Variant report

Variant rs9954994
Chromosome Location chr18:30336000-30336001
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:30328800-30336000 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr18:30333800-30341400 Weak transcription Fetal Kidney kidney
3 chr18:30334000-30336000 Enhancers HUES48 Cell Line embryonic stem cell
4 chr18:30334200-30338800 Weak transcription Dnd41 blood
5 chr18:30334600-30337400 Genic enhancers HepG2 liver
6 chr18:30334800-30336200 Weak transcription Primary B cells from cord blood blood
7 chr18:30335200-30336200 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr18:30335200-30339600 Weak transcription H1 Cell Line embryonic stem cell
9 chr18:30335200-30340000 Weak transcription Fetal Brain Male brain
10 chr18:30335200-30340400 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr18:30335600-30336000 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr18:30335600-30339800 Weak transcription iPS-15b Cell Line embryonic stem cell
13 chr18:30335600-30342200 Enhancers Primary B cells from peripheral blood blood
14 chr18:30335800-30339600 Weak transcription iPS-18 Cell Line embryonic stem cell
15 chr18:30336000-30336200 Enhancers HUES64 Cell Line embryonic stem cell
16 chr18:30336000-30337600 ZNF genes & repeats H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr18:30336000-30339600 Weak transcription HUES48 Cell Line embryonic stem cell

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