| Tag | Content |
|---|
EnhancerAtlas ID | HS151-09338 | Organism | Homo sapiens | Tissue/cell | OCI-LY1 | Coordinate | chr5:1764870-1766170 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr5:1765340-1765353 | TGCAGCTGTCTCC | + | 6.24 | | Myog | MA0500.1 | chr5:1765339-1765350 | CTGCAGCTGTC | - | 6.62 | | STAT3 | MA0144.2 | chr5:1766058-1766069 | TTTCTGGGAAG | + | 6.02 | | Tcf12 | MA0521.1 | chr5:1765339-1765350 | CTGCAGCTGTC | - | 6.14 | | YY1 | MA0095.2 | chr5:1765927-1765939 | CAAAATGGCTGC | + | 6.52 | | ZNF263 | MA0528.1 | chr5:1765496-1765517 | GGTGGAGGAGGAGGGGGGGCT | + | 6.13 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 1765291 | 1765456 | | chr5 | 1765231 | 1765394 |
| Enhancer Sequence | CGACTCCTCA CGTCCCCGCC TCCAACGCCA CAAGCCCGAC CGTCCTCCCC TTGGGTTCTG 60
CTTCTCCAAC ATCATTGCCA AAACCTCATT CATTACAAAT TCCAACTTTG TCCCAGAATA 120
ACAAGCACAG CTAGGACTGT TGGCCACTTG CTGGGCTGTG GTCCCTGCCC TGTGCTGGCT 180
GGTTGGCACA GATGCTCTTT AACCCTCCAA AGAAGCGTCC CCAGGAGCCC CTCCTCCTCC 240
TCCTGGCATG TCTGGATTCT CTGCAGGTAT TTGGGGTGAT ACACCCACCT GTCTTTCTTC 300
CCCCACAGGT GCTGGGTTCC TGAGGCAGGG GCTCAATGCG CATGGTCTTA GCATCTGACC 360
AGTGCCAAAA AGTGGCAGCA ATGTGGTGCC TGACTGACTT ATGAAAGAAT GCATCAGGCA 420
TGAGCTGGAC CTCAAGCTCT CCGCATTCCT CCTGGGTGGT CGCCTTAGTC TGCAGCTGTC 480
TCCACCAGGG AGGAAGGTAT GCAAAGCTAC AGAACCACAT AGGGTGGGGC CACAGCACGG 540
GCACCTCTCA GCTCCCCCTG AGTGAAACTT GCTTCACGGG GCCAGGTGTC AGGTGGAAAT 600
GTTCTCTTTG GTGCCACTGA TCCCATGGTG GAGGAGGAGG GGGGGCTGTT GCAGCAGCCC 660
AGGTGGGAGC TGCACACCCC TCTGGCCAGG TGGCGGGGAC GGCCGGCCTC TGTTCAGCAC 720
GGCCCACTGC ACAGGTGGGG GATGGCCAGC CTCTGTTCAG CACAGCCCGC TGCTGGCTGC 780
ACATCTCACG GGTCTTGTCC CAGCCTGTTT CTCCCACCAC CTCTCAACAG TTAGGGAGGT 840
TATGTTTTTA AAGATGTTTT TGCTGACTTC AGTGGTATGA CGGACTCCCA GAGACCAACC 900
CAGTCGAAGG ATTTGAACCT CTAGGGGTCT GTCACCCCTC ACACCTCCTA CAGGGTGGGA 960
GTTGGGCCAT TGCCAGGGCT GGGTCTGGTG CTCCATGAGT TAAAGACCAC GCTGTCTGTC 1020
TCTTGGTCTT CCCGTCATCC TTTGTTCCTC ATAGTTGCAA AATGGCTGCT GGAGCTCCAG 1080
ATGTGGGCCA CATCTCCCTT TTGTCAGAGC CCTTCTGACG GTGAATTTTA TGTATCAACT 1140
TGGTGAGGCC CTGGTGCTCA GCTGTTGAGT CAAATGCCAG CCTAGATGTT TCTGGGAAGG 1200
TATTTTTTAG ATGTGATTAA CATTTAAGCT AGCACACTTT GAGTAAATAG ATTACCACCT 1260
CCCCTCCCAC CATTGTGTGG TGGGCCCCAT CCAATCAGTT 1300
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