Tag | Content |
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EnhancerAtlas ID | HS158-30771 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr2:85945940-85947130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr2:85946383-85946398 | GGGGGTCAAAGTCCA | + | 6.86 | Hnf4a | MA0114.3 | chr2:85946384-85946400 | GGGGTCAAAGTCCACA | + | 8.37 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_32403 | chr2:85945927-85946380 | Gastric | SE_42161 | chr2:85946104-85947312 | Lung | SE_48223 | chr2:85946116-85947658 | Psoas_Muscle | SE_51392 | chr2:85945940-85947720 | Skeletal_Muscle |
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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 |
GH02I085718 | chr2 | 85945928 | 85947720 |
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Enhancer Sequence | CCAAAGTGCT GGGATTACAG GCGTGAGCCA CCTTGCCTGG CCTGTCCTGG TCCCTTGAGG 60 TGGCTTTCCT CCCTGAATCT GCTCCTGTAC AGTCCTTATG GTCCCCTGAT TTGCATCTTT 120 GCTCCTTCCT CCCCAGGCTG TGGGAACCTC CAAGAGAAGG GAGACGGAGA GCCCTGCTCA 180 GAACAAGTGG CCTATGAAGC TGTGGCTGGG TCCCCAGGGT CCTCGGCCTT CCTTGTTCAT 240 GGAGGGGGTG TCCTGTGGGT GTGGGGACAG TGGGCTCAGG TGGTCGGGCC AGCAGTGAGG 300 TCTGGCGAGT GAGCTGGTCA AGCAGGCAGA GTAACCAGAG GTGAAGATGA ACGCCATGGA 360 TTTGGGCACG CAAGAGCTGG CTCCTGGGAA AATCAGCTAG GGCTGGCAGC TTAAGACAGA 420 AAGGTTCTCC TAAGTCCAGG GAAGGGGGTC AAAGTCCACA AAGCAAGGAC CTTGCCCTCA 480 CCCTCCCAGT AAGTGACACA TAGATTAGGT CAGATACTTG AGCGGGGCTG TGAGACTTAG 540 GCACATCCCA CGTGTGGCAG ATACTGATGG GGTGAGACGC TGAACCTGGA ATGGAGCTCT 600 AAATTTGAAT TCCAGTTCAG CAGTAAACTC ACCACATGAC CTTGGAAGAG ACCGTGCACC 660 TCCCTGAGCC ACAGAGCCCT TTACTGCAAG CTGAGGATAA CACCCGTCCT CTGCACCCCA 720 GAAGTGTGTT GGGAGGAGAA AAGGTTAGAA GCCTGGGGGT TCCTTGTAAG CAGTGATGAA 780 TGGAGGGGTC TGTGAAGGGT GGCTGAAAAT CAGGGTGCTC CAGGCCAGGG GCAGGGATCC 840 TGGCAGTGGA GTGGGAGAGA GATTCAAGAA CAGAGTCTCT CCAGGTTTTG CCATCTGTAG 900 AGGTCAGAAG CACCCTGCCT TGACCTTGGG CTATTTCTAG AGAGCTGGCC AGGCATCTCT 960 CATGATGGCA GCAGCTGGCT GCCTCTCCTC TGGTGCTGGC TGCCTGCTCC TTGGCTCTGG 1020 CTGGACCTGC TCCAGGTTGA GGTCTCACCA GTTGAGCTGT CAGAGCCAAG GTAGGACAGA 1080 ACCCAGGCTG AGCCCTCTGG AGAACCCGCA GTATCTCAGA GGCACTTTAG CTTCTGAAGC 1140 GAGGAGAAAG CCTTGCAAGT TTAGTCCACG GTAGCCTGGA AGAAGCCGTC 1190
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