| Tag | Content |
|---|
EnhancerAtlas ID | HS158-04418 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:201279520-201280700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:201280331-201280342 | GGAGGGTGTGG | - | 6.32 | | Klf1 | MA0493.1 | chr1:201279913-201279924 | AGGGTGTGGCT | - | 6.02 | | Klf1 | MA0493.1 | chr1:201280333-201280344 | AGGGTGTGGCC | - | 6.32 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_26526 | chr1:201275996-201283211 | Esophagus | | SE_35843 | chr1:201275993-201282637 | HMEC | | SE_37062 | chr1:201275933-201282182 | HSMMtube | | SE_64243 | chr1:201275982-201282297 | NHEK |
|
| | 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 |
| GH01I201305 | chr1 | 201274996 | 201282487 |
|
Enhancer Sequence | GCAGGCTGGC TCCAGAGTCT GTGTTCTTGA CCTTGGGTCT TCCTCCAGTT TGTAGATCTC 60
AGCCCAGTGA GCTGGAGGAA GCACCTGGAT TCCCAGGCAG TTGCTGCCGT TTCAGCCTTC 120
AAGGCTGCAG GCTTCATCCA GGTCCCAGGC CAATTTGTGC AGGGAGAGCT GGTGGCAGTT 180
CACCTCCTTG TGCCTTGGAG GGAATCCAGG CCCCCTCATG GTACTTGGGG AGGACGGGGT 240
CTGAGAGGAG GCTTTACTCC TGCTTGTCAA AGTGACAGCA AAGGGCCATG ATGATGGGAG 300
AGAGTCATAC CCAGCTGTCC TCAGGCAGCA CAGCCCACCA GCACCATGAC ACTAGGAGCT 360
GGGGTGGGGT TCCCAGGAAT GGGTGACGCC ACTAGGGTGT GGCTGATGGT GGTAGGCTGG 420
GAAATGCAGT CCCACGGGGA TGTCTCTGCC TTCCCCACCT TGCCCGCTCC CCTGCAGGTG 480
CAGCCAATGC CCATTCCCTG TGGGCAGCCC ACCCTTGCTG AGACTTGGCA AGGCTGCCAG 540
CTGCTCCTTT TCCCAGCACA GGAAAGCAAA GCCCAAAGCC TCTGAGAGGC TCAATCAGCA 600
TGATCACATG TTTGCTGGTT TTGGGCCAGG ATGAGTGTTT GGGCTTCTCA TTAGGTGTCT 660
GAGATGACGT CCAGGCGTGT CGTTTATGGA GAACAAGGGT GCTCCTTGTT GCATTTCCAT 720
TTAAGGCTTA GCTGGCTCTT TGCCCTTTGG CAATGCTGGG CTTCCCCCTC CATGTTGTCA 780
TCTGCCACCT TCCTTCCCCT GAGAGGAGAA TGGAGGGTGT GGCCATTTGT AAAGGCTTTC 840
ATGGCATATT TTGCCTGTAA TCTGCAGGAC ACGCATTCCA TACCCAGATG CTCAGAAAAT 900
TGCCCAGCTG CTCTCCCCAT GCCTTGTGAT TGTCCATCTA TGCCTCTCCC AACAACCAGA 960
CACCAATTCT CTTTGGAGTA GGTTGGTTGA CCCAGTTTGG GGAAGAAAAT TATGCCTGCC 1020
TGAGTGCACA GCTGGGCGTG TGGGTGAAGG GGATGAGCAG GCTATTGCCA AGGTTAACAG 1080
TCTGTGGCTT CTGAGTTTTG GATGCAACTT CTGACTGGTG GTTTGACACC CAGTCTTTCT 1140
GGGAGCTCAA ACCATGGGAG TTTCCTGCTG TCTGTGACTC 1180
|
