Tag | Content |
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EnhancerAtlas ID | HS044-06278 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr18:47833420-47834860 |
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 | CCAACATTCT ACCGCGGGCG GCATTCCTTT GGTCTCCTCC ACAACCACAG TCCTTCCAGT 60 CTTTCATCCT TCCTCCAGTT TCCTGGTGTG TAGGGCCAGT TCTGCCAAGC AGCTCCCAGG 120 GGTGAACTGA TAACGAAATG CAGTCTTAGA AGGCTGAGAG ACAGAGGCTT GAGAGAAGCC 180 CACAGCTCCA TCACATTCCA CAAACCACTC TTCAGAGGAG CAGAGCGAGT TTCGGATCAC 240 AAAGCTGGGT AACGGCCAGT TCAGAGCCCA GATCTTCTGC CTCCCAGCCC TGTGTCCCTC 300 TTGGGACATA CACACCCCTT CACAAGGGGA CTGACCTTCT GGGTGACTTG CAGACTAATG 360 GGCCTTCAAG ACCCCAAGTG ACAATTTTCC AGAGACATAA TTTATGTATT AAAGCTGGCT 420 AGTGGGGGAT GTTTCTTGAA GGTAGGGTAG GTGGTTAACA GGTTTTCTTT ATATTTAATC 480 ACCTAACAAA TCTTATACCA GAGCACACTC CCCTTATAAA GGGAGGGCTG ATCGCGGTCT 540 AGGTGGGTGG GCTAGGCCTG GGGGCGGGTA AAGAAGGAAA ATTCTCAGGG TCTTGCACGC 600 TCCCCCAACT CCTGCGTTTA CCAGGATCAC CACGTTTAGA GTGGAGCCCT TTATCTTCCG 660 CAGCAAGGGG TCAAACGGCT GGCCTTATGC GTATTTTTGT CTTTCCTGGG TGCGCCCGGA 720 GCTAAGAAGG GAAACCGTGG CGGTTAGAGA CCAGAAGTAG GCTCTGTCAC TATGGAAACC 780 GAGGACGCTG GGGCTCGTGC CCTCCTATTG GGGCTGAGTT GCTGAGTCTG CGCAGTTTTC 840 ATCTCATGTC GGTCACGCCC CCAGCTGCGC TGCACGCTGG CTCTCGGGTT CAGCCCGAAA 900 AGTGGAGACT GAGGAAATAG GTGGTGGTGA ATACAACATT CTTTCTCATG AGACACTCAC 960 CGTGTGGTTG GAGAAATTAC GTAAAAAAAA ACAATTTCAG TTTTTAAAAA GTGCCATTAA 1020 TAACAGAGGA GTGCAAATCG AGACAGCACC TTCTGAAGGA TAAATAATTT ACCAGTGTAA 1080 TGTGTAGGAA TAACGGATGC TGTGGGGCAC CCGGTTCTAC TTCCAGACTC AAGAATGTGT 1140 TCCTCCAGTT GCAGGGTGTG TTGCTAGCAG AAAGCGTTGC TAGCAGAAAG CCTTCAATTG 1200 TAAGTCCTCT TCTGAGTTGC CTAAGCCAAA GAGAGTTACA CACTGAAGGT CACGCCCGTT 1260 TCCTGGACAG TTCACATCCA ATGACGCATC AGTGACATGG AGTATAAAGC CTTTCCTGAT 1320 TGCCTCAATC CTGGGCAATT CTTGCAGGTT GTCCCAGCTT CAGAGCTCCA TGTGCTGGGC 1380 GGTGGATTTC AACATCTCAT GTTGAACGGC TATGGCAGTT CAACATCTCA CTCTGCCCAA 1440
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