Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81608 |
| ensemblid | ENSG00000145216.17 |
| hgncid | 19124 |
| symbol | FIP1L1 |
| name | factor interacting with PAPOLA and CPSF1 |
| refseq_nuc | NM_030917.4 |
| refseq_prot | NP_112179.2 |
| ensembl_nuc | ENST00000337488.11 |
| ensembl_prot | ENSP00000336752.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 53377641 |
| end | 53460862 |
| strand | + |
| ver | v1.2 |
| region | chr4:53377641-53460862 |
| region5000 | chr4:53372641-53465862 |
| regionname0 | FIP1L1_chr4_53377641_53460862 |
| regionname5000 | FIP1L1_chr4_53372641_53465862 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1782 | 392 | 86 | 66 | 178 | 14 | 46 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | ATGTC others(1777): Show |
chr4 | 53372641 | 53465862 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3392 | 107 | 11 | 28 | 51 | 7 | 10 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0002 | 0/0 | 3396 | 77 | 26 | 2 | 33 | 0 | 16 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3391): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0003 | 1/1 | 3396 | 68 | 7 | 11 | 38 | 1 | 9 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3391): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0004 | 0/0 | 3392 | 60 | 10 | 15 | 28 | 4 | 3 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0005 | 0/0 | 3392 | 46 | 8 | 6 | 24 | 2 | 6 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0006 | 0/0 | 3392 | 15 | 13 | 2 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0007 | 0/0 | 3396 | 4 | 0 | 0 | 2 | 0 | 2 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3391): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0008 | 0/0 | 3392 | 3 | 3 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0009 | 0/0 | 3392 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0010 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3391): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0011 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3391): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0012 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0013 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0014 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0015 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0016 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0017 | 0/0 | 3396 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3391): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0018 | 0/0 | 3392 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3387): Show |
chr4 | 53372641 | 53465862 |
| a0001c0001t0019 | 0/0 | 3396 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | GCGCA others(3391): Show |
chr4 | 53372641 | 53465862 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0022 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0008g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0010g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0011g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0012g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0013g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0014g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0015g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0016g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0017g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0018g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0019g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0123 | EUR | GBR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0194 | EUR | FIN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0030 | EUR | FIN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0358 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00642 | hp2 | a0001 | c0001 | t0019 | g0363 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0129 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0273 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0148 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0338 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0252 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01243 | hp2 | a0001 | c0001 | t0018 | g0213 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0197 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0131 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0145 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0136 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0115 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0140 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0008 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01884 | hp2 | a0001 | c0001 | t0016 | g0033 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0117 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0128 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02015 | hp2 | a0001 | c0001 | t0017 | g0028 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0368 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0251 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | CDX | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0150 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0070 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0290 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0069 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0344 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02622 | hp1 | a0001 | c0001 | t0013 | g0235 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0365 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0149 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0352 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0072 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0314 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0134 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0366 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0250 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0364 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0092 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0351 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0349 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0212 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0353 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0071 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0367 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0362 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0073 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0312 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0369 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0211 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0233 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0342 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0356 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0370 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0124 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0135 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0122 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0321 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0337 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0313 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0333 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0326 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0009 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0063 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0232 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0226 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0355 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0361 | AFR | YRI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | YRI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | CHB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | CHB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0247 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0253 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0372 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0228 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0371 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18989 | hp2 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0373 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0271 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0018 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0094 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19072 | hp2 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0275 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0283 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0374 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19089 | hp1 | a0001 | c0001 | t0014 | g0287 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | YRI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0224 | AFR | ASW | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | ASW | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0218 | EUR | TSI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | GIH | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0335 | SAS | GIH | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0075 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0065 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | USA | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | USA | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0350 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0016 | REF | REF | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0022 | REF | REF | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:53377658 | C | T | 1 | a0001c0001t0019 | 1 | HG00642.hp2 | 5_prime_UTR_variant | MODIFIER | c.-181C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/18 | 181 | chr4 | 53377658 | ||||||
| chr4:53377662 | C | T | 1 | a0001c0001t0018 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-177C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/18 | 177 | chr4 | 53377662 | ||||||
| chr4:53377738 | T | C | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(8): Show |
239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-101T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/18 | 101 | chr4 | 53377738 | ||||||
| chr4:53459823 | T | C | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(12): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*374T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 374 | chr4 | 53459823 | ||||||
| chr4:53459921 | T | C | 2 | a0001c0001t0010 a0001c0001t0011 |
2 | HG02055.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*472T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 472 | chr4 | 53459921 | ||||||
| chr4:53459987 | C | T | 1 | a0001c0001t0011 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 538 | chr4 | 53459987 | ||||||
| chr4:53460048 | A | G | 1 | a0001c0001t0014 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*599A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 599 | chr4 | 53460048 | ||||||
| chr4:53460054 | T | C | 1 | a0001c0001t0016 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 605 | chr4 | 53460054 | ||||||
| chr4:53460055 | AAATT | A | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(12): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*616_*619delATTA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 616 | INFO_REALIGN_3_PRIME | chr4 | 53460055 | |||||
| chr4:53460150 | G | C | 1 | a0001c0001t0012 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*701G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 701 | chr4 | 53460150 | ||||||
| chr4:53460228 | C | CAGTT | 1 | a0001c0001t0007 | 4 | HG02683.hp2 HG03704.hp1 NA18963.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*781_*784dupGTTA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 785 | INFO_REALIGN_3_PRIME | chr4 | 53460228 | |||||
| chr4:53460228 | C | T | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0010 others(2): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*779C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 779 | chr4 | 53460228 | ||||||
| chr4:53460247 | A | G | 1 | a0001c0001t0015 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*798A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 798 | chr4 | 53460247 | ||||||
| chr4:53460357 | CAAAT | C | 2 | a0001c0001t0006 a0001c0001t0016 |
16 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*911_*914delATAA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 911 | INFO_REALIGN_3_PRIME | chr4 | 53460357 | |||||
| chr4:53460377 | A | G | 1 | a0001c0001t0013 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*928A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 928 | chr4 | 53460377 | ||||||
| chr4:53460383 | A | T | 1 | a0001c0001t0005 | 46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*934A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 934 | chr4 | 53460383 | ||||||
| chr4:53460624 | A | AAATC | 4 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(1): Show |
80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1177_*1180dupATCA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 1181 | INFO_REALIGN_3_PRIME | chr4 | 53460624 | |||||
| chr4:53460630 | T | A | 1 | a0001c0001t0017 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 1181 | chr4 | 53460630 | ||||||
| chr4:53460757 | G | C | 2 | a0001c0001t0008 a0001c0001t0015 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1308G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 1308 | chr4 | 53460757 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:53377935 | C | A | 1 | a0001c0001t0005g0014 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.85+12C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53377935 | |||||||
| chr4:53377935 | C | T | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | NA18973.hp1 NA18981.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+12C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53377935 | |||||||
| chr4:53377936 | C | A | 1 | a0001c0001t0005g0014 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.85+13C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53377936 | |||||||
| chr4:53378007 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.85+84G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378007 | |||||||
| chr4:53378109 | C | T | 1 | a0001c0001t0003g0370 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.85+186C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378109 | |||||||
| chr4:53378154 | C | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(226): Show |
239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.85+231C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378154 | |||||||
| chr4:53378156 | G | T | 76 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(73): Show |
80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.85+233G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378156 | |||||||
| chr4:53378251 | C | G | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.85+328C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378251 | |||||||
| chr4:53378268 | G | C | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+345G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378268 | |||||||
| chr4:53378271 | G | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.85+348G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378271 | |||||||
| chr4:53378299 | C | G | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.85+376C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378299 | |||||||
| chr4:53378534 | G | C | 1 | a0001c0001t0002g0297 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.86-539G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378534 | |||||||
| chr4:53378752 | T | C | 1 | a0001c0001t0006g0006 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.86-321T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378752 | |||||||
| chr4:53378841 | G | A | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.86-232G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378841 | |||||||
| chr4:53378842 | A | T | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.86-231A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378842 | |||||||
| chr4:53378862 | T | TA | 79 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(76): Show |
83 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.86-202dupA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 53378862 | ||||||
| chr4:53378894 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.86-179A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378894 | |||||||
| chr4:53379309 | A | T | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.170+45A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379309 | |||||||
| chr4:53379332 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.170+68A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379332 | |||||||
| chr4:53379379 | A | G | 6 | a0001c0001t0002g0013 a0001c0001t0002g0364 a0001c0001t0002g0365 others(3): Show |
7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+115A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379379 | |||||||
| chr4:53379516 | T | G | 1 | a0001c0001t0005g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.170+252T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379516 | |||||||
| chr4:53379582 | T | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.170+318T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379582 | |||||||
| chr4:53379608 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.170+344A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379608 | |||||||
| chr4:53379802 | G | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.170+538G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379802 | |||||||
| chr4:53380177 | G | A | 7 | a0001c0001t0004g0002 a0001c0001t0004g0104 a0001c0001t0004g0105 others(4): Show |
8 | NA18941.hp2 NA18956.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.170+913G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380177 | |||||||
| chr4:53380177 | GTGAAT | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.170+914_170+918del others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380177 | |||||||
| chr4:53380267 | G | T | 1 | a0001c0001t0004g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.170+1003G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380267 | |||||||
| chr4:53380405 | T | A | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.170+1141T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380405 | |||||||
| chr4:53380479 | G | T | 1 | a0001c0001t0001g0295 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.170+1215G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380479 | |||||||
| chr4:53380570 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.170+1306C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380570 | |||||||
| chr4:53380582 | G | A | 2 | a0001c0001t0002g0298 a0001c0001t0002g0299 |
2 | NA18960.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.170+1318G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380582 | |||||||
| chr4:53380656 | C | T | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG01358.hp2 HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.170+1392C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380656 | |||||||
| chr4:53380758 | A | G | 2 | a0001c0001t0002g0361 a0001c0001t0002g0362 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.170+1494A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380758 | |||||||
| chr4:53380789 | T | G | 2 | a0001c0001t0002g0361 a0001c0001t0002g0362 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.171-1489T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380789 | |||||||
| chr4:53380974 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.171-1304C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380974 | |||||||
| chr4:53380975 | G | A | 1 | a0001c0001t0004g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.171-1303G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380975 | |||||||
| chr4:53381417 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.171-861T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53381417 | |||||||
| chr4:53381615 | C | G | 3 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 |
3 | HG00558.hp1 NA18957.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.171-663C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53381615 | |||||||
| chr4:53381676 | T | A | 1 | a0001c0001t0019g0363 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.171-602T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53381676 | |||||||
| chr4:53381753 | C | CTTTT | 37 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(34): Show |
41 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.171-504_171-501dup others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTT | 20 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(17): Show |
21 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.171-505_171-501dup others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTT | 60 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(57): Show |
64 | HG00597.hp2 HG00642.hp2 HG01192.hp1 others(61): Show |
intron_variant | MODIFIER | c.171-506_171-501dup others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT | 8 | a0001c0001t0002g0297 a0001c0001t0002g0352 a0001c0001t0002g0353 others(5): Show |
8 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.171-507_171-501dup others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0299 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.171-510_171-501dup others(10): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0002g0362 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.171-511_171-501dup others(11): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(5): Show |
6 | a0001c0001t0001g0202 a0001c0001t0005g0197 a0001c0001t0005g0198 others(3): Show |
6 | HG01255.hp2 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.171-512_171-501dup others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(6): Show |
6 | a0001c0001t0001g0152 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG02145.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.171-513_171-501dup others(13): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(7): Show |
19 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0214 others(16): Show |
19 | HG00280.hp2 HG00597.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.171-514_171-501dup others(14): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(8): Show |
27 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0237 others(24): Show |
27 | HG00408.hp1 HG00544.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.171-515_171-501dup others(15): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(9): Show |
22 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(19): Show |
22 | HG00558.hp2 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.171-516_171-501dup others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(10): Show |
13 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(10): Show |
14 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.171-517_171-501dup others(17): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(11): Show |
7 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG01071.hp1 HG01433.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.171-518_171-501dup others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0289 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.171-519_171-501dup others(19): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0005g0290 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.171-520_171-501dup others(20): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.171-524_171-501dup others(24): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0294 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.171-501_171-500ins others(32): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | CT | C | 56 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(53): Show |
57 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.171-501delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0188 a0001c0001t0005g0189 |
2 | NA18988.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.171-511_171-501del others(11): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381753 | CTTTTTTT others(5): Show |
C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(36): Show |
44 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.171-512_171-501del others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | ||||||
| chr4:53381815 | A | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.171-463A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53381815 | |||||||
| chr4:53381929 | AT | A | 77 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(74): Show |
81 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.171-336delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381929 | ||||||
| chr4:53382109 | C | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.171-169C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53382109 | |||||||
| chr4:53382146 | A | AT | 3 | a0001c0001t0005g0225 a0001c0001t0005g0251 a0001c0001t0005g0271 |
3 | HG02132.hp1 NA19003.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.171-128dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53382146 | ||||||
| chr4:53382233 | C | T | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-45C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53382233 | |||||||
| chr4:53382239 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.171-39G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53382239 | |||||||
| chr4:53382251 | A | G | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.171-27A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53382251 | |||||||
| chr4:53382531 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.228+196A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382531 | |||||||
| chr4:53382565 | G | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0153 a0001c0001t0001g0154 others(10): Show |
15 | HG01346.hp1 HG01952.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.228+230G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382565 | |||||||
| chr4:53382863 | T | G | 1 | a0001c0001t0004g0139 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.228+528T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382863 | |||||||
| chr4:53382869 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.228+534T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382869 | |||||||
| chr4:53382873 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.228+538G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382873 | |||||||
| chr4:53382924 | A | G | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.228+589A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382924 | |||||||
| chr4:53383018 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(151): Show |
161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.228+683G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383018 | |||||||
| chr4:53383018 | GT | G | 6 | a0001c0001t0002g0013 a0001c0001t0002g0364 a0001c0001t0002g0365 others(3): Show |
7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.228+694delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 53383018 | ||||||
| chr4:53383066 | A | G | 1 | a0001c0001t0006g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.229-707A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383066 | |||||||
| chr4:53383068 | T | G | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.229-705T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383068 | |||||||
| chr4:53383106 | T | C | 74 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(71): Show |
78 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.229-667T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383106 | |||||||
| chr4:53383308 | T | C | 1 | a0001c0001t0002g0311 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.229-465T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383308 | |||||||
| chr4:53383421 | G | A | 2 | a0001c0001t0008g0005 a0001c0001t0008g0017 |
3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.229-352G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383421 | |||||||
| chr4:53383470 | T | C | 1 | a0001c0001t0008g0005 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.229-303T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383470 | |||||||
| chr4:53383560 | G | T | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.229-213G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383560 | |||||||
| chr4:53383697 | A | G | 1 | a0001c0001t0003g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.229-76A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383697 | |||||||
| chr4:53383887 | T | G | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.332+11T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53383887 | |||||||
| chr4:53383896 | G | A | 1 | a0001c0001t0003g0027 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.332+20G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53383896 | |||||||
| chr4:53384022 | T | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.332+146T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384022 | |||||||
| chr4:53384036 | A | G | 1 | a0001c0001t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332+160A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384036 | |||||||
| chr4:53384040 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+164T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384040 | |||||||
| chr4:53384058 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.332+182C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384058 | |||||||
| chr4:53384121 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+245G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384121 | |||||||
| chr4:53384188 | C | T | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.332+312C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384188 | |||||||
| chr4:53384257 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+381T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384257 | |||||||
| chr4:53384368 | C | T | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.332+492C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384368 | |||||||
| chr4:53384406 | C | T | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.332+530C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384406 | |||||||
| chr4:53384630 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+754G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384630 | |||||||
| chr4:53384687 | T | G | 3 | a0001c0001t0004g0103 a0001c0001t0004g0112 a0001c0001t0004g0113 |
3 | NA18944.hp2 NA18970.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.332+811T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384687 | |||||||
| chr4:53384761 | C | T | 46 | a0001c0001t0002g0012 a0001c0001t0002g0298 a0001c0001t0002g0299 others(43): Show |
47 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.332+885C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384761 | |||||||
| chr4:53384785 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+909G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384785 | |||||||
| chr4:53384996 | C | A | 1 | a0001c0001t0017g0028 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.332+1120C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384996 | |||||||
| chr4:53385028 | A | G | 1 | a0001c0001t0005g0250 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.332+1152A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385028 | |||||||
| chr4:53385130 | A | G | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+1254A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385130 | |||||||
| chr4:53385142 | C | T | 1 | a0001c0001t0012g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.332+1266C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385142 | |||||||
| chr4:53385238 | C | T | 1 | a0001c0001t0002g0306 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.332+1362C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385238 | |||||||
| chr4:53385427 | T | C | 1 | a0001c0001t0005g0226 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.332+1551T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385427 | |||||||
| chr4:53385491 | G | A | 76 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(73): Show |
80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.332+1615G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385491 | |||||||
| chr4:53385551 | A | G | 74 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(71): Show |
78 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.332+1675A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385551 | |||||||
| chr4:53386037 | A | AT | 79 | a0001c0001t0001g0164 a0001c0001t0001g0288 a0001c0001t0002g0004 others(76): Show |
83 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.332+2177dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53386037 | ||||||
| chr4:53386037 | A | ATT | 8 | a0001c0001t0006g0070 a0001c0001t0006g0071 a0001c0001t0006g0072 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.332+2176_332+2177d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53386037 | ||||||
| chr4:53386053 | T | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.332+2177T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386053 | |||||||
| chr4:53386055 | C | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.332+2179C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386055 | |||||||
| chr4:53386260 | A | G | 6 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
6 | HG00597.hp1 HG02165.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.332+2384A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386260 | |||||||
| chr4:53386268 | G | C | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.332+2392G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386268 | |||||||
| chr4:53386291 | G | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.332+2415G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386291 | |||||||
| chr4:53386347 | A | G | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.332+2471A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386347 | |||||||
| chr4:53386470 | G | C | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.332+2594G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386470 | |||||||
| chr4:53386490 | A | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.332+2614A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386490 | |||||||
| chr4:53386529 | A | G | 59 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0008 others(56): Show |
64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.332+2653A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386529 | |||||||
| chr4:53386675 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332+2799C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386675 | |||||||
| chr4:53386676 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+2800G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386676 | |||||||
| chr4:53386715 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+2839T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386715 | |||||||
| chr4:53386796 | A | G | 1 | a0001c0001t0004g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.332+2920A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386796 | |||||||
| chr4:53386817 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+2941T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386817 | |||||||
| chr4:53386945 | A | G | 1 | a0001c0001t0005g0206 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.333-2864A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386945 | |||||||
| chr4:53386955 | C | T | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.333-2854C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386955 | |||||||
| chr4:53387436 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.333-2373C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387436 | |||||||
| chr4:53387697 | C | T | 1 | a0001c0001t0005g0206 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.333-2112C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387697 | |||||||
| chr4:53387759 | G | C | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.333-2050G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387759 | |||||||
| chr4:53387806 | A | G | 1 | a0001c0001t0004g0148 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.333-2003A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387806 | |||||||
| chr4:53387824 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.333-1985G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387824 | |||||||
| chr4:53387864 | A | G | 1 | a0001c0001t0005g0206 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.333-1945A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387864 | |||||||
| chr4:53387979 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.333-1830G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387979 | |||||||
| chr4:53388005 | A | T | 1 | a0001c0001t0005g0218 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.333-1804A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388005 | |||||||
| chr4:53388207 | T | C | 75 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(72): Show |
76 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.333-1602T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388207 | |||||||
| chr4:53388344 | CT | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(281): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.333-1452delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53388344 | ||||||
| chr4:53388442 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.333-1367C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388442 | |||||||
| chr4:53388582 | G | A | 1 | a0001c0001t0002g0355 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.333-1227G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388582 | |||||||
| chr4:53388631 | G | A | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.333-1178G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388631 | |||||||
| chr4:53388635 | G | A | 1 | a0001c0001t0003g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.333-1174G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388635 | |||||||
| chr4:53388689 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(38): Show |
46 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.333-1120G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388689 | |||||||
| chr4:53388689 | G | T | 1 | a0001c0001t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.333-1120G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388689 | |||||||
| chr4:53388703 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.333-1106T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388703 | |||||||
| chr4:53388976 | GTATTA | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-827_333-823del others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53388976 | ||||||
| chr4:53389190 | G | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0282 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.333-619G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389190 | |||||||
| chr4:53389203 | A | G | 1 | a0001c0001t0017g0028 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.333-606A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389203 | |||||||
| chr4:53389455 | C | CT | 6 | a0001c0001t0001g0272 a0001c0001t0001g0282 a0001c0001t0002g0347 others(3): Show |
6 | HG02055.hp2 HG02970.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.333-343dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53389455 | ||||||
| chr4:53389455 | CT | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(276): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.333-343delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53389455 | ||||||
| chr4:53389599 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.333-210C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389599 | |||||||
| chr4:53389626 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.333-183T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389626 | |||||||
| chr4:53389700 | A | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.333-109A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389700 | |||||||
| chr4:53389720 | T | C | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.333-89T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389720 | |||||||
| chr4:53389789 | T | G | 9 | a0001c0001t0002g0303 a0001c0001t0002g0311 a0001c0001t0002g0321 others(6): Show |
9 | HG02129.hp2 HG03927.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.333-20T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389789 | |||||||
| chr4:53389892 | G | A | 1 | a0001c0001t0019g0363 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.397+19G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53389892 | |||||||
| chr4:53390000 | G | A | 45 | a0001c0001t0005g0011 a0001c0001t0005g0014 a0001c0001t0005g0151 others(42): Show |
46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.397+127G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390000 | |||||||
| chr4:53390024 | C | T | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.397+151C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390024 | |||||||
| chr4:53390080 | G | A | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.397+207G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390080 | |||||||
| chr4:53390088 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.397+215A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390088 | |||||||
| chr4:53390125 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0281 |
2 | NA18964.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.397+252A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390125 | |||||||
| chr4:53390232 | G | A | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.398-289G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390232 | |||||||
| chr4:53390283 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.398-238A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390283 | |||||||
| chr4:53390310 | G | A | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.398-211G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390310 | |||||||
| chr4:53390311 | C | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.398-210C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390311 | |||||||
| chr4:53390473 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.398-48T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390473 | |||||||
| chr4:53390677 | C | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+49C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390677 | |||||||
| chr4:53390859 | C | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.506-150C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390859 | |||||||
| chr4:53390867 | A | T | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.506-142A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390867 | |||||||
| chr4:53390870 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0002g0312 |
2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.506-139T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390870 | |||||||
| chr4:53390908 | A | G | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.506-101A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390908 | |||||||
| chr4:53390964 | A | T | 75 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(72): Show |
76 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.506-45A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390964 | |||||||
| chr4:53391216 | A | G | 2 | a0001c0001t0008g0005 a0001c0001t0008g0017 |
3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.636+77A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 8/17 | chr4 | 53391216 | |||||||
| chr4:53391304 | G | A | 10 | a0001c0001t0002g0303 a0001c0001t0002g0311 a0001c0001t0002g0321 others(7): Show |
10 | HG02129.hp2 HG03927.hp2 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.637-126G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 8/17 | chr4 | 53391304 | |||||||
| chr4:53391363 | G | A | 1 | a0001c0001t0002g0355 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.637-67G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 8/17 | chr4 | 53391363 | |||||||
| chr4:53391698 | A | G | 50 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(47): Show |
54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.705+200A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53391698 | |||||||
| chr4:53391844 | A | C | 1 | a0001c0001t0012g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.705+346A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53391844 | |||||||
| chr4:53391928 | G | A | 75 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(72): Show |
76 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.705+430G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53391928 | |||||||
| chr4:53391946 | A | G | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.705+448A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53391946 | |||||||
| chr4:53392382 | TG | T | 7 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0002g0314 others(4): Show |
7 | HG01261.hp1 HG02683.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.705+885delG | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53392382 | |||||||
| chr4:53392413 | C | G | 1 | a0001c0001t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.705+915C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53392413 | |||||||
| chr4:53392702 | T | C | 1 | a0001c0001t0010g0369 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.705+1204T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53392702 | |||||||
| chr4:53392715 | AAG | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+1221_705+1222d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53392715 | ||||||
| chr4:53392944 | T | C | 1 | a0001c0001t0002g0327 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.705+1446T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53392944 | |||||||
| chr4:53393239 | A | G | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.705+1741A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393239 | |||||||
| chr4:53393241 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.705+1743G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393241 | |||||||
| chr4:53393450 | G | A | 79 | a0001c0001t0001g0167 a0001c0001t0002g0004 a0001c0001t0002g0012 others(76): Show |
83 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.705+1952G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393450 | |||||||
| chr4:53393489 | A | T | 1 | a0001c0001t0003g0093 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.705+1991A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393489 | |||||||
| chr4:53393567 | G | GAAA | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.705+2070_705+2072d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393567 | ||||||
| chr4:53393616 | A | G | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.705+2118A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393616 | |||||||
| chr4:53393621 | G | A | 1 | a0001c0001t0018g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.705+2123G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393621 | |||||||
| chr4:53393695 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.705+2197C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393695 | |||||||
| chr4:53393762 | C | T | 1 | a0001c0001t0006g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.705+2264C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393762 | |||||||
| chr4:53393764 | G | GCCC | 14 | a0001c0001t0003g0020 a0001c0001t0003g0039 a0001c0001t0003g0040 others(11): Show |
15 | HG01175.hp2 HG01256.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.705+2281_705+2283d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | ||||||
| chr4:53393764 | G | GCCCC | 20 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0034 others(17): Show |
21 | HG00323.hp2 HG00741.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.705+2280_705+2283d others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | ||||||
| chr4:53393764 | G | GCCCCCCC others(3): Show |
1 | a0001c0001t0003g0029 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.705+2274_705+2283d others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | ||||||
| chr4:53393764 | G | GCCCCCCC others(4): Show |
1 | a0001c0001t0003g0077 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.705+2273_705+2283d others(13): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | ||||||
| chr4:53393764 | GCCCC | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(46): Show |
54 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.705+2280_705+2283d others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | ||||||
| chr4:53393764 | GCCCCC | G | 62 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0187 others(59): Show |
63 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.705+2279_705+2283d others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | ||||||
| chr4:53393764 | GCCCCCC | G | 23 | a0001c0001t0001g0152 a0001c0001t0001g0205 a0001c0001t0001g0208 others(20): Show |
23 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.705+2278_705+2283d others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | ||||||
| chr4:53393764 | GCCCCCCC others(3): Show |
G | 54 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0008 others(51): Show |
59 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.705+2274_705+2283d others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | ||||||
| chr4:53393764 | GCCCCCCC others(5): Show |
G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.705+2272_705+2283d others(14): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | ||||||
| chr4:53393776 | C | A | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.705+2278C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393776 | |||||||
| chr4:53393781 | C | G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG01167.hp2 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.705+2283C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393781 | |||||||
| chr4:53394383 | A | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0269 |
2 | NA18995.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.705+2885A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53394383 | |||||||
| chr4:53394508 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+3010A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53394508 | |||||||
| chr4:53394516 | C | T | 75 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(72): Show |
76 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.705+3018C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53394516 | |||||||
| chr4:53394745 | CTG | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.705+3249_705+3250d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53394745 | ||||||
| chr4:53394755 | T | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.705+3257T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53394755 | |||||||
| chr4:53394770 | C | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(100): Show |
108 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.705+3272C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53394770 | |||||||
| chr4:53395268 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.705+3770T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53395268 | |||||||
| chr4:53395479 | G | C | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.705+3981G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53395479 | |||||||
| chr4:53395575 | C | T | 75 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(72): Show |
76 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.705+4077C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53395575 | |||||||
| chr4:53395746 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.706-3984G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53395746 | |||||||
| chr4:53395756 | G | C | 1 | a0001c0001t0003g0048 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.706-3974G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53395756 | |||||||
| chr4:53395919 | A | AT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(209): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.706-3798dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53395919 | ||||||
| chr4:53395919 | A | ATT | 76 | a0001c0001t0001g0291 a0001c0001t0002g0004 a0001c0001t0002g0012 others(73): Show |
80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.706-3799_706-3798d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53395919 | ||||||
| chr4:53396009 | C | T | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.706-3721C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396009 | |||||||
| chr4:53396040 | G | A | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.706-3690G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396040 | |||||||
| chr4:53396138 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.706-3592C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396138 | |||||||
| chr4:53396153 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.706-3577A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396153 | |||||||
| chr4:53396296 | G | C | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.706-3434G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396296 | |||||||
| chr4:53396377 | T | C | 1 | a0001c0001t0002g0349 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.706-3353T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396377 | |||||||
| chr4:53396407 | CT | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.706-3314delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53396407 | ||||||
| chr4:53396459 | T | G | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.706-3271T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396459 | |||||||
| chr4:53396469 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.706-3261G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396469 | |||||||
| chr4:53396479 | C | A | 1 | a0001c0001t0012g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.706-3251C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396479 | |||||||
| chr4:53396550 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.706-3180C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396550 | |||||||
| chr4:53396657 | G | A | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.706-3073G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396657 | |||||||
| chr4:53396788 | A | C | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.706-2942A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396788 | |||||||
| chr4:53396829 | GTC | G | 46 | a0001c0001t0002g0012 a0001c0001t0002g0298 a0001c0001t0002g0299 others(43): Show |
47 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.706-2895_706-2894d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53396829 | ||||||
| chr4:53396917 | A | AT | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.706-2807dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53396917 | ||||||
| chr4:53397015 | A | G | 1 | a0001c0001t0005g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.706-2715A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397015 | |||||||
| chr4:53397186 | G | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.706-2544G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397186 | |||||||
| chr4:53397457 | G | A | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.706-2273G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397457 | |||||||
| chr4:53397465 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.706-2265C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397465 | |||||||
| chr4:53397591 | C | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.706-2139C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397591 | |||||||
| chr4:53397631 | A | G | 1 | a0001c0001t0002g0319 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.706-2099A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397631 | |||||||
| chr4:53397707 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.706-2023G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397707 | |||||||
| chr4:53397752 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.706-1978A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397752 | |||||||
| chr4:53397757 | T | C | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-1973T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397757 | |||||||
| chr4:53397825 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.706-1905G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397825 | |||||||
| chr4:53397938 | T | C | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.706-1792T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397938 | |||||||
| chr4:53397950 | G | A | 1 | a0001c0001t0004g0008 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.706-1780G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397950 | |||||||
| chr4:53397988 | G | A | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0256 others(1): Show |
4 | HG01109.hp2 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.706-1742G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397988 | |||||||
| chr4:53398007 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.706-1723C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398007 | |||||||
| chr4:53398022 | G | A | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.706-1708G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398022 | |||||||
| chr4:53398144 | A | G | 1 | a0001c0001t0003g0081 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.706-1586A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398144 | |||||||
| chr4:53398261 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.706-1469T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398261 | |||||||
| chr4:53398284 | A | C | 76 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(73): Show |
80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.706-1446A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398284 | |||||||
| chr4:53398376 | T | C | 76 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(73): Show |
80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.706-1354T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398376 | |||||||
| chr4:53398582 | T | C | 1 | a0001c0001t0013g0235 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.706-1148T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398582 | |||||||
| chr4:53398637 | A | AT | 61 | a0001c0001t0001g0152 a0001c0001t0001g0165 a0001c0001t0001g0166 others(58): Show |
61 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.706-1090dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53398637 | ||||||
| chr4:53398765 | G | C | 1 | a0001c0001t0002g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.706-965G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398765 | |||||||
| chr4:53398830 | A | C | 1 | a0001c0001t0003g0067 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.706-900A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398830 | |||||||
| chr4:53398875 | G | A | 4 | a0001c0001t0004g0109 a0001c0001t0004g0117 a0001c0001t0004g0140 others(1): Show |
4 | HG01074.hp2 HG01099.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-855G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398875 | |||||||
| chr4:53399166 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.706-564A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53399166 | |||||||
| chr4:53399271 | T | C | 1 | a0001c0001t0004g0105 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.706-459T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53399271 | |||||||
| chr4:53399320 | A | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0066 |
2 | HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.706-410A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53399320 | |||||||
| chr4:53399333 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.706-397A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53399333 | |||||||
| chr4:53399500 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.706-230G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53399500 | |||||||
| chr4:53399865 | T | C | 1 | a0001c0001t0004g0140 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.815+26T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53399865 | |||||||
| chr4:53399994 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.815+155C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53399994 | |||||||
| chr4:53400012 | A | G | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+173A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400012 | |||||||
| chr4:53400072 | G | T | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.815+233G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400072 | |||||||
| chr4:53400500 | A | G | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+661A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400500 | |||||||
| chr4:53400548 | G | A | 19 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0048 others(16): Show |
19 | HG00323.hp2 HG02004.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.815+709G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400548 | |||||||
| chr4:53400706 | C | T | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+867C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400706 | |||||||
| chr4:53400842 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.815+1003C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400842 | |||||||
| chr4:53400917 | A | G | 1 | a0001c0001t0002g0346 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.815+1078A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400917 | |||||||
| chr4:53400993 | A | G | 1 | a0001c0001t0002g0345 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.815+1154A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400993 | |||||||
| chr4:53401020 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.815+1181C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401020 | |||||||
| chr4:53401041 | G | A | 81 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(78): Show |
86 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.815+1202G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401041 | |||||||
| chr4:53401156 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.815+1317T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401156 | |||||||
| chr4:53401166 | G | T | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+1327G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401166 | |||||||
| chr4:53401267 | T | G | 2 | a0001c0001t0006g0032 a0001c0001t0016g0033 |
2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.815+1428T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401267 | |||||||
| chr4:53401268 | G | A | 1 | a0001c0001t0003g0040 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.815+1429G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401268 | |||||||
| chr4:53401363 | C | T | 1 | a0001c0001t0012g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.815+1524C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401363 | |||||||
| chr4:53401799 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+1960G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401799 | |||||||
| chr4:53402184 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.815+2345T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402184 | |||||||
| chr4:53402332 | TG | T | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+2498delG | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53402332 | ||||||
| chr4:53402377 | CAGG | C | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.815+2541_815+2543d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53402377 | ||||||
| chr4:53402536 | A | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+2697A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402536 | |||||||
| chr4:53402546 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.815+2707A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402546 | |||||||
| chr4:53402657 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+2818A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402657 | |||||||
| chr4:53402873 | A | G | 1 | a0001c0001t0004g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.815+3034A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402873 | |||||||
| chr4:53402929 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.815+3090G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402929 | |||||||
| chr4:53403006 | T | C | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.815+3167T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403006 | |||||||
| chr4:53403099 | T | C | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.815+3260T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403099 | |||||||
| chr4:53403107 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.815+3268A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403107 | |||||||
| chr4:53403402 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.815+3563G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403402 | |||||||
| chr4:53403478 | C | A | 1 | a0001c0001t0002g0308 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.815+3639C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403478 | |||||||
| chr4:53403529 | T | A | 74 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(71): Show |
78 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.815+3690T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403529 | |||||||
| chr4:53403531 | C | T | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+3692C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403531 | |||||||
| chr4:53403547 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+3708C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403547 | |||||||
| chr4:53403740 | G | C | 1 | a0001c0001t0003g0040 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.815+3901G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403740 | |||||||
| chr4:53403998 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.815+4159G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403998 | |||||||
| chr4:53404010 | C | CT | 110 | a0001c0001t0001g0157 a0001c0001t0001g0258 a0001c0001t0003g0373 others(107): Show |
117 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.815+4183dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53404010 | ||||||
| chr4:53404010 | C | CTT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(101): Show |
109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.815+4182_815+4183d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53404010 | ||||||
| chr4:53404010 | CT | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+4183delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53404010 | ||||||
| chr4:53404133 | T | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0203 |
2 | HG01255.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.815+4294T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404133 | |||||||
| chr4:53404177 | C | T | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.815+4338C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404177 | |||||||
| chr4:53404252 | T | C | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.815+4413T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404252 | |||||||
| chr4:53404256 | C | T | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+4417C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404256 | |||||||
| chr4:53404308 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.815+4469G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404308 | |||||||
| chr4:53404464 | A | G | 76 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(73): Show |
80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.815+4625A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404464 | |||||||
| chr4:53404489 | T | C | 1 | a0001c0001t0002g0313 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.815+4650T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404489 | |||||||
| chr4:53404516 | C | G | 1 | a0001c0001t0002g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.815+4677C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404516 | |||||||
| chr4:53404564 | A | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+4725A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404564 | |||||||
| chr4:53404564 | A | G | 15 | a0001c0001t0006g0006 a0001c0001t0006g0032 a0001c0001t0006g0064 others(12): Show |
16 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.815+4725A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404564 | |||||||
| chr4:53404612 | C | G | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.815+4773C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404612 | |||||||
| chr4:53404671 | G | C | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.815+4832G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404671 | |||||||
| chr4:53404870 | G | A | 1 | a0001c0001t0006g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.815+5031G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404870 | |||||||
| chr4:53404877 | T | C | 1 | a0001c0001t0012g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.815+5038T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404877 | |||||||
| chr4:53404889 | T | C | 1 | a0001c0001t0002g0364 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.815+5050T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404889 | |||||||
| chr4:53404910 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.815+5071C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404910 | |||||||
| chr4:53404933 | G | A | 1 | a0001c0001t0004g0120 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.815+5094G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404933 | |||||||
| chr4:53404952 | G | A | 1 | a0001c0001t0002g0301 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.815+5113G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404952 | |||||||
| chr4:53405030 | G | A | 1 | a0001c0001t0004g0121 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.815+5191G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405030 | |||||||
| chr4:53405054 | T | G | 1 | a0001c0001t0004g0122 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.815+5215T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405054 | |||||||
| chr4:53405090 | G | A | 1 | a0001c0001t0001g0288 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.815+5251G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405090 | |||||||
| chr4:53405103 | T | C | 1 | a0001c0001t0002g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.815+5264T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405103 | |||||||
| chr4:53405217 | C | T | 1 | a0001c0001t0004g0136 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.815+5378C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405217 | |||||||
| chr4:53405223 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.815+5384A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405223 | |||||||
| chr4:53405326 | C | T | 59 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0008 others(56): Show |
64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.815+5487C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405326 | |||||||
| chr4:53405330 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+5491A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405330 | |||||||
| chr4:53405440 | C | T | 1 | a0001c0001t0002g0344 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.815+5601C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405440 | |||||||
| chr4:53405441 | T | G | 1 | a0001c0001t0002g0344 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.815+5602T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405441 | |||||||
| chr4:53405444 | A | C | 59 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0008 others(56): Show |
64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.815+5605A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405444 | |||||||
| chr4:53405450 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.815+5611C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405450 | |||||||
| chr4:53405477 | C | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+5638C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405477 | |||||||
| chr4:53405488 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.815+5649C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405488 | |||||||
| chr4:53405534 | A | G | 1 | a0001c0001t0009g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.815+5695A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405534 | |||||||
| chr4:53405539 | G | C | 1 | a0001c0001t0002g0328 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.815+5700G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405539 | |||||||
| chr4:53405600 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.815+5761G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405600 | |||||||
| chr4:53405608 | A | G | 4 | a0001c0001t0002g0004 a0001c0001t0002g0297 a0001c0001t0002g0319 others(1): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.815+5769A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405608 | |||||||
| chr4:53405642 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.815+5803A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405642 | |||||||
| chr4:53405647 | A | C | 1 | a0001c0001t0011g0368 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.815+5808A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405647 | |||||||
| chr4:53405661 | G | C | 59 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0008 others(56): Show |
64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.815+5822G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405661 | |||||||
| chr4:53405667 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.815+5828G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405667 | |||||||
| chr4:53405682 | C | A | 1 | a0001c0001t0013g0235 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.815+5843C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405682 | |||||||
| chr4:53405683 | T | C | 1 | a0001c0001t0013g0235 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.815+5844T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405683 | |||||||
| chr4:53405735 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.815+5896G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405735 | |||||||
| chr4:53405839 | G | A | 1 | a0001c0001t0012g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.815+6000G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405839 | |||||||
| chr4:53405873 | T | C | 1 | a0001c0001t0003g0049 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.815+6034T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405873 | |||||||
| chr4:53405891 | A | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6052A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405891 | |||||||
| chr4:53405894 | T | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6055T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405894 | |||||||
| chr4:53405911 | G | C | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6072G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405911 | |||||||
| chr4:53405915 | C | T | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6076C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405915 | |||||||
| chr4:53405916 | A | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6077A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405916 | |||||||
| chr4:53405924 | G | T | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6085G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405924 | |||||||
| chr4:53405994 | C | G | 1 | a0001c0001t0002g0346 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.815+6155C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405994 | |||||||
| chr4:53406043 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(151): Show |
161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.815+6204A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406043 | |||||||
| chr4:53406076 | T | C | 1 | a0001c0001t0011g0368 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.815+6237T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406076 | |||||||
| chr4:53406087 | A | C | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+6248A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406087 | |||||||
| chr4:53406166 | A | G | 1 | a0001c0001t0002g0343 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.815+6327A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406166 | |||||||
| chr4:53406182 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.815+6343T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406182 | |||||||
| chr4:53406220 | AG | A | 76 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(73): Show |
80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.815+6384delG | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53406220 | ||||||
| chr4:53406222 | G | T | 1 | a0001c0001t0004g0105 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.815+6383G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406222 | |||||||
| chr4:53406236 | G | C | 46 | a0001c0001t0002g0012 a0001c0001t0002g0298 a0001c0001t0002g0299 others(43): Show |
47 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.815+6397G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406236 | |||||||
| chr4:53406255 | T | G | 3 | a0001c0001t0005g0151 a0001c0001t0005g0229 a0001c0001t0005g0230 |
3 | HG00408.hp1 HG02165.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.815+6416T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406255 | |||||||
| chr4:53406303 | A | G | 2 | a0001c0001t0007g0134 a0001c0001t0007g0135 |
2 | HG02683.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.815+6464A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406303 | |||||||
| chr4:53406323 | G | A | 81 | a0001c0001t0001g0202 a0001c0001t0001g0284 a0001c0001t0002g0004 others(78): Show |
85 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.815+6484G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406323 | |||||||
| chr4:53406403 | T | G | 50 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(47): Show |
54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.815+6564T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406403 | |||||||
| chr4:53406441 | G | C | 1 | a0001c0001t0006g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.815+6602G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406441 | |||||||
| chr4:53406449 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+6610G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406449 | |||||||
| chr4:53406492 | C | T | 50 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(47): Show |
54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.815+6653C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406492 | |||||||
| chr4:53406494 | G | A | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+6655G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406494 | |||||||
| chr4:53406533 | T | G | 1 | a0001c0001t0003g0078 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.815+6694T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406533 | |||||||
| chr4:53406554 | C | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+6715C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406554 | |||||||
| chr4:53406556 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+6717A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406556 | |||||||
| chr4:53406581 | A | T | 59 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0008 others(56): Show |
64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.815+6742A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406581 | |||||||
| chr4:53406604 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.815+6765C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406604 | |||||||
| chr4:53406617 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.815+6778C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406617 | |||||||
| chr4:53406715 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+6876A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406715 | |||||||
| chr4:53406743 | T | C | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.815+6904T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406743 | |||||||
| chr4:53406753 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.815+6914G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406753 | |||||||
| chr4:53406766 | A | C | 9 | a0001c0001t0003g0083 a0001c0001t0003g0085 a0001c0001t0003g0086 others(6): Show |
9 | HG02040.hp2 HG02074.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.815+6927A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406766 | |||||||
| chr4:53406802 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.815+6963T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406802 | |||||||
| chr4:53406881 | G | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.815+7042G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406881 | |||||||
| chr4:53406912 | T | C | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.815+7073T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406912 | |||||||
| chr4:53406925 | A | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+7086A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406925 | |||||||
| chr4:53406963 | G | C | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.815+7124G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406963 | |||||||
| chr4:53406999 | C | G | 9 | a0001c0001t0002g0303 a0001c0001t0002g0311 a0001c0001t0002g0321 others(6): Show |
9 | HG02129.hp2 HG03927.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.815+7160C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406999 | |||||||
| chr4:53407007 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0291 |
2 | HG00733.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.815+7168T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407007 | |||||||
| chr4:53407070 | C | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+7231C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407070 | |||||||
| chr4:53407107 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.815+7268G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407107 | |||||||
| chr4:53407292 | T | G | 61 | a0001c0001t0001g0152 a0001c0001t0001g0165 a0001c0001t0001g0166 others(58): Show |
61 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.816-7323T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407292 | |||||||
| chr4:53407320 | C | T | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.816-7295C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407320 | |||||||
| chr4:53407338 | C | G | 1 | a0001c0001t0011g0368 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.816-7277C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407338 | |||||||
| chr4:53407338 | C | T | 1 | a0001c0001t0003g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.816-7277C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407338 | |||||||
| chr4:53407432 | A | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-7183A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407432 | |||||||
| chr4:53407458 | G | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0181 a0001c0001t0001g0188 |
3 | HG00673.hp1 HG02083.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.816-7157G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407458 | |||||||
| chr4:53407527 | T | C | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.816-7088T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407527 | |||||||
| chr4:53407549 | A | G | 7 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0244 others(4): Show |
7 | NA18940.hp2 NA18945.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.816-7066A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407549 | |||||||
| chr4:53407581 | CGTT | C | 46 | a0001c0001t0001g0186 a0001c0001t0005g0011 a0001c0001t0005g0014 others(43): Show |
47 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.816-7032_816-7030d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53407581 | ||||||
| chr4:53407586 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.816-7029G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407586 | |||||||
| chr4:53407613 | T | TA | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-7000dupA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53407613 | ||||||
| chr4:53407724 | A | G | 4 | a0001c0001t0006g0006 a0001c0001t0006g0065 a0001c0001t0006g0069 others(1): Show |
5 | HG01358.hp1 HG01361.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.816-6891A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407724 | |||||||
| chr4:53407836 | G | C | 1 | a0001c0001t0002g0355 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.816-6779G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407836 | |||||||
| chr4:53407847 | G | T | 1 | a0001c0001t0002g0342 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.816-6768G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407847 | |||||||
| chr4:53407863 | C | G | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.816-6752C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407863 | |||||||
| chr4:53407987 | C | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0364 a0001c0001t0002g0366 others(1): Show |
5 | HG02717.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.816-6628C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407987 | |||||||
| chr4:53408015 | G | A | 1 | a0001c0001t0005g0250 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.816-6600G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408015 | |||||||
| chr4:53408017 | A | G | 365 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(362): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.816-6598A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408017 | |||||||
| chr4:53408017 | A | T | 1 | a0001c0001t0007g0135 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.816-6598A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408017 | |||||||
| chr4:53408085 | A | G | 1 | a0001c0001t0004g0109 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.816-6530A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408085 | |||||||
| chr4:53408087 | C | G | 1 | a0001c0001t0018g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.816-6528C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408087 | |||||||
| chr4:53408090 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-6525C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408090 | |||||||
| chr4:53408170 | G | A | 1 | a0001c0001t0002g0306 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.816-6445G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408170 | |||||||
| chr4:53408193 | G | T | 55 | a0001c0001t0001g0152 a0001c0001t0001g0195 a0001c0001t0001g0196 others(52): Show |
55 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.816-6422G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408193 | |||||||
| chr4:53408354 | G | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.816-6261G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408354 | |||||||
| chr4:53408356 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-6259A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408356 | |||||||
| chr4:53408399 | C | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.816-6216C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408399 | |||||||
| chr4:53408416 | C | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.816-6199C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408416 | |||||||
| chr4:53408435 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.816-6180C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408435 | |||||||
| chr4:53408457 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.816-6158C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408457 | |||||||
| chr4:53408462 | G | A | 2 | a0001c0001t0002g0348 a0001c0001t0003g0038 |
2 | HG02698.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.816-6153G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408462 | |||||||
| chr4:53408557 | G | A | 1 | a0001c0001t0002g0356 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.816-6058G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408557 | |||||||
| chr4:53408637 | A | T | 1 | a0001c0001t0002g0341 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.816-5978A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408637 | |||||||
| chr4:53408681 | G | A | 1 | a0001c0001t0018g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.816-5934G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408681 | |||||||
| chr4:53408773 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.816-5842T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408773 | |||||||
| chr4:53408814 | C | T | 3 | a0001c0001t0005g0211 a0001c0001t0005g0212 a0001c0001t0005g0233 |
3 | HG03017.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.816-5801C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408814 | |||||||
| chr4:53408832 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-5783G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408832 | |||||||
| chr4:53408843 | T | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0297 a0001c0001t0002g0319 others(1): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.816-5772T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408843 | |||||||
| chr4:53408844 | G | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0297 a0001c0001t0002g0319 others(1): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.816-5771G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408844 | |||||||
| chr4:53408888 | A | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.816-5727A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408888 | |||||||
| chr4:53408943 | TC | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.816-5670delC | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53408943 | ||||||
| chr4:53408951 | T | C | 1 | a0001c0001t0002g0308 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.816-5664T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408951 | |||||||
| chr4:53408955 | T | G | 1 | a0001c0001t0002g0355 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.816-5660T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408955 | |||||||
| chr4:53408971 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-5644G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408971 | |||||||
| chr4:53408982 | T | A | 46 | a0001c0001t0002g0012 a0001c0001t0002g0298 a0001c0001t0002g0299 others(43): Show |
47 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.816-5633T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408982 | |||||||
| chr4:53409042 | C | G | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.816-5573C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409042 | |||||||
| chr4:53409152 | G | T | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-5463G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409152 | |||||||
| chr4:53409262 | C | G | 2 | a0001c0001t0004g0107 a0001c0001t0004g0108 |
2 | NA18941.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.816-5353C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409262 | |||||||
| chr4:53409320 | A | T | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-5295A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409320 | |||||||
| chr4:53409326 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.816-5289G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409326 | |||||||
| chr4:53409362 | C | T | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.816-5253C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409362 | |||||||
| chr4:53409427 | G | A | 2 | a0001c0001t0001g0279 a0001c0001t0014g0287 |
2 | NA18939.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.816-5188G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409427 | |||||||
| chr4:53409434 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.816-5181C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409434 | |||||||
| chr4:53409477 | C | T | 3 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 |
3 | HG00558.hp1 NA18957.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.816-5138C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409477 | |||||||
| chr4:53409497 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-5118C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409497 | |||||||
| chr4:53409510 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.816-5105C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409510 | |||||||
| chr4:53409613 | C | G | 2 | a0001c0001t0005g0194 a0001c0001t0005g0277 |
2 | HG00323.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.816-5002C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409613 | |||||||
| chr4:53409640 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0153 a0001c0001t0001g0154 others(10): Show |
15 | HG01346.hp1 HG01952.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.816-4975C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409640 | |||||||
| chr4:53409696 | G | A | 1 | a0001c0001t0006g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.816-4919G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409696 | |||||||
| chr4:53409725 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.816-4890C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409725 | |||||||
| chr4:53409780 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-4835A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409780 | |||||||
| chr4:53409811 | C | T | 1 | a0001c0001t0002g0340 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.816-4804C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409811 | |||||||
| chr4:53409820 | C | T | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.816-4795C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409820 | |||||||
| chr4:53409915 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-4700A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409915 | |||||||
| chr4:53409931 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.816-4684C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409931 | |||||||
| chr4:53409975 | C | T | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.816-4640C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409975 | |||||||
| chr4:53409986 | C | T | 1 | a0001c0001t0004g0133 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.816-4629C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409986 | |||||||
| chr4:53410040 | C | T | 3 | a0001c0001t0006g0065 a0001c0001t0010g0369 a0001c0001t0011g0368 |
3 | HG02055.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.816-4575C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410040 | |||||||
| chr4:53410081 | G | A | 2 | a0001c0001t0004g0137 a0001c0001t0009g0149 |
2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.816-4534G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410081 | |||||||
| chr4:53410136 | C | G | 1 | a0001c0001t0001g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.816-4479C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410136 | |||||||
| chr4:53410151 | A | G | 3 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 |
3 | HG00558.hp1 NA18957.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.816-4464A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410151 | |||||||
| chr4:53410219 | A | C | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.816-4396A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410219 | |||||||
| chr4:53410236 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.816-4379T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410236 | |||||||
| chr4:53410273 | A | G | 4 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0067 others(1): Show |
4 | NA18968.hp1 NA19003.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.816-4342A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410273 | |||||||
| chr4:53410330 | G | A | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.816-4285G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410330 | |||||||
| chr4:53410341 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816-4274C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410341 | |||||||
| chr4:53410399 | A | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.816-4216A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410399 | |||||||
| chr4:53410476 | C | T | 2 | a0001c0001t0002g0317 a0001c0001t0002g0318 |
2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.816-4139C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410476 | |||||||
| chr4:53410495 | A | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.816-4120A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410495 | |||||||
| chr4:53410515 | G | C | 3 | a0001c0001t0002g0329 a0001c0001t0002g0346 a0001c0001t0002g0357 |
3 | NA18971.hp1 NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.816-4100G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410515 | |||||||
| chr4:53410556 | A | G | 1 | a0001c0001t0005g0255 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.816-4059A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410556 | |||||||
| chr4:53410741 | C | T | 59 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0008 others(56): Show |
64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.816-3874C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410741 | |||||||
| chr4:53410805 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-3810A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410805 | |||||||
| chr4:53410844 | C | T | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | NA18973.hp1 NA18981.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.816-3771C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410844 | |||||||
| chr4:53410908 | C | T | 1 | a0001c0001t0005g0276 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.816-3707C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410908 | |||||||
| chr4:53410967 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.816-3648A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410967 | |||||||
| chr4:53410971 | TG | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.816-3636delG | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53410971 | ||||||
| chr4:53410976 | G | A | 2 | a0001c0001t0002g0330 a0001c0001t0002g0345 |
2 | HG00597.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.816-3639G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410976 | |||||||
| chr4:53411022 | G | A | 15 | a0001c0001t0006g0006 a0001c0001t0006g0032 a0001c0001t0006g0064 others(12): Show |
16 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.816-3593G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411022 | |||||||
| chr4:53411133 | A | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0239 |
2 | HG00544.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.816-3482A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411133 | |||||||
| chr4:53411152 | G | A | 46 | a0001c0001t0001g0186 a0001c0001t0005g0011 a0001c0001t0005g0014 others(43): Show |
47 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.816-3463G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411152 | |||||||
| chr4:53411320 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.816-3295A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411320 | |||||||
| chr4:53411330 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-3285C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411330 | |||||||
| chr4:53411349 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.816-3266C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411349 | |||||||
| chr4:53411375 | G | A | 1 | a0001c0001t0006g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.816-3240G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411375 | |||||||
| chr4:53411480 | T | C | 3 | a0001c0001t0006g0032 a0001c0001t0006g0064 a0001c0001t0016g0033 |
3 | HG01884.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.816-3135T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411480 | |||||||
| chr4:53411481 | A | AT | 75 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(72): Show |
79 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.816-3126dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53411481 | ||||||
| chr4:53411550 | C | T | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.816-3065C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411550 | |||||||
| chr4:53411625 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.816-2990G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411625 | |||||||
| chr4:53411633 | A | C | 6 | a0001c0001t0004g0103 a0001c0001t0004g0112 a0001c0001t0004g0113 others(3): Show |
6 | NA18939.hp1 NA18940.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.816-2982A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411633 | |||||||
| chr4:53411701 | T | C | 2 | a0001c0001t0006g0072 a0001c0001t0006g0073 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.816-2914T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411701 | |||||||
| chr4:53411937 | C | G | 1 | a0001c0001t0002g0339 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.816-2678C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411937 | |||||||
| chr4:53411977 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-2638C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411977 | |||||||
| chr4:53411987 | A | AC | 9 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(6): Show |
9 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.816-2623dupC | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53411987 | ||||||
| chr4:53412006 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.816-2609A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412006 | |||||||
| chr4:53412052 | T | G | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.816-2563T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412052 | |||||||
| chr4:53412266 | A | G | 1 | a0001c0001t0005g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.816-2349A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412266 | |||||||
| chr4:53412563 | T | C | 1 | a0001c0001t0010g0369 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.816-2052T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412563 | |||||||
| chr4:53412623 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.816-1992A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412623 | |||||||
| chr4:53412739 | G | T | 2 | a0001c0001t0006g0072 a0001c0001t0006g0073 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.816-1876G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412739 | |||||||
| chr4:53412740 | C | T | 2 | a0001c0001t0006g0072 a0001c0001t0006g0073 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.816-1875C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412740 | |||||||
| chr4:53412954 | C | T | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.816-1661C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412954 | |||||||
| chr4:53413011 | G | A | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.816-1604G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413011 | |||||||
| chr4:53413032 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-1583G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413032 | |||||||
| chr4:53413036 | C | T | 1 | a0001c0001t0004g0007 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.816-1579C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413036 | |||||||
| chr4:53413125 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(151): Show |
161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.816-1490A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413125 | |||||||
| chr4:53413216 | T | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.816-1399T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413216 | |||||||
| chr4:53413602 | T | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-1013T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413602 | |||||||
| chr4:53413639 | G | T | 1 | a0001c0001t0005g0254 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.816-976G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413639 | |||||||
| chr4:53413656 | T | G | 1 | a0001c0001t0002g0355 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.816-959T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413656 | |||||||
| chr4:53413782 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-833T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413782 | |||||||
| chr4:53413826 | T | A | 1 | a0001c0001t0004g0138 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.816-789T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413826 | |||||||
| chr4:53413862 | A | G | 1 | a0001c0001t0004g0139 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.816-753A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413862 | |||||||
| chr4:53413921 | C | T | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-694C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413921 | |||||||
| chr4:53413932 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-683T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413932 | |||||||
| chr4:53414493 | G | T | 1 | a0001c0001t0004g0111 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.816-122G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53414493 | |||||||
| chr4:53414538 | GA | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(227): Show |
241 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.816-64delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53414538 | ||||||
| chr4:53414801 | A | C | 1 | a0001c0001t0005g0194 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.923+79A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53414801 | |||||||
| chr4:53414904 | C | G | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.923+182C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53414904 | |||||||
| chr4:53414908 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.923+186C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53414908 | |||||||
| chr4:53414985 | G | A | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG01358.hp2 HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.923+263G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53414985 | |||||||
| chr4:53415023 | C | T | 3 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0301 |
3 | NA18960.hp1 NA19079.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.923+301C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415023 | |||||||
| chr4:53415055 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.923+333C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415055 | |||||||
| chr4:53415061 | A | C | 1 | a0001c0001t0004g0139 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.923+339A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415061 | |||||||
| chr4:53415175 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.923+453A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415175 | |||||||
| chr4:53415185 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.923+463G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415185 | |||||||
| chr4:53415528 | T | G | 1 | a0001c0001t0003g0054 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.923+806T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415528 | |||||||
| chr4:53415529 | G | GT | 17 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(14): Show |
17 | HG01074.hp2 HG01099.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.923+818dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53415529 | ||||||
| chr4:53415529 | G | GTT | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(147): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.923+817_923+818dup others(2): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53415529 | ||||||
| chr4:53415530 | T | G | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.923+808T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415530 | |||||||
| chr4:53415547 | G | T | 1 | a0001c0001t0006g0006 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.923+825G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415547 | |||||||
| chr4:53415553 | G | T | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.923+831G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415553 | |||||||
| chr4:53415564 | T | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.923+842T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415564 | |||||||
| chr4:53415571 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.923+849C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415571 | |||||||
| chr4:53415824 | A | G | 1 | a0001c0001t0012g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923+1102A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415824 | |||||||
| chr4:53415976 | A | G | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.923+1254A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415976 | |||||||
| chr4:53416023 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.923+1301C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416023 | |||||||
| chr4:53416085 | A | C | 1 | a0001c0001t0009g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.923+1363A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416085 | |||||||
| chr4:53416119 | A | G | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.923+1397A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416119 | |||||||
| chr4:53416170 | A | G | 4 | a0001c0001t0004g0002 a0001c0001t0004g0104 a0001c0001t0007g0002 others(1): Show |
5 | NA18956.hp2 NA18963.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+1448A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416170 | |||||||
| chr4:53416236 | A | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.923+1514A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416236 | |||||||
| chr4:53416427 | C | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0364 a0001c0001t0002g0365 others(2): Show |
6 | HG00642.hp2 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+1705C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416427 | |||||||
| chr4:53416431 | A | G | 1 | a0001c0001t0003g0077 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.923+1709A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416431 | |||||||
| chr4:53416529 | G | A | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.923+1807G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416529 | |||||||
| chr4:53416987 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0185 |
2 | HG00280.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.923+2265A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416987 | |||||||
| chr4:53416999 | A | G | 1 | a0001c0001t0004g0132 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.923+2277A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416999 | |||||||
| chr4:53417146 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.923+2424C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417146 | |||||||
| chr4:53417182 | C | T | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+2460C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417182 | |||||||
| chr4:53417236 | T | C | 1 | a0001c0001t0004g0140 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.923+2514T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417236 | |||||||
| chr4:53417328 | C | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.923+2606C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417328 | |||||||
| chr4:53417407 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.923+2685C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417407 | |||||||
| chr4:53417629 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.923+2907C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417629 | |||||||
| chr4:53417642 | C | CA | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(107): Show |
116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.923+2944dupA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417642 | ||||||
| chr4:53417642 | C | CAA | 84 | a0001c0001t0001g0157 a0001c0001t0001g0167 a0001c0001t0001g0173 others(81): Show |
89 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.923+2943_923+2944d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417642 | ||||||
| chr4:53417642 | C | CAAA | 14 | a0001c0001t0001g0172 a0001c0001t0004g0007 a0001c0001t0004g0096 others(11): Show |
15 | HG02135.hp2 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+2942_923+2944d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417642 | ||||||
| chr4:53417642 | CA | C | 74 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(71): Show |
78 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(75): Show |
intron_variant | MODIFIER | c.923+2944delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417642 | ||||||
| chr4:53417662 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.923+2940A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417662 | |||||||
| chr4:53417702 | AGCTACTT others(9): Show |
A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG00280.hp1 HG01070.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+2997_923+3012d others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417702 | ||||||
| chr4:53417738 | A | AACACACA others(3): Show |
1 | a0001c0001t0011g0368 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.923+3033_923+3042d others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417738 | ||||||
| chr4:53417738 | A | AACACACA others(5): Show |
2 | a0001c0001t0002g0309 a0001c0001t0002g0351 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.923+3031_923+3042d others(14): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417738 | ||||||
| chr4:53417738 | A | AACACACA others(7): Show |
1 | a0001c0001t0002g0362 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.923+3029_923+3042d others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417738 | ||||||
| chr4:53417755 | ACACACAC others(31): Show |
A | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.923+3035_923+3072d others(40): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417755 | ||||||
| chr4:53417755 | ACACACAC others(33): Show |
A | 2 | a0001c0001t0008g0005 a0001c0001t0008g0017 |
3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.923+3035_923+3074d others(42): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417755 | ||||||
| chr4:53417759 | ACACACTC others(7): Show |
A | 2 | a0001c0001t0003g0087 a0001c0001t0003g0089 |
2 | NA18959.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.923+3039_923+3052d others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | ||||||
| chr4:53417759 | ACACACTC others(9): Show |
A | 6 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0083 others(3): Show |
6 | NA18944.hp1 NA18955.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+3039_923+3054d others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | ||||||
| chr4:53417759 | ACACACTC others(11): Show |
A | 9 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0047 others(6): Show |
9 | HG00621.hp1 HG00741.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+3039_923+3056d others(20): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | ||||||
| chr4:53417759 | ACACACTC others(13): Show |
A | 37 | a0001c0001t0003g0027 a0001c0001t0003g0030 a0001c0001t0003g0031 others(34): Show |
37 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.923+3039_923+3058d others(22): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | ||||||
| chr4:53417759 | ACACACTC others(15): Show |
A | 9 | a0001c0001t0003g0029 a0001c0001t0003g0040 a0001c0001t0006g0071 others(6): Show |
9 | HG00673.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+3039_923+3060d others(24): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | ||||||
| chr4:53417759 | ACACACTC others(17): Show |
A | 3 | a0001c0001t0006g0065 a0001c0001t0006g0069 a0001c0001t0006g0092 |
3 | HG02572.hp2 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.923+3039_923+3062d others(26): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | ||||||
| chr4:53417759 | ACACACTC others(19): Show |
A | 2 | a0001c0001t0003g0035 a0001c0001t0006g0006 |
3 | HG01358.hp1 HG01361.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.923+3039_923+3064d others(28): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | ||||||
| chr4:53417759 | ACACACTC others(21): Show |
A | 1 | a0001c0001t0003g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.923+3039_923+3066d others(30): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | ||||||
| chr4:53417761 | ACACTCTC others(9): Show |
A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0082 |
2 | HG02027.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.923+3041_923+3056d others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417761 | ||||||
| chr4:53417761 | ACACTCTC others(11): Show |
A | 4 | a0001c0001t0003g0046 a0001c0001t0003g0048 a0001c0001t0003g0063 others(1): Show |
4 | HG02056.hp1 HG04199.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+3041_923+3058d others(20): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417761 | ||||||
| chr4:53417761 | ACACTCTC others(23): Show |
A | 2 | a0001c0001t0004g0139 a0001c0001t0004g0148 |
2 | HG01099.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.923+3041_923+3070d others(32): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417761 | ||||||
| chr4:53417763 | ACTCT | A | 7 | a0001c0001t0001g0196 a0001c0001t0001g0263 a0001c0001t0002g0300 others(4): Show |
7 | HG02135.hp1 HG02280.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+3095_923+3098d others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCT | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0166 a0001c0001t0001g0172 others(7): Show |
10 | HG01081.hp1 HG01515.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.923+3093_923+3098d others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(1): Show |
A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0165 a0001c0001t0001g0171 others(16): Show |
19 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.923+3091_923+3098d others(10): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(3): Show |
A | 23 | a0001c0001t0001g0182 a0001c0001t0001g0195 a0001c0001t0001g0214 others(20): Show |
23 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.923+3089_923+3098d others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(5): Show |
A | 37 | a0001c0001t0001g0015 a0001c0001t0001g0167 a0001c0001t0001g0168 others(34): Show |
37 | HG00280.hp1 HG00558.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.923+3087_923+3098d others(14): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(7): Show |
A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0152 a0001c0001t0001g0179 others(29): Show |
33 | HG00140.hp2 HG00642.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.923+3085_923+3098d others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(9): Show |
A | 6 | a0001c0001t0001g0154 a0001c0001t0005g0014 a0001c0001t0005g0231 others(3): Show |
6 | HG02135.hp2 HG02451.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+3083_923+3098d others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(11): Show |
A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0153 a0001c0001t0001g0155 others(25): Show |
30 | HG00408.hp1 HG01346.hp1 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.923+3081_923+3098d others(20): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(13): Show |
A | 21 | a0001c0001t0001g0291 a0001c0001t0002g0318 a0001c0001t0002g0336 others(18): Show |
22 | HG00323.hp1 HG00733.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.923+3079_923+3098d others(22): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(15): Show |
A | 11 | a0001c0001t0001g0259 a0001c0001t0002g0313 a0001c0001t0002g0324 others(8): Show |
12 | HG02486.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+3077_923+3098d others(24): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(17): Show |
A | 12 | a0001c0001t0002g0004 a0001c0001t0002g0303 a0001c0001t0002g0306 others(9): Show |
12 | HG00597.hp2 HG02129.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.923+3075_923+3098d others(26): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(19): Show |
A | 25 | a0001c0001t0002g0012 a0001c0001t0002g0298 a0001c0001t0002g0299 others(22): Show |
26 | HG00558.hp1 HG01192.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.923+3073_923+3098d others(28): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(21): Show |
A | 7 | a0001c0001t0002g0004 a0001c0001t0002g0297 a0001c0001t0002g0339 others(4): Show |
8 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+3071_923+3098d others(30): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(23): Show |
A | 47 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(44): Show |
51 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.923+3069_923+3098d others(32): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(25): Show |
A | 2 | a0001c0001t0002g0304 a0001c0001t0002g0312 |
2 | HG02523.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.923+3067_923+3098d others(34): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417763 | ACTCTCTC others(27): Show |
A | 1 | a0001c0001t0004g0117 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.923+3065_923+3098d others(36): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | ||||||
| chr4:53417765 | T | A | 9 | a0001c0001t0002g0307 a0001c0001t0002g0308 a0001c0001t0002g0309 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+3043T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417765 | |||||||
| chr4:53417767 | T | A | 9 | a0001c0001t0002g0307 a0001c0001t0002g0308 a0001c0001t0002g0309 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+3045T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417767 | |||||||
| chr4:53417769 | T | A | 12 | a0001c0001t0001g0196 a0001c0001t0001g0263 a0001c0001t0002g0300 others(9): Show |
12 | HG02055.hp2 HG02109.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.923+3047T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417769 | |||||||
| chr4:53417771 | T | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0166 a0001c0001t0001g0172 others(16): Show |
19 | HG01081.hp1 HG01515.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.923+3049T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417771 | |||||||
| chr4:53417773 | T | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0165 a0001c0001t0001g0166 others(27): Show |
31 | HG00621.hp2 HG00673.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.923+3051T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417773 | |||||||
| chr4:53417775 | T | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0165 a0001c0001t0001g0171 others(43): Show |
46 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.923+3053T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417775 | |||||||
| chr4:53417777 | T | A | 54 | a0001c0001t0001g0015 a0001c0001t0001g0167 a0001c0001t0001g0168 others(51): Show |
54 | HG00280.hp1 HG00558.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.923+3055T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417777 | |||||||
| chr4:53417779 | T | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0152 others(61): Show |
66 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.923+3057T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417779 | |||||||
| chr4:53417781 | T | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0154 a0001c0001t0001g0179 others(47): Show |
51 | HG00140.hp2 HG00642.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.923+3059T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417781 | |||||||
| chr4:53417783 | T | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0153 a0001c0001t0001g0154 others(59): Show |
65 | HG00408.hp1 HG00642.hp2 HG01243.hp2 others(62): Show |
intron_variant | MODIFIER | c.923+3061T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417783 | |||||||
| chr4:53417785 | T | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0153 a0001c0001t0001g0154 others(53): Show |
60 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.923+3063T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417785 | |||||||
| chr4:53417787 | T | A | 44 | a0001c0001t0001g0259 a0001c0001t0001g0291 a0001c0001t0002g0013 others(41): Show |
46 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.923+3065T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417787 | |||||||
| chr4:53417789 | T | A | 38 | a0001c0001t0001g0291 a0001c0001t0002g0004 a0001c0001t0002g0013 others(35): Show |
39 | HG00597.hp2 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.923+3067T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417789 | |||||||
| chr4:53417791 | T | A | 58 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(55): Show |
60 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.923+3069T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417791 | |||||||
| chr4:53417793 | T | A | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.923+3071T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417793 | |||||||
| chr4:53417795 | T | A | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.923+3073T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417795 | |||||||
| chr4:53417797 | T | A | 66 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(63): Show |
70 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.923+3075T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417797 | |||||||
| chr4:53417799 | T | A | 66 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(63): Show |
70 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.923+3077T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417799 | |||||||
| chr4:53417801 | T | A | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.923+3079T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417801 | |||||||
| chr4:53417803 | T | A | 63 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(60): Show |
67 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.923+3081T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417803 | |||||||
| chr4:53417805 | T | A | 59 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
63 | HG00558.hp1 HG00642.hp2 HG01192.hp1 others(60): Show |
intron_variant | MODIFIER | c.923+3083T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417805 | |||||||
| chr4:53417807 | T | A | 24 | a0001c0001t0002g0004 a0001c0001t0002g0013 a0001c0001t0002g0297 others(21): Show |
27 | HG00642.hp2 HG01261.hp1 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.923+3085T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417807 | |||||||
| chr4:53417809 | T | A | 3 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0322 |
3 | HG02683.hp1 HG03239.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.923+3087T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417809 | |||||||
| chr4:53417811 | T | A | 3 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0322 |
3 | HG02683.hp1 HG03239.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.923+3089T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417811 | |||||||
| chr4:53417813 | T | A | 2 | a0001c0001t0002g0312 a0001c0001t0002g0314 |
2 | HG02683.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.923+3091T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417813 | |||||||
| chr4:53417820 | C | A | 1 | a0001c0001t0003g0035 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.923+3098C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417820 | |||||||
| chr4:53417849 | A | G | 1 | a0001c0001t0002g0313 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.923+3127A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417849 | |||||||
| chr4:53417891 | T | G | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.923+3169T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417891 | |||||||
| chr4:53418051 | A | G | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | HG01071.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.923+3329A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418051 | |||||||
| chr4:53418237 | G | A | 54 | a0001c0001t0002g0329 a0001c0001t0002g0346 a0001c0001t0002g0357 others(51): Show |
58 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.923+3515G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418237 | |||||||
| chr4:53418281 | C | CTAAA | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(38): Show |
46 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.923+3574_923+3577d others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53418281 | ||||||
| chr4:53418537 | A | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0066 |
2 | HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.923+3815A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418537 | |||||||
| chr4:53418700 | A | G | 8 | a0001c0001t0005g0197 a0001c0001t0005g0198 a0001c0001t0005g0199 others(5): Show |
8 | HG01255.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.923+3978A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418700 | |||||||
| chr4:53418738 | T | C | 1 | a0001c0001t0005g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.923+4016T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418738 | |||||||
| chr4:53418746 | G | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+4024G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418746 | |||||||
| chr4:53418858 | A | G | 1 | a0001c0001t0002g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.923+4136A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418858 | |||||||
| chr4:53419553 | A | G | 76 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(73): Show |
80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.923+4831A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419553 | |||||||
| chr4:53419600 | C | T | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.923+4878C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419600 | |||||||
| chr4:53419710 | C | G | 1 | a0001c0001t0018g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.923+4988C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419710 | |||||||
| chr4:53419725 | G | T | 1 | a0001c0001t0002g0300 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+5003G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419725 | |||||||
| chr4:53419739 | C | A | 1 | a0001c0001t0004g0114 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.923+5017C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419739 | |||||||
| chr4:53419785 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.923+5063A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419785 | |||||||
| chr4:53419846 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.923+5124C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419846 | |||||||
| chr4:53419886 | G | A | 1 | a0001c0001t0004g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.923+5164G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419886 | |||||||
| chr4:53419928 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.923+5206G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419928 | |||||||
| chr4:53419941 | G | A | 2 | a0001c0001t0002g0298 a0001c0001t0002g0299 |
2 | NA18960.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.923+5219G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419941 | |||||||
| chr4:53420054 | C | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.923+5332C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420054 | |||||||
| chr4:53420059 | G | A | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.923+5337G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420059 | |||||||
| chr4:53420069 | G | T | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.923+5347G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420069 | |||||||
| chr4:53420130 | G | A | 1 | a0001c0001t0006g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.923+5408G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420130 | |||||||
| chr4:53420156 | C | T | 2 | a0001c0001t0004g0007 a0001c0001t0004g0096 |
3 | HG02486.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.923+5434C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420156 | |||||||
| chr4:53420176 | C | T | 1 | a0001c0001t0004g0141 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.923+5454C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420176 | |||||||
| chr4:53420197 | C | CA | 73 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0152 others(70): Show |
76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.923+5503dupA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | ||||||
| chr4:53420197 | C | CAA | 71 | a0001c0001t0001g0003 a0001c0001t0001g0154 a0001c0001t0001g0155 others(68): Show |
74 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.923+5502_923+5503d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | ||||||
| chr4:53420197 | C | CAAA | 34 | a0001c0001t0001g0158 a0001c0001t0001g0196 a0001c0001t0001g0288 others(31): Show |
37 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.923+5501_923+5503d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | ||||||
| chr4:53420197 | C | CAAAA | 15 | a0001c0001t0004g0110 a0001c0001t0004g0111 a0001c0001t0004g0115 others(12): Show |
15 | HG00140.hp1 HG00423.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+5500_923+5503d others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | ||||||
| chr4:53420197 | CA | C | 65 | a0001c0001t0003g0023 a0001c0001t0003g0026 a0001c0001t0003g0027 others(62): Show |
66 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.923+5503delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | ||||||
| chr4:53420197 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0004g0002 a0001c0001t0004g0104 a0001c0001t0004g0105 others(3): Show |
7 | NA18941.hp2 NA18956.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+5495_923+5503d others(11): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | ||||||
| chr4:53420199 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0002g0355 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.923+5487_923+5488i others(13): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420199 | ||||||
| chr4:53420200 | A | AAAAAAAA others(3): Show |
12 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(9): Show |
12 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.923+5487_923+5488i others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420200 | ||||||
| chr4:53420201 | A | AAAAAAAA others(2): Show |
58 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0297 others(55): Show |
61 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.923+5487_923+5488i others(11): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420201 | ||||||
| chr4:53420210 | A | C | 6 | a0001c0001t0002g0013 a0001c0001t0002g0364 a0001c0001t0002g0365 others(3): Show |
7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+5488A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420210 | |||||||
| chr4:53420212 | A | C | 12 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(9): Show |
12 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.923+5490A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420212 | |||||||
| chr4:53420213 | A | C | 60 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0297 others(57): Show |
63 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(60): Show |
intron_variant | MODIFIER | c.923+5491A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420213 | |||||||
| chr4:53420217 | A | AAAAACAA others(2): Show |
6 | a0001c0001t0002g0013 a0001c0001t0002g0364 a0001c0001t0002g0365 others(3): Show |
7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+5499_923+5500i others(11): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420217 | ||||||
| chr4:53420226 | C | A | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.923+5504C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420226 | |||||||
| chr4:53420284 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.923+5562T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420284 | |||||||
| chr4:53420317 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.924-5555A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420317 | |||||||
| chr4:53420392 | G | T | 1 | a0001c0001t0005g0254 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.924-5480G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420392 | |||||||
| chr4:53420393 | C | T | 1 | a0001c0001t0005g0254 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.924-5479C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420393 | |||||||
| chr4:53420423 | C | G | 1 | a0001c0001t0003g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.924-5449C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420423 | |||||||
| chr4:53420429 | CA | C | 16 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(13): Show |
16 | HG01257.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.924-5424delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420429 | ||||||
| chr4:53420448 | AGAT | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(142): Show |
151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.924-5423_924-5421d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420448 | |||||||
| chr4:53420451 | TAAATC | T | 6 | a0001c0001t0001g0215 a0001c0001t0001g0238 a0001c0001t0001g0270 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-5419_924-5415d others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420451 | ||||||
| chr4:53420453 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(142): Show |
151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.924-5419A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420453 | |||||||
| chr4:53420455 | TC | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(142): Show |
151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.924-5416delC | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420455 | |||||||
| chr4:53420527 | T | G | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.924-5345T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420527 | |||||||
| chr4:53420563 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-5309A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420563 | |||||||
| chr4:53420589 | G | A | 1 | a0001c0001t0002g0355 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.924-5283G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420589 | |||||||
| chr4:53420614 | A | T | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.924-5258A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420614 | |||||||
| chr4:53420631 | C | G | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.924-5241C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420631 | |||||||
| chr4:53420718 | AG | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-5152delG | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420718 | ||||||
| chr4:53420736 | A | G | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.924-5136A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420736 | |||||||
| chr4:53420796 | A | G | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-5076A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420796 | |||||||
| chr4:53420807 | T | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.924-5065T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420807 | |||||||
| chr4:53421070 | G | T | 1 | a0001c0001t0001g0293 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.924-4802G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53421070 | |||||||
| chr4:53421382 | A | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.924-4490A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53421382 | |||||||
| chr4:53421530 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.924-4342T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53421530 | |||||||
| chr4:53421589 | T | A | 74 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(71): Show |
78 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.924-4283T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53421589 | |||||||
| chr4:53421874 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.924-3998G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53421874 | |||||||
| chr4:53422024 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.924-3848T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422024 | |||||||
| chr4:53422410 | A | G | 2 | a0001c0001t0008g0005 a0001c0001t0008g0017 |
3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.924-3462A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422410 | |||||||
| chr4:53422457 | C | G | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.924-3415C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422457 | |||||||
| chr4:53422639 | T | C | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.924-3233T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422639 | |||||||
| chr4:53422722 | A | T | 47 | a0001c0001t0004g0113 a0001c0001t0005g0011 a0001c0001t0005g0014 others(44): Show |
48 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.924-3150A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422722 | |||||||
| chr4:53422724 | T | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(108): Show |
116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.924-3148T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422724 | |||||||
| chr4:53422860 | A | C | 1 | a0001c0001t0002g0349 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.924-3012A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422860 | |||||||
| chr4:53422868 | C | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.924-3004C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422868 | |||||||
| chr4:53422880 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.924-2992G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422880 | |||||||
| chr4:53422913 | G | A | 1 | a0001c0001t0018g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.924-2959G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422913 | |||||||
| chr4:53423014 | G | A | 1 | a0001c0001t0010g0369 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.924-2858G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423014 | |||||||
| chr4:53423195 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(150): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.924-2677G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423195 | |||||||
| chr4:53423213 | G | A | 7 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0244 others(4): Show |
7 | NA18940.hp2 NA18945.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.924-2659G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423213 | |||||||
| chr4:53423463 | A | T | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.924-2409A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423463 | |||||||
| chr4:53423525 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.924-2347A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423525 | |||||||
| chr4:53423549 | C | T | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.924-2323C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423549 | |||||||
| chr4:53423564 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.924-2308T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423564 | |||||||
| chr4:53423574 | G | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-2298G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423574 | |||||||
| chr4:53423615 | T | G | 1 | a0001c0001t0003g0089 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.924-2257T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423615 | |||||||
| chr4:53423659 | G | A | 1 | a0001c0001t0011g0368 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.924-2213G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423659 | |||||||
| chr4:53423663 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.924-2209A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423663 | |||||||
| chr4:53423671 | A | C | 1 | a0001c0001t0005g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.924-2201A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423671 | |||||||
| chr4:53423772 | T | C | 1 | a0001c0001t0002g0330 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.924-2100T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423772 | |||||||
| chr4:53423811 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.924-2061T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423811 | |||||||
| chr4:53424035 | T | C | 1 | a0001c0001t0002g0300 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.924-1837T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53424035 | |||||||
| chr4:53424062 | A | G | 4 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(1): Show |
4 | NA18961.hp1 NA18974.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-1810A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53424062 | |||||||
| chr4:53424242 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.924-1630A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53424242 | |||||||
| chr4:53424310 | A | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.924-1562A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53424310 | |||||||
| chr4:53424510 | A | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.924-1362A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53424510 | |||||||
| chr4:53425053 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.924-819G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425053 | |||||||
| chr4:53425070 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.924-802C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425070 | |||||||
| chr4:53425197 | T | C | 1 | a0001c0001t0002g0354 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.924-675T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425197 | |||||||
| chr4:53425210 | A | T | 4 | a0001c0001t0005g0274 a0001c0001t0005g0275 a0001c0001t0005g0277 others(1): Show |
4 | NA18971.hp2 NA18990.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-662A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425210 | |||||||
| chr4:53425230 | G | C | 1 | a0001c0001t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.924-642G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425230 | |||||||
| chr4:53425294 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.924-578T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425294 | |||||||
| chr4:53425426 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0269 |
2 | NA18995.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.924-446T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425426 | |||||||
| chr4:53425595 | C | G | 4 | a0001c0001t0004g0109 a0001c0001t0004g0117 a0001c0001t0004g0140 others(1): Show |
4 | HG01074.hp2 HG01099.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-277C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425595 | |||||||
| chr4:53425833 | A | G | 8 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0060 others(5): Show |
8 | HG00544.hp1 HG00673.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.924-39A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425833 | |||||||
| chr4:53425837 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0182 a0001c0001t0001g0183 |
6 | HG00140.hp2 HG01169.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-35G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425837 | |||||||
| chr4:53426017 | A | G | 1 | a0001c0001t0002g0343 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1017+52A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426017 | |||||||
| chr4:53426109 | T | C | 1 | a0001c0001t0006g0006 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1017+144T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426109 | |||||||
| chr4:53426211 | T | C | 1 | a0001c0001t0002g0339 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1017+246T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426211 | |||||||
| chr4:53426278 | G | A | 2 | a0001c0001t0003g0055 a0001c0001t0003g0370 |
2 | HG00423.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1017+313G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426278 | |||||||
| chr4:53426624 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1017+659T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426624 | |||||||
| chr4:53426929 | CT | C | 8 | a0001c0001t0004g0009 a0001c0001t0004g0115 a0001c0001t0004g0122 others(5): Show |
9 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1017+971delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr4 | 53426929 | ||||||
| chr4:53426981 | G | A | 1 | a0001c0001t0005g0276 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1017+1016G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426981 | |||||||
| chr4:53427012 | A | G | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1018-1015A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427012 | |||||||
| chr4:53427170 | G | T | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1018-857G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427170 | |||||||
| chr4:53427223 | T | G | 1 | a0001c0001t0002g0352 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1018-804T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427223 | |||||||
| chr4:53427345 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1018-682A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427345 | |||||||
| chr4:53427376 | G | T | 1 | a0001c0001t0002g0349 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1018-651G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427376 | |||||||
| chr4:53427381 | T | G | 2 | a0001c0001t0004g0007 a0001c0001t0004g0096 |
3 | HG02486.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1018-646T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427381 | |||||||
| chr4:53427527 | C | G | 1 | a0001c0001t0002g0355 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1018-500C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427527 | |||||||
| chr4:53427777 | G | T | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1018-250G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427777 | |||||||
| chr4:53427865 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1018-162C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427865 | |||||||
| chr4:53427875 | A | T | 45 | a0001c0001t0005g0011 a0001c0001t0005g0014 a0001c0001t0005g0151 others(42): Show |
46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1018-152A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427875 | |||||||
| chr4:53428371 | A | G | 11 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(8): Show |
11 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174+188A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428371 | |||||||
| chr4:53428393 | A | G | 2 | a0001c0001t0008g0005 a0001c0001t0008g0017 |
3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1174+210A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428393 | |||||||
| chr4:53428423 | A | G | 1 | a0001c0001t0005g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1174+240A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428423 | |||||||
| chr4:53428439 | A | C | 75 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(72): Show |
76 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1174+256A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428439 | |||||||
| chr4:53428464 | A | G | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1174+281A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428464 | |||||||
| chr4:53428510 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1174+327G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428510 | |||||||
| chr4:53428595 | GTCT | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(34): Show |
42 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1174+419_1174+421d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53428595 | ||||||
| chr4:53428767 | T | A | 4 | a0001c0001t0001g0260 a0001c0001t0001g0264 a0001c0001t0001g0270 others(1): Show |
4 | NA18954.hp1 NA18956.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+584T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428767 | |||||||
| chr4:53428774 | G | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+591G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428774 | |||||||
| chr4:53428841 | G | A | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1174+658G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428841 | |||||||
| chr4:53429002 | G | A | 1 | a0001c0001t0002g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1174+819G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429002 | |||||||
| chr4:53429060 | G | C | 59 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0008 others(56): Show |
64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1174+877G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429060 | |||||||
| chr4:53429065 | G | A | 50 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(47): Show |
54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1174+882G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429065 | |||||||
| chr4:53429465 | T | G | 9 | a0001c0001t0005g0151 a0001c0001t0005g0189 a0001c0001t0005g0227 others(6): Show |
9 | HG00408.hp1 HG02165.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174+1282T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429465 | |||||||
| chr4:53429630 | G | A | 6 | a0001c0001t0002g0013 a0001c0001t0002g0364 a0001c0001t0002g0365 others(3): Show |
7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1447G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429630 | |||||||
| chr4:53429786 | T | C | 1 | a0001c0001t0013g0235 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1174+1603T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429786 | |||||||
| chr4:53429953 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(210): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1174+1770G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429953 | |||||||
| chr4:53429957 | C | T | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0256 others(1): Show |
4 | HG01109.hp2 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1774C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429957 | |||||||
| chr4:53430214 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1174+2031A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430214 | |||||||
| chr4:53430240 | A | G | 1 | a0001c0001t0003g0049 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1174+2057A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430240 | |||||||
| chr4:53430248 | C | G | 15 | a0001c0001t0006g0006 a0001c0001t0006g0032 a0001c0001t0006g0064 others(12): Show |
16 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1174+2065C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430248 | |||||||
| chr4:53430250 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+2067A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430250 | |||||||
| chr4:53430256 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1174+2073C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430256 | |||||||
| chr4:53430341 | C | CT | 62 | a0001c0001t0001g0015 a0001c0001t0001g0152 a0001c0001t0001g0157 others(59): Show |
63 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1174+2182dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53430341 | ||||||
| chr4:53430341 | CT | C | 121 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0002g0004 others(118): Show |
130 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.1174+2182delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53430341 | ||||||
| chr4:53430412 | G | A | 1 | a0001c0001t0005g0276 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1174+2229G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430412 | |||||||
| chr4:53430585 | C | T | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+2402C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430585 | |||||||
| chr4:53430825 | G | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1174+2642G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430825 | |||||||
| chr4:53430837 | A | G | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174+2654A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430837 | |||||||
| chr4:53430984 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1174+2801C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430984 | |||||||
| chr4:53431047 | A | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0364 a0001c0001t0002g0365 others(2): Show |
6 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174+2864A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431047 | |||||||
| chr4:53431073 | G | A | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | NA18973.hp1 NA18981.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+2890G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431073 | |||||||
| chr4:53431149 | T | A | 59 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0008 others(56): Show |
64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1174+2966T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431149 | |||||||
| chr4:53431277 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1174+3094A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431277 | |||||||
| chr4:53431353 | A | G | 1 | a0001c0001t0002g0304 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1174+3170A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431353 | |||||||
| chr4:53431366 | C | T | 1 | a0001c0001t0005g0226 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1174+3183C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431366 | |||||||
| chr4:53431541 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1174+3358A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431541 | |||||||
| chr4:53431582 | T | G | 1 | a0001c0001t0005g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174+3399T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431582 | |||||||
| chr4:53431584 | C | A | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1174+3401C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431584 | |||||||
| chr4:53431608 | TTTTTG | T | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.1174+3445_1174+344 others(9): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53431608 | ||||||
| chr4:53431633 | C | T | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.1174+3450C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431633 | |||||||
| chr4:53431652 | T | A | 1 | a0001c0001t0003g0054 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1174+3469T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431652 | |||||||
| chr4:53431737 | G | C | 1 | a0001c0001t0001g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1174+3554G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431737 | |||||||
| chr4:53431771 | A | T | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174+3588A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431771 | |||||||
| chr4:53431910 | T | G | 2 | a0001c0001t0002g0305 a0001c0001t0002g0332 |
2 | HG02056.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1174+3727T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431910 | |||||||
| chr4:53432086 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0181 |
2 | HG00673.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1174+3903A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432086 | |||||||
| chr4:53432157 | A | AGGCTGAG others(11): Show |
1 | a0001c0001t0004g0125 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1174+3975_1174+399 others(22): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432157 | ||||||
| chr4:53432171 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0152 others(216): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1174+3988A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432171 | |||||||
| chr4:53432199 | C | G | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1174+4016C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432199 | |||||||
| chr4:53432270 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0152 others(135): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1174+4087C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432270 | |||||||
| chr4:53432272 | C | T | 2 | a0001c0001t0008g0005 a0001c0001t0008g0017 |
3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1174+4089C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432272 | |||||||
| chr4:53432398 | CA | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0153 a0001c0001t0001g0154 others(113): Show |
119 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1174+4241delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | ||||||
| chr4:53432398 | CAA | C | 55 | a0001c0001t0001g0234 a0001c0001t0001g0239 a0001c0001t0001g0244 others(52): Show |
60 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1174+4240_1174+424 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | ||||||
| chr4:53432398 | CAAA | C | 70 | a0001c0001t0001g0152 a0001c0001t0001g0165 a0001c0001t0001g0166 others(67): Show |
71 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1174+4239_1174+424 others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | ||||||
| chr4:53432398 | CAAAA | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0168 others(117): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1174+4238_1174+424 others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | ||||||
| chr4:53432398 | CAAAAA | C | 8 | a0001c0001t0001g0170 a0001c0001t0001g0179 a0001c0001t0001g0185 others(5): Show |
8 | HG01070.hp2 HG01243.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+4237_1174+424 others(9): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | ||||||
| chr4:53432398 | CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0008g0005 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1174+4221_1174+424 others(25): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | ||||||
| chr4:53432438 | T | C | 1 | a0001c0001t0012g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1174+4255T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432438 | |||||||
| chr4:53432494 | G | A | 45 | a0001c0001t0005g0011 a0001c0001t0005g0014 a0001c0001t0005g0151 others(42): Show |
46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1174+4311G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432494 | |||||||
| chr4:53432679 | A | T | 6 | a0001c0001t0002g0013 a0001c0001t0002g0364 a0001c0001t0002g0365 others(3): Show |
7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+4496A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432679 | |||||||
| chr4:53432839 | G | A | 2 | a0001c0001t0003g0056 a0001c0001t0003g0057 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1174+4656G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432839 | |||||||
| chr4:53433156 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1174+4973C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433156 | |||||||
| chr4:53433189 | G | T | 1 | a0001c0001t0003g0081 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1174+5006G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433189 | |||||||
| chr4:53433213 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(220): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1174+5030T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433213 | |||||||
| chr4:53433304 | C | T | 1 | a0001c0001t0002g0336 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1174+5121C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433304 | |||||||
| chr4:53433402 | T | G | 1 | a0001c0001t0002g0328 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1174+5219T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433402 | |||||||
| chr4:53433438 | T | C | 45 | a0001c0001t0005g0011 a0001c0001t0005g0014 a0001c0001t0005g0151 others(42): Show |
46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1174+5255T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433438 | |||||||
| chr4:53433498 | GTCA | G | 75 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(72): Show |
76 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1174+5320_1174+532 others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53433498 | ||||||
| chr4:53433517 | AT | A | 364 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(361): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1174+5345delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53433517 | ||||||
| chr4:53433716 | G | A | 1 | a0001c0001t0002g0349 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1174+5533G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433716 | |||||||
| chr4:53433838 | C | T | 2 | a0001c0001t0008g0005 a0001c0001t0008g0017 |
3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1174+5655C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433838 | |||||||
| chr4:53433922 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1174+5739C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433922 | |||||||
| chr4:53433936 | T | C | 1 | a0001c0001t0002g0339 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1174+5753T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433936 | |||||||
| chr4:53433960 | G | C | 37 | a0001c0001t0005g0011 a0001c0001t0005g0014 a0001c0001t0005g0151 others(34): Show |
38 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1174+5777G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433960 | |||||||
| chr4:53434079 | C | T | 1 | a0001c0001t0004g0114 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1174+5896C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434079 | |||||||
| chr4:53434091 | G | A | 1 | a0001c0001t0002g0349 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1174+5908G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434091 | |||||||
| chr4:53434147 | T | TAC | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174+5964_1174+596 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434147 | |||||||
| chr4:53434252 | A | T | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174+6069A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434252 | |||||||
| chr4:53434354 | G | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1174+6171G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434354 | |||||||
| chr4:53434355 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1174+6172C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434355 | |||||||
| chr4:53434424 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1174+6241A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434424 | |||||||
| chr4:53434429 | G | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1174+6246G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434429 | |||||||
| chr4:53434471 | A | AT | 7 | a0001c0001t0005g0203 a0001c0001t0005g0226 a0001c0001t0005g0228 others(4): Show |
8 | HG01243.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+6305dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53434471 | ||||||
| chr4:53434471 | AT | A | 68 | a0001c0001t0001g0152 a0001c0001t0001g0195 a0001c0001t0001g0196 others(65): Show |
68 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1174+6305delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53434471 | ||||||
| chr4:53434618 | T | G | 6 | a0001c0001t0002g0013 a0001c0001t0002g0364 a0001c0001t0002g0365 others(3): Show |
7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+6435T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434618 | |||||||
| chr4:53434674 | G | A | 4 | a0001c0001t0001g0202 a0001c0001t0001g0284 a0001c0001t0012g0224 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+6491G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434674 | |||||||
| chr4:53434760 | G | A | 3 | a0001c0001t0005g0275 a0001c0001t0005g0277 a0001c0001t0005g0283 |
3 | NA18971.hp2 NA19082.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1174+6577G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434760 | |||||||
| chr4:53434889 | T | A | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1174+6706T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434889 | |||||||
| chr4:53434994 | A | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1174+6811A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434994 | |||||||
| chr4:53435826 | CGT | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(228): Show |
242 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1175-6819_1175-681 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53435826 | ||||||
| chr4:53435856 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1175-6797G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53435856 | |||||||
| chr4:53435885 | G | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0297 a0001c0001t0002g0319 others(1): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-6768G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53435885 | |||||||
| chr4:53435993 | A | G | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1175-6660A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53435993 | |||||||
| chr4:53436003 | A | G | 1 | a0001c0001t0002g0349 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1175-6650A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53436003 | |||||||
| chr4:53436077 | G | GT | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1175-6575dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53436077 | ||||||
| chr4:53436133 | A | T | 1 | a0001c0001t0001g0180 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1175-6520A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53436133 | |||||||
| chr4:53436530 | T | C | 3 | a0001c0001t0002g0313 a0001c0001t0002g0317 a0001c0001t0002g0318 |
3 | HG02698.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1175-6123T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53436530 | |||||||
| chr4:53436856 | AC | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1175-5792delC | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53436856 | ||||||
| chr4:53437098 | G | A | 3 | a0001c0001t0001g0246 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | NA18964.hp1 NA18987.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1175-5555G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437098 | |||||||
| chr4:53437147 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0002g0328 |
2 | HG00733.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1175-5506C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437147 | |||||||
| chr4:53437148 | G | A | 1 | a0001c0001t0002g0315 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1175-5505G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437148 | |||||||
| chr4:53437300 | A | G | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.1175-5353A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437300 | |||||||
| chr4:53437326 | C | CAA | 45 | a0001c0001t0003g0027 a0001c0001t0003g0030 a0001c0001t0003g0031 others(42): Show |
45 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1175-5301_1175-530 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | ||||||
| chr4:53437326 | C | CAAA | 12 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(9): Show |
12 | HG00741.hp2 HG01175.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1175-5302_1175-530 others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | ||||||
| chr4:53437326 | C | CAAAA | 7 | a0001c0001t0003g0029 a0001c0001t0006g0006 a0001c0001t0006g0065 others(4): Show |
8 | HG00673.hp2 HG01358.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-5303_1175-530 others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | ||||||
| chr4:53437326 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0006g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1175-5313_1175-530 others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | ||||||
| chr4:53437326 | CA | C | 14 | a0001c0001t0002g0315 a0001c0001t0002g0321 a0001c0001t0002g0326 others(11): Show |
15 | HG00423.hp2 HG01261.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.1175-5300delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | ||||||
| chr4:53437326 | CAA | C | 108 | a0001c0001t0001g0164 a0001c0001t0001g0172 a0001c0001t0001g0174 others(105): Show |
115 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.1175-5301_1175-530 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | ||||||
| chr4:53437326 | CAAA | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(142): Show |
152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1175-5302_1175-530 others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | ||||||
| chr4:53437326 | CAAAA | C | 10 | a0001c0001t0001g0234 a0001c0001t0001g0261 a0001c0001t0001g0291 others(7): Show |
11 | HG00642.hp2 HG00733.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.1175-5303_1175-530 others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | ||||||
| chr4:53437326 | CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0002g0300 a0001c0001t0002g0308 a0001c0001t0002g0309 others(6): Show |
9 | HG02630.hp2 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1175-5309_1175-530 others(14): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | ||||||
| chr4:53437326 | CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1175-5313_1175-530 others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | ||||||
| chr4:53437354 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1175-5299G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437354 | |||||||
| chr4:53437375 | T | C | 5 | a0001c0001t0002g0300 a0001c0001t0002g0352 a0001c0001t0002g0353 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175-5278T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437375 | |||||||
| chr4:53437659 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-4994A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437659 | |||||||
| chr4:53437699 | T | TTTTA | 60 | a0001c0001t0001g0202 a0001c0001t0002g0300 a0001c0001t0002g0307 others(57): Show |
64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1175-4931_1175-492 others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437699 | ||||||
| chr4:53437744 | G | A | 1 | a0001c0001t0005g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1175-4909G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437744 | |||||||
| chr4:53437881 | A | G | 11 | a0001c0001t0003g0048 a0001c0001t0003g0051 a0001c0001t0003g0052 others(8): Show |
11 | HG02074.hp1 NA18953.hp2 NA18968.hp1 others(8): Show |
intron_variant | MODIFIER | c.1175-4772A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437881 | |||||||
| chr4:53438017 | G | A | 1 | a0001c0001t0002g0329 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1175-4636G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438017 | |||||||
| chr4:53438053 | G | T | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1175-4600G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438053 | |||||||
| chr4:53438341 | A | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1175-4312A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438341 | |||||||
| chr4:53438668 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1175-3985T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438668 | |||||||
| chr4:53438752 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1175-3901A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438752 | |||||||
| chr4:53438758 | C | G | 15 | a0001c0001t0006g0006 a0001c0001t0006g0032 a0001c0001t0006g0064 others(12): Show |
16 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1175-3895C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438758 | |||||||
| chr4:53438806 | G | A | 2 | a0001c0001t0008g0005 a0001c0001t0008g0017 |
3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1175-3847G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438806 | |||||||
| chr4:53438889 | C | G | 1 | a0001c0001t0004g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1175-3764C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438889 | |||||||
| chr4:53439049 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1175-3604T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439049 | |||||||
| chr4:53439095 | T | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1175-3558T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439095 | |||||||
| chr4:53439237 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(104): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1175-3416A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439237 | |||||||
| chr4:53439312 | T | C | 1 | a0001c0001t0002g0365 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1175-3341T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439312 | |||||||
| chr4:53439450 | A | G | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1175-3203A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439450 | |||||||
| chr4:53439589 | T | C | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-3064T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439589 | |||||||
| chr4:53439729 | C | T | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1175-2924C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439729 | |||||||
| chr4:53439798 | T | TAG | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-2854_1175-285 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53439798 | ||||||
| chr4:53439935 | G | A | 1 | a0001c0001t0004g0147 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1175-2718G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439935 | |||||||
| chr4:53440049 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1175-2604C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440049 | |||||||
| chr4:53440074 | T | G | 1 | a0001c0001t0005g0228 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1175-2579T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440074 | |||||||
| chr4:53440097 | C | A | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1175-2556C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440097 | |||||||
| chr4:53440273 | A | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1175-2380A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440273 | |||||||
| chr4:53440422 | T | C | 1 | a0001c0001t0003g0077 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1175-2231T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440422 | |||||||
| chr4:53440436 | G | C | 1 | a0001c0001t0004g0127 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1175-2217G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440436 | |||||||
| chr4:53440794 | C | G | 1 | a0001c0001t0005g0194 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1175-1859C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440794 | |||||||
| chr4:53440804 | C | T | 1 | a0001c0001t0005g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1175-1849C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440804 | |||||||
| chr4:53440969 | T | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1175-1684T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440969 | |||||||
| chr4:53441102 | T | G | 1 | a0001c0001t0003g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1175-1551T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441102 | |||||||
| chr4:53441147 | T | TTTTA | 4 | a0001c0001t0004g0099 a0001c0001t0004g0100 a0001c0001t0004g0101 others(1): Show |
4 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1482_1175-147 others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53441147 | ||||||
| chr4:53441168 | T | C | 1 | a0001c0001t0003g0036 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1175-1485T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441168 | |||||||
| chr4:53441172 | T | C | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1481T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441172 | |||||||
| chr4:53441708 | C | T | 3 | a0001c0001t0005g0275 a0001c0001t0005g0277 a0001c0001t0005g0283 |
3 | NA18971.hp2 NA19082.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1175-945C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441708 | |||||||
| chr4:53441809 | A | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1175-844A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441809 | |||||||
| chr4:53441951 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1175-702A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441951 | |||||||
| chr4:53442240 | A | G | 1 | a0001c0001t0002g0366 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1175-413A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53442240 | |||||||
| chr4:53442255 | G | A | 2 | a0001c0001t0006g0072 a0001c0001t0006g0073 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1175-398G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53442255 | |||||||
| chr4:53442437 | G | A | 50 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(47): Show |
54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1175-216G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53442437 | |||||||
| chr4:53442975 | T | C | 45 | a0001c0001t0005g0011 a0001c0001t0005g0014 a0001c0001t0005g0151 others(42): Show |
46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1229+268T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53442975 | |||||||
| chr4:53443010 | A | C | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1229+303A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443010 | |||||||
| chr4:53443063 | G | A | 1 | a0001c0001t0009g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1229+356G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443063 | |||||||
| chr4:53443134 | A | G | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1229+427A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443134 | |||||||
| chr4:53443298 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1229+591G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443298 | |||||||
| chr4:53443372 | AAT | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1229+669_1229+670d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 53443372 | ||||||
| chr4:53443374 | T | C | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1229+667T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443374 | |||||||
| chr4:53443395 | T | C | 1 | a0001c0001t0010g0369 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1230-653T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443395 | |||||||
| chr4:53443477 | A | G | 45 | a0001c0001t0005g0011 a0001c0001t0005g0014 a0001c0001t0005g0151 others(42): Show |
46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230-571A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443477 | |||||||
| chr4:53443542 | C | T | 1 | a0001c0001t0002g0361 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1230-506C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443542 | |||||||
| chr4:53443549 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1230-499A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443549 | |||||||
| chr4:53443635 | A | G | 45 | a0001c0001t0005g0011 a0001c0001t0005g0014 a0001c0001t0005g0151 others(42): Show |
46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230-413A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443635 | |||||||
| chr4:53443669 | C | T | 2 | a0001c0001t0010g0369 a0001c0001t0011g0368 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1230-379C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443669 | |||||||
| chr4:53443891 | C | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(147): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1230-157C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443891 | |||||||
| chr4:53444019 | A | G | 1 | a0001c0001t0003g0039 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1230-29A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53444019 | |||||||
| chr4:53444021 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1230-27A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53444021 | |||||||
| chr4:53444114 | T | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(151): Show |
160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1285+11T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444114 | |||||||
| chr4:53444173 | TA | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1285+75delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53444173 | ||||||
| chr4:53444341 | C | T | 56 | a0001c0001t0001g0152 a0001c0001t0001g0187 a0001c0001t0001g0195 others(53): Show |
56 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1285+238C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444341 | |||||||
| chr4:53444379 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1285+276C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444379 | |||||||
| chr4:53444383 | A | G | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1285+280A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444383 | |||||||
| chr4:53444422 | G | A | 11 | a0001c0001t0004g0010 a0001c0001t0004g0114 a0001c0001t0004g0120 others(8): Show |
12 | HG00423.hp2 HG02080.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.1285+319G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444422 | |||||||
| chr4:53444466 | T | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(288): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1285+363T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444466 | |||||||
| chr4:53444585 | A | T | 63 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(60): Show |
67 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1285+482A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444585 | |||||||
| chr4:53444602 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1285+499A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444602 | |||||||
| chr4:53444811 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1285+708A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444811 | |||||||
| chr4:53445108 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1285+1005C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445108 | |||||||
| chr4:53445176 | G | C | 4 | a0001c0001t0004g0099 a0001c0001t0004g0100 a0001c0001t0004g0101 others(1): Show |
4 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+1073G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445176 | |||||||
| chr4:53445381 | C | A | 1 | a0001c0001t0003g0078 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1285+1278C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445381 | |||||||
| chr4:53445531 | A | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1285+1428A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445531 | |||||||
| chr4:53445706 | T | G | 1 | a0001c0001t0002g0302 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1285+1603T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445706 | |||||||
| chr4:53445813 | C | T | 1 | a0001c0001t0004g0109 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1285+1710C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445813 | |||||||
| chr4:53445836 | A | T | 1 | a0001c0001t0001g0280 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1285+1733A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445836 | |||||||
| chr4:53445902 | T | C | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1285+1799T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445902 | |||||||
| chr4:53445905 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1285+1802T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445905 | |||||||
| chr4:53445950 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1285+1847T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445950 | |||||||
| chr4:53446084 | C | T | 1 | a0001c0001t0015g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1285+1981C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446084 | |||||||
| chr4:53446147 | G | A | 1 | a0001c0001t0006g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1285+2044G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446147 | |||||||
| chr4:53446161 | T | C | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+2058T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446161 | |||||||
| chr4:53446170 | T | G | 1 | a0001c0001t0002g0316 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1285+2067T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446170 | |||||||
| chr4:53446199 | C | CT | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1285+2106dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53446199 | ||||||
| chr4:53446199 | CT | C | 75 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(72): Show |
76 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1285+2106delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53446199 | ||||||
| chr4:53446203 | T | A | 1 | a0001c0001t0018g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1285+2100T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446203 | |||||||
| chr4:53446539 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1285+2436A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446539 | |||||||
| chr4:53446585 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+2482A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446585 | |||||||
| chr4:53446830 | T | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1285+2727T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446830 | |||||||
| chr4:53446939 | TTTTTTGT others(5): Show |
T | 1 | a0001c0001t0001g0272 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1285+2854_1285+286 others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53446939 | ||||||
| chr4:53446945 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1285+2842G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446945 | |||||||
| chr4:53447549 | C | T | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285+3446C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447549 | |||||||
| chr4:53447610 | A | G | 3 | a0001c0001t0002g0337 a0001c0001t0002g0344 a0001c0001t0002g0350 |
3 | HG02602.hp2 HG03942.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1285+3507A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447610 | |||||||
| chr4:53447648 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1285+3545A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447648 | |||||||
| chr4:53447706 | C | T | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285+3603C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447706 | |||||||
| chr4:53447799 | G | A | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.1285+3696G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447799 | |||||||
| chr4:53447859 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1285+3756C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447859 | |||||||
| chr4:53447919 | A | G | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+3816A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447919 | |||||||
| chr4:53448020 | G | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+3917G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53448020 | |||||||
| chr4:53448095 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1285+3992A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53448095 | |||||||
| chr4:53448251 | T | C | 63 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(60): Show |
67 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1285+4148T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53448251 | |||||||
| chr4:53448383 | A | G | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285+4280A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53448383 | |||||||
| chr4:53448661 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1286-4259A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53448661 | |||||||
| chr4:53449100 | T | C | 1 | a0001c0001t0007g0135 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1286-3820T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449100 | |||||||
| chr4:53449432 | T | C | 1 | a0001c0001t0002g0334 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1286-3488T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449432 | |||||||
| chr4:53449602 | C | G | 1 | a0001c0001t0003g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1286-3318C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449602 | |||||||
| chr4:53449623 | T | C | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1286-3297T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449623 | |||||||
| chr4:53449703 | T | C | 1 | a0001c0001t0005g0229 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1286-3217T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449703 | |||||||
| chr4:53449751 | T | C | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1286-3169T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449751 | |||||||
| chr4:53449965 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1286-2955G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449965 | |||||||
| chr4:53450047 | T | C | 12 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0038 others(9): Show |
12 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1286-2873T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450047 | |||||||
| chr4:53450328 | T | G | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.1286-2592T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450328 | |||||||
| chr4:53450329 | A | G | 1 | a0001c0001t0017g0028 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1286-2591A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450329 | |||||||
| chr4:53450450 | C | G | 1 | a0001c0001t0004g0008 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1286-2470C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450450 | |||||||
| chr4:53450498 | C | T | 2 | a0001c0001t0005g0229 a0001c0001t0005g0230 |
2 | HG02165.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1286-2422C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450498 | |||||||
| chr4:53450529 | C | T | 2 | a0001c0001t0003g0062 a0001c0001t0003g0068 |
2 | HG02129.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1286-2391C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450529 | |||||||
| chr4:53450756 | T | C | 59 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0008 others(56): Show |
64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1286-2164T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450756 | |||||||
| chr4:53450764 | T | C | 1 | a0001c0001t0004g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1286-2156T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450764 | |||||||
| chr4:53450765 | C | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1286-2155C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450765 | |||||||
| chr4:53450815 | A | G | 8 | a0001c0001t0004g0009 a0001c0001t0004g0115 a0001c0001t0004g0122 others(5): Show |
9 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1286-2105A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450815 | |||||||
| chr4:53450963 | C | CT | 12 | a0001c0001t0001g0153 a0001c0001t0001g0267 a0001c0001t0002g0303 others(9): Show |
12 | HG02129.hp2 HG03130.hp1 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.1286-1941dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53450963 | ||||||
| chr4:53450963 | CTT | C | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1286-1942_1286-194 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53450963 | ||||||
| chr4:53450984 | T | C | 1 | a0001c0001t0002g0343 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1286-1936T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450984 | |||||||
| chr4:53451325 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1286-1595T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451325 | |||||||
| chr4:53451439 | T | G | 7 | a0001c0001t0002g0303 a0001c0001t0002g0322 a0001c0001t0002g0323 others(4): Show |
7 | HG02129.hp2 HG04184.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1286-1481T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451439 | |||||||
| chr4:53451568 | A | G | 1 | a0001c0001t0003g0055 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1286-1352A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451568 | |||||||
| chr4:53451575 | C | CT | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(228): Show |
242 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1286-1331dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53451575 | ||||||
| chr4:53451610 | A | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0096 a0001c0001t0004g0097 others(5): Show |
9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1286-1310A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451610 | |||||||
| chr4:53451885 | CT | C | 138 | a0001c0001t0001g0184 a0001c0001t0002g0004 a0001c0001t0002g0012 others(135): Show |
148 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.1286-1019delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53451885 | ||||||
| chr4:53451894 | T | G | 2 | a0001c0001t0005g0014 a0001c0001t0005g0276 |
2 | HG02135.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1286-1026T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451894 | |||||||
| chr4:53451898 | T | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(147): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1286-1022T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451898 | |||||||
| chr4:53452019 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1286-901G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452019 | |||||||
| chr4:53452039 | G | A | 2 | a0001c0001t0002g0361 a0001c0001t0002g0362 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1286-881G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452039 | |||||||
| chr4:53452143 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1286-777A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452143 | |||||||
| chr4:53452247 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0182 a0001c0001t0001g0183 |
6 | HG00140.hp2 HG01169.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286-673C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452247 | |||||||
| chr4:53452452 | G | A | 1 | a0001c0001t0002g0349 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1286-468G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452452 | |||||||
| chr4:53452584 | G | T | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1286-336G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452584 | |||||||
| chr4:53452608 | C | T | 2 | a0001c0001t0002g0333 a0001c0001t0002g0335 |
2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1286-312C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452608 | |||||||
| chr4:53452731 | T | G | 1 | a0001c0001t0001g0295 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1286-189T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452731 | |||||||
| chr4:53452805 | T | G | 1 | a0001c0001t0010g0369 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286-115T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452805 | |||||||
| chr4:53452844 | C | A | 366 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(363): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.1286-76C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452844 | |||||||
| chr4:53453195 | G | A | 1 | a0001c0001t0003g0048 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1499+62G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453195 | |||||||
| chr4:53453443 | T | C | 1 | a0001c0001t0005g0253 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1499+310T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453443 | |||||||
| chr4:53453565 | A | G | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1499+432A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453565 | |||||||
| chr4:53453669 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1499+536T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453669 | |||||||
| chr4:53453744 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1499+611C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453744 | |||||||
| chr4:53453872 | T | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0297 a0001c0001t0002g0319 others(1): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499+739T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453872 | |||||||
| chr4:53453921 | A | T | 5 | a0001c0001t0002g0307 a0001c0001t0002g0308 a0001c0001t0002g0309 others(2): Show |
5 | HG02109.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499+788A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453921 | |||||||
| chr4:53453968 | C | T | 9 | a0001c0001t0002g0303 a0001c0001t0002g0311 a0001c0001t0002g0321 others(6): Show |
9 | HG02129.hp2 HG03927.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.1499+835C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453968 | |||||||
| chr4:53454339 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1499+1206A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454339 | |||||||
| chr4:53454443 | C | T | 1 | a0001c0001t0012g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1499+1310C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454443 | |||||||
| chr4:53454450 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(229): Show |
243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1499+1317C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454450 | |||||||
| chr4:53454481 | C | A | 1 | a0001c0001t0003g0048 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1499+1348C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454481 | |||||||
| chr4:53454505 | T | C | 7 | a0001c0001t0006g0070 a0001c0001t0006g0071 a0001c0001t0006g0072 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1499+1372T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454505 | |||||||
| chr4:53454535 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1499+1402G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454535 | |||||||
| chr4:53454652 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1499+1519T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454652 | |||||||
| chr4:53454655 | A | G | 1 | a0001c0001t0003g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1499+1522A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454655 | |||||||
| chr4:53454993 | T | A | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499+1860T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454993 | |||||||
| chr4:53455030 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1499+1897C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455030 | |||||||
| chr4:53455149 | T | C | 57 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0297 others(54): Show |
60 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(57): Show |
intron_variant | MODIFIER | c.1499+2016T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455149 | |||||||
| chr4:53455270 | A | G | 31 | a0001c0001t0002g0012 a0001c0001t0002g0298 a0001c0001t0002g0299 others(28): Show |
32 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1499+2137A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455270 | |||||||
| chr4:53455446 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(103): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1499+2313G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455446 | |||||||
| chr4:53455531 | G | C | 1 | a0001c0001t0002g0315 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1499+2398G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455531 | |||||||
| chr4:53455835 | G | A | 1 | a0001c0001t0002g0367 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1499+2702G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455835 | |||||||
| chr4:53455847 | C | CT | 51 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 others(48): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1499+2720dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 53455847 | ||||||
| chr4:53455940 | A | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(287): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1500-2713A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455940 | |||||||
| chr4:53456237 | T | C | 3 | a0001c0001t0008g0005 a0001c0001t0008g0017 a0001c0001t0015g0018 |
4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500-2416T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53456237 | |||||||
| chr4:53456529 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1500-2124G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53456529 | |||||||
| chr4:53456545 | ATTTTAGC others(2): Show |
A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1500-2106_1500-209 others(13): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 53456545 | ||||||
| chr4:53456919 | G | A | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1500-1734G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53456919 | |||||||
| chr4:53457101 | T | C | 1 | a0001c0001t0005g0275 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1500-1552T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457101 | |||||||
| chr4:53457116 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1500-1537C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457116 | |||||||
| chr4:53457147 | C | G | 64 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1500-1506C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457147 | |||||||
| chr4:53457178 | A | G | 1 | a0001c0001t0002g0323 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1500-1475A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457178 | |||||||
| chr4:53457658 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1500-995T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457658 | |||||||
| chr4:53457740 | G | C | 1 | a0001c0001t0002g0349 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1500-913G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457740 | |||||||
| chr4:53458006 | G | GC | 10 | a0001c0001t0002g0300 a0001c0001t0002g0307 a0001c0001t0002g0308 others(7): Show |
10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1500-641dupC | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 53458006 | ||||||
| chr4:53458058 | A | G | 4 | a0001c0001t0001g0291 a0001c0001t0008g0005 a0001c0001t0008g0017 others(1): Show |
5 | HG00733.hp2 HG03130.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1500-595A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53458058 | |||||||
| chr4:53458212 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(75): Show |
82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1500-441A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53458212 | |||||||
| chr4:53458218 | A | C | 1 | a0001c0001t0005g0194 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1500-435A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53458218 | |||||||
| chr4:53458227 | T | C | 2 | a0001c0001t0009g0149 a0001c0001t0009g0150 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1500-426T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53458227 | |||||||
| chr4:53458284 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1500-369T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53458284 | |||||||
| chr4:53458824 | A | T | 57 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0297 others(54): Show |
60 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(57): Show |
intron_variant | MODIFIER | c.1637+34A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | chr4 | 53458824 | |||||||
| chr4:53458899 | G | C | 1 | a0001c0001t0001g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1637+109G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | chr4 | 53458899 | |||||||
| chr4:53458918 | C | T | 1 | a0001c0001t0004g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1637+128C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | chr4 | 53458918 | |||||||
| chr4:53459149 | AACTGATT others(7): Show |
A | 1 | a0001c0001t0001g0176 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1638-150_1638-137d others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 53459149 | ||||||
| chr4:53459255 | T | C | 1 | a0001c0001t0002g0339 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1638-47T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | chr4 | 53459255 | |||||||
| chr4:53459277 | C | CT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(94): Show |
102 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
splice_region_variant&intron_variant | LOW | c.1638-5dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 53459277 | ||||||
| chr4:53459277 | C | CTT | 121 | a0001c0001t0001g0155 a0001c0001t0001g0182 a0001c0001t0001g0183 others(118): Show |
126 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(123): Show |
splice_region_variant&intron_variant | LOW | c.1638-6_1638-5dupTT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 53459277 | ||||||
| chr4:53459277 | C | CTTT | 6 | a0001c0001t0001g0243 a0001c0001t0005g0228 a0001c0001t0008g0005 others(3): Show |
7 | HG02055.hp2 HG03130.hp1 HG03486.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1638-7_1638-5dupTT others(1): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 53459277 | ||||||
| chr4:53459277 | CT | C | 50 | a0001c0001t0003g0021 a0001c0001t0004g0002 a0001c0001t0004g0007 others(47): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
splice_region_variant&intron_variant | LOW | c.1638-5delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 53459277 |