Variant report

Variant	rs9504271
Chromosome Location	chr6:4853955-4853956
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:4847558..4849642-chr6:4852103..4854411,2	K562	blood:
2	chr6:4806891..4809234-chr6:4853712..4855967,2	K562	blood:
3	chr6:4853455..4855875-chr6:4862739..4864405,2	K562	blood:
4	chr6:4775945..4778797-chr6:4852829..4854855,2	MCF-7	breast:
5	chr6:4853835..4856430-chr6:4856609..4858869,2	MCF-7	breast:
6	chr6:4848197..4852151-chr6:4852565..4855208,4	MCF-7	breast:
7	chr6:4847745..4850576-chr6:4852287..4854812,4	K562	blood:

Variant related genes	Relation type
ENSG00000153046	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs13199417	1.00[CEU][hapmap]
rs13212871	1.00[CEU][hapmap]
rs1557032	1.00[EUR][1000 genomes]
rs17138859	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17138931	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17138959	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs17138966	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2235429	1.00[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2326553	1.00[CEU][hapmap]
rs4376391	1.00[EUR][1000 genomes]
rs56278978	1.00[EUR][1000 genomes]
rs58368827	1.00[EUR][1000 genomes]
rs60609172	1.00[EUR][1000 genomes]
rs60949901	1.00[EUR][1000 genomes]
rs61278797	1.00[EUR][1000 genomes]
rs6916304	1.00[EUR][1000 genomes]
rs6916467	1.00[EUR][1000 genomes]
rs6919412	1.00[EUR][1000 genomes]
rs73348304	0.81[AFR][1000 genomes]
rs73348319	1.00[EUR][1000 genomes]
rs73348345	1.00[EUR][1000 genomes]
rs73348361	1.00[EUR][1000 genomes]
rs73362530	1.00[EUR][1000 genomes]
rs73362564	1.00[EUR][1000 genomes]
rs73364523	1.00[EUR][1000 genomes]
rs73364567	1.00[EUR][1000 genomes]
rs73364571	1.00[EUR][1000 genomes]
rs7743735	1.00[EUR][1000 genomes]
rs7768749	1.00[EUR][1000 genomes]
rs811251	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs947151	1.00[EUR][1000 genomes]
rs9502239	1.00[EUR][1000 genomes]
rs9502244	0.89[EUR][1000 genomes]
rs9502247	1.00[EUR][1000 genomes]
rs9502248	1.00[EUR][1000 genomes]
rs9502249	1.00[EUR][1000 genomes]
rs9502250	1.00[CEU][hapmap]
rs9502251	0.87[EUR][1000 genomes]
rs9504262	1.00[EUR][1000 genomes]
rs9504269	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9504270	1.00[EUR][1000 genomes]
rs9504275	1.00[EUR][1000 genomes]
rs9504276	1.00[EUR][1000 genomes]
rs9504281	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9504284	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs9504286	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3366530	chr6:4471528-4865322	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	esv2422499	chr6:4745428-5073222	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1015888	chr6:4787784-4883663	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv966675	chr6:4819733-4855009	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv830577	chr6:4834567-5050544	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4844600-4859600	Weak transcription	Spleen	Spleen
2	chr6:4844800-4854000	Weak transcription	NHEK	skin
3	chr6:4844800-4856600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:4844800-4863000	Weak transcription	Primary B cells from peripheral blood	blood
5	chr6:4846400-4859000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:4847400-4854000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:4847400-4871000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr6:4847600-4854000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr6:4847600-4854000	Weak transcription	Lung	lung
10	chr6:4849000-4854000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr6:4849000-4854000	Weak transcription	Fetal Stomach	stomach
12	chr6:4849000-4854000	Weak transcription	Left Ventricle	heart
13	chr6:4849000-4854000	Weak transcription	Right Atrium	heart
14	chr6:4849000-4856000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr6:4849000-4856000	Weak transcription	Brain Angular Gyrus	brain
16	chr6:4849000-4856600	Weak transcription	Right Ventricle	heart
17	chr6:4849000-4857800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr6:4849000-4859000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr6:4849000-4863000	Weak transcription	Fetal Muscle Leg	muscle
20	chr6:4849200-4854000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:4849200-4854000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr6:4849200-4854000	Weak transcription	Gastric	stomach
23	chr6:4849200-4854000	Weak transcription	Ovary	ovary
24	chr6:4849200-4854000	Weak transcription	Psoas Muscle	Psoas
25	chr6:4849200-4854200	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr6:4849200-4857800	Weak transcription	Pancreas	Pancrea
27	chr6:4849200-4858200	Weak transcription	Fetal Muscle Trunk	muscle
28	chr6:4849200-4858600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:4849200-4858600	Weak transcription	Brain Substantia Nigra	brain
30	chr6:4849200-4859000	Weak transcription	Brain Anterior Caudate	brain
31	chr6:4849200-4859400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr6:4849200-4861400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr6:4849200-4863200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr6:4849200-4865400	Weak transcription	Aorta	Aorta
35	chr6:4849400-4862400	Weak transcription	Fetal Kidney	kidney
36	chr6:4849600-4854000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr6:4849600-4854000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr6:4849600-4854000	Weak transcription	Fetal Intestine Small	intestine
39	chr6:4849600-4854400	Weak transcription	Osteobl	bone
40	chr6:4849600-4861400	Weak transcription	Placenta	Placenta
41	chr6:4849800-4854000	Weak transcription	Duodenum Mucosa	Duodenum
42	chr6:4849800-4854000	Weak transcription	Fetal Intestine Large	intestine
43	chr6:4849800-4854000	Weak transcription	GM12878-XiMat	blood
44	chr6:4849800-4856000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr6:4849800-4858200	Weak transcription	Colon Smooth Muscle	Colon
46	chr6:4849800-4858400	Weak transcription	Small Intestine	intestine
47	chr6:4849800-4863800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr6:4849800-4868000	Weak transcription	Hela-S3	cervix
49	chr6:4850000-4854000	Weak transcription	NH-A	brain
50	chr6:4850000-4854400	Weak transcription	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links