Variant report

Variant rs77036213
Chromosome Location chr11:17781973-17781974
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:17771200-17782200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr11:17772400-17786800 Weak transcription Brain Inferior Temporal Lobe brain
3 chr11:17772400-17790600 Weak transcription Right Atrium heart
4 chr11:17773400-17795600 Weak transcription Brain Hippocampus Middle brain
5 chr11:17774000-17786000 Weak transcription Gastric stomach
6 chr11:17774000-17791600 Weak transcription Pancreas Pancrea
7 chr11:17776400-17785800 Weak transcription Brain Angular Gyrus brain
8 chr11:17777400-17782200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
9 chr11:17781000-17786400 Weak transcription Brain Germinal Matrix brain
10 chr11:17781800-17782000 Enhancers HUES48 Cell Line embryonic stem cell
11 chr11:17781800-17782000 Enhancers Skeletal Muscle Male skeletal muscle
12 chr11:17781800-17782000 Flanking Active TSS Hela-S3 cervix
13 chr11:17781800-17782200 Enhancers Fetal Brain Female brain
14 chr11:17781800-17782200 Enhancers GM12878-XiMat blood
15 chr11:17781800-17783400 Enhancers Skeletal Muscle Female skeletal muscle

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