| Tag | Content |
|---|
EnhancerAtlas ID | HS146-03627 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr12:64915710-64917010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr12:64916792-64916807 | AGTGCTGACTCATGC | - | 6.23 | | Nfe2l2 | MA0150.2 | chr12:64916794-64916809 | TGCTGACTCATGCCA | - | 6.17 | | Nr2f6(var.2) | MA0728.1 | chr12:64916969-64916984 | GAGGTCAGGAGTTCA | + | 6.22 | | TP53 | MA0106.3 | chr12:64916176-64916194 | AGCATGTTAGGGCATGCC | + | 6.13 | | TP53 | MA0106.3 | chr12:64916176-64916194 | AGCATGTTAGGGCATGCC | - | 6.58 | | TP63 | MA0525.2 | chr12:64916176-64916194 | AGCATGTTAGGGCATGCC | + | 6.09 | | ZNF263 | MA0528.1 | chr12:64916239-64916260 | TCCTATCCTCCCTCCTCCTCC | - | 7.59 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I064521 | chr12 | 64915742 | 64917005 |
|
Enhancer Sequence | AAATGCTGGG AACACAGCCC TTCTGCTGGC TTGGTTGATT CATCTCAATT GGAGAAGGGA 60
GTCTGTGAAA TTATACAACG CTCATCTTGT GAAGCTTCAA ATTTTGAGTT TCACACTTGA 120
AGTTCTTTAG GCACGGTAAA CTTTTTTGGA ACACCATGAA GCATGAAAGC AGATGCTTTT 180
GGAAATGAAC TGTTTTCTAT GACATGGTTT TCCAGACAGA TCTGGGAAGC TCAGTCAAAG 240
AAGAATGAAC ATCTTTGAAA ATATCAAAAA GTCTATGTTA CAGGGTGGAT ATTCTCCGGG 300
CTCAAAACTA TTCATTGCTT TCTTTTTTTT TGAGGGCATA TAAAATAAAA AACAGAAATT 360
GCAACAGAAC TTCTGTTCTC CAGCTGTCAA ATCTATTATT TTCCTCCCAG CTCCTGCTGG 420
GGGGATGTGG GGAGAAATCA GCAGGGACCC CTTTTCACTG TCCTTTAGCA TGTTAGGGCA 480
TGCCCAATGC TGATGATGAA ATATGTGGTT AAAAACGTTT AACCCTTTGT CCTATCCTCC 540
CTCCTCCTCC CACTCAGCCC AGCACGTTCA CAAAAGACCA CGAATGTTAC CCACACATAA 600
ACACTAGCAC CTACCAAGTC TCTTGTCAAA AGCCATTTTA GGATTGCAGC TACCAGATTG 660
TCTGAATGAT CTGCCGCCTT AGATTTTTTT ACTAAGAGGA TTGAGAGTTG ATTCATATAA 720
GGACTATGAA ACTTGTGTGC CAGGAGTCTC AACGCAAGAA ATAAAAAAAA CTGGAAGTTT 780
CACCCACCTA AATTATCCTT TTGGCTATTG TCATAGCCAT TCAGCTACTT GGTTTCAGCT 840
AAAGAGGCTG GGAGGACAGA AATTTCTCTG TCCCAGTAGG AGTTTAAGAT GCAACAAAAC 900
AAATGTAGAA CTAATAGGCT CCTGGGGGAA AGGTGGGGAA AAGTGTATCT TCATTTCCAT 960
TCCTCTCCCA CTCCTCCGGG CTGCTGGGAC CCTTTGGAAA TCCAGAAAAA GAGTGTTGCT 1020
TTTCCACCAA CTACATCCCC CAAGCCCAAG TCATCAGGCA CAGGGCCGGA GGGGTGGGGA 1080
AGAGTGCTGA CTCATGCCAG CGCAAAAGAA GATGCCCATA TTTTTTAAAA CTGCTGCCCT 1140
GTTCTTTTTC TGGAATGCTT TCTCTGTTGA TTTGCTCAAA AAAATAAGCT TCTGGCCAGG 1200
CACGGTGGCT CAAGCCTGTA ATCCCAGCAC TTTGGGAGAC TGAGGCAGGC AGATCACCTG 1260
AGGTCAGGAG TTCAAGACCA GCCTGGCCAA CATGGCGAAA 1300
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