Variant report

Variant	rs7096045
Chromosome Location	chr10:5076063-5076064
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	STAT3	chr10:5075491-5076099	Hela-S3	cervix:	n/a	chr10:5075719-5075728 chr10:5075718-5075727
2	GATA3	chr10:5075315-5076142	A549	lung:	n/a	n/a
3	CEBPB	chr10:5075471-5076090	A549	lung:	n/a	chr10:5075770-5075783
4	FOSL2	chr10:5075402-5076080	A549	lung:	n/a	chr10:5075722-5075734 chr10:5075719-5075727 chr10:5075719-5075728 chr10:5075717-5075729 chr10:5075718-5075727 chr10:5075720-5075727 chr10:5075718-5075728

No.	Distal block	Cell Line	Cell type
1	chr10:5073664..5075237-chr10:5075576..5077420,2	MCF-7	breast:
2	chr10:5067000..5068647-chr10:5074072..5076812,2	MCF-7	breast:
3	chr10:5074304..5076231-chr10:5473842..5475799,2	K562	blood:

Variant related genes	Relation type
AKR1C3	TF binding region

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10795225	0.82[AMR][1000 genomes]
rs10795226	0.82[AMR][1000 genomes]
rs10795228	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10795234	0.86[ASN][1000 genomes]
rs10795241	0.94[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10904392	0.82[AMR][1000 genomes]
rs10904400	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10904402	0.94[CHB][hapmap];0.91[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10904403	0.94[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10904406	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11252887	0.83[ASN][1000 genomes]
rs11492950	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11511653	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11599072	0.91[ASN][1000 genomes]
rs11817416	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12766479	0.80[AMR][1000 genomes]
rs1937880	0.80[AMR][1000 genomes]
rs2096422	0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2398187	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2398190	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2398191	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2398192	0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2398194	0.82[ASN][1000 genomes]
rs2801898	0.90[AMR][1000 genomes]
rs4143631	0.94[CHB][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs4525119	0.94[CHB][hapmap];0.87[YRI][hapmap];0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4880701	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4880702	0.92[ASN][1000 genomes]
rs4881379	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4881383	0.92[ASN][1000 genomes]
rs4881386	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4881387	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4881388	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4881394	0.88[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs6601893	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7074522	0.92[ASN][1000 genomes]
rs7080470	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7081949	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7087341	0.80[AMR][1000 genomes]
rs7088426	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7897300	0.88[AMR][1000 genomes]
rs7899089	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7915896	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894792	chr10:4832920-5498724	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv948794	chr10:4863093-5227382	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv1045155	chr10:4872239-5211318	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1040343	chr10:4872814-5196815	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv540462	chr10:4872814-5196815	Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv869470	chr10:4878904-5203685	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv466713	chr10:4901798-5319679	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	nsv549881	chr10:4901798-5319679	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
9	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
10	nsv1050246	chr10:4927428-5211318	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv549882	chr10:4943518-5203864	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
12	esv2763913	chr10:4961021-5321407	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
13	nsv894794	chr10:4972761-5121745	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
14	nsv430122	chr10:4986040-5134511	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
15	nsv1039386	chr10:5008383-5348491	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
16	nsv1036566	chr10:5037926-5261426	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
17	nsv549883	chr10:5037926-5275762	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
18	nsv831773	chr10:5069805-5109716	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5068000-5076800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr10:5074000-5078800	Weak transcription	Stomach Mucosa	stomach
3	chr10:5074800-5076600	Enhancers	Hela-S3	cervix
4	chr10:5075000-5076200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:5075000-5076200	Enhancers	NHDF-Ad	bronchial
6	chr10:5075000-5076400	Enhancers	HMEC	breast
7	chr10:5075000-5076800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr10:5075000-5076800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr10:5075200-5076200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:5075200-5076200	Enhancers	NHEK	skin
11	chr10:5075200-5076600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr10:5075200-5076600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr10:5075200-5076600	Enhancers	NH-A	brain
14	chr10:5075200-5077000	ZNF genes & repeats	Adipose Nuclei	Adipose
15	chr10:5075400-5076200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr10:5075400-5076200	Enhancers	HSMM	muscle
17	chr10:5075400-5076200	Enhancers	HUVEC	blood vessel
18	chr10:5075600-5076800	Enhancers	Osteobl	bone
19	chr10:5075800-5076200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr10:5076000-5076200	ZNF genes & repeats	A549	lung
21	chr10:5076000-5076200	Enhancers	NHLF	lung
22	chr10:5076000-5076800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links