| Tag | Content |
|---|
EnhancerAtlas ID | HS003-38188 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr5:158832070-158833380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr5:158832671-158832682 | TTTCCCAGAAG | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_58825 | chr5:158828929-158907311 | Ly3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 158832550 | 158832976 | | chr5 | 158832569 | 158832996 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I159405 | chr5 | 158832569 | 158832996 |
|
Enhancer Sequence | AGTAAAATCC AACCCCCGCC CCAATCTCCC AGGCCTTCTG ACAAATTACA GAGCACCCCA 60
GGCTCTCTTT CCACTTTGTA CATTGACCAT TGCTCCTTTT TCTGCCTAGA TCATTCTTCT 120
GCCCCCTCCT TGGAAGGGCC TTCCATGCCT TTCTAAGTAT ATGCTCCCCA ACATAGACAG 180
TGGTTAAGAC CCAGGCTCTG AAACACCACT CACGGGTTCA AGTTCGGCTC TGATACATAC 240
CAGTGAATTG ACCTTGGGCA ATCACCTGAC TTCTCTGCCA CAGTTCCCAC TTCCGTAAGA 300
TGGAAGTAAT AATTGTTTGT ACCTTACGGA GCAGTTGTGG AGAAAGGATG ACATTAATAG 360
TTGGCCATTA TTACTGTTTT TCAGAGCACT CTATTTCCCT TCTAGCGCTG CGGTCTGTAA 420
TTAATTTATT TGTATATATG TCCATTAACC ACCACCCGTA ATATCCTATT ATCTTCTATA 480
ATGGGATCTT TTAATAAGGG CAATGACCAT GTCTTTCTCA TCATCCTTAT ATAGCACAGT 540
GCCTGCGACT TAAAAAATGC TCAAGTCATA GTTGTTGGAT GAGGAATTCA CTGAACGGGT 600
ATTTCCCAGA AGTCTCAACA GCCTGTCCCC AGAGACAAGA AGGCACCACG AGGGGTGACT 660
GAGGCAGCCC TGCAGCCCCT CAGGGAAGAG CCAGGGAGCT TGTCAGATGG CCCTGTTTTG 720
CATTTCATTC TCCCGGTTGC AGGCTTTCAC TTATGTAATG AAATAGCAGT GAAACCCCAC 780
TGACACCTGA GTGCTTCCCC TCTAGCCAGC CCAGTATTTG ACCACAAAAA GGGGGAAGAA 840
AAAAATATAA GAAAAAAAGG AGCTTCAAAC CACATGCTTC TTGGGACACA CAGATGAGCT 900
GTCCTTTCCC CAGAGTCGTC TGAGCGTATT GTAGTAGCCT GGAGGGGTGT TTTGCTGAGC 960
CTGATCATTG TGACCAAGTG GTGAAAAATC AAGGTCCCCA GCCTGCGTGT CAGCAGTCGA 1020
GACTTTTTCC ACCTCTGCCC CTGACCTGCT GTGCAACCTT TTGCAAGTCA CCTTACCTGT 1080
CTGGGTCTCT TCAGTGACCC CATCTGCAAA TTGAGGGACT GAAATAGATG ATGAAAGTAG 1140
AGTAGCCATG CAGTTCTGGC TTTGCCTGTA GACTTGGTAG AATGATTAAT AATAACCTCT 1200
TTCATTCTTC TTTTTTTTGA GATGGAGTCT TGTTCTATCG CCCAGGCTGG AGTGCAGTGG 1260
TGTGATATTG GCTCACTGCA ACCTCCACCT CCCAGGTTCA AGCGATTCTC 1310
|
