Variant report

Variant	rs2576372
Chromosome Location	chr3:100639636-100639637
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs1036467	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10511181	0.89[EUR][1000 genomes]
rs13060137	0.94[EUR][1000 genomes]
rs13072000	0.94[EUR][1000 genomes]
rs13077353	0.94[EUR][1000 genomes]
rs13079002	0.98[EUR][1000 genomes]
rs13080859	0.88[EUR][1000 genomes]
rs13088524	0.89[EUR][1000 genomes]
rs13092605	0.96[EUR][1000 genomes]
rs13099053	0.94[EUR][1000 genomes]
rs13100301	0.94[EUR][1000 genomes]
rs17284842	0.94[EUR][1000 genomes]
rs17338506	0.84[EUR][1000 genomes]
rs17398421	0.89[EUR][1000 genomes]
rs17398684	0.87[EUR][1000 genomes]
rs2245266	0.96[EUR][1000 genomes]
rs2245473	0.94[EUR][1000 genomes]
rs2245556	0.96[EUR][1000 genomes]
rs2576365	0.96[EUR][1000 genomes]
rs2576369	0.96[EUR][1000 genomes]
rs2576377	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2576382	0.91[EUR][1000 genomes]
rs2576387	0.98[EUR][1000 genomes]
rs2576391	0.91[EUR][1000 genomes]
rs2595893	0.91[EUR][1000 genomes]
rs2595894	0.91[EUR][1000 genomes]
rs2713748	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2713764	0.91[EUR][1000 genomes]
rs2713782	0.98[EUR][1000 genomes]
rs2713786	0.91[EUR][1000 genomes]
rs2713787	0.96[EUR][1000 genomes]
rs2713788	0.93[EUR][1000 genomes]
rs2713789	0.96[EUR][1000 genomes]
rs2713793	0.96[EUR][1000 genomes]
rs34275644	0.91[EUR][1000 genomes]
rs34315591	0.92[EUR][1000 genomes]
rs34515751	0.91[EUR][1000 genomes]
rs34565718	0.94[EUR][1000 genomes]
rs34645172	0.83[EUR][1000 genomes]
rs34719725	0.89[EUR][1000 genomes]
rs34999788	0.91[EUR][1000 genomes]
rs35090886	0.83[EUR][1000 genomes]
rs35509049	0.89[EUR][1000 genomes]
rs35517882	0.85[EUR][1000 genomes]
rs35530876	0.89[EUR][1000 genomes]
rs35617051	0.88[EUR][1000 genomes]
rs35630894	0.89[EUR][1000 genomes]
rs35999953	0.96[EUR][1000 genomes]
rs36156426	0.94[EUR][1000 genomes]
rs36165056	0.96[EUR][1000 genomes]
rs36194526	0.91[EUR][1000 genomes]
rs4060963	0.96[EUR][1000 genomes]
rs41273553	0.94[EUR][1000 genomes]
rs4928096	0.94[EUR][1000 genomes]
rs62273925	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62273927	0.94[EUR][1000 genomes]
rs62273928	0.94[EUR][1000 genomes]
rs62273930	0.91[EUR][1000 genomes]
rs62273935	0.89[EUR][1000 genomes]
rs62275197	0.89[EUR][1000 genomes]
rs62275198	0.89[EUR][1000 genomes]
rs62275199	0.87[EUR][1000 genomes]
rs62275200	0.87[EUR][1000 genomes]
rs62275203	0.83[EUR][1000 genomes]
rs62275204	0.83[EUR][1000 genomes]
rs62277105	0.84[EUR][1000 genomes]
rs66852780	0.83[EUR][1000 genomes]
rs67946790	0.89[EUR][1000 genomes]
rs67991823	0.94[EUR][1000 genomes]
rs72928364	0.80[EUR][1000 genomes]
rs73137256	0.84[EUR][1000 genomes]
rs73137276	0.88[EUR][1000 genomes]
rs73143088	0.89[EUR][1000 genomes]
rs7431835	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9832195	0.96[EUR][1000 genomes]
rs9840644	0.96[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	nsv514163	chr3:100547342-100670846	Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv931417	chr3:100547347-101183844	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	esv2757881	chr3:100613387-100776497	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2759163	chr3:100613387-100776497	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100599600-100645400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr3:100617600-100641000	Weak transcription	Fetal Muscle Leg	muscle
3	chr3:100617800-100641000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr3:100630200-100673600	Weak transcription	Ovary	ovary
5	chr3:100630400-100647000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr3:100632400-100639800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr3:100633000-100640000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:100634400-100646400	Weak transcription	Aorta	Aorta
9	chr3:100634600-100646000	Weak transcription	Fetal Stomach	stomach
10	chr3:100634800-100643000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr3:100635000-100640800	Weak transcription	Osteobl	bone
12	chr3:100635000-100646600	Weak transcription	NHDF-Ad	bronchial
13	chr3:100635000-100647400	Weak transcription	Colon Smooth Muscle	Colon
14	chr3:100635200-100647600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr3:100636000-100644200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr3:100636600-100641200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr3:100637600-100660000	Weak transcription	HSMMtube	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links