Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 348751 |
| ensemblid | ENSG00000226124.10 |
| hgncid | 48661 |
| symbol | FTCDNL1 |
| name | formiminotransferase cyclodeaminase N-terminal like |
| refseq_nuc | NM_001363886.2 |
| refseq_prot | NP_001350815.1 |
| ensembl_nuc | ENST00000420128.6 |
| ensembl_prot | ENSP00000457780.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 199809272 |
| end | 199851192 |
| strand | - |
| ver | v1.2 |
| region | chr2:199809272-199851192 |
| region5000 | chr2:199804272-199856192 |
| regionname0 | FTCDNL1_chr2_199809272_199851192 |
| regionname5000 | FTCDNL1_chr2_199804272_199856192 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 138 | 383 | 80 | 66 | 190 | 10 | 35 | 152 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | MSSSR others(133): Show |
chr2 | 199804272 | 199856192 |
| a0002 | 0/0 | 138 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | MSSSR others(133): Show |
chr2 | 199804272 | 199856192 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 414 | 383 | 80 | 66 | 190 | 10 | 35 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | ATGTC others(409): Show |
chr2 | 199804272 | 199856192 | ||
| a0002c0002 | 0/0 | 414 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | ATGTC others(409): Show |
chr2 | 199804272 | 199856192 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4309 | 160 | 33 | 26 | 69 | 5 | 26 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0002 | 0/0 | 4309 | 66 | 7 | 13 | 42 | 0 | 4 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0003 | 0/0 | 4309 | 52 | 7 | 8 | 35 | 1 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0004 | 0/0 | 4309 | 15 | 0 | 0 | 15 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0005 | 0/0 | 4306 | 14 | 0 | 5 | 8 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4301): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0006 | 0/0 | 4279 | 7 | 6 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4274): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0007 | 1/0 | 4310 | 7 | 3 | 0 | 2 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4305): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0008 | 0/0 | 4279 | 6 | 4 | 1 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4274): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0009 | 0/0 | 4308 | 6 | 0 | 4 | 0 | 1 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4303): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0010 | 0/0 | 4309 | 6 | 6 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0011 | 0/0 | 4308 | 6 | 1 | 5 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4303): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0012 | 0/0 | 4310 | 4 | 1 | 2 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4305): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0013 | 0/0 | 4309 | 3 | 0 | 0 | 3 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0014 | 0/0 | 4309 | 3 | 0 | 0 | 3 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0015 | 0/0 | 4310 | 3 | 3 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4305): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0016 | 0/0 | 4310 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4305): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0017 | 0/0 | 4309 | 2 | 2 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0018 | 0/0 | 4309 | 2 | 2 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0019 | 0/0 | 4279 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4274): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0020 | 0/0 | 4280 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4275): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0021 | 0/0 | 4279 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4274): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0022 | 0/0 | 4309 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0023 | 0/0 | 4309 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0024 | 0/0 | 4306 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4301): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0025 | 0/0 | 4309 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0026 | 0/0 | 4307 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4302): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0027 | 0/0 | 4310 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4305): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0028 | 0/0 | 4309 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0029 | 0/0 | 4310 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4305): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0030 | 0/0 | 4309 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0031 | 0/0 | 4308 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4303): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0032 | 0/0 | 4309 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0033 | 0/0 | 4309 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0034 | 0/0 | 4309 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0035 | 0/0 | 4309 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0036 | 0/0 | 4340 | 1 | 0 | 0 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4335): Show |
chr2 | 199804272 | 199856192 |
| a0001c0001t0037 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4394): Show |
chr2 | 199804272 | 199856192 |
| a0002c0002t0001 | 0/0 | 4309 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | GGAGC others(4304): Show |
chr2 | 199804272 | 199856192 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0005 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0041 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0006g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0007g0027 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0007g0044 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0008g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0009g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0009g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0009g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0009g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0009g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0010g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0010g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0011g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0011g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0011g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0012g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0012g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0013g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0013g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0014g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0014g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0014g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0015g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0015g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0016g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0016g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0017g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0017g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0018g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0018g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0019g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0020g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0021g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0022g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0023g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0024g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0025g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0026g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0027g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0028g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0029g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0030g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0031g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0032g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0033g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0034g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0035g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0036g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0001c0001t0037g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00140 | hp2 | a0001 | c0001 | t0036 | g0292 | EUR | GBR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0147 | EUR | FIN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0132 | EUR | FIN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0044 | EUR | FIN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00408 | hp1 | a0001 | c0001 | t0013 | g0061 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00642 | hp2 | a0001 | c0001 | t0009 | g0171 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00741 | hp1 | a0001 | c0001 | t0012 | g0156 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01069 | hp1 | a0001 | c0001 | t0011 | g0047 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0048 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01071 | hp1 | a0001 | c0001 | t0011 | g0046 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0048 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01099 | hp2 | a0001 | c0001 | t0011 | g0047 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0276 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0034 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0034 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01261 | hp2 | a0001 | c0001 | t0009 | g0191 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0046 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01358 | hp2 | a0001 | c0001 | t0032 | g0247 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01361 | hp2 | a0001 | c0001 | t0012 | g0211 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01516 | hp1 | a0001 | c0001 | t0009 | g0188 | EUR | IBS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01884 | hp2 | a0001 | c0001 | t0015 | g0124 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0226 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02040 | hp2 | a0001 | c0001 | t0022 | g0060 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02056 | hp1 | a0001 | c0001 | t0014 | g0174 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0255 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02132 | hp1 | a0001 | c0001 | t0034 | g0290 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0055 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | CDX | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | CDX | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0181 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02273 | hp1 | a0001 | c0001 | t0024 | g0146 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0278 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0152 | AMR | PEL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0074 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02451 | hp2 | a0001 | c0001 | t0018 | g0099 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0073 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02622 | hp2 | a0001 | c0001 | t0017 | g0205 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0281 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02647 | hp1 | a0001 | c0001 | t0019 | g0053 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02683 | hp2 | a0001 | c0001 | t0009 | g0134 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02717 | hp2 | a0001 | c0001 | t0033 | g0207 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0279 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0215 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0027 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0054 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0125 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03209 | hp2 | a0001 | c0001 | t0037 | g0293 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03225 | hp2 | a0001 | c0001 | t0030 | g0162 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03239 | hp1 | a0001 | c0001 | t0028 | g0075 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03239 | hp2 | a0001 | c0001 | t0012 | g0184 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0269 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0282 | AFR | ESN | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0059 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0096 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | BEB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG04115 | hp1 | a0001 | c0001 | t0025 | g0095 | SAS | STU | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | STU | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | STU | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | YRI | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18522 | hp2 | a0001 | c0001 | t0015 | g0252 | AFR | YRI | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18949 | hp1 | a0001 | c0001 | t0016 | g0145 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18957 | hp1 | a0001 | c0001 | t0021 | g0056 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18964 | hp2 | a0001 | c0001 | t0031 | g0175 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18988 | hp2 | a0001 | c0001 | t0013 | g0023 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18993 | hp2 | a0001 | c0001 | t0013 | g0023 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19063 | hp1 | a0001 | c0001 | t0008 | g0058 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19066 | hp1 | a0001 | c0001 | t0016 | g0119 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19072 | hp2 | a0001 | c0001 | t0035 | g0291 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19078 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19078 | hp2 | a0001 | c0001 | t0026 | g0105 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19080 | hp2 | a0001 | c0001 | t0029 | g0106 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19081 | hp1 | a0001 | c0001 | t0027 | g0128 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19084 | hp1 | a0001 | c0001 | t0014 | g0163 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19087 | hp1 | a0001 | c0001 | t0023 | g0076 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19088 | hp2 | a0001 | c0001 | t0014 | g0176 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19090 | hp2 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19240 | hp1 | a0001 | c0001 | t0020 | g0051 | AFR | YRI | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | GIH | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | GIH | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02486 | hp2 | a0001 | c0001 | t0018 | g0160 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | USA | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | USA | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | USA | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0159 | AFR | USA | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0067 | AFR | LWK | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0041 | REF | REF | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0027 | REF | REF | FTCDNL1_chr2_199804272_199856192 | FTCDNL1 | chr2 | 199804272 | 199856192 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:199819716 | C | T | 1 | a0002 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.253G>A | p.Val85Met | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/5 | 713/4310 | 253/417 | 85/138 | chr2 | 199819716 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:199809443 | AAAG | A | 2 | a0001c0001t0001 a0001c0001t0006 |
7 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3259_*3261delCTT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 3259 | chr2 | 199809443 | ||||||
| chr2:199809467 | T | C | 3 | a0001c0001t0014 a0001c0001t0021 a0001c0001t0031 |
5 | HG02056.hp1 NA18957.hp1 NA18964.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3238A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 3238 | chr2 | 199809467 | ||||||
| chr2:199809565 | CATT | C | 3 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0026 |
16 | HG00280.hp1 HG00408.hp2 HG01069.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3137_*3139delAAT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 3137 | chr2 | 199809565 | ||||||
| chr2:199809599 | G | T | 1 | a0001c0001t0030 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3106C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 3106 | chr2 | 199809599 | ||||||
| chr2:199809899 | AT | A | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(24): Show |
355 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*2805delA | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2805 | chr2 | 199809899 | ||||||
| chr2:199809899 | ATT | A | 2 | a0001c0001t0009 a0001c0001t0031 |
7 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805delAA | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2804 | chr2 | 199809899 | ||||||
| chr2:199810029 | T | G | 1 | a0001c0001t0032 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2676A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2676 | chr2 | 199810029 | ||||||
| chr2:199810112 | G | A | 1 | a0001c0001t0011 | 6 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2593C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2593 | chr2 | 199810112 | ||||||
| chr2:199810115 | A | G | 1 | a0001c0001t0010 | 6 | HG02258.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2590T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2590 | chr2 | 199810115 | ||||||
| chr2:199810230 | C | A | 2 | a0001c0001t0004 a0001c0001t0027 |
16 | HG00609.hp2 HG02080.hp1 HG02135.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2475G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2475 | chr2 | 199810230 | ||||||
| chr2:199810247 | C | T | 1 | a0001c0001t0025 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2458G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2458 | chr2 | 199810247 | ||||||
| chr2:199810295 | T | A | 2 | a0001c0001t0004 a0001c0001t0027 |
16 | HG00609.hp2 HG02080.hp1 HG02135.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2410A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2410 | chr2 | 199810295 | ||||||
| chr2:199810564 | C | G | 1 | a0001c0001t0028 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2141G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2141 | chr2 | 199810564 | ||||||
| chr2:199810587 | C | T | 1 | a0001c0001t0024 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2118G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2118 | chr2 | 199810587 | ||||||
| chr2:199810608 | T | G | 1 | a0001c0001t0033 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2097A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2097 | chr2 | 199810608 | ||||||
| chr2:199810614 | G | A | 1 | a0001c0001t0015 | 3 | HG01884.hp2 HG03516.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2091C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 2091 | chr2 | 199810614 | ||||||
| chr2:199810907 | C | T | 1 | a0001c0001t0016 | 2 | NA18949.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1798G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 1798 | chr2 | 199810907 | ||||||
| chr2:199811151 | A | T | 1 | a0001c0001t0017 | 2 | HG02622.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1554T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 1554 | chr2 | 199811151 | ||||||
| chr2:199811379 | T | A | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(28): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*1326A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 1326 | chr2 | 199811379 | ||||||
| chr2:199811610 | C | G | 1 | a0001c0001t0034 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1095G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 1095 | chr2 | 199811610 | ||||||
| chr2:199811770 | T | C | 1 | a0001c0001t0018 | 2 | HG02451.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*935A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 935 | chr2 | 199811770 | ||||||
| chr2:199811879 | A | G | 1 | a0001c0001t0019 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*826T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 826 | chr2 | 199811879 | ||||||
| chr2:199812203 | A | C | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(11): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*502T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 502 | chr2 | 199812203 | ||||||
| chr2:199812292 | C | A | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0037 |
5 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*413G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 413 | chr2 | 199812292 | ||||||
| chr2:199812303 | C | G | 1 | a0001c0001t0023 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 402 | chr2 | 199812303 | ||||||
| chr2:199812371 | AT | A | 1 | a0001c0001t0011 | 6 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*333delA | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 5/5 | 333 | chr2 | 199812371 | ||||||
| chr2:199850811 | G | C | 1 | a0001c0001t0034 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/5 | 1849 | chr2 | 199850811 | ||||||
| chr2:199850893 | C | T | 1 | a0001c0001t0013 | 3 | HG00408.hp1 NA18988.hp2 NA18993.hp2 |
5_prime_UTR_variant | MODIFIER | c.-161G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/5 | 1931 | chr2 | 199850893 | ||||||
| chr2:199851060 | A | G | 1 | a0001c0001t0022 | 1 | HG02040.hp2 | 5_prime_UTR_variant | MODIFIER | c.-328T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/5 | 2098 | chr2 | 199851060 | ||||||
| chr2:199851107 | G | C | 1 | a0001c0001t0035 | 1 | NA19072.hp2 | 5_prime_UTR_variant | MODIFIER | c.-375C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/5 | 2145 | chr2 | 199851107 | ||||||
| chr2:199851119 | T | TCGCCGCC others(23): Show |
1 | a0001c0001t0036 | 1 | HG00140.hp2 | 5_prime_UTR_variant | MODIFIER | c.-417_-388dupGAGGCT others(24): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/5 | 2158 | chr2 | 199851119 | ||||||
| chr2:199851119 | T | TCGCCGCC others(83): Show |
1 | a0001c0001t0037 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-388_-387insGAGGCT others(84): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/5 | 2158 | chr2 | 199851119 | ||||||
| chr2:199851119 | TCGCCGCC others(23): Show |
T | 5 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0019 others(2): Show |
16 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-417_-388delGAGGCT others(24): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/5 | 2158 | chr2 | 199851119 | ||||||
| chr2:199851133 | G | A | 1 | a0001c0001t0001 | 2 | HG03453.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-401C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/5 | 2171 | chr2 | 199851133 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:199812815 | C | A | 1 | a0001c0001t0002g0249 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.398-91G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199812815 | |||||||
| chr2:199812902 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.398-178G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199812902 | |||||||
| chr2:199812917 | G | A | 1 | a0001c0001t0018g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.398-193C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199812917 | |||||||
| chr2:199812940 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.398-216A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199812940 | |||||||
| chr2:199813049 | C | G | 9 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0101 others(6): Show |
15 | HG00621.hp1 HG01361.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.398-325G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813049 | |||||||
| chr2:199813068 | T | C | 1 | a0001c0001t0030g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.398-344A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813068 | |||||||
| chr2:199813395 | CT | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.398-672delA | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813395 | |||||||
| chr2:199813641 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0010g0278 |
2 | HG01074.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.398-917C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813641 | |||||||
| chr2:199813688 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.398-964C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813688 | |||||||
| chr2:199813711 | G | C | 74 | a0001c0001t0002g0011 a0001c0001t0002g0015 a0001c0001t0002g0020 others(71): Show |
90 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.398-987C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813711 | |||||||
| chr2:199813748 | T | A | 8 | a0001c0001t0001g0250 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
9 | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.398-1024A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813748 | |||||||
| chr2:199813912 | C | CA | 34 | a0001c0001t0002g0045 a0001c0001t0002g0108 a0001c0001t0002g0111 others(31): Show |
38 | HG00597.hp2 HG00621.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.398-1189dupT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813912 | |||||||
| chr2:199813912 | C | CAA | 6 | a0001c0001t0002g0224 a0001c0001t0002g0264 a0001c0001t0002g0273 others(3): Show |
7 | HG01069.hp1 HG01099.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-1190_398-1189d others(4): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813912 | |||||||
| chr2:199813912 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0002g0110 a0001c0001t0002g0123 a0001c0001t0002g0244 others(3): Show |
6 | HG02080.hp2 HG02717.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-1197_398-1189d others(11): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813912 | |||||||
| chr2:199813912 | CAAAAAAA others(3): Show |
C | 28 | a0001c0001t0002g0011 a0001c0001t0002g0021 a0001c0001t0002g0039 others(25): Show |
35 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.398-1198_398-1189d others(12): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813912 | |||||||
| chr2:199813912 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.398-1201_398-1189d others(15): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813912 | |||||||
| chr2:199813912 | CAAAAAAA others(7): Show |
C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.398-1202_398-1189d others(16): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813912 | |||||||
| chr2:199813912 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0004g0130 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.398-1203_398-1189d others(17): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813912 | |||||||
| chr2:199813944 | T | A | 34 | a0001c0001t0002g0015 a0001c0001t0002g0020 a0001c0001t0002g0032 others(31): Show |
39 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.398-1220A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199813944 | |||||||
| chr2:199814401 | T | C | 4 | a0001c0001t0011g0046 a0001c0001t0011g0047 a0001c0001t0011g0067 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-1677A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199814401 | |||||||
| chr2:199814435 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.398-1711G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199814435 | |||||||
| chr2:199814606 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.398-1882T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199814606 | |||||||
| chr2:199814778 | T | C | 1 | a0001c0001t0002g0078 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.398-2054A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199814778 | |||||||
| chr2:199814911 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.398-2187C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199814911 | |||||||
| chr2:199815113 | G | GGATTTTA others(6): Show |
1 | a0001c0001t0003g0079 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.398-2402_398-2390d others(15): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199815113 | |||||||
| chr2:199815237 | T | C | 4 | a0001c0001t0002g0112 a0001c0001t0002g0116 a0001c0001t0002g0150 others(1): Show |
4 | HG01978.hp1 HG01993.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-2513A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199815237 | |||||||
| chr2:199815425 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.398-2701C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199815425 | |||||||
| chr2:199815430 | C | T | 1 | a0001c0001t0037g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.398-2706G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199815430 | |||||||
| chr2:199815431 | G | A | 11 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0029 others(8): Show |
17 | NA18941.hp1 NA18942.hp2 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.398-2707C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199815431 | |||||||
| chr2:199815636 | A | G | 40 | a0001c0001t0002g0015 a0001c0001t0002g0020 a0001c0001t0002g0032 others(37): Show |
49 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.398-2912T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199815636 | |||||||
| chr2:199815757 | T | G | 1 | a0001c0001t0002g0020 | 3 | NA18947.hp2 NA18971.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.398-3033A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199815757 | |||||||
| chr2:199815818 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.398-3094C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199815818 | |||||||
| chr2:199815835 | A | G | 33 | a0001c0001t0002g0011 a0001c0001t0002g0021 a0001c0001t0002g0039 others(30): Show |
40 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.398-3111T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199815835 | |||||||
| chr2:199816006 | A | AAAAG | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.398-3286_398-3283d others(6): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199816006 | |||||||
| chr2:199816276 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.397+3296G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199816276 | |||||||
| chr2:199816317 | C | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.397+3255G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199816317 | |||||||
| chr2:199816325 | G | A | 1 | a0001c0001t0005g0147 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.397+3247C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199816325 | |||||||
| chr2:199816338 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.397+3234A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199816338 | |||||||
| chr2:199816374 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.397+3198A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199816374 | |||||||
| chr2:199816431 | T | C | 1 | a0001c0001t0015g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.397+3141A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199816431 | |||||||
| chr2:199816574 | T | G | 13 | a0001c0001t0001g0109 a0001c0001t0005g0013 a0001c0001t0005g0034 others(10): Show |
16 | HG00280.hp1 HG00408.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.397+2998A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199816574 | |||||||
| chr2:199816823 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.397+2749C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199816823 | |||||||
| chr2:199816936 | A | G | 3 | a0001c0001t0015g0124 a0001c0001t0015g0252 a0001c0001t0015g0282 |
3 | HG01884.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.397+2636T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199816936 | |||||||
| chr2:199817030 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(158): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.397+2542G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199817030 | |||||||
| chr2:199817101 | T | C | 1 | a0001c0001t0037g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.397+2471A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199817101 | |||||||
| chr2:199817107 | T | C | 74 | a0001c0001t0002g0011 a0001c0001t0002g0015 a0001c0001t0002g0020 others(71): Show |
90 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.397+2465A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199817107 | |||||||
| chr2:199817425 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0035 others(3): Show |
16 | NA18953.hp1 NA18955.hp1 NA18956.hp2 others(13): Show |
intron_variant | MODIFIER | c.397+2147C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199817425 | |||||||
| chr2:199817437 | G | C | 1 | a0001c0001t0018g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.397+2135C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199817437 | |||||||
| chr2:199817515 | G | T | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.397+2057C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199817515 | |||||||
| chr2:199817589 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0169 a0001c0001t0001g0251 |
4 | HG02723.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1983T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199817589 | |||||||
| chr2:199817743 | CA | C | 7 | a0001c0001t0001g0231 a0001c0001t0002g0045 a0001c0001t0002g0272 others(4): Show |
11 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+1828delT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199817743 | |||||||
| chr2:199817920 | C | A | 1 | a0001c0001t0001g0284 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.397+1652G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199817920 | |||||||
| chr2:199817945 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.397+1627T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199817945 | |||||||
| chr2:199818175 | C | A | 8 | a0001c0001t0001g0250 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
9 | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+1397G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199818175 | |||||||
| chr2:199818175 | C | T | 6 | a0001c0001t0001g0187 a0001c0001t0001g0212 a0001c0001t0009g0048 others(3): Show |
7 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+1397G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199818175 | |||||||
| chr2:199818201 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.397+1371T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199818201 | |||||||
| chr2:199818489 | C | T | 4 | a0001c0001t0017g0205 a0001c0001t0017g0269 a0001c0001t0018g0099 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1083G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199818489 | |||||||
| chr2:199818596 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.397+976C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199818596 | |||||||
| chr2:199818608 | T | A | 1 | a0001c0001t0001g0236 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.397+964A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199818608 | |||||||
| chr2:199818920 | C | G | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.397+652G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199818920 | |||||||
| chr2:199819043 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.397+529G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199819043 | |||||||
| chr2:199819103 | A | T | 1 | a0001c0001t0035g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.397+469T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199819103 | |||||||
| chr2:199819152 | G | T | 1 | a0001c0001t0001g0242 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.397+420C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199819152 | |||||||
| chr2:199819155 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.397+417A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199819155 | |||||||
| chr2:199819209 | A | G | 1 | a0001c0001t0037g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.397+363T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199819209 | |||||||
| chr2:199819239 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.397+333G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199819239 | |||||||
| chr2:199819526 | T | TA | 10 | a0001c0001t0001g0068 a0001c0001t0002g0196 a0001c0001t0004g0130 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+45dupT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 4/4 | chr2 | 199819526 | |||||||
| chr2:199819981 | G | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.212-224C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199819981 | |||||||
| chr2:199820044 | A | T | 1 | a0001c0001t0037g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.212-287T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199820044 | |||||||
| chr2:199820057 | T | A | 1 | a0001c0001t0002g0121 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.212-300A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199820057 | |||||||
| chr2:199820146 | T | A | 2 | a0001c0001t0003g0010 a0001c0001t0003g0085 |
5 | NA18942.hp2 NA18952.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-389A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199820146 | |||||||
| chr2:199820415 | G | A | 3 | a0001c0001t0015g0124 a0001c0001t0015g0252 a0001c0001t0015g0282 |
3 | HG01884.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.212-658C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199820415 | |||||||
| chr2:199820417 | A | T | 4 | a0001c0001t0017g0205 a0001c0001t0017g0269 a0001c0001t0018g0099 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-660T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199820417 | |||||||
| chr2:199820661 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.212-904T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199820661 | |||||||
| chr2:199820910 | G | A | 28 | a0001c0001t0002g0015 a0001c0001t0002g0020 a0001c0001t0002g0032 others(25): Show |
33 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.212-1153C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199820910 | |||||||
| chr2:199820934 | G | A | 1 | a0001c0001t0010g0159 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.212-1177C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199820934 | |||||||
| chr2:199820940 | C | T | 1 | a0001c0001t0018g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.212-1183G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199820940 | |||||||
| chr2:199821180 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.212-1423G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199821180 | |||||||
| chr2:199821277 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.212-1520C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199821277 | |||||||
| chr2:199821316 | A | AT | 11 | a0001c0001t0002g0045 a0001c0001t0002g0123 a0001c0001t0002g0150 others(8): Show |
15 | HG00597.hp1 HG01109.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-1560dupA | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199821316 | |||||||
| chr2:199821316 | AT | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.212-1560delA | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199821316 | |||||||
| chr2:199821336 | T | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
266 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.212-1579A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199821336 | |||||||
| chr2:199821489 | G | A | 3 | a0001c0001t0003g0062 a0001c0001t0003g0064 a0001c0001t0003g0065 |
3 | HG02976.hp1 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.212-1732C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199821489 | |||||||
| chr2:199821665 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.212-1908C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199821665 | |||||||
| chr2:199822013 | C | T | 1 | a0001c0001t0010g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.212-2256G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822013 | |||||||
| chr2:199822044 | C | G | 1 | a0001c0001t0001g0286 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.212-2287G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822044 | |||||||
| chr2:199822113 | A | T | 1 | a0001c0001t0003g0026 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.212-2356T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822113 | |||||||
| chr2:199822181 | T | C | 1 | a0001c0001t0005g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.212-2424A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822181 | |||||||
| chr2:199822294 | C | T | 1 | a0001c0001t0017g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.212-2537G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822294 | |||||||
| chr2:199822314 | G | A | 1 | a0001c0001t0035g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.212-2557C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822314 | |||||||
| chr2:199822481 | G | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.212-2724C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822481 | |||||||
| chr2:199822525 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.212-2768G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822525 | |||||||
| chr2:199822580 | T | C | 1 | a0001c0001t0005g0104 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.212-2823A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822580 | |||||||
| chr2:199822605 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.212-2848C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822605 | |||||||
| chr2:199822651 | G | A | 40 | a0001c0001t0002g0015 a0001c0001t0002g0020 a0001c0001t0002g0032 others(37): Show |
49 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.212-2894C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199822651 | |||||||
| chr2:199823168 | G | A | 4 | a0001c0001t0011g0046 a0001c0001t0011g0047 a0001c0001t0011g0067 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-3411C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199823168 | |||||||
| chr2:199823221 | C | A | 1 | a0001c0001t0001g0204 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.212-3464G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199823221 | |||||||
| chr2:199823231 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.212-3474A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199823231 | |||||||
| chr2:199823337 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.212-3580G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199823337 | |||||||
| chr2:199823413 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.212-3656C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199823413 | |||||||
| chr2:199823554 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0204 a0001c0001t0001g0228 others(1): Show |
6 | NA18946.hp1 NA18960.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-3797A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199823554 | |||||||
| chr2:199823598 | T | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0035 others(4): Show |
17 | HG00609.hp1 NA18953.hp1 NA18955.hp1 others(14): Show |
intron_variant | MODIFIER | c.212-3841A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199823598 | |||||||
| chr2:199823725 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.212-3968A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199823725 | |||||||
| chr2:199823931 | G | A | 2 | a0001c0001t0003g0010 a0001c0001t0003g0085 |
5 | NA18942.hp2 NA18952.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-4174C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199823931 | |||||||
| chr2:199824013 | C | A | 1 | a0001c0001t0017g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.212-4256G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824013 | |||||||
| chr2:199824132 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.212-4375A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824132 | |||||||
| chr2:199824310 | T | C | 1 | a0001c0001t0026g0105 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.212-4553A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824310 | |||||||
| chr2:199824337 | G | C | 12 | a0001c0001t0004g0006 a0001c0001t0004g0070 a0001c0001t0004g0122 others(9): Show |
16 | HG00609.hp2 HG02080.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.212-4580C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824337 | |||||||
| chr2:199824417 | T | C | 1 | a0001c0001t0002g0078 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.212-4660A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824417 | |||||||
| chr2:199824540 | T | C | 1 | a0001c0001t0002g0230 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.212-4783A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824540 | |||||||
| chr2:199824624 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.212-4867A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824624 | |||||||
| chr2:199824664 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.212-4907C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824664 | |||||||
| chr2:199824674 | C | T | 3 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0019g0053 |
3 | HG02647.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.212-4917G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824674 | |||||||
| chr2:199824775 | T | A | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.212-5018A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824775 | |||||||
| chr2:199824829 | G | A | 3 | a0001c0001t0015g0124 a0001c0001t0015g0252 a0001c0001t0015g0282 |
3 | HG01884.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.212-5072C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824829 | |||||||
| chr2:199824832 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(158): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.212-5075C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199824832 | |||||||
| chr2:199825088 | T | A | 1 | a0001c0001t0005g0152 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.212-5331A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199825088 | |||||||
| chr2:199825129 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.212-5372G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199825129 | |||||||
| chr2:199825137 | C | CA | 7 | a0001c0001t0002g0179 a0001c0001t0011g0046 a0001c0001t0011g0047 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.212-5381dupT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199825137 | |||||||
| chr2:199825247 | G | T | 1 | a0001c0001t0002g0078 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.212-5490C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199825247 | |||||||
| chr2:199825281 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.212-5524T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199825281 | |||||||
| chr2:199825287 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.212-5530C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199825287 | |||||||
| chr2:199825379 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.212-5622G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199825379 | |||||||
| chr2:199825620 | T | C | 1 | a0001c0001t0018g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.212-5863A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199825620 | |||||||
| chr2:199825706 | GCTTCCTA others(4): Show |
G | 40 | a0001c0001t0002g0015 a0001c0001t0002g0020 a0001c0001t0002g0032 others(37): Show |
49 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.212-5960_212-5950d others(13): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199825706 | |||||||
| chr2:199825967 | T | TCACATGT others(6): Show |
9 | a0001c0001t0001g0042 a0001c0001t0001g0118 a0001c0001t0001g0189 others(6): Show |
10 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-6223_212-6211d others(15): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199825967 | |||||||
| chr2:199826048 | C | T | 33 | a0001c0001t0002g0011 a0001c0001t0002g0021 a0001c0001t0002g0039 others(30): Show |
40 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.212-6291G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826048 | |||||||
| chr2:199826216 | C | A | 4 | a0001c0001t0011g0046 a0001c0001t0011g0047 a0001c0001t0011g0067 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-6459G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826216 | |||||||
| chr2:199826368 | G | C | 1 | a0001c0001t0017g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.212-6611C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826368 | |||||||
| chr2:199826433 | G | GA | 78 | a0001c0001t0002g0011 a0001c0001t0002g0015 a0001c0001t0002g0020 others(75): Show |
96 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.212-6677dupT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826433 | |||||||
| chr2:199826482 | C | A | 1 | a0001c0001t0008g0009 | 4 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-6725G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826482 | |||||||
| chr2:199826488 | CA | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.212-6732delT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826488 | |||||||
| chr2:199826488 | CAA | C | 80 | a0001c0001t0001g0233 a0001c0001t0001g0267 a0001c0001t0002g0011 others(77): Show |
98 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.212-6733_212-6732d others(4): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826488 | |||||||
| chr2:199826500 | A | G | 1 | a0001c0001t0003g0079 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.212-6743T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826500 | |||||||
| chr2:199826663 | C | T | 1 | a0001c0001t0010g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.212-6906G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826663 | |||||||
| chr2:199826905 | C | A | 1 | a0001c0001t0017g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.212-7148G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826905 | |||||||
| chr2:199826949 | A | T | 1 | a0001c0001t0008g0058 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.212-7192T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826949 | |||||||
| chr2:199826970 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(81): Show |
120 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.212-7213A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199826970 | |||||||
| chr2:199827129 | A | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.212-7372T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199827129 | |||||||
| chr2:199827210 | G | A | 1 | a0001c0001t0003g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.212-7453C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199827210 | |||||||
| chr2:199827278 | T | A | 1 | a0001c0001t0018g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.212-7521A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199827278 | |||||||
| chr2:199827390 | G | T | 3 | a0001c0001t0015g0124 a0001c0001t0015g0252 a0001c0001t0015g0282 |
3 | HG01884.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.212-7633C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199827390 | |||||||
| chr2:199827436 | G | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.212-7679C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199827436 | |||||||
| chr2:199827872 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.212-8115G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199827872 | |||||||
| chr2:199828088 | C | T | 1 | a0001c0001t0001g0017 | 3 | NA18953.hp2 NA18998.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.212-8331G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199828088 | |||||||
| chr2:199828096 | CAAGGGCC others(6): Show |
C | 34 | a0001c0001t0002g0015 a0001c0001t0002g0020 a0001c0001t0002g0032 others(31): Show |
39 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.212-8352_212-8340d others(15): Show |
FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199828096 | |||||||
| chr2:199828704 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.212-8947A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199828704 | |||||||
| chr2:199828786 | AC | A | 5 | a0001c0001t0005g0013 a0001c0001t0005g0104 a0001c0001t0005g0107 others(2): Show |
7 | NA18939.hp2 NA18962.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-9030delG | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199828786 | |||||||
| chr2:199828846 | T | C | 6 | a0001c0001t0002g0045 a0001c0001t0002g0272 a0001c0001t0002g0273 others(3): Show |
10 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-9089A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199828846 | |||||||
| chr2:199828862 | G | A | 1 | a0001c0001t0003g0088 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.212-9105C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199828862 | |||||||
| chr2:199828891 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.212-9134G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199828891 | |||||||
| chr2:199828945 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.212-9188A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199828945 | |||||||
| chr2:199828997 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(243): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.212-9240T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199828997 | |||||||
| chr2:199829057 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.212-9300G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199829057 | |||||||
| chr2:199829131 | G | A | 33 | a0001c0001t0002g0011 a0001c0001t0002g0021 a0001c0001t0002g0039 others(30): Show |
40 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.212-9374C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199829131 | |||||||
| chr2:199829131 | GC | G | 4 | a0001c0001t0017g0205 a0001c0001t0017g0269 a0001c0001t0018g0099 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-9375delG | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199829131 | |||||||
| chr2:199829227 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.212-9470C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199829227 | |||||||
| chr2:199829478 | A | C | 2 | a0001c0001t0018g0099 a0001c0001t0018g0160 |
2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.212-9721T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199829478 | |||||||
| chr2:199829899 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-10142G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199829899 | |||||||
| chr2:199829946 | A | C | 1 | a0001c0001t0003g0071 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.212-10189T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199829946 | |||||||
| chr2:199830055 | G | C | 35 | a0001c0001t0002g0015 a0001c0001t0002g0020 a0001c0001t0002g0032 others(32): Show |
40 | HG00673.hp1 HG00673.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.212-10298C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830055 | |||||||
| chr2:199830072 | T | C | 1 | a0001c0001t0004g0127 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.212-10315A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830072 | |||||||
| chr2:199830269 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0242 a0001c0001t0025g0095 |
3 | HG01074.hp1 HG02083.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.212-10512A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830269 | |||||||
| chr2:199830301 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.212-10544C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830301 | |||||||
| chr2:199830628 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-10871C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830628 | |||||||
| chr2:199830661 | C | A | 1 | a0001c0001t0002g0123 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.212-10904G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830661 | |||||||
| chr2:199830704 | G | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0078 a0001c0001t0002g0121 others(3): Show |
8 | HG02040.hp1 HG02080.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-10947C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830704 | |||||||
| chr2:199830715 | T | C | 1 | a0001c0001t0002g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.212-10958A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830715 | |||||||
| chr2:199830717 | C | T | 1 | a0001c0001t0002g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.212-10960G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830717 | |||||||
| chr2:199830718 | T | C | 1 | a0001c0001t0002g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.212-10961A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830718 | |||||||
| chr2:199830767 | C | T | 1 | a0001c0001t0010g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.212-11010G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830767 | |||||||
| chr2:199830801 | A | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.212-11044T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830801 | |||||||
| chr2:199830855 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.212-11098C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199830855 | |||||||
| chr2:199831020 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0277 |
2 | HG02293.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.212-11263A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831020 | |||||||
| chr2:199831085 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.212-11328G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831085 | |||||||
| chr2:199831178 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.212-11421C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831178 | |||||||
| chr2:199831245 | C | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0230 a0001c0001t0008g0058 |
5 | NA18941.hp2 NA18947.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-11488G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831245 | |||||||
| chr2:199831629 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.212-11872A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831629 | |||||||
| chr2:199831646 | G | A | 83 | a0001c0001t0002g0011 a0001c0001t0002g0015 a0001c0001t0002g0020 others(80): Show |
101 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.212-11889C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831646 | |||||||
| chr2:199831656 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.212-11899C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831656 | |||||||
| chr2:199831664 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.212-11907C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831664 | |||||||
| chr2:199831723 | T | C | 80 | a0001c0001t0001g0153 a0001c0001t0002g0011 a0001c0001t0002g0015 others(77): Show |
98 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.212-11966A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831723 | |||||||
| chr2:199831758 | T | C | 1 | a0001c0001t0009g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.212-12001A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831758 | |||||||
| chr2:199831938 | C | G | 20 | a0001c0001t0003g0010 a0001c0001t0003g0012 a0001c0001t0003g0024 others(17): Show |
27 | HG01192.hp2 HG01346.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.212-12181G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199831938 | |||||||
| chr2:199832008 | A | T | 1 | a0001c0001t0002g0178 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.212-12251T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832008 | |||||||
| chr2:199832229 | T | C | 1 | a0001c0001t0018g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.212-12472A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832229 | |||||||
| chr2:199832335 | A | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.212-12578T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832335 | |||||||
| chr2:199832422 | A | T | 1 | a0001c0001t0003g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.212-12665T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832422 | |||||||
| chr2:199832523 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.212-12766C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832523 | |||||||
| chr2:199832807 | T | C | 4 | a0001c0001t0011g0046 a0001c0001t0011g0047 a0001c0001t0011g0067 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-13050A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832807 | |||||||
| chr2:199832816 | A | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.212-13059T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832816 | |||||||
| chr2:199832915 | A | C | 1 | a0001c0001t0012g0211 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.212-13158T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832915 | |||||||
| chr2:199832948 | A | G | 1 | a0001c0001t0037g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211+13127T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832948 | |||||||
| chr2:199832950 | T | G | 2 | a0001c0001t0017g0205 a0001c0001t0017g0269 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211+13125A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832950 | |||||||
| chr2:199832970 | AT | A | 9 | a0001c0001t0001g0098 a0001c0001t0001g0154 a0001c0001t0001g0204 others(6): Show |
9 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+13104delA | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199832970 | |||||||
| chr2:199833224 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
111 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.211+12851C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199833224 | |||||||
| chr2:199833441 | G | A | 1 | a0001c0001t0005g0147 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.211+12634C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199833441 | |||||||
| chr2:199833887 | A | G | 37 | a0001c0001t0001g0036 a0001c0001t0002g0015 a0001c0001t0002g0020 others(34): Show |
43 | HG00673.hp1 HG00673.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.211+12188T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199833887 | |||||||
| chr2:199834368 | C | G | 31 | a0001c0001t0002g0011 a0001c0001t0002g0021 a0001c0001t0002g0039 others(28): Show |
38 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.211+11707G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199834368 | |||||||
| chr2:199834394 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211+11681G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199834394 | |||||||
| chr2:199834563 | C | T | 1 | a0001c0001t0037g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211+11512G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199834563 | |||||||
| chr2:199834718 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.211+11357G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199834718 | |||||||
| chr2:199834734 | C | T | 1 | a0001c0001t0012g0215 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.211+11341G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199834734 | |||||||
| chr2:199834806 | T | C | 6 | a0001c0001t0002g0045 a0001c0001t0002g0272 a0001c0001t0002g0273 others(3): Show |
10 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+11269A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199834806 | |||||||
| chr2:199834825 | C | T | 1 | a0001c0001t0017g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.211+11250G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199834825 | |||||||
| chr2:199834878 | G | A | 1 | a0001c0001t0003g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.211+11197C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199834878 | |||||||
| chr2:199834880 | T | C | 4 | a0001c0001t0015g0124 a0001c0001t0015g0252 a0001c0001t0015g0282 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+11195A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199834880 | |||||||
| chr2:199834895 | G | A | 1 | a0001c0001t0037g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211+11180C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199834895 | |||||||
| chr2:199835010 | C | CA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0101 others(9): Show |
18 | HG00621.hp1 HG01361.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.211+11064dupT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835010 | |||||||
| chr2:199835104 | G | A | 3 | a0001c0001t0011g0046 a0001c0001t0011g0047 a0001c0001t0011g0276 |
5 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+10971C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835104 | |||||||
| chr2:199835183 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.211+10892T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835183 | |||||||
| chr2:199835229 | A | G | 5 | a0001c0001t0005g0275 a0001c0001t0011g0046 a0001c0001t0011g0047 others(2): Show |
7 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+10846T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835229 | |||||||
| chr2:199835324 | T | G | 1 | a0001c0001t0002g0114 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.211+10751A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835324 | |||||||
| chr2:199835363 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.211+10712T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835363 | |||||||
| chr2:199835434 | A | C | 1 | a0001c0001t0017g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.211+10641T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835434 | |||||||
| chr2:199835527 | T | C | 4 | a0001c0001t0005g0275 a0001c0001t0011g0046 a0001c0001t0011g0047 others(1): Show |
6 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.211+10548A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835527 | |||||||
| chr2:199835631 | G | T | 1 | a0001c0001t0002g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.211+10444C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835631 | |||||||
| chr2:199835887 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.211+10188A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835887 | |||||||
| chr2:199835962 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(129): Show |
168 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.211+10113A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199835962 | |||||||
| chr2:199836277 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.211+9798T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199836277 | |||||||
| chr2:199836499 | T | G | 2 | a0001c0001t0001g0250 a0001c0001t0017g0205 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.211+9576A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199836499 | |||||||
| chr2:199836527 | G | A | 3 | a0001c0001t0010g0125 a0001c0001t0030g0162 a0001c0001t0037g0293 |
3 | HG02976.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.211+9548C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199836527 | |||||||
| chr2:199836603 | C | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0097 a0001c0001t0001g0172 others(3): Show |
7 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+9472G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199836603 | |||||||
| chr2:199836643 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.211+9432C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199836643 | |||||||
| chr2:199836722 | T | C | 1 | a0001c0001t0015g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.211+9353A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199836722 | |||||||
| chr2:199836724 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.211+9351G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199836724 | |||||||
| chr2:199836892 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.211+9183T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199836892 | |||||||
| chr2:199836949 | G | A | 1 | a0001c0001t0009g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.211+9126C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199836949 | |||||||
| chr2:199837029 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.211+9046G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837029 | |||||||
| chr2:199837042 | T | C | 2 | a0001c0001t0002g0102 a0001c0001t0005g0107 |
2 | NA18962.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.211+9033A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837042 | |||||||
| chr2:199837065 | A | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(116): Show |
159 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.211+9010T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837065 | |||||||
| chr2:199837226 | C | G | 1 | a0001c0001t0003g0266 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.211+8849G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837226 | |||||||
| chr2:199837243 | T | C | 1 | a0001c0001t0004g0127 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.211+8832A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837243 | |||||||
| chr2:199837244 | AT | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0113 a0001c0001t0002g0114 |
5 | NA18949.hp2 NA18955.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+8830delA | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837244 | |||||||
| chr2:199837307 | T | A | 23 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0117 others(20): Show |
28 | HG00673.hp1 HG00673.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.211+8768A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837307 | |||||||
| chr2:199837443 | T | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0287 |
2 | HG02723.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.211+8632A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837443 | |||||||
| chr2:199837699 | A | T | 1 | a0001c0001t0011g0276 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.211+8376T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837699 | |||||||
| chr2:199837730 | T | A | 1 | a0001c0001t0002g0241 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.211+8345A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837730 | |||||||
| chr2:199837731 | A | T | 3 | a0001c0001t0016g0119 a0001c0001t0017g0269 a0001c0001t0018g0099 |
3 | HG02451.hp2 HG03486.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.211+8344T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837731 | |||||||
| chr2:199837788 | C | T | 2 | a0001c0001t0003g0024 a0001c0001t0035g0291 |
3 | NA18961.hp2 NA18979.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.211+8287G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837788 | |||||||
| chr2:199837860 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.211+8215A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837860 | |||||||
| chr2:199837862 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.211+8213T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199837862 | |||||||
| chr2:199838162 | G | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(71): Show |
97 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.211+7913C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199838162 | |||||||
| chr2:199838164 | A | G | 21 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0117 others(18): Show |
26 | HG00673.hp1 HG00673.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.211+7911T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199838164 | |||||||
| chr2:199838763 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.211+7312C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199838763 | |||||||
| chr2:199838788 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.211+7287C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199838788 | |||||||
| chr2:199838940 | C | T | 1 | a0001c0001t0003g0012 | 3 | NA18964.hp1 NA19067.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.211+7135G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199838940 | |||||||
| chr2:199839161 | TA | T | 10 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0045 others(7): Show |
14 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.211+6913delT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199839161 | |||||||
| chr2:199839224 | G | A | 4 | a0001c0001t0003g0028 a0001c0001t0003g0079 a0001c0001t0003g0080 others(1): Show |
5 | HG00621.hp2 NA18950.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+6851C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199839224 | |||||||
| chr2:199839255 | T | A | 1 | a0001c0001t0033g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.211+6820A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199839255 | |||||||
| chr2:199839345 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.211+6730A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199839345 | |||||||
| chr2:199839364 | T | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(40): Show |
60 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.211+6711A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199839364 | |||||||
| chr2:199839408 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.211+6667A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199839408 | |||||||
| chr2:199839944 | A | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG03098.hp1 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.211+6131T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199839944 | |||||||
| chr2:199839959 | A | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): Show |
157 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.211+6116T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199839959 | |||||||
| chr2:199840577 | A | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0015g0252 |
3 | HG01243.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.211+5498T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199840577 | |||||||
| chr2:199840585 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0120 others(11): Show |
19 | HG00735.hp1 HG01192.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.211+5490C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199840585 | |||||||
| chr2:199840679 | T | C | 1 | a0001c0001t0015g0252 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211+5396A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199840679 | |||||||
| chr2:199840709 | G | C | 2 | a0001c0001t0017g0269 a0001c0001t0018g0099 |
2 | HG02451.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211+5366C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199840709 | |||||||
| chr2:199840752 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.211+5323T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199840752 | |||||||
| chr2:199840900 | C | A | 132 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.211+5175G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199840900 | |||||||
| chr2:199840976 | C | A | 1 | a0001c0001t0001g0243 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.211+5099G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199840976 | |||||||
| chr2:199841050 | C | G | 22 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0117 others(19): Show |
27 | HG00673.hp2 HG00738.hp1 HG01993.hp1 others(24): Show |
intron_variant | MODIFIER | c.211+5025G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199841050 | |||||||
| chr2:199841213 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.211+4862A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199841213 | |||||||
| chr2:199841305 | T | C | 1 | a0001c0001t0018g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.211+4770A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199841305 | |||||||
| chr2:199841319 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.211+4756C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199841319 | |||||||
| chr2:199841417 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0217 a0001c0001t0001g0219 others(8): Show |
19 | HG00544.hp1 HG00609.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.211+4658T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199841417 | |||||||
| chr2:199841509 | T | A | 13 | a0001c0001t0002g0082 a0001c0001t0003g0010 a0001c0001t0003g0012 others(10): Show |
19 | NA18612.hp2 NA18941.hp1 NA18942.hp2 others(16): Show |
intron_variant | MODIFIER | c.211+4566A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199841509 | |||||||
| chr2:199841705 | C | T | 27 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0117 others(24): Show |
33 | HG00673.hp1 HG00673.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.211+4370G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199841705 | |||||||
| chr2:199842079 | C | T | 1 | a0001c0001t0011g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211+3996G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842079 | |||||||
| chr2:199842104 | C | CA | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(37): Show |
56 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.211+3970dupT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842104 | |||||||
| chr2:199842115 | A | C | 28 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0117 others(25): Show |
34 | HG00673.hp1 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.211+3960T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842115 | |||||||
| chr2:199842247 | G | A | 3 | a0001c0001t0006g0022 a0001c0001t0006g0050 a0001c0001t0006g0055 |
4 | HG02145.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+3828C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842247 | |||||||
| chr2:199842272 | A | C | 4 | a0001c0001t0001g0063 a0001c0001t0003g0062 a0001c0001t0003g0064 others(1): Show |
4 | HG02109.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+3803T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842272 | |||||||
| chr2:199842276 | T | A | 1 | a0001c0001t0003g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.211+3799A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842276 | |||||||
| chr2:199842297 | AT | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0097 a0001c0001t0001g0209 |
4 | HG02572.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+3777delA | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842297 | |||||||
| chr2:199842613 | A | T | 1 | a0001c0001t0017g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.211+3462T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842613 | |||||||
| chr2:199842741 | C | T | 2 | a0001c0001t0017g0269 a0001c0001t0018g0099 |
2 | HG02451.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211+3334G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842741 | |||||||
| chr2:199842883 | G | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0117 others(18): Show |
26 | HG00673.hp2 HG00738.hp1 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.211+3192C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842883 | |||||||
| chr2:199842928 | C | T | 4 | a0001c0001t0001g0140 a0001c0001t0002g0139 a0001c0001t0003g0137 others(1): Show |
4 | HG00642.hp1 HG02273.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+3147G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842928 | |||||||
| chr2:199842938 | C | CA | 58 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0019 others(55): Show |
76 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.211+3136dupT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842938 | |||||||
| chr2:199842938 | CA | C | 9 | a0001c0001t0001g0063 a0001c0001t0003g0062 a0001c0001t0003g0064 others(6): Show |
10 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+3136delT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842938 | |||||||
| chr2:199842955 | C | A | 1 | a0001c0001t0004g0131 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.211+3120G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842955 | |||||||
| chr2:199842956 | T | C | 1 | a0001c0001t0004g0131 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.211+3119A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842956 | |||||||
| chr2:199842958 | A | T | 1 | a0001c0001t0004g0131 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.211+3117T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199842958 | |||||||
| chr2:199843952 | GA | G | 138 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.211+2122delT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199843952 | |||||||
| chr2:199844157 | T | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0041 others(44): Show |
62 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.211+1918A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199844157 | |||||||
| chr2:199844159 | A | AT | 27 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0117 others(24): Show |
32 | HG00673.hp1 HG00673.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.211+1915dupA | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199844159 | |||||||
| chr2:199844376 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(68): Show |
96 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.211+1699A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199844376 | |||||||
| chr2:199844688 | C | T | 1 | a0001c0001t0014g0163 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.211+1387G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199844688 | |||||||
| chr2:199844883 | T | C | 6 | a0001c0001t0002g0045 a0001c0001t0002g0272 a0001c0001t0002g0273 others(3): Show |
10 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+1192A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199844883 | |||||||
| chr2:199845321 | C | T | 2 | a0001c0001t0017g0269 a0001c0001t0018g0099 |
2 | HG02451.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211+754G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845321 | |||||||
| chr2:199845385 | G | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(40): Show |
60 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.211+690C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845385 | |||||||
| chr2:199845421 | G | T | 1 | a0001c0001t0030g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.211+654C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845421 | |||||||
| chr2:199845426 | C | A | 2 | a0001c0001t0017g0269 a0001c0001t0018g0099 |
2 | HG02451.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211+649G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845426 | |||||||
| chr2:199845444 | G | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.211+631C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845444 | |||||||
| chr2:199845472 | G | A | 1 | a0001c0001t0003g0087 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.211+603C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845472 | |||||||
| chr2:199845575 | A | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(30): Show |
49 | HG00280.hp1 HG00642.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.211+500T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845575 | |||||||
| chr2:199845670 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0003g0062 a0001c0001t0003g0064 others(1): Show |
4 | HG02109.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+405G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845670 | |||||||
| chr2:199845833 | C | CA | 7 | a0001c0001t0001g0158 a0001c0001t0001g0251 a0001c0001t0003g0030 others(4): Show |
8 | HG01175.hp1 HG02015.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+241dupT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845833 | |||||||
| chr2:199845833 | CA | C | 6 | a0001c0001t0001g0161 a0001c0001t0002g0102 a0001c0001t0003g0066 others(3): Show |
7 | HG01081.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+241delT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845833 | |||||||
| chr2:199845866 | A | G | 1 | a0001c0001t0003g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211+209T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845866 | |||||||
| chr2:199845943 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0003g0062 a0001c0001t0003g0064 others(1): Show |
4 | HG02109.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+132G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845943 | |||||||
| chr2:199845983 | T | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(235): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.211+92A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 3/4 | chr2 | 199845983 | |||||||
| chr2:199846173 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03704.hp1 | splice_region_variant&intron_variant | LOW | c.116-3C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199846173 | |||||||
| chr2:199846281 | G | A | 1 | a0001c0001t0015g0252 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.116-111C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199846281 | |||||||
| chr2:199846296 | G | C | 21 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0117 others(18): Show |
26 | HG00673.hp2 HG00738.hp1 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.116-126C>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199846296 | |||||||
| chr2:199846464 | G | T | 1 | a0001c0001t0018g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.116-294C>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199846464 | |||||||
| chr2:199846565 | A | C | 1 | a0001c0001t0010g0159 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.116-395T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199846565 | |||||||
| chr2:199846626 | C | T | 23 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0117 others(20): Show |
29 | HG00673.hp2 HG00738.hp1 HG01993.hp1 others(26): Show |
intron_variant | MODIFIER | c.116-456G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199846626 | |||||||
| chr2:199846705 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.116-535G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199846705 | |||||||
| chr2:199846751 | A | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(34): Show |
53 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.116-581T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199846751 | |||||||
| chr2:199846840 | A | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(37): Show |
56 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.116-670T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199846840 | |||||||
| chr2:199846959 | C | T | 1 | a0001c0001t0005g0275 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.116-789G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199846959 | |||||||
| chr2:199847015 | A | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(34): Show |
53 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.116-845T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199847015 | |||||||
| chr2:199847281 | T | TA | 17 | a0001c0001t0001g0253 a0001c0001t0002g0021 a0001c0001t0002g0254 others(14): Show |
20 | HG00408.hp1 HG00597.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.116-1112dupT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199847281 | |||||||
| chr2:199847311 | T | C | 1 | a0001c0001t0001g0043 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.116-1141A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199847311 | |||||||
| chr2:199847418 | C | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(233): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.116-1248G>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199847418 | |||||||
| chr2:199847831 | T | C | 2 | a0001c0001t0001g0265 a0001c0001t0007g0044 |
3 | HG00323.hp1 NA18959.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.115+1017A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199847831 | |||||||
| chr2:199848311 | T | C | 1 | a0001c0001t0003g0266 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.115+537A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199848311 | |||||||
| chr2:199848401 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.115+447C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199848401 | |||||||
| chr2:199848468 | A | G | 4 | a0001c0001t0004g0129 a0001c0001t0004g0130 a0001c0001t0004g0131 others(1): Show |
4 | NA18992.hp2 NA19000.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+380T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199848468 | |||||||
| chr2:199848680 | C | G | 8 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0002g0045 others(5): Show |
9 | HG01243.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+168G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199848680 | |||||||
| chr2:199848708 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.115+140C>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199848708 | |||||||
| chr2:199848714 | A | G | 1 | a0001c0001t0004g0127 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.115+134T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199848714 | |||||||
| chr2:199848809 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.115+39T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199848809 | |||||||
| chr2:199848814 | A | G | 4 | a0001c0001t0010g0125 a0001c0001t0015g0124 a0001c0001t0018g0099 others(1): Show |
4 | HG01884.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+34T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 2/4 | chr2 | 199848814 | |||||||
| chr2:199849028 | A | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(28): Show |
48 | HG00673.hp2 HG00735.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.-7-59T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199849028 | |||||||
| chr2:199849413 | A | G | 2 | a0001c0001t0006g0022 a0001c0001t0006g0050 |
3 | HG02258.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-444T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199849413 | |||||||
| chr2:199849451 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-7-482T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199849451 | |||||||
| chr2:199849476 | A | T | 8 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0002g0045 others(5): Show |
9 | HG01243.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-507T>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199849476 | |||||||
| chr2:199849557 | TAA | T | 2 | a0001c0001t0006g0022 a0001c0001t0006g0050 |
3 | HG02258.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-590_-7-589delTT | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199849557 | |||||||
| chr2:199849614 | T | A | 1 | a0001c0001t0035g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-7-645A>T | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199849614 | |||||||
| chr2:199849723 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-7-754G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199849723 | |||||||
| chr2:199850043 | C | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(220): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-8+697G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199850043 | |||||||
| chr2:199850084 | T | C | 1 | a0001c0001t0005g0289 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-8+656A>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199850084 | |||||||
| chr2:199850141 | A | G | 1 | a0001c0001t0018g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8+599T>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199850141 | |||||||
| chr2:199850299 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+441G>A | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199850299 | |||||||
| chr2:199850440 | C | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0097 |
3 | HG02572.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-8+300G>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199850440 | |||||||
| chr2:199850549 | A | C | 3 | a0001c0001t0001g0094 a0001c0001t0025g0095 a0002c0002t0001g0096 |
3 | HG03654.hp1 HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-8+191T>G | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199850549 | |||||||
| chr2:199850665 | T | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.-8+75A>C | FTCDNL1 | ENSG00000226124.10 | transcript | ENST00000420128.6 | protein_coding | 1/4 | chr2 | 199850665 |