Variant report

Variant	rs555153161
Chromosome Location	chr1:94213683-94213684
allele	C/T
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	esv3320426	chr1:94212708-94213724	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94199400-94217400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:94208200-94215600	Weak transcription	Aorta	Aorta
3	chr1:94210800-94215600	Weak transcription	Thymus	Thymus
4	chr1:94211800-94215600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:94212400-94214400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:94212600-94215200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:94212600-94217200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr1:94213000-94216200	Weak transcription	Esophagus	oesophagus
9	chr1:94213200-94216800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:94213400-94215600	Weak transcription	HMEC	breast
11	chr1:94213400-94217800	Enhancers	Primary B cells from peripheral blood	blood
12	chr1:94213600-94215400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:94213600-94215600	Weak transcription	HepG2	liver

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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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