Tag | Content |
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EnhancerAtlas ID | HS108-26253 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr21:46449270-46450470 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PAX5 | MA0014.3 | chr21:46449815-46449827 | GAGCGTGACCCT | + | 6.92 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 46449400 | 46450000 | chr21 | 46450000 | 46450194 |
| | Number: 1 | ID | Chromosome | Start | End |
GH21I045029 | chr21 | 46449179 | 46454770 |
| Enhancer Sequence | CACTCCAGAG GGGTCCATTG AGCTGGGTCC TCTGCAGGGC TGTGGCCTGT GCTGGGTGGA 60 GACAGTCCTG GGGTGCTGGA GGCAAGCGGG GCTTCACTCA GGGCTGTATC TGGCTGCCTC 120 CGAATCGCAA CAGAAGCTCA ACAAGCCTGG AGCTCCCTCA GGGGGCTCAG TGGCCTCTGA 180 GACCTCCCAT CTTCCATTTT CCCCTAGAGC TGGCCATGCC TGGGGACTCT GACCATGGGC 240 CCCAGAGAGC GCTGCTCCCC TTTGGCCAGC GACAGGGTGG CCAGGCCCAG GATCTGGAGG 300 GAGAAAGCTG CTGGCCTTCT CCAGGGTGCA GCCTGGAGCT TCCCTGCTCT TCTGCAGCTG 360 TGCTCAGCTA CGCTCCAGGG CTGCGCTGAT TTCCGCTGTC AGTGACTTAA GCCAGCGTCC 420 ACGGCCAATC AGCACAGCAC TTCTGCCTGC TGCCTGCTGG GTTCAGACCA GGCTGGGTCT 480 GGTCCCTGAC GGAGGATGCA GTTCTCATCC TTCAAGCACA AGCCTACAGG CAGCCCCTTG 540 TCACCGAGCG TGACCCTGCC TCAAGGCCTC CTCCTCCCTC TCTTGAGTGA GTGGAGCAGA 600 GCTGGCCGTG GCCTCCCTGC CTCCGCTGAG CCCACCACCA GTGGGTTTTG TTCGGGGCTA 660 ATGAGGCGCG GGAAAGGCGG AAGGTGCCGG CGTGACAGCT CAGAAGATGG AACTAATGAG 720 ACCTTGTTGC TGGACAAAGG TGGCATTCAG GGTGTCCTTT TGGCCTCGGC CCCCGACTCC 780 CAAACGGGCC CCTCTAATCA CAGATGGTTC CCGGACCTGT CCCAGCAAAG GGTCCTGAAG 840 CCCCGGCTTT GCTGTGCAGA GGCTCCTCCC AACCTGGGTT TAGCCAGGCG CCTCCTCGCC 900 TGCCCCACCC CCTGCATCTG GTCACCTCAC CCCTCCAGGC GCAGTTTTGA TGGAGAAAAC 960 CAGACGCTGT GGGAGCCCAG GCCGGCGTCT GAAGTCCGAG GTTCCAGGGG CCACAGAGCC 1020 CCGGCCTGGA CTCACAGGGG AACTCCCTCA CGGCAGGTGG GCCTCCTGGG TCTTTGTCTT 1080 CCTCATCAAT TGGCAATAGC TAATCAGTGG TGGATTTCTG CAGGTTTGGC AGCTGCTGCT 1140 CCATTTGAAA CAGCTTAAAT GAGCTAAGAG CCAACTCAGC GGGTAAAACT GTAATCAGTG 1200
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