Tag | Content |
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EnhancerAtlas ID | HS197-13689 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr21:46806030-46808020 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr21:46806852-46806869 | AGGGTCACCGTGACCTT | - | 8.64 | ESR1 | MA0112.3 | chr21:46806852-46806869 | AGGGTCACCGTGACCTT | + | 8.87 | ESR2 | MA0258.2 | chr21:46806853-46806868 | GGGTCACCGTGACCT | - | 7.2 | ESR2 | MA0258.2 | chr21:46806853-46806868 | GGGTCACCGTGACCT | + | 7.52 | PPARG | MA0066.1 | chr21:46806850-46806870 | CGAGGGTCACCGTGACCTTG | - | 6.21 | PPARG | MA0066.1 | chr21:46806851-46806871 | GAGGGTCACCGTGACCTTGA | + | 6.36 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_44555 | chr21:46806116-46807932 | NHDF-Ad |
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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 |
GH21I045385 | chr21 | 46805134 | 46808785 |
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Enhancer Sequence | ATGTCATCAG TGCCTGCTTC CCTCCTTGTG GAGGGCTCTG ACGGCCGACC CCCAAAGTCC 60 ATCTTTCCCC CAGATGTCAT CAGTGCCTGC TTCCCTCCCT GTGGAGGGCT CTGAGGGCCG 120 ACCCCCAAAG TCCATCTTTC CCCCAGATGT CATCAGTACC TGCTTCCCTC CTTGTGGAGG 180 GCTCTGACGG CCGACCCCAG GGTGGGAGAG GGCCAGCCCC CCAGCAGCAG GAGCAGTTTA 240 AACTGCGGGT AAGTGTGCTC CAGGGGCCCT GGTTCTGCAG AGCCACACGC CGAGGCTCCT 300 GAGCTATGTG AGGAATCCAG GGTGCAGCTC ACTGCGTGTC GCCCAACTGC CCTGGGAACC 360 GGCACTGCAG GGTCAGGTGC ATCCCTTTCC ATGTGAGCTC CTGGCCAGCC CAGGCAGACA 420 GGGGAGGCCA CACAGCTTCC AGGCAGGCAG CGGCTGGGCC TGAGCTGGCC CATACCTGCC 480 GGGCTCCTGT CCCACCGGCT GTGTCCGGCC AGCCAGGGCT GGGGACATAC ACACCTGAGC 540 TGCTCTCAGG AGCACTTTTA CTGGAACCTC GAGGAACCTC AACCTCCTTG TTTCTAGGTT 600 GCAGCTCCAT TACGTGCTCT GCAAGTGAAA GATGCTGAGG TGGACACTAA CGTCGGGAGG 660 GAAGCCTAAA CATTGACGTC ATCTGTGCAA AAAGTCAGGA GCATCCACAG GTCCACTCTG 720 TCCCGGACAC GTTCTCAAAG TCAGGAGCAT CCACAGATCC ACTCTGTCCC GGACACGCTC 780 TCACGCTCTC TCCGGTTTGA CTTTGCAATA ACACAGCCCA CGAGGGTCAC CGTGACCTTG 840 AAACAGTCCT GGCTACTTTA AAATTAGCTG CCCCTAGGAG CATGGAAGAT GATTCATCCC 900 GTGACAAATC TTGCCTTATG TCTCTTTTAA ACACACACAT CTGGGTATCA GGCAGCCTCA 960 CGGGGGCAGC TTGGTTGTGC TGGAACTCAG CCTCATTGAC TCCGGTTTCA TGTGCACAGA 1020 AACTGACTTT GAAACTTGCA GGAAGAGGCT GTCCTGGAAG AAGCTGCAGC CTGCAGAGAC 1080 GGCCCTGGGC TTCCTGCATC GCTCCCTTCC TGCCACGGGG CTGTGCCAGG AGCTTCCATG 1140 CAGCTCTCAC ACACAAGGCA GGTCCCCAGC TGGCTCTCTG CAGAGCCTGA CCTGAGGCAC 1200 CCATTCGATG AGAGCAGGTT CTCTCAGTGT AGAACCCAGA CCAGCAGAAG CCGCATCACA 1260 GGGACGCTTC AGAGACGCAC TGCTCAGCCC AGAACTGCCA GGCCTGGCAG CCGGGGTGCG 1320 GGGACCCTGG GACCCTGATG TTGTGTGAGT TCAGGAAAAA CAGCGTTGCC TTCCTGAATG 1380 CTGTTCCATT TACTTCTAGC TCCTACGTGT TTCTTCAAGT AAAACACAGT CGAGCCTCAT 1440 TATTCATGGG CAAATTTGCC TACTTACTAG CATTTACCCT AACCCAGATT CAATACTCAG 1500 GGCACCTCCA CGGTCATTGG TGGACGTCAC AGCGTCACAG CAATGAGACG TGAGTTTCCT 1560 GACACGGTGT CTGGGCGGGG GCAGAACGAG CCATGCTTTG GTGTCTCGTT TGTGTGTGCG 1620 TGAGTGTGTG AATGTGGGAG TATGTGAGTG TGTGTTCATG TGTGTGTTCG TAAGCGTGTT 1680 CTCACCTCAA CACTAACAAC CCTGACTGGC ATGTGATGGC AGCCTCATGG GGCTCCAAGC 1740 CCATGTGTAT GGGCTCCCTG TCTGTGCTGG AAGGTTCTAC AGCAAAAATC AGCCCCTGCT 1800 CACCAGAGGC AAACTGAGCA TGAAAGGAAA TGAAAGACGT GAACTTTAAT GCCTCTCATG 1860 TGCCGGGAGA ACGAGGTCAC ACAGCAAATC ACGGCTCTTG GGAATCAGGA TGTGTTTGAA 1920 AACTTCAGGG GCTCTGAGCC CTCATGAACC CAACCGATGG GCAAGCAGCC CAGGCCCAGG 1980 CTGGAGATGG 1990
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