Tag | Content |
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EnhancerAtlas ID | HS019-00345 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr1:27830050-27831710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:27830565-27830583 | GGAACGAAAGCAGGAAGA | + | 6.13 | 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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I027502 | chr1 | 27828889 | 27832715 |
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Enhancer Sequence | CCTCAGCCTT CCAAGTAGCT GGGACTACAG GTGCGCACCA CCACGCCTGG CTAATTTTTG 60 TATTTTTAGT AGAGACGCGG TTTCACCATG TTGGCCAGGA TGATCTCGAT CTCTTGACCT 120 CGTGATCTGC CTGCCTCGGC CTCTCAGAGT GCTGGGATTA CAGGCGTGAG CCACCGCGCC 180 CAGCTCACTC TGAATATTTT GAGCGACCTA TTTATGATTT GAATTTATTC ATTCGAGAAG 240 CACCCCAACA TACCTCCTAT ATGTCAGGCA TGGACCCAGG AACTGTGACT ACAACAGATA 300 ATTAGGGGTT GGTTCCTCAG ACAGGACAAA GGGCAGGACA CTGAGTGCCA CCTCTACAGA 360 GGGGTCTGAC TGGATAAAGA CAAAGTGTGA AAGTGTATGA CTTTCACAAA ACAAGAAAGC 420 CAAGCCCCGT GTGGGGTGAC AGGGTGCAGG GATGGGAGAT GGCACTCAGG GAGCTAGCAC 480 TGGACAGGCC AGTGATTCCG AAGACAGAGG ATAAAGGAAC GAAAGCAGGA AGAGAGGGAA 540 TGAGTTATGG GTGAAATATT CGGATCCTGT AGCCTCCATA GAAGGTGGCC AAGTGGGCAG 600 GGGGCAAAGT CCCAGCCAAG CCCCTCAGCA CCCCCATGTG TTCCCAGCCC TGCTGAGCCC 660 TGCAGCTCGT CTCCTCCTGG CTCCAAAAGT CAGACCAAAC CCCGGAGAAC AGAGGCGGGT 720 GAGGAGGGGG CGGTGGGGTA CAAGCCCAGG CCTCTCACCC CAGCAAAGCC TGCCTTCCCA 780 GTGCCTGGGG CCAACCCAGC TGAGAAGCCA GAGGTTACAG GGAAAGGATT AAGGAGTTGC 840 TTGCTTTTTT ACCCAAACTC TGCTGTATTT CTCTGTCTTT CTTCAATCTC TCTCTCTCTC 900 TCTTTTTTTT TAAAGAAAAA TATTCCTGTA CACGCACCCA GAGGCTTTTG CAGGAGGCGG 960 CTGTTGGAGA ACTGGGAAAA CAAGCCAAGA AACAAGAGAG AGGAAAAAGA CCACGCCTCG 1020 CCTGGCAGAT TCCTAATGGC CCAGGAGACC TGAGGCTTTA CAGTGGGAGG CCGGTGGGGG 1080 CTGGCTCGGG TGGGAGGGAA GGGCAGGCCG AAGGACAGCC ACTTGCTGGC TGGTGACCTT 1140 GGGCGGGATA CTGCCTGCTT CCCTCTGGTG AGAATGGGGA GGAGGGAGGC AGGGGCAGGC 1200 CTGGCCGGCT GAGGTCACAG GAAGGCCCCT TCCAGCCTGA AACGCGATCT CGGGATGTGG 1260 GGCCTGCCAA CCTGCAGCGA CCCTGGGCCA GCAGAGATGA AAGGCTGCCT GTCCCCAGCT 1320 TCCGGACCCC CAAGGCCCCA CTGCCTCAAA GTTGGAGAGC AGCAGAGCTG TGTTGCCACT 1380 GGCTGGGGCC AGCTGCTGGG CTCCCCACCC CACCTTATGT CATCCAACCC TCCCTTCCCT 1440 GTTTTGCAGA GGACACTCAG GCCCAGAGAG GGTGGTGACC TGCCTGAGGT CACACAGCAA 1500 GCGGGAGTCT GAGCCAAGGC TCACCACAGT CTTTGGACTC CAAGTCCAGG CCTCCTGCCT 1560 TTCCCAGAAA CTTGGCTGCC TGGGGGCTTA CCCTGGGGAG TTGGAGAGAA CTAGGGCTGG 1620 GGAGGACACT TAGGAGCTGT GTCTGTTTGA AGTCACAACT 1660
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