Tag | Content |
---|
EnhancerAtlas ID | HS108-26565 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr22:23780080-23781010 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr22:23780574-23780589 | TTGCTGAGTCTGCGT | + | 6.08 | MAFG | MA0659.1 | chr22:23780571-23780592 | TGTTTGCTGAGTCTGCGTTAT | - | 6.33 | MAFG | MA0659.1 | chr22:23780571-23780592 | TGTTTGCTGAGTCTGCGTTAT | + | 6.63 | NFE2L1 | MA0089.2 | chr22:23780590-23780605 | ATTGATGAGTCATCG | - | 6.46 | USF1 | MA0093.2 | chr22:23780173-23780184 | GGTCACGTGGT | - | 6.32 | USF2 | MA0526.2 | chr22:23780170-23780186 | CGGGGTCACGTGGTAA | + | 6.38 | ZBTB18 | MA0698.1 | chr22:23780919-23780932 | CATCCAGATGTTG | + | 7.34 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACACAGTGCC GCTGTGAACA TTCGTGTACA AGCTTGTGTG TGGAAATGCA TTTTTGTTTC 60 TCTCGGGTGT ACACCCATAA GAGGAAGTGC CGGGGTCACG TGGTAATTTA ACGTTGAGCT 120 TTGTAAGGAG CTGCCTCTTC TCCCAGGTTC TCCCCGTCCT CCCCAACACG CGCCACTGTC 180 TGCTTTTATG ATGCTTTTCC ATCCCAGGGG CTGCGGGTGC CGCTGGGTTA CAGGGTCCGT 240 GAACCTCCTG AGATTCAAAT GCAAAATGTG AAGTGGGTGT TGGCGTGGGT TTCGGGTAGA 300 GGGACTGCAG CCCCTGCACG GGGTTAGGAA TATGTTTCCC AGTCCAGGCA GAGCTACGCA 360 GGAATCGCCT CTAGACACCC AAGAGGGAGC AGTTTTGTCT GGAGAAGTAG CCCACTGCCG 420 TGTTTCACCA GGCTGGCCTG TGATAGCTGG ACCTGCCCCG ATGCCACCAC CTCCTCCTGC 480 CAGGGCTTCC CTGTTTGCTG AGTCTGCGTT ATTGATGAGT CATCGTCTAT ATACACGCAC 540 CCGTGAGGCC GTCAAGGCAG TGAACAGACC CTTCGCCCCC AGATCCCAGG CCCTGTGCAG 600 CCTGCCTTGC CCCTCCCACT GCAACCCGAC CCCAAGCAGC CACTGATCCT TCTGTGTTTC 660 CTGTCACCAC GGGTTCATCC ATGTTTTCTA GAGTTTCTGT AAGTGGAATC ACGCAGTATC 720 TAGCCTTTCT CGTCTGGCTT CTTCCACTAA GCGTAGTTAG TTTGAGATTT ATCCATGTTG 780 CTGTGGTATC AACAGTTTAT CCCTTTACAG TCATACAGAT AGACCACAGT GTCTTCATCC 840 ATCCAGATGT TGACGGGCAT TCCGGTGGCT TCCAGCTTGG GGCTGTTGCA AATAAAGTGT 900 ACAGTGAACA TTCACATGCA AGCTTTGCAC 930
|
| |
|
|
|