Variant report

Variant	rs577819871
Chromosome Location	chr12:103663982-103663983
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv975641	chr12:103663103-103667663	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103662800-103666200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr12:103663200-103664000	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr12:103663400-103664000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr12:103663600-103664200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr12:103663600-103664600	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr12:103663800-103664200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr12:103663800-103664800	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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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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