Tag | Content |
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EnhancerAtlas ID | HS047-07490 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:12581800-12583060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr12:12582317-12582327 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr12:12582317-12582327 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr12:12582317-12582327 | AATGGAAAAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_19167 | chr12:12581915-12583217 | CD4p_CD25-_Il17p_PMAstim_Th17 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 12582379 | 12582901 | chr12 | 12581949 | 12583004 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I012428 | chr12 | 12581177 | 12583557 |
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Enhancer Sequence | TCATAATAAA GGGTAAAGCA GAAAAATCCT AAGTGTAAAA AACATTTATA AAACTATACA 60 AAAAATAATT TCAAGGTTCA TTCTCTATTA ATGGTATTGG AGTTGGTAGG AAATAATTAA 120 AATAGGAGTA TAAATCCAGA AGCCCGCAGA GGCCAGGCAG GTAATGTGGG TGAGTGGAGC 180 TGCCGGGCAT TGGACAGGAG GGAGATGGTG GGGACTGAGC AAACAGGCAA GTGCACAACT 240 CATTGAAAGC ATTCCAAAAA TTTAAAAAAT CTTAATGCTC ATTCAGAATG AAACACTTCA 300 GAGGACTGGA AGTTTGTGGT CTCCTAAAAA TGACAAAATT TACCGTCTCT AAATTTGCCC 360 AGCTTTCTGT CCTTCTCCCT CTTTTCAGAA GATCCAGGAG AGGCGTAGCT ATCAATACGA 420 GAGGGAGATG GTTTCCTGGC ACAAGAGGGT GATGGGAAAA CATTGTGTTC AATGCCTCTA 480 GAATTTGCCT GGGTTGCCAC AACTTTGTTG CTTCAGGAAT GGAAAATGTG GCCCATCTTC 540 TTATTTTCTC TGTCCTGTCT TGCTCCTGCT ATGACCCGGG GCAGGATTTG CGGTGGGTTT 600 ATGGAGATTC CTATGAGTCA AGGAAGCACA TTCTGAGGAT AGAGTCATGC ACCTGGGTTT 660 TGTTTTTAGA TGGTTAGAGG GAGGCTGCAA TTGTGATTTA TAAGAATGAC TTAAAGTGTA 720 ATTCCTTTGA TTTTGAAGTT GGCTAGGCAA CTTAATTTGA ACATCCTAGT GTGCCTATTA 780 GACCTGGCAA CCTTCTCAAA ATCCCCCTCC TACTTCCCTC GTTTCCCTCA CCCTCCACCT 840 TTTTCTCAAG AGGTAGAAGT GAGAGTTTTG TTTTGTGAGC TAAGGTTGGG TTCTGGGCCC 900 TCTGCTTCAG CCACCTGGCA GCTTGGGCTG GCCCTGTAGC CTTCCTCCAC TTCATTCTGC 960 GATTCAGGCT CCCAATAGTC TTCTGAAGCA CCGGAGAGCT TCCTCATGCA CCTTAGAAGA 1020 GCAGATTCAG ACTGAGACAA GGACTCGCTC TTAGGCATAT ATGCAGCCTA CAGAGATCCT 1080 GGGAAGCCTT TTTCCTCCTA ATATCTTCCT AGACTTATGC TTTCCTTGGA ATTCCAGCAA 1140 TAGAACTGCA TACTCGTACC CTAATCAAGA ACCTTTTATG TACTAGGTGC TCTACTAGAC 1200 ATGAGATAAA AAGATAAGCA AAACGTGGTC CCTGTCTTCA ACCAGCTCAC CATTTGTTAT 1260
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