Variant report

Variant rs7926718
Chromosome Location chr11:58409579-58409580
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr11:58407200-58409600 Enhancers Primary hematopoietic stem cells blood
5 chr11:58407200-58410000 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr11:58407600-58410800 Enhancers Rectal Mucosa Donor 31 rectum
7 chr11:58407800-58410400 Enhancers Fetal Intestine Large intestine
8 chr11:58407800-58410600 Enhancers Fetal Intestine Small intestine
9 chr11:58408000-58410000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr11:58408200-58409800 Enhancers Duodenum Mucosa Duodenum
11 chr11:58408800-58410200 Weak transcription Sigmoid Colon Sigmoid Colon
12 chr11:58408800-58413000 Weak transcription Primary T helper naive cells fromperipheralblood blood
13 chr11:58408800-58413000 Weak transcription Thymus Thymus
14 chr11:58409000-58411800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
15 chr11:58409200-58409600 Flanking Active TSS Rectal Mucosa Donor 29 rectum

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