Variant report

Variant	rs10851546
Chromosome Location	chr15:31689067-31689068
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:31666607..31669484-chr15:31689062..31691079,2	MCF-7	breast:
2	chr15:31619402..31621251-chr15:31688977..31690973,2	MCF-7	breast:
3	chr15:31684315..31687013-chr15:31687874..31690870,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000169926	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10047980	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11071016	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4261489	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4328401	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4354896	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4389106	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4586393	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4779873	0.86[CEU][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4779874	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62037901	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6493635	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6493639	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6493659	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7165145	0.97[EUR][1000 genomes]
rs7171213	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7174005	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7175258	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7182014	0.83[EUR][1000 genomes]
rs7402619	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv903831	chr15:30986051-31723279	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
2	nsv1054147	chr15:31014507-31972706	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv542306	chr15:31014507-31972706	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	nsv932896	chr15:31292475-31730445	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
5	esv1815415	chr15:31483843-31697213	Genic enhancers Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	esv34100	chr15:31496514-31792591	Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv903840	chr15:31589970-31800149	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
8	nsv903841	chr15:31616674-31697242	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv903842	chr15:31621321-31697242	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
10	nsv456748	chr15:31621321-31697642	Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
11	nsv568801	chr15:31621321-31697642	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
12	esv1810782	chr15:31633161-31697642	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
13	nsv903843	chr15:31672947-31723279	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31685000-31689600	Weak transcription	HSMM	muscle
2	chr15:31685200-31689400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr15:31685200-31689600	Weak transcription	Brain Angular Gyrus	brain
4	chr15:31685200-31689600	Weak transcription	Psoas Muscle	Psoas
5	chr15:31685400-31689200	Weak transcription	Left Ventricle	heart
6	chr15:31685400-31689200	Weak transcription	Ovary	ovary
7	chr15:31685400-31689600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr15:31685400-31689600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr15:31685400-31689600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr15:31685400-31689600	Weak transcription	Brain Hippocampus Middle	brain
11	chr15:31685400-31689800	Weak transcription	Small Intestine	intestine
12	chr15:31685400-31690200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr15:31685600-31689600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr15:31685600-31689600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr15:31685600-31689600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr15:31685600-31689600	Weak transcription	Brain Anterior Caudate	brain
17	chr15:31685600-31689600	Weak transcription	Colon Smooth Muscle	Colon
18	chr15:31685600-31689600	Weak transcription	Right Atrium	heart
19	chr15:31685600-31689600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr15:31685800-31689600	Weak transcription	Colonic Mucosa	Colon
21	chr15:31685800-31694000	Weak transcription	Aorta	Aorta
22	chr15:31686000-31689600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr15:31686000-31689600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr15:31686000-31689600	Weak transcription	Esophagus	oesophagus
25	chr15:31686000-31689600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr15:31686000-31689600	Weak transcription	Spleen	Spleen
27	chr15:31686000-31689600	Weak transcription	GM12878-XiMat	blood
28	chr15:31686000-31689600	Weak transcription	NH-A	brain
29	chr15:31686000-31689800	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr15:31686000-31690000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr15:31686000-31690200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr15:31686000-31696200	Weak transcription	Gastric	stomach
33	chr15:31686200-31689400	Weak transcription	Primary B cells from peripheral blood	blood
34	chr15:31686200-31689600	Weak transcription	Primary T cells from cord blood	blood
35	chr15:31686200-31689600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr15:31686200-31689600	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr15:31686200-31689600	Weak transcription	Right Ventricle	heart
38	chr15:31686200-31689800	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr15:31686200-31690000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr15:31686200-31690000	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr15:31686200-31690200	Weak transcription	Thymus	Thymus
42	chr15:31686400-31689200	Weak transcription	Pancreas	Pancrea
43	chr15:31686400-31689600	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr15:31686400-31689600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr15:31686400-31689600	Weak transcription	Fetal Thymus	thymus
46	chr15:31686400-31690200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr15:31686400-31690400	Weak transcription	Dnd41	blood
48	chr15:31686600-31689200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr15:31688000-31689200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr15:31688000-31689600	Enhancers	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links