Variant report

Variant rs116678119
Chromosome Location chr12:48335059-48335060
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:48328400-48337800 Enhancers Fetal Heart heart
2 chr12:48329400-48335200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr12:48332600-48339600 Weak transcription NHDF-Ad bronchial
4 chr12:48332800-48337400 Weak transcription HMEC breast
5 chr12:48332800-48337400 Weak transcription NHEK skin
6 chr12:48332800-48340200 Weak transcription Right Atrium heart
7 chr12:48333000-48335800 Weak transcription Right Ventricle heart
8 chr12:48333000-48339200 Weak transcription HSMM muscle
9 chr12:48333400-48335200 Weak transcription Fetal Muscle Leg muscle
10 chr12:48333400-48335800 Weak transcription Spleen Spleen
11 chr12:48333600-48336200 Weak transcription Small Intestine intestine
12 chr12:48333800-48337000 Weak transcription Hela-S3 cervix
13 chr12:48334000-48336800 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
14 chr12:48334200-48335200 Weak transcription HSMMtube muscle
15 chr12:48334200-48336600 Weak transcription Rectal Mucosa Donor 31 rectum
16 chr12:48334400-48336400 Weak transcription Colonic Mucosa Colon
17 chr12:48334600-48335800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
18 chr12:48334800-48335400 Enhancers Primary hematopoietic stem cells short term culture blood
19 chr12:48335000-48335800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
20 chr12:48335000-48336400 Enhancers Duodenum Mucosa Duodenum
21 chr12:48335000-48337000 Bivalent Enhancer Fetal Stomach stomach

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