| Tag | Content |
|---|
EnhancerAtlas ID | HS087-01996 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr1:167012840-167014220 |
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 | TTGGGCTCTA TCTTTGTCAC TAACCAGCTG CATGTTCCTT AACAAGTCAC TTTAATATCC 60
CGAGCGTTGG TTTCCTCATC TGTAAACTAA GATGAATAAT GCCTGGCTGA TAATGTGGCT 120
GTGAAGATTA AAATGGGTCA TGCCTTTGAA TATGCTTTAT AAAATTCAGT TCTTCTTTCA 180
TTTCCTCAGC CGATTGCTCA TGTTCCTCTA ATACACTGTC CCCACCCTGG ACAACCTCTA 240
GCAGGTATAT GCACACCTGA AGATACTGAG ACAGGGAGAC TGACTAGTTG AGATTCACTG 300
AGGCTGATGT GTCTAGAAAG TTGCTCACTA AGTATTCCCG CAGGGTGTTT GAAGCCTCTT 360
CCTGGATGCC TGGTGAGACG AGACACTTTG AATCCACCTT GCAAAGCTCC TGCTCCAAGA 420
CAGCTGCAGC TTGTGCTCTG TAGAGCGATA TGAAATAATT GCCCGTTGGC ACAATAAGCC 480
CATCTCCTCT CCGGGCAGCA CAAAAGAAAG CTCAAAAGCA TCTCCGGTTT TGATTGCCAA 540
GTGGGGGAGG CAGTGAAAGT ACACTAAATT ATGAGTCCAG GTGCCTCTCT ACAGAAATCC 600
ACTTCCGCCT CGCTGCCGCT CTGAAGGCGC GCAGTGGGTG TTGACGTCAC CTTCGGCCAC 660
AGGAGCTTGG AGAGGCTGGG GCCCTGACTC CCCGCGGGAT CCGCTGGTAG ACCAGGGCGT 720
GCTCTCAGAC TGGAAGTGCA GGAAGGCTCG CTTACTCTCG CCATAGACCA GACTGACAGG 780
GGTCTGCCAA GGCTGCTGGG AATGTGGGAA GTGAACTTTA GGTGGAAACA GAAAAGCTTC 840
TCTCTCCGTG GGTAGCCTTT TTTTTTTTTT TTTAGTTCAG GAGAGAAAAA AAAAATCATA 900
GAAGCCTGCC AAGCCAAATA AACTATGCTC AATTAAGTCT TTCAACTGTG CAATTCCTCT 960
TGTTGATTTT ATGAGGAAAA GGGCAGAATA GAAACATGAT GGGCTTGTTT AAAATACTTC 1020
AAAAGGGAAG AACCTATATT CTCCTGCTTC CCAGACCGAC CTCTTTCGGG CTTTCCTTTC 1080
CTCCAGCCAT GCTGCAGGCC TTTCACTGTC ATCTCCTCCA TCTGTGATAA AGCTGTCCAC 1140
AGAACCCGTC CTCAGCTGCT TTCTCACCAC ACACCCTCAC TCAGGGCATG TCCTCCATGT 1200
CATGCCCCTC ATCCAGGCCT GTGACTCCCA AGGAGCTGAA TCAGCCAAAA CTCTCCCTCC 1260
CCAACCCCAA CTCCAGGCGC TTATACCTCA CTCCCCACAG CTGTTTTTAT TATTCGTATT 1320
CACTGCTACT CAATCCCATC TTGTTTTCAA GAGGACTTAA GGTGGATTCC ACAAATACAT 1380
|
