Variant report

Variant rs17100699
Chromosome Location chr12:65222300-65222301
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:65212600-65239000 Weak transcription Hela-S3 cervix
2 chr12:65219800-65226000 Weak transcription Gastric stomach
3 chr12:65220200-65226400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr12:65220400-65229800 Weak transcription Pancreas Pancrea
5 chr12:65220600-65226200 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr12:65220600-65230400 Weak transcription Brain Inferior Temporal Lobe brain
7 chr12:65220600-65233000 Weak transcription HUVEC blood vessel
8 chr12:65220600-65237000 Weak transcription Brain Anterior Caudate brain
9 chr12:65221000-65226400 Weak transcription Spleen Spleen
10 chr12:65221200-65225800 Weak transcription Fetal Intestine Small intestine
11 chr12:65221400-65223200 Weak transcription Fetal Brain Male brain
12 chr12:65221600-65231200 Weak transcription Brain Angular Gyrus brain
13 chr12:65222000-65222400 Strong transcription Fetal Brain Female brain
14 chr12:65222000-65222400 Transcr. at gene 5' and 3' GM12878-XiMat blood
15 chr12:65222000-65223400 Strong transcription Brain Dorsolateral Prefrontal Cortex brain
16 chr12:65222200-65226000 Weak transcription Fetal Intestine Large intestine

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