Variant report

Variant rs10000829
Chromosome Location chr4:22340827-22340828
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:22329000-22389400 Weak transcription Pancreas Pancrea
2 chr4:22329800-22349800 Weak transcription Skeletal Muscle Female skeletal muscle
3 chr4:22331600-22343000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr4:22331600-22346200 Weak transcription Left Ventricle heart
5 chr4:22332200-22342600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr4:22332200-22349800 Weak transcription Liver Liver
7 chr4:22336600-22385400 Weak transcription Fetal Intestine Large intestine
8 chr4:22340000-22341800 Active TSS Brain Anterior Caudate brain
9 chr4:22340600-22341000 Enhancers Brain Substantia Nigra brain
10 chr4:22340600-22341400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr4:22340600-22341600 Enhancers Cortex derived primary cultured neurospheres brain
12 chr4:22340800-22341600 Enhancers Brain Cingulate Gyrus brain
13 chr4:22340800-22341800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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