Variant report

Variant rs61263516
Chromosome Location chr12:509780-509781
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:499200-510000 Weak transcription Primary T cells fromperipheralblood blood
2 chr12:499200-510000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
3 chr12:499200-510000 Weak transcription Placenta Placenta
4 chr12:499200-510000 Weak transcription Left Ventricle heart
5 chr12:499200-510000 Weak transcription Sigmoid Colon Sigmoid Colon
6 chr12:499400-510000 Weak transcription Primary hematopoietic stem cells blood
7 chr12:499400-510000 Weak transcription Primary T helper cells fromperipheralblood blood
8 chr12:499400-510000 Weak transcription Brain Substantia Nigra brain
9 chr12:499600-510000 Weak transcription Primary T cells from cord blood blood
10 chr12:499600-510000 Weak transcription Primary T helper naive cells from peripheral blood blood
11 chr12:499600-510000 Weak transcription Brain Anterior Caudate brain
12 chr12:499600-510000 Weak transcription Fetal Lung lung
13 chr12:499600-510000 Weak transcription Fetal Muscle Leg muscle
14 chr12:499600-510400 Weak transcription Fetal Brain Male brain
15 chr12:499800-510000 Weak transcription Fetal Adrenal Gland Adrenal Gland
16 chr12:499800-510000 Weak transcription A549 lung
17 chr12:505200-510200 Weak transcription Fetal Stomach stomach
18 chr12:509400-510000 Enhancers Fetal Intestine Small intestine
19 chr12:509400-510000 Enhancers K562 blood
20 chr12:509400-511800 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
21 chr12:509600-509800 Enhancers Dnd41 blood
22 chr12:509600-510000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
23 chr12:509600-510000 Enhancers Fetal Intestine Large intestine
24 chr12:509600-510000 Enhancers HepG2 liver

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