Variant report

Variant rs35454412
Chromosome Location chr6:45132270-45132271
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:45130200-45132600 Weak transcription Aorta Aorta
2 chr6:45130600-45133200 Enhancers Primary T helper cells PMA-I stimulated --
3 chr6:45131000-45133000 Enhancers ES-I3 Cell Line embryonic stem cell
4 chr6:45131200-45132400 Enhancers iPS-20b Cell Line embryonic stem cell
5 chr6:45131400-45133000 Enhancers HUES6 Cell Line embryonic stem cell
6 chr6:45131600-45132400 Enhancers HMEC breast
7 chr6:45131600-45132800 Enhancers Primary T killer naive cells fromperipheralblood blood
8 chr6:45131600-45132800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:45131600-45133000 Enhancers NHEK skin
10 chr6:45131800-45132400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
11 chr6:45131800-45133000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr6:45131800-45133000 Enhancers GM12878-XiMat blood
13 chr6:45132000-45132600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr6:45132000-45135400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr6:45132000-45141400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
16 chr6:45132200-45132800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr6:45132200-45137600 Weak transcription HUES64 Cell Line embryonic stem cell

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