Tag | Content |
---|
EnhancerAtlas ID | HS091-14339 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr15:25016480-25018720 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NRF1 | MA0506.1 | chr15:25018385-25018396 | GCGCCTGCGCG | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH15I024772 | chr15 | 25017241 | 25018946 |
| Enhancer Sequence | CCTAACATTG TTCCTCCTTT TCTTAATGTG TTTGGCTATT CTACTTTGAC TTTCTAATAC 60 AAATTTTAGA ATCTATTTGT CAATTTCTAC AAAAAAAAAT AATGGGATGT TGATTGAGGA 120 TTTAGTGAAT GCATAGATTA AAATGTAAGA ATCGCTCTCT TAATATTGAC CTTCCAATTC 180 ATGAAATTAG TGTATCGCTG TATTTATTTA GATCTTTTAA AACTAATCTC ATCAGTGTTT 240 CCTAATTCCC AGAGTACAAT TTTTGCCAGA TTTATCTCTA AGAATATCAT TTTTATATTG 300 CTGTAAATAT ATTTTAACTT CAATGCTCAA TTTTTCATTA TCGCTATAAG GGAAGACAGT 360 TGATTTTCAC CTATGCATTT TTGCAAACTA AGAAAATCTA GTGACAACCA TGTGGTATAT 420 ATATTGCTAC ATGTGAGGCA TGGACAAATG AACAACAAAC ATACATTTCT CCTATATCTG 480 AGACATCAGT CAAGCTGATA TTCGAACATA TAGGCAATAA AAATCAGATT AGAGAGGCTG 540 CATAGTTATG TGGAAATCCA CAAAATGCAT GTGCATACAA CACTAATTTA AATGGTCACT 600 GCAGGTATCC TGCAGGAAGT AATTTAAGAT TGAAAACATG AATAAGTAGC TGAAAAACGA 660 TGCAAATTTA AGCTGGGAAA GACAAAAGAA TGATTAGTAT TCATGTAGAA ACCATGACAT 720 GTATACAAGT CAAAATATTT GAGGCATCAC AAGAATAGCA ATTTCAGAAC ACATGAAGGA 780 AGTTACAAAT CTATGTCAGG GCTAGATTTT TAAGAAATTA TGTGGGGTTG AGGCTCAGCC 840 CCTGCATTGG CAAAGAAAAA GTTATGGGTG ATGAAAATAG ACAACCTAAA GTCCTGGAAA 900 AGAGTCCACA CAAAATTTTA GTATTTTCAA GGTAGAAGCT TCTCTTGACT CAGTTGGACC 960 TCCCTGTGAA AAATACGAAA TCAGAAAAGG AACTTTCCAC CTAGAAAACG AATTTCAGTA 1020 CCAAGCATAG GTTGCTTTCA CGCCTAAACC CCTCCTTACT TGAATTGCAG AAGTACCTGC 1080 TATACTGTAG TTTTTGGGCA TGAGGGACCC CTGTGCTCAC AGCGCCATCT AGCATCAACA 1140 GAAAGGGGGG CTGATGGCAA TAGAAAGGGG GGCTGATGGC AGCCTTAATA AATTCAGGAG 1200 AGGAAAAAAA AAAACACAAA ACAAAACAGA TGGCGGCCCA GCATCCAGGA ACTGCTGTGT 1260 TCATTTGAGT AGGATTTTTC TTATATTCGT TTAAAAACTG AAACATAATT CATAATTGCT 1320 GCAGGGGTTA GGGGTGAAAT GCAATTGGTA ACCATTCCCA GTAAAGACTC AGGGAATCCT 1380 GGCCCAAGAC CACATTTCCT GTCATTTAAC GCAAGGGTTA AAAGGTCGAA GTGAATCCCA 1440 TTACGCTAAC TGATTTCATT TACAAACATG GATGTATAGG AGTGTGTTAC TATGCACGGA 1500 ATCATACTTC GGATGTGAGT GTAAAACGAG TTCAGCTGAT TTTGCACTGT CACATTAAAC 1560 CCGGAACCAT GTGTTTCCAT ATACATCACG CTCCTCTTTG GTAGCACTAC AGTTCATAAG 1620 ATGAATGTAA TTTCTTAGAT TACAGCCTTA ACGGGTTATT ACTCTTTCAA TGTTTTCTAA 1680 TGTGATATAG ATGTCGGACG TATTCGCTCA AGTATACGTG GCGGGGCCGG GGTCCCGACC 1740 GTCTGTCGGA GCGAGCTGTG CCGCAAAGCC CAGCTACTCC GATCTCACAG GGATGGTGGC 1800 AGGAAATGCG CCATTGTTCG GCGCAGCGAA ACAGCCCGCA GTGCGCTGTA GGAAGGTCAC 1860 ATGACAGAGG GGGAAGACGG TGGCCGGCAG CAGCCGATCC ACTGCGCGCC TGCGCGGCTC 1920 CGGTGGCGTG AATGTCGCTG GTCTCCCGTC ACCGTTTCCG TTTCCGGGCG AGTCTGTTCG 1980 GCTTATGGCG TCTGCTAGGA GTCTCCTATC CGGCGTTTGT GCCGCAGAAA ACCTTTAACC 2040 TGCGTTTTAC CCGTAAACAT TTTCCTTTTT AGGCTTCCTA TCATTGTTTT GGTTCTTGCT 2100 CCTGTATTAA CTTTGTTTTT GGTTTTTTCT TTTTTTTTTT TTTTCAAGAC GGAGTCTCGC 2160 TCTGTCGCCC AGGCTGGAGT GCAGTGGTGC GATCTCGGCT CACTGCAAGC TCCGCCTCCC 2220 GCGTTCACGC TATTCTCCTA 2240
|
| |
|
|
|