| Tag | Content |
|---|
EnhancerAtlas ID | HS081-06053 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr14:39672840-39673850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr14:39673210-39673222 | TGTCAGGGGGTG | + | 6.22 | | NFE2L1 | MA0089.2 | chr14:39673311-39673326 | GCATGACTCAGCAGA | + | 7.23 | | Nfe2l2 | MA0150.2 | chr14:39673309-39673324 | CTGCATGACTCAGCA | + | 7.41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 39673031 | 39673603 | | chr14 | 39672861 | 39673002 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I039203 | chr14 | 39672488 | 39674045 |
|
Enhancer Sequence | ACCTGGAGCT GATTCAATTT AGACAGCCCA ACAAAATACA GGTGTAGAGG AAGCAGTAGG 60
AAAGGCCCTG GGAACTTGCT GGGTCCCCAG CAGGCCATTC CTGCCTGGCA CCACAGGGAT 120
CTATCAGGAG AGTGGGCAGA AGAGTGAGGG AAAACACCAC AGGGAGAAGG AAATCTCCAG 180
CTGAACTTTG TGACAATTTG AACCTGGTGA GAAGCCTCCT GGCCAGAACT CAGGGGAGGA 240
TGCATATCAG TGTGCAGACT CCACAGACTG GGGTAGAACT AAAGCCCTTT TATGTTGCAG 300
CTGGGAGGAG GGTAGCCTGG GGCAAGTTCT CAAGCCCAGC CCACCCACTG TCCAGAAACA 360
GACTTGACGC TGTCAGGGGG TGCATGGTGG GTGTGGGACC AGCTCTTTAG TTTGTGTGGG 420
AGGTGGATGA GGCCTGTGAC TGCCAGCTTT CCCCCACTTC CCTGACAACC TGCATGACTC 480
AGCAGAGGCA TCTATAATCC TCCTAGGTAC ACAACTCCAT TGACCTGGGA ACCTTACCCC 540
ATCCCCCACA GCAGCCACAG CAAGACCCGC CCAAGGATAG TCTGAGCTCA GACATGCCTA 600
GCCCTGCCCC CACCTGATGG GCCTTCCTTA TCCACTCTGG TAGCTGAAGA CAAAGGGCAT 660
ATAATCTTGG GACTTCAAGG GCCCCACCCA CCACTGGTTC CTCTCCATAC TACCATAGTT 720
GATGCTCTCT GGAAAGCATC ACCTCCCAGC AGGAGGCCAA CTAGCACAAA AATAGAGCAT 780
TTAAACCACC AAAGCTAAGA ACCCTCACAG AGCCCATTGC GCTCCCCTGC CACCTCCACC 840
AGAACAGGTG CTGGTATCCA TGTCTGAGAG ATCCATAGAC AGTTCACATC ACAGGGCTCT 900
GTGCAGACAA CTCCCAGTAC CAGCCCAGAG CTGGGTAGAC GTGCTGGGTG GCTCGATCCA 960
GAAGAAAGAC AACAATCACT GCAGTCTGGC TCACAGGAAG CCACATCCAT 1010
|
