| Tag | Content |
|---|
EnhancerAtlas ID | HS188-00227 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr1:26002080-26003660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:26002631-26002644 | AGAAACAGCTGCA | - | 6.29 | | Myog | MA0500.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.62 | | Znf423 | MA0116.1 | chr1:26002536-26002551 | TGCCCCCTGGGTGGC | - | 6.13 |
|
| | 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 |
| GH01I025675 | chr1 | 26002283 | 26003398 |
|
Enhancer Sequence | GGGGGGGAGG TGGTTACCCA GTGTGGGATT GCTGGATCAA ATGATAGTTC TACTTTTAGT 60
TCTTTAAGGA ATCTCCATAC TGTTTTCCAT AGTGGTTGTA CTAACTTATA TTCCCACCAG 120
CAGTGTAAAA GTGTTCACTT TTCACCACAT CCATGCCATG GCTGCTTTTT ATTGAGCACA 180
TATTATATAC GAGCCATTGT GCTCAACACT TTACATCTGT TATTTACTCT TAGGGTTATT 240
CTAAGGATTA AGTATTTCTG TCCTTTTACA GATGAGGAAA CTGAGACTTA CAGGGGTTAA 300
GTCACTCACT CAAGGCCACA CAGCCAGTAA GGTGGCAGAG CCCTAGAGCA GCCTCTCAAG 360
CTTCAATGTG CGTTTGAATC ACCTGGGGCT CTTGTTAAAC TGCTGCTACA GATTCAGCAG 420
GTGGGAGAGT GGAACTGAGG TACTCTGTTT CTGACGTGCC CCCTGGGTGG CCCTACTCCT 480
GGTCCCTGGA GCACTTTGAG CAGCGAGAGT TTCTCTGCCT GTATGGCCCA CACTCTCGAC 540
CCTGATGCCT TAGAAACAGC TGCAGACAGG ATGCGATTCC TGAGACTGCT CAAACCTGAA 600
ACCCCATGGG CAGGATGTGG GTGAGCTGTC TGGACCTCAG GTGGGTGGGA GTTGTATCAT 660
ATGCTCATTT CCCACATTGG CCTTTCAATA GCTTGAGTAA ACCCGAAACT GAGAGGGTTG 720
GAGGCAGCAT CTCCCCTTCT ACTCCCCCGC TTCACCTCCC CGGGCAACCA AACCCCACCC 780
GTGCCCAGCT TCTGAGCGAT AGACCTGGGC TGTGTATTTG CAGGAGCCTC ACTGGGGTCA 840
CCAACCAGGT CATGTTGTGT TGCCCCAATA AATGGAACTG GATCAGAAAA TCCAACGTGG 900
ATAGTTTTTA GGTGCCAAGC TGTCAGCTCT TCCCTTGGAC TGTGCTGAAA GTGGAAGAGG 960
AGAAAAAAAT CAACCCAATG TTCTAAGCTC TCTGTCTACA TAGTCATTAG ATCCCAGGAT 1020
CGTTAGAGAC CAAATCCCTT CCCACTTGGC CCCTGCAAAT GGGGCCAGGT GTCACTGCTG 1080
GGAGACGCCA GTAAGGCTGC ACGTCATGGT GTGAGCACTT GTCTTTAATG ACTGGGAAAA 1140
TCCATTTCCT TCCTTGGCAG CTTTGAATGT AGCAACTGTG GTTCTGGGTC ACTGCCAGAG 1200
CCAGCCTTGT GTGTATGTGT GTGATTTTTT AAAGTGGGGG AGAATGTCTC AATATTCAAT 1260
GCTCACCCCC TTCCTTCCAA GTTGTACCCC CAGAGAACTG TCCAACACAA ACTTTGGAGT 1320
TTTCCACTCT GGGAGTGGTC TGCTGGCACC CACGTGTCCT CCCCTCCTCT AATGCATCCT 1380
TTCTCTCTTG ATCTCATTGT TCTGGGGTCC TCAGCTGAGT GGGCATCTGT GCCTGGGTGA 1440
TCGATTCTAG TCTCTTTTCT GCAGGAGAGA ACTCTTGAGC TCTGAGACAG GTAGAAAGAA 1500
AATCTTAAAC CAAATAATAA TGTTCTGCCT CACACTAGTA AATATTTTGC ACTAAAAAAT 1560
TCCGTGTCAT TTTGATTTGT 1580
|
