Variant report

Variant	rs10072795
Chromosome Location	chr5:61926737-61926738
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:61925893..61927703-chr5:61935030..61937549,2	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10051492	0.83[CEU][hapmap]
rs10054305	0.96[CEU][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10058044	0.96[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10060589	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10065749	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10069745	0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs10071568	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12516160	0.83[CEU][hapmap]
rs12521329	0.83[CEU][hapmap]
rs13167856	0.80[CEU][hapmap]
rs13174978	0.91[CEU][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs149540	0.91[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs152184	0.91[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs152199	0.91[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs152215	0.91[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs1541677	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1562244	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs181912	0.83[CEU][hapmap]
rs247233	0.91[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap]
rs247240	0.91[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs26637	0.91[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs28539215	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28581963	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs32154	0.83[CEU][hapmap]
rs32155	0.83[CEU][hapmap]
rs32164	0.83[CEU][hapmap]
rs32171	0.87[CEU][hapmap]
rs32181	0.83[CEU][hapmap]
rs32187	0.83[CEU][hapmap]
rs34562047	0.81[EUR][1000 genomes]
rs366238	0.80[CEU][hapmap]
rs3776638	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs39923	0.83[CEU][hapmap]
rs39935	0.83[CEU][hapmap]
rs4700012	0.80[CEU][hapmap]
rs6449601	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6449602	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6881888	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6888641	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7706610	0.83[CEU][hapmap]
rs7717128	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7718484	0.83[CEU][hapmap]
rs7722692	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7729526	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7737525	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs784921	0.92[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs918606	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020255	chr5:61451792-62031365	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1027539	chr5:61457762-62000008	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS 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 lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv881731	chr5:61794164-61941043	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv881732	chr5:61811970-62063366	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	esv2763458	chr5:61852234-62157166	ZNF genes & repeats Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv1022817	chr5:61853619-62149259	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
7	nsv948334	chr5:61891622-62197219	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
8	nsv4858	chr5:61922306-61966961	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61848200-61939600	Weak transcription	Brain Anterior Caudate	brain
2	chr5:61864800-61945800	Weak transcription	HSMMtube	muscle
3	chr5:61881400-61939400	Weak transcription	Spleen	Spleen
4	chr5:61886800-61941200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr5:61888800-61928000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr5:61888800-61937000	Weak transcription	Gastric	stomach
7	chr5:61889600-61929200	Weak transcription	NH-A	brain
8	chr5:61889600-61936200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr5:61893000-61943200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr5:61899800-61928200	Weak transcription	Ovary	ovary
11	chr5:61899800-61928400	Weak transcription	Esophagus	oesophagus
12	chr5:61899800-61939600	Weak transcription	Pancreas	Pancrea
13	chr5:61902000-61934200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr5:61905200-61927600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr5:61905400-61939200	Weak transcription	Fetal Kidney	kidney
16	chr5:61905800-61927200	Weak transcription	Fetal Thymus	thymus
17	chr5:61905800-61927400	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr5:61905800-61927800	Weak transcription	Fetal Lung	lung
19	chr5:61906000-61927600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr5:61906000-61946000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr5:61910800-61928000	Weak transcription	Right Ventricle	heart
22	chr5:61910800-61929200	Weak transcription	HepG2	liver
23	chr5:61910800-61929400	Weak transcription	Fetal Muscle Leg	muscle
24	chr5:61910800-61929600	Weak transcription	Lung	lung
25	chr5:61911000-61928600	Weak transcription	Thymus	Thymus
26	chr5:61911000-61931200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr5:61911000-61933800	Weak transcription	Aorta	Aorta
28	chr5:61911000-61939200	Weak transcription	Fetal Stomach	stomach
29	chr5:61911000-61944200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr5:61911200-61941800	Weak transcription	Fetal Intestine Small	intestine
31	chr5:61913400-61943000	Weak transcription	Hela-S3	cervix
32	chr5:61916000-61928200	Weak transcription	Placenta	Placenta
33	chr5:61916600-61929000	Weak transcription	Brain Angular Gyrus	brain
34	chr5:61917200-61945800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr5:61920400-61942600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr5:61921400-61927800	Weak transcription	Brain Hippocampus Middle	brain
37	chr5:61923000-61926800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:61923000-61945400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr5:61923200-61928000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr5:61923200-61935000	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr5:61923200-61939000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr5:61923400-61941400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr5:61923800-61926800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:61923800-61935600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr5:61924000-61928000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr5:61924000-61928400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:61924000-61928600	Weak transcription	Fetal Muscle Trunk	muscle
48	chr5:61924000-61930600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr5:61924000-61936000	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr5:61924000-61944400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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