Variant report

Variant rs67983743
Chromosome Location chr2:99488199-99488200
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:99484000-99489000 Weak transcription Stomach Smooth Muscle stomach
2 chr2:99485000-99488200 Enhancers Fetal Muscle Leg muscle
3 chr2:99485600-99499800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
4 chr2:99485800-99488200 Enhancers Cortex derived primary cultured neurospheres brain
5 chr2:99485800-99491800 Weak transcription Brain Anterior Caudate brain
6 chr2:99486000-99488600 Weak transcription Right Atrium heart
7 chr2:99486200-99489800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr2:99486400-99489600 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr2:99486600-99489400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:99486600-99489800 Weak transcription NHEK skin
11 chr2:99486800-99489600 Weak transcription Placenta Placenta
12 chr2:99486800-99491000 Weak transcription GM12878-XiMat blood
13 chr2:99487000-99489600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:99487000-99489600 Weak transcription HMEC breast
15 chr2:99487600-99499400 Weak transcription Gastric stomach
16 chr2:99487800-99489000 Enhancers Pancreatic Islets Pancreatic Islet
17 chr2:99488000-99489600 Weak transcription Esophagus oesophagus

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