Variant report

Variant rs13015996
Chromosome Location chr2:187209035-187209036
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187188600-187216200 Weak transcription Primary hematopoietic stem cells blood
2 chr2:187192400-187211600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:187204800-187209800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr2:187207600-187213800 Weak transcription Small Intestine intestine
5 chr2:187207800-187212600 Weak transcription HepG2 liver
6 chr2:187207800-187214200 Weak transcription Fetal Stomach stomach
7 chr2:187208200-187213000 Weak transcription Fetal Intestine Small intestine
8 chr2:187208200-187219600 Weak transcription Right Atrium heart
9 chr2:187208600-187211200 Weak transcription Breast Myoepithelial Primary Cells Breast

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