Variant report

Variant rs73361875
Chromosome Location chr14:105068642-105068643
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105060800-105069000 Weak transcription Fetal Intestine Small intestine
2 chr14:105063800-105070000 Enhancers Fetal Brain Male brain
3 chr14:105064800-105068800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
4 chr14:105065200-105070800 Weak transcription Right Atrium heart
5 chr14:105065400-105070000 Weak transcription Fetal Heart heart
6 chr14:105066000-105069200 Bivalent Enhancer Placenta Placenta
7 chr14:105066800-105068800 Enhancers Brain Inferior Temporal Lobe brain
8 chr14:105066800-105069400 Enhancers Brain Angular Gyrus brain
9 chr14:105066800-105070400 Weak transcription Pancreas Pancrea
10 chr14:105067200-105069400 Enhancers Fetal Brain Female brain
11 chr14:105068000-105069800 Weak transcription Placenta Amnion Placenta Amnion
12 chr14:105068400-105068800 Enhancers Brain Germinal Matrix brain
13 chr14:105068400-105069400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr14:105068600-105070000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

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