Variant report

Variant	rs7028001
Chromosome Location	chr9:14144998-14144999
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10511591	0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10511592	0.93[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12552654	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12554151	0.93[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16931403	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs2382440	0.85[CEU][hapmap]
rs4237133	0.92[CEU][hapmap]
rs6474820	0.85[CEU][hapmap];0.82[JPT][hapmap];0.82[EUR][1000 genomes]
rs7029562	0.80[CEU][hapmap]
rs7031735	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7042127	1.00[CEU][hapmap];0.81[JPT][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7042365	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7044402	0.93[CHB][hapmap];0.86[JPT][hapmap]
rs7045411	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs723968	0.92[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73642095	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73642096	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73642097	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7863447	0.84[CEU][hapmap];0.84[EUR][1000 genomes]
rs7868947	1.00[CEU][hapmap];0.81[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]

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:52 , 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	chr9:14127000-14146000	Weak transcription	Osteobl	bone
12	chr9:14127000-14151200	Weak transcription	Aorta	Aorta
13	chr9:14127000-14156400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr9:14131800-14173200	Weak transcription	Pancreas	Pancrea
15	chr9:14133400-14153200	Weak transcription	Psoas Muscle	Psoas
16	chr9:14133800-14146000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr9:14133800-14146200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr9:14134000-14148000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr9:14134000-14151000	Weak transcription	Adipose Nuclei	Adipose
20	chr9:14134000-14181000	Weak transcription	Ovary	ovary
21	chr9:14134200-14145600	Weak transcription	Liver	Liver
22	chr9:14134200-14156200	Weak transcription	Right Ventricle	heart
23	chr9:14134200-14159400	Weak transcription	Fetal Stomach	stomach
24	chr9:14136000-14155000	Weak transcription	Brain Germinal Matrix	brain
25	chr9:14137200-14146200	Weak transcription	A549	lung
26	chr9:14137400-14145200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr9:14137600-14148200	Weak transcription	NHEK	skin
28	chr9:14137600-14153400	Weak transcription	HMEC	breast
29	chr9:14140200-14148000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr9:14140400-14147200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:14142200-14159000	Weak transcription	Brain Hippocampus Middle	brain
32	chr9:14143400-14145200	Enhancers	Rectal Smooth Muscle	rectum
33	chr9:14143800-14145000	Enhancers	Colon Smooth Muscle	Colon
34	chr9:14143800-14147000	Strong transcription	HUVEC	blood vessel
35	chr9:14144000-14157000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr9:14144200-14147000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:14144200-14152800	Weak transcription	Fetal Brain Male	brain
38	chr9:14144400-14145000	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr9:14144400-14147000	Strong transcription	HSMM	muscle
40	chr9:14144400-14148000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:14144400-14155000	Weak transcription	Brain Angular Gyrus	brain
42	chr9:14144400-14156400	Weak transcription	Brain Substantia Nigra	brain
43	chr9:14144600-14145000	Enhancers	Fetal Heart	heart
44	chr9:14144600-14145200	Genic enhancers	Fetal Brain Female	brain
45	chr9:14144600-14148000	Strong transcription	Fetal Lung	lung
46	chr9:14144800-14145400	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr9:14144800-14145400	Enhancers	Spleen	Spleen
48	chr9:14144800-14145600	Strong transcription	Left Ventricle	heart
49	chr9:14144800-14146800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr9:14144800-14146800	Strong transcription	Fetal Muscle Trunk	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links