Tag | Content |
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EnhancerAtlas ID | HS050-64510 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr7:151386420-151387720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr7:151387063-151387084 | GGAGGAAGAGAAGAGGAAGGA | + | 7.19 | ZNF263 | MA0528.1 | chr7:151387060-151387081 | GGAGGAGGAAGAGAAGAGGAA | + | 8.49 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_28925 | chr7:151386662-151395278 | Fetal_Intestine_Large | SE_40641 | chr7:151382877-151388315 | Left_Ventricle | SE_42300 | chr7:151384080-151387976 | Lung | SE_48572 | chr7:151384147-151388331 | Right_Atrium | SE_55969 | chr7:151380708-151389306 | u87 | SE_65578 | chr7:151384252-151387921 | Pancreatic_islets | SE_67703 | chr7:151380708-151389306 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I151685 | chr7 | 151383021 | 151388403 |
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Enhancer Sequence | GCACAGGTGG GAAGGGCTGT GGGTGATGCA GGGAGGGCTT TCAGTCACCA TCCCCTCCTG 60 GAAGTGTATC CCAAGCCATT TCCAGGTGTA CAGCTCTCAG GGGAGACAAG AATGCATTGT 120 TCTACCTGGC ACGATGGGGT GTGGGCCACG TGGGGTATGG GCCACAGAAG CACATTCCCA 180 AACCTCCACT TTGGAGAGCC ACGTACAGCG AAGCAGGAGA AGGCGGCAGA GGCGGGGATG 240 GGGAGACCGT CTGTGAGTGT GGTTCCTGCC CGGCTTTCCC CTTCCCGCCA GGTCTCCCAG 300 GAGGCCAGGT GGCGGCTGCA GCCGGTGGCA GACACTCCCT TCCTGGGGTG CTGGCTGCAG 360 CCGGCTGCCA TGGGACTCCA ACCAGGGCTC TCCTGGGGTT CTGTTGACTC AACACATCAT 420 CTGACGCCAC CCCGGCAGGC CCTCTGGGTG TCAGGTGCCA GTGAGACGGG TTGGGGAGGC 480 TGGGACGGTG TCCAGACTGC CGCCTCTGCC CCAGAGCTCG TTTCCATGGT GCCGTTCCCA 540 GCTCCAGGAG CTCTCCTCAT TCACATCATG AAGGGAGAGG CAGGGATCGT GAGCTCTAGT 600 GGTTGTCTGC CTCCAGTGAT TAATTGGTAC GATTCTCCAC GGAGGAGGAA GAGAAGAGGA 660 AGGAAAGCTG CAGATGAAAG GGAAATAAGC GTCTCGTGGT GGAAACAAAA GTATTGGTTG 720 CATCCTTTCA AAGACGATCT GGAATCTCAA ACCTAGGGTT TACCTCTGCC CCTCGATGGC 780 AACAACAATT CTGGGAGTTC AGGGCCATGA TAAAAAATGA CAGCATCACA CCTGAATTGC 840 TGCTAGTGTT TTTAATAGAC AGGTAACCAC TCATCCCGAG GGAGGTGGGA AAGGAGCCCT 900 CTTGCTAGGG AGCTTGGAAT TCCTAATGCT GCCTGTGTCT GATGGACAGT ACCTACCCCT 960 GGTAGAGCTC GCTTCGCGGG GAGGGAGAAC TCAGCCCTCT GTTTGCATGA TCTGAGGCTC 1020 TGGAAAGCCC CCTGCCCCCT TCCAGATACC TCATCTACTT GACAAACTTC CAAGATGCCC 1080 TGCCTCCCCT TTCTACACAT TGCTCTTCCC CGAAAGGTTC CTGCTCTGTT ATTCTTGGTC 1140 AATCTGCAGA AGGCAGGCCG GATACTCCAC AAAGGACCCA AGAGAGGAGC AGCCGTTAGG 1200 AAGGTGCAAG GCTGGGAGGG AAGGACAGGA CCAGGGTTCC CGGATTCAAT TGTACCACAT 1260 CATACATGTT GCCTCCATGC AATTTTCTCT TTAGTGCCAG 1300
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