Variant report

Variant rs12606529
Chromosome Location chr18:30340360-30340361
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:30333800-30341400 Weak transcription Fetal Kidney kidney
2 chr18:30335200-30340400 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr18:30335600-30342200 Enhancers Primary B cells from peripheral blood blood
4 chr18:30339400-30342200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
5 chr18:30339600-30341600 Genic enhancers HepG2 liver
6 chr18:30339600-30342000 Enhancers H1 Cell Line embryonic stem cell
7 chr18:30339600-30342000 Enhancers HUES48 Cell Line embryonic stem cell
8 chr18:30339600-30342000 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr18:30339600-30342200 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr18:30339800-30340800 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr18:30339800-30341000 Flanking Active TSS Dnd41 blood
12 chr18:30339800-30341400 Genic enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr18:30339800-30341600 Enhancers GM12878-XiMat blood
14 chr18:30339800-30341800 Enhancers iPS-15b Cell Line embryonic stem cell
15 chr18:30340000-30340400 Enhancers Fetal Brain Male brain
16 chr18:30340000-30340800 Enhancers Fetal Adrenal Gland Adrenal Gland
17 chr18:30340200-30340600 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
18 chr18:30340200-30341800 Flanking Active TSS Primary B cells from cord blood blood

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