Variant report

Variant	rs17168868
Chromosome Location	chr7:136685758-136685759
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs1424547	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17168865	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17168866	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17168883	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs421325	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv831147	chr7:136583444-136755741	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	esv2753059	chr7:136633745-136893745	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136674800-136694200	Weak transcription	Left Ventricle	heart
2	chr7:136682600-136685800	Weak transcription	NH-A	brain
3	chr7:136683200-136685800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:136683200-136685800	Weak transcription	Osteobl	bone
5	chr7:136683600-136685800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:136683800-136685800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr7:136683800-136685800	Weak transcription	NHLF	lung
8	chr7:136683800-136686000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:136684000-136685800	Weak transcription	HSMMtube	muscle
10	chr7:136684800-136689000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr7:136685200-136686600	Enhancers	Fetal Heart	heart
12	chr7:136685400-136686200	Enhancers	Stomach Smooth Muscle	stomach
13	chr7:136685400-136686600	Enhancers	Colon Smooth Muscle	Colon
14	chr7:136685400-136686800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:136685400-136688200	Enhancers	Rectal Smooth Muscle	rectum
16	chr7:136685600-136686600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:136685600-136688200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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