Variant report

Variant rs28585439
Chromosome Location chr4:3592160-3592161
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3587200-3593000 ZNF genes & repeats Fetal Brain Female brain
2 chr4:3587400-3592800 ZNF genes & repeats Brain Germinal Matrix brain
3 chr4:3589800-3593000 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
4 chr4:3591600-3592400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
5 chr4:3591800-3592400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr4:3591800-3592600 Flanking Active TSS Brain Inferior Temporal Lobe brain
7 chr4:3591800-3592600 Enhancers Brain Substantia Nigra brain
8 chr4:3591800-3592600 Strong transcription Fetal Intestine Small intestine
9 chr4:3591800-3592600 Bivalent Enhancer Fetal Muscle Trunk muscle
10 chr4:3591800-3592800 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
11 chr4:3592000-3592200 Active TSS Brain Anterior Caudate brain
12 chr4:3592000-3592200 Enhancers Brain Cingulate Gyrus brain
13 chr4:3592000-3592200 Active TSS Brain Dorsolateral Prefrontal Cortex brain
14 chr4:3592000-3592400 Flanking Active TSS Brain Angular Gyrus brain
15 chr4:3592000-3592400 Flanking Bivalent TSS/Enh Brain Hippocampus Middle brain
16 chr4:3592000-3592600 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
17 chr4:3592000-3592600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
18 chr4:3592000-3592600 Enhancers Fetal Brain Male brain
19 chr4:3592000-3595400 Weak transcription Fetal Intestine Large intestine

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