Variant report

Variant rs531758928
Chromosome Location chr11:10386723-10386724
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:10373600-10388000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr11:10376400-10388000 Weak transcription Psoas Muscle Psoas
3 chr11:10380600-10388000 Weak transcription Lung lung
4 chr11:10381000-10388000 Weak transcription Ovary ovary
5 chr11:10381000-10388200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr11:10381200-10387800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr11:10382200-10387200 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr11:10384600-10387600 Weak transcription NHEK skin
9 chr11:10384600-10388000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr11:10386400-10387200 Enhancers Small Intestine intestine
11 chr11:10386400-10387400 Enhancers Rectal Mucosa Donor 31 rectum
12 chr11:10386600-10386800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr11:10386600-10386800 Enhancers Duodenum Mucosa Duodenum
14 chr11:10386600-10386800 Enhancers Pancreas Pancrea
15 chr11:10386600-10386800 Enhancers Sigmoid Colon Sigmoid Colon
16 chr11:10386600-10386800 Enhancers A549 lung
17 chr11:10386600-10386800 Enhancers HUVEC blood vessel
18 chr11:10386600-10387000 Enhancers Fetal Intestine Large intestine
19 chr11:10386600-10387400 Enhancers Fetal Intestine Small intestine

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