Variant report

Variant	rs976216
Chromosome Location	chr15:92511796-92511797
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:92509487..92513090-chr15:92516971..92519490,3	MCF-7	breast:
2	chr15:92509773..92512510-chr15:92514174..92516460,3	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10454699	0.97[ASN][1000 genomes]
rs10852165	0.85[ASN][1000 genomes]
rs10852166	0.83[ASN][1000 genomes]
rs11635055	0.90[ASN][1000 genomes]
rs12439826	0.94[ASN][1000 genomes]
rs12901238	0.99[ASN][1000 genomes]
rs12902685	0.96[ASN][1000 genomes]
rs12905744	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12909480	0.96[ASN][1000 genomes]
rs12910715	0.92[ASN][1000 genomes]
rs12910862	0.93[ASN][1000 genomes]
rs12916491	0.90[ASN][1000 genomes]
rs1356417	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1400783	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1568210	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16946157	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16946164	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16946168	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2138849	0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs2176452	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28470895	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35973922	0.91[ASN][1000 genomes]
rs4312282	0.90[ASN][1000 genomes]
rs4932592	0.95[ASN][1000 genomes]
rs4932593	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62009549	0.95[ASN][1000 genomes]
rs7165760	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7171131	0.82[ASN][1000 genomes]
rs7171921	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7172099	0.96[ASN][1000 genomes]
rs7172159	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7178673	0.87[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs7178734	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7179815	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8025507	0.80[ASN][1000 genomes]
rs8027160	0.80[ASN][1000 genomes]
rs8040046	0.96[ASN][1000 genomes]
rs953888	0.95[ASN][1000 genomes]
rs9920069	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]

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	nsv1048635	chr15:92073294-92557339	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv870094	chr15:92367354-92631647	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv534110	chr15:92397220-92592961	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:92498200-92555000	Weak transcription	Gastric	stomach
2	chr15:92506000-92513600	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr15:92506000-92517600	Weak transcription	Colonic Mucosa	Colon
4	chr15:92507600-92512200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr15:92507600-92514400	Enhancers	Fetal Heart	heart
6	chr15:92507600-92516400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr15:92507800-92513200	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr15:92508000-92514000	Enhancers	Brain Angular Gyrus	brain
9	chr15:92508000-92515000	Enhancers	Brain Cingulate Gyrus	brain
10	chr15:92508600-92514200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr15:92508600-92517600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr15:92508800-92514400	Enhancers	Ovary	ovary
13	chr15:92508800-92517600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr15:92509000-92512000	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr15:92509000-92518400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr15:92509200-92513600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr15:92509600-92511800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr15:92509600-92512800	Weak transcription	Fetal Muscle Trunk	muscle
19	chr15:92509600-92512800	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr15:92509600-92512800	Weak transcription	Stomach Smooth Muscle	stomach
21	chr15:92509600-92513000	Weak transcription	NHLF	lung
22	chr15:92509600-92515400	Enhancers	Brain Substantia Nigra	brain
23	chr15:92509600-92519200	Enhancers	Brain Hippocampus Middle	brain
24	chr15:92509800-92512000	Enhancers	HMEC	breast
25	chr15:92509800-92512800	Weak transcription	Adipose Nuclei	Adipose
26	chr15:92509800-92513000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr15:92509800-92513000	Weak transcription	HSMM	muscle
28	chr15:92509800-92515200	Enhancers	Brain Anterior Caudate	brain
29	chr15:92510000-92513200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr15:92510000-92514200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr15:92510200-92511800	Weak transcription	Fetal Lung	lung
32	chr15:92510200-92511800	Weak transcription	Psoas Muscle	Psoas
33	chr15:92510200-92511800	Enhancers	Hela-S3	cervix
34	chr15:92510200-92512800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr15:92510200-92512800	Weak transcription	NHDF-Ad	bronchial
36	chr15:92510200-92513000	Weak transcription	HSMMtube	muscle
37	chr15:92510200-92513600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr15:92510800-92512000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr15:92510800-92512000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr15:92510800-92512000	Enhancers	A549	lung
41	chr15:92510800-92512000	Enhancers	NHEK	skin
42	chr15:92510800-92512200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:92510800-92512400	Enhancers	Spleen	Spleen
44	chr15:92510800-92514400	Enhancers	Left Ventricle	heart
45	chr15:92511000-92514000	Enhancers	Right Atrium	heart
46	chr15:92511200-92511800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr15:92511200-92511800	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr15:92511200-92512000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr15:92511200-92512200	Enhancers	Esophagus	oesophagus
50	chr15:92511200-92514000	Enhancers	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links