| Tag | Content |
|---|
EnhancerAtlas ID | HS093-14891 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr19:5077580-5078960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr19:5078239-5078249 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr19:5078239-5078249 | GGCACGTGCC | - | 6.02 | | Klf1 | MA0493.1 | chr19:5077881-5077892 | GGCCACACCCT | + | 6.32 | | Klf1 | MA0493.1 | chr19:5077732-5077743 | TGGGTGTGGCC | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65334 | chr19:5076889-5078643 | Pancreatic_islets |
|
| | 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 |
| GH19I005078 | chr19 | 5078341 | 5078450 |
|
Enhancer Sequence | GAGAAGTTTC TAGAACAGTG ATTAGCATGC CAGAGGAGGG CCGCATGGCT CAGCAGTTAG 60
CCTCCAGCTC TTCCACGGGG AAGCGAAGAT GGCAGAGCTT GAATCTGGCG GGGTGTTAAC 120
CTCCCCTCCC AAACCAAACC AAAACTTCCT CCTGGGTGTG GCCATCAGAG GCCCCTCCGC 180
AGGGGCTGCA GGGGTGGAAG GGCAGGGGCA GGCCCTGCTG ACCTGGCAGG AAGCTGCCAA 240
AGAAACAGAG GGCAGGGCCC CTCGTCCCGT GCAAGGTGGG AACCTGGTTC CTACCGCCCC 300
AGGCCACACC CTAAGTCTCA GGCACCCCCA CGGCCCATGT CACCCGGCCG TGGAGAGAAC 360
TGCCTGTTTA GAAGTGACAT TTCGGGCTCT CCTGCACCGT GAAGACTGTG AACTCATTCA 420
GTTCACTGCT TCAGGGGCTG CTGGTGGAGG CTGTGATGGA GGAGACCTGA GGCCGGGGGG 480
TGGGGCCTCC CTACACCTGA TTTGATGGAC AGCTGGGGTT TGGTGTCCCA GGAGCAGAGC 540
AGGCTGTGCT CAGGGTCCAG CTCAGCAACT GCACCCACTC GAGGCAGTTC CTTCCCCATG 600
GAGAAGCCTT TGTCCATGGG AGAGTCTAGG CCTGTGTCCC CAGCTCTGTC CAGGTGAGAG 660
GCACGTGCCA AGAACCTGCA AGGCAGGTCT GGGCCGCAGC CCAGCTCATG AGGTTCCACG 720
GGAAGAGTGA TGTGCAGGCT CGGGAGCGTG CTCTGTGGTG AGGCCCTGAG TGTCAGCCAG 780
CCGGAAATTG CTTGTGACAT TTCAATCAAA CCGCCAAAGC ATCAGCTCAC ACATCGGGGA 840
TCCGCTCTTC CTGGCGGGGC TGCAACCCAG AGGCCGCCTC CCAGCCGCTG CAGGCATTCA 900
TCAGACAGCA CAGATCTCGC TCGGAGAAGT GCGCATTTCC GGCCTTTCCT CTTCTCCCCC 960
GTCTTCTGGT TGGAACATCA TTCAGTACCA GCAAAACCAG ACAGATCACG GCATTGCTCA 1020
GGGAAGTGAG AAGTACTGAT TTTCTGGCTG GTTTGTCTAA AACCTTCTCC AAAGTGGTGC 1080
TTCCTGGAGG GGGGTGCCCA TCGAAGGGGT GGGCAGGCAG TGAGTGGCCT GGACTCCCAG 1140
GTCAGCATCT GTATCGCACT GCAGTTTATC TGTAAAGTTC CTGAACCTGA GCCAAAGGTG 1200
GCTCACCACC AGCCTCAGAG CGGCTGCTGG CACCATGCAT GGTAGCAGGC GGGGTCCAGG 1260
CAGTACGGCT GCGCTCCCCA ACACCGCCAG CTGGTTGCTG GGGCCGGGCG CCAGTTTCTC 1320
CAGAGGCTGC CACAGTGAAG GCCCCTGTCC CACTGCAGCG AACAGCACCC TGTGCCGCCC 1380
|
