Variant report

Variant rs12166716
Chromosome Location chr22:29236217-29236218
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:29214800-29242200 Weak transcription Aorta Aorta
2 chr22:29216000-29238600 Weak transcription Spleen Spleen
3 chr22:29224000-29237400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
4 chr22:29225400-29242000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr22:29226000-29248800 Weak transcription Primary T cells from cord blood blood
6 chr22:29226200-29239600 Weak transcription Rectal Mucosa Donor 29 rectum
7 chr22:29226200-29242800 Weak transcription Stomach Smooth Muscle stomach
8 chr22:29226600-29241800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr22:29226600-29242200 Weak transcription Fetal Muscle Leg muscle
10 chr22:29229400-29241800 Weak transcription Fetal Adrenal Gland Adrenal Gland
11 chr22:29230400-29236800 Weak transcription Fetal Stomach stomach
12 chr22:29231200-29239200 Weak transcription Brain Inferior Temporal Lobe brain
13 chr22:29234000-29251600 Weak transcription Fetal Lung lung
14 chr22:29234200-29236400 Weak transcription Dnd41 blood
15 chr22:29234800-29237600 Enhancers Breast Myoepithelial Primary Cells Breast
16 chr22:29235200-29243200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr22:29235800-29237000 Weak transcription HepG2 liver
18 chr22:29236000-29236400 Strong transcription Fetal Intestine Small intestine

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