Variant report

Variant rs10792174
Chromosome Location chr11:58410118-58410119
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58406000-58410200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
2 chr11:58406200-58411200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr11:58406200-58413000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr11:58407600-58410800 Enhancers Rectal Mucosa Donor 31 rectum
5 chr11:58407800-58410400 Enhancers Fetal Intestine Large intestine
6 chr11:58407800-58410600 Enhancers Fetal Intestine Small intestine
7 chr11:58408800-58410200 Weak transcription Sigmoid Colon Sigmoid Colon
8 chr11:58408800-58413000 Weak transcription Primary T helper naive cells fromperipheralblood blood
9 chr11:58408800-58413000 Weak transcription Thymus Thymus
10 chr11:58409000-58411800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
11 chr11:58409600-58410200 Enhancers Rectal Mucosa Donor 29 rectum
12 chr11:58409800-58410200 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr11:58410000-58410200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr11:58410000-58410600 Enhancers K562 blood

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