Variant report

Variant rs12205473
Chromosome Location chr6:34082944-34082945
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:34025000-34101800 Weak transcription Right Atrium heart
2 chr6:34051400-34089000 Weak transcription H9 Cell Line embryonic stem cell
3 chr6:34067000-34097000 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr6:34067200-34089000 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr6:34067400-34089000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr6:34078800-34083600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr6:34080800-34088200 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr6:34081600-34083000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr6:34081800-34083600 Enhancers Fetal Brain Female brain
10 chr6:34082000-34083200 Enhancers Spleen Spleen
11 chr6:34082400-34083800 Enhancers Fetal Brain Male brain
12 chr6:34082800-34083000 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
13 chr6:34082800-34083000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
14 chr6:34082800-34083600 Bivalent Enhancer Brain Germinal Matrix brain

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