Variant report

Variant rs567862869
Chromosome Location chr14:105066960-105066961
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105060800-105069000 Weak transcription Fetal Intestine Small intestine
2 chr14:105063000-105067400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
3 chr14:105063800-105070000 Enhancers Fetal Brain Male brain
4 chr14:105064000-105067400 Bivalent Enhancer Fetal Muscle Leg muscle
5 chr14:105064000-105068600 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr14:105064400-105068600 Enhancers Cortex derived primary cultured neurospheres brain
7 chr14:105064600-105067600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr14:105064800-105068800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
9 chr14:105065200-105070800 Weak transcription Right Atrium heart
10 chr14:105065400-105070000 Weak transcription Fetal Heart heart
11 chr14:105066000-105069200 Bivalent Enhancer Placenta Placenta
12 chr14:105066200-105067000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr14:105066200-105067400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr14:105066400-105067200 Flanking Active TSS Brain Germinal Matrix brain
15 chr14:105066400-105067200 Flanking Active TSS Fetal Brain Female brain
16 chr14:105066400-105067400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
17 chr14:105066800-105067000 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
18 chr14:105066800-105067000 Enhancers Brain Anterior Caudate brain
19 chr14:105066800-105067200 Enhancers Brain Hippocampus Middle brain
20 chr14:105066800-105067800 Enhancers Brain Cingulate Gyrus brain
21 chr14:105066800-105068800 Enhancers Brain Inferior Temporal Lobe brain
22 chr14:105066800-105069400 Enhancers Brain Angular Gyrus brain
23 chr14:105066800-105070400 Weak transcription Pancreas Pancrea

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