| Tag | Content |
|---|
EnhancerAtlas ID | HS187-11624 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr18:72706320-72707760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ONECUT1 | MA0679.1 | chr18:72706851-72706865 | ATTATTGATTTATC | - | 6 | | ONECUT2 | MA0756.1 | chr18:72706851-72706865 | ATTATTGATTTATC | - | 6.16 | | ONECUT3 | MA0757.1 | chr18:72706851-72706865 | ATTATTGATTTATC | - | 6.44 | | Stat6 | MA0520.1 | chr18:72706444-72706459 | CATTTCCAGAGAAAT | + | 8.18 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr18 | 72706567 | 72706772 | | chr18 | 72706946 | 72707254 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I074993 | chr18 | 72705624 | 72708651 |
|
Enhancer Sequence | CGCTTAAAAA GTTACAAAAA ATAAGATCAA GATCCAGGTT GTGTCAAAGG GCTGTTTGCT 60
GAAAAGCATG CAAATTTCCT GTGAGGAAAT AACTGGGAAG AGCCACAGAA GTGATGAAAA 120
TGAACATTTC CAGAGAAATT GTGTCTGGAA AGTCTGCATC CTTGTTTAAA GCAAACAGTC 180
AGGAAGGAGG CCAGTGGCAG AAGGGGAGGC AGTTCGACCC TGAATGTGGA CTGTCCCTGC 240
TGGTGTGTGT CCATCTGTGC AGAGAGCAGG GCTCATGTTT AGATTCTCAA ACGGTAGGGA 300
GTATTACAGT GCAGTTCACT TTGGACACGT GTCCTATGAC CAGGAAACCA TATGCAAAAG 360
ACGGCAGCGG CACTCAGGAC CCAGCGACAG GAAGAATAGA TGATGGAAAG GGCCGGGGAG 420
GGCACTCGTG GGCAGTGAGC GGCCACAGCA CAGTGTGGAC AGAATTCTGG GAGTGACTTT 480
GAAGACAGAG TTGAGATTTT TTTCTACAAT TGATGAGGGT GGAAGAAGTT TATTATTGAT 540
TTATCAACTA TCTAGACATA AAAGCAACGA AATTTCAAGG AGACGAAATG GTGTCCAAAT 600
GTTAGAGAAG TGACAAGCCG TGGTTCTGCA GCTGTATTCA TTTTAAGCAG GCTAGAAATC 660
TTTACTCAAT GTATGTATTT TCTTTCTCTG ACTTCCTGTG TGAAAAAACA GTTTGACACC 720
CTGAAATGAC TCACATCCTG AATATGTTGC TAATTGAATA TTTATCGAAG GCTGACTTAT 780
ATTTGCAAAT TCATGGAATG TAAAGGACAG TGGAGCTAGA TCTGCGTGAC TGCAGGGGCA 840
AGTGTGAACG GCAGGGCCTG GCTTGGGCGA TTTGAGTGTG CCAGGAGCCG TGGCACCTTA 900
GGGCTAAAGG AGACCACATC CATGGTAAAC AGCATTCTGG ATGCTGTGTG GAGAGTGGCC 960
AGAGGGTCAC AAAAGGGGCA GCCAAGAGAC AGGTTCAGAG ACTACTGCAG TAACCGAGCT 1020
GAGGGTGATT CGATCCTACA CTGGGTTGCA GTGTGGGTGG ACCAGTTGTG AAGTGGGCAG 1080
GTTCTAAAAA AAGCATTAGG CTATCAAAGA AACCTTAACA CTGATCCTCA CAGAAAATAG 1140
TATTTTATTC GCTTCCTAAA TTATTTTGCT GACCGTGCTG TTTGTAGCTC TGGGTCAGCT 1200
CTGTCTCACT GTGCATTTGT TATATTTCTT TTTTCTTTCT GTTTTCTAGA TTATTATCAA 1260
TGAAGTCTTA ATCTTTTTTA ATGAAATCAT TTGGAAGAGG CTTTGGTGGG AGAGGCAGAA 1320
GGGAGGGTGA CAATGCTGGG CCCTTCCTCT GTCTTTTTCT GGGCAGTTCA TTCGGCTGTG 1380
CTCTGAGGCT ACCATTTCTT GTTTAAGAGA TACCGAGGGA CTTGTGCTTG GCTCTGCTTT 1440
|
