| Tag | Content |
|---|
EnhancerAtlas ID | HS076-41802 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr3:184218050-184218960 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr3:184218483-184218498 | ATGCTGATTCAGCGT | - | 6.42 | | MAFF | MA0495.3 | chr3:184218483-184218498 | ATGCTGATTCAGCGT | + | 6.43 | | MAFG | MA0659.1 | chr3:184218480-184218501 | CAGATGCTGATTCAGCGTTTC | - | 6.13 | | MAFG | MA0659.1 | chr3:184218480-184218501 | CAGATGCTGATTCAGCGTTTC | + | 6.32 | | MAFK | MA0496.2 | chr3:184218481-184218500 | AGATGCTGATTCAGCGTTT | + | 6.23 | | MAFK | MA0496.2 | chr3:184218481-184218500 | AGATGCTGATTCAGCGTTT | - | 6.2 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGGAGCCTC TGTTCCTGTA GCAGGGCCAG AGACACCAGC ACCATATAGT AGAGTGAGTA 60
GAGAAGGAAG AACATTGCTG GCAGCAGGTG TCCCTCGAGG GTGCCCATGG CTTTAGTGTG 120
TGTGTTGGGG CCAACGGGGC GAGAGCTGGT AGATGAGCAG CAACCTCACA CACACATGAC 180
CGGCATCCTC ACAGGCAGGA GTGGCTGCCT CTGAACCACG GAGAGATCAT GCTGACGAGC 240
CCCACCCCTG CCTCCCACAC ACAGAAAGGA ATAGGTCTTG TTGCAGAAAC CTGAGCCACA 300
CCCCAGGGTG GGACGCCTTT AAGAGGGTCC TCCAGGGTGG GACCGCTGCA GCCACCTTGC 360
TCTGCTCCTT ACTTAAATCG GCTAGGCCCA GCATTTCAAT CTGTGCACCT CACTGCAGAT 420
GTCAGTTTCA CAGATGCTGA TTCAGCGTTT CTTTCACCAG CCCCTCTGCC ACAGCGCCCT 480
ACCCCTGCAG AGAGGAAACA AAGAGAGTGA AGGAGCTCCA GCAAAGAGGA GTAGGGCTGA 540
CTCTCAGGCT GACTTTTCTC TCAGTGCTTG GCACAGTACA TACTTTTCTC TCATTTAACA 600
ACTCTATGAG GGAGGTGTTA TTAGGTGAAA TTTTACAAGT GAAATGAAGG TCCAGAGCGG 660
TGCAGAGACA TGCACAAAGT GGTCCATCTG CCAGCTGGCA CAGCAGAGCC AGGACGTGGA 720
CCCGGGTCTG CTCATCCAAC AAAGCCTGAA GTTTATGCAC AGCAAAACTA CTGACATTCA 780
CTTCCAACCC CGTAATCATG ACTGTGGGGA ATTTACTTGG TCTTCTTGAG TCTCAGCTTC 840
CTGATGTGTA GAATGGGAAT AATAATTACT TCATAGATTT GTTATGAGAA TTAAATGGGA 900
TTATATATAA 910
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