Variant report

Variant	rs10756534
Chromosome Location	chr9:14180089-14180090
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10122366	0.83[AMR][1000 genomes]
rs10124557	0.83[AMR][1000 genomes]
rs10125399	0.91[AMR][1000 genomes]
rs10738354	1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10756538	1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10810102	0.91[AMR][1000 genomes]
rs10961397	0.83[AMR][1000 genomes]
rs12001507	0.83[EUR][1000 genomes]
rs12344948	0.83[AMR][1000 genomes]
rs2890981	1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs73411963	0.83[AMR][1000 genomes]
rs73645005	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033764	chr9:13764918-14226168	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv892593	chr9:13948798-14233159	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1023303	chr9:14025605-14286269	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv540069	chr9:14025605-14286269	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv1029491	chr9:14033607-14942373	Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv429998	chr9:14043516-14214688	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
7	nsv892596	chr9:14145487-14208724	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv892597	chr9:14163383-14233159	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14123800-14198600	Weak transcription	Gastric	stomach
2	chr9:14134000-14181000	Weak transcription	Ovary	ovary
3	chr9:14159800-14180200	Weak transcription	Fetal Stomach	stomach
4	chr9:14160600-14181400	Weak transcription	HSMM	muscle
5	chr9:14165000-14180200	Weak transcription	Brain Angular Gyrus	brain
6	chr9:14165800-14180200	Weak transcription	Brain Anterior Caudate	brain
7	chr9:14165800-14181800	Weak transcription	Psoas Muscle	Psoas
8	chr9:14166200-14183200	Weak transcription	Esophagus	oesophagus
9	chr9:14170400-14186200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr9:14170800-14180200	Weak transcription	Right Atrium	heart
11	chr9:14171400-14180200	Weak transcription	Fetal Muscle Leg	muscle
12	chr9:14171800-14180800	Weak transcription	Osteobl	bone
13	chr9:14172200-14181800	Weak transcription	Right Ventricle	heart
14	chr9:14174000-14180600	Weak transcription	Pancreas	Pancrea
15	chr9:14174800-14180200	Weak transcription	Small Intestine	intestine
16	chr9:14176600-14180800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr9:14177200-14180600	Weak transcription	Left Ventricle	heart
18	chr9:14177200-14203400	Weak transcription	Fetal Muscle Trunk	muscle
19	chr9:14178000-14181400	Enhancers	Stomach Mucosa	stomach
20	chr9:14178200-14180200	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr9:14178600-14180600	Strong transcription	HUVEC	blood vessel
22	chr9:14178800-14180200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr9:14178800-14180200	Enhancers	Brain Germinal Matrix	brain
24	chr9:14178800-14180400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr9:14178800-14181400	Active TSS	Aorta	Aorta
26	chr9:14179000-14180600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr9:14179000-14181600	Enhancers	A549	lung
28	chr9:14179200-14180200	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr9:14179200-14180200	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr9:14179200-14180200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr9:14179200-14180200	Weak transcription	Stomach Smooth Muscle	stomach
32	chr9:14179400-14180200	Enhancers	HepG2	liver
33	chr9:14179400-14180200	Genic enhancers	NHEK	skin
34	chr9:14179400-14180400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr9:14179400-14180600	Enhancers	Adipose Nuclei	Adipose
36	chr9:14179600-14180200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr9:14179600-14180200	Enhancers	HMEC	breast
38	chr9:14179600-14180400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr9:14179600-14180400	Enhancers	Brain Substantia Nigra	brain
40	chr9:14179600-14180400	Enhancers	Duodenum Mucosa	Duodenum
41	chr9:14179600-14180400	Enhancers	Fetal Brain Female	brain
42	chr9:14179600-14180400	Enhancers	Rectal Smooth Muscle	rectum
43	chr9:14179600-14180600	Enhancers	Brain Cingulate Gyrus	brain
44	chr9:14179600-14181000	Genic enhancers	Fetal Lung	lung
45	chr9:14179600-14183400	Enhancers	Fetal Heart	heart
46	chr9:14179600-14183400	Enhancers	NH-A	brain
47	chr9:14179800-14180200	Enhancers	Fetal Brain Male	brain
48	chr9:14179800-14180400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr9:14180000-14180600	Flanking Active TSS	Colon Smooth Muscle	Colon
50	chr9:14180000-14180800	Enhancers	Brain Hippocampus Middle	brain

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