| Tag | Content |
|---|
EnhancerAtlas ID | HS098-23537 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:20811490-20812650 |
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 |
|
| | 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 | TCGGGAGGCT GAGACACGAG AATCGCTTGA ACCCAGGAGA CGGAGGTTGC AGTGAACCGA 60
GATCATGCCT CTGCACTCCA GCCTGGGCAA CAAAGCAAGA CCTTGTCTCA AAAAAACAAA 120
AATTACGCAT GCCTGTTTTA CTTGTTTTCC AGACTTGTCT CTGGCTTGAT CAGGGCATAT 180
AACTATGTAT TTTTTGTATC TGTGTAACAA AAAATATGTT GGTTTTTAAA AATAAAAACA 240
TAAAAGGAGC CTCCAGCCCG CAGCGGCTGG AGCCGGAGGG TGCGCTTGAA CAGGCCAGGG 300
AGCCACGAGG CGGCGCAGGA CCTGAGCCCA GAGAAACGAC CTGGAAAGGA AGCTTCTCAC 360
AGAATGCGGC GCGGACAGCG GCTGCCGAGC AGGGGATCTG GAAAGCACTG GCCCCTGAGC 420
CCCAGCGCAG CGCAGGGTGT CGCAGGGGTT AGCCCGGGTG GCGGGAAGAG CCCAGGGAGC 480
AAGGCCCCCC CCCACGCGCA GGCGCGCTGC GCTCCCCCGC GCTGTGACAT CATTGATGAC 540
CCCGCGCAGA GGCCTCCTCA ATGCAGGCGC CTCCCTCTCA GCGCTAGAGC CCAGGCCACT 600
GCCAGGGAAG TGTCCCTACC AGGCGAGTGG CCCTGCCAGG CCCTCCTGCT GCTGCTCGCG 660
GTCGCTCGCC AGGAAAATTT TATGTGGCAT GTCCCCTAAA AGCGCTCGCA TTTCAGGGTA 720
AAATGTTTTA ATTATGTTGC AGCCCTTTAA AACAATCGCT GATCATTATT GATTTCCTCA 780
GGTATTTATT GTCACAATAT TAATCATGAT GACCTCGCTC GGTATTAATA TGCATGTCCC 840
AACTAGTTCT TGCAGTGATT AATTGCACAA TTATTTTAAG GGTTACCAGT TTTCCTCATG 900
TCTCCTACGT GGCAGGAGTT TGGGTTGCAT TTTTGCAGAT ACAGGGTGCA GCAGGTACAC 960
TTGTCCTCTA CCTTCGGGGT CAAAATCAGT CCTGTGTTTA AATCTCACAG GCTACTTGAG 1020
CTCCTTGCTC TCCGTTTTCA TTCGTAGTCT CAATATGCCA ACTTTATTAA TCTTTTAAAG 1080
ATTACTCATC CAATACAGGT GACTGTACAT TAAATATGGA TGGAAGTTGG CCTGTGAGGA 1140
AATACATTAT TTTTTAAAAG 1160
|
