Tag | Content |
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EnhancerAtlas ID | HS050-21094 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr14:75662870-75663960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr14:75663381-75663395 | CACTTCCTCTTTCC | - | 6.1 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09622 | chr14:75662710-75664246 | CD14 |
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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 |
GH14I075196 | chr14 | 75662904 | 75663990 |
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Enhancer Sequence | GTTGCATTCT TGGTCTGGGC CTTCCGAGAA AATGTCCTTT TCTCAGAGGT GATGAATCAG 60 GCCACATTCC TCCTCCACCT TCCTGAGAAG CTCTCTCAAA TGCTACCTCT GTTCCCAGGG 120 TCTCCCAAAC CCAAATGCCG CCTGGCCCAG CATCCCCATT CAGAGTCCTC TCCTCACACA 180 CAGCCACTCT GGCTGGCTTC CCCCACAGCC CCCAGGTGAC CCTGTGTCCA TTGAGAGGCT 240 GCCTCCCTCT CACTCCCCTG TGTCTCTGTT GCTCCTTCTA GTGGAAGAAC CTGAAGGTCT 300 TGATGCCGGG GAGCTGGCAA TCAGTCAACC CTCAGGATGT CCCTCCTATC CTCCACTATA 360 TCCAGGGTCT CTTGGGCACC ACAGTTCTTC CCTTAGCCCT GTTAGGGCAG GCGTCTCGCA 420 CTGCCCCCCT CTGCTGCCCA CCTCCCACTC TCACCACTGG CCCAGGGCAT GGGGTGTACC 480 ATCAGGCACA TAGGCCTTAT CACTGTGCAA ACACTTCCTC TTTCCCCAGT GCTGGTTCTC 540 ACACAATTGG TAATCAGTGT AAACTTCCTC TGACAATTTA CTGAGCAAAC ATTTACCATA 600 CAACTGCCCT ATGTAGGGCT CTGTGCTAAG GCCCATGGGG AACCCAAGCC TGGTCTCCAC 660 CTTGGGGCAT CTCGAGTCTG GTAGAGATGA GGCACATGAG GCGTCTCAGA TGCCGCGGGT 720 CTTGCGGACC AGAGCACCGC GGACTGGAAT CCCATTTCTG CTCTCTACTC CCTGTCTTAC 780 CTTGGAGCAA GTGACATCCT TTCTGATCTT GAATTTCCTT AGCTGTGAAA TGGGAGTAAT 840 GCTGTCTAGG TTTGTTGTGA GGACTAACTA AGATCCCTAG AGGGCCTGGC AGAGCACCTG 900 AGATAAGGAC ATTCCACAGT CCCTGTGGTG CCACCTTTCA GATATGAATT GAGGGGTCCC 960 TATATACTAC AGGGTCAGCC AATCATCTAG TCAACAAGAA CACATTCAAA ACGGAAGTGT 1020 TGGGTAAGTG GGGAACACAC ATGAACATAA CACACATACA CATAAGGGTA TAAACATAAC 1080 CCTTTAGTTT 1090
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