Tag | Content |
---|
EnhancerAtlas ID | HS003-29763 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr20:39190020-39191640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr20:39190677-39190688 | AGCCACACCCA | + | 6.14 | STAT3 | MA0144.2 | chr20:39190123-39190134 | TTTCTGGGAAG | + | 6.02 | Stat4 | MA0518.1 | chr20:39190123-39190137 | TTTCTGGGAAGTGG | + | 6.14 |
|
| 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 |
GH20I040561 | chr20 | 39190381 | 39192721 |
|
Enhancer Sequence | GCCAGCAACT AGTGACACAG CATCTGGTAC TGAAGCCAAT CAATGAAGTG CAAAGAACCC 60 AGGAAGGGGG ACCAACCAGC CTCCTTTGCC TGAGACTGGG GAGTTTCTGG GAAGTGGAAT 120 TTATAGGTTT TTTGGGTTTT TTTTAGATGA AGTTTCACTC TTGTCGCCCA GGCTGGAGTT 180 CAATGACACA ATCTCAGCTC ACCGCAACCT CCGCCTCCCA GGTTCAAGCG ATTCTCCCGC 240 CTCAGCCTCC TGAGTAGCTG TGATTACGGG CATGTGCCAC CAAGCCCGGC TAATTTTGTA 300 TTTTTAGTAG AGATGGGGTT TCTCCATGTT GGTCAGGCCG GTCTCAAATT CCCCGACCTC 360 AGGTGATCTG CCTGCCTTAA AGTGCTGGGA TTACAGGCAT GAGCCACTGC GCCCTTCCAA 420 TTTTTAGTTT TTAAAACAAG GCAGGCCTAG GCAAGCGAAA ATAAGCTGTT CACCCTAGAC 480 CCAGGTATGC ACGTGAGACC TGATTCTCAG GGGTCCTAGG GCAGACCAAC CCTCCCACCC 540 ACCAACAGAG CCTTGAGATA TTTGTGGGAT GTGCAGGGCA AATATAAAAA TTCCAACCGC 600 TGCAGGCCTC ACCTGGGCCA CTGCCTTCCC TGAAACAGGT GAAAACTGAA ATTCTCAAGC 660 CACACCCACT AGAGCAGCAG GAGGAAGAAT GGGGGAAACC CTTTAGCAGT GATTTGGAAT 720 CCCACTGTGT CCCTCCTCCA TGAGCTGTCT GTGTGTGACT GAGCAGCTCG CTTCCCTCAC 780 TCTCTGGGGG TGGGGTCAGG GTGGGGAGTC TGTCTGACTC ACTGCCCAAG CCACAGGCCT 840 GTCTGCTTGT CCCCAGACAG GGGACCTACC TACCCACTGT CCTTCAGCTC TGTTGTCAGC 900 CACAGGCTGT GCCCAAGAGG GCACATGGGG TTGGTGTGGG GAGGAGGGTA GGTTTCCTTG 960 GCTGAGGCAG AGGAAGTTGC TTTCTGTCTC AAGTTCTGCT CACAGGTCAG ACATTACCGG 1020 CCTTGTGATC ATCAATCTCC CATTGTGTCC TTTCAACACG TACCAGTGTC TTCAACACTA 1080 AGTCCCTTGC AGAGGGAATG GGATAGGGAC CGAACCTCAC ATGCTTTTCT GCTTCCCTGT 1140 GGATTTGTGA GGCTGATATC CAGGTGAAGA GATCAAGTAG AGTTTTGTTC ATTCACTCAA 1200 ATGTTCACTG TGCCTAGTAA CAGGCAGACA CTGAGAAAAT TGCTAGAAAT ACAACAATGA 1260 ACAAAGTTCC TGCACTCATG ATGCTTACTG TCTACTGGGG GAAACCAACG ATAAAAGAGT 1320 CAGTACAAAA AAAATTAATA AGTGTTAGGG GAGGAGAAGA GCTGGGTACT GTGAGAACAC 1380 ATATCCAAGG ATCTATCGTA TTCTGGGCAA TCATGGAGTA CTTCCATGAG GAAGCATGGT 1440 TTATGTTGAG ACCCAAAATG AGGAAGAGTT AACATATACT TAACTGTGTG CCCTAGACCT 1500 TCAAGGATGG GGACTGCCTC TCTGAGCAGC TGCAGGGAGG CCTCTGGAGA GGTCTCTACA 1560 CTGTGATGCT GGGTTAGCCT TACCTATGAG CTGATACACG CAGGCCTCAG AGCAGGGCCT 1620
|