Variant report

Variant	rs201218009
Chromosome Location	chrX:57333159-57333160
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	esv3337471	chrX:57332477-57334575	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:57316400-57336800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chrX:57316600-57339400	Weak transcription	Primary T cells from cord blood	blood
3	chrX:57319600-57337800	Weak transcription	Fetal Intestine Large	intestine
4	chrX:57321000-57337800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chrX:57322200-57339200	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chrX:57322400-57338000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chrX:57322400-57341400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chrX:57323200-57337600	Weak transcription	Pancreas	Pancrea
9	chrX:57329400-57339200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chrX:57329400-57339800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chrX:57329600-57337800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chrX:57330200-57339200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chrX:57330800-57337200	Weak transcription	Liver	Liver
14	chrX:57331000-57339600	Weak transcription	Left Ventricle	heart
15	chrX:57331600-57339400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chrX:57333000-57333200	Enhancers	HUES64 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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