Variant report

Variant rs17034363
Chromosome Location chr12:104071956-104071957
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:104064000-104072000 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr12:104065800-104075200 Enhancers Fetal Intestine Large intestine
3 chr12:104066800-104074600 Enhancers Rectal Mucosa Donor 31 rectum
4 chr12:104068000-104073800 Weak transcription Spleen Spleen
5 chr12:104068400-104073200 Weak transcription Sigmoid Colon Sigmoid Colon
6 chr12:104070200-104072400 Enhancers Fetal Intestine Small intestine
7 chr12:104070600-104072200 Enhancers Duodenum Mucosa Duodenum
8 chr12:104070800-104073600 Weak transcription Pancreatic Islets Pancreatic Islet
9 chr12:104071000-104072000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr12:104071400-104072200 Flanking Active TSS Rectal Mucosa Donor 29 rectum
11 chr12:104071400-104074000 Weak transcription Fetal Muscle Leg muscle
12 chr12:104071600-104072000 Weak transcription Colonic Mucosa Colon
13 chr12:104071600-104072800 Weak transcription Fetal Brain Male brain
14 chr12:104071600-104074400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr12:104071600-104074400 Weak transcription Brain Germinal Matrix brain
16 chr12:104071800-104072200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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