Tag | Content |
---|
EnhancerAtlas ID | HS108-14457 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:3213140-3214560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr16:3213921-3213931 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr16:3213921-3213931 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr16:3213921-3213931 | ATTTTCCATT | + | 6.02 | NRF1 | MA0506.1 | chr16:3213405-3213416 | GCGCCTGCGCG | + | 6.14 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34540 | chr16:3212796-3214677 | HCT-116 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 3213388 | 3213840 | chr16 | 3214190 | 3214464 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I003163 | chr16 | 3213001 | 3213902 |
|
Enhancer Sequence | TTGAGACGGA GTTGCCCAGG CTGGAGTGCA GTGGTGCCAT CTCGGCTCAC TACAACCTCC 60 GCCTCTGGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG ATTACAGGCG 120 GGTGCCACCA CGCCTGGCTA ATTTTTTGTA TTTTTAGTAG AGACGGAGTT TCATCATGTT 180 GGCCAGGCTG GTCTCCAGCT CCTCACCTCA GGTGATCCAC CCGCCTCAGC CTCCCAAAGT 240 GCTGGGATTA CAGGCGTGAG CCCCCGCGCC TGCGCGCCCG GCCTGATTGA CATTTTCAAG 300 CTGGGATTTT CCAGGCTTTG AGAATGACCA GGTCTGCGAT GACACTCCCT GGCTGGGAGC 360 AGGAGGGACT CCTGAGACTG CTCCCCTTGT GGACAAAGAG GAAGTTGGGC CGATGGCCGA 420 TGACGGCCAG GCCGCGAGGC TGCTGCTGGG CCCTGGGTCA CAGGTCGAGG TGTCAGGCCT 480 CTGAGCCTAA AGCTCAACCA TTATAACCCC TGTGACCTGC ACATATACGT GCAGATGGCC 540 TGCAGGAGCC AAGAAGTCTG AAGAAGCCAA AAAAACCACA AAGAAGTATA ACAGCCGGTT 600 CCTGCCTTAA GTGATTAACC AACATTACAA CATTCTACCA CTGTGACTTG TCCCTGCCCT 660 ACCTTGGCTG ATCAATCGAC TTTGTGACAT TCTTCTTTTG GACAATAAAT CTTATGACCT 720 CCCTACCACA TACCTTGTGA CCCCCTCCTC TGCTAACAAT AGATAACCAC CTTTTACTGT 780 AATTTTCCAT TACCTACCCA ACTCCTACAA AGCAACCCCT TCCCCATCTC CCTTCGCTGA 840 CTCCTTTTTC GGACTCAGTC CGCCTGCACC CAGGTGATTA AAAAAGTTTT ACTGCTTACA 900 CAAAGCCTGT TTGGTGGTCT CTTCTCACAG ATGTGCTTGA CAGAGGCCGC CCTGCAGTTC 960 CTGTTCCGAT CTAAGGAAGG GAAGGGGAGG CGAGGAAGAA CTGGGTCCCA AGACAAGAGG 1020 GTCCATTTCG TGAGGCACAC ACTCAGGACA GACCCTACCC CGCTGCTCTA CTCTTTCGCT 1080 TCAGTCCCTC CTTCCCGGCC TCCGCTGGCC CCCTGACCCC GCACTGATCA TTAATGCAGA 1140 AGCAGCGCAG ACCAGCAGCC GGGATCGCCG GTAATCCCAG CACTTTGGGA GGCGGAGGCG 1200 GGCGGATCAC CGGAGGTCGG CAGTTCTGAG GTCGGCAGTT CGAGACCAGC CTGACCAACA 1260 TGGAGAAACC TCTGTCATGA GCCGCTTGCC TCCACCGTGC ATGCAGATCT GCAGGGGAGT 1320 GGGAAGAGGC AGGTTCTTTG GGTCATTTGA AACGGTTTGG AGATATGCAG AGGCTGGGCT 1380 CAATATTAAG TAGGAATTGG GATTTATATT GGCAGCGAAG 1420
|