The 2.0 version of rSNPBase

Variant report

Variant esv1251832
Chromosome Location chr2:114064913-114064914
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:114058200-114067200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr2:114060800-114065400 Weak transcription Gastric stomach
3 chr2:114062800-114067000 Weak transcription Skeletal Muscle Female skeletal muscle
4 chr2:114063000-114066000 Weak transcription HSMMtube muscle
5 chr2:114063000-114067200 Weak transcription Esophagus oesophagus
6 chr2:114063400-114066000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:114063400-114066200 Weak transcription HMEC breast
8 chr2:114063400-114066200 Weak transcription NHEK skin
9 chr2:114063400-114066400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:114063800-114066200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr2:114063800-114067000 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr2:114064600-114082000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr2:114064800-114067400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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Last update: Aug 31, 2015