Variant report
Variant | rs10751337 |
---|---|
Chromosome Location | chr10:44223771-44223772 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | MAX | chr10:44223722-44224007 | K562 | blood: | n/a | chr10:44223865-44223874 |
No data |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr10:44222418..44225154-chr10:44227350..44232031,4 | K562 | blood: |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-ZNF485-7 | chr10:44223665-44224176 | NONHSAT012989 |
No data |
No data |
Variant related genes | Relation type |
---|---|
UQCRHP3 | TF binding region |
ENSG00000224162 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10751332 | 0.89[ASN][1000 genomes] |
rs10751339 | 0.88[CEU][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs10751340 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs10751342 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs10751343 | 0.88[ASN][1000 genomes] |
rs10793470 | 0.86[ASN][1000 genomes] |
rs10793471 | 0.88[ASN][1000 genomes] |
rs10793476 | 0.99[ASN][1000 genomes] |
rs10793477 | 0.88[CEU][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs10793478 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs10793479 | 0.83[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs10793483 | 0.87[ASN][1000 genomes] |
rs10793484 | 0.88[ASN][1000 genomes] |
rs10793489 | 0.85[ASN][1000 genomes] |
rs10793496 | 0.88[MEX][hapmap] |
rs10793498 | 0.88[MEX][hapmap] |
rs10899861 | 0.88[ASN][1000 genomes] |
rs10899864 | 0.89[ASN][1000 genomes] |
rs10899890 | 0.90[ASN][1000 genomes] |
rs10899891 | 0.88[ASN][1000 genomes] |
rs10899893 | 0.88[ASN][1000 genomes] |
rs10899894 | 0.88[ASN][1000 genomes] |
rs10899896 | 0.83[ASN][1000 genomes] |
rs10899897 | 0.87[ASN][1000 genomes] |
rs10899900 | 0.85[ASN][1000 genomes] |
rs10899901 | 0.85[ASN][1000 genomes] |
rs1107925 | 0.92[ASN][1000 genomes] |
rs11238637 | 0.88[ASN][1000 genomes] |
rs11238672 | 0.88[CEU][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs11238705 | 0.85[ASN][1000 genomes] |
rs12218690 | 0.87[ASN][1000 genomes] |
rs12258494 | 0.94[ASN][1000 genomes] |
rs12413246 | 0.89[ASN][1000 genomes] |
rs12570501 | 0.92[ASN][1000 genomes] |
rs1335894 | 0.94[ASN][1000 genomes] |
rs1335896 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs1537797 | 0.94[ASN][1000 genomes] |
rs1537798 | 0.94[ASN][1000 genomes] |
rs1537800 | 0.88[CEU][hapmap] |
rs1572377 | 0.94[ASN][1000 genomes] |
rs17154279 | 0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes] |
rs2050503 | 0.85[ASN][1000 genomes] |
rs2152456 | 0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap] |
rs2297724 | 0.85[ASN][1000 genomes] |
rs4080021 | 0.85[ASN][1000 genomes] |
rs4245608 | 0.83[ASN][1000 genomes] |
rs4534528 | 0.93[ASN][1000 genomes] |
rs4536161 | 0.82[AMR][1000 genomes] |
rs4536162 | 0.83[AMR][1000 genomes] |
rs4948756 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs4948758 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs4948759 | 0.94[ASN][1000 genomes] |
rs4948766 | 0.92[ASN][1000 genomes] |
rs4948767 | 0.87[ASN][1000 genomes] |
rs4948768 | 0.88[ASN][1000 genomes] |
rs4948771 | 0.85[ASN][1000 genomes] |
rs4948772 | 0.83[ASN][1000 genomes] |
rs4948774 | 0.85[ASN][1000 genomes] |
rs58086514 | 0.99[ASN][1000 genomes] |
rs60407866 | 0.93[ASN][1000 genomes] |
rs7101084 | 0.87[ASN][1000 genomes] |
rs74138024 | 0.92[ASN][1000 genomes] |
rs74138025 | 0.92[ASN][1000 genomes] |
rs7903170 | 1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs7911606 | 0.92[ASN][1000 genomes] |
rs883474 | 0.92[ASN][1000 genomes] |
rs951259 | 0.88[ASN][1000 genomes] |
rs951798 | 0.85[ASN][1000 genomes] |
rs964877 | 0.85[ASN][1000 genomes] |
rs980445 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs980446 | 0.94[ASN][1000 genomes] |
rs980447 | 0.94[ASN][1000 genomes] |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:44223600-44224000 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr10:44223600-44224200 | Bivalent Enhancer | Placenta | Placenta |