| Tag | Content |
|---|
EnhancerAtlas ID | HS165-14823 | Organism | Homo sapiens | Tissue/cell | Ramos | Coordinate | chr8:6777600-6778810 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYCN | MA0104.4 | chr8:6778387-6778399 | GGCCACGTGGTC | + | 6.52 | | MYCN | MA0104.4 | chr8:6778387-6778399 | GGCCACGTGGTC | - | 6.52 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATACTGTAAC CCTGAATATG CGTACGTCTA TTCAATAGTT ACCCTCACCC TAGTGTTCCC 60
TCAGAGGGGC ACACAGAATC CTGGTTGCTA AGCATTGCTT TGGTGCATGC TGAAGATCCC 120
AGTAACTTCA AGCTCTCTTT ATTTTGAATT GTATGTCTAC TAAGGGGAGT GACCTGGGTT 180
CCAGTGAAAT GGTTTCCACT GCACCTGCTC CTTTCACTTC CTCCCCTGCT CTGTCCTCCC 240
CTTGCTCACC TCTCTTTCAA TTTCTCCTTA GCCTGCCTTG CCTTTAGCAG GAGAAGAATG 300
GTGAGAATAG AGAGAATCTA GTCCTGAGCA TGGTCGACCT GGGTTCTGGG CAGGTTACCT 360
GTGCCATGCC CTTATTCTAC CCGTTGGCCT GTGCAGGGAG GTGAGCACTG AGGAAAGACA 420
GGTGTGTTCA CTCTGCCCAG GTGAGCTCCG GGATGGGACT CCCTAGGAGG GATCGTGGGG 480
AGGGACGTCC AGGCTACCAT TCAGGGCTGG CCATCTGGGC TTCAGGGACA TCCTGACGTC 540
TTTGCCTTGT CCTGTGGTCT CCACAGAGAC AGTGTTGGGG CTCCCCTGAG TTGCTGTAAT 600
TCCACAAGTG GGGAGCTCCC CTCACATCTC TCTGCTTCCT CGGCCAACCC TCCTCTCCAG 660
CTGCCAGGGC CCTGTCTACC TGACACTTGG ACCTTGCTGC ATATTTCTCA GCTTCCGTCC 720
ACCTCTCCCA TCTGGCTGTC TTTGTGTGTG TGTGTGTGTG GCTTTGTCAG TTACGGCGGG 780
GTTTCTGGGC CACGTGGTCC GTGCTGTTTG AGCCATCCTG AGCTAGAGGC TGTACCATGT 840
CTCTAGGGGA AGGGGTGGGT ATGAGGCCTG GAGAACTTTC AGGGCTGTCT TGCGTGGAGG 900
ACTGTCTACA AGGTTTAGGA GCCGGGATAA AGGTAGTCCC TGCAAAGCCC GGACAGCCAC 960
AGCCCACCTC GGGGGCCATC GAGTGCTACC TGGGAGGTCT CCTCCCCATC ATTTGCTCAG 1020
GCTACGTGTT AGTCAGGTTC TCCAGAGAAG CAGAACCAAT TCCTTAACTG TGTGGTGTGG 1080
TGAGCCACAG GCCAGCAGGC TGGAGACCCG GGGAGGAGCT GCAGGCCAGT CCCGAGGCCA 1140
CCTGCTGCCA GAACTCCCTC TTGCTCTGGG GAGGTCAGTC TTTGTTCCAT TCATGTCCCC 1200
TCCTCATTAT 1210
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