| Tag | Content |
|---|
EnhancerAtlas ID | HS095-02249 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:167012780-167014110 |
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 | TTCTGGGGAA AAAAAAAAAA TCTATAAGAC AGCCCAGAAC TAACATAGTT AGACCTGAGT 60
TTGGGCTCTA TCTTTGTCAC TAACCAGCTG CATGTTCCTT AACAAGTCAC TTTAATATCC 120
CGAGCGTTGG TTTCCTCATC TGTAAACTAA GATGAATAAT GCCTGGCTGA TAATGTGGCT 180
GTGAAGATTA AAATGGGTCA TGCCTTTGAA TATGCTTTAT AAAATTCAGT TCTTCTTTCA 240
TTTCCTCAGC CGATTGCTCA TGTTCCTCTA ATACACTGTC CCCACCCTGG ACAACCTCTA 300
GCAGGTATAT GCACACCTGA AGATACTGAG ACAGGGAGAC TGACTAGTTG AGATTCACTG 360
AGGCTGATGT GTCTAGAAAG TTGCTCACTA AGTATTCCCG CAGGGTGTTT GAAGCCTCTT 420
CCTGGATGCC TGGTGAGACG AGACACTTTG AATCCACCTT GCAAAGCTCC TGCTCCAAGA 480
CAGCTGCAGC TTGTGCTCTG TAGAGCGATA TGAAATAATT GCCCGTTGGC ACAATAAGCC 540
CATCTCCTCT CCGGGCAGCA CAAAAGAAAG CTCAAAAGCA TCTCCGGTTT TGATTGCCAA 600
GTGGGGGAGG CAGTGAAAGT ACACTAAATT ATGAGTCCAG GTGCCTCTCT ACAGAAATCC 660
ACTTCCGCCT CGCTGCCGCT CTGAAGGCGC GCAGTGGGTG TTGACGTCAC CTTCGGCCAC 720
AGGAGCTTGG AGAGGCTGGG GCCCTGACTC CCCGCGGGAT CCGCTGGTAG ACCAGGGCGT 780
GCTCTCAGAC TGGAAGTGCA GGAAGGCTCG CTTACTCTCG CCATAGACCA GACTGACAGG 840
GGTCTGCCAA GGCTGCTGGG AATGTGGGAA GTGAACTTTA GGTGGAAACA GAAAAGCTTC 900
TCTCTCCGTG GGTAGCCTTT TTTTTTTTTT TTTAGTTCAG GAGAGAAAAA AAAAATCATA 960
GAAGCCTGCC AAGCCAAATA AACTATGCTC AATTAAGTCT TTCAACTGTG CAATTCCTCT 1020
TGTTGATTTT ATGAGGAAAA GGGCAGAATA GAAACATGAT GGGCTTGTTT AAAATACTTC 1080
AAAAGGGAAG AACCTATATT CTCCTGCTTC CCAGACCGAC CTCTTTCGGG CTTTCCTTTC 1140
CTCCAGCCAT GCTGCAGGCC TTTCACTGTC ATCTCCTCCA TCTGTGATAA AGCTGTCCAC 1200
AGAACCCGTC CTCAGCTGCT TTCTCACCAC ACACCCTCAC TCAGGGCATG TCCTCCATGT 1260
CATGCCCCTC ATCCAGGCCT GTGACTCCCA AGGAGCTGAA TCAGCCAAAA CTCTCCCTCC 1320
CCAACCCCAA 1330
|
