Variant report

Variant	rs7915707
Chromosome Location	chr10:49810977-49810978
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:49803449..49806328-chr10:49810436..49812286,2	K562	blood:

Extended variants
information (count: 6 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs7914253	0.95[CHD][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs7914646	0.87[LWK][hapmap];0.92[YRI][hapmap];0.86[AFR][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	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	nsv540623	chr10:49805087-49819765	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv540624	chr10:49805087-49822634	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7915707	ARHGAP22	cis	cerebellum	SCAN

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49797400-49812200	Weak transcription	Right Atrium	heart
2	chr10:49805600-49811000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:49807000-49811000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr10:49807600-49811600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr10:49808000-49811400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:49808000-49811800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr10:49808000-49811800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:49808000-49812000	Weak transcription	Ovary	ovary
9	chr10:49808400-49811600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr10:49809200-49812200	Weak transcription	Aorta	Aorta
11	chr10:49809800-49812600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr10:49810000-49811200	Flanking Active TSS	NHDF-Ad	bronchial
13	chr10:49810000-49811400	Transcr. at gene 5' and 3'	HSMM	muscle
14	chr10:49810000-49812000	Transcr. at gene 5' and 3'	NHLF	lung
15	chr10:49810000-49812400	Flanking Active TSS	Osteobl	bone
16	chr10:49810000-49813000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr10:49810200-49811600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr10:49810200-49811600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr10:49810400-49813000	Flanking Active TSS	HUVEC	blood vessel
20	chr10:49810600-49811000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:49810600-49811000	Enhancers	Brain Anterior Caudate	brain
22	chr10:49810600-49811200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:49810600-49811200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr10:49810600-49811200	Flanking Active TSS	Brain Hippocampus Middle	brain
25	chr10:49810600-49811200	Flanking Active TSS	HSMMtube	muscle
26	chr10:49810600-49811400	Flanking Active TSS	Brain Substantia Nigra	brain
27	chr10:49810600-49811600	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr10:49810600-49812800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr10:49810600-49812800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr10:49810600-49813000	Flanking Active TSS	HMEC	breast
31	chr10:49810800-49811000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr10:49810800-49811000	Active TSS	Brain Cingulate Gyrus	brain
33	chr10:49810800-49811000	Bivalent Enhancer	Right Ventricle	heart
34	chr10:49810800-49811200	Flanking Active TSS	Brain Angular Gyrus	brain
35	chr10:49810800-49811200	Enhancers	Gastric	stomach
36	chr10:49810800-49811600	Active TSS	NH-A	brain

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