Tag | Content |
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EnhancerAtlas ID | HS158-01205 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:27830510-27832190 |
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 | GGCACTCAGG GAGCTAGCAC TGGACAGGCC AGTGATTCCG AAGACAGAGG ATAAAGGAAC 60 GAAAGCAGGA AGAGAGGGAA TGAGTTATGG GTGAAATATT CGGATCCTGT AGCCTCCATA 120 GAAGGTGGCC AAGTGGGCAG GGGGCAAAGT CCCAGCCAAG CCCCTCAGCA CCCCCATGTG 180 TTCCCAGCCC TGCTGAGCCC TGCAGCTCGT CTCCTCCTGG CTCCAAAAGT CAGACCAAAC 240 CCCGGAGAAC AGAGGCGGGT GAGGAGGGGG CGGTGGGGTA CAAGCCCAGG CCTCTCACCC 300 CAGCAAAGCC TGCCTTCCCA GTGCCTGGGG CCAACCCAGC TGAGAAGCCA GAGGTTACAG 360 GGAAAGGATT AAGGAGTTGC TTGCTTTTTT ACCCAAACTC TGCTGTATTT CTCTGTCTTT 420 CTTCAATCTC TCTCTCTCTC TCTTTTTTTT TAAAGAAAAA TATTCCTGTA CACGCACCCA 480 GAGGCTTTTG CAGGAGGCGG CTGTTGGAGA ACTGGGAAAA CAAGCCAAGA AACAAGAGAG 540 AGGAAAAAGA CCACGCCTCG CCTGGCAGAT TCCTAATGGC CCAGGAGACC TGAGGCTTTA 600 CAGTGGGAGG CCGGTGGGGG CTGGCTCGGG TGGGAGGGAA GGGCAGGCCG AAGGACAGCC 660 ACTTGCTGGC TGGTGACCTT GGGCGGGATA CTGCCTGCTT CCCTCTGGTG AGAATGGGGA 720 GGAGGGAGGC AGGGGCAGGC CTGGCCGGCT GAGGTCACAG GAAGGCCCCT TCCAGCCTGA 780 AACGCGATCT CGGGATGTGG GGCCTGCCAA CCTGCAGCGA CCCTGGGCCA GCAGAGATGA 840 AAGGCTGCCT GTCCCCAGCT TCCGGACCCC CAAGGCCCCA CTGCCTCAAA GTTGGAGAGC 900 AGCAGAGCTG TGTTGCCACT GGCTGGGGCC AGCTGCTGGG CTCCCCACCC CACCTTATGT 960 CATCCAACCC TCCCTTCCCT GTTTTGCAGA GGACACTCAG GCCCAGAGAG GGTGGTGACC 1020 TGCCTGAGGT CACACAGCAA GCGGGAGTCT GAGCCAAGGC TCACCACAGT CTTTGGACTC 1080 CAAGTCCAGG CCTCCTGCCT TTCCCAGAAA CTTGGCTGCC TGGGGGCTTA CCCTGGGGAG 1140 TTGGAGAGAA CTAGGGCTGG GGAGGACACT TAGGAGCTGT GTCTGTTTGA AGTCACAACT 1200 TAATGTTGAC TAAAGTGCTT TTTTTTTAAA AGACAAAAAG AAAATTCCCA GCCCCTGCCA 1260 TAAGCCTGGA CTTGCTCACT GGCAGGGGAA GGAATGCAGC TCTGGCCACC ACAGCTGCTG 1320 GTGGCCAGCT GCAGCCTCAG CTTCTGCTGC TCCCGCCCCA GCCGGCAAAG GGACAAAGGC 1380 CTCTTCTCAG GCCTGTCCTC TCCAGCCCCC TGGATCAGCT GGCAGAACAT TGACGGAGCC 1440 TCCTCTGTCA CAGACCTGCT AAGTCATTGT TCCTCTCTGG GCCTTAGTGC CGTTTCTGTA 1500 AAATGGGGGC ATAGTATCTG CCTGACCTAC TTCTCAGCAC TGTTTTGAGG CTCCAAGTAA 1560 AGTTCTGGAA ATACAAAGCT CTCAGCGCCT CCTTCCACCT GCGGGTCTGC CTTCTCACTG 1620 TGCCCTTTGC CTCGACCACC CCTCCCTCCC TCATGCTTTC CCTGGCCAGC CCCAACTCAC 1680
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