| Tag | Content |
|---|
EnhancerAtlas ID | HS078-00883 | Organism | Homo sapiens | Tissue/cell | H2171 | Coordinate | chr1:47973500-47974870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:47973961-47973972 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr1:47973962-47973972 | GGGGCGGGGC | - | 6.02 | | SP3 | MA0746.2 | chr1:47973960-47973973 | GGGGGGCGGGGCG | - | 6.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCTCCCGCT CAGCGGGGCT GAGGGGCTGG GGGCCTCGAG TCTCAGCTGG ACTGTGGCAT 60
CAGGCCGGGG CTGAGCTGGG CCTTCCCCTG TGGGAGCAGA AATGGACTCC TGGGAACAAG 120
TTTGCAAGGG ATGCGGCCGG GCGGGGTTGT TCAGAGGACT CTGAAGGGGA CTGTCGCCAG 180
GAGAAAGCTC TCTCTGAGCT CAGTGGAAGC GCCGCGGGCG TCCTTCGCCT GGCCGGTTCC 240
GGCGCTCTTA TCTGGCGGGA AAGCCAGCTC CTCTACCGTG TCCCCTGTGC GCCCGCGGTC 300
CTCTGAGGAC GCCCGCCCCG TACCAACCCG TCCTGGCTTC CACTCGGCCC CGGAGACAGG 360
GCGGGCGGGT GGCACCTTCG GGCCCCGCGG GGCGCCCGCC GCGGCGTGGG GCGTGGAGAG 420
GGTGGCGACA GAGCGCGGGC GGGGACAGCG CGTGGGCCGC GGGGGGCGGG GCGCGGTGGC 480
GAAATGGCTT TTCCAGATTA GGGGCCCAGC CCGCACTGTT GACACAGTCA TAAGTTTTAA 540
TGAGAAATTT TGAGTATTTG TGTGGGAGAC GCAGCCTCTG TGCACAGATG CTGCGGGCGG 600
GCGGCGCGGG GGGCCGTCCC TCCCTGGGGC CGCCGCGGCC GCAGGCCCGG CACGGATTCC 660
TTTCAGGCAG AGGGGAAACA TTTAAACTCG CTCACCTTTG AACTGCCAGG GACGCTGTTT 720
ACCTTGGCTG CCCGAGTGGC AGTTTTACAG ATATTAAATA CCGACCCGAG GCTGAGCCGG 780
GGCTCCTTCG CTCCCCGCCC CCGCCGGGGG GCTGCGCTGG GCACGCCGAG GCCCGGGATG 840
CCCGTTCCAC CGGGGGTCAT CTCAGTGAGG GTCCCGAGCC CCTTTCTGCA GATGGTTTCT 900
GTAATCTGTG CTGGGGAGAC GCCCTGGGGC TCTCCGTTCT CGTCCACTCC TCAGCCTATT 960
CATCTCCTAA TTCGATTTTC TATGTCAGGG CGGAGCAGTG TGGAGGCTGA GAGCTGTCTG 1020
GGCCCTGCTC ACCCATTTTT TTTTTTTTTT TTGGCATTTC TGCATCTAGA AAGGGGATGT 1080
CATAAGCGAG GCACCTCCTA AGTAGGGGCT CCGGTGGCCT GGCTCTGTCT TTTCAAGGAA 1140
CAGAGGAGAC CTCTCTCTCC GAAGATGTCT ATGGGACAGA GGAGGGCTCT GCCTGAGCCG 1200
CAGTCTTCAG CGGGCAGGCA GAGGGCTCCC TGCAGAGGCA CAAGCCATGT TGATTTTACG 1260
GAGCAGGCTG CTATGCACAT TTCACTCCTG ATTTATTGGT TTTTAACTAG ATCCTTATGC 1320
TGGGCTAAAA AAGCCATCTT GCACTTTGCA AGGCTCTGCT GACTGCTGCC 1370
|
| |
|
|
|
