Tag | Content |
---|
EnhancerAtlas ID | HS196-28953 | Organism | Homo sapiens | Tissue/cell | ZR75-1 | Coordinate | chr7:33276500-33277670 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr7:33276578-33276589 | TAATTTAATCA | + | 6.62 | SPI1 | MA0080.4 | chr7:33276883-33276897 | AACTTCCTCATTTC | - | 6.43 | ZNF263 | MA0528.1 | chr7:33277566-33277587 | TCTCTTCTCTTCCTCTCCTCC | - | 6.04 | ZNF263 | MA0528.1 | chr7:33277569-33277590 | CTTCTCTTCCTCTCCTCCCTC | - | 6.32 | ZNF263 | MA0528.1 | chr7:33277576-33277597 | TCCTCTCCTCCCTCATCCTCA | - | 6.93 | ZNF263 | MA0528.1 | chr7:33277573-33277594 | TCTTCCTCTCCTCCCTCATCC | - | 7.81 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGAAACTTT GTACCCTTTT ACCTCATCAT TTTTAATGAC GTACAATTTG TGTTTTACAC 60 ATGCATACAC ATTATAATTA ATTTAATCAG TCATCTGTTG ATGTATATCT AATGCTTTCA 120 ATAGTTTTTA TATTTATAAA TCATTGAACT TATTTGTAAT TCTTTATATA TTAAAAATAT 180 AAAATGAATA CATTTTTATT AAACCAAAAC TGAAAAGTTC CTTTTCATTT CCCTTCTGCA 240 GATGAAATCT CACTCTTGTG CCAAGGTAAA TAAAATAGTG AGCAACCTTG CAGTTGGATA 300 CAATGTTCAA TGCGTTTATA AACATATTTG GTTCTGTTTT ATGTTGTTTT ACATAAATGA 360 GGTCACTCTG TATATTAGCT TGTAACTTCC TCATTTCAGT TACACGGACA TCTTTTCATG 420 TCCAAACACA CAGACTTTTG TTCTTCTTTG AGCTATGTAC AATTCTATAT TTGGATATTT 480 CATTATTTAG TCATTGAGAT TGCTTCTAAA ATTTCAATTA TGGACAGTGT GTTTTTGCAG 540 TGGCTCACTC TGCCTTAGTA TATGCCTTTA CAGTAAAGCC CATGGGTGTG TATCCTCTTG 600 ATCTGTCTGT GACATACATT TTAGCATTTA CATTTAATTT CACTTAAGAG TAGTGGTATG 660 TGTTGATCTT GTGGTGGAAA ATAGAGGCAG TTGGCTAAAT ATTCTAGAAA GTTTGCAGAG 720 AGCTTGATCA AATAAGCTCA GAGGAAGAGG TTCCTCACTT CAGGATTACC ACATTCATCT 780 AGTACCTTCT TCAACAACCA TTTAAATTAA CCTTCTCACT GAAAGCCCAT TTGGCTAATG 840 GAAGATTTTC ACTGACTTTT CACTCTATGA AAATAAATTG ATAAAGATTC AGGAGTTATC 900 AGCTCTAGGT ATGCTTCTCA GTAATGGATG CTTATTCAAA CTTTTACTCT TGTGACAATC 960 AAGATCAGTA GAAGTCTGGT TTTTTGATGG TTCAGATGAC AAATTTCAGT GGATAGAAAT 1020 TGTGTCAACT GCTTTCTGAT GAGGTGAAAG CCTGCTCTTT CTGTCCTCTC TTCTCTTCCT 1080 CTCCTCCCTC ATCCTCAAGA ATAGAGAGCC ATTTCATATA CAGTGGACAT TGTTTGCTCC 1140 ATTAAATAAC AATAGTCTTT TCAGACTGAC 1170
|
| |
|
|
|