Variant report

Variant	rs3740787
Chromosome Location	chr11:45128302-45128303
allele	C/T
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	chr11:45123400-45132200	Enhancers	Fetal Muscle Leg	muscle
2	chr11:45124600-45130000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:45124800-45128400	Weak transcription	HepG2	liver
4	chr11:45124800-45129600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr11:45124800-45129600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:45124800-45129800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:45124800-45131400	Weak transcription	Brain Angular Gyrus	brain
8	chr11:45124800-45133800	Weak transcription	Right Atrium	heart
9	chr11:45125000-45129800	Weak transcription	HMEC	breast
10	chr11:45126800-45132200	Enhancers	Fetal Intestine Small	intestine
11	chr11:45126800-45132400	Enhancers	Fetal Intestine Large	intestine
12	chr11:45127600-45128800	Weak transcription	Fetal Brain Male	brain
13	chr11:45127800-45128800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr11:45128200-45128400	Enhancers	Fetal Brain Female	brain

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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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