| Tag | Content |
|---|
EnhancerAtlas ID | HS158-01129 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:26248860-26250020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr1:26249280-26249290 | GACACGTGCC | + | 6.02 | | Npas2 | MA0626.1 | chr1:26249280-26249290 | GACACGTGCC | - | 6.02 | | TFAP4 | MA0691.1 | chr1:26249156-26249166 | AACAGCTGAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_03348 | chr1:26248429-26249442 | Brain_Angular_Gyrus | | SE_03348 | chr1:26249453-26250112 | Brain_Angular_Gyrus | | SE_04754 | chr1:26248435-26250710 | Brain_Anterior_Caudate | | SE_05300 | chr1:26248205-26250482 | Brain_Cingulate_Gyrus | | SE_07163 | chr1:26248199-26250726 | Brain_Hippocampus_Middle_150 | | SE_37807 | chr1:26248263-26250260 | HSMMtube |
|
| | 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 |
| GH01I025922 | chr1 | 26248542 | 26250508 |
|
Enhancer Sequence | GTGGGTTAGG TTCAGGGTCA AGACTAGACC CCACATCGCT TGGGGAAAGG AAAGGCCACG 60
GTGTGAGAGG GAGTTGGCGG GGAGGGAATG GCTGAAATTA AACATGGTGA TTATCCCACC 120
ATCAGTGGAA GTTATCCAGC AGCAGTGGAC ATGACTGCGA ATCCTCCAGA AAATGGCTTC 180
GCTGCGCTCC ACGGATCTGC TCTCCCACCC CACCTGCGGC TTGCACAGCG ACACACAAGC 240
GTTGTGATTG GCTCTTCCTT GGCTGAGACA AGGGTGGGGA CCGAAATGGC GTCTCTAACA 300
GCTGATTTTT CAGGGCAGCA GCTCTGTGCT AGGAGAAGAG AAGGCCGGGC TCACTGGCGG 360
TGCGGAGCCC GCCAGGGCCA ATCCGCATCC GGGCGGAGGT GCAAGCCCGA CCGCAGTACT 420
GACACGTGCC GCGACGTCCC CTCCCGGCAG CTCGCGGGGA CCTGGGAGCG GGTGGGGTCT 480
CTGGCTGGCG GGGAGCCAGG GCTGCGGGAA ACCGCACGAG GTCGCGTTCG CGAGTGGCGG 540
AGAAGCCCAG ACCCCCGGGC GCACGCGGCC GCGCCCACCC AGGTCGCTGG GAGGTGCCCG 600
CCCGGGAGGC GCCGCGGCCA GTGCCTGCCG TTAGCTTCAG GAAGAACTAG GATTGAGTAA 660
GAAACGACTA GGGATGGAAG CACTTGGCAC TCCGGGTCTC GGAGCAGGCT GGGGACGCCC 720
GCGGCAGGAA CCTGGTCCTC CACTCCGGGT GCGGACCAAA GTCTGCTAGG GCTTCCCCGA 780
AGTGGATTCA GTGACTCGGG AGAGGACCCA GCCCCTAGGC CCCATCCCCG GTTAAGGGCC 840
AGTCTTGGTC TGGGTGTTTC TCTCCGGGAG CTGGTCGCAG GTTTCCGTTT TCCTCTTCAA 900
GGAAGGAAAG ACCAGCGAGA GAATTCGAGG GAAAGAACAA AAGCCGCCGG CACCGCCCAG 960
CCCAATTTTT GGAGCCTGGG AGGCTGGCTC CCTTCCTCTG ACCGCTGGGA CGACTCGGAG 1020
GGCTGGCGCT TTTTCCTTCA CCACCATTTC TTCCCAGCGA CCAACTTTTG AGTCCTTGCT 1080
GTGTGCCAAG CACTTCACTG AGTGTCATAT CTCACTTCCT CCCCACGACA ATTGTAAGAC 1140
ATGACAGGCT TGGAAAGGAG 1160
|
