| Tag | Content |
|---|
EnhancerAtlas ID | HS159-00111 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr1:26002400-26003960 |
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 | CAGCCAGTAA GGTGGCAGAG CCCTAGAGCA GCCTCTCAAG CTTCAATGTG CGTTTGAATC 60
ACCTGGGGCT CTTGTTAAAC TGCTGCTACA GATTCAGCAG GTGGGAGAGT GGAACTGAGG 120
TACTCTGTTT CTGACGTGCC CCCTGGGTGG CCCTACTCCT GGTCCCTGGA GCACTTTGAG 180
CAGCGAGAGT TTCTCTGCCT GTATGGCCCA CACTCTCGAC CCTGATGCCT TAGAAACAGC 240
TGCAGACAGG ATGCGATTCC TGAGACTGCT CAAACCTGAA ACCCCATGGG CAGGATGTGG 300
GTGAGCTGTC TGGACCTCAG GTGGGTGGGA GTTGTATCAT ATGCTCATTT CCCACATTGG 360
CCTTTCAATA GCTTGAGTAA ACCCGAAACT GAGAGGGTTG GAGGCAGCAT CTCCCCTTCT 420
ACTCCCCCGC TTCACCTCCC CGGGCAACCA AACCCCACCC GTGCCCAGCT TCTGAGCGAT 480
AGACCTGGGC TGTGTATTTG CAGGAGCCTC ACTGGGGTCA CCAACCAGGT CATGTTGTGT 540
TGCCCCAATA AATGGAACTG GATCAGAAAA TCCAACGTGG ATAGTTTTTA GGTGCCAAGC 600
TGTCAGCTCT TCCCTTGGAC TGTGCTGAAA GTGGAAGAGG AGAAAAAAAT CAACCCAATG 660
TTCTAAGCTC TCTGTCTACA TAGTCATTAG ATCCCAGGAT CGTTAGAGAC CAAATCCCTT 720
CCCACTTGGC CCCTGCAAAT GGGGCCAGGT GTCACTGCTG GGAGACGCCA GTAAGGCTGC 780
ACGTCATGGT GTGAGCACTT GTCTTTAATG ACTGGGAAAA TCCATTTCCT TCCTTGGCAG 840
CTTTGAATGT AGCAACTGTG GTTCTGGGTC ACTGCCAGAG CCAGCCTTGT GTGTATGTGT 900
GTGATTTTTT AAAGTGGGGG AGAATGTCTC AATATTCAAT GCTCACCCCC TTCCTTCCAA 960
GTTGTACCCC CAGAGAACTG TCCAACACAA ACTTTGGAGT TTTCCACTCT GGGAGTGGTC 1020
TGCTGGCACC CACGTGTCCT CCCCTCCTCT AATGCATCCT TTCTCTCTTG ATCTCATTGT 1080
TCTGGGGTCC TCAGCTGAGT GGGCATCTGT GCCTGGGTGA TCGATTCTAG TCTCTTTTCT 1140
GCAGGAGAGA ACTCTTGAGC TCTGAGACAG GTAGAAAGAA AATCTTAAAC CAAATAATAA 1200
TGTTCTGCCT CACACTAGTA AATATTTTGC ACTAAAAAAT TCCGTGTCAT TTTGATTTGT 1260
TCAGGTAGAC AAGAACATCT TTTGTTTGAG GAAGAACTGA AGAGATTTCT TGGGATTCAG 1320
CTCCGATGGC TCTGCCTGTA TCTCTCTATC ATTGGAGCTT TGTTTTCCAC CTTTGCAAGA 1380
CTTGAGTGAA GGGAAGGCTT TGTGGTCTAT TGTTAGGTGC TCTTTGAATC TATAAATCAC 1440
AGGCTACAGG AAGGGAGGGG CTTCCAGAGA CCATCTAGAG CCACCCTCTA TCTCTAGCAG 1500
GGACACACAC ACACACACAC ACGTACACAC ACACAATGAC TGCCTGTTGC GCGTTTCTAG 1560
|
