Variant report

Variant rs16898351
Chromosome Location chr6:57370692-57370693
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:57358800-57372000 Weak transcription iPS-20b Cell Line embryonic stem cell
2 chr6:57366000-57371800 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr6:57367400-57371800 Weak transcription Aorta Aorta
4 chr6:57369400-57372600 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
5 chr6:57369800-57370800 Enhancers HUES48 Cell Line embryonic stem cell
6 chr6:57369800-57370800 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr6:57369800-57370800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr6:57369800-57370800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr6:57370000-57370800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr6:57370400-57370800 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr6:57370400-57370800 Enhancers NHDF-Ad bronchial
12 chr6:57370400-57374200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr6:57370400-57380200 Weak transcription ES-WA7 Cell Line embryonic stem cell
14 chr6:57370600-57370800 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr6:57370600-57372000 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr6:57370600-57372200 Weak transcription Cortex derived primary cultured neurospheres brain

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