Variant report

Variant	rs7005799
Chromosome Location	chr8:87402140-87402141
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs17608967	0.80[EUR][1000 genomes]
rs55727343	0.83[EUR][1000 genomes]
rs56096624	0.82[EUR][1000 genomes]
rs57644875	0.82[EUR][1000 genomes]
rs7006017	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932023	chr8:86845979-87490694	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	nsv429926	chr8:87161695-87429872	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	esv3349873	chr8:87185763-87603726	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	esv3360246	chr8:87200232-87419244	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87355800-87405600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:87356800-87403800	Weak transcription	Aorta	Aorta
3	chr8:87357400-87403400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr8:87357800-87413600	Weak transcription	Pancreas	Pancrea
5	chr8:87366800-87423800	Weak transcription	Colonic Mucosa	Colon
6	chr8:87375600-87403000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr8:87378600-87402200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr8:87378600-87402200	Weak transcription	Spleen	Spleen
9	chr8:87378800-87403800	Weak transcription	Psoas Muscle	Psoas
10	chr8:87379600-87444000	Weak transcription	Brain Germinal Matrix	brain
11	chr8:87379800-87403800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr8:87380800-87403600	Weak transcription	Stomach Mucosa	stomach
13	chr8:87381000-87403600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr8:87381000-87404000	Weak transcription	Small Intestine	intestine
15	chr8:87381000-87430800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr8:87381200-87425600	Weak transcription	K562	blood
17	chr8:87382400-87444000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr8:87383000-87403200	Weak transcription	Osteobl	bone
19	chr8:87383000-87406000	Weak transcription	HUVEC	blood vessel
20	chr8:87383000-87415000	Weak transcription	NHDF-Ad	bronchial
21	chr8:87383400-87404400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:87385000-87438000	Weak transcription	Fetal Brain Male	brain
23	chr8:87386000-87403800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr8:87386200-87403600	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr8:87387400-87403200	Weak transcription	NH-A	brain
26	chr8:87388200-87403400	Weak transcription	Colon Smooth Muscle	Colon
27	chr8:87388200-87410600	Weak transcription	HMEC	breast
28	chr8:87388200-87415200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr8:87388400-87406200	Weak transcription	HSMM	muscle
30	chr8:87388400-87430600	Weak transcription	Fetal Kidney	kidney
31	chr8:87388600-87441200	Weak transcription	Right Ventricle	heart
32	chr8:87389000-87403400	Weak transcription	Brain Angular Gyrus	brain
33	chr8:87389400-87404400	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr8:87391000-87403400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr8:87391800-87403400	Weak transcription	Brain Anterior Caudate	brain
36	chr8:87392200-87409000	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr8:87392400-87404400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr8:87392400-87407000	Strong transcription	Primary T helper cells PMA-I stimulated	--
39	chr8:87393000-87403400	Weak transcription	Brain Substantia Nigra	brain
40	chr8:87393200-87403400	Weak transcription	Brain Cingulate Gyrus	brain
41	chr8:87393200-87403400	Weak transcription	Brain Hippocampus Middle	brain
42	chr8:87393600-87404600	Strong transcription	Liver	Liver
43	chr8:87394600-87403400	Weak transcription	HSMMtube	muscle
44	chr8:87395400-87406000	Weak transcription	Hela-S3	cervix
45	chr8:87396200-87415600	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr8:87396400-87406000	Weak transcription	Left Ventricle	heart
47	chr8:87397400-87431200	Weak transcription	Fetal Brain Female	brain
48	chr8:87397800-87402400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:87398000-87402800	Weak transcription	Fetal Heart	heart
50	chr8:87398800-87403000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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