| Tag | Content |
|---|
EnhancerAtlas ID | HS077-00145 | Organism | Homo sapiens | Tissue/cell | H128 | Coordinate | chr1:11434850-11436920 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr1:11436028-11436042 | ATTCCCTGGGGAAT | + | 6.72 | | EBF1 | MA0154.3 | chr1:11436028-11436042 | ATTCCCTGGGGAAT | - | 7.73 | | IRF1 | MA0050.2 | chr1:11435055-11435076 | CTGCACTTTCTTTTTCTTTTT | + | 7.02 | | Myod1 | MA0499.1 | chr1:11435858-11435871 | AGTGACAGCTGCA | - | 6.78 | | STAT3 | MA0144.2 | chr1:11434880-11434891 | TTTCCCAGAAG | - | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGAATCCAC CAAAGGCCTT TTTGGTTTGT TTTCCCAGAA GCCCATCAGT CACCATCTGG 60
GGAGGACAAG GAGGGAGCAG GGCTGATCCA AGGAGCTCTG GGGCAGATGG ACTGTCCCTG 120
TCACGGCTTC TTTTACTGGT AGTAATGACT CCCACTGGTT GAGTATGCAG GCGCCACTTT 180
GCTCCATGCC AGGTACCATC CATGCCTGCA CTTTCTTTTT CTTTTTGTTT TTTGAGATGG 240
AGTCCCGCTG TGTTGCCCAG GCTGGAGTGC AGTGGCGAGA TCTTGACTCA CTGCAACCTC 300
CACCTCCTGG GTTCAAGTGA TGCTCCTGCC TCAGTCTCCT GAGTAGCTCG GATTACAGGC 360
ATGCACCACC ATGCCCGGCT AATTTTTGTA TTTTTAATAG AGATGGGTTT CACCGTGTTG 420
GTCAGGATGG TCTCGATCTC CTGACCTCAT GATCCGCCCA CCTTGGCCTT CCAAAGTGCT 480
GGGATTACAG GCGTGAGCCA CCGCACTTGG CCCATGCCAG CACTTTCTAG GTATAATCTC 540
ACTTGATCCC ATCCGGCTCT TTGAGGCAGG CTATATGATC ATGCCCATTT TGCAAATCAG 600
GGAGCTGAGC CTGAGGAGCT GGGGTCCTTG CCCAGTCACA CAGCCAGTAA CAGCAAGAGT 660
TCTGATTTAC CCCTAGCTGG TCTGGATTCT CTTGGTCCCC TTATACACCT GTTCCCTGCT 720
GGGGGAAGTC AGCTGGGGGC GTGGAGACTG CCTTGGAAGG TGGCTGCTGC AGCCCCCCAG 780
ACCTCCGGCA ATAGAATTCC CTATAATTCG GTTATAAATC ATGTTCCTAA CTAAGCCAGC 840
TCTGAAGGTC ACCGGTAATC AAACTGTCAG CAGGCCATCT TCAGCGGCTG CCGTGGTCAG 900
GGCCCTGAGC CAGGAGAGCC CAGGGAATCA AGCTTCCAGC CCGCACCTTT ACAAGTGGGT 960
AAGAGGCTGG AAATGGGAAC AGGTTAAGAG GGCTTGGGGC TGGGGCCGAG TGACAGCTGC 1020
ACTTCTGACT TCAAGATAAT GAGGAGGAGA GAAGCTCCAG CCTCGCTTCT GAGCTATCTC 1080
GGTCCTTCCT GTTGTTGGTA GCATTGAACC TCCTGATCCG TGGAAGGTGG CTGCTTGCAA 1140
AGTTCTGATG ACATCACATG GATGTGTGTT GGCCGGGTAT TCCCTGGGGA ATGAGCTTAG 1200
CGCGGAAGCA GAAGAGTTGC ATTTTCTAAA CCACCAGCTA AGTGGCAGGT GCGTACACAT 1260
CATCCTGTGT AATCCCTAAG CTTGTCCCAT GTGGTAGCAA GTTCCTTTTA TTATCTCCAT 1320
CTCCTGGAGG CTCAGATTGG CAAAGGGGAC AGAGCTTGCA AGCATTCAGG TTGGCATTCA 1380
GGCTTACATC TGGGTTTTTT CCTTTTAATT CTTTTTTTTT TTTTTTTTTT TTTTTTTTGA 1440
GACAGAGTCT CACTCTGTTG TCCAGGCTGG AGTGTAGTGG CGCGATCTCA GCTCACAGCA 1500
ACCTCTGCCT CCCGGGTTGA ATTATCCTGC CTCAGCCTCC CGAGTAGCTA GGATTACAGG 1560
CATGTGCCAC CACATCCGGC TAATTTTTGT ATTTTTAGTA GAGACGGGGT TTCACCTTGT 1620
TGGCCAGCCT GGTCTCGAAC TCCTGACCTC AAGTGATCTG CCCACCTCGG CCTCCCAAAG 1680
TGCTGGGATT ACAGGCGTAA GCCACTGCAC CTGGCCTTCT TTTGACTCTT ACCAGTATTT 1740
TCCAATTTTG ACATTTTGAA ATAATGCTGG GAAATGCTGG TTAAACCAAG AGAAACAAGA 1800
TTCCTGTCCG CATGACTTTT CAGAGCCTTT AATAAATTGG ATCACGATTC TTCATGCACA 1860
GAGAGATGGG ATGCCAGGGT GGAGGCCTTG GAGGCTCTGG CAGAGAGGAG ATTAGTACTC 1920
CATTCCTACC CCAGTTCTGC AGGGGAGCAT GGCTGGCTTG CTCTTGAAGC CCTGGCCCCC 1980
CTCATCTGGA TGCAGCCTAC AGTGGGGTGA GCTGAGGCCT GGCTCCACAC ACCTCACAGG 2040
AACTCCTAGA AGAAGGGAGG CTGTCAGGTA 2070
|
| |
|
|
|
