Tag | Content |
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EnhancerAtlas ID | HS158-18431 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr14:104196180-104197400 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP8 | MA0747.1 | chr14:104196470-104196482 | AGGGGGCGTGGG | - | 6.04 | ZNF263 | MA0528.1 | chr14:104196761-104196782 | CCCTCTCTGCCTGCCTCCTCC | - | 6.25 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_03053 | chr14:104196382-104197392 | Bladder | SE_06305 | chr14:104194098-104197464 | Brain_Hippocampus_Middle | SE_08167 | chr14:104194332-104197262 | Brain_Inferior_Temporal_Lobe | SE_26911 | chr14:104194299-104197024 | Esophagus | SE_32310 | chr14:104194384-104197255 | Gastric | SE_41604 | chr14:104193490-104197468 | LNCaP | SE_46928 | chr14:104196993-104197228 | Ovary | SE_53673 | chr14:104196363-104197507 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 104196804 | 104197391 | chr14 | 104196508 | 104196729 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I103729 | chr14 | 104196035 | 104197416 |
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Enhancer Sequence | AAGGTCAGCC TCTTCCTCCT CACCGGGGCT CCCCGCATGC AGCGGGCCCG TTCCTCCCCT 60 CGCCACCTGG CTTCTGTCCA CGGGGTGGTC CATGCCAAGG TTCTTTGTGA AACCTGAATT 120 CACTTACTTT GGTTGACTTA AGAGAGATGT TGGATCTGAT AAGTGGGTTT ATAAAGCATA 180 AATGAAGATA CCGCAGCAGA TGTACTTTCT CAGTTCTGTC TCAGCGGGAG GGTTACCCAG 240 CAATTGACAG CTCTCTGTCA GTACCTGCCA GCCCTGAACA GGCTGAGGCC AGGGGGCGTG 300 GGGGCTCACC TGCCCTTGGG AGCCTCTGCC AACACTGCCC TTCCCCCCGA GGCCTGCTGC 360 TCCCCAGCTC AGTGTGGCCT CCTGGGACCC CTGACTCTCC TGGCACTTCT GTCAGCCTCC 420 TGGATGGTGA GGTGAGATGC CCAGGCCAGT GTTCTGTCCT GAGCTCAGGG ATGTGTGTGG 480 AGCCGGGATG GCATCAAGCT GGTTGCCTTG AGCAGGCTGC AAGGTATAGA TGCCCAGGTG 540 CAAAGGGTAG GGTCTGGAGA AGCGGGGGTC ACCCCAGGCA CCCCTCTCTG CCTGCCTCCT 600 CCTGGGGAGC CTGAGGCTCA GATGAAGGCC AGTGTTTAGG GGCATCAGAT GAAGGCCAGT 660 GCCTCAGGAG GCCAGGGCAA CACAGCCTCC CGGACTGCTC TCCCGGGCAG ACCCTCCCCA 720 GGGCTTCTGG CACTGTGTCC CCCTTGTGGT GGCTTGGGGG GTGCAGTGAG CCCCGCTCTG 780 CCCAGTCTCA GTAGAGCCCT TCAGACCCCA GCACCCTGTC TTCCGGTGGG GGTGGGGACA 840 ATAGGAACAG TCCCCTGACC TGAAGGCAGC CAAGGGGCCG CCTGCCAGCC TGGGCCCTGT 900 AGGGCAGGCC ACACACTCAT TCTTTCAAGG CCAGATAGTA AACCTTTGCC AGCCACGTGT 960 GCTGTGGTGA AGGCGGAGGC GGCTGCAGAA GACAGGGTGA CAGACGGCCA TGGCTATGAT 1020 CCAGTGGTGC TTTATCAGGC AAATGCAGGC GGTAGGCAGA GCCATGGTCG CCCTGCTCTA 1080 GAGCCTAGGC AGGACGTTAC ACTGACAGGC AAGGTTCCCC AGTGTTGGGG GTGGGGGTGC 1140 GTGCCCTAAC CACAGAACCG GGCTTATGAA AGTGTGGTTC TAGAGGCCCG GCATGGTGGC 1200 CCACGCCTGT AACCCCAGCA 1220
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