Tag | Content |
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EnhancerAtlas ID | HS038-21737 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr8:131057790-131059200 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr8:131058105-131058116 | GAGCCATAAAA | + | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_00708 | chr8:131057605-131059064 | Adipose_Nuclei | SE_58319 | chr8:130983513-131114285 | Ly1 | SE_58914 | chr8:130970257-131059501 | Ly3 | SE_59893 | chr8:131020352-131075191 | Ly4 |
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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 |
GH08I130045 | chr8 | 131057569 | 131059297 |
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Enhancer Sequence | GTCTTTGGCC AATGTATGTC ACATTTCCAC TCAAGAATCT ATGGGTCACA GAACACGAGT 60 ATGTCCAGCT TGAGTAGATA TGTAGCCGAC TTCACTTTGA CTCTATTCCT GTTCTCTGCC 120 TCCTATCCCA TGCCCTTAAC TTCCCTTTCC TTGCAAGCAA GCAGGGTCAC CACCCTGGCA 180 TCTTCCACTC TGGGGCAGAC CAGACAGGGC CTGGGTTTTG CGTGGGAAAG TAAACCCCAG 240 GCCACTGGGA CTAGTTGGTG GGTAACCCTG GAGGCACCGC TGTTCCTTCA TCTTCAGAGC 300 TCACTTAGGG TGGCAGAGCC ATAAAAGGAG CTTCAGATAG GGAAGTAGCT GGTAACCGGA 360 GGTGGAGCCA GCCAGGGTAG TCTCGGTGTC TGACGTTTCT AAGTGCTTCC AGCTGAGCAG 420 GAACCAGGCT TGCACATTCA GACAATGTAT TCCTGTGAAT CTGTTCAGCG GCTTAATGCA 480 CCATAAAAAG AGGTCCATTG TCAAGCAGCC TGTTTCCCGG GTGGGAGTCA GCAATATGCA 540 GCGTAAGTGG GTAGAGCCAC TGTGGCTCAG AGGCTCCCCG GCTTTGGCCC TCGGTTGGGG 600 GCGGGTGCTG CCCATGCTTT TGAAAGGAGA GCAGCTAATG TGACTCCCTG GACTCCGCCC 660 CTTTCAACAG CGGGCGCTCT GCTCGTTATT TTTGACCGGT TTCATGTGCT CACTCGTTCA 720 AGAAATACTC TTGTGATCAC CAACTGCAGG TCAAGCATGG AGGAGGTTTA TGTCTCTAAT 780 TTATCACTTG TCACCGGGGA AGGTGAGGAG TTTTCAAAGT TCTAGTCATT TTATTATTCT 840 ATTTTGCACA TGGTGGTCAG TGTGCAAGTT CTCATCATTT TTGAAGTGGT GAGTGCTGAG 900 GATTAGTATT CTGTGCTACT TTGTGTTAGG CACTAGGACA AGCATGTTAC ATGTACCGTC 960 ACATCAGTGA TGTCATTTAT CACACCAATT CTATGATACT AAGACTACCA TTATCCCATT 1020 TGGGCAAAGG AAAAATGCTG AGGCTTGAAG AGGTTAAGGC TCAGCACATT GTTTTCTGAT 1080 TTCAAAGTCC AGACTCTTAC CCTCCCCTGA TCCTATCCCT CTGGACCCAG GTAACAAATG 1140 GCTGTGGCTG GCCCAGCCAG GCTACCAAGC TGCCACCCTT AGGGATGAAC AGAAGCTGTG 1200 CTGCAGGTGA TGAAAGTCCC AGGCCCTGCA TCCAGTTCAC ACTGCACGGA GAAGCCAGTG 1260 GCTACGCATG GACAGTGTGT GTCTGGCTTT ATAGAGATGG TCACACAGCA TTGGGCGGGT 1320 CACTGAGCAC TGTTCCACCT TCCAGCCCAC AGACTCCCAA GCTGTGTCAC ATCTAATGGA 1380 ACTTGAGGCT CAGAGCTCAG TCCATGTGCC 1410
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