Variant report

Variant	rs62171762
Chromosome Location	chr2:114596068-114596069
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114574200-114603600	Weak transcription	Primary B cells from cord blood	blood
2	chr2:114586400-114601000	Weak transcription	Primary T cells from cord blood	blood
3	chr2:114589200-114596400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:114589200-114600200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr2:114589200-114600200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:114589200-114600200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr2:114591600-114597800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr2:114592000-114596200	Weak transcription	Fetal Intestine Large	intestine
9	chr2:114592400-114597600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr2:114592600-114597400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:114592800-114599400	Weak transcription	Placenta	Placenta
12	chr2:114595600-114598600	Enhancers	HepG2	liver

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

what's new

Quick links