Tag | Content |
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EnhancerAtlas ID | HS040-01139 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:27830220-27832620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:27830565-27830583 | GGAACGAAAGCAGGAAGA | + | 6.13 | Nfe2l2 | MA0150.2 | chr1:27831966-27831981 | TGCTAAGTCATTGTT | - | 6.36 | STAT1 | MA0137.3 | chr1:27831609-27831620 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr1:27831609-27831620 | TTTCCCAGAAA | - | 6.32 | ZNF263 | MA0528.1 | chr1:27831218-27831239 | TGAGAATGGGGAGGAGGGAGG | + | 6.04 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_02913 | chr1:27830213-27831026 | Bladder | SE_02913 | chr1:27831120-27832355 | Bladder | SE_05196 | chr1:27829210-27833352 | Brain_Cingulate_Gyrus | SE_05814 | chr1:27829181-27832931 | Brain_Hippocampus_Middle | SE_06945 | chr1:27829261-27832857 | Brain_Hippocampus_Middle_150 | SE_07770 | chr1:27829738-27832662 | Brain_Inferior_Temporal_Lobe | SE_23188 | chr1:27830280-27832092 | Colon_Crypt_1 | SE_24033 | chr1:27830527-27830952 | Colon_Crypt_2 | SE_24033 | chr1:27830969-27832275 | Colon_Crypt_2 | SE_24711 | chr1:27830217-27832142 | Colon_Crypt_3 | SE_25901 | chr1:27830171-27832637 | Duodenum_Smooth_Muscle | SE_26518 | chr1:27830129-27832742 | Esophagus | SE_27625 | chr1:27830080-27832462 | Fetal_Intestine | SE_28547 | chr1:27830055-27832555 | Fetal_Intestine_Large | SE_29557 | chr1:27829444-27832772 | Fetal_Muscle | SE_31394 | chr1:27830159-27832397 | Gastric | SE_33477 | chr1:27830354-27831735 | H2171 | SE_34755 | chr1:27830079-27832086 | HeLa | SE_35950 | chr1:27830256-27832335 | HMEC | SE_36974 | chr1:27829579-27833069 | HSMMtube | SE_39896 | chr1:27830278-27832548 | K562 | SE_40593 | chr1:27829483-27832634 | Left_Ventricle | SE_42106 | chr1:27830105-27832560 | Lung | SE_48058 | chr1:27830093-27832593 | Psoas_Muscle | SE_48567 | chr1:27830115-27832554 | Right_Atrium | SE_50130 | chr1:27830153-27832341 | Sigmoid_Colon | SE_51091 | chr1:27829612-27832640 | Skeletal_Muscle | SE_52467 | chr1:27830150-27832427 | Small_Intestine | SE_62718 | chr1:27801410-27856116 | Tonsil | SE_65253 | chr1:27830186-27832347 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 27830304 | 27830805 | chr1 | 27830808 | 27832117 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I027502 | chr1 | 27828889 | 27832715 |
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Enhancer Sequence | CCACCGCGCC CAGCTCACTC TGAATATTTT GAGCGACCTA TTTATGATTT GAATTTATTC 60 ATTCGAGAAG CACCCCAACA TACCTCCTAT ATGTCAGGCA TGGACCCAGG AACTGTGACT 120 ACAACAGATA ATTAGGGGTT GGTTCCTCAG ACAGGACAAA GGGCAGGACA CTGAGTGCCA 180 CCTCTACAGA GGGGTCTGAC TGGATAAAGA CAAAGTGTGA AAGTGTATGA CTTTCACAAA 240 ACAAGAAAGC CAAGCCCCGT GTGGGGTGAC AGGGTGCAGG GATGGGAGAT GGCACTCAGG 300 GAGCTAGCAC TGGACAGGCC AGTGATTCCG AAGACAGAGG ATAAAGGAAC GAAAGCAGGA 360 AGAGAGGGAA TGAGTTATGG GTGAAATATT CGGATCCTGT AGCCTCCATA GAAGGTGGCC 420 AAGTGGGCAG GGGGCAAAGT CCCAGCCAAG CCCCTCAGCA CCCCCATGTG TTCCCAGCCC 480 TGCTGAGCCC TGCAGCTCGT CTCCTCCTGG CTCCAAAAGT CAGACCAAAC CCCGGAGAAC 540 AGAGGCGGGT GAGGAGGGGG CGGTGGGGTA CAAGCCCAGG CCTCTCACCC CAGCAAAGCC 600 TGCCTTCCCA GTGCCTGGGG CCAACCCAGC TGAGAAGCCA GAGGTTACAG GGAAAGGATT 660 AAGGAGTTGC TTGCTTTTTT ACCCAAACTC TGCTGTATTT CTCTGTCTTT CTTCAATCTC 720 TCTCTCTCTC TCTTTTTTTT TAAAGAAAAA TATTCCTGTA CACGCACCCA GAGGCTTTTG 780 CAGGAGGCGG CTGTTGGAGA ACTGGGAAAA CAAGCCAAGA AACAAGAGAG AGGAAAAAGA 840 CCACGCCTCG CCTGGCAGAT TCCTAATGGC CCAGGAGACC TGAGGCTTTA CAGTGGGAGG 900 CCGGTGGGGG CTGGCTCGGG TGGGAGGGAA GGGCAGGCCG AAGGACAGCC ACTTGCTGGC 960 TGGTGACCTT GGGCGGGATA CTGCCTGCTT CCCTCTGGTG AGAATGGGGA GGAGGGAGGC 1020 AGGGGCAGGC CTGGCCGGCT GAGGTCACAG GAAGGCCCCT TCCAGCCTGA AACGCGATCT 1080 CGGGATGTGG GGCCTGCCAA CCTGCAGCGA CCCTGGGCCA GCAGAGATGA AAGGCTGCCT 1140 GTCCCCAGCT TCCGGACCCC CAAGGCCCCA CTGCCTCAAA GTTGGAGAGC AGCAGAGCTG 1200 TGTTGCCACT GGCTGGGGCC AGCTGCTGGG CTCCCCACCC CACCTTATGT CATCCAACCC 1260 TCCCTTCCCT GTTTTGCAGA GGACACTCAG GCCCAGAGAG GGTGGTGACC TGCCTGAGGT 1320 CACACAGCAA GCGGGAGTCT GAGCCAAGGC TCACCACAGT CTTTGGACTC CAAGTCCAGG 1380 CCTCCTGCCT TTCCCAGAAA CTTGGCTGCC TGGGGGCTTA CCCTGGGGAG TTGGAGAGAA 1440 CTAGGGCTGG GGAGGACACT TAGGAGCTGT GTCTGTTTGA AGTCACAACT TAATGTTGAC 1500 TAAAGTGCTT TTTTTTTAAA AGACAAAAAG AAAATTCCCA GCCCCTGCCA TAAGCCTGGA 1560 CTTGCTCACT GGCAGGGGAA GGAATGCAGC TCTGGCCACC ACAGCTGCTG GTGGCCAGCT 1620 GCAGCCTCAG CTTCTGCTGC TCCCGCCCCA GCCGGCAAAG GGACAAAGGC CTCTTCTCAG 1680 GCCTGTCCTC TCCAGCCCCC TGGATCAGCT GGCAGAACAT TGACGGAGCC TCCTCTGTCA 1740 CAGACCTGCT AAGTCATTGT TCCTCTCTGG GCCTTAGTGC CGTTTCTGTA AAATGGGGGC 1800 ATAGTATCTG CCTGACCTAC TTCTCAGCAC TGTTTTGAGG CTCCAAGTAA AGTTCTGGAA 1860 ATACAAAGCT CTCAGCGCCT CCTTCCACCT GCGGGTCTGC CTTCTCACTG TGCCCTTTGC 1920 CTCGACCACC CCTCCCTCCC TCATGCTTTC CCTGGCCAGC CCCAACTCAC TCAGCTCAGC 1980 TCAGTGGGAC CATCACCTGC TCTAAAACCT GCCCTCAACT TCTGAAGGAG GCACCTTCAG 2040 AAGAAAAAAG ACGGCAGTGC TGTATTTATC ATGGTTGTAC ATAATTAAAT AATTGGCCAG 2100 TGTGGTGCCT CAGGCCTGTA ATCCCAACAC TTTGGGAGGC TGAGGTGGGA GGATTACTTG 2160 AAGCCAGGTG TTCAAGACCA GCCTGGGCAA CATGGCAAAA CCCTGTCTCT ACAAAAAATA 2220 AATTAGCTGG GCATGGTGGC ATGTGCCTGT AGTCCCTGCT ACTCGGGAGG CTGAGGTGGT 2280 AGGATGGATT GAGCCTGGGA GGTTGAGGAG TGACCTGCAG TGAGCTGTAA CTGTGCCACT 2340 GAACTCCAGC CTGGGTGACG GAGTGAGGCC CTGTCTCAAA CATAAAAATA AAAATAAATT 2400
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