Variant report

Variant rs532294878
Chromosome Location chr6:121774676-121774677
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:121764200-121775200 Weak transcription Psoas Muscle Psoas
2 chr6:121769200-121776800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr6:121769200-121776800 Weak transcription Esophagus oesophagus
4 chr6:121769400-121776400 Weak transcription Aorta Aorta
5 chr6:121769400-121779000 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr6:121770200-121774800 Weak transcription Ovary ovary
7 chr6:121770800-121778800 Weak transcription A549 lung
8 chr6:121771000-121776800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr6:121771400-121774800 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr6:121771400-121775200 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr6:121771400-121777200 Weak transcription HUES48 Cell Line embryonic stem cell
12 chr6:121771600-121774800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr6:121772200-121777200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr6:121772200-121777200 Weak transcription Osteobl bone
15 chr6:121773400-121775000 Enhancers HUVEC blood vessel
16 chr6:121774000-121775000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr6:121774600-121774800 Enhancers Muscle Satellite Cultured Cells --
18 chr6:121774600-121775000 Enhancers Breast Myoepithelial Primary Cells Breast

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