Variant report

Variant	rs2622710
Chromosome Location	chr3:137798064-137798065
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:137797953..137799816-chr3:137805788..137808409,2	MCF-7	breast:
2	chr3:137796613..137798345-chr3:137800057..137802193,2	MCF-7	breast:
3	chr3:137795704..137798653-chr3:137818142..137820266,2	K562	blood:

Variant related genes	Relation type
ENSG00000158163	Chromatin interaction

Extended variants
information (count: 117 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:108)

rs_ID	r²[population]
rs1107422	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11719358	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13100360	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1351446	0.86[ASN][1000 genomes]
rs1444577	0.85[ASN][1000 genomes]
rs1444578	0.83[ASN][1000 genomes]
rs1545816	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1564496	0.83[ASN][1000 genomes]
rs17838821	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs179282	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2170309	0.83[ASN][1000 genomes]
rs2246945	0.83[ASN][1000 genomes]
rs2589259	0.85[ASN][1000 genomes]
rs2622697	0.83[ASN][1000 genomes]
rs2622698	0.86[ASN][1000 genomes]
rs2622704	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2622705	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2622706	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2622707	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2622709	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2622711	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2622713	0.94[EUR][1000 genomes]
rs2622714	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2622715	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2622716	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2622717	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2622718	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2622719	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2622720	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2622724	0.89[ASN][1000 genomes]
rs2622725	0.89[ASN][1000 genomes]
rs2622726	0.89[ASN][1000 genomes]
rs2622727	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2622728	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2622729	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2622730	0.92[ASN][1000 genomes]
rs2622746	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2724679	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2724687	0.86[ASN][1000 genomes]
rs2724693	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2724694	0.95[ASN][1000 genomes]
rs2724695	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2724697	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2724698	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2724699	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2724700	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2724701	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2724702	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2724703	0.94[ASN][1000 genomes]
rs2724704	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2724705	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2724706	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2724707	0.94[ASN][1000 genomes]
rs2724708	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2724713	0.90[ASN][1000 genomes]
rs2724716	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2724717	0.92[ASN][1000 genomes]
rs2724720	0.89[ASN][1000 genomes]
rs2724721	0.89[ASN][1000 genomes]
rs2724722	0.89[ASN][1000 genomes]
rs2724723	0.89[ASN][1000 genomes]
rs2724729	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28480035	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs329381	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs329382	0.86[ASN][1000 genomes]
rs329383	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs329384	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs329385	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs329388	0.89[ASN][1000 genomes]
rs329389	0.91[ASN][1000 genomes]
rs329390	0.91[ASN][1000 genomes]
rs329391	0.91[ASN][1000 genomes]
rs365504	0.94[ASN][1000 genomes]
rs367439	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs374045	0.94[ASN][1000 genomes]
rs382629	0.94[ASN][1000 genomes]
rs384828	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs389697	0.92[ASN][1000 genomes]
rs390729	0.92[ASN][1000 genomes]
rs405265	0.92[ASN][1000 genomes]
rs405517	0.89[ASN][1000 genomes]
rs405602	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs407009	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs419075	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs425938	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs436145	0.89[ASN][1000 genomes]
rs442800	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs445025	0.94[ASN][1000 genomes]
rs446644	0.94[ASN][1000 genomes]
rs452195	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs453023	0.94[ASN][1000 genomes]
rs4678403	0.83[ASN][1000 genomes]
rs618553	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6809258	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7613955	0.92[ASN][1000 genomes]
rs7629243	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7639197	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs899983	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9812778	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9814877	0.90[ASN][1000 genomes]
rs9834462	0.88[ASN][1000 genomes]
rs9834670	0.90[ASN][1000 genomes]
rs9842648	0.87[ASN][1000 genomes]
rs9842918	0.84[ASN][1000 genomes]
rs9857908	0.87[ASN][1000 genomes]
rs9860229	0.88[ASN][1000 genomes]
rs9860630	0.84[ASN][1000 genomes]
rs996432	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530056	chr3:137312356-138161861	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2757890	chr3:137611789-137933835	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	esv2759180	chr3:137611789-137933835	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	esv2751978	chr3:137715302-137890750	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1007857	chr3:137767454-137843106	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1008563	chr3:137776151-137801394	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1002136	chr3:137776151-137806500	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv519971	chr3:137782655-137801213	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv522591	chr3:137782655-137801213	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:137778200-137800600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr3:137778800-137800400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr3:137780000-137813400	Weak transcription	HUVEC	blood vessel
4	chr3:137780600-137811600	Weak transcription	Psoas Muscle	Psoas
5	chr3:137780800-137800600	Weak transcription	Brain Hippocampus Middle	brain
6	chr3:137781000-137833200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr3:137782600-137800600	Weak transcription	Placenta	Placenta
8	chr3:137783000-137802000	Weak transcription	Fetal Brain Female	brain
9	chr3:137783200-137811600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr3:137783200-137821200	Weak transcription	Colonic Mucosa	Colon
11	chr3:137785000-137801000	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr3:137785400-137805600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr3:137785600-137800600	Weak transcription	Rectal Smooth Muscle	rectum
14	chr3:137785800-137799000	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr3:137786000-137802000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr3:137786200-137798200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr3:137787200-137800400	Weak transcription	Gastric	stomach
18	chr3:137787600-137806600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:137787800-137800400	Weak transcription	Brain Cingulate Gyrus	brain
20	chr3:137787800-137800400	Weak transcription	Brain Substantia Nigra	brain
21	chr3:137787800-137802600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr3:137787800-137805200	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr3:137788000-137800400	Weak transcription	Stomach Mucosa	stomach
24	chr3:137789800-137803200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr3:137789800-137803600	Strong transcription	Fetal Lung	lung
26	chr3:137790400-137798200	Weak transcription	Pancreas	Pancrea
27	chr3:137790800-137798800	Weak transcription	Right Ventricle	heart
28	chr3:137790800-137802400	Weak transcription	Fetal Intestine Large	intestine
29	chr3:137790800-137802800	Weak transcription	Brain Germinal Matrix	brain
30	chr3:137792000-137802000	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr3:137792000-137802800	Weak transcription	Liver	Liver
32	chr3:137792000-137820600	Weak transcription	Esophagus	oesophagus
33	chr3:137792200-137805200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr3:137792400-137818200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr3:137792600-137802000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr3:137793600-137801400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:137793800-137803600	Strong transcription	Fetal Muscle Trunk	muscle
38	chr3:137794200-137801200	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr3:137794400-137800200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr3:137794600-137800000	Strong transcription	Ovary	ovary
41	chr3:137794600-137803400	Strong transcription	Fetal Muscle Leg	muscle
42	chr3:137794600-137803400	Strong transcription	Fetal Stomach	stomach
43	chr3:137794800-137798400	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr3:137795000-137801200	Strong transcription	Stomach Smooth Muscle	stomach
45	chr3:137795400-137799400	Strong transcription	Left Ventricle	heart
46	chr3:137795800-137803400	Strong transcription	Aorta	Aorta
47	chr3:137796000-137799800	Strong transcription	Colon Smooth Muscle	Colon
48	chr3:137796200-137801600	Weak transcription	Fetal Kidney	kidney
49	chr3:137796200-137801800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:137796200-137802400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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