Variant report

Variant rs6675368
Chromosome Location chr1:220718372-220718373
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220703400-220724400 Weak transcription Aorta Aorta
2 chr1:220706000-220723800 Weak transcription Fetal Brain Male brain
3 chr1:220715600-220718600 Enhancers HUES48 Cell Line embryonic stem cell
4 chr1:220716000-220722400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr1:220716600-220718600 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr1:220717600-220718800 Strong transcription Cortex derived primary cultured neurospheres brain
7 chr1:220717800-220718800 Enhancers HUES64 Cell Line embryonic stem cell
8 chr1:220718000-220718400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:220718000-220718600 Enhancers Fetal Heart heart
10 chr1:220718000-220722200 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr1:220718000-220722200 Weak transcription Brain Angular Gyrus brain
12 chr1:220718000-220738600 Weak transcription iPS-20b Cell Line embryonic stem cell
13 chr1:220718200-220718400 Enhancers HUES6 Cell Line embryonic stem cell
14 chr1:220718200-220718400 Weak transcription Esophagus oesophagus
15 chr1:220718200-220718600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr1:220718200-220726200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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