| Tag | Content |
|---|
EnhancerAtlas ID | HS145-09090 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr16:30834540-30836050 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr16:30835076-30835091 | GTGTCAAAAATAGAA | + | 6.38 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGGATTACA GGCATGAGCC ACCACGCCCA GCCTTTTTTT TTTTCTTATG TTAAATAAAC 60
AACAAAGAAC TGTGAAATAA AATATATAAC AATACAAGGA AAAACATGAG AAACAGTTTT 120
ATTGGAAATA TTCTAACACA TTTTCTGAAC AAATAATCAA AAAATAAATA AGGACATAGA 180
AAATATGAAC ATATAAATTT CTTACCCTGA AAACAAACAG TACACCTTCT TTTCAAGTTT 240
CATGGACAGT GGACAAAATT AAATAATTAT TAAGCTACAA AGAATATTTT GGTAAATTTT 300
GAAAAGTAGA AATTCTAGAA ACCATTCTCA GATCAAAATG CAATACAACT AACAATAATG 360
TAAAACATAC CACTTAGAAA TTTTGAAACG TAAGTAGCAC CTCAAATTAT CCTTAGGACA 420
AGATGTAAAT CAAGAGTTAA AAAAATTAAA AAACAGACGA TTTAGAAAAT AATTTAAAAA 480
GTAGGATTAA CAGCCAAAGC TATATGCAGA GGTAAAAACA GCATTAAATG CTTTTAGTGT 540
CAAAAATAGA AGAAAAATGA AACGAATTAA GCATGCTTGC AAGTTGGGAT TTTGGAAAGT 600
AGTATAAAAA CAGTTCCTCC AAAAATGGGA GAAATGGAAT ATTTGAAATA GAAAACAGAA 660
AAAGCAAACA CTCAGAGGCC TGAGAGGTGG TGGGATGAGT TTTCTGCCTG TGGACAGAGA 720
CACGCTTGGA GGCATCCCCG CGGGCTTGGT CCCCTGGCGT GTGTCATCAG GCCTGTCCCC 780
TCTCACTCCT CGAGCCCCGC CTGGTGTCCT CTCCTGTTCC CAGGGCTGAA GCTCCTGTGT 840
CTGTGTCATC ACCGCATCTT GAACATCCTG TGCCTTGATT GTGGCACTCT ACAGGTTTCT 900
CTACAACTAA TTCTTTTCAC TTATGACTCA CTTACTAGTA GACTTGACAG GACAGGAACC 960
ATGTCCTGAT ACTCATTGGA TCCACAGGGC CCGGTAGGCA TTGAGTTCTT AATAGACATT 1020
ATGAGTGGAA GAAAATGAGC AGATGGACTC AAGCACTGAT TCCTGAGTTG CATCTGGCCC 1080
CATTGCCCAG CCACAGGCTG GAAGCCCATG TCCTGAGGCC TGGAATGAAT TAGTCCAACA 1140
ATAAGAGGAC TAACTATGCA GGATCCACCT AATAGATTGT TATGCAACCT ATAATGGCTG 1200
TGTTGACAAT GTCAATAAAA TATGAGGAAG TGGGGCTTTG ATTGTTTTTC TTTTTCCTTT 1260
TTTTTTTTTT TTTTTTTTTG AGATGAAGTC TCGCTCTGTC GTCCAGGCTG GAGTGCACTG 1320
GCGCTACCTC AGCTCACTGC AAACTCCGCC TCCCGAGTTC AAGTGATTCT CCTGCCTCAG 1380
CCTCCGGAGT AGCTGGGATT ACAGACACCT GCCACCACAC CCGGCTAATT TTTGTAGTTT 1440
TAGTAAAAAC AGGGTTTCAC CATATTGGCC AGGCTGGTCT CGAGTTTCTG ACCTCATGAT 1500
CCACCCACCT 1510
|
| |
|
|
|
