Variant report

Variant rs17123428
Chromosome Location chr11:119759344-119759345
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:119746000-119762400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr11:119747200-119768200 Weak transcription Fetal Intestine Small intestine
3 chr11:119747600-119762400 Weak transcription Esophagus oesophagus
4 chr11:119749600-119760000 Enhancers Fetal Heart heart
5 chr11:119755200-119760400 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr11:119757400-119760400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr11:119757600-119760000 Bivalent Enhancer Fetal Muscle Leg muscle
8 chr11:119758400-119759600 Enhancers Spleen Spleen
9 chr11:119758400-119760000 Enhancers Left Ventricle heart
10 chr11:119758400-119760000 Enhancers Right Atrium heart
11 chr11:119758600-119759400 Enhancers Rectal Mucosa Donor 31 rectum
12 chr11:119758600-119759800 Enhancers Fetal Brain Male brain
13 chr11:119758600-119761600 Enhancers Right Ventricle heart
14 chr11:119758800-119764000 Enhancers Brain Hippocampus Middle brain
15 chr11:119759200-119759400 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
16 chr11:119759200-119759800 Bivalent Enhancer Fetal Muscle Trunk muscle
17 chr11:119759200-119759800 Bivalent Enhancer Fetal Stomach stomach
18 chr11:119759200-119760200 Weak transcription Brain Cingulate Gyrus brain

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