Variant report

Variant rs396330
Chromosome Location chr22:21405555-21405556
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:21400600-21405600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr22:21400600-21405800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr22:21400600-21405800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr22:21400600-21406000 Weak transcription NHEK skin
5 chr22:21400800-21405800 Weak transcription H9 Cell Line embryonic stem cell
6 chr22:21400800-21405800 Weak transcription HSMM muscle
7 chr22:21400800-21406000 Weak transcription NH-A brain
8 chr22:21400800-21410200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr22:21403800-21407400 Enhancers Placenta Placenta
10 chr22:21404200-21406200 Weak transcription Right Atrium heart
11 chr22:21405000-21406000 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr22:21405200-21406400 Enhancers Fetal Thymus thymus
13 chr22:21405200-21406800 Enhancers H1 Cell Line embryonic stem cell
14 chr22:21405200-21406800 Enhancers GM12878-XiMat blood
15 chr22:21405400-21406800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
16 chr22:21405400-21406800 Bivalent Enhancer K562 blood
17 chr22:21405400-21407000 Enhancers ES-I3 Cell Line embryonic stem cell
18 chr22:21405400-21407000 Enhancers iPS-18 Cell Line embryonic stem cell

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