Variant report

Variant rs652996
Chromosome Location chr6:167627931-167627932
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167615800-167628800 Weak transcription Right Atrium heart
2 chr6:167623000-167629200 Enhancers Fetal Brain Male brain
3 chr6:167623600-167628200 Enhancers Fetal Brain Female brain
4 chr6:167624600-167632800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr6:167625600-167630000 Weak transcription Rectal Smooth Muscle rectum
6 chr6:167626200-167635000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr6:167626600-167631000 Weak transcription Placenta Amnion Placenta Amnion
8 chr6:167627400-167628000 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr6:167627600-167628000 Enhancers Brain Cingulate Gyrus brain
10 chr6:167627600-167629000 Enhancers HepG2 liver
11 chr6:167627800-167628000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr6:167627800-167628000 Enhancers Brain Substantia Nigra brain
13 chr6:167627800-167628200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
14 chr6:167627800-167628200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
15 chr6:167627800-167628200 Bivalent Enhancer Brain Anterior Caudate brain
16 chr6:167627800-167628200 Enhancers Brain Germinal Matrix brain
17 chr6:167627800-167628200 Bivalent Enhancer Brain Hippocampus Middle brain
18 chr6:167627800-167628200 Enhancers Brain Inferior Temporal Lobe brain

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