Variant report

Variant	rs12096956
Chromosome Location	chr1:215213672-215213673
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11120469	0.80[AFR][1000 genomes]
rs11120470	1.00[AFR][1000 genomes]
rs11120471	1.00[AFR][1000 genomes]
rs11120472	0.87[YRI][hapmap]
rs11120474	0.87[YRI][hapmap]
rs12061587	0.87[YRI][hapmap]
rs12062465	0.87[YRI][hapmap]
rs12066174	1.00[YRI][hapmap]
rs12069528	0.82[ASW][hapmap];0.87[YRI][hapmap]
rs12069674	0.87[YRI][hapmap]
rs12078139	0.87[YRI][hapmap]
rs12082755	0.80[AFR][1000 genomes]
rs12087979	1.00[AFR][1000 genomes]
rs12088528	0.82[ASW][hapmap];0.87[YRI][hapmap];0.80[AFR][1000 genomes]
rs12089490	0.80[AFR][1000 genomes]
rs12090549	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs12092077	0.80[AFR][1000 genomes]
rs12097853	0.87[YRI][hapmap]

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	nsv468105	chr1:215167236-215248417	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv549182	chr1:215167236-215248417	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 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	chr1:215206800-215213800	Weak transcription	Osteobl	bone
2	chr1:215206800-215216000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:215213200-215214400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:215213200-215214800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:215213400-215214000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:215213600-215214000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr1:215213600-215214000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr1:215213600-215214000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr1:215213600-215214000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr1:215213600-215214000	Genic enhancers	NHDF-Ad	bronchial
11	chr1:215213600-215214200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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