Variant report

Variant rs9378374
Chromosome Location chr6:422408-422409
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:420200-423400 Weak transcription Placenta Amnion Placenta Amnion
2 chr6:421600-423200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr6:422000-424200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr6:422200-423400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr6:422200-423600 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr6:422200-423800 Enhancers Primary Natural Killer cells fromperipheralblood blood
7 chr6:422200-423800 Enhancers Muscle Satellite Cultured Cells --
8 chr6:422400-422600 Active TSS A549 lung
9 chr6:422400-422800 Enhancers Primary T helper cells fromperipheralblood blood
10 chr6:422400-422800 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr6:422400-423200 Enhancers Primary T helper 17 cells PMA-I stimulated --
12 chr6:422400-423400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr6:422400-423600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr6:422400-423600 Enhancers NH-A brain
15 chr6:422400-423600 Enhancers Osteobl bone
16 chr6:422400-423800 Enhancers Primary T helper cells PMA-I stimulated --
17 chr6:422400-423800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
18 chr6:422400-423800 Enhancers HepG2 liver

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