Variant report

Variant	rs72491139
Chromosome Location	chr3:119028661-119028662
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs6803331	1.00[AMR][1000 genomes]
rs7646935	1.00[AMR][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	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv829694	chr3:119011488-119153579	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119014200-119029800	Weak transcription	Gastric	stomach
2	chr3:119014200-119032800	Weak transcription	Pancreas	Pancrea
3	chr3:119015000-119041200	Weak transcription	Aorta	Aorta
4	chr3:119015200-119041000	Weak transcription	Fetal Kidney	kidney
5	chr3:119016000-119035400	Weak transcription	Fetal Brain Male	brain
6	chr3:119016000-119041000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr3:119016400-119040800	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr3:119016400-119041000	Weak transcription	Fetal Intestine Small	intestine
9	chr3:119017400-119029800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr3:119017400-119040600	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr3:119017600-119032400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr3:119018800-119032800	Weak transcription	Thymus	Thymus
13	chr3:119019200-119040800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr3:119020400-119029800	Weak transcription	Colonic Mucosa	Colon
15	chr3:119020400-119040600	Weak transcription	Esophagus	oesophagus
16	chr3:119020800-119030400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr3:119020800-119032400	Weak transcription	Fetal Muscle Trunk	muscle
18	chr3:119021000-119030400	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr3:119021000-119032400	Weak transcription	Primary T cells from cord blood	blood
20	chr3:119021200-119041000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr3:119021200-119041000	Weak transcription	Fetal Thymus	thymus
22	chr3:119022000-119032400	Weak transcription	Duodenum Mucosa	Duodenum
23	chr3:119022200-119029000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr3:119022200-119040800	Weak transcription	Brain Angular Gyrus	brain
25	chr3:119022400-119029000	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr3:119022400-119040600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:119022400-119041000	Weak transcription	Primary B cells from cord blood	blood
28	chr3:119022400-119041000	Weak transcription	Fetal Intestine Large	intestine
29	chr3:119022400-119041200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr3:119022600-119028800	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr3:119022600-119029000	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr3:119022600-119029000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:119022600-119029000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr3:119022600-119032600	Weak transcription	Stomach Smooth Muscle	stomach
35	chr3:119022600-119040600	Weak transcription	Primary B cells from peripheral blood	blood
36	chr3:119023600-119029000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr3:119023600-119029000	Weak transcription	Spleen	Spleen
38	chr3:119023600-119029000	Weak transcription	NHEK	skin
39	chr3:119023600-119032800	Weak transcription	Ovary	ovary
40	chr3:119024200-119028800	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr3:119024200-119029000	Weak transcription	Placenta	Placenta
42	chr3:119024400-119040600	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr3:119024600-119028800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:119024800-119029000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr3:119024800-119029000	Weak transcription	Fetal Heart	heart
46	chr3:119024800-119029000	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr3:119024800-119029200	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr3:119024800-119029200	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr3:119024800-119032400	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr3:119024800-119032600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links