Variant report

Variant	rs2146921
Chromosome Location	chr6:1972034-1972035
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs17134537	1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57256628	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7450779	1.00[YRI][hapmap];0.98[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530548	chr6:1441421-2351608	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv869043	chr6:1744238-2006788	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv931941	chr6:1768439-2246781	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv531295	chr6:1773436-2724986	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
5	nsv1032149	chr6:1848148-2006021	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1032727	chr6:1900622-2064690	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv538095	chr6:1900622-2064690	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv883386	chr6:1910108-2122454	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:1915800-1972800	Weak transcription	Colonic Mucosa	Colon
2	chr6:1947400-1980000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:1953400-1977800	Weak transcription	Fetal Intestine Small	intestine
4	chr6:1961600-1972200	Weak transcription	Stomach Mucosa	stomach
5	chr6:1967400-1977800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:1967400-1978000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr6:1969600-1972200	Enhancers	Primary hematopoietic stem cells	blood
8	chr6:1969600-1972400	Enhancers	Fetal Lung	lung
9	chr6:1969800-1972400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr6:1969800-1972400	Enhancers	Dnd41	blood
11	chr6:1970800-1972400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr6:1971000-1972400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:1971000-1975000	Weak transcription	Esophagus	oesophagus
14	chr6:1971000-1979000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:1971000-1979400	Weak transcription	Primary T cells from cord blood	blood
16	chr6:1971800-1972400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:1971800-1972400	Enhancers	Stomach Smooth Muscle	stomach
18	chr6:1971800-1972400	Enhancers	HSMMtube	muscle
19	chr6:1971800-1973200	Genic enhancers	HepG2	liver
20	chr6:1972000-1973400	Enhancers	Liver	Liver
21	chr6:1972000-1978000	Weak transcription	Fetal Stomach	stomach
22	chr6:1972000-1978200	Weak transcription	Pancreas	Pancrea
23	chr6:1972000-1992200	Weak transcription	Gastric	stomach

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