Variant report

Variant	rs17694606
Chromosome Location	chr8:69990385-69990386
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11774326	0.93[EUR][1000 genomes]
rs13249703	0.95[EUR][1000 genomes]
rs13254975	0.97[EUR][1000 genomes]
rs13256879	0.94[EUR][1000 genomes]
rs13258843	0.93[EUR][1000 genomes]
rs13264794	0.95[CEU][hapmap];0.97[EUR][1000 genomes]
rs13264856	0.93[EUR][1000 genomes]
rs13269711	0.93[EUR][1000 genomes]
rs13270005	0.92[EUR][1000 genomes]
rs13272514	0.95[EUR][1000 genomes]
rs13274778	0.97[EUR][1000 genomes]
rs13276126	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13277901	0.97[EUR][1000 genomes]
rs13280997	0.95[CEU][hapmap];0.97[EUR][1000 genomes]
rs1365415	0.97[EUR][1000 genomes]
rs1426596	0.97[EUR][1000 genomes]
rs1541763	0.97[EUR][1000 genomes]
rs7014382	0.96[EUR][1000 genomes]
rs7829232	0.95[EUR][1000 genomes]

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	nsv1031633	chr8:69766575-70322790	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv890987	chr8:69959105-70004698	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69985000-69991600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr8:69985600-69992800	Enhancers	Muscle Satellite Cultured Cells	--
3	chr8:69986800-69991600	Weak transcription	HSMMtube	muscle
4	chr8:69987000-69991400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:69987200-69991600	Weak transcription	NH-A	brain
6	chr8:69988000-69990400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr8:69988000-69991400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr8:69988000-69992200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:69988200-69990600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:69988200-69990600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr8:69988200-69991400	Weak transcription	NHLF	lung
12	chr8:69988200-69991600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr8:69988800-69990800	Weak transcription	NHDF-Ad	bronchial
14	chr8:69988800-69993600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr8:69989200-69990400	Enhancers	Fetal Stomach	stomach
16	chr8:69989600-69993400	Enhancers	Osteobl	bone
17	chr8:69989800-69990800	Weak transcription	Fetal Lung	lung
18	chr8:69990000-69993800	Enhancers	HSMM	muscle
19	chr8:69990200-69992400	Enhancers	Fetal Heart	heart

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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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