Variant report
Variant | rs1523583 |
---|---|
Chromosome Location | chr18:30338058-30338059 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:30333800-30341400 | Weak transcription | Fetal Kidney | kidney |
2 | chr18:30334200-30338800 | Weak transcription | Dnd41 | blood |
3 | chr18:30335200-30339600 | Weak transcription | H1 Cell Line | embryonic stem cell |
4 | chr18:30335200-30340000 | Weak transcription | Fetal Brain Male | brain |
5 | chr18:30335200-30340400 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
6 | chr18:30335600-30339800 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
7 | chr18:30335600-30342200 | Enhancers | Primary B cells from peripheral blood | blood |
8 | chr18:30335800-30339600 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
9 | chr18:30336000-30339600 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
10 | chr18:30336200-30339400 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
11 | chr18:30336200-30339600 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
12 | chr18:30336200-30339800 | Genic enhancers | Primary B cells from cord blood | blood |
13 | chr18:30336400-30338400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
14 | chr18:30337400-30339600 | Strong transcription | HepG2 | liver |
15 | chr18:30337600-30339800 | Strong transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
16 | chr18:30337800-30338200 | Enhancers | Fetal Heart | heart |
17 | chr18:30337800-30339400 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |