Tag | Content |
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EnhancerAtlas ID | HS047-16018 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr18:47833580-47834890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr18:47833958-47833973 | CTAGGTGGGTGGGCT | - | 6.38 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_59642 | chr18:47812066-47884052 | Ly4 | SE_61249 | chr18:47823747-47848177 | HBL1 | SE_61714 | chr18:47823714-47861915 | Toledo | SE_65778 | chr18:47833408-47834751 | Pancreatic_islets |
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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 |
GH18I050306 | chr18 | 47833285 | 47835497 |
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Enhancer Sequence | ACAGAGGCTT GAGAGAAGCC CACAGCTCCA TCACATTCCA CAAACCACTC TTCAGAGGAG 60 CAGAGCGAGT TTCGGATCAC AAAGCTGGGT AACGGCCAGT TCAGAGCCCA GATCTTCTGC 120 CTCCCAGCCC TGTGTCCCTC TTGGGACATA CACACCCCTT CACAAGGGGA CTGACCTTCT 180 GGGTGACTTG CAGACTAATG GGCCTTCAAG ACCCCAAGTG ACAATTTTCC AGAGACATAA 240 TTTATGTATT AAAGCTGGCT AGTGGGGGAT GTTTCTTGAA GGTAGGGTAG GTGGTTAACA 300 GGTTTTCTTT ATATTTAATC ACCTAACAAA TCTTATACCA GAGCACACTC CCCTTATAAA 360 GGGAGGGCTG ATCGCGGTCT AGGTGGGTGG GCTAGGCCTG GGGGCGGGTA AAGAAGGAAA 420 ATTCTCAGGG TCTTGCACGC TCCCCCAACT CCTGCGTTTA CCAGGATCAC CACGTTTAGA 480 GTGGAGCCCT TTATCTTCCG CAGCAAGGGG TCAAACGGCT GGCCTTATGC GTATTTTTGT 540 CTTTCCTGGG TGCGCCCGGA GCTAAGAAGG GAAACCGTGG CGGTTAGAGA CCAGAAGTAG 600 GCTCTGTCAC TATGGAAACC GAGGACGCTG GGGCTCGTGC CCTCCTATTG GGGCTGAGTT 660 GCTGAGTCTG CGCAGTTTTC ATCTCATGTC GGTCACGCCC CCAGCTGCGC TGCACGCTGG 720 CTCTCGGGTT CAGCCCGAAA AGTGGAGACT GAGGAAATAG GTGGTGGTGA ATACAACATT 780 CTTTCTCATG AGACACTCAC CGTGTGGTTG GAGAAATTAC GTAAAAAAAA ACAATTTCAG 840 TTTTTAAAAA GTGCCATTAA TAACAGAGGA GTGCAAATCG AGACAGCACC TTCTGAAGGA 900 TAAATAATTT ACCAGTGTAA TGTGTAGGAA TAACGGATGC TGTGGGGCAC CCGGTTCTAC 960 TTCCAGACTC AAGAATGTGT TCCTCCAGTT GCAGGGTGTG TTGCTAGCAG AAAGCGTTGC 1020 TAGCAGAAAG CCTTCAATTG TAAGTCCTCT TCTGAGTTGC CTAAGCCAAA GAGAGTTACA 1080 CACTGAAGGT CACGCCCGTT TCCTGGACAG TTCACATCCA ATGACGCATC AGTGACATGG 1140 AGTATAAAGC CTTTCCTGAT TGCCTCAATC CTGGGCAATT CTTGCAGGTT GTCCCAGCTT 1200 CAGAGCTCCA TGTGCTGGGC GGTGGATTTC AACATCTCAT GTTGAACGGC TATGGCAGTT 1260 CAACATCTCA CTCTGCCCAA TTCTGCTTTC TTCCACTCTG TACGTTTTTC 1310
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