Tag | Content |
---|
EnhancerAtlas ID | HS118-10914 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr2:219170250-219171870 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr2:219170572-219170584 | TTTATTTTTAGC | - | 6.04 | MEF2C | MA0497.1 | chr2:219170571-219170586 | ATTTATTTTTAGCCT | - | 6.03 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 219171031 | 219171361 | chr2 | 219170512 | 219170566 |
| Enhancer Sequence | TTTTTGTAGA GGTGGGGTCT CACTGTGTTG CCCAGGCTGG TCTTGAATTT CTAGACAATT 60 TTCCGATCCA TCATCCCGCC TTGGCCTTCC AAAGTGCTGG GATTACATGC ATGAGCCACC 120 ACCCCCAGCC CAGAGGTCAG AGTCTTGTAA AGAAAAGGCT ATGGCTCCTC TGGGTGTGCC 180 CCCTTCCGCC CCCACCATAG CCAAACCATT CGTTTCTGTT TGGCTGTGAG ATGACATTTT 240 TTCCAGGGTC TGGAGTTAGA GTAGTGACCA GGCAGTGCAA ATAATTGTGG TAATCAGAAA 300 AGCCTTCGAA GAGGAGGTTG AATTTATTTT TAGCCTTAAA GAAACTGGAC TAAAAGGAAA 360 GGCATTATCA GCCTCCTTGA GAACTGAACT CATTCTCCTC CCTCCTCTGT TGAGAGCTGC 420 CAGACTCCCT AGATTGAGAA TTGGACCTTC ATTAGTTATG GTTACTCCTG GAAGGGTATC 480 ACATCCCCGG GGGCATGGTA GGGCTGGAAG GTACCTGGTA TCTTGAGGAA GCTGCCTAAA 540 AGGATTTCTC CAGGTGGCAT GGGGCAGAAA TCTAGGATAG TGATCAGGGC AGGCTGGCAG 600 ACGGGACACA TGTGGAGGGG AGCAGCAGGA ACGCCACACA CTAGAGAACT GGGCTGAGAC 660 CATGTCGCTA AAACAAGGGA TGCAAATTTG ATTGTGTAGA CACTGGCTTT GAGCAGGGGG 720 AGCCCCTGCT TGAAACTGAT GGCTAGGGGC TGCAGGTGCC TGCAATGGGC CAGGCATGAG 780 GACCCAAGGG CCTGATTTGG GATGATGCAA TGGGAAATGG AGGCAAAGGT CACACCCTCT 840 TATCATTTCA GTCATAAAAT ATTTACTTGA GCACCCACCA GGACAGATGC TGATGTTGCA 900 AGAATGAGAT CAATAATATC AAGGAACATG TGTGGAGTAC TTGAAACGGC CCAGGCAAGG 960 TGTCCTTTCT CTGGGTAATC ACGGTTAATC CTCCGAGTAG CTCCATGCAA ATTACCAGTC 1020 CCTCGTGGAG AGAAAGAGAA TGAGGTTTGA GTAGATTAAG AACATTGCCC CAAGGTGCAG 1080 AGTTCCTAGT GGAGCCAGGG TTCTAAGCTG GTCATTCCAA GTCTAGCACA CAACCCCCAA 1140 ACCCGATTCC ACTCCCTCCC CGACAGTTCA CCCTCCTTAC CCACAAGGCA CTTGAAGTGT 1200 TATGGGGCAG CGCCAGGAAT TACTGCACAG CCTAAGGACC ATCACAGAGA CATGTGTGCA 1260 ATGAAGTGTG CAAGTCATTA CCTAGGCCTA AGAGATGCCC TCACCCAGGA GCTAGGTGTC 1320 GGGATTGGTT TGTTTGGTCA TCTGACAAAC ACAGATGCTT CCTAACTTAT AGAGTGGTTA 1380 CATCCCAATA AACTCATCCT AAATTGAAAA TATCCTAAGT GGAAAATGCA TTAAATACAC 1440 CTAAACCTAC CAAACATCAT AGCCTAGCCT AGCCTGCCTT AAACATGCAC AAAACAATGA 1500 CATTCGTTTA CAGTTGGGCA AAATCATCTG GAAACACAGA TGATGCCGTT GGCCAAGTTG 1560 GCAGACCTGA AGGAGAGGGT TGGGGTCACA TGAGGATGAG GAGGTAGCTT TGGACAAATC 1620
|
| |
|
|
|