Variant report

Variant	rs9642177
Chromosome Location	chr7:83812258-83812259
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11976488	1.00[ASN][1000 genomes]
rs12234403	0.87[ASN][1000 genomes]
rs13231195	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34183115	0.80[AFR][1000 genomes]
rs34446199	0.80[AFR][1000 genomes]
rs34753507	0.80[AFR][1000 genomes]
rs35157722	0.80[AFR][1000 genomes]
rs35192141	0.80[AFR][1000 genomes]
rs36005262	0.80[AFR][1000 genomes]
rs36075153	0.80[AFR][1000 genomes]
rs73709589	1.00[ASN][1000 genomes]
rs9642176	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83792200-83820600	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr7:83800800-83816600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr7:83803400-83816200	Weak transcription	Fetal Brain Male	brain
4	chr7:83803400-83821800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:83803600-83813400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:83803600-83816200	Weak transcription	NHLF	lung
7	chr7:83803600-83816400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:83803600-83816400	Weak transcription	NH-A	brain
9	chr7:83803800-83820600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr7:83804600-83813600	Weak transcription	Fetal Lung	lung
11	chr7:83804600-83816200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr7:83805000-83816200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:83805000-83817200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:83805200-83813200	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr7:83806400-83815400	Weak transcription	Fetal Stomach	stomach
16	chr7:83806800-83816200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:83807600-83813200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr7:83807600-83814000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:83809000-83816200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:83809200-83813800	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr7:83810200-83814000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:83811400-83812600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr7:83811400-83813600	Weak transcription	Rectal Smooth Muscle	rectum
24	chr7:83811600-83816400	Weak transcription	Colon Smooth Muscle	Colon
25	chr7:83811800-83813200	Enhancers	Fetal Heart	heart
26	chr7:83812000-83812600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:83812000-83812800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:83812000-83816200	Weak transcription	A549	lung
29	chr7:83812000-83816400	Weak transcription	NHDF-Ad	bronchial
30	chr7:83812000-83819600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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