Tag | Content |
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EnhancerAtlas ID | HS182-19149 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr6:137077160-137078620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr6:137077922-137077933 | CATGAGTCACT | - | 6.14 | JUN(var.2) | MA0489.1 | chr6:137077923-137077937 | ATGAGTCACTTTTT | - | 6.86 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09572 | chr6:137075976-137080210 | CD14 | SE_59682 | chr6:137063070-137114568 | Ly4 |
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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 |
GH06I136756 | chr6 | 137077340 | 137079137 |
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Enhancer Sequence | AATGGGCTAG AAATATGTAC TTGAAAGTCA CTGTCACACT TTGGGAGGCC AAAATGGGCA 60 GATCGCTTGA GCCCAGGAGT TCAAGACGAG CCTAGGCAAC ATGGCAAAAC CCCGCCTCTA 120 CAGAAAAAAA AAAAACACTA CAAAAATAAG CCAGGCATGG TGGTGCATGC CTGTAGTCCT 180 AGCTACTGGA GAGACTGAGG TGAGAGGATC ACTTAAGCCT GGTAGGCAGA CGTTGCAGTG 240 AGCTGAGATG GTACCTCTGC ACTCCAAACT GCATGACAGA GCCAGACCTG TCTCAAAAAA 300 ACAAAATGCA GGTCACTTTC ATTGAGCTGG GCATGGATGC TATACAGCTA AGTCAGAGTG 360 CAATGAAATG ATCTCTCTGA ATATGTCTTT CCAACTAGAC TAGAAGCTCC TTAAGGGTAT 420 TGCCTTTTTG TTGCTGTTGT TGTTGAGACA GTCTCTCTCA CTGTCGCCCA GGCTGGAGTG 480 CAGTGGCGCA ATCTCGGCTC ACTGCAACCT CCGCCTCCCT GCAACCTCCG CCTCCCGGAA 540 GGGTATTGCC TGTGTTGTAC TCATCTCTTT ATCATAAGTG TCCTAAATAA TGAAAGAACA 600 ATTCTTCAAG AGAAAAGGAG TGGTCAGCCC CTTTACCCTC CTGTCAAGGA AAATTAAGCC 660 TGAAGGTCAT ACTATTGGAT GCTTAAAGGC CCTGCCGATT CATCACAAGA CAGTTTCCAC 720 AAACTGATGG GAGAGAGACA CTTGCAAGGC TTAGGTGAGT AACATGAGTC ACTTTTTCTA 780 GATTATCAGA GCATTGTCAG CACTGAGGGG CTGATGGCCC GGTGCATGTG GATAAGGTCT 840 CCTTTTCCTC TTCCATCTCA TTAGGAAGAC TGACCCCAAG ACTCCAAGAG ACACTTTCTC 900 AAGTGTGCAT AGGCTTTCTC TTCAGAACCA CACGAAGCTC AGAAGCAAAG CTCATTTTGG 960 CTTTCCAGTA TCTCTATGGT TTTCCAGCAA ATCAAGGTGA ACACCCGAGA AAACTCAGGT 1020 TTCAGTGCTG CAGTAGAAAT CGATAGGAAG ACTTTGGCCT GCTTTGGTTC TAGACCATTC 1080 AAGTCATCTA GCCCAGGGAA GGTGTCGTAG GGTTCCAGCC TGGCTCACCA GAGTTTTATG 1140 CTGGGACGTG GGGCAAGAGC CACGTGCAAT AATCAAGAGA TGCTTTGCCT TGGTTTATTT 1200 TCTGACTACA TACCTACCTC TAGGACTTTT CAAGAAAATA AGTTCCAGGG AAAGATTGTG 1260 GTATTCCTTA GCAACCCAGC CAAATACAAC TATAACAGCA TCTCAGTTTC AACACAGTTT 1320 ACAGGAAGTA AGAGAGTCAG GGCTGGGTCT TTGGAGAAAT AAGCTCAAGG GAGATGTTTC 1380 TGTGTTGGGA AGCAAGAATT TATGAGCTGT CTGTCTAGTC AGATAGCATC ACAGATTTGT 1440 AAATAATGTT CATAATAATT 1460
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