Variant report

Variant rs11118570
Chromosome Location chr1:220718000-220718001
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr1:220708800-220718000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:220715600-220718600 Enhancers HUES48 Cell Line embryonic stem cell
5 chr1:220716000-220718200 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr1:220716000-220722400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr1:220716600-220718600 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr1:220716800-220718000 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr1:220717600-220718800 Strong transcription Cortex derived primary cultured neurospheres brain
10 chr1:220717800-220718000 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr1:220717800-220718200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:220717800-220718800 Enhancers HUES64 Cell Line embryonic stem cell
13 chr1:220718000-220718400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:220718000-220718600 Enhancers Fetal Heart heart
15 chr1:220718000-220722200 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr1:220718000-220722200 Weak transcription Brain Angular Gyrus brain
17 chr1:220718000-220738600 Weak transcription iPS-20b Cell Line embryonic stem cell

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