Variant report

Variant rs4795369
Chromosome Location chr17:37609120-37609121
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:37608200-37611000 Enhancers Fetal Intestine Large intestine
2 chr17:37608400-37612000 Enhancers Liver Liver
3 chr17:37608400-37616800 Weak transcription Fetal Adrenal Gland Adrenal Gland
4 chr17:37608400-37617200 Weak transcription Primary hematopoietic stem cells short term culture blood
5 chr17:37608600-37609800 Weak transcription A549 lung
6 chr17:37608600-37614000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr17:37608600-37616800 Weak transcription Hela-S3 cervix
8 chr17:37608600-37617200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr17:37608800-37610200 Weak transcription K562 blood
10 chr17:37608800-37616800 Weak transcription Right Ventricle heart
11 chr17:37609000-37610800 Enhancers Fetal Intestine Small intestine
12 chr17:37609000-37610800 Flanking Active TSS HepG2 liver

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