Variant report

Variant rs183552977
Chromosome Location chr2:10970738-10970739
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:10961200-10972400 Weak transcription Right Atrium heart
2 chr2:10963600-10971800 Weak transcription Brain Anterior Caudate brain
3 chr2:10968200-10973000 Enhancers Liver Liver
4 chr2:10968200-10973200 Enhancers Spleen Spleen
5 chr2:10968400-10972400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr2:10968600-10971000 Enhancers Gastric stomach
7 chr2:10968800-10972400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr2:10969000-10970800 Enhancers Rectal Mucosa Donor 31 rectum
9 chr2:10969200-10971000 Enhancers Stomach Mucosa stomach
10 chr2:10970000-10970800 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
11 chr2:10970000-10973200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr2:10970200-10972600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr2:10970200-10973600 Bivalent Enhancer Fetal Muscle Trunk muscle
14 chr2:10970600-10972400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
15 chr2:10970600-10972400 Weak transcription Pancreas Pancrea

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