Tag | Content |
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EnhancerAtlas ID | HS078-01228 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:109797250-109799120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr1:109797876-109797887 | CTTTCCCGCCC | - | 6.32 | Klf12 | MA0742.1 | chr1:109797324-109797339 | AGTCAGGGCGTGGCC | - | 6.2 | NR2C2 | MA0504.1 | chr1:109798293-109798308 | TGGGGTCAGAGGCCA | + | 6.3 | Sox3 | MA0514.1 | chr1:109797839-109797849 | CCTTTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_05978 | chr1:109790351-109821764 | Brain_Hippocampus_Middle | SE_08846 | chr1:109796444-109797562 | Brain_Mid_Frontal_Lobe | SE_08846 | chr1:109797563-109797759 | Brain_Mid_Frontal_Lobe | SE_08846 | chr1:109797826-109798479 | Brain_Mid_Frontal_Lobe | SE_26927 | chr1:109795303-109798511 | Esophagus | SE_36073 | chr1:109796174-109797974 | HMEC | SE_43475 | chr1:109795151-109799177 | MCF-7 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 109797745 | 109797906 | chr1 | 109797912 | 109798355 | chr1 | 109798400 | 109798790 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I109252 | chr1 | 109795621 | 109798890 |
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Enhancer Sequence | GAAAAGAAGA GGCTGGCAGG CCCCTACTCC CACCCCAGGG AGTGTGGCCT GAAGGGGAAG 60 GAGGGGTATG CCAGAGTCAG GGCGTGGCCT CACTCAGGGT CCTTGCTGGA CAGATGCCTC 120 CCTGCCCCAC CCTTCAAAGT AGCCACAGGA ACCAGGAAGC AGGAGCTTTT CAGGGACTGT 180 GGCTGAGGTT CTGAGCCTCC TGAGACTTCA GTTTCCCCTC CAGGAGGCGG AAGAGGGAGG 240 CTGGAGCTCC TGTGTCCTCA ACTGTGCCTG GGCACTTGAG ACAAGTGGGA AGGAGGTGGG 300 AAGGAGGGCC TCTCCCTCTG GTCCTCCACA CCCAGCCTGC CTTTGGTGAG CGTGGCCAGG 360 CACTGGCAGA GAAGCGCCCC CATTAAGCCT TCGGTCTCCC ACCAGGGCAG AGCCCTAGAC 420 CTTGGTTCCC TAGTCTAGAG AAGGCTCGGG GCAACATCCA GGACGGCTCC TCCTGGCCCG 480 GCAGCTCTGG CCCCACCCTC TCCCTTCGGC CCTGACCCTT GGAGGCAGTC ACCACGGCAA 540 CCCCAAAGTT CAGGGAGGCC GGGGTGAGGG GGAGCTGACT CCCACTGCCC CTTTGTTTTC 600 CTCCTCTTGT TCTTTGTCTC TTCTTTCTTT CCCGCCCCTG CCCATGCGGA GCCCTGCAGC 660 ACTGCCTCTC TCCGGTGCCC TCTCCCTGCT CCTGCGGCTC TCCGGCTCTC CCACTTGCCC 720 ATTGCTGGCT CCTCTCCTGA GGCTTTGTCT TCCCCTGTTT GGTCTCCGTG TTTGTGCCTC 780 CACTCTCTTC CCTATGGCTG CAGCTGCCCC AGCCTGGGCC GATGGCTCCC CTGGAGGCTG 840 AATTCTCCTC GCCTCTTTCT TCCTCTGCTC AGACACGCAG CAGCTCCTGT CCATGGTCTG 900 GGCAGCTCCC AGAACAGCAG AGCCCTCTTG GCCTCCAGTC TCCGCTGGCA CATCTGCCAG 960 GGGAAGAGAG GCTGGGAGGC TGACCGGGAC CTGGCACTTT TCCAGGTGTG CCTGGCTAAG 1020 CTTGGGACAC AGGTGGCATT TCCTGGGGTC AGAGGCCATC CCAGCTGTTC CTTTTCTGTC 1080 CAGGAAGACA GCTCAGGCAA CGTACTCCCC ACCCCTGTTC CCATCCTGCC TTTGCACCTG 1140 AGGGGTGACC TAGGTCAAGG CAGGGGAGGG TGATATAGAA AGGAGAGAGC AGTGGGTTGA 1200 CTGTTGGGGA TGGGGGACAA CAGCAGAGGG GGCAGGTGGC CACAGATGGT GGACCAGATG 1260 GGAAGCAACA GAGACATGCT GGGAGAGGGG CCCAGGCGGG GCCTAAGACG ATGGCGGTGG 1320 GGGACACAGG GAGAAGTGTT TGTTCCCAGG GCTGAGGGGT GGCAAAGTTT CTCCCGCTCC 1380 ATGGCCTTGG TTGCCCCCTC TCCTCTCTTA ATCAGTTATG GGCACTGTGT GTGGAGTCTT 1440 GGGCTGCTTT CTGCCTGGAG GGAATATCCC GTCAAGGAAT CATTAGGCAG ATATACCAGG 1500 TATACAAGAG CTCTGTGCCA GCTGAGCATC CTGGTGCGGG GAAGTCTGAA ACGGAGAGGA 1560 AAGTAGAGCC TGATGACATA AATCTGGGCA GGCTTCCTGG AGCAGGTGAG CTAGGGCAGG 1620 TTAGAAGACT CAGAGGACTG TGGGCTGGTG TCTGGGTGGG AAGGAACAGC CTGTGCAGCA 1680 GCTTTGAGAC GAGAGCAGGA GGAACAGAAG TGGGTGATGA CAAGCAGGCT TGCTGGTGAG 1740 AGCTAGTGAG AATAAGCAAG TGATGAGGCT GGAGGGTAGG TGGGCAGTCG GCTGAGGACA 1800 TGGCTGAGAT GGGGGTCTGC TTTCAGCCTT CCCGGCTTCA GCTGAGCCAC CGCTGGTACA 1860 GTCAGCCACC 1870
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