179-8069C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868252 | |||||||
| chr4:122868298 | G | A | 16 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(13): Show |
17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-8023G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868298 | |||||||
| chr4:122868428 | T | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-7893T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868428 | |||||||
| chr4:122868481 | C | T | 5 | a0001c0001t0010g0219 a0001c0001t0010g0220 a0001c0001t0010g0221 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-7840C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868481 | |||||||
| chr4:122868543 | C | T | 1 | a0001c0001t0013g0243 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.179-7778C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868543 | |||||||
| chr4:122868667 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-7654C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868667 | |||||||
| chr4:122868781 | T | C | 23 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(20): Show |
25 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.179-7540T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868781 | |||||||
| chr4:122868912 | T | C | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-7409T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868912 | |||||||
| chr4:122868976 | G | C | 2 | a0001c0001t0028g0203 a0001c0001t0041g0225 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.179-7345G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868976 | |||||||
| chr4:122869085 | G | A | 1 | a0001c0001t0006g0039 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.179-7236G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869085 | |||||||
| chr4:122869281 | C | T | 7 | a0001c0001t0010g0168 a0001c0001t0010g0205 a0001c0001t0010g0219 others(4): Show |
7 | HG02572.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-7040C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869281 | |||||||
| chr4:122869336 | T | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-6985T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869336 | |||||||
| chr4:122869430 | A | G | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-6891A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869430 | |||||||
| chr4:122869444 | G | A | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-6877G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869444 | |||||||
| chr4:122869606 | C | T | 2 | a0001c0001t0019g0023 a0001c0001t0019g0024 |
2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.179-6715C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869606 | |||||||
| chr4:122869774 | A | G | 1 | a0001c0001t0008g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.179-6547A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869774 | |||||||
| chr4:122869821 | C | G | 68 | a0001c0001t0002g0005 a0001c0001t0002g0045 a0001c0001t0002g0046 others(65): Show |
69 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.179-6500C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869821 | |||||||
| chr4:122869897 | C | A | 2 | a0001c0001t0002g0005 a0001c0001t0002g0085 |
3 | NA18972.hp1 NA18984.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.179-6424C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869897 | |||||||
| chr4:122869914 | A | G | 122 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(119): Show |
128 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.179-6407A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869914 | |||||||
| chr4:122869960 | G | A | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-6361G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869960 | |||||||
| chr4:122870019 | T | C | 3 | a0001c0001t0017g0124 a0001c0001t0017g0131 a0001c0001t0017g0150 |
3 | HG01975.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.179-6302T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870019 | |||||||
| chr4:122870093 | C | T | 1 | a0001c0001t0004g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.179-6228C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870093 | |||||||
| chr4:122870170 | C | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-6151C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870170 | |||||||
| chr4:122870198 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.179-6123G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870198 | |||||||
| chr4:122870237 | G | T | 1 | a0001c0001t0003g0044 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.179-6084G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870237 | |||||||
| chr4:122870329 | G | A | 54 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(51): Show |
54 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.179-5992G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870329 | |||||||
| chr4:122870555 | A | G | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-5766A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870555 | |||||||
| chr4:122870556 | C | T | 68 | a0001c0001t0002g0005 a0001c0001t0002g0045 a0001c0001t0002g0046 others(65): Show |
69 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.179-5765C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870556 | |||||||
| chr4:122870882 | T | G | 11 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(8): Show |
12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-5439T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870882 | |||||||
| chr4:122870911 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.179-5410T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870911 | |||||||
| chr4:122870991 | T | C | 1 | a0001c0001t0042g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.179-5330T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870991 | |||||||
| chr4:122871064 | C | T | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-5257C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871064 | |||||||
| chr4:122871173 | C | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-5148C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871173 | |||||||
| chr4:122871188 | C | CTGTT | 31 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(28): Show |
33 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.179-5132_179-5129d others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871188 | ||||||
| chr4:122871209 | T | C | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-5112T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871209 | |||||||
| chr4:122871277 | G | A | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-5044G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871277 | |||||||
| chr4:122871302 | T | TGGGGTC | 3 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 |
3 | HG01243.hp1 HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.179-5014_179-5013i others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871302 | ||||||
| chr4:122871465 | T | A | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.179-4856T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871465 | |||||||
| chr4:122871528 | C | T | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-4793C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871528 | |||||||
| chr4:122871673 | C | T | 1 | a0001c0001t0010g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.179-4648C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871673 | |||||||
| chr4:122871692 | T | A | 16 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(13): Show |
17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-4629T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871692 | |||||||
| chr4:122871781 | C | CA | 13 | a0001c0001t0001g0057 a0001c0001t0001g0093 a0001c0001t0002g0062 others(10): Show |
13 | HG00741.hp1 HG01167.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-4523dupA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | ||||||
| chr4:122871781 | C | CAA | 44 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(41): Show |
47 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.179-4524_179-4523d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | ||||||
| chr4:122871781 | C | CAAA | 8 | a0001c0001t0005g0106 a0001c0001t0010g0219 a0001c0001t0010g0220 others(5): Show |
8 | HG01175.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-4525_179-4523d others(5): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | ||||||
| chr4:122871781 | C | CAAAA | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01106.hp1 HG01192.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-4526_179-4523d others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | ||||||
| chr4:122871781 | CA | C | 8 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0081 others(5): Show |
8 | HG01346.hp1 HG01361.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-4523delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | ||||||
| chr4:122871781 | CAA | C | 17 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(14): Show |
18 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.179-4524_179-4523d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | ||||||
| chr4:122871809 | GCAA | G | 16 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(13): Show |
17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-4503_179-4501d others(5): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871809 | ||||||
| chr4:122871915 | GA | G | 228 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(225): Show |
236 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.179-4403delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871915 | ||||||
| chr4:122871923 | C | T | 1 | a0001c0001t0033g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.179-4398C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871923 | |||||||
| chr4:122871932 | G | T | 71 | a0001c0001t0002g0005 a0001c0001t0002g0045 a0001c0001t0002g0046 others(68): Show |
73 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.179-4389G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871932 | |||||||
| chr4:122872010 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.179-4311A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872010 | |||||||
| chr4:122872258 | T | C | 20 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(17): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.179-4063T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872258 | |||||||
| chr4:122872294 | C | T | 1 | a0001c0001t0012g0012 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.179-4027C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872294 | |||||||
| chr4:122872335 | T | G | 2 | a0001c0001t0008g0204 a0001c0001t0019g0015 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.179-3986T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872335 | |||||||
| chr4:122872385 | G | A | 20 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(17): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.179-3936G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872385 | |||||||
| chr4:122872396 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.179-3925C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872396 | |||||||
| chr4:122872691 | A | G | 2 | a0001c0001t0020g0010 a0001c0001t0020g0238 |
3 | HG02145.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.179-3630A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872691 | |||||||
| chr4:122872718 | A | C | 13 | a0001c0001t0010g0168 a0001c0001t0010g0205 a0001c0001t0010g0219 others(10): Show |
13 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-3603A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872718 | |||||||
| chr4:122872813 | A | G | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-3508A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872813 | |||||||
| chr4:122872829 | G | A | 1 | a0001c0001t0029g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.179-3492G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872829 | |||||||
| chr4:122872858 | C | A | 121 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(118): Show |
126 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.179-3463C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872858 | |||||||
| chr4:122872858 | C | T | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-3463C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872858 | |||||||
| chr4:122872972 | T | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-3349T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872972 | |||||||
| chr4:122873015 | C | A | 71 | a0001c0001t0002g0005 a0001c0001t0002g0045 a0001c0001t0002g0046 others(68): Show |
73 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.179-3306C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122873015 | |||||||
| chr4:122873297 | C | G | 1 | a0001c0001t0015g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.179-3024C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122873297 | |||||||
| chr4:122873556 | CA | C | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-2763delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122873556 | ||||||
| chr4:122873597 | A | G | 12 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(9): Show |
13 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-2724A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122873597 | |||||||
| chr4:122873807 | T | A | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-2514T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122873807 | |||||||
| chr4:122873830 | AATGGAAA others(1): Show |
A | 15 | a0001c0001t0010g0168 a0001c0001t0010g0205 a0001c0001t0010g0219 others(12): Show |
15 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.179-2489_179-2482d others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122873830 | ||||||
| chr4:122873952 | A | G | 5 | a0001c0001t0004g0193 a0001c0001t0004g0194 a0001c0001t0004g0195 others(2): Show |
5 | HG01168.hp1 HG02818.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-2369A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122873952 | |||||||
| chr4:122874120 | C | G | 1 | a0001c0001t0027g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.179-2201C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874120 | |||||||
| chr4:122874182 | A | T | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-2139A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874182 | |||||||
| chr4:122874253 | G | A | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-2068G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874253 | |||||||
| chr4:122874288 | C | T | 3 | a0001c0001t0027g0202 a0001c0001t0036g0199 a0001c0001t0044g0192 |
3 | HG02622.hp2 HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.179-2033C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874288 | |||||||
| chr4:122874353 | T | C | 16 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(13): Show |
17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-1968T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874353 | |||||||
| chr4:122874498 | A | G | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-1823A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874498 | |||||||
| chr4:122874663 | T | C | 1 | a0001c0001t0003g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.179-1658T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874663 | |||||||
| chr4:122874729 | A | T | 209 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(206): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.179-1592A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874729 | |||||||
| chr4:122874749 | A | G | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-1572A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874749 | |||||||
| chr4:122874813 | C | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1508C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874813 | |||||||
| chr4:122874952 | T | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-1369T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874952 | |||||||
| chr4:122875107 | C | A | 1 | a0001c0001t0015g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.179-1214C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875107 | |||||||
| chr4:122875308 | C | G | 23 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(20): Show |
25 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.179-1013C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875308 | |||||||
| chr4:122875386 | G | A | 68 | a0001c0001t0002g0005 a0001c0001t0002g0045 a0001c0001t0002g0046 others(65): Show |
69 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.179-935G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875386 | |||||||
| chr4:122875427 | C | CAAAAAAA others(270): Show |
1 | a0001c0001t0001g0081 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.179-877_179-876ins others(277): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122875427 | ||||||
| chr4:122875427 | C | CAAAAAAA others(271): Show |
47 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0047 others(44): Show |
48 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.179-877_179-876ins others(278): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122875427 | ||||||
| chr4:122875427 | C | CAAAAAAA others(272): Show |
7 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0103 others(4): Show |
7 | HG01358.hp1 HG01517.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-877_179-876ins others(279): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122875427 | ||||||
| chr4:122875580 | A | G | 31 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(28): Show |
33 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.179-741A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875580 | |||||||
| chr4:122875590 | C | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-731C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875590 | |||||||
| chr4:122875633 | G | A | 1 | a0001c0001t0003g0147 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.179-688G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875633 | |||||||
| chr4:122875635 | G | A | 1 | a0001c0001t0034g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-686G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875635 | |||||||
| chr4:122875697 | C | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-624C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875697 | |||||||
| chr4:122875801 | C | T | 1 | a0001c0001t0039g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-520C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875801 | |||||||
| chr4:122875843 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.179-478G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875843 | |||||||
| chr4:122875944 | C | T | 1 | a0001c0001t0009g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-377C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875944 | |||||||
| chr4:122876028 | C | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-293C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122876028 | |||||||
| chr4:122876099 | A | T | 2 | a0001c0001t0002g0076 a0001c0001t0006g0028 |
2 | NA18957.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.179-222A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122876099 | |||||||
| chr4:122876273 | G | T | 11 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(8): Show |
12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-48G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122876273 | |||||||
| chr4:122876313 | C | T | 1 | a0001c0001t0037g0102 | 1 | NA18966.hp1 | splice_region_variant&intron_variant | LOW | c.179-8C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122876313 | |||||||
| chr4:122876449 | C | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+25C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876449 | |||||||
| chr4:122876700 | T | G | 2 | a0001c0001t0003g0173 a0001c0001t0003g0174 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.282+276T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876700 | |||||||
| chr4:122876756 | T | C | 1 | a0001c0001t0037g0102 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.282+332T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876756 | |||||||
| chr4:122876768 | G | A | 23 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(20): Show |
25 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.282+344G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876768 | |||||||
| chr4:122876787 | A | G | 209 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(206): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.282+363A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876787 | |||||||
| chr4:122876796 | G | A | 2 | a0001c0001t0002g0134 a0001c0001t0002g0212 |
2 | HG01168.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.282+372G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876796 | |||||||
| chr4:122877028 | C | T | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.282+604C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877028 | |||||||
| chr4:122877105 | CT | C | 6 | a0001c0001t0003g0173 a0001c0001t0010g0219 a0001c0001t0010g0220 others(3): Show |
6 | HG01257.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+691delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122877105 | ||||||
| chr4:122877115 | T | C | 2 | a0001c0001t0027g0202 a0001c0001t0049g0229 |
2 | HG01106.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+691T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877115 | |||||||
| chr4:122877116 | C | CT | 34 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(31): Show |
37 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.282+703dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122877116 | ||||||
| chr4:122877116 | C | T | 2 | a0001c0001t0027g0202 a0001c0001t0049g0229 |
2 | HG01106.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+692C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877116 | |||||||
| chr4:122877150 | C | T | 1 | a0001c0001t0015g0200 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.282+726C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877150 | |||||||
| chr4:122877151 | G | A | 1 | a0001c0001t0012g0032 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.282+727G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877151 | |||||||
| chr4:122877211 | G | A | 20 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(17): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.282+787G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877211 | |||||||
| chr4:122877273 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(83): Show |
89 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.282+849T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877273 | |||||||
| chr4:122877310 | G | A | 1 | a0001c0001t0027g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.282+886G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877310 | |||||||
| chr4:122877532 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.282+1108G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877532 | |||||||
| chr4:122877556 | T | C | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.282+1132T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877556 | |||||||
| chr4:122877628 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.282+1204A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877628 | |||||||
| chr4:122877695 | A | C | 1 | a0001c0001t0047g0184 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.282+1271A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877695 | |||||||
| chr4:122877719 | C | T | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+1295C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877719 | |||||||
| chr4:122877838 | A | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+1414A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877838 | |||||||
| chr4:122877846 | A | C | 17 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(14): Show |
18 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.282+1422A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877846 | |||||||
| chr4:122877875 | A | T | 1 | a0001c0001t0009g0201 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.282+1451A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877875 | |||||||
| chr4:122878092 | C | A | 1 | a0001c0001t0002g0075 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.282+1668C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878092 | |||||||
| chr4:122878170 | A | G | 25 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(22): Show |
27 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.282+1746A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878170 | |||||||
| chr4:122878320 | G | T | 2 | a0001c0001t0028g0203 a0001c0001t0041g0225 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.282+1896G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878320 | |||||||
| chr4:122878342 | T | A | 1 | a0001c0001t0008g0161 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.282+1918T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878342 | |||||||
| chr4:122878499 | G | A | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+2075G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878499 | |||||||
| chr4:122878651 | G | A | 20 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(17): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.282+2227G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878651 | |||||||
| chr4:122878752 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.282+2328G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878752 | |||||||
| chr4:122878832 | A | G | 208 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(205): Show |
216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.282+2408A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878832 | |||||||
| chr4:122878893 | G | A | 16 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(13): Show |
17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.282+2469G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878893 | |||||||
| chr4:122879126 | C | A | 1 | a0001c0001t0007g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.282+2702C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879126 | |||||||
| chr4:122879177 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.282+2753A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879177 | |||||||
| chr4:122879251 | A | C | 209 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(206): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.282+2827A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879251 | |||||||
| chr4:122879389 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.282+2965A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879389 | |||||||
| chr4:122879462 | A | G | 20 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(17): Show |
22 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.282+3038A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879462 | |||||||
| chr4:122879581 | A | G | 1 | a0001c0001t0012g0012 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.282+3157A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879581 | |||||||
| chr4:122879613 | A | C | 71 | a0001c0001t0002g0005 a0001c0001t0002g0045 a0001c0001t0002g0046 others(68): Show |
73 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.282+3189A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879613 | |||||||
| chr4:122879614 | T | A | 2 | a0001c0001t0028g0203 a0001c0001t0041g0225 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.282+3190T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879614 | |||||||
| chr4:122879731 | A | G | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+3307A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879731 | |||||||
| chr4:122879752 | G | A | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+3328G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879752 | |||||||
| chr4:122879777 | G | T | 209 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(206): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.282+3353G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879777 | |||||||
| chr4:122879935 | A | T | 1 | a0001c0001t0033g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.282+3511A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879935 | |||||||
| chr4:122880075 | A | C | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+3651A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880075 | |||||||
| chr4:122880201 | C | T | 11 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(8): Show |
12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.282+3777C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880201 | |||||||
| chr4:122880245 | C | CT | 40 | a0001c0001t0001g0053 a0001c0001t0001g0104 a0001c0001t0004g0226 others(37): Show |
42 | HG01109.hp1 HG01192.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.282+3840dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122880245 | ||||||
| chr4:122880245 | C | CTT | 5 | a0001c0001t0005g0003 a0001c0001t0005g0106 a0001c0001t0008g0117 others(2): Show |
6 | HG01106.hp1 HG01175.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+3839_282+3840d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122880245 | ||||||
| chr4:122880278 | G | A | 14 | a0001c0001t0010g0168 a0001c0001t0010g0205 a0001c0001t0010g0219 others(11): Show |
14 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.282+3854G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880278 | |||||||
| chr4:122880339 | C | T | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+3915C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880339 | |||||||
| chr4:122880347 | C | T | 17 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(14): Show |
18 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.282+3923C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880347 | |||||||
| chr4:122880373 | A | G | 1 | a0001c0001t0010g0223 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.282+3949A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880373 | |||||||
| chr4:122880407 | C | T | 23 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(20): Show |
25 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.282+3983C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880407 | |||||||
| chr4:122880528 | G | A | 13 | a0001c0001t0010g0168 a0001c0001t0010g0205 a0001c0001t0010g0219 others(10): Show |
13 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+4104G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880528 | |||||||
| chr4:122880737 | T | C | 2 | a0001c0001t0003g0240 a0001c0001t0003g0241 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.282+4313T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880737 | |||||||
| chr4:122880757 | T | A | 1 | a0001c0001t0009g0201 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.282+4333T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880757 | |||||||
| chr4:122880803 | C | T | 1 | a0001c0001t0008g0117 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.282+4379C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880803 | |||||||
| chr4:122880848 | C | T | 2 | a0001c0001t0006g0037 a0001c0001t0038g0031 |
2 | HG01255.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.282+4424C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880848 | |||||||
| chr4:122881009 | C | T | 2 | a0001c0001t0011g0008 a0001c0001t0011g0188 |
3 | HG01891.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.282+4585C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881009 | |||||||
| chr4:122881015 | GA | G | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+4593delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122881015 | ||||||
| chr4:122881060 | G | A | 1 | a0001c0001t0007g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.282+4636G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881060 | |||||||
| chr4:122881164 | A | T | 5 | a0001c0001t0010g0219 a0001c0001t0010g0220 a0001c0001t0010g0221 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+4740A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881164 | |||||||
| chr4:122881277 | C | T | 1 | a0001c0001t0047g0184 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.282+4853C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881277 | |||||||
| chr4:122881537 | G | A | 2 | a0001c0001t0028g0203 a0001c0001t0041g0225 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.282+5113G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881537 | |||||||
| chr4:122881576 | G | A | 1 | a0001c0001t0029g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.282+5152G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881576 | |||||||
| chr4:122881600 | A | G | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+5176A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881600 | |||||||
| chr4:122881620 | G | A | 1 | a0001c0001t0005g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.282+5196G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881620 | |||||||
| chr4:122881624 | TTCATTGT others(5): Show |
T | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+5206_282+5217d others(14): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122881624 | ||||||
| chr4:122881710 | C | T | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+5286C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881710 | |||||||
| chr4:122881774 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+5350C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881774 | |||||||
| chr4:122881775 | G | A | 7 | a0001c0001t0009g0007 a0001c0001t0009g0170 a0001c0001t0009g0181 others(4): Show |
8 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+5351G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881775 | |||||||
| chr4:122881813 | C | A | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.282+5389C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881813 | |||||||
| chr4:122881939 | G | A | 20 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(17): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.282+5515G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881939 | |||||||
| chr4:122881977 | A | G | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+5553A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881977 | |||||||
| chr4:122882124 | C | T | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+5700C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882124 | |||||||
| chr4:122882215 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+5791C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882215 | |||||||
| chr4:122882518 | A | G | 20 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(17): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.282+6094A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882518 | |||||||
| chr4:122882573 | T | C | 5 | a0001c0001t0007g0148 a0001c0001t0007g0152 a0001c0001t0007g0153 others(2): Show |
5 | HG02809.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+6149T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882573 | |||||||
| chr4:122882716 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.282+6292G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882716 | |||||||
| chr4:122882829 | C | T | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+6405C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882829 | |||||||
| chr4:122883207 | C | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+6783C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883207 | |||||||
| chr4:122883366 | C | G | 15 | a0001c0001t0010g0168 a0001c0001t0010g0205 a0001c0001t0010g0219 others(12): Show |
15 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.282+6942C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883366 | |||||||
| chr4:122883394 | G | T | 1 | a0001c0001t0002g0237 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.282+6970G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883394 | |||||||
| chr4:122883487 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.282+7063T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883487 | |||||||
| chr4:122883553 | G | A | 1 | a0001c0001t0019g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.282+7129G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883553 | |||||||
| chr4:122883666 | G | A | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+7242G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883666 | |||||||
| chr4:122883794 | C | A | 17 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(14): Show |
18 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.282+7370C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883794 | |||||||
| chr4:122884009 | C | G | 1 | a0001c0001t0003g0044 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.282+7585C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884009 | |||||||
| chr4:122884073 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.282+7649G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884073 | |||||||
| chr4:122884226 | G | A | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+7802G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884226 | |||||||
| chr4:122884276 | T | C | 6 | a0001c0001t0008g0006 a0001c0001t0008g0159 a0001c0001t0008g0161 others(3): Show |
7 | HG02280.hp1 HG03098.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+7852T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884276 | |||||||
| chr4:122884314 | C | T | 15 | a0001c0001t0010g0168 a0001c0001t0010g0205 a0001c0001t0010g0219 others(12): Show |
15 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.282+7890C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884314 | |||||||
| chr4:122884422 | G | A | 16 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(13): Show |
17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.283-7789G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884422 | |||||||
| chr4:122884710 | C | T | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-7501C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884710 | |||||||
| chr4:122884757 | TAGGAGTG others(34): Show |
T | 1 | a0001c0001t0015g0200 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.283-7451_283-7411d others(43): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122884757 | ||||||
| chr4:122884776 | T | C | 1 | a0001c0001t0003g0101 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.283-7435T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884776 | |||||||
| chr4:122884796 | G | A | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.283-7415G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884796 | |||||||
| chr4:122884853 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.283-7358G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884853 | |||||||
| chr4:122884914 | A | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.283-7297A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884914 | |||||||
| chr4:122884940 | G | C | 2 | a0001c0001t0028g0203 a0001c0001t0041g0225 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.283-7271G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884940 | |||||||
| chr4:122885233 | G | C | 2 | a0001c0001t0028g0203 a0001c0001t0041g0225 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.283-6978G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122885233 | |||||||
| chr4:122885383 | T | C | 1 | a0001c0001t0049g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.283-6828T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122885383 | |||||||
| chr4:122885722 | A | T | 2 | a0001c0001t0005g0003 a0001c0001t0005g0106 |
3 | HG01175.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.283-6489A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122885722 | |||||||
| chr4:122885913 | C | CT | 38 | a0001c0001t0002g0046 a0001c0001t0002g0054 a0001c0001t0003g0120 others(35): Show |
40 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.283-6275dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122885913 | ||||||
| chr4:122885913 | C | CTT | 7 | a0001c0001t0004g0198 a0001c0001t0007g0169 a0001c0001t0011g0185 others(4): Show |
7 | HG01106.hp1 HG01361.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-6276_283-6275d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122885913 | ||||||
| chr4:122885913 | CT | C | 43 | a0001c0001t0002g0138 a0001c0001t0002g0178 a0001c0001t0003g0002 others(40): Show |
46 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.283-6275delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122885913 | ||||||
| chr4:122885913 | CTTTTTTT others(1): Show |
C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(54): Show |
59 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.283-6282_283-6275d others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122885913 | ||||||
| chr4:122885914 | T | C | 5 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(2): Show |
5 | HG01192.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-6297T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122885914 | |||||||
| chr4:122885995 | C | T | 2 | a0001c0001t0017g0131 a0001c0001t0017g0150 |
2 | HG01975.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.283-6216C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122885995 | |||||||
| chr4:122886005 | A | G | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-6206A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886005 | |||||||
| chr4:122886039 | C | T | 1 | a0001c0001t0007g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.283-6172C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886039 | |||||||
| chr4:122886107 | G | A | 69 | a0001c0001t0002g0005 a0001c0001t0002g0045 a0001c0001t0002g0046 others(66): Show |
70 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.283-6104G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886107 | |||||||
| chr4:122886124 | T | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.283-6087T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886124 | |||||||
| chr4:122886217 | A | G | 208 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(205): Show |
216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.283-5994A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886217 | |||||||
| chr4:122886348 | T | C | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-5863T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886348 | |||||||
| chr4:122886562 | A | G | 4 | a0001c0001t0014g0128 a0001c0001t0014g0144 a0001c0001t0014g0158 others(1): Show |
4 | HG03195.hp1 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-5649A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886562 | |||||||
| chr4:122886581 | T | A | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-5630T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886581 | |||||||
| chr4:122886622 | C | G | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-5589C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886622 | |||||||
| chr4:122886623 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.283-5588C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886623 | |||||||
| chr4:122886677 | A | C | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-5534A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886677 | |||||||
| chr4:122886926 | CTAAGCT | C | 8 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(5): Show |
8 | HG01106.hp1 HG01192.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-5278_283-5273d others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122886926 | ||||||
| chr4:122886973 | G | A | 12 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(9): Show |
13 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.283-5238G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886973 | |||||||
| chr4:122887111 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(56): Show |
60 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.283-5100C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887111 | |||||||
| chr4:122887230 | C | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-4981C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887230 | |||||||
| chr4:122887291 | G | T | 23 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(20): Show |
25 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.283-4920G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887291 | |||||||
| chr4:122887350 | G | A | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-4861G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887350 | |||||||
| chr4:122887395 | A | G | 15 | a0001c0001t0010g0168 a0001c0001t0010g0205 a0001c0001t0010g0219 others(12): Show |
15 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.283-4816A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887395 | |||||||
| chr4:122887470 | G | A | 1 | a0001c0001t0020g0010 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.283-4741G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887470 | |||||||
| chr4:122887801 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.283-4410A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887801 | |||||||
| chr4:122887841 | T | G | 2 | a0001c0001t0005g0107 a0001c0001t0026g0108 |
2 | HG00099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.283-4370T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887841 | |||||||
| chr4:122887921 | AAAT | A | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-4289_283-4287d others(5): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887921 | |||||||
| chr4:122887967 | A | G | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-4244A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887967 | |||||||
| chr4:122888123 | C | T | 20 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(17): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.283-4088C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888123 | |||||||
| chr4:122888466 | G | C | 1 | a0001c0002t0022g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283-3745G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888466 | |||||||
| chr4:122888550 | C | T | 2 | a0001c0001t0022g0235 a0001c0002t0022g0017 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.283-3661C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888550 | |||||||
| chr4:122888804 | G | A | 1 | a0001c0001t0005g0058 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.283-3407G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888804 | |||||||
| chr4:122888843 | A | G | 1 | a0001c0001t0048g0020 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.283-3368A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888843 | |||||||
| chr4:122888987 | G | T | 2 | a0001c0001t0028g0203 a0001c0001t0041g0225 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.283-3224G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888987 | |||||||
| chr4:122889173 | T | C | 23 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(20): Show |
25 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.283-3038T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889173 | |||||||
| chr4:122889212 | A | G | 20 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(17): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.283-2999A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889212 | |||||||
| chr4:122889281 | T | C | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-2930T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889281 | |||||||
| chr4:122889302 | G | A | 1 | a0001c0001t0037g0102 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.283-2909G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889302 | |||||||
| chr4:122889457 | T | A | 1 | a0001c0001t0037g0102 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.283-2754T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889457 | |||||||
| chr4:122889467 | A | G | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-2744A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889467 | |||||||
| chr4:122889513 | AC | A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(82): Show |
88 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.283-2697delC | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889513 | |||||||
| chr4:122889579 | C | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(54): Show |
58 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.283-2632C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889579 | |||||||
| chr4:122889660 | T | A | 1 | a0001c0001t0030g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.283-2551T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889660 | |||||||
| chr4:122889845 | T | A | 7 | a0001c0001t0009g0007 a0001c0001t0009g0170 a0001c0001t0009g0181 others(4): Show |
8 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-2366T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889845 | |||||||
| chr4:122889848 | A | C | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-2363A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889848 | |||||||
| chr4:122889861 | C | A | 2 | a0001c0001t0028g0203 a0001c0001t0041g0225 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.283-2350C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889861 | |||||||
| chr4:122889911 | G | A | 2 | a0001c0001t0003g0240 a0001c0001t0003g0241 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.283-2300G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889911 | |||||||
| chr4:122889956 | G | A | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-2255G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889956 | |||||||
| chr4:122890272 | C | T | 4 | a0001c0001t0022g0235 a0001c0001t0028g0203 a0001c0001t0041g0225 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-1939C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890272 | |||||||
| chr4:122890316 | A | G | 1 | a0001c0001t0009g0201 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.283-1895A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890316 | |||||||
| chr4:122890317 | T | C | 23 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(20): Show |
25 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.283-1894T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890317 | |||||||
| chr4:122890452 | T | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.283-1759T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890452 | |||||||
| chr4:122890537 | C | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1674C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890537 | |||||||
| chr4:122890543 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1668T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890543 | |||||||
| chr4:122890545 | C | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1666C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890545 | |||||||
| chr4:122890548 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1663T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890548 | |||||||
| chr4:122890550 | G | C | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1661G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890550 | |||||||
| chr4:122890554 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1657G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890554 | |||||||
| chr4:122890556 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1655T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890556 | |||||||
| chr4:122890557 | G | T | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1654G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890557 | |||||||
| chr4:122890559 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1652G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890559 | |||||||
| chr4:122890561 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1650C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890561 | |||||||
| chr4:122890565 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1646T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890565 | |||||||
| chr4:122890579 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1632T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890579 | |||||||
| chr4:122890581 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1630C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890581 | |||||||
| chr4:122890582 | T | G | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1629T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890582 | |||||||
| chr4:122890583 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1628T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890583 | |||||||
| chr4:122890587 | C | T | 1 | a0001c0001t0012g0032 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.283-1624C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890587 | |||||||
| chr4:122890592 | T | G | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1619T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890592 | |||||||
| chr4:122890593 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1618T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890593 | |||||||
| chr4:122890594 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1617T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890594 | |||||||
| chr4:122890597 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1614T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890597 | |||||||
| chr4:122890601 | C | G | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1610C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890601 | |||||||
| chr4:122890604 | TTTTGTTA others(3): Show |
T | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1605_283-1596d others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122890604 | ||||||
| chr4:122890620 | G | C | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1591G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890620 | |||||||
| chr4:122890622 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1589T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890622 | |||||||
| chr4:122890624 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1587T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890624 | |||||||
| chr4:122890625 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1586T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890625 | |||||||
| chr4:122890630 | T | G | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1581T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890630 | |||||||
| chr4:122890631 | T | TCTCCCCC others(6): Show |
1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1580_283-1579i others(15): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890631 | |||||||
| chr4:122890632 | G | C | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1579G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890632 | |||||||
| chr4:122890634 | T | G | 1 | a0001c0001t0002g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1577T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890634 | |||||||
| chr4:122890859 | C | T | 20 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(17): Show |
22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.283-1352C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890859 | |||||||
| chr4:122890888 | G | A | 8 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(5): Show |
8 | HG01106.hp1 HG01192.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-1323G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890888 | |||||||
| chr4:122891013 | CA | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(98): Show |
105 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.283-1196delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891013 | ||||||
| chr4:122891017 | T | C | 11 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(8): Show |
12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.283-1194T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891017 | |||||||
| chr4:122891021 | C | CT | 52 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(49): Show |
53 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.283-1176dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891021 | ||||||
| chr4:122891021 | CT | C | 22 | a0001c0001t0003g0044 a0001c0001t0004g0231 a0001c0001t0007g0148 others(19): Show |
24 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.283-1176delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891021 | ||||||
| chr4:122891031 | T | G | 28 | a0001c0001t0003g0182 a0001c0001t0005g0003 a0001c0001t0005g0058 others(25): Show |
30 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.283-1180T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891031 | |||||||
| chr4:122891032 | T | G | 7 | a0001c0001t0006g0019 a0001c0001t0006g0033 a0001c0001t0006g0036 others(4): Show |
8 | HG00639.hp1 HG01106.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-1179T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891032 | |||||||
| chr4:122891032 | TTTTG | T | 14 | a0001c0001t0008g0006 a0001c0001t0008g0117 a0001c0001t0008g0159 others(11): Show |
15 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.283-1175_283-1172d others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891032 | ||||||
| chr4:122891035 | TG | T | 5 | a0001c0001t0002g0067 a0001c0001t0002g0111 a0001c0001t0006g0040 others(2): Show |
5 | HG00408.hp2 HG02723.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-1175delG | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891035 | |||||||
| chr4:122891036 | G | T | 134 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(131): Show |
136 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.283-1175G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891036 | |||||||
| chr4:122891037 | T | G | 1 | a0001c0001t0010g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283-1174T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891037 | |||||||
| chr4:122891041 | G | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(71): Show |
76 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.283-1170G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891041 | |||||||
| chr4:122891044 | T | G | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-1167T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891044 | |||||||
| chr4:122891046 | G | T | 2 | a0001c0001t0037g0102 a0001c0001t0049g0229 |
2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-1165G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891046 | |||||||
| chr4:122891053 | T | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(54): Show |
58 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.283-1158T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891053 | |||||||
| chr4:122891054 | T | G | 4 | a0001c0001t0008g0117 a0001c0001t0019g0023 a0001c0001t0019g0024 others(1): Show |
4 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-1157T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891054 | |||||||
| chr4:122891129 | C | T | 17 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(14): Show |
18 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.283-1082C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891129 | |||||||
| chr4:122891134 | A | G | 17 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0152 others(14): Show |
18 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.283-1077A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891134 | |||||||
| chr4:122891202 | G | A | 2 | a0001c0001t0008g0006 a0001c0001t0008g0161 |
3 | HG03491.hp1 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.283-1009G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891202 | |||||||
| chr4:122891283 | G | T | 6 | a0001c0001t0013g0242 a0001c0001t0013g0243 a0001c0001t0013g0244 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-928G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891283 | |||||||
| chr4:122891424 | C | CT | 11 | a0001c0001t0013g0242 a0001c0001t0013g0244 a0001c0001t0013g0245 others(8): Show |
12 | HG01106.hp1 HG01192.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.283-771dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891424 | ||||||
| chr4:122891424 | C | CTT | 19 | a0001c0001t0001g0079 a0001c0001t0007g0148 a0001c0001t0007g0149 others(16): Show |
20 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.283-772_283-771dup others(2): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891424 | ||||||
| chr4:122891424 | C | CTTT | 54 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(51): Show |
55 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.283-773_283-771dup others(3): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891424 | ||||||
| chr4:122891424 | CT | C | 13 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0044 others(10): Show |
15 | HG01167.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.283-771delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891424 | ||||||
| chr4:122891583 | T | A | 1 | a0001c0001t0010g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283-628T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891583 | |||||||
| chr4:122891642 | G | C | 23 | a0001c0001t0005g0003 a0001c0001t0005g0058 a0001c0001t0005g0060 others(20): Show |
25 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.283-569G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891642 | |||||||
| chr4:122891726 | C | CCTT | 65 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(62): Show |
66 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.283-482_283-480dup others(3): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891726 | ||||||
| chr4:122891854 | G | A | 137 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(134): Show |
143 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.283-357G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891854 | |||||||
| chr4:122892002 | T | C | 1 | a0001c0001t0032g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.283-209T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122892002 |