Variant report

Variant	rs9613785
Chromosome Location	chr22:29439201-29439202
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:29436637..29439256-chr22:29468690..29471478,2	MCF-7	breast:
2	chr22:29436800..29439536-chr22:29439547..29442052,2	K562	blood:
3	chr22:29426264..29428504-chr22:29439113..29440872,2	K562	blood:
4	chr22:29195509..29198134-chr22:29437512..29441446,4	K562	blood:
5	chr22:29195462..29200064-chr22:29436514..29439223,5	MCF-7	breast:
6	chr22:29437866..29439720-chr22:29487851..29489925,2	MCF-7	breast:
7	chr22:29436460..29439991-chr22:29442261..29446083,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000177993	Chromatin interaction
ENSG00000100219	Chromatin interaction
ENSG00000226471	Chromatin interaction
ENSG00000183762	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs12484832	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12485244	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17440734	0.96[CEU][hapmap];0.81[CHD][hapmap];0.89[GIH][hapmap];0.87[MEX][hapmap]
rs1977047	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1983553	0.93[CEU][hapmap];0.86[JPT][hapmap];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2064084	0.93[CEU][hapmap];0.81[CHD][hapmap];0.91[GIH][hapmap];0.87[MEX][hapmap]
rs2072774	0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs2103544	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2347789	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2347790	1.00[ASW][hapmap];0.96[CEU][hapmap];0.81[CHD][hapmap];0.91[GIH][hapmap];0.81[LWK][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28541979	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4140643	0.96[CEU][hapmap];0.80[GIH][hapmap];0.83[TSI][hapmap]
rs4333023	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4404379	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4594553	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4616575	0.85[AMR][1000 genomes]
rs469994	0.96[CEU][hapmap]
rs4820794	0.96[CEU][hapmap];0.86[JPT][hapmap];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4823002	1.00[CEU][hapmap];0.80[GIH][hapmap];0.85[TSI][hapmap]
rs4823003	0.93[CEU][hapmap];0.82[JPT][hapmap]
rs4823005	0.93[CEU][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs5997430	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs5997431	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs5997432	0.82[ASN][1000 genomes]
rs5997433	0.93[CEU][hapmap]
rs5997434	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs5997435	0.89[EUR][1000 genomes]
rs6005955	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6005956	0.96[CEU][hapmap];0.92[YRI][hapmap];0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6005958	0.92[CEU][hapmap]
rs6005959	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6005964	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs6005965	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6005967	1.00[ASW][hapmap];1.00[CEU][hapmap];0.83[CHB][hapmap];0.91[GIH][hapmap];0.93[LWK][hapmap];0.96[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs713834	1.00[CEU][hapmap];0.87[GIH][hapmap];0.86[JPT][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs727892	0.88[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7284304	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7287517	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7290304	0.93[CEU][hapmap];0.82[JPT][hapmap];0.80[ASN][1000 genomes]
rs738246	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8137254	0.96[CEU][hapmap];0.85[TSI][hapmap];0.88[EUR][1000 genomes]
rs8137499	0.96[CEU][hapmap]
rs8142591	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs874915	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs874916	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs874917	0.82[ASN][1000 genomes]
rs9608719	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs9608721	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9613768	0.83[TSI][hapmap]
rs9613771	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9613776	0.96[CEU][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9613777	1.00[ASW][hapmap];0.96[CEU][hapmap];0.81[CHD][hapmap];0.89[GIH][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];0.82[MKK][hapmap];0.95[TSI][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9613782	0.83[MEX][hapmap];0.83[TSI][hapmap]
rs9613784	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs964589	1.00[CEU][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][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	nsv1064079	chr22:29065528-29456059	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv531586	chr22:29252132-29902266	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29427400-29448400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr22:29427800-29451400	Weak transcription	Psoas Muscle	Psoas
3	chr22:29428000-29441800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr22:29428600-29440400	Weak transcription	Esophagus	oesophagus
5	chr22:29428600-29440800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr22:29428800-29443600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr22:29429000-29440600	Weak transcription	Colonic Mucosa	Colon
8	chr22:29429000-29444000	Weak transcription	Right Ventricle	heart
9	chr22:29429800-29439400	Weak transcription	Aorta	Aorta
10	chr22:29433800-29440600	Weak transcription	Lung	lung
11	chr22:29435400-29440000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr22:29435400-29440400	Weak transcription	Gastric	stomach
13	chr22:29436400-29440800	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr22:29436600-29439600	Weak transcription	Left Ventricle	heart
15	chr22:29436600-29440000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr22:29436800-29439400	Weak transcription	Placenta	Placenta
17	chr22:29436800-29441200	Genic enhancers	HepG2	liver
18	chr22:29436800-29442600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr22:29436800-29443800	Weak transcription	Hela-S3	cervix
20	chr22:29436800-29445600	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr22:29437200-29439400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr22:29437200-29439400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr22:29437200-29439400	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr22:29437200-29439400	Weak transcription	NHEK	skin
25	chr22:29437200-29439600	Weak transcription	Fetal Kidney	kidney
26	chr22:29437200-29440000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr22:29437200-29440000	Weak transcription	Ovary	ovary
28	chr22:29437200-29440000	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr22:29437200-29440400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr22:29437200-29440400	Weak transcription	Rectal Smooth Muscle	rectum
31	chr22:29437200-29440600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr22:29437200-29440600	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr22:29437200-29441400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr22:29437200-29442200	Weak transcription	Small Intestine	intestine
35	chr22:29437200-29443000	Weak transcription	K562	blood
36	chr22:29437200-29443200	Weak transcription	Brain Angular Gyrus	brain
37	chr22:29437200-29443800	Weak transcription	Fetal Heart	heart
38	chr22:29437200-29450800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr22:29437400-29439400	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr22:29437400-29439400	Weak transcription	A549	lung
41	chr22:29437400-29439600	Weak transcription	Brain Substantia Nigra	brain
42	chr22:29437400-29440000	Weak transcription	Brain Cingulate Gyrus	brain
43	chr22:29437600-29439400	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr22:29437600-29439600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr22:29437600-29440400	Weak transcription	Fetal Brain Female	brain
46	chr22:29437600-29440800	Weak transcription	Adipose Nuclei	Adipose
47	chr22:29437800-29439600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr22:29437800-29439600	Weak transcription	HSMMtube	muscle
49	chr22:29437800-29439800	Weak transcription	Stomach Mucosa	stomach
50	chr22:29437800-29440000	Weak transcription	Fetal Lung	lung

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