Variant report

Variant rs77007428
Chromosome Location chr11:59616555-59616556
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:59614200-59619400 Enhancers Primary neutrophils fromperipheralblood blood
2 chr11:59614600-59622000 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr11:59614600-59624800 Weak transcription HUES48 Cell Line embryonic stem cell
4 chr11:59616000-59616600 Enhancers Pancreas Pancrea
5 chr11:59616000-59617200 Enhancers Rectal Mucosa Donor 31 rectum
6 chr11:59616000-59617400 Enhancers Fetal Intestine Large intestine
7 chr11:59616000-59617400 Enhancers Fetal Intestine Small intestine
8 chr11:59616000-59617400 Enhancers Sigmoid Colon Sigmoid Colon
9 chr11:59616200-59616600 Enhancers Duodenum Mucosa Duodenum
10 chr11:59616200-59616600 Enhancers Small Intestine intestine
11 chr11:59616200-59617000 Enhancers Stomach Mucosa stomach
12 chr11:59616200-59617200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr11:59616200-59617200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr11:59616200-59617400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr11:59616400-59616600 Flanking Active TSS Rectal Mucosa Donor 29 rectum
16 chr11:59616400-59617000 Enhancers K562 blood
17 chr11:59616400-59618200 Weak transcription Colonic Mucosa Colon

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