| Tag | Content |
|---|
EnhancerAtlas ID | HS154-16512 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr4:4576440-4577770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr4:4576692-4576704 | TGCAGTGATTTT | - | 6.11 | | RREB1 | MA0073.1 | chr4:4576611-4576631 | ACACAACACACACACACACA | + | 6.19 | | SREBF2 | MA0596.1 | chr4:4577738-4577748 | ATCACCCCAT | - | 6.02 | | ZNF263 | MA0528.1 | chr4:4576576-4576597 | CTCCTTCCTCCCCCTTCCTCC | - | 6.37 | | ZNF263 | MA0528.1 | chr4:4576575-4576596 | CCTCCTTCCTCCCCCTTCCTC | - | 6.44 | | ZNF263 | MA0528.1 | chr4:4576569-4576590 | TGCCCTCCTCCTTCCTCCCCC | - | 6.53 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I004574 | chr4 | 4576041 | 4577727 |
|
Enhancer Sequence | CAGGGCCTTA GGGGAGGGTA GGTCATTAGG TAGAAAGTTG GGCATTGCAA GGCGAGAAAA 60
CAGTGTATGA GCTGCTGTGA AAGACATGGG AAGGGGAGAA GCTCAGGCTG TTTCTCCTCC 120
ACCAGAGAAT GCCCTCCTCC TTCCTCCCCC TTCCTCCCAA CACACACACA CACACAACAC 180
ACACACACAC ACACACACAC ACCAGTTTTC TCCCGGAAAC TGAGCTAATC CAGCCACGCC 240
CCGACAGACA TTTGCAGTGA TTTTACACAC ACACACACAC ACACACACAC ACACCAGTTT 300
TCTCCCTGAA ATTGAACTAA TTCAGCCAGG GCCCCCCTAC AAACGTTTGT AGTGATTTTA 360
CTCCCAGCGT GGACTCTCCT GCCCGGTCAG CTTCAAGGAT TCCTTTGGTC CCAGAAATAG 420
CCAAGGTGGC GGTGAAGGGA GGAGCTGTTT CATTTCCGAA ATGAAAAAGT TTAAGATAAT 480
TACACAGACG GCTTGAGCCT GCAATGGACA AAAAGTTTCA TTATTGGACC CCTTTGGGGA 540
AGGCGCCTCC CATCCCCAAA GGAGCGGGTT AACCGCTCGG CTGGCGCGGC CCCGCCCGGG 600
TCGCCGTCTG AGAGGGACGG TCGCGCCCCC TTTGAAGTGC GGCCGCGCCT AATGAGGGAC 660
TCGCTGGGCC TCGGGATCAA GTGTCAGCGC CGCCCCAGAC GCCGCAGGGC AGACAAAGGG 720
CGCGGGCCGC CTGGCGGCGC TGGGAGGAGC GTGCGGCCCG CGGCGCTGAG CGGGACAAAG 780
GCGGAGACGG GCGCGCGGCG GGGTCCCACG GGCAGAAGAG CCTGGCCTCC AGCGCCCGGC 840
GCCCGGTTCG CTGCCTCCGG AGCCCCCAAG AGCCTCTCTG AGGGCGGGAG CGGTAGCGCA 900
GGCCACGCCG ACGGCGACCA CAACGCGCCT GCGCCAAGCC CCGGCCCCAG CGTAACCTCG 960
TGGGTGACAG TGTGACCTGG GTTTTCTCCG ATACGCGCGA TGTGCCCGCT GAGGGCAATA 1020
TAGCACCCCC CTCGCACCTC ACCCTTAGGC GTGCCAGGCA CTCTTCTAAA TCCGAGCTTC 1080
TATTAACCCA TTTCCTGTCC TGCATCACTT TGCAAGGTGG GTGGGGTGAG TAGCCCCATT 1140
GTCCAGCTCA CTCCATTCTA CAGATCAACC CATTGTATAG CTCACCCCAC TGTCCAGCTC 1200
ACCACATTGT ACACGTCACT TCATTGTACA CATCAGCCAT TGTACAGACC ACCCCATTGT 1260
ACAGATCACC TCGTTGTACA GATCACCTCA TTGCACAGAT CACCCCATTG TACAGATCAC 1320
CTCATTGTAC 1330
|
