Variant report

Variant	rs7811968
Chromosome Location	chr7:83803627-83803628
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10229639	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11971977	1.00[EUR][1000 genomes]
rs11976214	0.98[EUR][1000 genomes]
rs11976275	1.00[EUR][1000 genomes]
rs12707623	1.00[EUR][1000 genomes]
rs12707624	1.00[EUR][1000 genomes]
rs12707625	0.98[EUR][1000 genomes]
rs12707626	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12707627	1.00[EUR][1000 genomes]
rs13224698	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs13230138	0.87[EUR][1000 genomes]
rs13231088	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13231114	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13231702	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13234305	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13242741	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs1557936	1.00[EUR][1000 genomes]
rs17158699	1.00[ASW][hapmap];0.83[LWK][hapmap];0.83[AFR][1000 genomes]
rs28464975	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34054916	1.00[EUR][1000 genomes]
rs34183115	1.00[EUR][1000 genomes]
rs34231292	0.95[EUR][1000 genomes]
rs34406409	1.00[EUR][1000 genomes]
rs34445481	1.00[EUR][1000 genomes]
rs34446199	1.00[EUR][1000 genomes]
rs34586908	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34753507	1.00[EUR][1000 genomes]
rs34798940	1.00[EUR][1000 genomes]
rs34843693	1.00[EUR][1000 genomes]
rs34998443	0.98[EUR][1000 genomes]
rs35088033	1.00[EUR][1000 genomes]
rs35157722	1.00[EUR][1000 genomes]
rs35192141	1.00[EUR][1000 genomes]
rs35241002	1.00[EUR][1000 genomes]
rs35276675	0.98[EUR][1000 genomes]
rs35473465	1.00[EUR][1000 genomes]
rs35732081	1.00[EUR][1000 genomes]
rs35743946	0.98[EUR][1000 genomes]
rs35815557	1.00[EUR][1000 genomes]
rs35912238	1.00[EUR][1000 genomes]
rs35929386	1.00[EUR][1000 genomes]
rs35947091	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36005262	1.00[EUR][1000 genomes]
rs36075153	1.00[EUR][1000 genomes]
rs71522694	0.95[EUR][1000 genomes]
rs71558711	1.00[EUR][1000 genomes]
rs71558712	1.00[EUR][1000 genomes]
rs71558713	1.00[EUR][1000 genomes]
rs71558715	1.00[EUR][1000 genomes]
rs71558716	1.00[EUR][1000 genomes]
rs71558719	0.93[EUR][1000 genomes]
rs7784725	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv888629	chr7:83722691-83896025	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1017884	chr7:83724138-83972995	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong 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	1 gene(s)	inside rSNPs	diseases
4	nsv538995	chr7:83724138-83972995	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv888630	chr7:83782839-83809111	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83787800-83804600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:83792200-83820600	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr7:83797400-83804600	Weak transcription	Colon Smooth Muscle	Colon
4	chr7:83800800-83816600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr7:83801600-83805800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:83802000-83807400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:83802800-83804600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
8	chr7:83803000-83803800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr7:83803000-83803800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr7:83803000-83803800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:83803000-83803800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr7:83803000-83803800	ZNF genes & repeats	Fetal Muscle Trunk	muscle
13	chr7:83803000-83803800	ZNF genes & repeats	Fetal Muscle Leg	muscle
14	chr7:83803000-83803800	ZNF genes & repeats	A549	lung
15	chr7:83803000-83804600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
16	chr7:83803000-83805000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:83803000-83805000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
18	chr7:83803000-83805200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
19	chr7:83803400-83803800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:83803400-83803800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:83803400-83804600	Strong transcription	Fetal Lung	lung
22	chr7:83803400-83805000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:83803400-83806000	Weak transcription	Fetal Stomach	stomach
24	chr7:83803400-83806200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr7:83803400-83816200	Weak transcription	Fetal Brain Male	brain
26	chr7:83803400-83821800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr7:83803600-83805800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:83803600-83806000	Weak transcription	NHDF-Ad	bronchial
29	chr7:83803600-83813400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr7:83803600-83816200	Weak transcription	NHLF	lung
31	chr7:83803600-83816400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr7:83803600-83816400	Weak transcription	NH-A	brain

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