Tag | Content |
---|
EnhancerAtlas ID | HS102-14810 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr21:34754350-34756980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr21:34754590-34754608 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr21:34754594-34754612 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr21:34754670-34754688 | AGAAGGGAAGAAGGAAAG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr21:34754578-34754596 | GAAAGGGAGGGAGGAAGG | + | 7.45 | EWSR1-FLI1 | MA0149.1 | chr21:34754582-34754600 | GGGAGGGAGGAAGGAAGG | + | 8.32 | EWSR1-FLI1 | MA0149.1 | chr21:34754598-34754616 | GGAAGGAAGGAAGGAAAA | + | 9.07 | EWSR1-FLI1 | MA0149.1 | chr21:34754586-34754604 | GGGAGGAAGGAAGGAAGG | + | 9.47 | Foxd3 | MA0041.1 | chr21:34756589-34756601 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr21:34756593-34756605 | GTTTGTTTGTTT | + | 6.32 | IRF1 | MA0050.2 | chr21:34754551-34754572 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | Klf1 | MA0493.1 | chr21:34756066-34756077 | AGCCACACCCT | + | 6.02 | USF1 | MA0093.2 | chr21:34755676-34755687 | GCCACGTGACC | + | 6.62 | USF2 | MA0526.2 | chr21:34755674-34755690 | GCGCCACGTGACCCAG | - | 6.69 | ZNF263 | MA0528.1 | chr21:34754580-34754601 | AAGGGAGGGAGGAAGGAAGGA | + | 6.09 | ZNF263 | MA0528.1 | chr21:34754575-34754596 | GAAGAAAGGGAGGGAGGAAGG | + | 6.23 | ZNF263 | MA0528.1 | chr21:34754595-34754616 | GAAGGAAGGAAGGAAGGAAAA | + | 6.56 | ZNF263 | MA0528.1 | chr21:34754591-34754612 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr21:34754584-34754605 | GAGGGAGGAAGGAAGGAAGGA | + | 7.08 | ZNF263 | MA0528.1 | chr21:34754587-34754608 | GGAGGAAGGAAGGAAGGAAGG | + | 7.42 |
|
| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_00219 | chr21:34750982-34756583 | Adipose_Nuclei | SE_09780 | chr21:34750609-34758167 | CD14 | SE_10653 | chr21:34751101-34757835 | CD19_Primary | SE_10924 | chr21:34750502-34759616 | CD20 | SE_27036 | chr21:34754548-34756615 | Esophagus | SE_36753 | chr21:34754454-34756616 | HMEC | SE_53413 | chr21:34751185-34757173 | Spleen | SE_58466 | chr21:34731200-34786233 | Ly1 | SE_60169 | chr21:34732700-34761220 | Ly4 | SE_60632 | chr21:34732666-34757447 | DHL6 | SE_61512 | chr21:34731229-34778660 | Toledo | SE_64665 | chr21:34754499-34756570 | NHEK |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 34754708 | 34755048 | chr21 | 34755296 | 34756154 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH21I033378 | chr21 | 34751108 | 34757769 |
|
Enhancer Sequence | AAGACCAGCC TGCCCAACAT GGTGAAACTC TGTCTCTACT AAAAATACAA AAAAATTAGC 60 CGAGCATGGT GGCGGGCACC TGTAATCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATTG 120 CTTGAACCTG GGAGGTGGAG GTTGCAGTGA GCCGAGATTG TGCTACTACA CTCCTGCCTG 180 GGCGGCAGAG ACCCTGTCTC AAAAAAAAAA AAGAAAGAAA GAAAAGAAGA AAGGGAGGGA 240 GGAAGGAAGG AAGGAAGGAA GGAAAAAGAA AAGTAAAGAA CAGAAAAAGA AGAAAGGAAA 300 AGAAAAGAAA GGAAAAGAAA AGAAGGGAAG AAGGAAAGAG CAGAGAGGCC CAGTCGCTCT 360 TCTCAGAGTC TCCGTGGCAT CTCGGTAGAT TTGCTGATCC CTTTACATAA CCCAAGTTGA 420 GGCATGCCCT AATTTCACCC ACAAATGCTA CTAAGCCCAG GCCCTTATCC AGCCAAAACC 480 ATCCTGCCAA GCTCCCACCA CCACCATCAG CATCATTTTC AGGTTGTTGG TCATCACTGG 540 TTGTTGGTCA TCACTGGTTG TTGGTCATCT ATGTCACCTA ACAGGCCACT CATGACGTTA 600 GCCCTTGACT TCAAAAAGGA CCTCAAAGAA AATTCCAGTT TTCACTCCAA AAGGAGAAAT 660 CAGGCCGAGC TGTGATGGCT CATGCCTGTA TTCCCAGCAC TATGGGAGGC TGAGGCAGGC 720 GGATCGCTTG AGCCCAGGAG TTTGAGACCA CCCTGGGCAA ACCTATCTTT CCAAAAAAAT 780 ACAAAAAGAT TAGCTGGGCA TGGTGGTGCG TGCCTGTAGT CTCAGCTAGT CAGGAGGCTG 840 AGGTGGGAGG ATCACTTAAG CCTGGAAGGT TGAGGCTGCA GTGAGCGGTG ATGGTGCCAC 900 TGCACTCCAG CCTGGATAAC AGAGCAAGAT GCTGTCTCAA AAACTAGCAA ACGAAACAAA 960 AGGAGAAACT GCTGGCAGCC CCTAATCTAG TACTGTCCCG GCTCCACCCA CCTTCAGATC 1020 CAGCCTCCTC CCCTGGCACA CGGGAGCCCC CTCCTCTGAC TGTGCTGAAA GTGAGGGAAG 1080 ATCCCCTCTG GGGAGAGAGC TGTAGCCTTG ACCTCTGCAC ACCTTACTTA TCCAGAGCAC 1140 GAGGCAGGGC CGCTGACTCA TCCTGGTTTA CCCTGGGCTT TCCCAGTTTC AGCACTGAAA 1200 GTCCCGCATC TGGAAAAGCC CCTGAGTCGC TGACAAACCA GACAGTCCGG ACCATGCAAA 1260 GCACAGTGCA TGGTGCTTTA GCCACAAAGT TGATTGAAAA GTCAGAGGCA GTGAGCCACA 1320 GGAAGCGCCA CGTGACCCAG ACTGCGAGGA GGACACAGGA AACCAACCCT CACTGTGTCC 1380 TGCTAGGGGG TTAACCCGTC TACAAGCATC AGGGTTGCCA TTTCAGAGAT CAGCAAACTG 1440 AACAGCAGTC GTGACTTGTC CTCGCCTGCA AGACAAGCGA GTAACAAATC CATGAAGGGA 1500 AGGACACGGA ATTGAGCAAG GGGGCAGGGC CGGATGTCAT TTTGGCGTTT TTTTTTCTTT 1560 CAGTGATTGA GGTAAAATTC ACATAACATA AATTAACCAT TTTAAAGTGT ACGATTCAGA 1620 GGCATTTGGT ACATTCACAC TGTTGTGCAA GCACCACCTG TATCTCGTTC CAAAATATTT 1680 TCACTTCCCC AAAAGGAAAC TGTGTCCCCA TCAAGCAGCC ACACCCTACT CCCTCACCCC 1740 CGCCCCCAGC CTCTGACAAC CACCAATGTA CCTTTTGTCT CTATGGATTT GCCTTTACTG 1800 AACAATTCAT AGTAATGGAA CCATACAATA TGTAGTCCTT TGCGACTGGC TTTTTTTACT 1860 CAGCATCAAT TTTTTTTTCT TTTTCTTCGA GACAGAGTCT TGCTCTGTCA CCCCGGCTGG 1920 AGTGCAGTGG CATGATCTCG GCTCACTGCA ACCTCCACCT CCTGGGCTCA AGCGATTCAC 1980 ATGCTTCAGC CTTCTGAGTA GCTGGGACTG CAGGTGTGCA CCACCATGCA TGGCTAAATT 2040 TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTAG AGAGGGAGGT CTTACTACAT 2100 TGCCCAGACT GGTCTCAAAC TCCTGGCCTC AAGCAATCCT CCTTCCTCGG CTTCTCAAAG 2160 TGCTGGGATT ACAGGCTTGA GCCATCACGC CCAGCCTATC ATCCTAGTTT TGTTTTTTGG 2220 GTTTTTTGTT TGTTGGTTGG TTTGTTTGTT TGTTTTTGAG ACCTAGTTTC ACTCTTGTCA 2280 CCCAGGCTGG AGTGCAATGG TGCAATCTTG GCTCACTGCA ACCTCCGCCT CCTGGGTTCA 2340 AGTGATTCTC CTGCCTCAGC CTCTCAAGTA GTTGTGACTA CAAGCATGCG CCACCACACC 2400 TGGCTAATTT TTGTATTTTT AGTAGAGACA GGGTTTCACC ATATTGTCCA GCCTGATCTC 2460 AAACCCCTGA TCTCAAGTGA TCCTCCCACT TTGGCCTCCC AAAGTGCTGG GATTTCAAGT 2520 GTGAGCCACC GTGCCCGGCT GCCTCATCAA TTCTCTATAA ACAGTTATTA ATGAGAAGTC 2580 AGTTGAGCTG TTTCTATGTA TTTGTTTCCA GAAAGAAACA GGGTGCACCT 2630
|