Tag | Content |
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EnhancerAtlas ID | HS051-00852 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr1:45314460-45316190 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:45316107-45316127 | GGGCTGTGGGTGAGGTGGGG | - | 6.46 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTCTGCCTG CCTTGCTTTT CTGATTTCTG TCCATGGAGA GGTGGCCGGC CAGTGGACAT 60 TCAGTTGCTC ACTATGTTTC AGACATACTC AGCCCCTCTG TAGCTGCTAC CAAAAGAAAA 120 CAAAAACTGT CCCTGCCTTC TGGCAGACAA ACAGGGCAAA GAGAAGAAAA ATCAAAGCAT 180 CTTGGGCACC CAGCCAGTCC TGGAACTGTC AGACAATAGC AGCAGTGTCC TGAGCTGGGG 240 GCTGCTCCCA GCTGGGACTC AAACTCAACA ACACCTTCCT CTGGGAAAGC TTTTACCTTT 300 TGTTTTCTCC AGCTCCTTCC TTTCCTTGAT GCAGAGGCCG TTCCATGGAC TTGTGCAAAG 360 GGAAGGCACA GGAGAGGTTT TTCCTCTGTC TCACTGTCAG GGGTTCTAAG GGCTCCATGG 420 GGAAGGACAG GAAAGGGTAC ATAGGAGGGC TCTGAGACAG TTTAATCAAT GCCCTTTACT 480 CCTCCACCGC ACTTTCCCTC CCAACCCTTT TCTCTGCTCA AGGAGCAATC TTCTGGCTCC 540 TTGGGAGACC CTAAGGGGAA GAAAGCTCTG GGAAAGAGGA CAAAACCTGA GAAACAGAAG 600 GGCCTTTAAC ATTCAAACAG TCGAACTTTC TCATTTTGCA GATGGAAACA CTCAAGGTCA 660 GAGAGGAGAG AGTGATTTGA CCCAAACCAA ACAACATTAC AGAGGACAGA TTTTCTTCCA 720 CCCAGGCCAG GACTCTGTCT CCAGCACCAT CTAGGCCCCA CCAATTTAAT TTCAGTTCCA 780 AAGGGGACCA TGTTGGGCAC CACCACAGCT CTTTATCCCC ACATCCCTCT CAGCCCTATT 840 GGTTTCAACC ACTTCTGCCG GGCCATTTCA GCTCCTGCCT GATTAGGGCA AACTTTCAGG 900 AGCCTTGTTC TGACCAGTGG GAGCACCAGG GCTCTCAAGA AGGCTGACAG AGGTGGAGAT 960 CCCCCAGGGT AGAAATACTC ACGGAGTCTC TCACAAGTTC TATGACTAAG ATAGGCAAGA 1020 TTACTCAAGT AAACTTGAGA GCCTTGAGGT TTTTGAAGCA ATGCAGAAAC CAGTATTTCA 1080 AATAATTCTT TCTAATTACT GCCACCCACA GTGAAGACAT CAAGAGAAGC CTTTACTTTG 1140 ATAATTCTAG GAGGTGAAAT CTCACCCCAG GAACCACTTT TATCTTCCAC CAAACACCTG 1200 CAGGCTGTAA AAGCAATGCA GGGAGAGAGC AGAGTGAATG TGTGTTTGGG AGCAGGGGTG 1260 GTGGAGGGAA GGTGGATAGG CCTCTAGAAG GGCTGTGAGT ATGGAAATTT CATTCCTCAA 1320 TTATCTGAAG CAGGAGAGTC TGCAGAATTA GGATATAAAG GAGTGCAGCT GGAGGAGAGT 1380 CAGAAGGAAT TTCAAGCCAT GATACAGGTT CCTGGCTCTT CCTTCCCAGG TTGGGCAAAC 1440 CTCAGTGAGG TGAGGTGCAG CGGGGTCTGG CTTGGCTCAG ACCATGGCTC TTCATGTTCT 1500 TATCTCCACT AGAACCTGTG GGAATAGGCT TGTTGGCTAG GCAGGGGCTG CCCCTGCTTC 1560 TGTTCAGTCT CCAAGGGATA TTAGTTGAAC TAGGGAAAAT GGCTAGAGGC TGGGAGGAGA 1620 GGGAGTGAAT GGTGAGCATG GAGGGTGGGG CTGTGGGTGA GGTGGGGGAA GGGGCTGGGA 1680 ATCTGTATGG TAGGTATGGG AGCAGAGTCC TGGGCTGATG CTCAGGCGTG 1730
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