Variant report

Variant	rs10259357
Chromosome Location	chr7:84812188-84812189
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10248667	1.00[AMR][1000 genomes]
rs10262095	1.00[AMR][1000 genomes]
rs28369275	1.00[AMR][1000 genomes]
rs28419570	1.00[AMR][1000 genomes]
rs28528166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7778124	1.00[AMR][1000 genomes]
rs7811875	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422324	chr7:84530290-84944913	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
2	nsv916645	chr7:84678606-85420011	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv869255	chr7:84678606-85444155	Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv888645	chr7:84738495-84842884	Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv888646	chr7:84754151-84905855	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84802000-84814200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:84802400-84814000	Weak transcription	HMEC	breast
3	chr7:84808600-84813400	Weak transcription	Fetal Kidney	kidney
4	chr7:84808600-84814000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:84808600-84814000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:84808600-84814200	Weak transcription	Brain Substantia Nigra	brain
7	chr7:84808800-84813800	Weak transcription	HUVEC	blood vessel
8	chr7:84808800-84814000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:84808800-84814200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr7:84808800-84814200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:84809000-84813600	Weak transcription	Fetal Stomach	stomach
12	chr7:84810600-84812400	Weak transcription	Fetal Lung	lung

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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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