Tag | Content |
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EnhancerAtlas ID | HS047-09291 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr13:44765540-44768280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr13:44766333-44766351 | AGAAGGAAGTTAGGAAGG | + | 6.53 | EWSR1-FLI1 | MA0149.1 | chr13:44766345-44766363 | GGAAGGAAGGAAGGAGAA | + | 7.67 | EWSR1-FLI1 | MA0149.1 | chr13:44766341-44766359 | GTTAGGAAGGAAGGAAGG | + | 7.74 | EWSR1-FLI1 | MA0149.1 | chr13:44766337-44766355 | GGAAGTTAGGAAGGAAGG | + | 7.92 | HNF1A | MA0046.2 | chr13:44767180-44767195 | AATTAAACATTAACA | + | 6.48 | HSF1 | MA0486.2 | chr13:44767814-44767827 | TTCCAGAAGGTTC | + | 6.15 | IRF1 | MA0050.2 | chr13:44766369-44766390 | AGAAAGAAAGAGAAAGAAAGA | - | 6.76 | IRF1 | MA0050.2 | chr13:44766355-44766376 | AAGGAGAAAGAGAAAGAAAGA | - | 6.81 | NFAT5 | MA0606.1 | chr13:44766595-44766605 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr13:44766595-44766605 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr13:44766595-44766605 | ATTTTCCATT | + | 6.02 | RFX1 | MA0509.2 | chr13:44768050-44768066 | TGTTACCATGGAAACT | + | 6.39 | RFX1 | MA0509.2 | chr13:44768050-44768066 | TGTTACCATGGAAACT | - | 6.4 | RFX2 | MA0600.2 | chr13:44768050-44768066 | TGTTACCATGGAAACT | - | 6.62 | RFX2 | MA0600.2 | chr13:44768050-44768066 | TGTTACCATGGAAACT | + | 6.65 | RFX5 | MA0510.2 | chr13:44768050-44768066 | TGTTACCATGGAAACT | + | 6.54 | RFX5 | MA0510.2 | chr13:44768050-44768066 | TGTTACCATGGAAACT | - | 6.54 | ZNF263 | MA0528.1 | chr13:44766492-44766513 | AGAGGAGGAGTGGGGAGTGAG | + | 6.07 | ZNF263 | MA0528.1 | chr13:44766354-44766375 | GAAGGAGAAAGAGAAAGAAAG | + | 6.75 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_03282 | chr13:44765085-44766383 | Brain_Angular_Gyrus | SE_05255 | chr13:44764499-44767547 | Brain_Cingulate_Gyrus | SE_07866 | chr13:44763936-44767524 | Brain_Inferior_Temporal_Lobe |
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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 |
GH13I044191 | chr13 | 44765201 | 44766883 |
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Enhancer Sequence | CCTCTAAGCA TACAAGGAAG AACAGAGATT TCAACCATTA TTTCTCAGTG AACTAAACAT 60 CAAACTATAA GTTTTCAAGT CAGCCATGAC CTGGCATCTC TCCGTCTTTT GAAAACGAAG 120 CCAAACAATC TATGGTGCGG TCTCCTTAAG CTGTGTCCGA AATATGCAGG GTTGTGCAAT 180 ATGCAATGTT TTGGTCAGTC ACTAGGTGGC ATCTAATTGA GGCACCGGGT GAACTCTCCC 240 AGAAGGAGCG TGTTTTAGAG CACACCACAG TTCTCCATTT TGGCTGCCAT TGTTTGGTGG 300 GCGTGTTGGA GTTAATCCAT TGCCATCTGT CTTTATTTTG CTAACTTACT CAGTCGGACG 360 CCACACAATT GAGTTCTGCA AATGTCGGCT CTCCAGTACA GCAATTACCG AGTCTCTCTC 420 TAAACAATAT CACCGCACGG CATTCTTCCT GCCTTGCCTA GAGCTTGAAA CATTCAGGCT 480 CATTTTGACT TTCTTTGCTT ATAGCGCTTG TCATCTTCAA AGATGAAAGA AAAATGGTCT 540 GAACTCAAAG CCACAACAAG GCATGGCTTC TCTTTCCAAA CTGAGTACAT ACCAATCAAC 600 ATGTTCCTAT TACATAAAAA CCCCAGGCAA CACAGCCAAG GATGTGGGCT TGTGCTTGTG 660 CAGTCCAGGA AGACACCACC GCCTCCTCCA GGATGCAGAC AGAGTGCATT TTGTTGTTGA 720 TGATGATGTT GTTCTTTTAA TATTTGAGGG ACTGGTGGGA GAGGTGGCAA GTGAGGCACA 780 TGGAAGTAAT AGGAGAAGGA AGTTAGGAAG GAAGGAAGGA GAAAGAGAAA GAAAGAAAGA 840 GAAAGAAAGA AAGAAAGAGA GAGAGAGAGA GAGAGAGAGA AAGAAAGAAA GAAAGAAAGA 900 AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA AAGAAAGGAT ATAGAGGAGG 960 AGTGGGGAGT GAGCTGATAT TTGAAGGACC TAACTTCCAT TGCTGTTCCA GAAGAGGGAT 1020 GAATTAATAA TCTCAGTAAC CTAGAAATGG TGTTTATTTT CCATTGTTTG CTCATTTCAT 1080 TCATTCACGC ATTGTGTATT GAAGACCTAC TCTGTGTGTC AGGCAGTGTA TGAGATGTTC 1140 CAGATACAAG TGGGATCGAT TCATCAAGAT TCATTGTCTT CTTTGAGCTT ACATTTTGTG 1200 GGGAGACAGA CATTGATCAA GTAAACACAA GCATGATAGC TGTTGTGAAA TAGACACAAA 1260 AACACACAGG GTGTTGCACA AGCACACAAT GGGTGCCCTC ACCTAGTCTG GGGGCCAGGA 1320 AAGGATCTCT GAGATAGGTG AAGATGAAGG GGGTTTTTAG AGTATCATTC TTCTTTGTTG 1380 AACTCTCACG TGCCAAATAC TCTGCTTTGC AATTAGCAGA TGCTAGATTC ATATTTGGTG 1440 ACCAACTAGC AAGTGAGGAA GATCTAGCAG GATGAGAACC AGTGAAAATA CAGCCCAGTC 1500 CCTGATGGGA CTAATTCCTC CTTAATCCTT TGCTTTTGCC TTTTTTTCCT GCCAAAATTA 1560 TATAAAGATT TGCATCCATC TTTTATCTTT ATTTAAGTCC ATTTTGTTCA AAGTTTTCAA 1620 TGCCTGGTAA ACCAAAAGTG AATTAAACAT TAACATATTA GTTTACATTG CTATCTACTG 1680 TAGTTCTTCA GAATCGATTC ACTGTTTAAA TTTTAGAAAA TAGGAGGCAA TTTGGGGAGC 1740 AAAGAAGAGG AAGCCAGAAA AAAAGGGAAC ATACTGTGTT TGTCTTCTCC GCTGTATTAC 1800 CATATTTTCA AATGTAATTT CTGTCTTCAG GGTTTCCACT ATGAAGCAGA GGGAGTCCAT 1860 ATCCTATGTA TTGACATAAG ATTCGAGCAA AGGCAAACCC ACGAATATGC AGTTTTTGGG 1920 AACTGTAAAC TCCCTGAGTT TCATTACAGG TGCTGGAATA GGTGGATATT GAAAGGATTT 1980 AATGTGGTCT CACTACTTAC CAGTGCATTT GTGAATGACC CATTCTTGTA GGACTTTATC 2040 TTGTCAACCA AGTCTATTTG TCATTAAATA TTTGTGGTCT GAGTCCTTTA AAGTCATCTC 2100 CTGGGAGAAC TGCATTGCCA GGTAGTTTGA AGACCAACGC CAGCTACATA GTAACATAAG 2160 GAGCCTTTGC CTTGCTTTAT TTTGGTCTTA ACTCATTGCT CCCCTAAGCT GAATAGGGAA 2220 TGTCAGGCAG CTGTCCTTCA TGCCACTGAG ATTCTCCTGC CTGAGGCCCC AACCTTCCAG 2280 AAGGTTCAGG TGGCTGGGGC CTTCCAGGGG GAGTGGCTGG GTCTGTGAGG TGGCCCATGG 2340 ATAGAGCTGG GGTACCCTCT TCCTCCCACC TCTCTGGGAT CTGCCTGCAC TGTGGACCTG 2400 GTCATGTCCT GGGGTGGGGG TGCAGAGGGC AAGTGGGGAT ACCAGGGGAA GAAGAAATGT 2460 CACTTGAGCT GTGGCAGACA CTGGAGGGCC AGGCCCTGCA CAACAACCAC TGTTACCATG 2520 GAAACTCCCA AGGAGACCGC CGAAGGCCAC TAGAAGCAGC CTTGGTAACA TTCTTCCATT 2580 TCTGACCTCT CATTACATTT GACATAATTG ACCAATCTCA TTCTGGAGAC TTCTCCTTCC 2640 TCGGTTTATG TGACATGAAC CCTCTTGGTT CTGCTCCTCT CACCCTGAGT GACCTCTGTC 2700 AGCCTCTTTT GCAGACACTT ACTTCACTCT CTCTTCATTC 2740
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