Variant report

Variant rs749676
Chromosome Location chr18:30339291-30339292
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:30333800-30341400 Weak transcription Fetal Kidney kidney
2 chr18:30335200-30339600 Weak transcription H1 Cell Line embryonic stem cell
3 chr18:30335200-30340000 Weak transcription Fetal Brain Male brain
4 chr18:30335200-30340400 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr18:30335600-30339800 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chr18:30335600-30342200 Enhancers Primary B cells from peripheral blood blood
7 chr18:30335800-30339600 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr18:30336000-30339600 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr18:30336200-30339400 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr18:30336200-30339600 Weak transcription iPS-20b Cell Line embryonic stem cell
11 chr18:30336200-30339800 Genic enhancers Primary B cells from cord blood blood
12 chr18:30337400-30339600 Strong transcription HepG2 liver
13 chr18:30337600-30339800 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr18:30337800-30339400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
15 chr18:30338800-30339800 Enhancers Dnd41 blood

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