Tag | Content |
---|
EnhancerAtlas ID | HS076-12927 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr12:14093770-14095260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr12:14094870-14094889 | TACTGCCCTCTCCTGGGCA | - | 6.07 | HNF1A | MA0046.2 | chr12:14094951-14094966 | AGTTAATCTTTAATC | - | 6.43 | MEF2A | MA0052.3 | chr12:14094162-14094174 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr12:14094162-14094174 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr12:14094161-14094176 | TTCTATTTTTAGTAT | - | 7.21 |
|
| 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 |
GH12I013941 | chr12 | 14093936 | 14095370 |
|
Enhancer Sequence | CCTGCCCCAC CCTGACATAT ACCCCACAAT CACCCATGCT CTCCACACAC CTTCCAACAT 60 GATGATTGAA ACTAGGGGAC TCTCCACACA CCTTACAGGG ACTTTGGGGC TCCAATTCAC 120 ATTAACCCTC TCTCCAATTT CCCTTCATTT CCCACATTTT CTTTCACTAA CCATTATTAT 180 TTATGCTAGT GCCCCACTAG CTTCCCCAGG GAAAGCAGAC ACACATATGT TCACACACAC 240 ACACACACAC ACAGTAGGTA GGAGGTAGAT AGGAGGGTGG GTAGACAGGG GATTCACACT 300 CTCTGTGGCC GTTGGATAGA GCTGGGCCAG TTACCAAGAA TGACCAAAAC AGTACTGCTA 360 GATATTGAGA ATTAGCTTAT ATTTCATTGC CTTCTATTTT TAGTATTTTG ATACTCCTTT 420 ATGTTCCCAC ATTGAACCTG GTCAAAAGCT AAAAATGCCT GTAACTAGCA CACAGCTCCC 480 CACAAACCTT GCAGCCAGAA AGTTGTCCCA GAAGAAAAGC TGACAACTCC AGTCATATGC 540 ATGATAAGGC TGAGGCAGGT TGCCAAACCC TCCTGCTGTG AAGATGGACA AAGGGACAAG 600 AAAAAAATCA CAATGATGCT CTGATTTCAA AGCCAGGTGA GGAACGGGAT TGGGTGTGAC 660 CTTTTGTTTC TGAGTCTGAG GTGTAAAATT CTGTGGGGTA GGATGGAGGA TATAAACTGT 720 GGGGAGCATG ACTTGATAGT CTAGAGAAGT TGGGGACAGG ACAGCCACCT CAGTGGCTGA 780 GGTAGATCGG CATAAACTGC CCTTAAACTG GACCCACAGG GAAGTGGTGG CCGAGGCATG 840 CAGCATTCAC AGCATCAAAC CCAGGGGACC ATCACTGCAG ATTTCCAGTC TGTTAGCGTC 900 CTAAGGACAA ATGAAAAGTG TCACTTCTAG ATCTACGTGT GTGCAAACCA TGGTAGCCGA 960 AGGCTGAAAA CAACTAAACA TAAGATTGAA AGCTGATCAG GTGAGAATGA AAATGAGGCC 1020 CAACTGTGAC TAATTCTATG CTGGCTCCCG CAGCGCAGTG TCTGCTAAGG ACAACTGGAA 1080 AAGCTTAAAT GTTAGCATGT TACTGCCCTC TCCTGGGCAA AAGGTCAAAG TCGGTACAAA 1140 TGTTTGAGTC ACAACTTGTT CAAGTTTGTG TGCCCCATAG CAGTTAATCT TTAATCCACT 1200 CTTTTACAAG CCTTTGAAAA AAGGTCTGCT TTTACCGTCT TCCACGTGCA AACCTCTCTC 1260 CATGACCACC ACCATGTTAC TTTTTCCATT GGAACCAAGG GCTTCTGAGA TCACAGACTT 1320 CATCGGGGGT CATAAGTAAT TGTGGGAAAG GGATTAGCAT CATTTGCCAG AAGAGCTGAT 1380 ATGACAGGGG TGGGGAGGAC AGCCCAGAAC TTCAGAGCTG ATCTACTCTT TAAGCAAGAA 1440 CCCCCTTTTT CTGTTTATTG CCCTGCAACT GTTCTAGGCA ATTCTGGGTC 1490
|