Variant report

Variant	rs6569051
Chromosome Location	chr6:119445798-119445799
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs597392	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs630954	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs649979	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs653796	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs661645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs676491	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs677341	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7759325	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7776256	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs808038	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025995	chr6:119407742-119709548	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119439200-119448400	Weak transcription	K562	blood
2	chr6:119440600-119448400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:119441400-119449200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:119441400-119450200	Weak transcription	NH-A	brain
5	chr6:119441800-119450400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr6:119444800-119449600	Weak transcription	Fetal Lung	lung
7	chr6:119445400-119445800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:119445400-119446000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr6:119445400-119446200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr6:119445400-119446200	Enhancers	HUVEC	blood vessel
11	chr6:119445400-119446200	Enhancers	NHEK	skin
12	chr6:119445400-119446400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr6:119445600-119445800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr6:119445600-119446200	Enhancers	ES-I3 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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