Tag | Content |
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EnhancerAtlas ID | HS177-12975 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr2:189315460-189316440 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr2:189315998-189316013 | TTGCTGAGTGAGCAT | - | 6.08 | MAFF | MA0495.3 | chr2:189315998-189316013 | TTGCTGAGTGAGCAT | + | 6.11 | MAFG | MA0659.1 | chr2:189315995-189316016 | GGATTGCTGAGTGAGCATATT | - | 6.44 | MAFG | MA0659.1 | chr2:189315995-189316016 | GGATTGCTGAGTGAGCATATT | + | 6.79 | MAFK | MA0496.2 | chr2:189315996-189316015 | GATTGCTGAGTGAGCATAT | - | 6.48 | MAFK | MA0496.2 | chr2:189315996-189316015 | GATTGCTGAGTGAGCATAT | + | 6.66 |
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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 | TATTAAGTGC ATTTGTACTT AATAAACTTT CCAAAAGAAT TGCTCTTCTA TAGTTCAGTT 60 TGGGACCCAC AGAAGCAAGA GTAGGATTAC TCCATGTTTC AGGAGCCTCA ACTTTACTAT 120 TCAACAAGGA TTGCAATTCG AGCACCATCT GCTTCACAGC TGAGAATCAT TAAGCTTCAG 180 CAACATTTCC CCATCTCAGC ACCTGACTTC TGCCAAGCAA GTAGGAAGTT TTGCCTTCAC 240 CTTCACCTTT CAGCAAATTA CTCAATTAGT AAATGGGTAT ATGCTACCAT TTAAACTCCA 300 AAATGTAGTG ACTCTTTTTA GCTGAAAACA AACCACCATT GGTATCTAAA TTAACATTGT 360 ATTTTGCTGA TGATTTCTAA ACTTGAATTG TTTTTAAATG CTACTTTTCT ACTTAATTTT 420 TCCTAACAAT TTATGATGTA AAACACATGG TACATTCGGG AGGAAAGCAT GTTGTTTCAC 480 TTTACCTGAC CAATGTTGGC ATGATCAAAG ACATTCACAA ATGTTCACTT TTGTTGGATT 540 GCTGAGTGAG CATATTTGTG TGATGTTAAA GGAATGAGCT TGGGCTGTAT GTTGCCACAT 600 ATGGTTTGCA TTATGATAAA TGAATGTTAA TAGGAAAAAA AAAGTAAAGC ATTGGAAACA 660 TGAGAAAACT CCAGATTTAT TTCTCTTTAA AAGAAAGTTT TTATTTTACA TCTACCAAGA 720 CAGGACATCT TTGTAACAGG GCATATACTA CATTTTTATC ATTAAGTAAT TATTATCTGC 780 TGCTTATTCT ATTAAATGAG TTAAGTGAAT ATTTTCCAGC ACTCAAAATG TGTTTACATT 840 TTATGGATAG TCTCATAATT TTAAAACTGA TTATTTTAAT TTAGGCTTTT TGGTTTTCTC 900 AATATTAATG TCAAAATTGA AAATACAATG TTTTTAAAGT GTGCTTTGCC TGCACTTTGT 960 AAACTATGTA ACTGGAAATT 980
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