Variant report
Variant | rs13223314 |
---|---|
Chromosome Location | chr7:153109508-153109509 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:43)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:43 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | NR2F2 | chr7:153109141-153110241 | K562 | blood: | n/a | n/a |
2 | BCL3 | chr7:153109499-153110250 | K562 | blood: | n/a | n/a |
3 | BCLAF1 | chr7:153107687-153111130 | K562 | blood: | n/a | n/a |
4 | POLR2A | chr7:153109094-153111262 | K562 | blood: | n/a | n/a |
5 | PML | chr7:153099702-153111270 | K562 | blood: | n/a | n/a |
6 | E2F6 | chr7:153109093-153109550 | K562 | blood: | n/a | n/a |
7 | MAZ | chr7:153109075-153112076 | K562 | blood: | n/a | n/a |
8 | ZNF384 | chr7:153109228-153109525 | K562 | blood: | n/a | n/a |
9 | HEY1 | chr7:153106358-153111237 | K562 | blood: | n/a | n/a |
10 | NR2F2 | chr7:153109468-153111493 | K562 | blood: | n/a | n/a |
11 | HCFC1 | chr7:153109116-153109519 | K562 | blood: | n/a | n/a |
12 | TBP | chr7:153109098-153111653 | K562 | blood: | n/a | n/a |
13 | RCOR1 | chr7:153109089-153111415 | K562 | blood: | n/a | n/a |
14 | YY1 | chr7:153109081-153111497 | K562 | blood: | n/a | chr7:153109966-153109978 chr7:153109908-153109920 chr7:153109939-153109951 |
15 | POLR2A | chr7:153106565-153111352 | K562 | blood: | n/a | n/a |
16 | TAL1 | chr7:153107838-153111161 | K562 | blood: | n/a | n/a |
17 | TEAD4 | chr7:153107711-153111655 | K562 | blood: | n/a | n/a |
18 | UBTF | chr7:153108965-153109512 | K562 | blood: | n/a | n/a |
19 | CBX3 | chr7:153109019-153109556 | K562 | blood: | n/a | n/a |
20 | MYC | chr7:153109127-153112213 | K562 | blood: | n/a | n/a |
21 | POLR2A | chr7:153106387-153111222 | K562 | blood: | n/a | n/a |
22 | POLR2A | chr7:153099644-153111299 | K562 | blood: | n/a | n/a |
23 | POLR2A | chr7:153099580-153111354 | K562 | blood: | n/a | n/a |
24 | ZNF143 | chr7:153109105-153109531 | K562 | blood: | n/a | n/a |
25 | YY1 | chr7:153109196-153111377 | K562 | blood: | n/a | chr7:153109966-153109978 chr7:153109908-153109920 chr7:153109939-153109951 |
26 | CHD2 | chr7:153108792-153111309 | K562 | blood: | n/a | n/a |
27 | TBL1XR1 | chr7:153109114-153111156 | K562 | blood: | n/a | n/a |
28 | POLR2A | chr7:153105460-153111327 | K562 | blood: | n/a | n/a |
29 | POLR2A | chr7:153099546-153111466 | K562 | blood: | n/a | n/a |
30 | POLR2A | chr7:153099728-153111351 | K562 | blood: | n/a | n/a |
31 | MYC | chr7:153109086-153112044 | K562 | blood: | n/a | n/a |
32 | UBTF | chr7:153109143-153109526 | K562 | blood: | n/a | n/a |
33 | POLR2A | chr7:153099807-153111353 | K562 | blood: | n/a | n/a |
34 | ZMIZ1 | chr7:153109264-153111164 | K562 | blood: | n/a | n/a |
35 | POLR2A | chr7:153099579-153111215 | K562 | blood: | n/a | n/a |
36 | POLR2A | chr7:153073454-153111170 | K562 | blood: | n/a | n/a |
37 | RFX5 | chr7:153109334-153110084 | K562 | blood: | n/a | n/a |
38 | YY1 | chr7:153109138-153109568 | K562 | blood: | n/a | n/a |
39 | HEY1 | chr7:153105465-153111229 | K562 | blood: | n/a | n/a |
40 | POLR2A | chr7:153100654-153111363 | K562 | blood: | n/a | n/a |
41 | MAX | chr7:153109075-153109531 | K562 | blood: | n/a | n/a |
42 | TRIM28 | chr7:153107652-153111711 | K562 | blood: | n/a | n/a |
43 | CEBPB | chr7:153109256-153109540 | K562 | blood: | n/a | n/a |
No data |
(count:5 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:64297147..64300786-chr7:153106859..153112225,9 | K562 | blood: | |
2 | chr7:64297147..64300763-chr7:153106859..153112373,8 | K562 | blood: | |
3 | chr1:113496225..113498697-chr7:153107803..153110252,2 | K562 | blood: | |
4 | chr7:152160161..152162874-chr7:153109419..153112345,3 | K562 | blood: | |
5 | chr2:84103331..84106345-chr7:153106704..153111137,6 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000234722 | TF binding region |
ENSG00000155380 | Chromatin interaction |
ENSG00000223700 | Chromatin interaction |
ENSG00000261455 | Chromatin interaction |
ENSG00000234338 | Chromatin interaction |
ENSG00000236198 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10239341 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10246632 | 0.96[CEU][hapmap];0.86[CHB][hapmap];0.95[EUR][1000 genomes] |
rs10278147 | 0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1037004 | 0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs11760609 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs12154671 | 0.81[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs12703288 | 0.84[ASN][1000 genomes] |
rs12703290 | 0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12703292 | 0.84[ASN][1000 genomes] |
rs12703293 | 0.83[ASN][1000 genomes] |
rs12703294 | 0.84[ASN][1000 genomes] |
rs12703295 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12703296 | 0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12703297 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12703298 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12703299 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12703300 | 0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12703301 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12703302 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12703303 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12703304 | 0.96[CEU][hapmap];0.86[CHB][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs12703305 | 0.96[CEU][hapmap];0.86[CHB][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs12703306 | 0.96[CEU][hapmap];0.86[CHB][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs1319653 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs13224388 | 0.84[ASN][1000 genomes] |
rs13226467 | 0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs13230671 | 0.96[CEU][hapmap];0.85[CHB][hapmap];0.95[EUR][1000 genomes] |
rs13231619 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs13231707 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs13233777 | 0.96[CEU][hapmap];0.86[CHB][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs13234416 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs13235094 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs13238866 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs13242507 | 0.88[EUR][1000 genomes] |
rs13245532 | 0.85[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1444458 | 0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1444462 | 0.84[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1444463 | 0.96[CEU][hapmap];0.87[CHB][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs1992624 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs2312340 | 0.84[ASN][1000 genomes] |
rs2312341 | 0.84[ASN][1000 genomes] |
rs2312342 | 0.84[ASN][1000 genomes] |
rs2312343 | 0.84[ASN][1000 genomes] |
rs2312352 | 0.98[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs28648695 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs28671105 | 0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs28675346 | 0.89[EUR][1000 genomes] |
rs2872007 | 0.84[ASN][1000 genomes] |
rs2872011 | 0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs34123236 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs34140991 | 0.84[ASN][1000 genomes] |
rs34396242 | 0.84[ASN][1000 genomes] |
rs34628166 | 0.84[ASN][1000 genomes] |
rs34726402 | 0.87[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs35425384 | 0.84[ASN][1000 genomes] |
rs35444218 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs35792470 | 0.83[ASN][1000 genomes] |
rs4563798 | 0.88[EUR][1000 genomes] |
rs55838859 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs6464332 | 0.84[ASN][1000 genomes] |
rs6955304 | 0.80[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs6965505 | 0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6966291 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6971281 | 0.96[CEU][hapmap];0.87[CHB][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs6971902 | 0.96[CEU][hapmap];0.87[CHB][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs6974731 | 0.96[CEU][hapmap];0.86[CHB][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7779733 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7780839 | 0.89[EUR][1000 genomes] |
rs7784310 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7785341 | 0.94[EUR][1000 genomes] |
rs7785383 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7785473 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7787854 | 0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7791985 | 0.81[ASN][1000 genomes] |
rs7798819 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7800637 | 0.96[CEU][hapmap];0.95[CHB][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7800865 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7803966 | 0.95[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7804377 | 0.95[EUR][1000 genomes] |
rs7805371 | 0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7805698 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7811018 | 0.84[ASN][1000 genomes] |
rs880798 | 0.84[ASN][1000 genomes] |
rs880799 | 0.84[ASN][1000 genomes] |
rs884852 | 0.95[EUR][1000 genomes] |
rs884853 | 0.96[CEU][hapmap];0.91[CHB][hapmap];0.95[EUR][1000 genomes] |
rs895002 | 0.82[ASN][1000 genomes] |
rs987673 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs987674 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs987675 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs989754 | 0.95[CHB][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532222 | chr7:152504090-153450290 | Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
2 | nsv1034277 | chr7:152932263-153526276 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
3 | nsv1023927 | chr7:152938365-153526276 | Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
4 | nsv609072 | chr7:152942680-153527304 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
5 | nsv1028109 | chr7:152945148-153526276 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
6 | nsv1034036 | chr7:152954795-153379878 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
7 | nsv539211 | chr7:152954795-153379878 | Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
8 | nsv1032443 | chr7:152988419-153450150 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
9 | nsv539212 | chr7:152988419-153450150 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
10 | esv2758141 | chr7:153001173-153298779 | Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
11 | esv2759576 | chr7:153001173-153298779 | Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
12 | nsv889510 | chr7:153050837-153413046 | Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
13 | nsv889511 | chr7:153076838-153201572 | Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
14 | nsv889512 | chr7:153088772-153662151 | Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
15 | esv16065 | chr7:153106266-153111170 | Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:153106800-153110000 | Transcr. at gene 5' and 3' | K562 | blood |