| Tag | Content |
|---|
EnhancerAtlas ID | HS154-09154 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr17:20811310-20812780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr17:20811984-20811995 | CGCGCAGGCGC | - | 6.14 | | TP63 | MA0525.2 | chr17:20812320-20812338 | TGCATGTCCCAACTAGTT | - | 6.1 | | Zfx | MA0146.2 | chr17:20811361-20811375 | GAGGCCGGGGCCGG | - | 6.14 |
|
| | 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 |
| GH17I020907 | chr17 | 20811041 | 20812752 |
|
Enhancer Sequence | ATTAGGGATG GGCCTGCGCG GTGGCTCACG TCTGTAATCC CAGCACTTTG GGAGGCCGGG 60
GCCGGCAGAT CACGAGGTCA GGAGTTAGTG ACCAGTCTGG CCAACATGGT GAAACCCCGT 120
CTCCACTAAA AATACAAAAA TTAGCTGGGC ATGGTGTTGA ATGCCTGTAA TCCCACCTAC 180
TCGGGAGGCT GAGACACGAG AATCGCTTGA ACCCAGGAGA CGGAGGTTGC AGTGAACCGA 240
GATCATGCCT CTGCACTCCA GCCTGGGCAA CAAAGCAAGA CCTTGTCTCA AAAAAACAAA 300
AATTACGCAT GCCTGTTTTA CTTGTTTTCC AGACTTGTCT CTGGCTTGAT CAGGGCATAT 360
AACTATGTAT TTTTTGTATC TGTGTAACAA AAAATATGTT GGTTTTTAAA AATAAAAACA 420
TAAAAGGAGC CTCCAGCCCG CAGCGGCTGG AGCCGGAGGG TGCGCTTGAA CAGGCCAGGG 480
AGCCACGAGG CGGCGCAGGA CCTGAGCCCA GAGAAACGAC CTGGAAAGGA AGCTTCTCAC 540
AGAATGCGGC GCGGACAGCG GCTGCCGAGC AGGGGATCTG GAAAGCACTG GCCCCTGAGC 600
CCCAGCGCAG CGCAGGGTGT CGCAGGGGTT AGCCCGGGTG GCGGGAAGAG CCCAGGGAGC 660
AAGGCCCCCC CCCACGCGCA GGCGCGCTGC GCTCCCCCGC GCTGTGACAT CATTGATGAC 720
CCCGCGCAGA GGCCTCCTCA ATGCAGGCGC CTCCCTCTCA GCGCTAGAGC CCAGGCCACT 780
GCCAGGGAAG TGTCCCTACC AGGCGAGTGG CCCTGCCAGG CCCTCCTGCT GCTGCTCGCG 840
GTCGCTCGCC AGGAAAATTT TATGTGGCAT GTCCCCTAAA AGCGCTCGCA TTTCAGGGTA 900
AAATGTTTTA ATTATGTTGC AGCCCTTTAA AACAATCGCT GATCATTATT GATTTCCTCA 960
GGTATTTATT GTCACAATAT TAATCATGAT GACCTCGCTC GGTATTAATA TGCATGTCCC 1020
AACTAGTTCT TGCAGTGATT AATTGCACAA TTATTTTAAG GGTTACCAGT TTTCCTCATG 1080
TCTCCTACGT GGCAGGAGTT TGGGTTGCAT TTTTGCAGAT ACAGGGTGCA GCAGGTACAC 1140
TTGTCCTCTA CCTTCGGGGT CAAAATCAGT CCTGTGTTTA AATCTCACAG GCTACTTGAG 1200
CTCCTTGCTC TCCGTTTTCA TTCGTAGTCT CAATATGCCA ACTTTATTAA TCTTTTAAAG 1260
ATTACTCATC CAATACAGGT GACTGTACAT TAAATATGGA TGGAAGTTGG CCTGTGAGGA 1320
AATACATTAT TTTTTAAAAG GCAACCAACA AGTACTAGTT CTTAACTAAA AAGTGGGGGC 1380
AAGCTGAGAA ACTAAAGCAG AAAAGGAAAT TTTACCAGTC CGAAATAGAT CCATTCTCGG 1440
AATTCACAGA ATTTTCATAA CATCTGACTC 1470
|
