Variant report

Variant rs138599819
Chromosome Location chr6:32362187-32362188
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:32351400-32365000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr6:32356400-32364200 Weak transcription Fetal Lung lung
3 chr6:32360800-32362800 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr6:32360800-32362800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr6:32360800-32362800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr6:32360800-32362800 Enhancers Esophagus oesophagus
7 chr6:32361000-32362200 Flanking Active TSS NHEK skin
8 chr6:32361000-32370600 Weak transcription Spleen Spleen
9 chr6:32361200-32366000 Weak transcription Fetal Muscle Trunk muscle
10 chr6:32361400-32363000 Strong transcription Fetal Stomach stomach
11 chr6:32361400-32366800 Weak transcription Fetal Kidney kidney
12 chr6:32361600-32366800 Weak transcription Fetal Brain Male brain
13 chr6:32361800-32364600 Weak transcription Primary B cells from peripheral blood blood
14 chr6:32362000-32362400 Enhancers HUVEC blood vessel
15 chr6:32362000-32362800 Enhancers HMEC breast
16 chr6:32362000-32364200 Weak transcription GM12878-XiMat blood
17 chr6:32362000-32365000 Weak transcription Hela-S3 cervix

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