| Tag | Content |
|---|
EnhancerAtlas ID | HS187-22812 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr7:75795410-75796350 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr7:75796011-75796022 | GCGCATGCGCA | + | 6.32 |
| | | 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 |
| GH07I076162 | chr7 | 75791992 | 75796918 |
| Enhancer Sequence | CCGGCCAGCC CTATTTATTT AAGCCTATAC ATTTTGCACT TGTTAAAAGT ATTTGAACAT 60
ACAATTACCA TGTTTTCTTT AAGCGGTCCC TCCCTGTTGC ACACTTGGAT AGTTTATTTT 120
TTTAGACAAG GTTTACTTCA GTCTCGCAGG ATAGAGTGCT GTGATGGGAT CATAGCTCAT 180
TGCAGCCTTG AACCTTGGGG TTCAAGTATC TGGGAAGCTG AGGAGGGACT ACAGAGATGG 240
AGTCGCGCCA TGTTGCCCAG GCCGCTCTTT AACTCCTGGC CTGAAGGGAT CCTTCCGCCT 300
CGGCGGAGCC CGGACATAGT TTTCTAGTTT TGACCCACAG AAACACTGTG CTGGGTCGGA 360
GTTTGTCAAC TACCCTTCTC CAGCCAGCAA CACACAGAAC ATGGCGGGGA AGTCACGGTC 420
ACCAGGCTCC AAACCGAGGA GAAAACAGCC CAGCTCCAGG CACTGTAGCG TCACTGTGAC 480
ATCGCCGAAG GCCGGCGCTA TTACGTCGCC GGAAGGCCCG CGCCTGTGAC GTCAGCGGAG 540
GCGCGCCCCT TCTGTAGAAC CAATCGGAAC TCGAGGCGCG GCGGCTGGGT ATTCCAGGAG 600
AGCGCATGCG CAGACGCGTG GCCACAGACT GCCGGTCAGT GTCAGTAGGC GGCGGGTTAG 660
TGTCCGCAGG CTCCGACTCG GCCGCCGACA CCAATAAGCT ACAAGGACGA GCTTTACCAC 720
TGCCTGTACT ACTGCTACCT GCGCGACTTC CCAGCCTGCG GCGTAGGGCG CAGCAAGGGC 780
CTGACGCTGA GCGAGTAGGC GCTGCGCACC AAGCGGCTGT GGCCCGGAGG GCACTGTCGG 840
GCAGAAGCTC CTCAGTGGCC ACCACAAGCC CGCTAGCTCC GGCTACAGCC CTTGCCGCAC 900
ACTCGCGTCA CCTGAGCCTG TGTAGGTGCG CCCCCCCAAC 940
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