Variant report

Variant	rs11091385
Chromosome Location	chrX:55147923-55147924
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:55143600-55149000	Weak transcription	Fetal Heart	heart
2	chrX:55144000-55150400	Enhancers	K562	blood
3	chrX:55145600-55148200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chrX:55145800-55150200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chrX:55146400-55148600	Enhancers	HUVEC	blood vessel
6	chrX:55146800-55148200	Enhancers	Fetal Intestine Large	intestine
7	chrX:55147200-55148000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chrX:55147200-55148200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chrX:55147800-55149600	Weak transcription	Fetal Intestine Small	intestine

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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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