Tag | Content |
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EnhancerAtlas ID | HS182-16959 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr4:38874450-38875790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr4:38874460-38874476 | CCATATGTAAACAAAG | + | 6.55 | FOXP2 | MA0593.1 | chr4:38874464-38874475 | ATGTAAACAAA | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_25214 | chr4:38874412-38875029 | Colon_Crypt_3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr4 | 38874665 | 38875086 | chr4 | 38875223 | 38875374 | chr4 | 38875379 | 38875472 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I038871 | chr4 | 38873462 | 38875744 |
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Enhancer Sequence | CATGACGGTC CCATATGTAA ACAAAGGGTG TATCTCTGGT CCAATAAAAC TGTGTTTACC 60 AAAACAGGCA GAGGACAAGA GTTGGCCAGC AGACTGGTTT GCCAACACCC TGTCCTAGGC 120 TAGTCCTGAT TCAGAGAGAG GTTTTCACAA AGATTTTGTA AACTTCCAAA TGACAACAGC 180 CTTTTTAGCA GCCCCCATCA ATTCTACTCA CCTCCCATAA ACCACCCACA ATACTACCCC 240 TTCTCTATAC AGTGGGTTTC TATCGTTCTT TACTATTTCA GCTAGGCTTG AACCTGGCTC 300 CTTGACAGCC CACGGCCAAC CTTGAATATC CTAAACTTTG TATACCAGCT CAAGGGAAGT 360 CTGCATTCGT TGCCATTCTT ACATGTAGAC TTGTTTACAG GAATATTATC ACTGAATTCA 420 AGGTCTGGCA GATATTTTTG CTTACACAAA TACATTCTAA CTCAATTAAC TGGGAGGTGA 480 AGGAAAAAAG AAAGACAATA CGGAAATGTC AAGTCATTTG GAACCATCTG CTGTAAGAGA 540 GCTCCTGAGT GTCTGTACAC AAATATTAAT CTAACTCAAC AGGCATATTT GTTGAGCTTC 600 CTACTATGCA CAGGAAGCCA TGCCAAGTAC TATGTAGAAT ATGAATACAA AACAAGGAAG 660 GTCTTTGTCT TTATAGAATT TACAAATCAT AGGAAAAACT GAAGCAACTC TAATCAAAGA 720 GGACTTTAAC TGTCTAAAGT AAGATAAACA CAAAATGCCC TCAGAAGGGT TCAGAAGGAA 780 AATGTTCAAC CTGGAGGAAC AAAGAATGGA GGAGGCGGTT ATTTTAACTG GGTCTTCAAT 840 GTGCAAAAGA ACAACATATG GAACTAACAG CCCCCGAGGG TCTCTTGTGG ATGTGCCAGG 900 CATTGCACAG ATATTTACAC TGTCTCATTT AAGGTTTTAT AGGAAATCGT GGGAGGTAAG 960 CCTGGTGGGA TCAGAGCACA GAGGTCCCTG GATACTAGCT GAAGCATGTG GCCTCATCTC 1020 AGGAGGGAGA GGAAGGGGAA GCTCCTGAGG ATGTGTGAGC AGGAGAGCCA TGTAATTAGA 1080 GCCGTGAGGT GAAGGATGGG AAGTAAGGGG AAGAGCTGCA GTGAACAGGG GAACCCAATA 1140 CTGAAATAGT CATCATGAAC CATAATGAGG ACCTTGCCAT GAGAATAGGA GTAAAAGAAT 1200 GTAGATAGAT TCTCAATAAA GAGCCTCTAG GATTTGGCCA CTGACTGAAT GTAAGAAAAG 1260 AGGCAGATGG CATTGCTGAT AGGGCTCTGA TGTGGTTCAG TCTCAAAGTC AGACACGGGT 1320 TCAAATTTCA AATGTAGAAT 1340
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