| Tag | Content |
|---|
EnhancerAtlas ID | HS105-49604 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr20:25841860-25843010 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr20:25842306-25842317 | CGCGCATGCGC | - | 6.02 | | NRF1 | MA0506.1 | chr20:25842307-25842318 | GCGCATGCGCA | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACACACACAC ACACAGAGTC CTTGAGCAGA GGCATTGAAA CACACACCCT AAGGCAACCC 60
CTGAGGCTTC GGGGTTCTGC TCTTGGCGAG ATCGACCCTC GGGTGAGGGA GCACCGCAGG 120
GGTACTCAGG CCGACCAGTC CTCGAGGTCA CGGCGGCACG ACTTTTGGCG AGACTCACCC 180
CAACCAACAC CGTCCGGGCA GCCCTGAGGC TGGGATGCCG TGCTGCCTCC CCCGGACTCC 240
GCCTGGGATT TCCTCATTCT TGTCAGCCCT TTGCGAGTCC TGGCATCCGG AGACGTTCCC 300
GTCGACCCCG AGGAGAGGTC AGGCCGGAGC CTCAGAGCTC CGACACACAA GCACTGCCAC 360
GAAGGGCTCC TGCTTTGCCA AGCCTCGGGG ACTGGTTTCT AAGACAACCG TGGGAACCAC 420
TGTGACGGGA GAAGAGGCTC GCGCCTCGCG CATGCGCATT GGCCCGCCCG ACTGGCGCTC 480
CGCTCCTGGC GGTCAGGCTG CGTCCCCTTT AAATAACGCC ACCGCAGCGC GGCGGCAGCG 540
AGCCTCCTGC TGCAGCCGCG GCGGCGGCTG GATCCGGGCT CCAGTTTGTG GCGGCTTGGG 600
AGACCGGACC GTGGGTGTCT TGTCCTGTCC CAGGGCCAAA CCCCCAGGAG TCCTGTCCTC 660
AGGAACTCCT TGAGCTGACT TCCACCGAGG GAGGGAGGGG GAGCTTCAGG ACGCCTGCTG 720
TGTTCTCAGG ACACCCCTTC AGATCCCATT TCGGCCCCCA CTGAGTGAGA TAGGATGGGC 780
TCGCCACATG CGCTGAGGCA GGCAGGGCCT CGCTGCAGCC AAGAATGATC CCATAGGTCT 840
CGAGGCCAAG TGTCCGCTGC AAATTCACTG ATCCTTCAAC CCTCTGCCTC CCTCCTCCTT 900
TGAAAGAGCA GTGGCCTACC CCTCTTCTAA AAGCCCTGGG GCTCAGGAAA GCCGACCGCG 960
CTTTACAGGA CTCGTGCAAA CAAGAACAGG GGAGATTGCG AGGTGGAGAC CATGTGAACA 1020
CGAATGGCAC TGGCGTATCC CACAGCAGAT GGTGTGAACG TGTGTCACCG GAGGCAAACC 1080
GGGCGACAGC GAAAGAAACG GTGGTGTCCA GGCATGTGCC GGTGCAAGGG GGGAACGAGT 1140
GACCTATCCA 1150
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