Variant report

Variant rs3018047
Chromosome Location chr4:100014510-100014511
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:100011400-100025800 Weak transcription Esophagus oesophagus
2 chr4:100011600-100025600 Weak transcription Primary T cells from cord blood blood
3 chr4:100011800-100020600 Weak transcription Fetal Intestine Small intestine
4 chr4:100012200-100015000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr4:100012800-100063800 Weak transcription Aorta Aorta
6 chr4:100013000-100014800 Weak transcription Fetal Lung lung
7 chr4:100013000-100020200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr4:100013200-100015400 Weak transcription Rectal Smooth Muscle rectum
9 chr4:100013400-100014600 Flanking Active TSS K562 blood
10 chr4:100014000-100022000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr4:100014200-100014800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr4:100014400-100021200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr4:100014400-100024000 Weak transcription HMEC breast

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