Variant report

Variant rs13259038
Chromosome Location chr8:10547526-10547527
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:10543200-10548000 Weak transcription A549 lung
2 chr8:10543200-10548200 Weak transcription Duodenum Mucosa Duodenum
3 chr8:10543600-10548200 Weak transcription Liver Liver
4 chr8:10546200-10547800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr8:10546400-10548000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr8:10546600-10548000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr8:10546800-10549600 Enhancers Primary B cells from peripheral blood blood
8 chr8:10547000-10547600 Enhancers K562 blood
9 chr8:10547200-10547600 Enhancers Primary T killer naive cells fromperipheralblood blood
10 chr8:10547200-10551000 Enhancers Spleen Spleen
11 chr8:10547400-10547600 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr8:10547400-10549000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr8:10547400-10551600 Enhancers Esophagus oesophagus

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