Tag | Content |
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EnhancerAtlas ID | HS042-34526 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr4:16746400-16747900 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PAX6 | MA0069.1 | chr4:16747002-16747016 | AAGTCAAGCGTGAA | - | 7.64 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 16746759 | 16746814 | chr4 | 16746791 | 16746894 |
| | Number: 1 | ID | Chromosome | Start | End |
GH04I016745 | chr4 | 16746759 | 16746814 |
| Enhancer Sequence | GTCACGTGTT TTATGAAGAA TTAGGAAACA TTAATTTGAA TCCTGACTTT ATTACCAGCT 60 AGCTGGGTTG CCTTGAGCAA GTCAAAGCCA AGTCAATTTT TTGGTTTGTT AGCTGTACAT 120 ATAAATACAG ATTATAATAG CTATTACTTA TTGAAAAACT CCTGTGTATC AGGGATTGTA 180 TGTATGTTAC TCACAAATAC TATAGTAACA GTGTCAGATA GACACTATTT TCATTATACA 240 GATCAAAATG GTGAGACTCA GAGAAATTAG GTGTAACATC CGAGGTCATA TGGTAACTGC 300 AGGACAGGGT CGTGATTTGA AGCCAAGCTT GTCTGACTCA CAAGCCTGGG CTATTTGCCT 360 TTAAAGTGAG GGGTTATGTA AGGCATTCTC TAATTGGGTC ATCCTGGAAA TACAGACTGA 420 GTATGTGATT TCCACAGAAC AAGGCAGGCA GAAGGCCCTC CTCCTCTACA CCTCAGAGGT 480 AAGTCACATC TCAGTTCCTG TTGGTCCAAA TGAATGCAGG CTGAGGCAAT GGCAGAGACC 540 CAGAGCCCAG GCGGGGAGAC TGCGGGGATT TAAGAACTCG TTTACTTAGA ACAGTGAAAA 600 GGAAGTCAAG CGTGAACTTT CTGAGCTCCA AAGATATTCT CAGGGCCCAT TTGCGAATAA 660 GCATAAATCT TCAAATTTAT CCAAAGTTTA GCAAATTCAC AATGACAAAT GTAACAGTTC 720 CTCTAAATTG AAGTTCATCT CCTGGCAGTT TTGGAGGCTT GGAGAAAATG CCAGCAACAA 780 GGACTTGGAA GGAAATAAAT CTTTAGATTC CCTGAAAACA CAGAGAGTTA TTGTGGAAGA 840 CATATGGAGG ACCCCATACT GCGTTAAGAA AGAAAATTTA TAAATGTCAG CTTCATAGCA 900 GCAATGTCGA AGGGATTTCA GCAATCCACA CTTAACTACA ATAAGAAAAA CAGGCTGCAG 960 GTACACATTT GCCACGAAGA ACTAATTATG CTTAACCTGT GCTCTTTCTG GGAGGAGCAA 1020 ATGAGGAGAG AAGGAGGTAA GTGTCCAGGA TCCAGAGTAA GACATTAGAA TTTTTTTTTA 1080 ATCCAAACAG GTCACGTTTA AAGATTCTCT ATTGTTGAAA AAAAAAAAAA AGTTCTGAAT 1140 AGTGGGATGG TAAAGGGTAC ACAGTATGGG CCTATATGGC AGAAGAGTTG AATTCTGCAT 1200 CTTTGAAGGC CTCGCTTTTG TCGTCTCTTC AACACTAATG ATCAATCTGA CACCTGCTCC 1260 CAGGTTTGTA CTGATGATGG AATGACGCAT GGTCACCAAG TACTACTCAG CAAATATTGA 1320 CCATGGGCCT TTCTGTATCA CAGAAACAGG CACAGTGACT ACAAAGGTGA ATGACACACA 1380 GTCCCCACCC TCAGTAAGCT TACAGATGGT CCTGATTTAT GAAAGCATTT CATAAACTGT 1440 AAAGCATTAT TAGAATGTTT ATCATTTTAA CTTATTAACT AATCCAGTAA GTCATTATTG 1500
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