Tag | Content |
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EnhancerAtlas ID | HS074-01378 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:228929490-228930930 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:228930211-228930231 | TGGTGGTTGTTGGCTTGTGG | - | 6.48 |
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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 |
GH01I228791 | chr1 | 228927141 | 228930766 |
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Enhancer Sequence | ACAAAACGGG GAATGTGTGC TAGAGTCAGA GGAGGATTTT TGAAGAAGAA GGAGGAGGAA 60 TGAACATCTG TATAAAATTG TTGCACAGAA GTGATTTTAT TTAAACATTA AACATTAAAA 120 CATTTACTAG CCTTCCACTA TATGACAATT GCTATACCAG GAATAGGGTT ATCAGAAGTA 180 AATCAGGTTC AGTCCCTGCC TGTAAGGATC CTCCAGTCTA GTAGAAGATA AAAACATAAA 240 TAGACAAGTG GAATAAATTG TAGGTTACAC AGAGAACTAA AAATCAAACA TATTGAACAG 300 GTGGGAACAG ACTTCCATGG CTTCAGAAAG GTGATGACTT TCAAGACCAG ACAGGAGCTA 360 TGTGCAGGTG TCCACAAGGT GAACCATCGG AGAGTTTCAG AGAGAGGAAG GACTAGGAGC 420 TCCCACAGAG CTGGTAGAGT AAGTATGGCC AAGGATGAAG GATGAAGTAA GGGGCAGAGA 480 GAGACATGAG TTTGAAGAAT GTTCATGGTT CAGACTACTG AGGGCTTTGT AGTTTGGAGC 540 AACAGGATTT TTGCTCATTT GTGAGTTTCC TGTGCCAAAC CACAAATGGA GTGACTCAAA 600 ACAAGAGAAA TTTATTTTCT CACAATTCTG AAAGTCAAAA GTCTTAAATC CAGGTGTGAG 660 CAGGGCTGCA CAGCCTCTAG GGGCTCTAGG GAAGAATCTG TTTGTAGCCT TTTCCATCTT 720 CTGGTGGTTG TTGGCTTGTG GCCACAACAC TTCAAACTAT CCCTCTGTGG TGACATCGCC 780 TCCTTCTTTC ACTGTGATCT CCCCCTTCCT CCCTCTTATA AAGATACTTG TGATGGCATT 840 TAGGGCCATG GTTCAAGCTT ATCTCCACAT CTCAAGATTC TTAACTCATT TGCAAAACCC 900 CTTTTTCCAT ATAAGCTCAC ATTTATAGGC TTCAGGGATT AGGACCTGCA TATATTTGGG 960 GGCTGTAATT CAGCTTGCTA CAGTCAGGGT TGGCAATTAG TTATACCTTC CTGGGAGTAA 1020 AAGACAGAAT GGATTGGAGA GACCCATACT GGAGTCAAGA ACATCATCAC TTTGGAGATT 1080 ACAGAAGACA TACAGGTTAA GAGGTGACTG AGACCTGAAC TAAGAGAGCA GTGGAGGTGG 1140 GGATGGGAGT GAGATCTCAG TGGAAAAGTG TCAGTAGGGT TGGGTGGTTC TCAGTGTCTC 1200 AGTGGGGTCC TGGGGACAGA AGCCCAATCA CACATATCGA AAGCGACAGC AGATTTCACT 1260 TCTTTTCAGT CATCTACCGG GTACTGAGCT AGTTGTCAAA GGCAATGATA AGCCAGCATG 1320 TGTCTGATAG CGTGGGAAGG AGCTCTGAAA ACAGGACCAG AAAGGAAACG GAGGTGGGGA 1380 AACAGATTCT CTAATTCCTG AGCATCTTTG AAGAAATCCA CTGTAGGCTG TGTCATTCTG 1440
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