| Tag | Content |
|---|
EnhancerAtlas ID | HS113-16417 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr18:10558260-10559290 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr18:10559126-10559140 | TTGTGACGTGGCAC | - | 6.72 | | TP53 | MA0106.3 | chr18:10558829-10558847 | GACATGCACGTACATGTT | + | 7.07 | | TP53 | MA0106.3 | chr18:10558829-10558847 | GACATGCACGTACATGTT | - | 7 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAAGAGCACT TGTTAGTACT GAAGGACTGA GTGCGCCCCC ACCACCATTC CTATTTTCAG 60
AGCTGAGCAT CATCTTAAAT AATGTAATGC TATGATCCTA ACTGATTGAT TCTCTTGACA 120
AAAAGAGTGA GTTAATGTAT CCCTATTATC AGAGAAGAGA GTGGACAGTA CAAGAAGAGG 180
AAGTGAGTGG GGCAAAGGTG TTAGCATAGT CCCACTGAGA CACATGAGGC TCCTCACACC 240
TCAGTCCTTG TTCTTGCGGT GAGCATGGGC TGAGAGTCTC CATATGGACA GAGTGGCAAG 300
CTGTGACCTC TGGCCCACAG GGACTCACTG GCCACCAGAC CCTGGCTCTG TCCCCATCCT 360
CTCAGCTCCT TACCTCCTCC ATGTGCCTTG TAGACAGCTA CAGGAGAGAC AGAAAATTCA 420
CAGGCACAGA TTGCTCTGAT GGTCACCAGA AATTCCAGTG AGAATAGGGA CAGGATGACA 480
GAAGTTACTT GACAAGTGGA AATCAGCGTG GCCCAGGCAT CTGGAGGGAG TTCCCTGACA 540
TCTCTGAGCT GCACAGCCAC CTGGTCCAGG ACATGCACGT ACATGTTCCC CAAGTGAGCT 600
AGAATGGTAG GGGTGCCAAA AGTTTCCAGA AGCTGCTGGT AATCCATCCT GGTCCGGGTG 660
ACTCCAGCCG GCAGTGACCC TGGAGTTAGG GGGTGCTCTA CAGCCAGGCT GGCTACATGA 720
TTTGCAGGGC CCAGTGCAAA ATGAACATGC AGGAAATGCA GAGACCTCCC TCTGCAGTCA 780
CTCTGTTGAC CTGCCATGGT GTTTTTCGTT TGCTATTCCA TGTCTTGCTT CAGGAACAGA 840
CCTGCGTGGG TGTGTGGACC CATGCCTTGT GACGTGGCAC AAGGTGTGCA TCCAGCCCAA 900
CCCTCCCTGT GCCCATCTCT GATGGGGAGT GCAGCTGCAC TTTCTGGGCA GGGTCGGGGA 960
GTGGGCTGCC AATGGCCCAT TATTGGATGG ACCCTGCAGG AGGATGCAGC CTCCACTGTC 1020
CCATCAGACT 1030
|
