| Tag | Content |
|---|
EnhancerAtlas ID | HS003-36051 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr5:392120-393540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr5:393142-393152 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr5:393142-393152 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr5:393142-393152 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_03106 | chr5:393118-393835 | Bladder | | SE_34945 | chr5:392406-393774 | HeLa | | SE_37211 | chr5:393298-397341 | HSMMtube | | SE_44252 | chr5:392826-397128 | NHDF-Ad | | SE_45637 | chr5:392344-397415 | Osteoblasts | | SE_58626 | chr5:366707-441100 | Ly1 | | SE_59696 | chr5:390329-441740 | Ly4 |
|
| | 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 |
| GH05I000390 | chr5 | 390969 | 397295 |
|
Enhancer Sequence | CCAGAGCGTG CACGGGCGCA GGGCGAGGAG GGCGCAGGGT GAGGCAGGGC CAGAGCGTGC 60
ACGAACACAC GGGTGCAGGG CGAGGCAGGC GCAGGGCGAG GCAGGGCCAG AGCGTGCACG 120
GACGCAGGGC GAGGAGGGCG CAGGGCGAGG CAGGGCCAGA GCGTGCACGG GCGCAGGGCG 180
AGGAGGGCGC AGGGCGAGGC AGGGCCAGAG CGTGCACGGG CGCAGGGCGA TGAGGGCGCA 240
GGGCGAGGCA GGGCCAGAGC GTGCACGGGC GCAGGGCGAG GAGGGCGCAG GGCGAGGCAG 300
GGCCAGAGCG TGCACGGGCG CAGGGCGAGG AGGGCGCAGG GCGAGGCAGG GCCAGAGCGT 360
GCACGGGCGC AGGGCGAGGA GGGCGCAGGG TGAGGCAGGG CCAGAGCGTG CACGAACACA 420
CGGGTGCAGG GCGAGGCAGG CGCAGGGCGA GGCAGGGCCA GAGTGTGCAC GGGCGCAGGG 480
CGAGGTGGGT GCAGATGTGG CAGGTGCAGA CGCGGCGTCC ACAGCCAGGC CTAAAGACGG 540
TGTCTGAAGC TGGGGAAACC CAACAGTGAC TCGTTATGTA AGCGTGTGAC TTAGCAAGAC 600
AGAGGAAAAT GCCCAAACCG CCGGTGAGAA GGGCTCAAAG CAGTCGCTCA AAGCAGCAGG 660
AAGTGATGTG GCGGGAAGGC TGGTTTTAGG GACAACGGCT GAGTTTCGGT GGAGGCTTGC 720
ATGCTGTGTG ACTCTTCAGA CCTGGCTCAT TTCACGTCGA CTCTTCTTGC CCATTACGTC 780
ATTTCATCAG GCCTTACCGC GACTGCCTCA GGCCTTACCG TGGCCGCCCC AGGCTTACTT 840
TGGTTCTTGG CTGCTTGGAC TGTCTCCCCC ATGCCTTCAT TTTCTGCGTT TCCTTCTCGG 900
TGTAGGTGCC TCTTGCAGGT GACGGGTCAA GGGATCTCCC CCCACACCAA GCGCCGTCTT 960
TCACTGGGGC CCACCTACTT CTTGTGATTC TTTAGGAGCT GATTTCTGTC ATCCTATTTT 1020
GTATTTTCCA TTCACTGCAC ATCCTTTGGG TTTTTTCCTC CCCTAACCCT CTGTTAGATA 1080
AATTGAGCTT TCTTGAACTG AAGGTGCACA TTCTGCTTTT GTTCTCATGG GGATGCCTTT 1140
GAAATGAGAG CTTTCAGGTT GATTTGCTGT TTCTCAGGCT CTTCTGCGGT GATGTTCCCC 1200
CAGCAGGGCC TGTGCCGGCA CAGACGCGTC CTCCGGCCCT CCCCACGTTG GCAGCACGTT 1260
GACTGTGTCT GAAGCTTAAT CCCGATGTCA CAGATTCTTG TCTTTGCACC TAACGTTACG 1320
TGTCTCATCC AGCCCAGGGC ACCCGATCAC GTCGCTCACT AACCGATCCT TCCTCCTCCC 1380
GAGTGTTCCT CTAGCAGTCT GCTGTGGGCC TTGCTGTGAA 1420
|
