Variant report

Variant	rs7868947
Chromosome Location	chr9:14144376-14144377
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10511591	0.81[JPT][hapmap]
rs10511592	0.92[CEU][hapmap];0.81[JPT][hapmap];0.87[YRI][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12004755	0.81[CHB][hapmap];0.83[AMR][1000 genomes]
rs12552654	1.00[CEU][hapmap];0.81[JPT][hapmap];0.95[YRI][hapmap];0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12554151	0.92[CEU][hapmap];0.81[JPT][hapmap]
rs13300925	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs16931403	0.81[JPT][hapmap];0.85[YRI][hapmap]
rs2382437	0.94[JPT][hapmap];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2382438	0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs2382439	0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs2382440	0.84[CEU][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs4237133	0.92[CEU][hapmap]
rs4740559	0.85[AMR][1000 genomes]
rs6474820	0.84[CEU][hapmap];1.00[JPT][hapmap]
rs7028001	1.00[CEU][hapmap];0.81[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7029562	0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs7030475	0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs7031735	1.00[CEU][hapmap];0.84[JPT][hapmap];0.82[EUR][1000 genomes]
rs7042127	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7042365	1.00[CEU][hapmap];0.81[JPT][hapmap];0.93[EUR][1000 genomes]
rs7045411	1.00[CEU][hapmap];0.81[JPT][hapmap];0.89[EUR][1000 genomes]
rs723968	0.92[CEU][hapmap];0.81[JPT][hapmap];0.85[YRI][hapmap];0.82[EUR][1000 genomes]
rs73642095	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73642096	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73642097	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7863447	0.83[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv892595	chr9:14129951-14168029	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14116600-14159200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr9:14116600-14179200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr9:14116800-14156000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:14117000-14171200	Weak transcription	Hela-S3	cervix
5	chr9:14120200-14159000	Weak transcription	NHLF	lung
6	chr9:14120600-14151600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr9:14120600-14154800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr9:14120600-14159000	Weak transcription	NH-A	brain
9	chr9:14123800-14198600	Weak transcription	Gastric	stomach
10	chr9:14126400-14148200	Weak transcription	Placenta	Placenta
11	chr9:14126800-14144800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr9:14127000-14146000	Weak transcription	Osteobl	bone
13	chr9:14127000-14151200	Weak transcription	Aorta	Aorta
14	chr9:14127000-14156400	Weak transcription	Duodenum Mucosa	Duodenum
15	chr9:14131800-14173200	Weak transcription	Pancreas	Pancrea
16	chr9:14132000-14144600	Weak transcription	Fetal Brain Female	brain
17	chr9:14133000-14144800	Weak transcription	Left Ventricle	heart
18	chr9:14133400-14153200	Weak transcription	Psoas Muscle	Psoas
19	chr9:14133800-14146000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr9:14133800-14146200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr9:14134000-14148000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr9:14134000-14151000	Weak transcription	Adipose Nuclei	Adipose
23	chr9:14134000-14181000	Weak transcription	Ovary	ovary
24	chr9:14134200-14144400	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr9:14134200-14144600	Weak transcription	Fetal Heart	heart
26	chr9:14134200-14145600	Weak transcription	Liver	Liver
27	chr9:14134200-14156200	Weak transcription	Right Ventricle	heart
28	chr9:14134200-14159400	Weak transcription	Fetal Stomach	stomach
29	chr9:14136000-14155000	Weak transcription	Brain Germinal Matrix	brain
30	chr9:14137200-14146200	Weak transcription	A549	lung
31	chr9:14137400-14145200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr9:14137600-14148200	Weak transcription	NHEK	skin
33	chr9:14137600-14153400	Weak transcription	HMEC	breast
34	chr9:14140200-14148000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr9:14140400-14144400	Weak transcription	HSMM	muscle
36	chr9:14140400-14147200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr9:14141000-14144800	Weak transcription	Fetal Muscle Trunk	muscle
38	chr9:14141200-14144800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:14141200-14144800	Weak transcription	Fetal Muscle Leg	muscle
40	chr9:14142200-14159000	Weak transcription	Brain Hippocampus Middle	brain
41	chr9:14143000-14144600	Weak transcription	Fetal Lung	lung
42	chr9:14143200-14144400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr9:14143400-14145200	Enhancers	Rectal Smooth Muscle	rectum
44	chr9:14143600-14144400	Enhancers	Brain Angular Gyrus	brain
45	chr9:14143800-14144800	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr9:14143800-14144800	Enhancers	Brain Anterior Caudate	brain
47	chr9:14143800-14145000	Enhancers	Colon Smooth Muscle	Colon
48	chr9:14143800-14147000	Strong transcription	HUVEC	blood vessel
49	chr9:14144000-14157000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr9:14144200-14144400	Enhancers	Brain Substantia Nigra	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links