Variant report

Variant	rs7649027
Chromosome Location	chr3:60046404-60046405
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:6)

rs_ID	r²[population]
rs17061982	0.83[AMR][1000 genomes]
rs17061988	0.83[AMR][1000 genomes]
rs17062003	0.83[AMR][1000 genomes]
rs7625054	0.83[AMR][1000 genomes]
rs7625055	0.83[AMR][1000 genomes]
rs7627449	0.83[AMR][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	nsv428085	chr3:59782509-60070116	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014983	chr3:59884024-60558331	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv590387	chr3:59890976-60481459	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv834707	chr3:60005679-60184046	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60041000-60049000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr3:60042000-60051600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr3:60042800-60046800	Weak transcription	Thymus	Thymus
4	chr3:60042800-60050200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr3:60043000-60051400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr3:60043200-60046600	Weak transcription	Fetal Thymus	thymus
7	chr3:60043600-60047400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr3:60044000-60048200	Genic enhancers	Dnd41	blood
9	chr3:60044800-60050200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr3:60045000-60054200	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr3:60045200-60046600	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr3:60045600-60050200	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr3:60045800-60052400	Enhancers	Primary T cells from cord blood	blood
14	chr3:60046400-60046600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
15	chr3:60046400-60046600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr3:60046400-60048200	Enhancers	Primary T helper cells fromperipheralblood	blood

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

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