Variant report

Variant	rs9470907
Chromosome Location	chr6:38585653-38585654
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs4711553	0.89[ASW][hapmap]
rs4714173	0.89[ASW][hapmap]
rs7775968	0.89[ASW][hapmap]
rs9296255	0.89[ASW][hapmap]
rs9470893	1.00[AMR][1000 genomes]
rs9470916	0.89[ASW][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021991	chr6:37893949-38738720	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv534620	chr6:38049585-38602064	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38565400-38589200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr6:38572000-38591600	Weak transcription	Fetal Intestine Small	intestine
3	chr6:38580600-38600200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:38580600-38601800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:38580800-38585800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr6:38580800-38589400	Weak transcription	Right Atrium	heart
7	chr6:38580800-38594000	Weak transcription	Small Intestine	intestine
8	chr6:38580800-38604400	Weak transcription	Ovary	ovary
9	chr6:38581000-38585800	Weak transcription	HSMMtube	muscle
10	chr6:38581000-38586200	Weak transcription	Osteobl	bone
11	chr6:38581200-38585800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:38581400-38585800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:38581800-38585800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:38582200-38587200	Weak transcription	Psoas Muscle	Psoas
15	chr6:38582600-38587200	Weak transcription	Right Ventricle	heart
16	chr6:38583000-38599200	Weak transcription	Primary B cells from peripheral blood	blood
17	chr6:38583400-38600400	Weak transcription	Left Ventricle	heart
18	chr6:38583800-38602000	Weak transcription	Primary T cells from cord blood	blood
19	chr6:38585200-38588600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr6:38585400-38586400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:38585600-38585800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:38585600-38586800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr6:38585600-38586800	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr6:38585600-38587600	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links