Tag | Content |
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EnhancerAtlas ID | HS191-26561 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr3:119894420-119897380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:119895065-119895083 | TCTTCCTTCCTTCCTTCC | - | 10.05 | EWSR1-FLI1 | MA0149.1 | chr3:119895069-119895087 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr3:119895061-119895079 | CTCATCTTCCTTCCTTCC | - | 6.35 | EWSR1-FLI1 | MA0149.1 | chr3:119895109-119895127 | CCTCTCTCCCTTCCTTCC | - | 6.73 | EWSR1-FLI1 | MA0149.1 | chr3:119895113-119895131 | TCTCCCTTCCTTCCTTCT | - | 6.82 | EWSR1-FLI1 | MA0149.1 | chr3:119895117-119895135 | CCTTCCTTCCTTCTTTTT | - | 6.84 | EWSR1-FLI1 | MA0149.1 | chr3:119895092-119895110 | CCCTCCTTCCCTCCCTCC | - | 7.36 | EWSR1-FLI1 | MA0149.1 | chr3:119895077-119895095 | CCTTCCTTCCTACCTCCC | - | 7.88 | EWSR1-FLI1 | MA0149.1 | chr3:119895073-119895091 | CCTTCCTTCCTTCCTACC | - | 9.17 | RARA(var.2) | MA0730.1 | chr3:119896101-119896118 | GGGTCATATTCAGGTCA | + | 6.16 | SPIB | MA0081.2 | chr3:119896950-119896962 | AAAGGGGAAGTG | + | 6.07 | TCF7L2 | MA0523.1 | chr3:119895798-119895812 | TTCCTTTCATGTTT | - | 6.07 | ZNF263 | MA0528.1 | chr3:119895100-119895121 | CCCTCCCTCCCTCTCTCCCTT | - | 6.03 | ZNF263 | MA0528.1 | chr3:119895088-119895109 | ACCTCCCTCCTTCCCTCCCTC | - | 6.3 | ZNF263 | MA0528.1 | chr3:119895109-119895130 | CCTCTCTCCCTTCCTTCCTTC | - | 6.5 | ZNF263 | MA0528.1 | chr3:119895105-119895126 | CCTCCCTCTCTCCCTTCCTTC | - | 6.95 | ZNF263 | MA0528.1 | chr3:119895065-119895086 | TCTTCCTTCCTTCCTTCCTTC | - | 7.03 | ZNF263 | MA0528.1 | chr3:119895080-119895101 | TCCTTCCTACCTCCCTCCTTC | - | 7.07 | ZNF263 | MA0528.1 | chr3:119895092-119895113 | CCCTCCTTCCCTCCCTCCCTC | - | 8.31 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_36203 | chr3:119895522-119897331 | HMEC | SE_64843 | chr3:119895578-119897171 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 119895587 | 119896680 | chr3 | 119896703 | 119897072 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I120175 | chr3 | 119894683 | 119897644 |
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Enhancer Sequence | AATGTAATCA CAAGAATCCT TATAGGAGGG AGGGAGGAGA GCCAGAGTTG GAGAAGGAGA 60 TGTGACAATG GAAACAGGGG CGAGAGAGAG AAAGATTTGA ATCTCTTCTG GCAGATTTGA 120 ACCTGGCTGG CTTAGAAGGT GGAGGAGGGG ACAATAAGCA CAAGAATGCA GACGGCCTCT 180 AGAAGCTGAA AAAGACAAGG AAACAGATTC TCCCCTTGCA TCTCTGGAGG GAATACAGAC 240 TTCCTGACAC CTTAAGTTTA GCCAAATAAG ACCTATTTCA GATTTCTGAC CTCCAAAATT 300 TTAAGATAAT AAACTTGTAT TATTTTAAGC CACTAAGCTT GTGGGAATTT GTTATAGCAG 360 CAGTGGGAAA CTAATATGGT GGGACTAAAT GTCAACTCTT TAACAGGGTC CAGCAGGGCC 420 TCAGAAGCTC CCCAGGTGTG TCTCTCCCCA GTCCTGTCAT TCTCCCCCTG GTTTCCATTT 480 GTGCTTCAAA AATAACAAAG ACCATGGTGC TCCAAACATA CGCTACTCTC TTTCTAGCCT 540 CCCTGCCTCT GGTCATGATG TTATTCCATC AGAAATGCCA CCTACTTTCC CCCATCTCTT 600 CAATGAACTC TTATGTTTCC TTCAAGACTG AGCTCGAACA CCTCATCTTC CTTCCTTCCT 660 TCCTTCCTAC CTCCCTCCTT CCCTCCCTCC CTCTCTCCCT TCCTTCCTTC TTTTTTTTTT 720 TTTTTGAGAC AGGGTCTTAC TCTGTCTGGA GTGCAGTGGC ACAATCACAG CTCACTGCAG 780 CCTCAACCTC CTGGGCTCAG GTGATCCTCC TACTTCAGCC TCCTGGGTAG CTGGGACCAG 840 AGGCATGCAC CACCATGCCT GGCTAATTTT TGCTTTATAT TTTTTGAGAC AGTCTCACTC 900 TGTCTCTGGC TGGAGTGCAA TGGCACAATC TCGGCTCACT GCAACCCTTG TCTCCCGGTT 960 TAAGCAACTC TCCTGCCTCA GCCTCCCAAG TAGCTGGATT ACAGGCGCCC GCCACCACAC 1020 CCAGCTAATT TTTTGTATTT TTAGTAGAGA CGGGGTTTTA CCATGTTGGC CAGGCTGGTC 1080 TCAAACTCCT GACTTCACGT GATCTGCCCG CCTTGTCCTC CCAAACTGCT GGAATTACAG 1140 GCGTGAGCCA CCACGTCTAG CCAATTTTTG CATTTTTTGC AGAGACCAGG TTTCACCATG 1200 TTGACCAGGT TGCTCTCGAA CTCTTGGGCT CAAGCGATCT ACCCGCCTCA GCCTTGAAAA 1260 GTGCTGGGAT TATAAGCATG AGCCACCATG CCCAGCCTCA TTTTCTGAGA AGGTGCCACT 1320 GAGTTCTCAG ATGGGCTGGG GAAGGCCTTT CTCAAAGCTC TTAACACATG TATGATAATT 1380 CCTTTCATGT TTGCTCCCCA CTAGACCTAG AGGCGGACTC TGTGTTTAAG TGCATGTACC 1440 CAGCAGTTAA TAAGTGGATG GATGGATGCA TGCATGAACA AATGAAGGAA GCTTTCTTTA 1500 AAATGCTCAC TGGTCTAGTA GGGGTGCTGG GACATATACA TATAATTATA AGGCAGATTA 1560 GAAAGGCCTG CACATCTTCA GGGAGGAGCA GATGAAATGC TTTCGGGGTT AGAGGAGAGA 1620 GAAAACAATG TCCTACCTTA GGACCTGCCT GCCTCTCTGA GGGAGCAGAG GGCTGGGGGA 1680 TGGGTCATAT TCAGGTCAGA ACAGCAGCGG CTGGCTGACT TCTAGTGATG ACCTCAGTGC 1740 TTGGCATAAA CACTCAGGCA TTTCCTGAGT GCCTGTGTAA AGAAGGCTTC TTGGGCCCCT 1800 TGTCTCCTTA GTAATGTCAT CCATTTCACC CGCTCTCTGG CGCTGCCTCG CTGCCCTGGG 1860 GGTATCTGTG CCTTTGCTTT CACAAACTCC TCCCATCACA GTCATGTCTG AAAGCTCACT 1920 GGCAAGAAGG AACCCCGTTT TGCTGCAACC CCCAACCCTT ACCCAGATAG TTCCCCTCAC 1980 CCACTTTCCC AAATTTACTC AAATTACTTT CCCAAATTAT CTTCTAGGAA TACACAGTGC 2040 AAGTATCACA GGGAGAATCG TTCTTCTACC AAAGACCTCG GAGCCAGAGG GAAACACACA 2100 GAAACCTAAC AAACCTCAGT TTCTTTTATA TTTTGAAAAA GAACTACTTA CCATCTAAAC 2160 CTAAAATACA ACAGACTACA AAATATATTT TTTAGTTTCA CATCATGGTC AGTTAGTTCC 2220 AGAGGAGAAA AAAAAAAAAC ACAAGGGAGA AAATGGAAGA GGAAAGACAG AGTAAGAGAA 2280 AGGAAGCTTA AGAAAGCTAG GAGGGAAAGA GGGAGTGAGA TAGAAGGAAA GCAAGGCCAG 2340 TGCAGTCCAT CCACCCAATT CCTGTACCTC ATAATCATTC CATTTCCATT CCCAATTCAA 2400 CAAATCAAGT GTTTGTTGCT TAGTGAAAAC CTGGAAGGCA GATTTCAAGC AGCACTTCAT 2460 TCTGCATTTT TGTGTGTAGA GTACCCAGAT GTCACAATTG TCCTAGCTGC TGAGGACTCA 2520 AACACCAGGC AAAGGGGAAG TGATGTGGCT GAGGCTTACG ATGCAAGGGG GCAGTGGTGA 2580 GAGGTGAGGA TGGAGAGAGG AGCAGTAAGC AGGGCGCCAT CATGGAGATT GCCAATTCAT 2640 TCAGTTTTCT GACCAAGGCT TTGTTTGTTC AGAAACATTT TCCTCTGATA GCTCTTTGAT 2700 AATGACTTCT GCCCCAAATT ATTTTGTTCT CTTTCAGAGA CTCCTATCAG CTCTCAATTG 2760 TATTCCTAGA TGTTTTCCAT ATTTTATTTT TTTCTTTTTA TTTTATTTTT TGAGACAGAT 2820 TTTCGCTCTT GTTGCCCAGG CTGGAGTGCA ATGGCGTGAT CTTGGCTCAC TGCAACCTCT 2880 GCCTCCTGGG TTCAGGCGAT TCTCCTGCCT CAGTCTCCCT AGTAGCTGGG ATTACAGATG 2940 GATGCCACAA CGCCCAGCTA 2960
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