| Tag | Content |
|---|
EnhancerAtlas ID | HS158-00016 | Organism | Homo sapiens | Tissue/cell | Pancreas | Coordinate | chr1:1207560-1208640 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr1:1208600-1208611 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr1:1208600-1208611 | TTTCCCAGAAA | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTGAGAACA GAGTTTGAAG CATATGTGCC TCGGGTTCCC TTCAAACATC CCCACAGACA 60
AAGGACACCA AGCATATCAT CCTGCTGAGA GAAAGAGTTG GCGATTTTAA AACAAAAAGG 120
CACAGGAAAA AAAAATGTTC ACACACAGAA ACTGCATTAA AGCAGCGTGA ATCACCGAGG 180
GCAGCTGTGC CCAGGTGCTG AGGCAGTGGC TGCCCAGCGT CCCTCACCCG TCCCTCTTTG 240
TCTGGACAGC TCTTTCCTGC TTAGGGGATG TGGCAGGAAA CCTTGGCCTG ACCCATCGGC 300
CAGGCGCATG GCACACCCAG GTCCAGGACT GCCAGGGAAG TCTCTGCCTT CTCCACCAGA 360
CTGCTCCGGA GGCTGGACGG AAGCCCGGGC CGATGGAAAT GGGACACTCA CCTGCGACTC 420
ACACATGCAC CTGCCTGGGT CACCTGCCTG TCACTCATCC ACGCACCTAC CTGCCTGGCT 480
CACCTGCCTG TCACTCAAGC ACTCACCTAC CTGCCTGGCT CACCTGCCTG TCACTCACGC 540
ACATCCCTGC CGAGAGTGGA ACTGCTAAGG AGGTCAGCGG TGCCAGGCCG TGCAGATGAC 600
GGACTGCAAG TTCCGGGCAC CCAGACCCAA CCACGCCCTA GGCTCAGGTG CTAGACTAAG 660
CGAGATACTC ACGATCCTTT CTTCGGAAGC CAGATTACAC AGTCTGGTTC CCCTGGAGCA 720
GGGCGCGGGG CCACCGACCT GCCCCAGCCA AGCCCGCTGT ACACTCTTCG CTGCCCACCT 780
CCCACCGGGC TGAGGCCCGA CCTTTCAGCC GCTTCCTATC TGGGTCTGGC AAGAGGATGG 840
CAACCGGACT AGAGTTAAAT ACACACGCAC TAAGTGGCAG GCACTGAAAA GGACGCCAGG 900
AGGTGACACC TGGCCAGGGG CTGAAAGGAT GCAGGGAACT GGCAGGTGTG GATGGCGAGG 960
CCCGGCGCCG CTTAGAGACT TGTTCCGGGC TCGTGTCTCA CTCGCCGGCC GGCGGTGGTC 1020
TCCCACTGTC ACCGCCCGGG TTTCCCAGAA ACGCTGGCCC TAAGCACAGT CCCGGGCACG 1080
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