Variant report

Variant	rs181637192
Chromosome Location	chr1:166710152-166710153
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	esv3386869	chr1:166708278-166710626	Enhancers Bivalent/Poised TSS	n/a	n/a	inside rSNPs	diseases
3	esv3420512	chr1:166708778-166710176	Enhancers Bivalent/Poised TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166709600-166710400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr1:166710000-166710200	Bivalent/Poised TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr1:166710000-166710400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr1:166710000-166710400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr1:166710000-166710400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr1:166710000-166710600	Enhancers	H1 Cell Line	embryonic stem cell

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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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