Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51077 |
| ensemblid | ENSG00000119616.11 |
| hgncid | 20220 |
| symbol | FCF1 |
| name | FCF1 rRNA-processing protein |
| refseq_nuc | NM_015962.5 |
| refseq_prot | NP_057046.1 |
| ensembl_nuc | ENST00000341162.8 |
| ensembl_prot | ENSP00000344393.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 74713144 |
| end | 74738620 |
| strand | + |
| ver | v1.2 |
| region | chr14:74713144-74738620 |
| region5000 | chr14:74708144-74743620 |
| regionname0 | FCF1_chr14_74713144_74738620 |
| regionname5000 | FCF1_chr14_74708144_74743620 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 198 | 360 | 94 | 71 | 151 | 14 | 28 | 118 | FCF1_chr14_74708144_74743620 | FCF1 | MGKQK others(193): Show |
chr14 | 74708144 | 74743620 |
| a0002 | 0/0 | 198 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | MGKQK others(193): Show |
chr14 | 74708144 | 74743620 |
| a0003 | 0/0 | 198 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | MGKQK others(193): Show |
chr14 | 74708144 | 74743620 |
| a0004 | 0/0 | 198 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | MGKQK others(193): Show |
chr14 | 74708144 | 74743620 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 594 | 357 | 93 | 71 | 151 | 14 | 26 | FCF1_chr14_74708144_74743620 | FCF1 | ATGGG others(589): Show |
chr14 | 74708144 | 74743620 | ||
| a0001c0003 | 0/0 | 594 | 2 | 0 | 0 | 0 | 0 | 2 | FCF1_chr14_74708144_74743620 | FCF1 | ATGGG others(589): Show |
chr14 | 74708144 | 74743620 | ||
| a0001c0004 | 0/0 | 594 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | ATGGG others(589): Show |
chr14 | 74708144 | 74743620 | ||
| a0002c0002 | 0/0 | 594 | 2 | 0 | 0 | 2 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | ATGGG others(589): Show |
chr14 | 74708144 | 74743620 | ||
| a0003c0005 | 0/0 | 594 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | ATGGG others(589): Show |
chr14 | 74708144 | 74743620 | ||
| a0004c0006 | 0/0 | 594 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | ATGGG others(589): Show |
chr14 | 74708144 | 74743620 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4340 | 93 | 22 | 16 | 37 | 3 | 15 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0002 | 0/1 | 4341 | 85 | 1 | 15 | 55 | 7 | 6 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0003 | 1/0 | 4341 | 78 | 16 | 19 | 36 | 3 | 3 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0004 | 0/0 | 4340 | 37 | 20 | 10 | 7 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0005 | 0/0 | 4341 | 6 | 6 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0006 | 0/0 | 4341 | 5 | 0 | 4 | 0 | 1 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0007 | 0/0 | 4341 | 4 | 0 | 0 | 4 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0008 | 0/0 | 4340 | 4 | 3 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0009 | 0/0 | 4340 | 3 | 3 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0010 | 0/0 | 4341 | 3 | 1 | 1 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0011 | 0/0 | 4342 | 3 | 3 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4337): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0012 | 0/0 | 4340 | 3 | 0 | 1 | 1 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0013 | 0/0 | 4339 | 3 | 0 | 0 | 3 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4334): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0014 | 0/0 | 4340 | 3 | 3 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0015 | 0/0 | 4341 | 2 | 0 | 0 | 2 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0016 | 0/0 | 4341 | 2 | 1 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0017 | 0/0 | 4340 | 2 | 0 | 0 | 2 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0018 | 0/0 | 4340 | 2 | 2 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0019 | 0/0 | 4341 | 2 | 2 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0020 | 0/0 | 4340 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0021 | 0/0 | 4340 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0022 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0023 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0024 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0025 | 0/0 | 4342 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4337): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0026 | 0/0 | 4340 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0027 | 0/0 | 4340 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0029 | 0/0 | 4340 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0030 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0031 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0032 | 0/0 | 4340 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0033 | 0/0 | 4340 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0034 | 0/0 | 4339 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4334): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0035 | 0/0 | 4342 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4337): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0036 | 0/0 | 4340 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0001t0037 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0001c0003t0001 | 0/0 | 4340 | 2 | 0 | 0 | 0 | 0 | 2 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0001c0004t0004 | 0/0 | 4340 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4335): Show |
chr14 | 74708144 | 74743620 |
| a0002c0002t0002 | 0/0 | 4341 | 2 | 0 | 0 | 2 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0003c0005t0028 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| a0004c0006t0003 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | GTAGA others(4336): Show |
chr14 | 74708144 | 74743620 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 22 | 8 | 2 | 7 | 2 | 3 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0008 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0014 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0021 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0001 | 0/0 | 32 | 0 | 4 | 24 | 2 | 2 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0004 | 0/0 | 7 | 0 | 2 | 4 | 1 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0024 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0003 | 1/0 | 13 | 0 | 4 | 6 | 1 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0005 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0006 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0007g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0008g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0009g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0010g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0010g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0012g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0012g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0013g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0013g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0013g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0014g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0014g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0014g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0015g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0015g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0016g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0016g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0017g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0017g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0018g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0018g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0019g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0019g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0021g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0022g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0023g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0024g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0025g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0026g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0027g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0029g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0030g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0031g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0032g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0033g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0034g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0035g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0036g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0001t0037g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0001c0004t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0003c0005t0028g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| a0004c0006t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0034 | EUR | GBR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0068 | EUR | FIN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0075 | EUR | FIN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00639 | hp1 | a0001 | c0001 | t0027 | g0180 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0077 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0036 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01106 | hp2 | a0003 | c0005 | t0028 | g0032 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01168 | hp2 | a0001 | c0001 | t0024 | g0018 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01175 | hp1 | a0001 | c0001 | t0012 | g0126 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01255 | hp2 | a0001 | c0001 | t0010 | g0051 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01361 | hp2 | a0001 | c0001 | t0037 | g0072 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0172 | AMR | CLM | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0081 | EUR | IBS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | IBS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01884 | hp1 | a0001 | c0001 | t0029 | g0140 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01884 | hp2 | a0001 | c0001 | t0020 | g0054 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01943 | hp1 | a0001 | c0001 | t0016 | g0006 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0067 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0056 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0023 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02055 | hp2 | a0001 | c0001 | t0019 | g0099 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02056 | hp1 | a0001 | c0001 | t0026 | g0059 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02129 | hp2 | a0001 | c0001 | t0010 | g0023 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0157 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0147 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0152 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0160 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02615 | hp1 | a0001 | c0001 | t0023 | g0005 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02630 | hp1 | a0001 | c0001 | t0018 | g0199 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02630 | hp2 | a0001 | c0001 | t0036 | g0156 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0047 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0039 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0163 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0175 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02818 | hp2 | a0001 | c0004 | t0004 | g0153 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02886 | hp2 | a0001 | c0001 | t0025 | g0018 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0049 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0166 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02976 | hp2 | a0001 | c0001 | t0035 | g0039 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0167 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03225 | hp2 | a0001 | c0001 | t0034 | g0007 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03453 | hp2 | a0001 | c0001 | t0021 | g0017 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03491 | hp2 | a0001 | c0001 | t0012 | g0005 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0048 | AFR | GWD | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03831 | hp1 | a0001 | c0001 | t0022 | g0026 | SAS | BEB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | BEB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | STU | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0019 | SAS | STU | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0038 | AFR | YRI | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | YRI | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | YRI | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18942 | hp2 | a0001 | c0001 | t0013 | g0009 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18946 | hp1 | a0001 | c0001 | t0033 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18946 | hp2 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18963 | hp2 | a0001 | c0001 | t0017 | g0108 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18969 | hp2 | a0001 | c0001 | t0013 | g0022 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18972 | hp2 | a0001 | c0001 | t0015 | g0092 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18978 | hp2 | a0001 | c0001 | t0007 | g0208 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18986 | hp2 | a0001 | c0001 | t0013 | g0019 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18993 | hp2 | a0001 | c0001 | t0015 | g0100 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19009 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19012 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | LWK | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | LWK | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | LWK | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19043 | hp2 | a0001 | c0001 | t0031 | g0165 | AFR | LWK | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19058 | hp2 | a0001 | c0001 | t0012 | g0138 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19076 | hp2 | a0001 | c0001 | t0032 | g0002 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19084 | hp1 | a0004 | c0006 | t0003 | g0115 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19091 | hp1 | a0001 | c0001 | t0017 | g0139 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | YRI | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0038 | AFR | YRI | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | ASW | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA20129 | hp2 | a0001 | c0001 | t0019 | g0116 | AFR | ASW | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | TSI | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0129 | EUR | TSI | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02486 | hp1 | a0001 | c0001 | t0018 | g0195 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0050 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03471 | hp1 | a0001 | c0001 | t0030 | g0158 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | USA | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | USA | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | USA | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | USA | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0024 | REF | REF | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0003 | REF | REF | FCF1_chr14_74708144_74743620 | FCF1 | chr14 | 74708144 | 74743620 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74723299 | T | C | 1 | a0003 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.320T>C | p.Met107Thr | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/8 | 374/4341 | 320/597 | 107/198 | chr14 | 74723299 | |||
| chr14:74734077 | A | T | 1 | a0004 | 1 | NA19084.hp1 | missense_variant&splice_region_variant | MODERATE | c.455A>T | p.His152Leu | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 509/4341 | 455/597 | 152/198 | chr14 | 74734077 | |||
| chr14:74734121 | A | T | 1 | a0004 | 1 | NA19084.hp1 | stop_gained | HIGH | c.499A>T | p.Arg167* | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 553/4341 | 499/597 | 167/198 | chr14 | 74734121 | |||
| chr14:74734123 | A | T | 1 | a0004 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.501A>T | p.Arg167Ser | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 555/4341 | 501/597 | 167/198 | chr14 | 74734123 | |||
| chr14:74734124 | A | C | 1 | a0004 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.502A>C | p.Ile168Leu | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 556/4341 | 502/597 | 168/198 | chr14 | 74734124 | |||
| chr14:74734151 | A | G | 1 | a0002 | 2 | HG00423.hp2 NA19077.hp2 |
missense_variant | MODERATE | c.529A>G | p.Met177Val | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 583/4341 | 529/597 | 177/198 | chr14 | 74734151 | |||
| chr14:74734154 | T | C | 1 | a0004 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.532T>C | p.Tyr178His | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 586/4341 | 532/597 | 178/198 | chr14 | 74734154 | |||
| chr14:74734158 | T | G | 1 | a0004 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.536T>G | p.Ile179Ser | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 590/4341 | 536/597 | 179/198 | chr14 | 74734158 | |||
| chr14:74734160 | T | G | 1 | a0004 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.538T>G | p.Ser180Ala | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 592/4341 | 538/597 | 180/198 | chr14 | 74734160 | |||
| chr14:74734161 | C | G | 1 | a0004 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.539C>G | p.Ser180Cys | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 593/4341 | 539/597 | 180/198 | chr14 | 74734161 | |||
| chr14:74734168 | T | A | 1 | a0004 | 1 | NA19084.hp1 | missense_variant&splice_region_variant | MODERATE | c.546T>A | p.His182Gln | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 600/4341 | 546/597 | 182/198 | chr14 | 74734168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74723276 | C | A | 1 | a0001c0004 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.297C>A | p.Ile99Ile | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/8 | 351/4341 | 297/597 | 99/198 | chr14 | 74723276 | |||
| chr14:74723321 | G | T | 1 | a0001c0003 | 2 | HG02738.hp2 HG04228.hp1 |
synonymous_variant | LOW | c.342G>T | p.Gly114Gly | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/8 | 396/4341 | 342/597 | 114/198 | chr14 | 74723321 | |||
| chr14:74734078 | T | C | 1 | a0004c0006 | 1 | NA19084.hp1 | splice_region_variant&synonymous_variant | LOW | c.456T>C | p.His152His | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 510/4341 | 456/597 | 152/198 | chr14 | 74734078 | |||
| chr14:74734138 | T | A | 1 | a0004c0006 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.516T>A | p.Pro172Pro | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 570/4341 | 516/597 | 172/198 | chr14 | 74734138 | |||
| chr14:74734162 | T | G | 1 | a0004c0006 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.540T>G | p.Ser180Ser | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/8 | 594/4341 | 540/597 | 180/198 | chr14 | 74734162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74713155 | G | A | 1 | a0001c0001t0009 | 3 | HG02723.hp2 NA18522.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-43G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 1/8 | 43 | chr14 | 74713155 | ||||||
| chr14:74713171 | C | T | 1 | a0001c0001t0037 | 1 | HG01361.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-27C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 1/8 | chr14 | 74713171 | |||||||
| chr14:74735426 | A | G | 1 | a0001c0001t0019 | 2 | HG02055.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*496A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 496 | chr14 | 74735426 | ||||||
| chr14:74735441 | A | G | 1 | a0001c0001t0018 | 2 | HG02486.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*511A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 511 | chr14 | 74735441 | ||||||
| chr14:74735540 | A | G | 1 | a0001c0001t0014 | 3 | HG02559.hp1 HG02895.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*610A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 610 | chr14 | 74735540 | ||||||
| chr14:74735670 | A | G | 1 | a0001c0001t0036 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*740A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 740 | chr14 | 74735670 | ||||||
| chr14:74735964 | C | T | 1 | a0001c0001t0035 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1034C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 1034 | chr14 | 74735964 | ||||||
| chr14:74735988 | G | A | 1 | a0001c0001t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1058G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 1058 | chr14 | 74735988 | ||||||
| chr14:74736270 | G | A | 1 | a0001c0001t0021 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1340G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 1340 | chr14 | 74736270 | ||||||
| chr14:74736409 | CA | C | 6 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0031 others(3): Show |
9 | HG03225.hp2 NA18942.hp2 NA18946.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1494delA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 1494 | INFO_REALIGN_3_PRIME | chr14 | 74736409 | |||||
| chr14:74736702 | G | A | 1 | a0001c0001t0022 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1772G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 1772 | chr14 | 74736702 | ||||||
| chr14:74736750 | G | A | 1 | a0001c0001t0023 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1820G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 1820 | chr14 | 74736750 | ||||||
| chr14:74736768 | C | T | 9 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0016 others(6): Show |
48 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1838C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 1838 | chr14 | 74736768 | ||||||
| chr14:74737040 | G | A | 1 | a0001c0001t0029 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2110G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2110 | chr14 | 74737040 | ||||||
| chr14:74737255 | T | A | 1 | a0001c0001t0005 | 6 | HG02109.hp1 HG02145.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2325T>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2325 | chr14 | 74737255 | ||||||
| chr14:74737333 | C | T | 1 | a0003c0005t0028 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2403 | chr14 | 74737333 | ||||||
| chr14:74737464 | G | C | 2 | a0001c0001t0006 a0001c0001t0037 |
6 | HG00323.hp1 HG00738.hp2 HG01257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2534G>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2534 | chr14 | 74737464 | ||||||
| chr14:74737626 | C | T | 1 | a0001c0001t0008 | 4 | HG01081.hp1 HG02451.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2696C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2696 | chr14 | 74737626 | ||||||
| chr14:74737749 | A | G | 1 | a0001c0001t0009 | 3 | HG02723.hp2 NA18522.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2819A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2819 | chr14 | 74737749 | ||||||
| chr14:74737764 | C | T | 1 | a0001c0001t0008 | 4 | HG01081.hp1 HG02451.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2834C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2834 | chr14 | 74737764 | ||||||
| chr14:74737812 | A | G | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(24): Show |
263 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*2882A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2882 | chr14 | 74737812 | ||||||
| chr14:74737883 | G | A | 1 | a0001c0001t0032 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2953G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2953 | chr14 | 74737883 | ||||||
| chr14:74737884 | A | G | 1 | a0001c0001t0032 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2954A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2954 | chr14 | 74737884 | ||||||
| chr14:74737917 | A | G | 1 | a0001c0001t0027 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2987A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 2987 | chr14 | 74737917 | ||||||
| chr14:74737936 | G | A | 1 | a0001c0001t0024 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3006G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 3006 | chr14 | 74737936 | ||||||
| chr14:74737991 | CA | C | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(15): Show |
159 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3080delA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 3080 | INFO_REALIGN_3_PRIME | chr14 | 74737991 | |||||
| chr14:74738083 | A | AT | 5 | a0001c0001t0011 a0001c0001t0025 a0001c0001t0030 others(2): Show |
7 | HG02723.hp1 HG02886.hp2 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3167dupT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 3168 | INFO_REALIGN_3_PRIME | chr14 | 74738083 | |||||
| chr14:74738134 | C | T | 1 | a0001c0001t0015 | 2 | NA18972.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3204C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 3204 | chr14 | 74738134 | ||||||
| chr14:74738135 | G | A | 3 | a0001c0001t0011 a0001c0001t0031 a0001c0001t0035 |
5 | HG02723.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3205G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 3205 | chr14 | 74738135 | ||||||
| chr14:74738162 | C | T | 1 | a0001c0001t0030 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3232C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 3232 | chr14 | 74738162 | ||||||
| chr14:74738413 | G | A | 19 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(16): Show |
162 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*3483G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 3483 | chr14 | 74738413 | ||||||
| chr14:74738541 | A | G | 2 | a0001c0001t0010 a0003c0005t0028 |
4 | HG01106.hp2 HG01255.hp2 HG02055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3611A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 8/8 | 3611 | chr14 | 74738541 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74713428 | A | T | 3 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 |
3 | HG02559.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4-57A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 1/7 | chr14 | 74713428 | |||||||
| chr14:74713610 | G | A | 2 | a0001c0001t0005g0045 a0001c0001t0005g0046 |
2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.71+58G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | chr14 | 74713610 | |||||||
| chr14:74713639 | G | GT | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.71+93dupT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 74713639 | ||||||
| chr14:74713698 | G | T | 3 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 |
3 | NA18956.hp2 NA18967.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.71+146G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | chr14 | 74713698 | |||||||
| chr14:74713888 | G | C | 1 | a0001c0001t0008g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.71+336G>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | chr14 | 74713888 | |||||||
| chr14:74713976 | A | G | 2 | a0001c0001t0005g0045 a0001c0001t0005g0046 |
2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.71+424A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | chr14 | 74713976 | |||||||
| chr14:74714268 | A | G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(5): Show |
9 | HG02738.hp2 HG04228.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-604A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | chr14 | 74714268 | |||||||
| chr14:74714329 | C | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0171 others(2): Show |
10 | HG01243.hp1 HG01496.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-543C>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | chr14 | 74714329 | |||||||
| chr14:74714398 | A | C | 5 | a0001c0001t0003g0018 a0001c0001t0003g0169 a0001c0001t0003g0170 others(2): Show |
5 | HG01168.hp2 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-474A>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | chr14 | 74714398 | |||||||
| chr14:74714683 | T | G | 3 | a0001c0001t0014g0048 a0001c0001t0014g0049 a0001c0001t0014g0050 |
3 | HG02559.hp1 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.72-189T>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | chr14 | 74714683 | |||||||
| chr14:74714716 | C | G | 3 | a0001c0001t0014g0048 a0001c0001t0014g0049 a0001c0001t0014g0050 |
3 | HG02559.hp1 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.72-156C>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | chr14 | 74714716 | |||||||
| chr14:74714778 | CA | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(100): Show |
166 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.72-79delA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 74714778 | ||||||
| chr14:74715100 | T | C | 1 | a0001c0001t0029g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.143+157T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 3/7 | chr14 | 74715100 | |||||||
| chr14:74715305 | A | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.143+362A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 3/7 | chr14 | 74715305 | |||||||
| chr14:74715394 | T | C | 1 | a0001c0001t0027g0180 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.143+451T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 3/7 | chr14 | 74715394 | |||||||
| chr14:74715610 | T | G | 1 | a0001c0001t0001g0181 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.144-341T>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 3/7 | chr14 | 74715610 | |||||||
| chr14:74715612 | T | G | 3 | a0001c0001t0003g0052 a0001c0001t0010g0023 a0001c0001t0010g0051 |
4 | HG01192.hp2 HG01255.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-339T>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 3/7 | chr14 | 74715612 | |||||||
| chr14:74715632 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0174 others(4): Show |
8 | HG02738.hp2 HG04228.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.144-319C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 3/7 | chr14 | 74715632 | |||||||
| chr14:74715633 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.144-318G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 3/7 | chr14 | 74715633 | |||||||
| chr14:74715913 | G | A | 1 | a0001c0001t0003g0053 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.144-38G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 3/7 | chr14 | 74715913 | |||||||
| chr14:74716125 | G | A | 1 | a0001c0001t0020g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.292+26G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74716125 | |||||||
| chr14:74716234 | G | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(146): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.292+135G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74716234 | |||||||
| chr14:74716247 | A | G | 1 | a0001c0001t0020g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.292+148A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74716247 | |||||||
| chr14:74716315 | A | G | 8 | a0001c0001t0004g0017 a0001c0001t0004g0159 a0001c0001t0004g0160 others(5): Show |
10 | HG01109.hp2 HG02572.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+216A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74716315 | |||||||
| chr14:74716396 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292+297A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74716396 | |||||||
| chr14:74716510 | C | T | 1 | a0001c0001t0030g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292+411C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74716510 | |||||||
| chr14:74716536 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.292+437G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74716536 | |||||||
| chr14:74716797 | C | T | 2 | a0001c0001t0012g0138 a0001c0001t0017g0139 |
2 | NA19058.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.292+698C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74716797 | |||||||
| chr14:74716798 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.292+699G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74716798 | |||||||
| chr14:74716891 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.292+792C>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74716891 | |||||||
| chr14:74717020 | GC | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(146): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.292+924delC | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74717020 | ||||||
| chr14:74717024 | A | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(146): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.292+925A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717024 | |||||||
| chr14:74717051 | G | A | 1 | a0001c0001t0006g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.292+952G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717051 | |||||||
| chr14:74717054 | C | T | 1 | a0001c0001t0003g0035 | 2 | NA18953.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.292+955C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717054 | |||||||
| chr14:74717121 | A | T | 1 | a0001c0001t0030g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292+1022A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717121 | |||||||
| chr14:74717180 | AC | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.292+1085delC | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74717180 | ||||||
| chr14:74717226 | C | T | 11 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(8): Show |
13 | HG02145.hp2 HG02630.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.292+1127C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717226 | |||||||
| chr14:74717364 | A | C | 1 | a0001c0001t0003g0137 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.292+1265A>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717364 | |||||||
| chr14:74717392 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0044 others(4): Show |
13 | NA18939.hp1 NA18941.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.292+1293C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717392 | |||||||
| chr14:74717503 | A | C | 4 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0136 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+1404A>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717503 | |||||||
| chr14:74717693 | T | A | 1 | a0001c0001t0002g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.292+1594T>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717693 | |||||||
| chr14:74717795 | A | G | 2 | a0001c0001t0003g0132 a0001c0001t0003g0133 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.292+1696A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717795 | |||||||
| chr14:74717936 | G | C | 1 | a0001c0001t0003g0088 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.292+1837G>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717936 | |||||||
| chr14:74717960 | C | T | 2 | a0001c0001t0003g0130 a0001c0001t0003g0131 |
2 | HG01074.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.292+1861C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74717960 | |||||||
| chr14:74718065 | A | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
9 | HG02056.hp2 HG02132.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.292+1966A>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718065 | |||||||
| chr14:74718238 | G | T | 2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | HG02809.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.292+2139G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718238 | |||||||
| chr14:74718476 | A | AAT | 18 | a0001c0001t0001g0183 a0001c0001t0004g0006 a0001c0001t0004g0007 others(15): Show |
27 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.292+2390_292+2391d others(4): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74718476 | ||||||
| chr14:74718517 | G | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG01978.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.292+2418G>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718517 | |||||||
| chr14:74718531 | T | G | 5 | a0001c0001t0004g0017 a0001c0001t0004g0159 a0001c0001t0004g0160 others(2): Show |
6 | HG01109.hp2 HG02572.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+2432T>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718531 | |||||||
| chr14:74718609 | G | T | 1 | a0001c0001t0004g0161 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.292+2510G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718609 | |||||||
| chr14:74718619 | G | T | 1 | a0001c0001t0003g0127 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.292+2520G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718619 | |||||||
| chr14:74718647 | TGTAAA | T | 17 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0040 others(14): Show |
26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.292+2552_292+2556d others(7): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74718647 | ||||||
| chr14:74718691 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.292+2592C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718691 | |||||||
| chr14:74718692 | G | A | 3 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 |
3 | NA18956.hp2 NA18967.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.292+2593G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718692 | |||||||
| chr14:74718765 | C | A | 1 | a0001c0001t0030g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292+2666C>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718765 | |||||||
| chr14:74718776 | T | G | 17 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0040 others(14): Show |
26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.292+2677T>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718776 | |||||||
| chr14:74718823 | C | A | 2 | a0001c0001t0010g0023 a0001c0001t0010g0051 |
3 | HG01255.hp2 HG02055.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.292+2724C>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718823 | |||||||
| chr14:74718913 | G | T | 1 | a0001c0001t0016g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+2814G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718913 | |||||||
| chr14:74718928 | G | A | 2 | a0001c0001t0005g0045 a0001c0001t0005g0046 |
2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.292+2829G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718928 | |||||||
| chr14:74718996 | A | G | 1 | a0001c0001t0001g0041 | 2 | NA18973.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.292+2897A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74718996 | |||||||
| chr14:74719045 | T | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
263 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.292+2946T>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719045 | |||||||
| chr14:74719097 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.292+2998T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719097 | |||||||
| chr14:74719129 | C | CA | 77 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0174 others(74): Show |
102 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.292+3053dupA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74719129 | ||||||
| chr14:74719129 | C | CAA | 14 | a0001c0001t0002g0058 a0001c0001t0002g0177 a0001c0001t0004g0141 others(11): Show |
15 | HG00741.hp1 HG01081.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.292+3052_292+3053d others(4): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74719129 | ||||||
| chr14:74719295 | T | TA | 8 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(5): Show |
9 | HG02738.hp2 HG04228.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.292+3210dupA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74719295 | ||||||
| chr14:74719307 | A | G | 52 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0015 others(49): Show |
95 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.292+3208A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719307 | |||||||
| chr14:74719307 | AAAG | A | 34 | a0001c0001t0003g0093 a0001c0001t0003g0106 a0001c0001t0004g0006 others(31): Show |
47 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.292+3223_292+3225d others(5): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74719307 | ||||||
| chr14:74719325 | A | G | 2 | a0001c0001t0002g0058 a0001c0001t0002g0065 |
2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.292+3226A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719325 | |||||||
| chr14:74719370 | T | C | 1 | a0001c0001t0008g0036 | 2 | HG01081.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.292+3271T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719370 | |||||||
| chr14:74719381 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+3282G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719381 | |||||||
| chr14:74719679 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.292+3580C>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719679 | |||||||
| chr14:74719722 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.293-3550G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719722 | |||||||
| chr14:74719747 | G | A | 32 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0016 others(29): Show |
45 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.293-3525G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719747 | |||||||
| chr14:74719877 | G | A | 4 | a0001c0001t0003g0107 a0001c0001t0008g0036 a0001c0001t0008g0047 others(1): Show |
5 | HG01081.hp1 HG02071.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-3395G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719877 | |||||||
| chr14:74719911 | C | T | 3 | a0001c0001t0008g0036 a0001c0001t0008g0047 a0001c0001t0008g0152 |
4 | HG01081.hp1 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-3361C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719911 | |||||||
| chr14:74719955 | A | G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(5): Show |
9 | HG02738.hp2 HG04228.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-3317A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74719955 | |||||||
| chr14:74720096 | C | G | 1 | a0001c0001t0030g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.293-3176C>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720096 | |||||||
| chr14:74720204 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.293-3068C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720204 | |||||||
| chr14:74720391 | A | C | 11 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(8): Show |
12 | HG02559.hp1 HG02738.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-2881A>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720391 | |||||||
| chr14:74720399 | T | TC | 2 | a0001c0001t0001g0010 a0001c0001t0001g0181 |
6 | NA18939.hp1 NA18966.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-2872dupC | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74720399 | ||||||
| chr14:74720415 | T | C | 1 | a0001c0001t0003g0094 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.293-2857T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720415 | |||||||
| chr14:74720550 | C | T | 1 | a0001c0001t0003g0035 | 2 | NA18953.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.293-2722C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720550 | |||||||
| chr14:74720570 | A | C | 1 | a0001c0001t0030g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.293-2702A>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720570 | |||||||
| chr14:74720771 | T | C | 1 | a0001c0001t0004g0143 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.293-2501T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720771 | |||||||
| chr14:74720871 | T | G | 1 | a0001c0001t0002g0066 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.293-2401T>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720871 | |||||||
| chr14:74720879 | G | GT | 6 | a0001c0001t0002g0065 a0001c0001t0002g0084 a0001c0001t0002g0085 others(3): Show |
6 | HG01175.hp1 HG01175.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-2376dupT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74720879 | ||||||
| chr14:74720879 | G | T | 5 | a0001c0001t0005g0031 a0001c0001t0005g0045 a0001c0001t0005g0046 others(2): Show |
6 | HG02109.hp1 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-2393G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720879 | |||||||
| chr14:74720879 | GT | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
148 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.293-2376delT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74720879 | ||||||
| chr14:74720879 | GTT | G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(5): Show |
9 | HG02738.hp2 HG04228.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-2377_293-2376d others(4): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74720879 | ||||||
| chr14:74720928 | G | C | 6 | a0001c0001t0004g0037 a0001c0001t0008g0036 a0001c0001t0008g0047 others(3): Show |
8 | HG01081.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-2344G>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720928 | |||||||
| chr14:74720972 | G | A | 2 | a0001c0001t0003g0110 a0001c0001t0017g0108 |
2 | NA18963.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.293-2300G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74720972 | |||||||
| chr14:74721044 | A | AT | 27 | a0001c0001t0001g0183 a0001c0001t0001g0203 a0001c0001t0002g0064 others(24): Show |
38 | HG00423.hp1 HG01243.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.293-2210dupT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74721044 | ||||||
| chr14:74721044 | AT | A | 6 | a0001c0001t0005g0031 a0001c0001t0005g0045 a0001c0001t0005g0046 others(3): Show |
7 | HG00323.hp1 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-2210delT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74721044 | ||||||
| chr14:74721302 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.293-1970C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74721302 | |||||||
| chr14:74721371 | A | T | 3 | a0001c0001t0014g0048 a0001c0001t0014g0049 a0001c0001t0014g0050 |
3 | HG02559.hp1 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.293-1901A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74721371 | |||||||
| chr14:74721419 | G | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.293-1853G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74721419 | |||||||
| chr14:74721811 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.293-1461G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74721811 | |||||||
| chr14:74722047 | C | CT | 130 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
234 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.293-1207dupT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74722047 | ||||||
| chr14:74722047 | C | CTT | 13 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0187 others(10): Show |
14 | HG00597.hp1 HG00597.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.293-1208_293-1207d others(4): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74722047 | ||||||
| chr14:74722112 | G | A | 3 | a0001c0001t0008g0036 a0001c0001t0008g0047 a0001c0001t0008g0152 |
4 | HG01081.hp1 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-1160G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74722112 | |||||||
| chr14:74722123 | A | G | 2 | a0001c0001t0003g0104 a0001c0001t0003g0124 |
2 | HG01074.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.293-1149A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74722123 | |||||||
| chr14:74722235 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.293-1037G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74722235 | |||||||
| chr14:74722523 | A | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
162 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.293-749A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74722523 | |||||||
| chr14:74722677 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0189 |
7 | HG00280.hp2 HG00741.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-595G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74722677 | |||||||
| chr14:74723020 | A | G | 3 | a0001c0001t0004g0037 a0001c0001t0016g0157 a0001c0001t0036g0156 |
4 | HG02145.hp2 HG02630.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-252A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74723020 | |||||||
| chr14:74723029 | G | A | 5 | a0001c0001t0005g0031 a0001c0001t0005g0045 a0001c0001t0005g0046 others(2): Show |
6 | HG02109.hp1 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-243G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74723029 | |||||||
| chr14:74723095 | C | A | 1 | a0001c0001t0004g0144 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.293-177C>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | chr14 | 74723095 | |||||||
| chr14:74723255 | A | AT | 5 | a0001c0001t0004g0007 a0001c0001t0004g0040 a0001c0001t0004g0171 others(2): Show |
10 | HG01243.hp1 HG01496.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-10dupT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 74723255 | ||||||
| chr14:74723752 | T | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
263 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.365+408T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74723752 | |||||||
| chr14:74723773 | A | C | 1 | a0001c0001t0002g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.365+429A>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74723773 | |||||||
| chr14:74723784 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.365+440C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74723784 | |||||||
| chr14:74723824 | G | T | 52 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0015 others(49): Show |
95 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.365+480G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74723824 | |||||||
| chr14:74723828 | C | CA | 52 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0004 others(49): Show |
95 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.365+499dupA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74723828 | ||||||
| chr14:74724675 | C | A | 1 | a0001c0001t0002g0069 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.365+1331C>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74724675 | |||||||
| chr14:74724895 | ACT | A | 6 | a0001c0001t0004g0037 a0001c0001t0008g0036 a0001c0001t0008g0047 others(3): Show |
8 | HG01081.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+1554_365+1555d others(4): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74724895 | ||||||
| chr14:74724911 | A | C | 1 | a0002c0002t0002g0080 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.365+1567A>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74724911 | |||||||
| chr14:74725052 | C | T | 4 | a0001c0001t0003g0103 a0001c0001t0003g0122 a0001c0001t0003g0123 others(1): Show |
4 | HG02040.hp2 NA18951.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+1708C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725052 | |||||||
| chr14:74725069 | T | TA | 77 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0015 others(74): Show |
131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.365+1736dupA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74725069 | ||||||
| chr14:74725150 | G | A | 14 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0150 others(11): Show |
18 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.365+1806G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725150 | |||||||
| chr14:74725349 | G | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(8): Show |
12 | HG01168.hp1 HG01361.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.365+2005G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725349 | |||||||
| chr14:74725376 | A | G | 1 | a0001c0001t0003g0121 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.365+2032A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725376 | |||||||
| chr14:74725380 | T | G | 1 | a0001c0001t0003g0128 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.365+2036T>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725380 | |||||||
| chr14:74725439 | C | A | 1 | a0001c0001t0012g0126 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.365+2095C>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725439 | |||||||
| chr14:74725441 | C | T | 1 | a0001c0001t0006g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.365+2097C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725441 | |||||||
| chr14:74725480 | C | CA | 20 | a0001c0001t0002g0064 a0001c0001t0002g0070 a0001c0001t0003g0032 others(17): Show |
21 | HG00140.hp2 HG01106.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.365+2165dupA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74725480 | ||||||
| chr14:74725480 | CA | C | 89 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0182 others(86): Show |
134 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.365+2165delA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74725480 | ||||||
| chr14:74725480 | CAA | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(64): Show |
123 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.365+2164_365+2165d others(4): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74725480 | ||||||
| chr14:74725480 | CAAA | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(7): Show |
11 | HG01496.hp2 HG02559.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.365+2163_365+2165d others(5): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74725480 | ||||||
| chr14:74725547 | G | A | 2 | a0001c0001t0002g0062 a0001c0001t0030g0158 |
2 | HG00597.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.365+2203G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725547 | |||||||
| chr14:74725687 | C | A | 3 | a0001c0001t0004g0151 a0001c0001t0004g0154 a0001c0004t0004g0153 |
3 | HG02818.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.365+2343C>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725687 | |||||||
| chr14:74725731 | G | A | 2 | a0001c0001t0018g0195 a0001c0001t0018g0199 |
2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.365+2387G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725731 | |||||||
| chr14:74725807 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.365+2463C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725807 | |||||||
| chr14:74725808 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.365+2464G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725808 | |||||||
| chr14:74725825 | G | T | 1 | a0001c0001t0002g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.365+2481G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725825 | |||||||
| chr14:74725860 | C | T | 1 | a0001c0001t0004g0149 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.365+2516C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725860 | |||||||
| chr14:74725868 | G | A | 1 | a0001c0001t0004g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365+2524G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725868 | |||||||
| chr14:74725890 | C | T | 3 | a0001c0001t0014g0048 a0001c0001t0014g0049 a0001c0001t0014g0050 |
3 | HG02559.hp1 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.365+2546C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725890 | |||||||
| chr14:74725935 | C | CA | 17 | a0001c0001t0001g0205 a0001c0001t0003g0088 a0001c0001t0004g0016 others(14): Show |
21 | HG01109.hp2 HG01884.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.365+2605dupA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74725935 | ||||||
| chr14:74725985 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG00639.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.365+2641G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74725985 | |||||||
| chr14:74726150 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0058 a0001c0001t0002g0065 |
3 | HG00741.hp1 HG01175.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.365+2806G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74726150 | |||||||
| chr14:74726228 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.365+2884G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74726228 | |||||||
| chr14:74726603 | CT | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(57): Show |
108 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.365+3274delT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74726603 | ||||||
| chr14:74726852 | C | T | 4 | a0001c0001t0003g0103 a0001c0001t0003g0122 a0001c0001t0003g0123 others(1): Show |
4 | HG02040.hp2 NA18951.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+3508C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74726852 | |||||||
| chr14:74726929 | C | T | 6 | a0001c0001t0004g0037 a0001c0001t0008g0036 a0001c0001t0008g0047 others(3): Show |
8 | HG01081.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+3585C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74726929 | |||||||
| chr14:74727038 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
162 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.365+3694A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74727038 | |||||||
| chr14:74727069 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.365+3725A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74727069 | |||||||
| chr14:74727405 | C | T | 2 | a0001c0001t0003g0102 a0001c0001t0003g0119 |
2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.365+4061C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74727405 | |||||||
| chr14:74727512 | T | C | 1 | a0001c0001t0001g0012 | 4 | HG00741.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+4168T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74727512 | |||||||
| chr14:74727796 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
263 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.365+4452A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74727796 | |||||||
| chr14:74727845 | C | A | 1 | a0001c0001t0002g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.365+4501C>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74727845 | |||||||
| chr14:74728043 | C | CTCCAGCT others(8): Show |
1 | a0001c0001t0003g0098 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.366-4686_366-4672d others(17): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74728043 | ||||||
| chr14:74728130 | A | G | 1 | a0001c0001t0003g0113 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.366-4601A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74728130 | |||||||
| chr14:74728402 | G | C | 2 | a0001c0001t0009g0038 a0001c0001t0009g0163 |
3 | HG02723.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.366-4329G>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74728402 | |||||||
| chr14:74728511 | A | G | 1 | a0001c0001t0003g0121 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.366-4220A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74728511 | |||||||
| chr14:74728512 | A | G | 1 | a0001c0001t0011g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-4219A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74728512 | |||||||
| chr14:74728732 | A | G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(5): Show |
9 | HG02738.hp2 HG04228.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.366-3999A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74728732 | |||||||
| chr14:74728833 | G | T | 1 | a0001c0001t0004g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.366-3898G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74728833 | |||||||
| chr14:74728883 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.366-3848T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74728883 | |||||||
| chr14:74728907 | T | C | 1 | a0001c0001t0004g0147 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.366-3824T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74728907 | |||||||
| chr14:74728916 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
162 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.366-3815A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74728916 | |||||||
| chr14:74729124 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0176 |
2 | NA18949.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.366-3607G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74729124 | |||||||
| chr14:74729452 | C | T | 3 | a0001c0001t0004g0037 a0001c0001t0016g0157 a0001c0001t0036g0156 |
4 | HG02145.hp2 HG02630.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-3279C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74729452 | |||||||
| chr14:74729517 | C | T | 1 | a0001c0001t0006g0077 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.366-3214C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74729517 | |||||||
| chr14:74729539 | G | T | 17 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0040 others(14): Show |
26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.366-3192G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74729539 | |||||||
| chr14:74729582 | T | C | 2 | a0001c0001t0003g0103 a0001c0001t0003g0122 |
2 | NA18951.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.366-3149T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74729582 | |||||||
| chr14:74729698 | G | C | 1 | a0001c0001t0002g0078 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.366-3033G>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74729698 | |||||||
| chr14:74729832 | A | C | 2 | a0001c0001t0004g0159 a0001c0001t0004g0160 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.366-2899A>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74729832 | |||||||
| chr14:74729861 | C | G | 3 | a0001c0001t0008g0036 a0001c0001t0008g0047 a0001c0001t0008g0152 |
4 | HG01081.hp1 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-2870C>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74729861 | |||||||
| chr14:74730005 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0075 |
3 | HG00323.hp2 HG01934.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.366-2726G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74730005 | |||||||
| chr14:74730206 | C | CT | 24 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0001t0002g0026 others(21): Show |
25 | HG00621.hp1 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.366-2502dupT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74730206 | ||||||
| chr14:74730206 | CT | C | 53 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0044 others(50): Show |
70 | HG00323.hp1 HG00423.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.366-2502delT | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74730206 | ||||||
| chr14:74730206 | CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0005g0031 a0001c0001t0005g0045 a0001c0001t0005g0046 others(2): Show |
6 | HG02109.hp1 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.366-2512_366-2502d others(13): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74730206 | ||||||
| chr14:74730275 | C | G | 11 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(8): Show |
12 | HG02559.hp1 HG02738.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.366-2456C>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74730275 | |||||||
| chr14:74730409 | T | A | 2 | a0001c0001t0002g0071 a0001c0001t0002g0074 |
2 | HG01192.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.366-2322T>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74730409 | |||||||
| chr14:74730418 | A | T | 1 | a0001c0001t0004g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.366-2313A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74730418 | |||||||
| chr14:74730419 | T | A | 2 | a0001c0001t0010g0023 a0001c0001t0010g0051 |
3 | HG01255.hp2 HG02055.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.366-2312T>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74730419 | |||||||
| chr14:74730502 | C | T | 3 | a0001c0001t0005g0031 a0001c0001t0005g0089 a0001c0001t0005g0164 |
4 | HG02109.hp1 HG02145.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-2229C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74730502 | |||||||
| chr14:74730611 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.366-2120T>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74730611 | |||||||
| chr14:74730738 | G | A | 3 | a0001c0001t0004g0037 a0001c0001t0016g0157 a0001c0001t0036g0156 |
4 | HG02145.hp2 HG02630.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-1993G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74730738 | |||||||
| chr14:74730828 | C | T | 4 | a0001c0001t0011g0039 a0001c0001t0011g0167 a0001c0001t0031g0165 others(1): Show |
4 | HG02723.hp1 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-1903C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74730828 | |||||||
| chr14:74730953 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.366-1778G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74730953 | |||||||
| chr14:74730998 | CA | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0198 a0001c0001t0001g0201 |
6 | HG00733.hp2 HG01261.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-1719delA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74730998 | ||||||
| chr14:74731742 | C | T | 1 | a0001c0001t0003g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.366-989C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74731742 | |||||||
| chr14:74731772 | G | A | 1 | a0001c0001t0004g0162 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.366-959G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74731772 | |||||||
| chr14:74732066 | A | G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(5): Show |
9 | HG02738.hp2 HG04228.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.366-665A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74732066 | |||||||
| chr14:74732154 | T | TTA | 49 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
96 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.366-563_366-562dup others(2): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74732154 | ||||||
| chr14:74732154 | T | TTATATA | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
3 | HG02257.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.366-567_366-562dup others(6): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 74732154 | ||||||
| chr14:74732156 | A | T | 2 | a0001c0001t0003g0093 a0001c0001t0003g0106 |
2 | NA18967.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.366-575A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74732156 | |||||||
| chr14:74732160 | A | G | 3 | a0001c0001t0008g0036 a0001c0001t0008g0047 a0001c0001t0008g0152 |
4 | HG01081.hp1 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-571A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74732160 | |||||||
| chr14:74732195 | A | G | 1 | a0001c0001t0002g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.366-536A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74732195 | |||||||
| chr14:74732282 | C | G | 17 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0040 others(14): Show |
26 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.366-449C>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74732282 | |||||||
| chr14:74732297 | A | T | 1 | a0001c0001t0003g0098 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.366-434A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 5/7 | chr14 | 74732297 | |||||||
| chr14:74733067 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.453+249T>C | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 6/7 | chr14 | 74733067 | |||||||
| chr14:74733178 | G | A | 2 | a0001c0001t0005g0045 a0001c0001t0005g0046 |
2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.453+360G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 6/7 | chr14 | 74733178 | |||||||
| chr14:74733801 | G | A | 8 | a0001c0001t0004g0017 a0001c0001t0004g0159 a0001c0001t0004g0160 others(5): Show |
10 | HG01109.hp2 HG02572.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.454-275G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 6/7 | chr14 | 74733801 | |||||||
| chr14:74733836 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.454-240A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 6/7 | chr14 | 74733836 | |||||||
| chr14:74733950 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.454-126C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 6/7 | chr14 | 74733950 | |||||||
| chr14:74733994 | G | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(151): Show |
261 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.454-82G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 6/7 | chr14 | 74733994 | |||||||
| chr14:74734034 | CTCAGTGA others(34): Show |
C | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.454-41_454-1delTCA others(38): Show |
FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 6/7 | chr14 | 74734034 | |||||||
| chr14:74734171 | G | A | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | splice_donor_variant&intron_variant | HIGH | c.548+1G>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734171 | |||||||
| chr14:74734172 | T | A | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | splice_donor_variant&intron_variant | HIGH | c.548+2T>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734172 | |||||||
| chr14:74734176 | A | T | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | splice_region_variant&intron_variant | LOW | c.548+6A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734176 | |||||||
| chr14:74734179 | T | G | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+9T>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734179 | |||||||
| chr14:74734182 | C | T | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+12C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734182 | |||||||
| chr14:74734227 | A | T | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+57A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734227 | |||||||
| chr14:74734232 | G | T | 1 | a0001c0001t0004g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.548+62G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734232 | |||||||
| chr14:74734264 | A | T | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+94A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734264 | |||||||
| chr14:74734265 | A | T | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+95A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734265 | |||||||
| chr14:74734273 | T | G | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+103T>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734273 | |||||||
| chr14:74734276 | C | A | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+106C>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734276 | |||||||
| chr14:74734288 | T | A | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+118T>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734288 | |||||||
| chr14:74734289 | A | T | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+119A>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734289 | |||||||
| chr14:74734297 | T | A | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+127T>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734297 | |||||||
| chr14:74734299 | G | T | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+129G>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734299 | |||||||
| chr14:74734300 | A | G | 1 | a0004c0006t0003g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+130A>G | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734300 | |||||||
| chr14:74734368 | TA | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.548+201delA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 74734368 | ||||||
| chr14:74734399 | T | TA | 8 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0173 others(5): Show |
9 | HG02738.hp2 HG04228.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.548+230dupA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 74734399 | ||||||
| chr14:74734413 | TA | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
9 | HG02056.hp2 HG02132.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.548+246delA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 74734413 | ||||||
| chr14:74734519 | T | TA | 53 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(50): Show |
101 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.549-350dupA | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 74734519 | ||||||
| chr14:74734542 | C | T | 1 | a0001c0001t0020g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.549-340C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734542 | |||||||
| chr14:74734645 | C | A | 1 | a0001c0001t0030g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.549-237C>A | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734645 | |||||||
| chr14:74734856 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.549-26C>T | FCF1 | ENSG00000119616.11 | transcript | ENST00000341162.8 | protein_coding | 7/7 | chr14 | 74734856 |