Variant report

Variant rs3857962
Chromosome Location chr8:67666408-67666409
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:67647800-67671000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr8:67652200-67672400 Weak transcription Fetal Intestine Small intestine
3 chr8:67656400-67679000 Weak transcription Sigmoid Colon Sigmoid Colon
4 chr8:67656600-67670400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr8:67660800-67667800 Weak transcription Brain Angular Gyrus brain
6 chr8:67661000-67668000 Weak transcription Brain Substantia Nigra brain
7 chr8:67661000-67673400 Weak transcription Brain Hippocampus Middle brain
8 chr8:67664600-67668200 Weak transcription Brain Inferior Temporal Lobe brain
9 chr8:67664600-67686400 Weak transcription Right Atrium heart
10 chr8:67664800-67670800 Weak transcription Brain Anterior Caudate brain
11 chr8:67665000-67671600 Weak transcription Monocytes-CD14+_RO01746 blood
12 chr8:67665800-67667000 Enhancers Primary neutrophils fromperipheralblood blood
13 chr8:67665800-67673000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr8:67666000-67673200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr8:67666200-67666600 Enhancers HepG2 liver
16 chr8:67666400-67666600 Enhancers K562 blood

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