Variant report

Variant rs3814504
Chromosome Location chr9:139941948-139941949
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139941200-139942200 Enhancers Right Ventricle heart
2 chr9:139941200-139942800 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr9:139941200-139943000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr9:139941200-139943200 Weak transcription K562 blood
5 chr9:139941200-139943400 Weak transcription HMEC breast
6 chr9:139941200-139943600 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr9:139941200-139944000 Weak transcription A549 lung
8 chr9:139941200-139944800 Bivalent Enhancer Placenta Placenta
9 chr9:139941200-139947800 Weak transcription Right Atrium heart
10 chr9:139941400-139942200 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
11 chr9:139941400-139942200 Enhancers Hela-S3 cervix
12 chr9:139941400-139942600 Weak transcription Pancreas Pancrea
13 chr9:139941400-139943200 Weak transcription Gastric stomach
14 chr9:139941400-139943600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
15 chr9:139941600-139942000 Bivalent Enhancer Lung lung
16 chr9:139941600-139943200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
17 chr9:139941800-139942000 Bivalent/Poised TSS Brain Dorsolateral Prefrontal Cortex brain
18 chr9:139941800-139942000 Bivalent/Poised TSS Fetal Brain Female brain
19 chr9:139941800-139942400 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell

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