Variant report

Variant rs12435534
Chromosome Location chr14:104653844-104653845
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104643800-104662200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr14:104645400-104655000 Weak transcription Gastric stomach
3 chr14:104648200-104655000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr14:104648400-104654400 Weak transcription Brain Germinal Matrix brain
5 chr14:104651600-104654200 Weak transcription Rectal Mucosa Donor 29 rectum
6 chr14:104651600-104655000 Weak transcription Fetal Intestine Small intestine
7 chr14:104652200-104654400 Enhancers Hela-S3 cervix
8 chr14:104652400-104655800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr14:104652600-104660400 Weak transcription Spleen Spleen
10 chr14:104653000-104654000 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr14:104653400-104654400 Weak transcription Esophagus oesophagus
12 chr14:104653400-104655400 Bivalent Enhancer Placenta Placenta
13 chr14:104653600-104654400 Enhancers Fetal Brain Male brain
14 chr14:104653600-104655000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
15 chr14:104653600-104656200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
16 chr14:104653800-104654800 Bivalent Enhancer NHEK skin
17 chr14:104653800-104655000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr14:104653800-104655400 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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