Variant report

Variant	rs1556149
Chromosome Location	chr9:85986905-85986906
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10441792	0.92[CEU][hapmap]
rs10746703	0.84[CEU][hapmap]
rs10780596	0.82[CEU][hapmap]
rs10867999	0.83[CEU][hapmap]
rs10868000	0.82[CEU][hapmap]
rs10868001	0.83[CEU][hapmap]
rs11140041	0.83[CEU][hapmap]
rs11140045	0.82[CEU][hapmap]
rs11140046	0.82[CEU][hapmap]
rs11140056	0.81[CEU][hapmap]
rs13439910	0.82[CEU][hapmap]
rs1536888	0.83[CEU][hapmap]
rs1536889	0.82[CEU][hapmap]
rs2375886	0.82[CEU][hapmap]
rs3860903	0.82[CEU][hapmap]
rs3915916	0.82[CEU][hapmap]
rs4877253	0.82[CEU][hapmap]
rs7847924	0.81[JPT][hapmap]

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	nsv1046491	chr9:85861492-86063992	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85937400-85998000	Weak transcription	Aorta	Aorta
2	chr9:85958200-86007600	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr9:85977000-85990200	Weak transcription	Right Ventricle	heart
4	chr9:85977400-85994600	Weak transcription	Pancreas	Pancrea
5	chr9:85977600-85990000	Weak transcription	Spleen	Spleen
6	chr9:85981000-85997800	Weak transcription	Left Ventricle	heart
7	chr9:85982000-85987000	Weak transcription	Fetal Muscle Leg	muscle
8	chr9:85982200-85987800	Weak transcription	HepG2	liver
9	chr9:85982400-85987400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:85982400-85987600	Weak transcription	Fetal Stomach	stomach
11	chr9:85982600-85998800	Weak transcription	Ovary	ovary
12	chr9:85983000-85998400	Weak transcription	Fetal Brain Male	brain
13	chr9:85986400-85989200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:85986600-85987200	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr9:85986800-85989200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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