Variant report

Variant	rs12667612
Chromosome Location	chr7:128369870-128369871
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10253936	0.85[CHB][hapmap];0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs339077	0.87[CHD][hapmap]
rs35845194	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs62479561	0.80[ASN][1000 genomes]
rs6947749	0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6949056	0.81[CHB][hapmap];0.82[CHD][hapmap];0.84[JPT][hapmap]
rs6952563	0.93[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.87[TSI][hapmap];0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs750464	1.00[CHB][hapmap];0.94[JPT][hapmap];0.93[YRI][hapmap];0.88[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	nsv427806	chr7:128179989-128428182	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv1016979	chr7:128333070-128534438	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128349400-128378600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr7:128349800-128378200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:128349800-128378400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:128361600-128378600	Weak transcription	Right Atrium	heart
5	chr7:128366200-128374400	Weak transcription	Primary B cells from peripheral blood	blood
6	chr7:128367000-128370200	Enhancers	HSMM	muscle
7	chr7:128367400-128370000	Weak transcription	Spleen	Spleen
8	chr7:128368400-128370000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr7:128368400-128372600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr7:128368800-128370000	Enhancers	Osteobl	bone
11	chr7:128368800-128370200	Enhancers	Fetal Muscle Leg	muscle
12	chr7:128368800-128370400	Enhancers	Fetal Muscle Trunk	muscle
13	chr7:128368800-128370600	Enhancers	HSMMtube	muscle
14	chr7:128369000-128370200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr7:128369000-128371000	Weak transcription	K562	blood
16	chr7:128369200-128377800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:128369400-128370200	Bivalent Enhancer	HepG2	liver
18	chr7:128369400-128377800	Weak transcription	HMEC	breast

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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