Tag | Content |
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EnhancerAtlas ID | HS037-16762 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr18:47833550-47834700 |
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 | TAACGAAATG CAGTCTTAGA AGGCTGAGAG ACAGAGGCTT GAGAGAAGCC CACAGCTCCA 60 TCACATTCCA CAAACCACTC TTCAGAGGAG CAGAGCGAGT TTCGGATCAC AAAGCTGGGT 120 AACGGCCAGT TCAGAGCCCA GATCTTCTGC CTCCCAGCCC TGTGTCCCTC TTGGGACATA 180 CACACCCCTT CACAAGGGGA CTGACCTTCT GGGTGACTTG CAGACTAATG GGCCTTCAAG 240 ACCCCAAGTG ACAATTTTCC AGAGACATAA TTTATGTATT AAAGCTGGCT AGTGGGGGAT 300 GTTTCTTGAA GGTAGGGTAG GTGGTTAACA GGTTTTCTTT ATATTTAATC ACCTAACAAA 360 TCTTATACCA GAGCACACTC CCCTTATAAA GGGAGGGCTG ATCGCGGTCT AGGTGGGTGG 420 GCTAGGCCTG GGGGCGGGTA AAGAAGGAAA ATTCTCAGGG TCTTGCACGC TCCCCCAACT 480 CCTGCGTTTA CCAGGATCAC CACGTTTAGA GTGGAGCCCT TTATCTTCCG CAGCAAGGGG 540 TCAAACGGCT GGCCTTATGC GTATTTTTGT CTTTCCTGGG TGCGCCCGGA GCTAAGAAGG 600 GAAACCGTGG CGGTTAGAGA CCAGAAGTAG GCTCTGTCAC TATGGAAACC GAGGACGCTG 660 GGGCTCGTGC CCTCCTATTG GGGCTGAGTT GCTGAGTCTG CGCAGTTTTC ATCTCATGTC 720 GGTCACGCCC CCAGCTGCGC TGCACGCTGG CTCTCGGGTT CAGCCCGAAA AGTGGAGACT 780 GAGGAAATAG GTGGTGGTGA ATACAACATT CTTTCTCATG AGACACTCAC CGTGTGGTTG 840 GAGAAATTAC GTAAAAAAAA ACAATTTCAG TTTTTAAAAA GTGCCATTAA TAACAGAGGA 900 GTGCAAATCG AGACAGCACC TTCTGAAGGA TAAATAATTT ACCAGTGTAA TGTGTAGGAA 960 TAACGGATGC TGTGGGGCAC CCGGTTCTAC TTCCAGACTC AAGAATGTGT TCCTCCAGTT 1020 GCAGGGTGTG TTGCTAGCAG AAAGCGTTGC TAGCAGAAAG CCTTCAATTG TAAGTCCTCT 1080 TCTGAGTTGC CTAAGCCAAA GAGAGTTACA CACTGAAGGT CACGCCCGTT TCCTGGACAG 1140 TTCACATCCA 1150
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