| Tag | Content |
|---|
EnhancerAtlas ID | HS193-12414 | Organism | Homo sapiens | Tissue/cell | U87 | Coordinate | chr16:19016600-19018110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2B | MA0660.1 | chr16:19017024-19017036 | GCTAATAATAGC | + | 6.07 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr16 | 19016606 | 19017680 | | chr16 | 19017780 | 19017800 | | chr16 | 19017800 | 19017874 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH16I019005 | chr16 | 19016524 | 19018195 |
| Enhancer Sequence | TGGGGTTTCA CCATGTTAGC AGGATGGTCT TGATCTCCTG ACCTCGTGAT CCACTCGCCT 60
CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA CGCCTGGCCC GCATGTTAAA 120
TACTTTAAAT GGCCTGGTAC AAGGTAGGCA AGTACTCAAT AAATCTTAGC CAGTGTTGTT 180
CATGTTGTTT GCAACTCCTT CCTCACCATC ATGCTGATGA GGCCCATGGT ATTAGATCCT 240
CCATTCCCGA GATGAGAAAA ATGTGACTCT GAGGCAGCTG TGGTCTCTCC TGGGGTGGCT 300
TGGCTGGTGG GTGACAGGCC AGTATTTTAA ACCAACCCAG GCTCCAGCCT GGGGCCCCTG 360
ACCCCACAGC TGTTGAATAT TCAGTAGGTC CATGCTGTTC TATATTCAAA GACCTTTGTT 420
TGTGGCTAAT AATAGCTCTT TGTTTCTGCT TGCAGGAGGG TAGCCTCCAT GCAGGGCTTA 480
GACCCTTTTC CTTTTCAGGG ACCACACCCA CCCTACCCTC ATATTGGCTC TAGGGAGCCA 540
CTGCCACTAA TGGAAGTGTG TCATATCCTC AGGGTGTGCC AGGCAGGGAG GTAGAAGGGT 600
GGGTGAGGCT CGTAGACTTG CACATGGTGA TTGGCAGGGC CCCAGCCACG TGTCCATGTG 660
TCATCTACAG TGGGACAGCT GCTCCATTGT GTCTGAACTT GCCTATCCGA GAAAGGCAAA 720
GATTACAGTG TCAGAGCCAG GCCTTGACCG GTCCCCACCT GGCCCTGCCC CTGCCCATCC 780
TCATCCGGTT GGTGCCTTTA TGGAGCTCTG TGTGTGCCGA GCACTGCCTG GGACCTTCTA 840
CCCATGTGAT CCCCTTTAAT GTTCATAAAC AGGCTGTGTA GCAAGTCCTG ACCCCAGCCT 900
TGCCCTTGCA GCCTCCAGGG TGACCTTTTT TTTTTTTTTT GGACGGAGTT TCGCTCTTGT 960
TGCCCAGGCT GGAGTGCAAT GGCACGATCT CGGCTCACTG CAACCTCCGC CTCCTGGGTT 1020
CAAGCGATCC TAAATAGCTG GGATTACAGG CACGCGCTAG CGTGCCCAGC TAATTTTGTA 1080
TTTTTAGTAG AGACAGCGTT TCTCCATGTT GGTCAGGCTG GTCTTGGACT CCCAACCTCA 1140
GGTGATCCCC TTGCCTTGGC CTCCCAAAGT GCTGGAATTA CAGGCGTGAG CCACCGTGCC 1200
CGGCCCAGGG TGACCTTTTA AAATGCAGTC AAAGCACAAC ATCCCAAGGT CCTGCCACAG 1260
TCTACAAAGC CTGACTTGGT TCGACCCCAG CCACCCCTCT GACTTTAACG TTTCCATTCT 1320
CCCTGTCCTA AATACCTATT GTTGCTCAAC ACACTGCTCC AAATGTGCTG GCTTAAGCCA 1380
TGTTGTTATT TCTGCTGATT CTGTGCATCA GGGACGATGC AGGGCACGGG GGAGCCCGCT 1440
TGCACTGCTG CCTGGGATGT CTGCTGGCGC TGGAGCACCC AAGATGGCCT CATCATGGCG 1500
ATGCCTGGTG 1510
|
| |
|
|
|
