Tag | Content |
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EnhancerAtlas ID | HS187-25368 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr9:130796930-130797970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mafb | MA0117.2 | chr9:130797696-130797708 | AAACTGCTGACT | + | 6.22 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_23076 | chr9:130796969-130797632 | Colon_Crypt_1 | SE_47183 | chr9:130796622-130798148 | Panc1 | SE_62942 | chr9:130767703-130798071 | 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: 1 | ID | Chromosome | Start | End |
GH09I128034 | chr9 | 130797001 | 130798210 |
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Enhancer Sequence | TTTTCATGGT TTTAGTAGGA AGATAAATTA GGCATGTATG ATTGCCCCCT CATCTTAACA 60 AGGAATTTCT CTCAGCTCAT TTTCTTCAGG GGAGAATTCT CTCCCACCCT GCCTTGCACC 120 TGCTTCTGAC CCAAGGACAT GGCAGAAGGA GCTAGGAGTT CCAGCTTTCA CTCCTGGCTC 180 CAACCCCTCA GTTGTATAGC CTTTGGAAAG TCACTTAATC CTTTTGGGCC TCAGTTTCCC 240 CATCTAGGGA ATAAGGGAAT GTCATGATCT CAGAGGAGGT GGCACAGTCT GATAGGGAGA 300 GGGCTGTCCC AGGGCTCCCA GCTGCCTCTT GGGCAGGGCA GGTCTAGGCT GTCTGGCCCC 360 CTCAGAGCCT TGACTGTCAG GGCCCAGGCT GAGCAGGCTC CCATGACCCC ACTGCGTGGC 420 AGGGAGATTA AGGCCAAGAA AGGGAGGGGG CCAGAATCGC ACAGCTTGCC CAGGCAGAAT 480 GGGCCCCTGC CTTCTGTTCC TGAGCTTTCT CCCTGCACCA GAGCCATCTC CGGGCTAGAC 540 AGGCTGGTAG AACCAGCCAC GTCCTCTCCC TGGGGTGGAG GAAGAGCCTG CTCCGCACAG 600 GGCCAGAACT TTCCAGCCAT CTCCCTCCAG CCTCACCAGT CCCCACCCAG AGCCTGAAAC 660 TCAGGGCTGT CTGTGCCCAG GGCTGCACCT GACTTTGGTT ATCTAGCACC ACCTACAGGA 720 TATATTGAGA ACAACATGCC ACATGGCTTC AAGCCCCAGA TTCCAGAAAC TGCTGACTGG 780 GAAGACGCCC ATTCATGGAT CGCACCTGGT ATGCCCGGGC CAGAGCTCTG TGCCCTGCAT 840 GAGCCTCTGC CCTGATCTGC ACCACAGGCC CTTAAGGCAG GAACTACATT ATAGTATTGA 900 ATCAATATAA CACCCTTTCA TAAGGGATAC AAATGTAGTT GTTAGATAAA AGGTATAACT 960 TCTGTTGTTC ACAGCAGAGT AGAGTGACTA CAGATAACAA TGTATTGTAT ATTTCAAAGT 1020 AGCTAGAAGA GAGGACATAA 1040
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