Variant report

Variant	rs183467035
Chromosome Location	chrX:104785541-104785542
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv432352	chrX:104346855-104831855	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv3348185	chrX:104784046-104786044	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:104780800-104785600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chrX:104785400-104786200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chrX:104785400-104786200	Enhancers	HMEC	breast
4	chrX:104785400-104786400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chrX:104785400-104787600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chrX:104785400-104787600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chrX:104785400-104791400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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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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