Variant report

Variant rs12088390
Chromosome Location chr1:246599821-246599822
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246581000-246608200 Weak transcription Aorta Aorta
2 chr1:246582000-246601600 Weak transcription Primary T cells from cord blood blood
3 chr1:246589200-246602000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr1:246596000-246602800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr1:246597200-246602000 Enhancers NHDF-Ad bronchial
6 chr1:246597400-246614200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr1:246598200-246600000 Enhancers HUES64 Cell Line embryonic stem cell
8 chr1:246598200-246602600 Weak transcription Thymus Thymus
9 chr1:246598400-246600000 Enhancers HUES48 Cell Line embryonic stem cell
10 chr1:246598400-246600000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:246598400-246600000 Enhancers A549 lung
12 chr1:246599200-246600800 Enhancers H9 Cell Line embryonic stem cell
13 chr1:246599400-246600200 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr1:246599400-246600600 Weak transcription NHLF lung
15 chr1:246599400-246601800 Weak transcription H1 Cell Line embryonic stem cell
16 chr1:246599400-246610800 Weak transcription Osteobl bone
17 chr1:246599600-246600600 Weak transcription iPS-15b Cell Line embryonic stem cell
18 chr1:246599800-246600000 Genic enhancers HSMM muscle

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