Variant report

Variant	rs708015
Chromosome Location	chr6:36998537-36998538
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:36995831..36998687-chr6:37023860..37026177,3	K562	blood:
2	chr6:36998393..36999918-chr6:37001477..37003042,2	K562	blood:
3	chr6:36573133..36574893-chr6:36998270..37000354,2	K562	blood:
4	chr6:36998448..37001378-chr6:37003343..37005292,2	K562	blood:
5	chr6:36995372..37000472-chr6:37174362..37180086,7	K562	blood:
6	chr6:36995831..36998687-chr6:37024606..37026177,2	K562	blood:
7	chr6:36996688..36999703-chr6:37014680..37019381,6	K562	blood:
8	chr6:36953033..36955715-chr6:36997324..37000089,2	K562	blood:
9	chr6:36993041..37002133-chr6:37135266..37141596,21	K562	blood:
10	chr6:36996690..36999564-chr6:37000125..37002261,3	MCF-7	breast:
11	chr6:36997224..37001862-chr6:37173680..37176936,6	K562	blood:
12	chr6:36993956..36998841-chr6:37016055..37021281,5	K562	blood:
13	chr6:36997259..36998862-chr6:37140083..37143068,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000137193	Chromatin interaction
ENSG00000137409	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs831496	0.86[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs831503	0.95[JPT][hapmap];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs831504	0.81[CEU][hapmap]
rs831505	0.84[EUR][1000 genomes];0.80[ASN][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	nsv1030015	chr6:36818510-37104446	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv916833	chr6:36826524-37029833	Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv518386	chr6:36942746-37037670	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	nsv885816	chr6:36965099-36999682	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36986800-37006600	Weak transcription	Colonic Mucosa	Colon
2	chr6:36988600-37006600	Weak transcription	Fetal Intestine Small	intestine
3	chr6:36990200-37006600	Weak transcription	Duodenum Mucosa	Duodenum
4	chr6:36991000-37001600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr6:36992600-37005800	Weak transcription	Liver	Liver
6	chr6:36992800-37006600	Weak transcription	Gastric	stomach
7	chr6:36993800-37001200	Weak transcription	Pancreas	Pancrea
8	chr6:36993800-37018200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr6:36995800-37006600	Weak transcription	Lung	lung
10	chr6:36996200-36999400	Weak transcription	Spleen	Spleen
11	chr6:36997400-37002400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr6:36997400-37013800	Weak transcription	Esophagus	oesophagus
13	chr6:36997600-36998600	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr6:36997600-37000800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr6:36997600-37001800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr6:36998000-36998800	ZNF genes & repeats	GM12878-XiMat	blood
17	chr6:36998000-36999000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
18	chr6:36998000-36999000	ZNF genes & repeats	K562	blood
19	chr6:36998000-37001200	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr6:36998200-36999400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr6:36998200-37001200	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr6:36998200-37001200	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr6:36998400-36998800	ZNF genes & repeats	Primary B cells from cord blood	blood
24	chr6:36998400-36998800	ZNF genes & repeats	Adipose Nuclei	Adipose
25	chr6:36998400-37001200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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