Variant report

Variant rs893607
Chromosome Location chr7:149490874-149490875
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:149473800-149534800 Weak transcription Right Atrium heart
2 chr7:149487600-149518400 Weak transcription Gastric stomach
3 chr7:149488000-149506400 Weak transcription Fetal Lung lung
4 chr7:149488400-149503600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
5 chr7:149488600-149491800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr7:149488600-149495000 Weak transcription Brain Angular Gyrus brain
7 chr7:149489200-149491200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr7:149489200-149507000 Weak transcription Spleen Spleen
9 chr7:149490400-149491200 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr7:149490400-149491200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr7:149490400-149491400 Enhancers HMEC breast
12 chr7:149490600-149491200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr7:149490600-149491400 Bivalent Enhancer Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr7:149490600-149520200 Weak transcription Brain Anterior Caudate brain
15 chr7:149490800-149491000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
16 chr7:149490800-149491000 Bivalent Enhancer NHEK skin
17 chr7:149490800-149492000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
18 chr7:149490800-149514400 Weak transcription Brain Hippocampus Middle brain

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