Variant report

Variant	rs6470367
Chromosome Location	chr8:126608587-126608588
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:126608438..126611381-chr8:126617335..126619462,2	K562	blood:
2	chr8:126440732..126445779-chr8:126600349..126612045,20	MCF-7	breast:
3	chr8:126585008..126593535-chr8:126599853..126611131,18	MCF-7	breast:
4	chr8:126601013..126605207-chr8:126607092..126609721,3	MCF-7	breast:
5	chr8:126440111..126444206-chr8:126606253..126610724,8	MCF-7	breast:

Variant related genes	Relation type
ENSG00000173334	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1031496	0.92[TSI][hapmap];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1454621	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[MKK][hapmap];0.92[TSI][hapmap]
rs4871620	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4871622	0.94[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs7001297	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7002040	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs897159	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[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	nsv891437	chr8:126470817-126629328	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv6377	chr8:126579620-126639253	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv38	chr8:126593465-126639253	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1015513	chr8:126602536-126618074	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126602200-126608600	Enhancers	Placenta	Placenta
2	chr8:126604000-126608800	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr8:126605600-126608800	Enhancers	Sigmoid Colon	Sigmoid Colon
4	chr8:126606600-126608600	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr8:126606600-126608600	Enhancers	Small Intestine	intestine
6	chr8:126606600-126613800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:126606800-126609000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:126606800-126609000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr8:126606800-126610400	Weak transcription	NHEK	skin
10	chr8:126606800-126610800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:126606800-126612800	Weak transcription	Spleen	Spleen
12	chr8:126606800-126613600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr8:126606800-126614800	Weak transcription	Osteobl	bone
14	chr8:126607400-126608600	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr8:126607400-126608800	Enhancers	Primary B cells from peripheral blood	blood
16	chr8:126607600-126609200	Enhancers	Fetal Heart	heart
17	chr8:126607800-126608800	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr8:126607800-126609000	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr8:126607800-126614000	Weak transcription	Hela-S3	cervix
20	chr8:126607800-126614600	Weak transcription	A549	lung
21	chr8:126608000-126608600	Enhancers	Esophagus	oesophagus
22	chr8:126608200-126609400	Weak transcription	Lung	lung
23	chr8:126608200-126613400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr8:126608400-126609600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr8:126608400-126612200	Weak transcription	Primary B cells from cord blood	blood
26	chr8:126608400-126613200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr8:126608400-126613600	Weak transcription	Pancreas	Pancrea
28	chr8:126608400-126618400	Weak transcription	Colonic Mucosa	Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links