Variant report

Variant rs10495148
Chromosome Location chr1:220720407-220720408
allele A/C
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 chr1:220716000-220722400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr1:220718000-220722200 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr1:220718000-220722200 Weak transcription Brain Angular Gyrus brain
6 chr1:220718000-220738600 Weak transcription iPS-20b Cell Line embryonic stem cell
7 chr1:220718200-220726200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:220718400-220726200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:220718600-220722200 Weak transcription HUES48 Cell Line embryonic stem cell
10 chr1:220718600-220724200 Weak transcription Fetal Heart heart
11 chr1:220718600-220731200 Weak transcription Esophagus oesophagus
12 chr1:220718600-220738600 Weak transcription iPS-15b Cell Line embryonic stem cell
13 chr1:220718600-220739000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr1:220718800-220723400 Weak transcription Cortex derived primary cultured neurospheres brain
15 chr1:220719000-220725200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr1:220719400-220722200 Weak transcription HUES64 Cell Line embryonic stem cell
17 chr1:220719400-220723800 Weak transcription Left Ventricle heart

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