Variant report

Variant rs111435960
Chromosome Location chr8:19128767-19128768
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:19121600-19129400 Weak transcription Spleen Spleen
2 chr8:19122400-19129800 Weak transcription Pancreas Pancrea
3 chr8:19123200-19129800 Weak transcription Gastric stomach
4 chr8:19125400-19129200 Weak transcription Primary hematopoietic stem cells blood
5 chr8:19125600-19128800 Weak transcription HMEC breast
6 chr8:19125600-19129400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr8:19125600-19129400 Weak transcription NHEK skin
8 chr8:19125600-19131200 Weak transcription Fetal Heart heart
9 chr8:19125600-19131200 Weak transcription Right Atrium heart
10 chr8:19125600-19131400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr8:19125800-19128800 Weak transcription A549 lung
12 chr8:19125800-19131000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr8:19125800-19131000 Weak transcription Fetal Lung lung
14 chr8:19125800-19131200 Weak transcription Adipose Nuclei Adipose
15 chr8:19126000-19129200 Weak transcription HUVEC blood vessel
16 chr8:19126000-19129400 Weak transcription Stomach Mucosa stomach
17 chr8:19126000-19129400 Weak transcription Hela-S3 cervix
18 chr8:19126000-19131200 Weak transcription Rectal Mucosa Donor 31 rectum
19 chr8:19126400-19129200 Weak transcription HepG2 liver
20 chr8:19127800-19133400 Enhancers Liver Liver
21 chr8:19128600-19128800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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