Tag | Content |
---|
EnhancerAtlas ID | HS108-11701 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:20997230-21000090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6 | MA0463.2 | chr14:20998066-20998082 | TTTTCCTAGAAAGCTT | - | 6.8 | CTCF | MA0139.1 | chr14:20999314-20999333 | GTGCCACCAGATGGCGCCA | + | 7.28 | EWSR1-FLI1 | MA0149.1 | chr14:20999087-20999105 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr14:20999034-20999052 | GAAAGAAAGAAAGGAAGA | + | 6.22 | EWSR1-FLI1 | MA0149.1 | chr14:20999038-20999056 | GAAAGAAAGGAAGAAAGA | + | 6.22 | EWSR1-FLI1 | MA0149.1 | chr14:20998974-20998992 | GAAAGGAAGAAAGGAAGA | + | 7.18 | EWSR1-FLI1 | MA0149.1 | chr14:20999091-20999109 | GGAAGGAAGGAAGGGGGA | + | 7.23 | EWSR1-FLI1 | MA0149.1 | chr14:20999083-20999101 | AAAAGGAAGGAAGGAAGG | + | 7.95 | Foxd3 | MA0041.1 | chr14:20998448-20998460 | GTTTGTTTGTTT | + | 6.32 | IRF1 | MA0050.2 | chr14:20999049-20999070 | AGAAAGAAAAAGAAAGAAAGA | - | 6.14 | IRF1 | MA0050.2 | chr14:20998542-20998563 | TGTTTCTTTCACTTTATGTTT | + | 6.28 | IRF1 | MA0050.2 | chr14:20998941-20998962 | AGAAAGAAAGAGAAAGAGAGG | - | 6.39 | IRF1 | MA0050.2 | chr14:20999023-20999044 | AGAGAGAAAGAGAAAGAAAGA | - | 6.86 | Mecom | MA0029.1 | chr14:20998301-20998315 | TATTATCTTTTCTT | - | 6.46 | STAT1 | MA0137.3 | chr14:20998067-20998078 | TTTCCTAGAAA | - | 6.14 | Stat4 | MA0518.1 | chr14:20998064-20998078 | CCTTTTCCTAGAAA | - | 6.34 | ZNF263 | MA0528.1 | chr14:20999012-20999033 | GAGGGAGGGAAAGAGAGAAAG | + | 6.06 | ZNF263 | MA0528.1 | chr14:20999084-20999105 | AAAGGAAGGAAGGAAGGAAGG | + | 6.16 | ZNF263 | MA0528.1 | chr14:20999092-20999113 | GAAGGAAGGAAGGGGGAAGAA | + | 6.33 | ZNF263 | MA0528.1 | chr14:20999008-20999029 | AAAGGAGGGAGGGAAAGAGAG | + | 7.09 | ZNF263 | MA0528.1 | chr14:20999088-20999109 | GAAGGAAGGAAGGAAGGGGGA | + | 7.14 |
|
| 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 |
GH14I020531 | chr14 | 20999241 | 20999410 |
|
Enhancer Sequence | ATAACACCAT ACAGCCTAAA ATAGCATTAT GTGTTTCCTG GAGTTTATTG CTAACTTTTT 60 TTTTTTTTTT TTTTGAGAAG GAGTCTTGCT CTGCTGCCAG GCTGGAGGGC AGTGGCGCGA 120 TCTTGGCTCA CTGCAATCTC TGCTTCCCAG GTTCAAGCAA TTCTCCTGCT CGGCCCCACA 180 AGTAGCTGGG ACTACAGGCG CACGCCACCA TGTCCGGCTA ATTTTTGTGT TTTTAGTAGA 240 GACGGGGTGT CACCATGTTG GCCAGTTTGG GCTCAATCTC TTGACCTCGT GATTTGCCCA 300 CCTCAGCATC CCAAAGTGCT GGGATTACAG GCATGAGCCA CCGTGCCTGG CCTATTGTTA 360 CCTTTTAATT TTCTTACACT TTGTGCAGGC CTTATATCCT CAAACTCATC CATCTTCTCA 420 GTCAAGTTGT GTTTCCTATT AGCTACTTGC CTTTTTCCTA GAGATTTTTG TCCTTGAGCC 480 TCTGCCTCAA TAAATCTGCT CTGCAGCTAT AATCCTGTAA TCAGTGTTAC CCAGATCTCA 540 TGTTTCCTTT TCCTTGGTCT ACTCTTCTCT GTTTATTCCT GATTTTTTTT GGAGCATATC 600 CCGAAGTACA TTCATAAGAA AGTGTGCTTG GGAGGTACAT TTTGTGTGTT CTTCCATATC 660 TGAAAATGTA TTTATTCTAT TCTCTGATTT GATTAATAAT TTGCCAGAGT ATGGAATTAT 720 AGAGTTACAA TTCCTCCACA GAATTGTGAA AATGCATTGC TTCAGAGTCA TCTATCATCC 780 AGTTCTATTG TTGAGAAGCC TGACGCCATT TTGAATCTTT GAAATTGATG CTTCCCTTTT 840 CCTAGAAAGC TTACAGGATC TTTTTATGCC TCTGTTCTCA ATCTTCACAG TGACATGCTT 900 AGGTACGAGT CATTGTATCC TGCACTGGGG ATGGGGGTGG GGTTAATTTG GAAACTCAAC 960 TTTTCGGGTA TGGGAAATTT ACTTCAGTAA ATTTCCAATT TCTGTTTCCC TCTCTCCTCT 1020 CTTCCTGGAA CTCTATTAGT CAAATATTGA ATCTCTTGGA TTGCTCTACT GTATTATCTT 1080 TTCTTCTGTT TTTCCTCTTT TGGAAGTCAT TTCTTTGACT TTATCTTTTG AACCTAATAC 1140 TAATTCTTCC ACTCCTGCTA TTTTATATAT TTATTTTCCA AGTGCTTGTT CTTTTTTGCT 1200 TTCCTTTTAC AAGTTTTTGT TTGTTTGTTT TGAAAACAAT AGTTCCCCAA ATAACTCGGA 1260 ATATACTAAC TAGAGGTTAT TAAGGCTTTA TCCTCTGTTC TCTGCTTTGT GATGTTTCTT 1320 TCACTTTATG TTTTTAAATT ACAGTCTTCA CAGAATTATG GAGACTGTCG AGTATGTGTG 1380 GAGAATGGAC CTTGCAAACA AATAAAACCA ATTTTGTAGA CTTTGACGAA TAAATTTCTC 1440 TTTAAAATAA AGATAGCTCA ATGTTGTTAA AATTATATAC ACACATACAA TTCTAAGCAC 1500 ATGGTAGGCG CTGAATTTAT GGTAGCTCCA GTCTTTTCTC TTTTATGAAT CAATTTCTCA 1560 AAAATATTTA AAGTGGCCAG TGCAGTGACT CACACCTGTA ATCCCAGCAC TTTGGGAGGT 1620 GAAAACGAGC GGATCACTTG AGCCCAGGAG TTTGAGACCA ACCTGGACAA CATAGGGAGA 1680 TTCTGTCTCT ACGAGAAAAA AAAAAGAGGA AAGAAAGAAA GAGAAAGAGA GGGAAAGAGA 1740 GAGAGAAAGG AAGAAAGGAA GAAGAAAGAA AAGAAAGAAA AGGAGGGAGG GAAAGAGAGA 1800 AAGAGAAAGA AAGAAAGGAA GAAAGAAAAA GAAAGAAAGA GAGAGAAAGA AAGAAAAGGA 1860 AGGAAGGAAG GAAGGGGGAA GAAAGAAATG AGTCGGTGTG GTAGTTCATG CCTGTGGTAC 1920 CAGCTACTTG GGAGGCTGAC GCGGGAGGAT CACTTGAGCT CAGGAAGTTG AGGCTGCAGT 1980 GAACTATGAT TGTGCCACTG CACTCCAGCC TGGATGGCAG AGCGAGACCT TGTCTTAAAT 2040 GATGATCATG ATAAAACCCC CAGTATCTAC AACGTGCGTG AGATGTGCCA CCAGATGGCG 2100 CCATGATTGG AACTGTAACA TGGAAGAACT CCAACTCCCT TCTTTAATAT TTCTGCAGAT 2160 TTCTGGTGAG GCTTTTATCC TTATGATCCG CTCTGCTTTT TGGATACTTT TTTTGCATGT 2220 GAGGTCCCAT GTTGACCCCA TTCCTGAAAC CCAGCTCCTT TCTTAACTCT TATTTATACC 2280 TGTCCCCTTC TGCTACACAC ACCCCAACTC AGGTAAAGTC TTCAGGAGTA GATTTGGAAG 2340 TTAAAGAGTA AATGAGGGTT TATGTTTTTG TGTTGAGAAA ACTTTTTATT TTACCCAGAT 2400 TACATCTCTT TTCTTAAAAT GTAATTGGCC ACACCATCTT CAGTTCACTG GCCCTTCATC 2460 TTGTACAGTT CTCAACCTTA CACTTTCTTG CTGGCTTGTG ATTTTTTTAT ATCCACACAC 2520 ACAGTCCCTC TGTTTCGTCC CCTCTTCCTT AGAACAAAAC AAATTATTTT CCTTGATTTC 2580 TGCTATATTT AAGGCACATA TTTATTATGT AACTTCCTGT GACATGTATG GCCTTAACAT 2640 CTTACCTGCT AGGTGAGCAG CATATGATGT TATTTTCCCA AAAAGAGTTA CTTTACTTCC 2700 TAAGAAAAGC TGTTGTCAGT TATTTAGGAT AGTAATATTT TTACCTCATC ATTCAGGTTT 2760 CTACAAATCT GAGGGAAAAA AGGAAAATAT CTGAAATCAA GAAAAGAGAA CTAACTTAAG 2820 TGTGTGGGGA TATAGGGAGG GCAAGAGAGG TGATGACTGA 2860
|