Variant report

Variant rs531073812
Chromosome Location chr14:105067407-105067408
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr14:105064000-105068600 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr14:105064400-105068600 Enhancers Cortex derived primary cultured neurospheres brain
5 chr14:105064600-105067600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr14:105064800-105068800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
7 chr14:105065200-105070800 Weak transcription Right Atrium heart
8 chr14:105065400-105070000 Weak transcription Fetal Heart heart
9 chr14:105066000-105069200 Bivalent Enhancer Placenta Placenta
10 chr14:105066800-105067800 Enhancers Brain Cingulate Gyrus brain
11 chr14:105066800-105068800 Enhancers Brain Inferior Temporal Lobe brain
12 chr14:105066800-105069400 Enhancers Brain Angular Gyrus brain
13 chr14:105066800-105070400 Weak transcription Pancreas Pancrea
14 chr14:105067000-105067600 Bivalent Enhancer Brain Anterior Caudate brain
15 chr14:105067200-105068200 Enhancers Brain Germinal Matrix brain
16 chr14:105067200-105068200 Bivalent Enhancer Brain Hippocampus Middle brain
17 chr14:105067200-105069400 Enhancers Fetal Brain Female brain
18 chr14:105067400-105068200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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