Variant report

Variant rs200474885
Chromosome Location chr10:42738907-42738908
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:42732400-42742600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr10:42737400-42739000 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr10:42737600-42739200 Active TSS Ovary ovary
4 chr10:42737800-42739200 Active TSS Aorta Aorta
5 chr10:42737800-42739200 Bivalent/Poised TSS Psoas Muscle Psoas
6 chr10:42737800-42739200 Active TSS Right Atrium heart
7 chr10:42738000-42739000 Bivalent Enhancer Primary T cells fromperipheralblood blood
8 chr10:42738000-42739000 Bivalent Enhancer Placenta Placenta
9 chr10:42738000-42739000 Bivalent/Poised TSS A549 lung
10 chr10:42738000-42739200 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
11 chr10:42738200-42739000 Active TSS Primary T regulatory cells fromperipheralblood blood
12 chr10:42738200-42739000 Bivalent/Poised TSS Fetal Muscle Leg muscle
13 chr10:42738200-42739000 Weak transcription HSMM muscle
14 chr10:42738200-42739200 Active TSS Right Ventricle heart
15 chr10:42738400-42739000 Active TSS Cortex derived primary cultured neurospheres brain
16 chr10:42738400-42739200 Active TSS Ganglion Eminence derived primary cultured neurospheres brain
17 chr10:42738400-42739200 Active TSS HepG2 liver
18 chr10:42738600-42739000 Active TSS Primary T helper naive cells fromperipheralblood blood
19 chr10:42738600-42739200 Bivalent/Poised TSS Monocytes-CD14+_RO01746 blood
20 chr10:42738800-42739000 Bivalent/Poised TSS Foreskin Melanocyte Primary Cells skin03 Skin

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