Tag | Content |
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EnhancerAtlas ID | HS101-30566 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr3:125782960-125784260 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr3:125783255-125783270 | TGCTGACTCACTCTG | - | 6.69 |
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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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Enhancer Sequence | CTGGCATCGA GGCATCAAGG GGTCAATGGT GGGGTAAGGC CTAAAACTAC GAAGTGCGGC 60 CTCAACACCT GGAGAAAGCA AGATAATGTG AGCGGCGCGT TCCCCTCCTG ACTCTGCTCC 120 TGTGGATGAG GTTCCCAGCC CAAGAGCCTC CTTATCTCAG GGCAGGAACT GTCCCTCCAC 180 ATCCCCGAGG AGCACGCTTC AGTTTCTGCC ACCCTGTGGA ATTACGCATA TAGTCAGGAA 240 TGGAGGGCAG GTTTCCCACT CTCTTGTTAT GACAAATCTT GCCCCCCACA TCCCCTGCTG 300 ACTCACTCTG CTCCCCAGTG GCCCCGCAAG GTGTGCAGCA TCCTCCTGCC TGGGTGACTG 360 GTATGAGGAC TAACAAATTG CCGTGGTCCT CACCTGTCCA GAGCCAGGTG TTGAGTGTCC 420 ACCATCCCCA TAACCCTAGG GCAGGACTCC CCACCCTCAC CAGCAGAGTA AAGAGGAGGC 480 AATTAAAACA GGCTGCTCTC ACCTCCTCCC GCACCCCCAG TCTTCTCTCT CTGCCCACAT 540 GAAACACCCC TCCAGCCAGC CCTCTTGCCC TCCTGGCCTT TCTAGACCGC TCGGTGTCTC 600 TGTAAGGCCA TAGCTTGCCT GGAGACCCCC GTTCTTCCCG GCACATGCAC ACAATGCTCA 660 TCCCAGTCCA CCCACAGAGC CCAGGACTGC ATCAGTTTCT GGAGACTGCT GCCATTCCTG 720 CCTGCTCCAC GCATTCCAGT GAGGAGTCCT GGTGGAATTT CAGAAAGATT AACTTGGAGG 780 AGCTTGGCGT CATCAGGTAA ACCCTTTAAA GGGAGCAGGT GCTTCCTGAA GTCAGAGAGG 840 GATTTCACCC AAGGGAGGTT TCTCCACTGC TGCCTTTGAA GATGGAAGGG CCACAAGGCA 900 AGACGTAGGA GTGGCCTCGA GAAGTGAAGT GCAGCCCCTG GCTGATAGCC AGCAAGGAAA 960 TGGAACTGCA GTCCTTCAAC CTCAGGGAGG AACCCAGCAC CAGGAGGTGA GTTCTGAAGA 1020 CAGGACTATG CTTAGAAGTG GATGTTCCCC CAGAGCCTCA TGAAGAGAAT GCATCCTGGC 1080 CAGCACGTGG ATTTCAGCTG TTGAGACCCT GAGCAGAGAT CCCAGCCATA CCATGCCTGC 1140 CCTCTGCCTT ACAGAACTAT GAGCTAATCA ATGCGTGCTG TTTTAAGCTG TTAAATTTGT 1200 GGTAATGTGG AACACAGCGA TATAAAACTG ATACAAAAAC CACATGTTGC CAAATCTTCT 1260 GAGTTTTAAA GAGGAGCTGA ATATAAGCAC TTTAATGAAA 1300
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