Tag | Content |
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EnhancerAtlas ID | HS051-26185 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr8:38823120-38824310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr8:38823461-38823474 | GAACCTTCTGGAA | - | 6.15 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_10253 | chr8:38818344-38824429 | CD19_Primary | SE_10916 | chr8:38778152-38824593 | CD20 | SE_20358 | chr8:38822359-38823290 | CD56 | SE_40765 | chr8:38823299-38824306 | Left_Ventricle | SE_43830 | chr8:38818934-38824182 | MM1S | SE_53542 | chr8:38823713-38824257 | Spleen | SE_62854 | chr8:38792840-38824305 | Tonsil |
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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 |
GH08I038965 | chr8 | 38822617 | 38823549 | GH08I038966 | chr8 | 38823918 | 38824230 |
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Enhancer Sequence | CAAATTCAAA ATAACCTTTT TTTTAACCTC CAAATACATG ATCTTATTTG ATCTTGATGA 60 TTTGATCTTT GAGGTAGGAA TTAGCTGCAG TTTGAGGATG AGGAAACTGA GAAAAGGTCT 120 TCTTATGGAG AGGGCAATGC GCTTATCTGT AAATGGTGGC GTTTAAGGCT TCATTTTTTT 180 GTCGCATATC ATATAATACC AGTGAAAACA ACAATAATAT CTGCTACTTA CAGAGCCCAT 240 TCTGTGCGTT CGGCCCTGTT TCAATAGTTT TTCCTAATTG AGGTCATTTA ATTCCCTCAA 300 TAATTAAGCT TGTGGAACAG GCCAGCCCTG ATATTTGTAA AGAACCTTCT GGAAGGATCT 360 TGGAGTCCTT ATCCTGGTGA TCTTTTTGGA CAAAGGATGG GTTTGTCTTT TTCTTGGGAA 420 ACCACCAGAT TGTCAAATAA CTGGAAAAAG TCAAGCGGGG AGACAGCGCT AGTAAGTTTG 480 CAGGCAGAGC ACACGTTAGA GAGGTGTTCA CTTTGGCCAC TTGTCACTAC ACCCTTTTTG 540 CCCTCGTGCA CCAGGACCTG AACGGTTTTC CTTGTAGGTG CACACATCTA ACCAAGGAGG 600 GTTTGTTTTG GGGTGACAGG AAGGGGTAGG GATGCAGGTT TGAGAATTTT TGTTTTACTG 660 TCTTTTCCTG ATAGAATGCA AAGAGGAGGG GTCACTTTGG GGATGGGGGG ATGAGGGGGG 720 ATGTGGAGTC CTTTGGGGGC TAGTGTGTGG TGGTGGCACA TACATCTGCA TGTGCACACC 780 AATGCACGCG TGTGTGTTTT GGTGGGACTG TTAGGGGATG ATGCTGGAGA CAGAGGAAGG 840 CTAACATGCA TATTTCTGGA GATTCTGCCT GGTCCCATTG CTGTGTCTGG CACCTGATGC 900 AGCATGTAAC ACCGGGTGGG GCCCTTAGCC AGCGTTTGCT CTGTTCACTT GAACTCAACC 960 CCTATAAAGC TGGAGGGCAC TGACAGGCTC CACCGGCAGT AGCGAGGCCG CTGGAGTTTC 1020 CTCCCTTTTT TCATAGAGCC GCTGCTGCCC CCTTCTGGGG TTTATAGGTT GTTTCTGGGA 1080 GGAAATAAGT AACTCGGCTT CATCCTTCAC ATACTGTGAA GCTTGGTGCT GCGAGTCCCA 1140 CAACTCTTTA AATTTTTTTA AAAGTTTTAT TCACAATAGC AAAGTCACAA 1190
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