Tag | Content |
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EnhancerAtlas ID | HS182-00557 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:27830090-27832760 |
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 | Nr2f6(var.2) | MA0728.1 | chr1:27830156-27830171 | CGATCTCTTGACCTC | - | 6 | 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 | CCACGCCTGG CTAATTTTTG TATTTTTAGT AGAGACGCGG TTTCACCATG TTGGCCAGGA 60 TGATCTCGAT CTCTTGACCT CGTGATCTGC CTGCCTCGGC CTCTCAGAGT GCTGGGATTA 120 CAGGCGTGAG CCACCGCGCC CAGCTCACTC TGAATATTTT GAGCGACCTA TTTATGATTT 180 GAATTTATTC ATTCGAGAAG CACCCCAACA TACCTCCTAT ATGTCAGGCA TGGACCCAGG 240 AACTGTGACT ACAACAGATA ATTAGGGGTT GGTTCCTCAG ACAGGACAAA GGGCAGGACA 300 CTGAGTGCCA CCTCTACAGA GGGGTCTGAC TGGATAAAGA CAAAGTGTGA AAGTGTATGA 360 CTTTCACAAA ACAAGAAAGC CAAGCCCCGT GTGGGGTGAC AGGGTGCAGG GATGGGAGAT 420 GGCACTCAGG GAGCTAGCAC TGGACAGGCC AGTGATTCCG AAGACAGAGG ATAAAGGAAC 480 GAAAGCAGGA AGAGAGGGAA TGAGTTATGG GTGAAATATT CGGATCCTGT AGCCTCCATA 540 GAAGGTGGCC AAGTGGGCAG GGGGCAAAGT CCCAGCCAAG CCCCTCAGCA CCCCCATGTG 600 TTCCCAGCCC TGCTGAGCCC TGCAGCTCGT CTCCTCCTGG CTCCAAAAGT CAGACCAAAC 660 CCCGGAGAAC AGAGGCGGGT GAGGAGGGGG CGGTGGGGTA CAAGCCCAGG CCTCTCACCC 720 CAGCAAAGCC TGCCTTCCCA GTGCCTGGGG CCAACCCAGC TGAGAAGCCA GAGGTTACAG 780 GGAAAGGATT AAGGAGTTGC TTGCTTTTTT ACCCAAACTC TGCTGTATTT CTCTGTCTTT 840 CTTCAATCTC TCTCTCTCTC TCTTTTTTTT TAAAGAAAAA TATTCCTGTA CACGCACCCA 900 GAGGCTTTTG CAGGAGGCGG CTGTTGGAGA ACTGGGAAAA CAAGCCAAGA AACAAGAGAG 960 AGGAAAAAGA CCACGCCTCG CCTGGCAGAT TCCTAATGGC CCAGGAGACC TGAGGCTTTA 1020 CAGTGGGAGG CCGGTGGGGG CTGGCTCGGG TGGGAGGGAA GGGCAGGCCG AAGGACAGCC 1080 ACTTGCTGGC TGGTGACCTT GGGCGGGATA CTGCCTGCTT CCCTCTGGTG AGAATGGGGA 1140 GGAGGGAGGC AGGGGCAGGC CTGGCCGGCT GAGGTCACAG GAAGGCCCCT TCCAGCCTGA 1200 AACGCGATCT CGGGATGTGG GGCCTGCCAA CCTGCAGCGA CCCTGGGCCA GCAGAGATGA 1260 AAGGCTGCCT GTCCCCAGCT TCCGGACCCC CAAGGCCCCA CTGCCTCAAA GTTGGAGAGC 1320 AGCAGAGCTG TGTTGCCACT GGCTGGGGCC AGCTGCTGGG CTCCCCACCC CACCTTATGT 1380 CATCCAACCC TCCCTTCCCT GTTTTGCAGA GGACACTCAG GCCCAGAGAG GGTGGTGACC 1440 TGCCTGAGGT CACACAGCAA GCGGGAGTCT GAGCCAAGGC TCACCACAGT CTTTGGACTC 1500 CAAGTCCAGG CCTCCTGCCT TTCCCAGAAA CTTGGCTGCC TGGGGGCTTA CCCTGGGGAG 1560 TTGGAGAGAA CTAGGGCTGG GGAGGACACT TAGGAGCTGT GTCTGTTTGA AGTCACAACT 1620 TAATGTTGAC TAAAGTGCTT TTTTTTTAAA AGACAAAAAG AAAATTCCCA GCCCCTGCCA 1680 TAAGCCTGGA CTTGCTCACT GGCAGGGGAA GGAATGCAGC TCTGGCCACC ACAGCTGCTG 1740 GTGGCCAGCT GCAGCCTCAG CTTCTGCTGC TCCCGCCCCA GCCGGCAAAG GGACAAAGGC 1800 CTCTTCTCAG GCCTGTCCTC TCCAGCCCCC TGGATCAGCT GGCAGAACAT TGACGGAGCC 1860 TCCTCTGTCA CAGACCTGCT AAGTCATTGT TCCTCTCTGG GCCTTAGTGC CGTTTCTGTA 1920 AAATGGGGGC ATAGTATCTG CCTGACCTAC TTCTCAGCAC TGTTTTGAGG CTCCAAGTAA 1980 AGTTCTGGAA ATACAAAGCT CTCAGCGCCT CCTTCCACCT GCGGGTCTGC CTTCTCACTG 2040 TGCCCTTTGC CTCGACCACC CCTCCCTCCC TCATGCTTTC CCTGGCCAGC CCCAACTCAC 2100 TCAGCTCAGC TCAGTGGGAC CATCACCTGC TCTAAAACCT GCCCTCAACT TCTGAAGGAG 2160 GCACCTTCAG AAGAAAAAAG ACGGCAGTGC TGTATTTATC ATGGTTGTAC ATAATTAAAT 2220 AATTGGCCAG TGTGGTGCCT CAGGCCTGTA ATCCCAACAC TTTGGGAGGC TGAGGTGGGA 2280 GGATTACTTG AAGCCAGGTG TTCAAGACCA GCCTGGGCAA CATGGCAAAA CCCTGTCTCT 2340 ACAAAAAATA AATTAGCTGG GCATGGTGGC ATGTGCCTGT AGTCCCTGCT ACTCGGGAGG 2400 CTGAGGTGGT AGGATGGATT GAGCCTGGGA GGTTGAGGAG TGACCTGCAG TGAGCTGTAA 2460 CTGTGCCACT GAACTCCAGC CTGGGTGACG GAGTGAGGCC CTGTCTCAAA CATAAAAATA 2520 AAAATAAATT AAATAGGTCA GGGGTGGCGG TGGCTCACAC CTGTAATCCC AGCACTTTGG 2580 GAGGCTGAGG CAGACAGATC ACCTGAGGCC AGGAGTTTGA GACCAGCCTG GCCAAAATGG 2640 TGAAACCCCG TCTCTACTAA AAGTACAAAA 2670
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