Tag | Content |
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EnhancerAtlas ID | HS182-10821 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:6774940-6776290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:6774995-6775010 | TGAACTCCTGACCTC | - | 6.22 | Nr5a2 | MA0505.1 | chr19:6774987-6775002 | GCTGGCCTTGAACTC | - | 8.25 | RARA | MA0729.1 | chr19:6774992-6775010 | CCTTGAACTCCTGACCTC | - | 6.73 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_17561 | chr19:6774722-6776103 | CD4p_CD25-_CD45RAp_Naive | SE_18804 | chr19:6774749-6775928 | CD4p_CD25-_Il17-_PMAstim_Th |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 6775833 | 6775873 | chr19 | 6775936 | 6775976 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I006774 | chr19 | 6774821 | 6775506 |
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Enhancer Sequence | TTTTTTTTGT ATTTTTAGTA GAGATGGGGT TTTCCCATGT TGACCAAGCT GGCCTTGAAC 60 TCCTGACCTC AGGTGATCTG ACCACCTCGG CCTCTCGAAA GGCTGGGATT ACAGGCATGA 120 GCCACCATGC CCGGCCCTTC TGTTTCTTTA GTGCCAGGGG ATTACACTGT CCTCAGCTGG 180 GACAGGGCTT CCTGAAAGGA GAAGGCACTC CCCCCACCAA CCTAAGCATC CATCCTCTGG 240 CCACAGCCCA TCCCAGCTTT GCCTACATTT GCTTAATCTT CTGGTTTCTA GGGCATGAGG 300 AAGTAGTCAT GGGATCTGTT AGGCCCCATC TGTTAGACCT GGCAGGGAGT CAAGCTCTCT 360 GTGATGCTTC AATAGCAGCT AATGGGAAAG TGGATAGACT TAAGGATGAA CTTCCATTCT 420 TGTGTATGTC TTAGCTAAAG CTAGTTTTTG GATGAAGGAC GAGGGTGCAT GATGCTAATC 480 CCTGGGAGAG CAGCTGCACT CCAAATACAG TCCTAATCCT CTGTAACAGG GAACAACGGG 540 AACCCAGATG GGGTCAGGCT TTATGCAAGA GGGGACATTT GTGCTGGGGT TTTGAAGAGT 600 AAATAGGAGT TTTTCTCATT GTTCTGGCTT CCTGTGCCCA GCTGTATCAG GCTCCAGGCT 660 GGGCATCGGT GTACCCAGAC CCTTTCCCTC TTCGAGGGGG CACATTCCTG CCCCTACCCA 720 TTTTGTTGCC CTTTGAAGCC CGGCCGTGTG TCTGGTATGT AGTGGGGACG TGTGAGGGAA 780 GGTAAGAGGT CTTGACAAGA AGCCAGAGGA AGCTGCCACA GGAACAACCT CTCTGGGTTT 840 CTGGGTGCCT AACTGTCCAC AGATTGAAGC AGAGCTGTGA ATGCCCCATG GGATGTGAAA 900 GGGTAGAGGG AAAAAGGAAA GGTGCTCCTG TGGAGGAAAT GGCATAAATA AAGGTGTGCA 960 GGCTGGAATG AGAATTCTTC CCAGTTTCTG TCATTTCTCT TCGGAGTCCT TCTCTTTTTT 1020 CTCAGTTGTT TCTTGGGAAG AGGGTGGAAA GAACATATTC ATCCATCCGT TCATCCACCC 1080 ATCCACTCAT TCATCCACTC ATCTATCCCT CCAATTATCC ATCCATCTAC CCATCCATCC 1140 ATCCATTTAT CCATCCATCC ATCCATCCAT CCATCCATCC ATCCATCCAT CCATCTGCTC 1200 ATCCATTCAT CCATCTGCTC ATCTATCCAC CCATCCATCC ATCCATCCAT CCATCCATCC 1260 ATCCACTCCT CCATCCATCT GCTCATCCAT TTATCCATCC ACTCATCTAT CCATCCATCC 1320 ATCCATCCAT CTGCTCATCC ATTCATCTAT 1350
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