Variant report

Variant rs7901797
Chromosome Location chr10:22767954-22767955
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:22765800-22806600 Weak transcription Right Atrium heart
2 chr10:22766000-22768200 Bivalent Enhancer Placenta Placenta
3 chr10:22766800-22769200 Enhancers Placenta Amnion Placenta Amnion
4 chr10:22767000-22768200 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
5 chr10:22767600-22768000 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
6 chr10:22767600-22768000 Enhancers Brain Angular Gyrus brain
7 chr10:22767600-22768000 Enhancers Brain Inferior Temporal Lobe brain
8 chr10:22767600-22768800 Enhancers Brain Cingulate Gyrus brain
9 chr10:22767600-22769000 Enhancers Dnd41 blood
10 chr10:22767600-22769200 Enhancers Brain Anterior Caudate brain
11 chr10:22767600-22769800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
12 chr10:22767600-22771600 Enhancers Brain Substantia Nigra brain
13 chr10:22767800-22768600 Enhancers Brain Hippocampus Middle brain
14 chr10:22767800-22769000 Enhancers HSMMtube muscle
15 chr10:22767800-22769600 Enhancers K562 blood

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