Variant report

Variant	rs7700002
Chromosome Location	chr4:175595307-175595308
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10008774	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10022789	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs28363675	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28776253	0.97[ASN][1000 genomes]
rs4695782	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55780848	0.98[ASN][1000 genomes]
rs59690175	0.98[ASN][1000 genomes]
rs61258069	0.98[ASN][1000 genomes]
rs6553806	0.90[CHB][hapmap]
rs6838560	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1018390	chr4:175475505-175969742	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv880584	chr4:175505749-175644689	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175591000-175595400	Weak transcription	Hela-S3	cervix
2	chr4:175594600-175595400	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr4:175594600-175595400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr4:175594600-175595400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr4:175594600-175595600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:175594600-175596800	Enhancers	K562	blood
7	chr4:175595000-175595400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr4:175595000-175595400	Enhancers	A549	lung
9	chr4:175595000-175596200	Enhancers	Fetal Intestine Small	intestine
10	chr4:175595200-175595400	Enhancers	Fetal Intestine Large	intestine
11	chr4:175595200-175596200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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