Tag | Content |
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EnhancerAtlas ID | HS133-00919 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:27830310-27832610 |
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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I027502 | chr1 | 27828889 | 27832715 |
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Enhancer Sequence | ATGTCAGGCA TGGACCCAGG AACTGTGACT ACAACAGATA ATTAGGGGTT GGTTCCTCAG 60 ACAGGACAAA GGGCAGGACA CTGAGTGCCA CCTCTACAGA GGGGTCTGAC TGGATAAAGA 120 CAAAGTGTGA AAGTGTATGA CTTTCACAAA ACAAGAAAGC CAAGCCCCGT GTGGGGTGAC 180 AGGGTGCAGG GATGGGAGAT GGCACTCAGG GAGCTAGCAC TGGACAGGCC AGTGATTCCG 240 AAGACAGAGG ATAAAGGAAC GAAAGCAGGA AGAGAGGGAA TGAGTTATGG GTGAAATATT 300 CGGATCCTGT AGCCTCCATA GAAGGTGGCC AAGTGGGCAG GGGGCAAAGT CCCAGCCAAG 360 CCCCTCAGCA CCCCCATGTG TTCCCAGCCC TGCTGAGCCC TGCAGCTCGT CTCCTCCTGG 420 CTCCAAAAGT CAGACCAAAC CCCGGAGAAC AGAGGCGGGT GAGGAGGGGG CGGTGGGGTA 480 CAAGCCCAGG CCTCTCACCC CAGCAAAGCC TGCCTTCCCA GTGCCTGGGG CCAACCCAGC 540 TGAGAAGCCA GAGGTTACAG GGAAAGGATT AAGGAGTTGC TTGCTTTTTT ACCCAAACTC 600 TGCTGTATTT CTCTGTCTTT CTTCAATCTC TCTCTCTCTC TCTTTTTTTT TAAAGAAAAA 660 TATTCCTGTA CACGCACCCA GAGGCTTTTG CAGGAGGCGG CTGTTGGAGA ACTGGGAAAA 720 CAAGCCAAGA AACAAGAGAG AGGAAAAAGA CCACGCCTCG CCTGGCAGAT TCCTAATGGC 780 CCAGGAGACC TGAGGCTTTA CAGTGGGAGG CCGGTGGGGG CTGGCTCGGG TGGGAGGGAA 840 GGGCAGGCCG AAGGACAGCC ACTTGCTGGC TGGTGACCTT GGGCGGGATA CTGCCTGCTT 900 CCCTCTGGTG AGAATGGGGA GGAGGGAGGC AGGGGCAGGC CTGGCCGGCT GAGGTCACAG 960 GAAGGCCCCT TCCAGCCTGA AACGCGATCT CGGGATGTGG GGCCTGCCAA CCTGCAGCGA 1020 CCCTGGGCCA GCAGAGATGA AAGGCTGCCT GTCCCCAGCT TCCGGACCCC CAAGGCCCCA 1080 CTGCCTCAAA GTTGGAGAGC AGCAGAGCTG TGTTGCCACT GGCTGGGGCC AGCTGCTGGG 1140 CTCCCCACCC CACCTTATGT CATCCAACCC TCCCTTCCCT GTTTTGCAGA GGACACTCAG 1200 GCCCAGAGAG GGTGGTGACC TGCCTGAGGT CACACAGCAA GCGGGAGTCT GAGCCAAGGC 1260 TCACCACAGT CTTTGGACTC CAAGTCCAGG CCTCCTGCCT TTCCCAGAAA CTTGGCTGCC 1320 TGGGGGCTTA CCCTGGGGAG TTGGAGAGAA CTAGGGCTGG GGAGGACACT TAGGAGCTGT 1380 GTCTGTTTGA AGTCACAACT TAATGTTGAC TAAAGTGCTT TTTTTTTAAA AGACAAAAAG 1440 AAAATTCCCA GCCCCTGCCA TAAGCCTGGA CTTGCTCACT GGCAGGGGAA GGAATGCAGC 1500 TCTGGCCACC ACAGCTGCTG GTGGCCAGCT GCAGCCTCAG CTTCTGCTGC TCCCGCCCCA 1560 GCCGGCAAAG GGACAAAGGC CTCTTCTCAG GCCTGTCCTC TCCAGCCCCC TGGATCAGCT 1620 GGCAGAACAT TGACGGAGCC TCCTCTGTCA CAGACCTGCT AAGTCATTGT TCCTCTCTGG 1680 GCCTTAGTGC CGTTTCTGTA AAATGGGGGC ATAGTATCTG CCTGACCTAC TTCTCAGCAC 1740 TGTTTTGAGG CTCCAAGTAA AGTTCTGGAA ATACAAAGCT CTCAGCGCCT CCTTCCACCT 1800 GCGGGTCTGC CTTCTCACTG TGCCCTTTGC CTCGACCACC CCTCCCTCCC TCATGCTTTC 1860 CCTGGCCAGC CCCAACTCAC TCAGCTCAGC TCAGTGGGAC CATCACCTGC TCTAAAACCT 1920 GCCCTCAACT TCTGAAGGAG GCACCTTCAG AAGAAAAAAG ACGGCAGTGC TGTATTTATC 1980 ATGGTTGTAC ATAATTAAAT AATTGGCCAG TGTGGTGCCT CAGGCCTGTA ATCCCAACAC 2040 TTTGGGAGGC TGAGGTGGGA GGATTACTTG AAGCCAGGTG TTCAAGACCA GCCTGGGCAA 2100 CATGGCAAAA CCCTGTCTCT ACAAAAAATA AATTAGCTGG GCATGGTGGC ATGTGCCTGT 2160 AGTCCCTGCT ACTCGGGAGG CTGAGGTGGT AGGATGGATT GAGCCTGGGA GGTTGAGGAG 2220 TGACCTGCAG TGAGCTGTAA CTGTGCCACT GAACTCCAGC CTGGGTGACG GAGTGAGGCC 2280 CTGTCTCAAA CATAAAAATA 2300
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