| Tag | Content |
|---|
EnhancerAtlas ID | HS064-01021 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr1:167012660-167013780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:167013258-167013269 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr1:167013258-167013269 | GACAGCTGCAG | + | 6.14 |
|
| | 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 |
| GH01I167043 | chr1 | 167012838 | 167014050 |
|
Enhancer Sequence | AGGAAGGCTG CCCTGAGCTG ATAAACCATA TAGATTGTTC CTGAAGGGAG AGACTAAGGC 60
TCATGGTATG AATTGTACTT AAGCAACTAA CATCTTTATT TAAGGGTTCT CTCAATCTCT 120
TTCTGGGGAA AAAAAAAAAA TCTATAAGAC AGCCCAGAAC TAACATAGTT AGACCTGAGT 180
TTGGGCTCTA TCTTTGTCAC TAACCAGCTG CATGTTCCTT AACAAGTCAC TTTAATATCC 240
CGAGCGTTGG TTTCCTCATC TGTAAACTAA GATGAATAAT GCCTGGCTGA TAATGTGGCT 300
GTGAAGATTA AAATGGGTCA TGCCTTTGAA TATGCTTTAT AAAATTCAGT TCTTCTTTCA 360
TTTCCTCAGC CGATTGCTCA TGTTCCTCTA ATACACTGTC CCCACCCTGG ACAACCTCTA 420
GCAGGTATAT GCACACCTGA AGATACTGAG ACAGGGAGAC TGACTAGTTG AGATTCACTG 480
AGGCTGATGT GTCTAGAAAG TTGCTCACTA AGTATTCCCG CAGGGTGTTT GAAGCCTCTT 540
CCTGGATGCC TGGTGAGACG AGACACTTTG AATCCACCTT GCAAAGCTCC TGCTCCAAGA 600
CAGCTGCAGC TTGTGCTCTG TAGAGCGATA TGAAATAATT GCCCGTTGGC ACAATAAGCC 660
CATCTCCTCT CCGGGCAGCA CAAAAGAAAG CTCAAAAGCA TCTCCGGTTT TGATTGCCAA 720
GTGGGGGAGG CAGTGAAAGT ACACTAAATT ATGAGTCCAG GTGCCTCTCT ACAGAAATCC 780
ACTTCCGCCT CGCTGCCGCT CTGAAGGCGC GCAGTGGGTG TTGACGTCAC CTTCGGCCAC 840
AGGAGCTTGG AGAGGCTGGG GCCCTGACTC CCCGCGGGAT CCGCTGGTAG ACCAGGGCGT 900
GCTCTCAGAC TGGAAGTGCA GGAAGGCTCG CTTACTCTCG CCATAGACCA GACTGACAGG 960
GGTCTGCCAA GGCTGCTGGG AATGTGGGAA GTGAACTTTA GGTGGAAACA GAAAAGCTTC 1020
TCTCTCCGTG GGTAGCCTTT TTTTTTTTTT TTTAGTTCAG GAGAGAAAAA AAAAATCATA 1080
GAAGCCTGCC AAGCCAAATA AACTATGCTC AATTAAGTCT 1120
|
