Variant report

Variant	rs935286
Chromosome Location	chr10:49796046-49796047
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	POLR2A	chr10:49795056-49798551	U87	brain:	n/a	n/a
2	CEBPB	chr10:49795893-49796226	A549	lung:	n/a	chr10:49796069-49796080 chr10:49796071-49796082 chr10:49796069-49796082
3	CEBPB	chr10:49795889-49796260	HepG2	liver:	n/a	chr10:49796069-49796080 chr10:49796071-49796082 chr10:49796069-49796082
4	POLR2A	chr10:49796010-49796129	HUVEC	blood vessel:	n/a	n/a
5	CEBPB	chr10:49795942-49796213	K562	blood:	n/a	chr10:49796069-49796080 chr10:49796071-49796082 chr10:49796069-49796082
6	CEBPB	chr10:49795893-49796258	IMR90	lung:	n/a	chr10:49796069-49796080 chr10:49796071-49796082 chr10:49796069-49796082
7	CEBPB	chr10:49796007-49796120	Hela-S3	cervix:	n/a	chr10:49796069-49796080 chr10:49796071-49796082 chr10:49796069-49796082
8	POLR2A	chr10:49795663-49797029	U87	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:49794436..49796437-chr10:49820833..49823076,2	K562	blood:

Variant related genes	Relation type
ARHGAP22	TF binding region

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10857607	0.86[EUR][1000 genomes]
rs11592077	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs11594078	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs12412298	0.86[EUR][1000 genomes]
rs1345107	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1806438	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1965169	0.87[CEU][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2377517	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4572084	0.87[CEU][hapmap]
rs61838376	0.98[EUR][1000 genomes]
rs61838387	0.97[EUR][1000 genomes]
rs61841202	0.85[EUR][1000 genomes]
rs61841203	0.85[EUR][1000 genomes]
rs7079932	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7909968	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1046588	chr10:49790254-49806169	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49787800-49796800	Weak transcription	Right Atrium	heart
2	chr10:49788800-49797200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr10:49791000-49796200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr10:49791400-49798400	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr10:49792200-49796600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr10:49792200-49797200	Weak transcription	Brain Anterior Caudate	brain
7	chr10:49792400-49796400	Weak transcription	Brain Angular Gyrus	brain
8	chr10:49792800-49796800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr10:49792800-49796800	Weak transcription	HUVEC	blood vessel
10	chr10:49794000-49796600	Weak transcription	HSMMtube	muscle
11	chr10:49794000-49796800	Weak transcription	NH-A	brain
12	chr10:49794400-49810600	Enhancers	Brain Substantia Nigra	brain
13	chr10:49794600-49796200	Strong transcription	HSMM	muscle
14	chr10:49794800-49799200	Enhancers	Brain Hippocampus Middle	brain
15	chr10:49795000-49797000	Genic enhancers	Muscle Satellite Cultured Cells	--
16	chr10:49795000-49797200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr10:49795000-49797400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr10:49795000-49799400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr10:49795200-49803800	Enhancers	NHDF-Ad	bronchial
20	chr10:49795600-49796200	Genic enhancers	Osteobl	bone
21	chr10:49795600-49797200	Enhancers	Adipose Nuclei	Adipose
22	chr10:49795600-49798800	Genic enhancers	NHLF	lung
23	chr10:49795800-49796200	Genic enhancers	Brain Inferior Temporal Lobe	brain
24	chr10:49795800-49796400	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr10:49795800-49797200	Enhancers	Left Ventricle	heart
26	chr10:49795800-49798800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr10:49795800-49798800	Enhancers	Brain Cingulate Gyrus	brain
28	chr10:49795800-49798800	Enhancers	HMEC	breast
29	chr10:49796000-49796200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr10:49796000-49796200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr10:49796000-49796200	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr10:49796000-49796200	Enhancers	Spleen	Spleen
33	chr10:49796000-49796800	Weak transcription	Gastric	stomach
34	chr10:49796000-49798200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:49796000-49798400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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