Variant report

Variant rs58449502
Chromosome Location chr6:4466035-4466036
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:4460000-4472400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr6:4461400-4466400 Weak transcription NHLF lung
3 chr6:4461600-4466400 Weak transcription Brain Anterior Caudate brain
4 chr6:4461600-4466400 Weak transcription HMEC breast
5 chr6:4461600-4466600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr6:4461800-4466400 Weak transcription Brain Angular Gyrus brain
7 chr6:4461800-4466400 Weak transcription Brain Hippocampus Middle brain
8 chr6:4461800-4466600 Weak transcription Brain Cingulate Gyrus brain
9 chr6:4461800-4466600 Weak transcription Colon Smooth Muscle Colon
10 chr6:4462000-4466400 Weak transcription Brain Inferior Temporal Lobe brain
11 chr6:4462000-4466400 Weak transcription Brain Substantia Nigra brain
12 chr6:4462200-4466400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr6:4462200-4466400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
14 chr6:4462400-4466200 Weak transcription Cortex derived primary cultured neurospheres brain
15 chr6:4462400-4469400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr6:4465200-4466200 Weak transcription HUVEC blood vessel
17 chr6:4465600-4466600 Enhancers Stomach Smooth Muscle stomach
18 chr6:4465600-4467400 Enhancers Breast Myoepithelial Primary Cells Breast
19 chr6:4465800-4466600 Enhancers Spleen Spleen
20 chr6:4466000-4466400 Weak transcription Placenta Placenta

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