Variant report

Variant rs554078285
Chromosome Location chr6:161775101-161775102
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:161763400-161782000 Weak transcription Skeletal Muscle Male skeletal muscle
2 chr6:161771400-161780200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr6:161773200-161776000 Weak transcription Primary monocytes fromperipheralblood blood
4 chr6:161773200-161776000 Weak transcription Monocytes-CD14+_RO01746 blood
5 chr6:161774000-161775800 Enhancers Placenta Placenta
6 chr6:161774200-161775200 Enhancers Brain Angular Gyrus brain
7 chr6:161774200-161775200 Enhancers Brain Anterior Caudate brain
8 chr6:161774200-161775800 Enhancers HUES48 Cell Line embryonic stem cell
9 chr6:161774600-161775200 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr6:161774800-161775200 Enhancers Brain Inferior Temporal Lobe brain
11 chr6:161774800-161775400 Enhancers Brain Cingulate Gyrus brain
12 chr6:161774800-161775600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr6:161774800-161775600 Enhancers Fetal Muscle Leg muscle
14 chr6:161775000-161775200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr6:161775000-161775200 Flanking Active TSS Brain Substantia Nigra brain
16 chr6:161775000-161775200 Enhancers Fetal Heart heart
17 chr6:161775000-161775600 Enhancers Brain Hippocampus Middle brain
18 chr6:161775000-161776200 Enhancers HSMMtube muscle
19 chr6:161775000-161777400 Weak transcription K562 blood

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