Variant report
Variant | rs10174735 |
---|---|
Chromosome Location | chr2:188326005-188326006 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:188325986..188328358-chr2:188338477..188341086,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10174456 | 0.90[ASN][1000 genomes] |
rs10179705 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10181823 | 0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10181845 | 0.81[ASN][1000 genomes] |
rs10191833 | 0.81[ASN][1000 genomes] |
rs10194145 | 0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10194247 | 0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10201618 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10203398 | 0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10203781 | 0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10931288 | 0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10931289 | 0.84[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11685426 | 0.86[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11689123 | 0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11691442 | 0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11894589 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11897572 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11903296 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12693471 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12987470 | 0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13019491 | 0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs13024536 | 0.89[ASN][1000 genomes] |
rs13028645 | 0.91[ASN][1000 genomes] |
rs13392310 | 0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs13409829 | 0.80[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs13411274 | 0.81[EUR][1000 genomes] |
rs13418253 | 0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13424790 | 0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13425233 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13430354 | 0.80[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs13430665 | 0.80[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1355519 | 0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1355520 | 0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1398061 | 0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1528233 | 0.90[ASN][1000 genomes] |
rs1528236 | 0.81[ASN][1000 genomes] |
rs1609268 | 0.90[ASN][1000 genomes] |
rs1632282 | 0.90[ASN][1000 genomes] |
rs16829016 | 0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1706261 | 0.90[ASN][1000 genomes] |
rs1706262 | 0.80[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1706273 | 0.81[ASN][1000 genomes] |
rs1706276 | 0.90[ASN][1000 genomes] |
rs1728678 | 0.81[ASN][1000 genomes] |
rs1728680 | 0.90[ASN][1000 genomes] |
rs1728690 | 0.90[ASN][1000 genomes] |
rs17367055 | 0.84[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs17464221 | 0.97[ASN][1000 genomes] |
rs17756804 | 0.81[ASN][1000 genomes] |
rs1912846 | 0.81[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs1912847 | 0.81[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs1912848 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1983492 | 0.80[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2030976 | 0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs2058670 | 0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2349315 | 0.86[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs35056802 | 0.91[ASN][1000 genomes] |
rs35721125 | 0.81[ASN][1000 genomes] |
rs35870933 | 0.91[ASN][1000 genomes] |
rs36110670 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36146505 | 0.92[ASN][1000 genomes] |
rs3771058 | 0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs3771059 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs3771061 | 0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs3771067 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs3771078 | 0.86[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs3821180 | 0.86[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs3821184 | 0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4140885 | 0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4667160 | 0.81[ASN][1000 genomes] |
rs59400383 | 0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6434219 | 0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6719550 | 0.84[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs67285003 | 0.86[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6744012 | 0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6753700 | 0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs696092 | 0.90[ASN][1000 genomes] |
rs698579 | 0.80[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs698582 | 0.80[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs698583 | 0.92[ASN][1000 genomes] |
rs698588 | 0.92[ASN][1000 genomes] |
rs698590 | 0.92[ASN][1000 genomes] |
rs698592 | 0.80[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs698593 | 0.89[ASN][1000 genomes] |
rs72902495 | 0.86[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7576066 | 0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7586970 | 0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7591567 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7598858 | 0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs8176472 | 0.84[ASN][1000 genomes] |
rs8176498 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs8176501 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs8176506 | 0.97[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs8176525 | 0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs8176526 | 0.87[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs8176528 | 0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs8176541 | 0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs8176546 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs8176547 | 0.82[ASN][1000 genomes] |
rs8176548 | 0.82[ASN][1000 genomes] |
rs8176580 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs8176583 | 0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs8176592 | 0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs840564 | 0.81[ASN][1000 genomes] |
rs840567 | 0.81[ASN][1000 genomes] |
rs840569 | 0.81[ASN][1000 genomes] |
rs840570 | 0.81[ASN][1000 genomes] |
rs840571 | 0.81[ASN][1000 genomes] |
rs840572 | 0.81[ASN][1000 genomes] |
rs840574 | 0.81[ASN][1000 genomes] |
rs840576 | 0.81[ASN][1000 genomes] |
rs840577 | 0.81[ASN][1000 genomes] |
rs840578 | 0.81[ASN][1000 genomes] |
rs840583 | 0.87[ASN][1000 genomes] |
rs840584 | 0.87[ASN][1000 genomes] |
rs840585 | 0.87[ASN][1000 genomes] |
rs840586 | 0.80[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs840587 | 0.80[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs840588 | 0.80[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs840589 | 0.87[ASN][1000 genomes] |
rs840590 | 0.87[ASN][1000 genomes] |
rs840591 | 0.86[ASN][1000 genomes] |
rs840593 | 0.87[ASN][1000 genomes] |
rs840595 | 0.80[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs840596 | 0.87[ASN][1000 genomes] |
rs840597 | 0.80[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs840609 | 0.80[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs840610 | 0.90[ASN][1000 genomes] |
rs840611 | 0.90[ASN][1000 genomes] |
rs840616 | 0.90[ASN][1000 genomes] |
rs858744 | 0.80[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs858756 | 0.80[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs858758 | 0.93[ASN][1000 genomes] |
rs858759 | 0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs860846 | 0.80[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs860859 | 0.90[ASN][1000 genomes] |
rs863972 | 0.80[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs865763 | 0.81[ASN][1000 genomes] |
rs880890 | 0.87[ASN][1000 genomes] |
rs907463 | 0.80[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs9288140 | 0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949700 | chr2:187713412-188361211 | Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
2 | nsv834487 | chr2:188182556-188353363 | Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 2 gene(s) | inside rSNPs | diseases |
3 | nsv875557 | chr2:188219052-188370232 | Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
4 | nsv875558 | chr2:188219052-188388311 | Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
5 | nsv875559 | chr2:188219052-188390112 | Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
6 | nsv875560 | chr2:188219052-188508011 | Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
7 | nsv875561 | chr2:188226900-188440752 | Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
8 | nsv584036 | chr2:188256158-188369841 | Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
9 | nsv875562 | chr2:188258904-188370232 | Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
10 | nsv875563 | chr2:188258904-188388311 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
11 | nsv875564 | chr2:188258904-188414161 | Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
12 | nsv875565 | chr2:188258904-188440752 | Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
13 | nsv875566 | chr2:188258904-188626214 | Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
14 | nsv875567 | chr2:188258904-188673462 | Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
15 | nsv834488 | chr2:188268434-188415496 | Enhancers Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
16 | nsv875568 | chr2:188291105-188653806 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
17 | nsv1011800 | chr2:188301324-188340396 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 1 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:188313000-188326200 | Weak transcription | Right Ventricle | heart |
2 | chr2:188313400-188340000 | Weak transcription | Fetal Brain Male | brain |
3 | chr2:188313600-188330400 | Weak transcription | Muscle Satellite Cultured Cells | -- |
4 | chr2:188324600-188332400 | Weak transcription | HUVEC | blood vessel |
5 | chr2:188325200-188326200 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
6 | chr2:188325400-188330400 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
7 | chr2:188325400-188334200 | Weak transcription | Primary hematopoietic stem cells | blood |
8 | chr2:188326000-188326200 | Weak transcription | Right Atrium | heart |
9 | chr2:188326000-188326200 | Active TSS | HepG2 | liver |
10 | chr2:188326000-188327000 | Active TSS | Foreskin Keratinocyte Primary Cells skin02 | Skin |
11 | chr2:188326000-188327200 | Active TSS | Fetal Intestine Large | intestine |
12 | chr2:188326000-188327400 | Active TSS | ES-I3 Cell Line | embryonic stem cell |