Variant report

Variant rs7621026
Chromosome Location chr3:49975334-49975335
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:49967600-49977400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr3:49967800-49977000 Weak transcription Primary B cells from cord blood blood
3 chr3:49967800-49977000 Weak transcription NHLF lung
4 chr3:49968000-49976600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr3:49968800-49976800 Weak transcription HepG2 liver
6 chr3:49969200-49977000 Weak transcription K562 blood
7 chr3:49973600-49976200 Enhancers Primary monocytes fromperipheralblood blood
8 chr3:49974200-49975400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr3:49974400-49975400 Enhancers Fetal Intestine Small intestine
10 chr3:49974400-49975600 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr3:49974600-49977000 Weak transcription Fetal Intestine Large intestine
12 chr3:49974800-49976800 Weak transcription GM12878-XiMat blood
13 chr3:49975000-49975600 Enhancers Monocytes-CD14+_RO01746 blood
14 chr3:49975000-49976800 Weak transcription Skeletal Muscle Female skeletal muscle
15 chr3:49975000-49977000 Enhancers Primary neutrophils fromperipheralblood blood
16 chr3:49975000-49977400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
17 chr3:49975200-49977000 Weak transcription Adipose Nuclei Adipose

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