Variant report

Variant rs13242576
Chromosome Location chr7:139897310-139897311
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:139888600-139905000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr7:139893000-139900000 Weak transcription Esophagus oesophagus
3 chr7:139895400-139900200 Weak transcription Rectal Mucosa Donor 29 rectum
4 chr7:139896400-139897400 Enhancers Placenta Placenta
5 chr7:139896400-139897600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr7:139896400-139897600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr7:139896600-139897600 Enhancers HMEC breast
8 chr7:139896600-139898000 Enhancers NHEK skin
9 chr7:139896600-139898600 Enhancers HepG2 liver
10 chr7:139896600-139899200 Weak transcription Osteobl bone
11 chr7:139896800-139897600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr7:139897000-139898800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr7:139897000-139899200 Weak transcription K562 blood
14 chr7:139897000-139900000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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