Tag | Content |
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EnhancerAtlas ID | HS051-18569 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr22:37373300-37374730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr22:37374272-37374291 | TGCTGCCACCTACAGGTCA | - | 6.73 | IRF1 | MA0050.2 | chr22:37374058-37374079 | AAATTAAAAAAGAAAGAAAGA | - | 6.18 | ZNF263 | MA0528.1 | chr22:37374217-37374238 | CCTCCCAGCCCCGCCTCCTTC | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I036976 | chr22 | 37373021 | 37374830 |
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Enhancer Sequence | GGTTGGAGGG AGACCACGGG GGATGGAGGC TAGTGGGGCT GCCACACTTC CACCCCATGA 60 CGCCACAGGA TGAAGGAGCT TCCAAAATGC ACGTGGACCC CAAGGAAGGG AGTGAGGCGT 120 GAGTGGCCAC GCAGAGCCCA TCCAAGGGGG CAGACAACTG GGTGAGAACA CCCCAGCAGG 180 CCAAGGCTGT GGGGTGTGCC CTAGAGGAGG GCAGGACCCG AGGCAGTATG GGGAGCTGCT 240 GAGCCAGTGC ATCTCCCTCA CGGGGGCGCT GTGCAGTGTA GGTGCCCCTA TGGGACACGC 300 ACACCTCCTC CAAGAGCGGC CCCCGCAGCG GAGCAGAGCT GGCCAGAGGA GCACTAAGTA 360 AGCCAGGCTG ACAGAGGTGC TGGAAAAGAG GTCCAAGGGG GAGCTGGAAC TGTTACAGGC 420 ATTCAAACCA GAGTGACTCC ATTTTGAACA GGGGCTGGGC TACTGGGCTG CGTTCCCAGG 480 AAGTCAGGCA TTGTTAGCCA CGGGATGAAA TAGAAAAAAA AAAGTTAGCC AGGTCTGGTG 540 GCGCACACCT GTAGTCCCCG GAAGGATCGC TTGAGCCCAG GAGTTCGAGG CAGCATTGAG 600 CTAAGATCTC GCCATTGCAC TCGGCCTGGG TGACCGAGTG AGACCCTGAC TCTAAAATAA 660 GTAAATAAAA AGAACCAAAA AGTATCTAAT TATGGATGAT TTTTACTTTC GTTTAGACGC 720 TATTCTCTAT AATAAAAAAT GTTGCATTTG TAATCAGAAA ATTAAAAAAG AAAGAAAGAA 780 AGAAAGAAAG AAAACTGTTA AAACTGAATT GGTAGAAGAA TGGGTTAGTG AGACAATCCC 840 TCGCAGAATC TTGTGCTTTG GGAAATCTCC GTGCCGTTTG TAGAAGGATT GCACCAGTGA 900 CGCGGTGACA CCCATCTCCT CCCAGCCCCG CCTCCTTCCT TCCGGTCCGC TGCTGAGGCT 960 TGGCTCGGCT TGTGCTGCCA CCTACAGGTC AGCGACAGAC ATTACTTCAA CCCCCCTTCC 1020 GCAGGGGCAG CCGCTCCCAG CTGCAGTTTT CCCTTTTCAT TTTAAGCCCT TGGATTTCAG 1080 AGTTGAGGAT GGAGATGTGT GGGAACTTCC AATGTGAAGT CAAGATAGGG GAGAGGGCAA 1140 GACAGAATGA GATAGAGAAC ACCTGTGTGT GCATCTGTAC ATGCAGGGCC CAGTGCAAAA 1200 TGAAGATGTG GGGGCCCCTT GTTCAAAAAT TATTAAGAAT CTCAATATTG TAACAGTAGG 1260 GCATTAAATC AAGTGCAGCG CCCTCTGAGA ATGAGCCGTC TGGGACTGCA CAGGTTATAG 1320 GCTGCATGCC CATGAAGCCG ACTGGCAACC TTGTATTTGG ACTTAAGTTA GCAATGCTTT 1380 CGTATGCTGT GCCTAGGTGT GTATGTGTAC AAATATGTAT ATTTGTGTGT 1430
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