Variant report

Variant rs11974612
Chromosome Location chr7:16953573-16953574
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:16942600-16961600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr7:16945200-16954000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr7:16945400-16955200 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr7:16945600-16955400 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr7:16946400-16955600 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr7:16947000-16955600 Weak transcription Stomach Mucosa stomach
7 chr7:16952200-16956200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr7:16952200-16957000 Enhancers Placenta Placenta
9 chr7:16952600-16955200 Weak transcription Fetal Kidney kidney
10 chr7:16953000-16953800 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr7:16953200-16953600 Enhancers HUES48 Cell Line embryonic stem cell
12 chr7:16953200-16953600 Enhancers HUES6 Cell Line embryonic stem cell
13 chr7:16953200-16953800 Enhancers H1 Cell Line embryonic stem cell
14 chr7:16953200-16955800 Enhancers Placenta Amnion Placenta Amnion
15 chr7:16953400-16953600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr7:16953400-16954200 Weak transcription Breast Myoepithelial Primary Cells Breast
17 chr7:16953400-16956200 Weak transcription iPS-18 Cell Line embryonic stem cell

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