Tag | Content |
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EnhancerAtlas ID | HS187-10944 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:73319220-73320080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr17:73319750-73319762 | GAGCACGTGGCT | - | 6.04 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_09177 | chr17:73302035-73320268 | CD14 | SE_10509 | chr17:73319249-73320057 | CD19_Primary | SE_14041 | chr17:73319343-73320076 | CD34_Primary_RO01536 | SE_25706 | chr17:73318350-73320087 | DND41 | SE_54131 | chr17:73319199-73319933 | Spleen | SE_61022 | chr17:73284104-73345918 | HBL1 | SE_62513 | chr17:73287335-73369120 | Tonsil |
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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 |
GH17I075322 | chr17 | 73318761 | 73320159 |
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Enhancer Sequence | AAAGGCATTC TCTGAGAGTG CTTGTTCAAT GAATGAATGA GTCCCTCCTC TCCTTCAGTC 60 TTTCAGCTGA TGGAAACCAA AGGCTTCAGA AAATCAATCC GGCAGGTGGC AGCACTGAGC 120 CTCAAGGAAG CCACTCAGCA CAAGATGCCT CGCATTTGGA AAAAATACTG CTTTACATGT 180 TAAGACAAAA TGTGGAAGGT GAGAAAGCTT CATTAGCAAG GGTATATTCC ACGGCACTTC 240 TGGCCCCACA GAGGCCCACT TCCACCCATG CAATGCAGGT GGTTTCTAAG AGCCCAGGGC 300 CCCAATAATG AGCAGTGTTT CAAATCACAG GCTCAAAACA TCCTAAAACT AAGAAACATC 360 TGACAACTGT TGATTCTTGA ACCTTTTTTG CAGAGGTGTG TGTGTTGTTA AAGAGAGTCA 420 TGACACCTGC TTTGCTTCTA AAACAATAAA TGCATTAAAT CCTTAAAAGA TTCTACTTGA 480 GAAAATGGAA GTTTGAGAGT TTCTGCTGAG CAAACAGGCA GCGTCCAGCC GAGCACGTGG 540 CTGCCCCCGT GGTTTTGGCC ACCACCCAGT GATTTACTGC TTGTTCCCCT CATCTTATAA 600 GGTTTCAGTT ACACTTGGGT CAGTATAAAA CTAAAGAAAG ACAGGTGTCA CACATGTTTT 660 TCTTTTCTTT TTTTTTTTTT TTTAAAGATG GATGGAGTCT TGCTCTTTCA CCCAGGCTGG 720 AATGCAATGG CTCAGTCTCG GCTCACTGCA ACCTCTGCCT CCTAGGTTCA AGTGATTCTC 780 CTGCTTCAGC CTCCGGAGTA GCTGGGAATA CAGGCATGTG CCACCACGCC TGGCTAATTT 840 TTGTATTTTT TTAGTAGGGA 860
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