Tag | Content |
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EnhancerAtlas ID | HS105-21078 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:124440620-124442100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr12:124441754-124441764 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr12:124441754-124441764 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr12:124441754-124441764 | ATTTTCCATT | + | 6.02 |
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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 | GAGATCTTTG AAATTATTAA AATAGTCCAA CAACAGTCAC TTCAGTAAAT AAAGTCACCA 60 TGACCAGGCA TTTAATTTTA GTACTTACAT ACCTTCTGGT GATCAATAAT CAGATATTTG 120 TTGTTATTGA ACATTTATTT ATTTGGAATA ACACAGCCTA AGTACCAATA TTTTTAAAAG 180 ATAAACTTAT ATTTTTAAGA GGGCATTTAC CATTTTCCTA GATCATTTCC TAGAGGTTTT 240 TTTCTGTTTT GTTTTTTGAT GGCTTCAGCA CGTCCATGTA AGGGTGTTTG ACCTCTGACT 300 TTCCATCTAG TGATCTGAGA GCTCCAGCGT GGATTATTCA GTTCAAGCGT CCTCTCCGCA 360 AACTTCCTGT GCTGCGTAGA ATAGGTGAGG CACGCTTACT GACGGCATTT ATGACTGACC 420 CCCATAAAGT TCTTCCCACT CACAATCACT CTTTATTATG TCAGGGAACA AGAGAATTCC 480 CAGAATCGTA TGTTTCAGCT CTCTGGGAAA TCACGCATTA AGTTCCAGGG GAAGGGAAAA 540 GCTTCCCACA AAACAGCTAT CCATTAAGAA TGTCTGTTGT TTAAAATGCA CCAGCAATTC 600 TAACATCCAG AGACCAGTGA GAGAACGGTA GAAGGCAAAT AGGTGTTACT TTAGGGCTGT 660 CTTTGCAACC AAATTTTGAT CATCGTAGAT AAATGAGCCA TTAGTGCATT AACCCAGTCA 720 AAATAAATGA AAACAAATAA TGACAAGTAA AATAAGGGGC AGGACAACTG TATTTCATAG 780 ATTATTTATC AGCTGTGGGA GGAGAGTGAA ATAAATTGGG GAAGGTAGAA AATCACTACA 840 TCTGATATTC ATTAGGATTT TTCAGAGAAT GAGAGGCAAT CCAGTATTTT CTTATTCTTA 900 CTGTCCTTGC CTTGTTAAAG GTCATCATTT TTCATTTGCA CTTTTTCCAT TTGTACAACT 960 GACTTTGTTT TTTCCTCTTA TATTTGACCT TGTGCCCCCA TAATGGGGTT AATTATAATC 1020 CTTGGTTCAT GACACACTCT TTAAGGGCCC ACTTTCATTT AGATACTTTT ACAAATAAGC 1080 ACCCGATGTA TCCAACATTT TTGGAACTTA GCAATTTTGG TTTAGAGTGC CCAGATTTTC 1140 CATTTGAAGT TCGAAATTCT TAGGTTGGAT GTTTCAGCTT CTTCTGGTTG ATCCAGCTCT 1200 GGTGAAGCCT ACTGGCCAGT CAGGAGCCTG GAGAGTTTGA CTTCCCAGTT TTCAGAATGC 1260 ACAGGATGGT CACCTGAGGT CATACCTGGC AGCCACTGCC CTTGCTGGTT GTGGGGGAGT 1320 GTGAGGCAGC TTCCATCTTT GCAAGCAGCT GCTATGTGCA CGCCCCACGA TGCCTTTCAG 1380 TTGGTTCTGC CTGGCTTCTC AAGGGTGTGA TCACTGCACT GTAAAGGGTG GTAACAGCAA 1440 TCATGTTTGA GGATAACTGT CCTAACACAT TCCCTGGGTC 1480
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