Variant report

Variant rs17649700
Chromosome Location chr17:43997901-43997902
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:43992200-44000000 Weak transcription HepG2 liver
2 chr17:43994600-44000200 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr17:43994800-44001400 Weak transcription Fetal Brain Female brain
4 chr17:43995000-44000600 Weak transcription Right Atrium heart
5 chr17:43996600-44002800 Enhancers Brain Substantia Nigra brain
6 chr17:43996600-44003000 Enhancers Brain Angular Gyrus brain
7 chr17:43996800-43998200 Strong transcription Brain Germinal Matrix brain
8 chr17:43996800-43999200 Enhancers Brain Anterior Caudate brain
9 chr17:43996800-44002600 Enhancers Brain Cingulate Gyrus brain
10 chr17:43997400-43998000 Enhancers Psoas Muscle Psoas
11 chr17:43997400-43998800 Genic enhancers Brain Inferior Temporal Lobe brain
12 chr17:43997600-43998600 Weak transcription Brain Hippocampus Middle brain
13 chr17:43997600-44002800 Enhancers Skeletal Muscle Male skeletal muscle
14 chr17:43997800-43998000 Bivalent Enhancer Fetal Muscle Trunk muscle
15 chr17:43997800-43998000 Flanking Active TSS Skeletal Muscle Female skeletal muscle
16 chr17:43997800-43998000 Enhancers Spleen Spleen
17 chr17:43997800-43998200 Enhancers Right Ventricle heart
18 chr17:43997800-43999800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
19 chr17:43997800-44000400 Strong transcription Liver Liver

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