Tag | Content |
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EnhancerAtlas ID | HS187-15935 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr21:45967260-45968240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr21:45967281-45967291 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr21:45967281-45967291 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr21:45967281-45967291 | 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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| Number: 1 | ID | Chromosome | Start | End |
GH21I044547 | chr21 | 45967256 | 45968095 |
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Enhancer Sequence | ATTCTGGGCT TCCTCAGGAA GATTTTCCAT TAATTGCTTT CCCCCCATGA GTAGCTCATA 60 TTTCTTCCCA CTTTGTCTGG TGAAAACCAG ACAGTGACTA TTACAATGGG ATATTTCTGG 120 GTATCAGGTT CTCCTCCCTC TGTGCAGTTT GCTGTTGCTG ATTGTTGTGG ATTGTGGTTG 180 TTTTTGCTTG TTTATGTCAA GTTAAAAAAT AGTTTCTTCA TCATGTGTGC TCACTTTCTA 240 TTAGCTTGGT GCTAAGACAG TAATTTGACA GAGAGTTCCT TAAACGCCTG GAATCAAAAA 300 ATTGTTTTTC TTCAGGGTTT GTAGCTGGGC TCTGTGTATT GGTCCACACC CCCCAGCACT 360 CGGCTGGGGA GTTTGCGACT CTGCCTTCCC CTTCACTTCC TGCTTGCATC TTCACTTCCT 420 GCTTGCACCT TTACTTCCTG CTTGCACCTT CCCTTCCTGC TTGCTCAGAG CCTGAAGTTC 480 AGCCAGAGGT GAGCACTGAG AGCTTCTCAG GTCTTTTCTG AGCTGGTGCC CCATCATGGG 540 CATGCGTGGG GGCCTTCTGG ACTCCCAAGA GTAAGTGGGA TCTCCCACCT CCCTTATTCC 600 TCAAAGCATG TCATCTTCCA GCTTTTCCTC CCAGGCTTTT TGGGCATGCC CAATGTTTTC 660 TGGCTGATAC CTTTGGCCCC AGGTGGCATT GACTGTTTAA TGTTCTGACA AAGCCTCAGT 720 GTAGCTGCTC TCTGCCTTGA GTCTGATTTG GTGAAATAAG GCAAGCCCTG TGTGTTAGTC 780 CTTCAGGGAG CCACCAGATG GGTAGAAACA GACAACTGCA CTGCCTTGCA AACAAGGTCC 840 CCTCTGCTTC CCTGGCAACA GCATCCCACA TCAGAAACTC GGGCTGCTGC CTTCCTGACT 900 GTCACCCAGC TGGGGAGTGG GGGATGGGGC AAGGGGGAGT TAAAATCCAC AAGGTTGTCC 960 TATTGGGTTG TGCTGCTTTT 980
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