Variant report

Variant	rs55718554
Chromosome Location	chr1:47871581-47871582
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47847600-47872800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:47868800-47873800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:47869200-47872400	Weak transcription	Fetal Intestine Small	intestine
4	chr1:47870800-47872000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:47871000-47871800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr1:47871200-47872200	Bivalent Enhancer	Fetal Lung	lung
7	chr1:47871400-47871800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr1:47871400-47871800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr1:47871400-47871800	Bivalent Enhancer	Placenta	Placenta
10	chr1:47871400-47871800	Bivalent Enhancer	Fetal Stomach	stomach
11	chr1:47871400-47871800	Enhancers	Placenta Amnion	Placenta Amnion

Quick Search:

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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