| Tag | Content |
|---|
EnhancerAtlas ID | HS076-52860 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr7:158702780-158704170 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr7:158704087-158704097 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr7:158704087-158704097 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr7:158704087-158704097 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr7:158704087-158704097 | AACAGCTGTT | - | 6.02 |
|
| | 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 |
| GH07I158911 | chr7 | 158703941 | 158704090 |
|
Enhancer Sequence | TCTGCCCTTG CGAGTTTATA TCCCAGTGAG GAGTAACAAA CAAATATCTT AAGGATTTGA 60
CCCCGGGCAC ACTAATGTTA GGGTGAAACT TAGGAAAGGA AAACCCAGCA CAGGCGATGG 120
AAAAGGAACT GTTTGTGAAG CAAGAGGAAG CCACGTGGGT GCGGCGTTTC GGGGCCTGTG 180
GGCAGAGGGC CATCGGCCGT GTCAGGCCTG TGGGTGCAGG GCCATTGGCT GTGTCAGGTC 240
TGTGGGTGGA GCATGATGGG CTGTGTCAGG CCTGTGGGCT GAGGGCGATT GGAGGGCGAT 300
CAGCTGTGTC AGACCTGTGG GAGCGCGATT GGCTGTGTCA GGCCTGTGGG CCGAGGGCAA 360
TTGGCTATGT CAGGCCTGTG GGCCGAGTGC GATTGGCTGT GTCAGGCCTG TGGGTGGAGG 420
GCCATTGGCT GTGTCAGGCT TGTGGGCGGA GCACGATTGG CTGTGTCAGG CCTGTGGGCT 480
GAGGGTGATT GGAGGGCCAT CAGCTGTGTC AGGCCTGTGG GCCGAGGGCA CTTGGCTGTG 540
TCAGGCCTGT GGGCCGAGGG CAATTGGAGG GCAATTGGCT GTGTCAGGCT CGTGGGCCGA 600
TCACTATTTG CTGTGTCAGA CCTGTGGGCG GAGGACGATT AGAGGGCAGT TGGCTGTGTC 660
AGACCTGTGG GTGGAGGGCC ATTGGCTGTG TCAGGCCTGT GTGCGCAGGG CGATTGGCTG 720
TGTCAGCCTG TGGGCCAAGG GTGATTGGCT GTGTCAGGCC TGTGGGCGGA GGGCGATTGG 780
CTGTGTCAGG CCTGTGAGCG AGGAGCGTTG GCTGTGTCAG GCCTGTGGGA GGAGTGCGAT 840
TGGCTGTGTC AGGCTTGTGG GCCAAGGGCG ATTGGCTGTT TCAGGCCTGT GGGAGGAGCG 900
CGAATGGCTG TTTCAGGCCC GTGGGCCGAG GGCGATTGGC TGTGTCAGGC CTGTGGGCGG 960
AGGGCGATTG GAGCGTGAAA GGCAGGTCAA GTCCTGGGGG AAGCACAGAG GTTGGCTGTG 1020
GCCTGGAAAA GAGCGTGGCC CAAAACACTT ACTGGCTGCG TGGTCCGACC ATGGTGCAGG 1080
TGATTGCATA GTCAGTATGT CAGCTCCTGA AGTCAAATGA ATTAGTCCTT AGGAACATCC 1140
CAGGCATATA TGTTGTGTGA CTTGATTTTG TGTTAGCTCA GGCATACGCA TTAGAACGGT 1200
CACACATGAG GTTCGTGACA CACACACGAG GCAGTCGGGG AGCAGAATCA CCAAATGCCA 1260
AGGTCACACA CCAGGTTCCC ACGACTGTCT ACTACTCAGT TATTTTTAAC AGCTGTTAAA 1320
TATCTCAGAC TCACCCCAGC CTGAAGCTAG GTTTCTGACA ATAACATGCA TTTAACTCTA 1380
AGTTTACTTC 1390
|
