Tag | Content |
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EnhancerAtlas ID | HS051-26653 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr8:125721360-125722520 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr8:125722262-125722280 | TGAAGGGAGGAAGGAAAA | + | 6.4 | EWSR1-FLI1 | MA0149.1 | chr8:125722258-125722276 | GAAATGAAGGGAGGAAGG | + | 7.05 | HSF1 | MA0486.2 | chr8:125722120-125722133 | TTCTGGAACATTC | + | 6.67 | KLF4 | MA0039.3 | chr8:125722026-125722037 | CCACACCCTGT | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_05555 | chr8:125721851-125723879 | Brain_Cingulate_Gyrus | SE_10859 | chr8:125712814-125729740 | CD20 | SE_33465 | chr8:125721578-125724787 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr8 | 125721699 | 125722377 | chr8 | 125721868 | 125722267 | chr8 | 125721421 | 125721613 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I124708 | chr8 | 125720497 | 125724067 |
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Enhancer Sequence | GAAAGGCAGC AGAGAAAAAG TCCTGCCTTT TGGACAGCAA GACTACATAA AGGAGACCAT 60 ACTCAAGTTT CAAAAGAAAC CCGCAACCCA AGACACTGGA AGCTCTTAGA GCCCTTTAGA 120 AAGCAATTCC CCAACTGTCC TTGGTTTTTG CATCTGCATC CACCCACCAA GAAGTCCCCA 180 GAAAGTTCAT TCCTGAGGTT GCTGGCTGAG CTCTGTCCCC ATTTGAGGAA ATCCCTCGGA 240 ATGCACTCCC AGAGCCGTGA AAACAATTCA ACACAGACCC CACTGTGGAT TTCACCTGAG 300 AACACATAAA GGCTTCACAA CGTTCCAGAC AGACCCAAAT CAAAGAAAAC AAAACTCCCG 360 CCACGCCCCG GCTTCTGCCA AGTCCAAAGT CACAAGGCAA AATGAGAAGG CGCACCTCCT 420 CCAGGAGCCC CCTGAATTTC TTCAGAGAGG AGAGCCAGGA GTTTCTGGAG CCCTTGGCAG 480 TGCGTTCGTT GAAAATACAA CTCAGATTAC ACTGGGTTCT AAGAAAGGAA AAGGTCCCTA 540 TTAAAGAAAC GGGAAGAGAA AGCCAGTTTG TTTACAAGCG TGTAAAGAGG ACTCCCTCCA 600 TCACTTCCTT GGGTGAGAGA TGGGGCTTCC CTGAACACGT GATCTCACCC ACACTCCCCA 660 CACACACCAC ACCCTGTGGC TGCTTCTCTT CAAATCTCCA GGGGGATTCA GCAATATTGA 720 AAACTCCTAT TCAGCTGTCA CTACCCAGCT GTGACACTTC TTCTGGAACA TTCTCTGACA 780 CACCCCCTTC CCACCTACCC TCTGGTTTAG CTGCACCTAC TCCCCAACTT ATCACATCAT 840 ACAGTTTGCT GTCTATAAGC CTGAGGGCTT CCCCTTTGGA CTGTGGAACA AGGACTGAGA 900 AATGAAGGGA GGAAGGAAAA GTACTTCTGG TAGGGGGTGC AGCTGACACA AAAGGAGGCA 960 GGGAACACTG ACCAGCTCTC TCCAAGGGAC ACTGGAGTGA CACATTTATG CTGGCCACTC 1020 CTCCAGGCAG GACATGGGCG AAGTGGCCCA GGTGGGCAAG GGCAGCCTTC CAGGGCAAGA 1080 CCCAGGGTGG GGACTTGGGA CAGGTGAGGA AGACCGGGGT GGCCTTCATT CAGACAGTGA 1140 GTGACATAAA TTCCAGACCA 1160
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