| Tag | Content |
|---|
EnhancerAtlas ID | HS002-05326 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr2:71927190-71928690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIL3 | MA0025.1 | chr2:71927458-71927469 | TTATGTAACGT | + | 6.32 | | ZNF263 | MA0528.1 | chr2:71927793-71927814 | GGGGGAGGCGGTGGGGGGAGG | + | 6.66 | | ZNF263 | MA0528.1 | chr2:71927809-71927830 | GGAGGCGGGGGAGGGGGAGGT | + | 6.93 | | ZNF263 | MA0528.1 | chr2:71927806-71927827 | GGGGGAGGCGGGGGAGGGGGA | + | 8.36 |
|
| | 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 |
| GH02I071700 | chr2 | 71927537 | 71928621 |
|
Enhancer Sequence | CCAGGTCCTC CTCTGCTTCA GTCTTAGCTG GCTGCCAGAG GGGCTGGTTG TCTGCCCACC 60
AGAGCAGAGA GAGGTGAGTG GGCTGGGGAC ATTCCTGCCC TCCCCAACCC GCCCCATGCT 120
ACTCCCTCTG GCAGCAGACC AGAGGAATCC AGGAGCCAGA GGTGGACCCG GGGCTTGTGG 180
CTAGGATCCC TGCCTGGCCC TGTGCAAGAA GGCATTGAGT TTTCATTCCT CAGGGGAGCT 240
ACAAATTTCC TGACGAGCGT GGTTGGGTTT ATGTAACGTA AACACCTCAG CACACAGTGT 300
TCCACCTGCA GGGGGGACAG GTGGGGGCCT CAAGTGCTGG CTGCTGGAGG TAAGAACTGA 360
GGAAAAGCTG GCCTCACCCG GGAGCCAGGT AGGAGCCACC TAACCGGTGT GCCAGCCAGG 420
CTGGTGCAGA GTCTGAAAGT CACCCATCAG TGTTCATTCA CTGGCTTCAG CAACGACCTC 480
TCCCGGATAA GGGTCACTGA GCAGATCTCC CCACCTCAGG GCAGGCGAGA TGAGACCCTG 540
TACGCCTCCC TCTGCTTTCT CCATTCTCAG ACTCTGATGG CCCAGGGCAT CCCCAGGAAC 600
CCCGGGGGAG GCGGTGGGGG GAGGCGGGGG AGGGGGAGGT GGGGCTTGAC CAGGAATGGC 660
TGGGGAAGGG CTTCAGGAAT CTCCACTTCT GTTCTGAGCT GACATTGTTC ACAAGGCAGG 720
GACAGAAGTG AGTGTCAGGG GCAGAGCCGG GGAGAAATGT GACGGCCCTG GTGGGGCCCC 780
TTCCGGGGAT GCTCTGACTC GCTCCTTGGT CTGAGGCCCG CCTGACCTGG TGCTGCATGG 840
GGGCTGCCTG GGTGGCCCTC CGCTGGTCTG GGCTGTCCCT AGGCTGGGAC TAGGCCCTGG 900
GTGGCTGCAC TGGGATTCAC TCAAAGCCAC CGCTGACCTG TCTCCCGGTC TGCCAGGGTA 960
AAAATAGATG TTTCCACTGC GGCCACCTCC GCAGCATCAA CTTTCTCCTA CTTGAGCCCC 1020
TGCCAGTGCT CGGCTCAGGG ACTGGAGCAT GAATTACAGG GCTGAGCTTG GCGTCGGGGC 1080
CTGGCGTCAG GGCCCTGCTG TGGAGCCAGG CTGCTCATGA ATGCCCTATT GTTTGGGGAA 1140
GTGACCCTGT GTGTCCCTCC TCGGGGCCTG GGGCCTGCCC TGCTCACCTC CAGGCCTCTT 1200
CCCATTCCCT TTGGCTTTGT GCCCGCCTGG CCTCTGAGTT CCTCACCTGC CGCCTCATCT 1260
TACAGGGGAG GCACAGTCCC TTCCATACAG GGCCAGCTCT ACGGGCATGT GACTTATGCA 1320
GTCACACAGG GCTCCACGCT CAGAAGGGCC CCACGCTTGG CTTAATGCCC TACTATCACC 1380
ACCTTGACTT TCCCAATAAT TTTGGAAAAA GGCACATTTG TATTTTGTAC TTGGCCCTAT 1440
GAATTACGTA GGTGGGCCTG CTCTATTAGG AACCACTAGT CTGATGAGGG AGCCACGGCC 1500
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