Variant report
Variant | rs528083159 |
---|---|
Chromosome Location | chr1:76693049-76693050 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:76687400-76695000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr1:76689000-76693800 | Enhancers | Primary neutrophils fromperipheralblood | blood |
3 | chr1:76690000-76694800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
4 | chr1:76692000-76694400 | Weak transcription | HUVEC | blood vessel |
5 | chr1:76692200-76693800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
6 | chr1:76692200-76696000 | Enhancers | Fetal Thymus | thymus |
7 | chr1:76692400-76695600 | Enhancers | H9 Cell Line | embryonic stem cell |
8 | chr1:76692400-76698200 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
9 | chr1:76692600-76698000 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
10 | chr1:76692600-76698200 | Enhancers | HUES48 Cell Line | embryonic stem cell |
11 | chr1:76692600-76698400 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
12 | chr1:76692800-76693400 | Enhancers | HUES6 Cell Line | embryonic stem cell |
13 | chr1:76692800-76694600 | Enhancers | Fetal Heart | heart |
14 | chr1:76692800-76695600 | Enhancers | Primary T cells from cord blood | blood |
15 | chr1:76692800-76695600 | Enhancers | Thymus | Thymus |
16 | chr1:76692800-76698000 | Enhancers | HUES64 Cell Line | embryonic stem cell |
17 | chr1:76693000-76694600 | Weak transcription | H1 Cell Line | embryonic stem cell |
18 | chr1:76693000-76694600 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
19 | chr1:76693000-76694800 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
20 | chr1:76693000-76695000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |