Variant report

Variant	rs6533485
Chromosome Location	chr4:110927563-110927564
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110895000-110928600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:110901000-110929600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:110907000-110932400	Weak transcription	Psoas Muscle	Psoas
4	chr4:110910400-110935200	Weak transcription	Pancreas	Pancrea
5	chr4:110910600-110929800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:110919000-110935200	Weak transcription	Left Ventricle	heart
7	chr4:110920800-110935800	Strong transcription	Skeletal Muscle Female	skeletal muscle
8	chr4:110921000-110927600	Weak transcription	Fetal Intestine Small	intestine
9	chr4:110925600-110928400	Weak transcription	Fetal Intestine Large	intestine
10	chr4:110926800-110927600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:110926800-110927600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:110926800-110927600	Enhancers	Duodenum Mucosa	Duodenum
13	chr4:110926800-110927600	Enhancers	GM12878-XiMat	blood
14	chr4:110926800-110930000	Enhancers	HepG2	liver
15	chr4:110926800-110930400	Enhancers	Fetal Heart	heart
16	chr4:110926800-110931200	Enhancers	Liver	Liver
17	chr4:110927400-110931000	Strong transcription	Skeletal Muscle Male	skeletal muscle

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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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