| Tag | Content |
|---|
EnhancerAtlas ID | HS098-25359 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr17:78429970-78431580 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr17:78430881-78430893 | CGCCCCCAGACA | - | 6.52 | | ZNF263 | MA0528.1 | chr17:78431129-78431150 | GGAGGAGGAGTTGGGAGAGGC | + | 6.54 | | ZNF740 | MA0753.2 | chr17:78430161-78430174 | CCCCCCCCCCCAC | + | 6.92 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCATGAGGCC TGAGGGGCCT GCTAGTGCAG GGGAGGAAGG GAAGTTCAAG CAAGCAGGCT 60
CAACGGAGGG CTCCACCCTC CAGGTACGGC CAGGTCCTGG GAGAAGGAGG GGAAGCAGTC 120
TGGTCCAGGA GAGAGGCAGC AAGGGCAGAT GCTAAGCCTT TGCCTCTGCA CTCCCTGGGG 180
ACCTCTGGGG ACCCCCCCCC CCACCCAGCA CTAGTAATCA AAGGAGGACA GACACCTACA 240
CACGTGTCCC ATATGTCTCA CCCTAGCAGG CAGCGAGAGG ATGCCCAGTG TTACTCTGGC 300
CCCCTGGAAG GCTAGCTTGC TCTCCTGGGC ACAAGTCAGA AGCAGTGTGA ACTGGAGTGG 360
GTGGTGGGGG ACACCCCTCC CGGTGAGCCC CCCCTCCGAC CCGGCTGTCA GTGATCCACA 420
AGTCTGGCCC ATCAGCCCTC CCTGCTGAGC ACACAGTCCA CTGACCCTTC TTCAGAATTG 480
TGGGAATGAC CTCACTGCCC CTCCAAGCAA CGTGTTGTGC TGCCGCCCAC ATCAGACATC 540
CGGGGAATGG ACTGCACAGC CTCCATGTGT GCTGGCTCCT TGGCGCCTGC AGAGCCGGGT 600
TGATTCTGTC TTTCCCTTCA ACTCTTGTCT TAAAGGATAT CCTGAGCGTG CCGGCTCCTC 660
TGCTCAGAGG GTGTTAGGGT GGCGGTGGCA GTGGGCACCT CTCTGCTCCT CGGCTGGGTG 720
CTCAGCCTCG CCAGGCTGCC TGGAGCTGGT GGAGCAACAG CCTTGTCCCC CGTCCAGCTC 780
TCTGCAGCTG CCCTCTCCTG TCAGAAGCTC CTGGAAAGCA TTTCTGGCAC ATAGAGGCCA 840
TCTGCATGTT CTCCTCCTGC CCGCCCCACC CCGAGTAGCC ACAGAGGATC TTCCCCAGCT 900
GCCTTCACCT CCGCCCCCAG ACAGAGCCTC CTGGCTACTC CCCCAGATAG TGTCTCCAAA 960
ATCACTTCCA TTTCTCCTCT GCTCGCAGCC ACTCAGTGGC TTTCGTTATC ATTCAGAATA 1020
AAACCAAAGC GTCCATTACC ATCCAACCAA AGACCCCAGG AACGCGCTGC AGTGGAATCA 1080
AGCCACGTCT GTTGACTGGT TGCTGTGAGA GGATGTTAGG AAGGACCCGC AAGTCTCCTC 1140
GTGTTGGGAG AGCATGGTGG GAGGAGGAGT TGGGAGAGGC TCAAGGCAGC AGGGCTGACT 1200
CCACAGCTGG GTATCTTGAT AACTTTTATC TAGAAGGCAG GAAGAACAAA ATGCAGCTGA 1260
AGCTGAAATT GATCAAGCAG CAGCGGTCAT TCAAATTAGC CAGGACGGGG TGGTTTGGTG 1320
ACCCTTGAGG TCTGGCCGAT GCTCATGTTC TGCCTATGCT CTGACACGAT CCTGTGTATC 1380
TTGCCCCATC TCGGGCACAC AGTGGTCTTG TCTGGTGTTG GTGTTCAGTG ACATTGCTTA 1440
GCCATGAAAT TGTCTCCAGG TTAGTGACTA GTGACGCCAG GGTGGGTGGC TCTTCTCTTT 1500
TTCAAGACCT GGGTGTCACC TGACCCCCAG CTGCCTCTGA CTCACCTGCC ACTGCCCTTC 1560
TTATCCACAC TCTTCCTGAC AAGCTGGTTT CCTGTGTGGC CGAACAGTTT 1610
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