Variant report

Variant	rs2499551
Chromosome Location	chrX:57310083-57310084
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:57308800-57310600	Enhancers	Dnd41	blood
2	chrX:57309200-57310600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chrX:57309200-57310600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chrX:57309200-57310600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chrX:57309400-57311600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chrX:57309600-57310400	Active TSS	HepG2	liver
7	chrX:57309600-57311400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chrX:57309600-57311800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chrX:57309800-57310200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chrX:57309800-57312800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chrX:57310000-57310600	Enhancers	Fetal Thymus	thymus
12	chrX:57310000-57313000	Weak transcription	Primary T cells from cord blood	blood
13	chrX:57310000-57313000	Weak transcription	Primary T cells fromperipheralblood	blood
14	chrX:57310000-57313000	Weak transcription	Primary T regulatory cells fromperipheralblood	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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