Variant report

Variant	rs7350424
Chromosome Location	chr10:49765730-49765731
allele	A/C
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	chr10:49765698-49765785	HUVEC	blood vessel:	n/a	n/a
2	POLR2A	chr10:49763949-49765858	U87	brain:	n/a	n/a
3	POLR2A	chr10:49764894-49765858	U87	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:49765600..49767473-chr10:49859240..49861901,2	K562	blood:

Variant related genes	Relation type
ARHGAP22	TF binding region
ENSG00000128805	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10491040	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10776614	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10776615	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10776616	0.89[ASN][1000 genomes]
rs10857592	0.86[ASN][1000 genomes]
rs10857596	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10857598	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11101362	0.86[ASN][1000 genomes]
rs11101364	0.86[ASN][1000 genomes]
rs11101368	0.86[ASN][1000 genomes]
rs11101377	0.89[ASN][1000 genomes]
rs11101381	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11101384	0.91[ASN][1000 genomes]
rs11591281	0.86[ASN][1000 genomes]
rs12358311	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12358315	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12412164	0.89[ASN][1000 genomes]
rs1345104	0.91[ASN][1000 genomes]
rs1345109	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1345110	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1345111	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1445148	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1445154	0.83[ASN][1000 genomes]
rs1473323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1838568	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1838569	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1838570	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1838573	0.88[ASN][1000 genomes]
rs1838574	0.90[ASN][1000 genomes]
rs1838579	0.91[ASN][1000 genomes]
rs1900021	0.88[ASN][1000 genomes]
rs1965170	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2077152	1.00[ASN][1000 genomes]
rs2120910	0.91[ASN][1000 genomes]
rs34983450	0.86[ASN][1000 genomes]
rs4084916	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4101278	0.88[ASN][1000 genomes]
rs41510345	0.84[ASN][1000 genomes]
rs4450130	0.86[ASN][1000 genomes]
rs4838421	0.91[ASN][1000 genomes]
rs4838422	0.91[ASN][1000 genomes]
rs4838617	0.89[ASN][1000 genomes]
rs4838623	0.91[ASN][1000 genomes]
rs56058334	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56080723	0.88[ASN][1000 genomes]
rs56248718	0.88[ASN][1000 genomes]
rs57601353	0.86[ASN][1000 genomes]
rs6537568	0.85[ASN][1000 genomes]
rs66695288	0.86[ASN][1000 genomes]
rs67372461	0.86[ASN][1000 genomes]
rs7071095	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7071480	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7074631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7085183	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7085335	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7088010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7089439	0.82[ASN][1000 genomes]
rs7094216	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7096053	0.85[ASN][1000 genomes]
rs7098068	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72785120	0.83[ASN][1000 genomes]
rs7350439	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs747533	0.85[ASN][1000 genomes]
rs7894707	0.87[ASN][1000 genomes]
rs7894971	0.91[ASN][1000 genomes]
rs7896644	0.91[ASN][1000 genomes]
rs7904456	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7905247	0.91[ASN][1000 genomes]
rs7916108	0.91[ASN][1000 genomes]
rs935271	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49742600-49774800	Weak transcription	Aorta	Aorta
2	chr10:49751200-49771600	Weak transcription	Pancreas	Pancrea
3	chr10:49757400-49782200	Weak transcription	HSMMtube	muscle
4	chr10:49759200-49770400	Weak transcription	NH-A	brain
5	chr10:49760800-49768800	Weak transcription	Ovary	ovary
6	chr10:49761600-49780600	Weak transcription	HUVEC	blood vessel
7	chr10:49762600-49772600	Weak transcription	Brain Angular Gyrus	brain
8	chr10:49763200-49780800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr10:49763800-49772600	Weak transcription	Brain Substantia Nigra	brain
10	chr10:49764400-49777800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr10:49764800-49766400	Weak transcription	Osteobl	bone
12	chr10:49765000-49773400	Weak transcription	NHLF	lung
13	chr10:49765000-49776400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr10:49765400-49765800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr10:49765400-49765800	Strong transcription	HMEC	breast
16	chr10:49765400-49766200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr10:49765400-49767400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr10:49765400-49767400	Weak transcription	HSMM	muscle
19	chr10:49765400-49768400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr10:49765400-49774000	Weak transcription	NHDF-Ad	bronchial
21	chr10:49765600-49765800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr10:49765600-49766000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr10:49765600-49766000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr10:49765600-49766000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr10:49765600-49766000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr10:49765600-49766600	Genic enhancers	Muscle Satellite Cultured Cells	--

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