Tag | Content |
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EnhancerAtlas ID | HS020-00905 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr1:27830450-27832880 |
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: 2 | ID | Chromosome | Start | End |
GH01I027502 | chr1 | 27828889 | 27832715 | GH01I027506 | chr1 | 27832804 | 27834041 |
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Enhancer Sequence | CTTTCACAAA ACAAGAAAGC CAAGCCCCGT GTGGGGTGAC AGGGTGCAGG GATGGGAGAT 60 GGCACTCAGG GAGCTAGCAC TGGACAGGCC AGTGATTCCG AAGACAGAGG ATAAAGGAAC 120 GAAAGCAGGA AGAGAGGGAA TGAGTTATGG GTGAAATATT CGGATCCTGT AGCCTCCATA 180 GAAGGTGGCC AAGTGGGCAG GGGGCAAAGT CCCAGCCAAG CCCCTCAGCA CCCCCATGTG 240 TTCCCAGCCC TGCTGAGCCC TGCAGCTCGT CTCCTCCTGG CTCCAAAAGT CAGACCAAAC 300 CCCGGAGAAC AGAGGCGGGT GAGGAGGGGG CGGTGGGGTA CAAGCCCAGG CCTCTCACCC 360 CAGCAAAGCC TGCCTTCCCA GTGCCTGGGG CCAACCCAGC TGAGAAGCCA GAGGTTACAG 420 GGAAAGGATT AAGGAGTTGC TTGCTTTTTT ACCCAAACTC TGCTGTATTT CTCTGTCTTT 480 CTTCAATCTC TCTCTCTCTC TCTTTTTTTT TAAAGAAAAA TATTCCTGTA CACGCACCCA 540 GAGGCTTTTG CAGGAGGCGG CTGTTGGAGA ACTGGGAAAA CAAGCCAAGA AACAAGAGAG 600 AGGAAAAAGA CCACGCCTCG CCTGGCAGAT TCCTAATGGC CCAGGAGACC TGAGGCTTTA 660 CAGTGGGAGG CCGGTGGGGG CTGGCTCGGG TGGGAGGGAA GGGCAGGCCG AAGGACAGCC 720 ACTTGCTGGC TGGTGACCTT GGGCGGGATA CTGCCTGCTT CCCTCTGGTG AGAATGGGGA 780 GGAGGGAGGC AGGGGCAGGC CTGGCCGGCT GAGGTCACAG GAAGGCCCCT TCCAGCCTGA 840 AACGCGATCT CGGGATGTGG GGCCTGCCAA CCTGCAGCGA CCCTGGGCCA GCAGAGATGA 900 AAGGCTGCCT GTCCCCAGCT TCCGGACCCC CAAGGCCCCA CTGCCTCAAA GTTGGAGAGC 960 AGCAGAGCTG TGTTGCCACT GGCTGGGGCC AGCTGCTGGG CTCCCCACCC CACCTTATGT 1020 CATCCAACCC TCCCTTCCCT GTTTTGCAGA GGACACTCAG GCCCAGAGAG GGTGGTGACC 1080 TGCCTGAGGT CACACAGCAA GCGGGAGTCT GAGCCAAGGC TCACCACAGT CTTTGGACTC 1140 CAAGTCCAGG CCTCCTGCCT TTCCCAGAAA CTTGGCTGCC TGGGGGCTTA CCCTGGGGAG 1200 TTGGAGAGAA CTAGGGCTGG GGAGGACACT TAGGAGCTGT GTCTGTTTGA AGTCACAACT 1260 TAATGTTGAC TAAAGTGCTT TTTTTTTAAA AGACAAAAAG AAAATTCCCA GCCCCTGCCA 1320 TAAGCCTGGA CTTGCTCACT GGCAGGGGAA GGAATGCAGC TCTGGCCACC ACAGCTGCTG 1380 GTGGCCAGCT GCAGCCTCAG CTTCTGCTGC TCCCGCCCCA GCCGGCAAAG GGACAAAGGC 1440 CTCTTCTCAG GCCTGTCCTC TCCAGCCCCC TGGATCAGCT GGCAGAACAT TGACGGAGCC 1500 TCCTCTGTCA CAGACCTGCT AAGTCATTGT TCCTCTCTGG GCCTTAGTGC CGTTTCTGTA 1560 AAATGGGGGC ATAGTATCTG CCTGACCTAC TTCTCAGCAC TGTTTTGAGG CTCCAAGTAA 1620 AGTTCTGGAA ATACAAAGCT CTCAGCGCCT CCTTCCACCT GCGGGTCTGC CTTCTCACTG 1680 TGCCCTTTGC CTCGACCACC CCTCCCTCCC TCATGCTTTC CCTGGCCAGC CCCAACTCAC 1740 TCAGCTCAGC TCAGTGGGAC CATCACCTGC TCTAAAACCT GCCCTCAACT TCTGAAGGAG 1800 GCACCTTCAG AAGAAAAAAG ACGGCAGTGC TGTATTTATC ATGGTTGTAC ATAATTAAAT 1860 AATTGGCCAG TGTGGTGCCT CAGGCCTGTA ATCCCAACAC TTTGGGAGGC TGAGGTGGGA 1920 GGATTACTTG AAGCCAGGTG TTCAAGACCA GCCTGGGCAA CATGGCAAAA CCCTGTCTCT 1980 ACAAAAAATA AATTAGCTGG GCATGGTGGC ATGTGCCTGT AGTCCCTGCT ACTCGGGAGG 2040 CTGAGGTGGT AGGATGGATT GAGCCTGGGA GGTTGAGGAG TGACCTGCAG TGAGCTGTAA 2100 CTGTGCCACT GAACTCCAGC CTGGGTGACG GAGTGAGGCC CTGTCTCAAA CATAAAAATA 2160 AAAATAAATT AAATAGGTCA GGGGTGGCGG TGGCTCACAC CTGTAATCCC AGCACTTTGG 2220 GAGGCTGAGG CAGACAGATC ACCTGAGGCC AGGAGTTTGA GACCAGCCTG GCCAAAATGG 2280 TGAAACCCCG TCTCTACTAA AAGTACAAAA ATTAGCCAGG CATGGTGGCA CACGCCTGTA 2340 GTCTCAGCTA CTCAGGAGGC TGAGGCAGGA GAGTCGCTTG AATCCAGGAG ACGGAGTTTG 2400 CAGTGAGCCA AGATCGCGCC ACTGCACTCT 2430
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