Variant report

Variant	rs10236054
Chromosome Location	chr7:8002535-8002536
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs16872351	1.00[CEU][hapmap]
rs17141597	1.00[CEU][hapmap]
rs17141876	1.00[CEU][hapmap]
rs17142053	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs17142255	1.00[CEU][hapmap];0.92[MEX][hapmap]
rs17142349	1.00[CEU][hapmap];0.92[MEX][hapmap]
rs17142477	1.00[CEU][hapmap]
rs58145708	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58707745	0.81[AMR][1000 genomes]
rs59427694	0.81[AMR][1000 genomes]
rs59697814	0.81[AMR][1000 genomes]
rs62433384	0.81[AMR][1000 genomes]
rs62433385	0.81[AMR][1000 genomes]
rs62433442	0.81[AMR][1000 genomes]
rs6463760	1.00[CEU][hapmap]
rs6955803	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs6956133	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs6956783	0.84[EUR][1000 genomes]
rs9640055	1.00[CEU][hapmap];0.85[MEX][hapmap];0.88[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026758	chr7:7187491-8075259	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
2	nsv1032670	chr7:7535515-8017077	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
3	esv2752177	chr7:7729247-8177689	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv917172	chr7:7854632-8807385	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	nsv1030180	chr7:7860424-8059221	Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
6	esv3346837	chr7:7915187-8068557	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv1020161	chr7:7929384-8047553	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7985000-8003800	Weak transcription	Primary B cells from cord blood	blood
2	chr7:7985400-8007600	Weak transcription	Psoas Muscle	Psoas
3	chr7:7986800-8007800	Weak transcription	Ovary	ovary
4	chr7:7996800-8007400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:8000200-8003600	Enhancers	GM12878-XiMat	blood
6	chr7:8001400-8002600	Weak transcription	NH-A	brain
7	chr7:8001800-8003000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr7:8002000-8002600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:8002000-8003200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr7:8002200-8002600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:8002200-8002600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:8002200-8003000	Enhancers	NHDF-Ad	bronchial
13	chr7:8002200-8003200	Enhancers	Osteobl	bone
14	chr7:8002400-8003000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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