| Tag | Content |
|---|
EnhancerAtlas ID | HS176-43806 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chrX:129090690-129092040 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chrX:129091649-129091662 | AATCCAGATGTGT | + | 6.59 | | ZNF263 | MA0528.1 | chrX:129091231-129091252 | GCCTCCTCCCCCTCCCCCTCC | - | 6.32 | | ZNF263 | MA0528.1 | chrX:129091234-129091255 | TCCTCCCCCTCCCCCTCCGCC | - | 6.56 | | ZNF263 | MA0528.1 | chrX:129091580-129091601 | CCTTCCCCCGCTCCCTCCCTC | - | 6.72 | | ZNF263 | MA0528.1 | chrX:129091237-129091258 | TCCCCCTCCCCCTCCGCCCCT | - | 6.77 | | ZNF263 | MA0528.1 | chrX:129091576-129091597 | TCTCCCTTCCCCCGCTCCCTC | - | 6.82 | | Zfx | MA0146.2 | chrX:129091261-129091275 | CAGGCCCCGGCTCC | - | 6.13 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTATTCGGA TTTAACCACC TTCCTGGATT TAACCATCTT TCCAAAGCTT CTCCTCTCTA 60
ACGTTGAAGC GGGAGCTAAG TAGCAGCAAT GGGTTCCCTC CCCACCTCCC CCCCACCCCC 120
GCAACCTTAT GCAGCCGATC TTAAGGACCA GGTACTGAGG AATGGGCTGT CCTTTCCGAC 180
CTGCACCCCT CAACGATTGG GATCGCTTTA GTTTCTCCCT GGAGTCGAGC ATTTGCCTGC 240
ACTTAAAAAA AAAAATCCCA AACCTGGACC CCCTTTGGGG AGGGGGTTAA CAGTTTCCTT 300
AAGTTTTCTC TAGTCTGAGT AAAGAAGGAC TTCCTTCTAC TCGTCCTCAA CTATCCCCTG 360
GGGCTTCAGC GGGGCGCGAG AGCTCGGGTC TGGGCCGGGG GCCGAGCAGG CTGCGCTGCC 420
CCTCCAGGAT TTCCTGCACT CGACGCGGCG AGGCCGGCTC GAACTTCGGC CTCCGACGAA 480
GGCAACTCCG CTTCCCTTTA AAATGCAGCA ACTCCCGGCC CCCGCCCCCG CCCCTCGGGC 540
CGCCTCCTCC CCCTCCCCCT CCGCCCCTGC CCAGGCCCCG GCTCCTCCCC GAGCCCTCGG 600
CGTGGGGGCC TCCTTGCCAC CTGCCCGCTG CCCATCCCAC ATGCAAAGCG TGACCGCCGG 660
GGAAGGAAGC CGAGCGCGCG CGCCCACACC GGCCCTGCGC CGCGGCGACA GCGAGCAGCT 720
CGCCTACTCC GTCCGTCTGC GCTTACCCAG CATGCACTTC CAGGCCCTGA GCTATCTCGG 780
AGCCGCAGCC CCGGGGTCAG AGCGGCCGGA AGAAACAGGA AGTTTGGGAC GGTCCTAGTC 840
GTGGGGCCGG GAGTCCTAAA AGACAGGCCC TGAACTCCGT GCTGCCTCTC CCTTCCCCCG 900
CTCCCTCCCT CTGGCGGACT TCCCTGGGGT CCGTTTCGGG GGCTGGCCTG AACTCCGAAA 960
ATCCAGATGT GTTTGGGGGT CATTCAAGGC ACACTCCCAG GGTTCCCTTC GCGGTAGCAT 1020
CTCCTGGCTT TATGGATCGA GGGGTGGGAG GAGGAGGGAG TGCTCCCGCC CTGGTGGGGT 1080
GGTAGTCCCC GAGGGGGCGT TGTCTTCTGC CCGCCGAGAG GGGGAAGGAC GCTAGATTGG 1140
GGTGGAGGTT GGGGGGCTGG AGATTTGTCT CCCACGGCCA ATTCCTGGGC GGATAGGGCA 1200
GTGGTTAGAA CCTATGGCGG AGTCCGGACT TACTGGCTCT CCTTCCCACT GCCAGTTAGC 1260
TTTGCTCTAA TCTGCCCTCC ACATTGACTT AGGCTGCCCC ATTACCCTCA GCACTATCTC 1320
ACAGACCTGC GCTGCTGCTC ACCAGGGGCA 1350
|
| |
|
|
|
