Variant report

Variant	rs7592323
Chromosome Location	chr2:179693338-179693339
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11693372	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs12464151	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12465459	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs12469367	1.00[CHB][hapmap];0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12471428	1.00[CHB][hapmap];0.85[YRI][hapmap];0.87[ASN][1000 genomes]
rs12992014	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13006510	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1844334	0.87[ASN][1000 genomes]
rs1994546	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs2366912	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3769858	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs6715406	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs6729746	0.87[ASN][1000 genomes]
rs6733291	1.00[CHB][hapmap];0.80[YRI][hapmap];0.80[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7561149	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7591782	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7600330	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834470	chr2:179555152-179728726	Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv934108	chr2:179556852-179729925	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179659400-179698000	Weak transcription	Primary B cells from cord blood	blood
2	chr2:179685000-179693800	Weak transcription	HSMM	muscle
3	chr2:179685000-179694000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr2:179685200-179694000	Weak transcription	Primary B cells from peripheral blood	blood
5	chr2:179685200-179694000	Weak transcription	HSMMtube	muscle
6	chr2:179685200-179698800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr2:179685600-179698200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr2:179685800-179693400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr2:179685800-179698000	Weak transcription	Fetal Heart	heart
10	chr2:179689400-179693800	Enhancers	HUVEC	blood vessel
11	chr2:179690400-179694000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr2:179690600-179701800	Weak transcription	Lung	lung
13	chr2:179690600-179701800	Weak transcription	Pancreas	Pancrea
14	chr2:179691400-179694400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:179692000-179693400	Strong transcription	Primary T cells from cord blood	blood
16	chr2:179692200-179694600	Enhancers	Psoas Muscle	Psoas
17	chr2:179692400-179694200	Enhancers	NH-A	brain
18	chr2:179692400-179694600	Enhancers	Brain Germinal Matrix	brain
19	chr2:179692600-179693400	Enhancers	Right Ventricle	heart
20	chr2:179692600-179693400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
21	chr2:179692600-179693400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
22	chr2:179692600-179693400	Enhancers	Spleen	Spleen
23	chr2:179692600-179694200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr2:179692600-179695600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr2:179692600-179695600	Enhancers	Fetal Lung	lung
26	chr2:179692600-179695800	Enhancers	Fetal Brain Male	brain
27	chr2:179692600-179695800	Enhancers	Fetal Brain Female	brain
28	chr2:179692800-179693400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr2:179692800-179693400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:179692800-179694000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr2:179693000-179693800	Enhancers	Left Ventricle	heart
32	chr2:179693000-179695200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:179693000-179701600	Weak transcription	Adipose Nuclei	Adipose
34	chr2:179693000-179709200	Weak transcription	Aorta	Aorta
35	chr2:179693200-179693400	Enhancers	Primary hematopoietic stem cells	blood
36	chr2:179693200-179693400	Enhancers	Fetal Muscle Trunk	muscle
37	chr2:179693200-179693400	Enhancers	Fetal Muscle Leg	muscle
38	chr2:179693200-179693400	Flanking Active TSS	Right Atrium	heart
39	chr2:179693200-179693400	Enhancers	Osteobl	bone
40	chr2:179693200-179694200	Enhancers	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links