Variant report

Variant rs12662527
Chromosome Location chr6:31190897-31190898
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:31179200-31195000 Weak transcription H9 Cell Line embryonic stem cell
2 chr6:31183200-31192600 Weak transcription Spleen Spleen
3 chr6:31189000-31196400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:31189800-31191000 Enhancers GM12878-XiMat blood
5 chr6:31190000-31192800 Weak transcription Primary neutrophils fromperipheralblood blood
6 chr6:31190400-31191000 Enhancers Fetal Lung lung
7 chr6:31190400-31191600 Enhancers Fetal Stomach stomach
8 chr6:31190600-31191000 Enhancers Lung lung
9 chr6:31190800-31191000 Enhancers Colonic Mucosa Colon
10 chr6:31190800-31191200 Bivalent Enhancer Placenta Placenta
11 chr6:31190800-31197600 Weak transcription Right Atrium heart

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