Variant report

Variant rs10899929
Chromosome Location chr10:44373192-44373193
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44360000-44392200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:44364200-44374000 Weak transcription NHLF lung
3 chr10:44365000-44373400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr10:44365000-44373400 Weak transcription Right Ventricle heart
5 chr10:44367200-44373200 Weak transcription Left Ventricle heart
6 chr10:44367200-44373200 Weak transcription Right Atrium heart
7 chr10:44367200-44373200 Weak transcription Spleen Spleen
8 chr10:44367400-44373600 Weak transcription Fetal Stomach stomach
9 chr10:44368400-44373600 Weak transcription Brain Cingulate Gyrus brain
10 chr10:44368400-44377200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr10:44370800-44373200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr10:44371400-44375200 Enhancers Fetal Kidney kidney
13 chr10:44371800-44373200 Weak transcription NHDF-Ad bronchial
14 chr10:44371800-44373600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr10:44373000-44374800 Enhancers Fetal Heart heart

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