Variant report

Variant rs17036571
Chromosome Location chr4:106983114-106983115
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:106959600-106983400 Weak transcription HepG2 liver
2 chr4:106967600-106983600 Weak transcription Skeletal Muscle Female skeletal muscle
3 chr4:106967600-106983800 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr4:106967800-106984200 Weak transcription Primary hematopoietic stem cells blood
5 chr4:106967800-106994600 Weak transcription Rectal Mucosa Donor 29 rectum
6 chr4:106968000-106984600 Weak transcription Primary B cells from cord blood blood
7 chr4:106972400-106997000 Weak transcription Sigmoid Colon Sigmoid Colon
8 chr4:106979400-106983800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr4:106980400-106986600 Weak transcription Pancreatic Islets Pancreatic Islet
10 chr4:106982800-106983200 Enhancers H9 Cell Line embryonic stem cell
11 chr4:106983000-106983200 Bivalent Enhancer HSMM muscle
12 chr4:106983000-106983400 Weak transcription Fetal Lung lung
13 chr4:106983000-106983600 Weak transcription Fetal Kidney kidney

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