Variant report

Variant	rs11596684
Chromosome Location	chr10:91218525-91218526
allele	C/T
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	JUND	chr10:91218079-91218624	SK-N-SH	brain:	n/a	chr10:91218285-91218292 chr10:91218285-91218293 chr10:91218279-91218288
2	STAT3	chr10:91218212-91218733	Hela-S3	cervix:	n/a	chr10:91218667-91218678
3	STAT3	chr10:91218466-91218869	MCF10A-Er-Src	breast:	n/a	chr10:91218667-91218678
4	STAT3	chr10:91218278-91218844	MCF10A-Er-Src	breast:	n/a	chr10:91218667-91218678
5	NFIC	chr10:91217918-91218594	ECC-1	luminal epithelium:	n/a	n/a
6	FOS	chr10:91218001-91218624	HUVEC	blood vessel:	n/a	chr10:91218285-91218292 chr10:91218285-91218293 chr10:91218279-91218288
7	FOS	chr10:91218092-91218669	MCF10A-Er-Src	breast:	n/a	chr10:91218285-91218292 chr10:91218285-91218293 chr10:91218279-91218288
8	TEAD4	chr10:91217998-91218836	ECC-1	luminal epithelium:	n/a	n/a
9	JUND	chr10:91218033-91218688	SK-N-SH	brain:	n/a	chr10:91218285-91218292 chr10:91218285-91218293 chr10:91218279-91218288
10	STAT3	chr10:91218279-91218835	MCF10A-Er-Src	breast:	n/a	chr10:91218667-91218678
11	NFIC	chr10:91217841-91218567	ECC-1	luminal epithelium:	n/a	n/a
12	GATA3	chr10:91217978-91218590	SK-N-SH	brain:	n/a	n/a

Variant related genes	Relation type
ENSG00000234452	TF binding region

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11203135	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11203136	0.80[CEU][hapmap];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11593758	0.92[ASN][1000 genomes]
rs11594380	0.90[GIH][hapmap];0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs17387244	0.86[CEU][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3740029	0.82[CEU][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59542683	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91179600-91225600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:91198800-91223600	Weak transcription	Left Ventricle	heart
3	chr10:91214000-91223600	Weak transcription	Pancreas	Pancrea
4	chr10:91214200-91223400	Weak transcription	Placenta	Placenta
5	chr10:91217400-91219200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:91217400-91219200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr10:91217600-91218600	Enhancers	NHDF-Ad	bronchial
8	chr10:91217600-91218800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr10:91217600-91219000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr10:91217600-91219000	Enhancers	HMEC	breast
11	chr10:91217600-91219000	Enhancers	HSMM	muscle
12	chr10:91217600-91219200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr10:91217600-91219400	Enhancers	Fetal Heart	heart
14	chr10:91217600-91219400	Enhancers	Hela-S3	cervix
15	chr10:91217600-91220000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr10:91217800-91218800	Enhancers	HSMMtube	muscle
17	chr10:91217800-91219000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr10:91217800-91219200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr10:91218000-91218600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr10:91218000-91218600	Flanking Active TSS	NHLF	lung
21	chr10:91218000-91218800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr10:91218000-91218800	Enhancers	Aorta	Aorta
23	chr10:91218200-91218600	Enhancers	A549	lung
24	chr10:91218200-91218600	Flanking Active TSS	HUVEC	blood vessel
25	chr10:91218200-91218600	Flanking Active TSS	Osteobl	bone
26	chr10:91218200-91218800	Flanking Active TSS	NH-A	brain
27	chr10:91218400-91218600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr10:91218400-91218600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr10:91218400-91218600	Flanking Active TSS	NHEK	skin
30	chr10:91218400-91219200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr10:91218400-91226200	Weak transcription	Fetal Lung	lung

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