Tag | Content |
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EnhancerAtlas ID | HS136-09723 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr19:41701210-41702840 |
SNPs | Number: 1 | 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 | chr19:41702757-41702775 | GGGTGGATGGAAGGAAGG | + | 6.59 | EWSR1-FLI1 | MA0149.1 | chr19:41702765-41702783 | GGAAGGAAGGAAGGAGGA | + | 8.78 | EWSR1-FLI1 | MA0149.1 | chr19:41702761-41702779 | GGATGGAAGGAAGGAAGG | + | 9.17 | Foxd3 | MA0041.1 | chr19:41701790-41701802 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr19:41701794-41701806 | AAACAAACAAAC | - | 6.32 | ZNF263 | MA0528.1 | chr19:41702762-41702783 | GATGGAAGGAAGGAAGGAGGA | + | 6.21 | ZNF263 | MA0528.1 | chr19:41702758-41702779 | GGTGGATGGAAGGAAGGAAGG | + | 6.28 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_69064 | chr19:41700891-41701913 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 41702000 | 41702400 | chr19 | 41702138 | 41702290 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I041195 | chr19 | 41701168 | 41702771 |
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Enhancer Sequence | AAGCCCTCGA ATAATAGAAA CAGTTCTCTG TATTACAACA GAAAGCAGGA GGCCCATGCT 60 GGGTGCTGCC AGGAACTCAG TAGTAACTAA GACAGCACCG GTGCTGCTTC CCCAGCGCAC 120 CTAGGCCAGT GGGGAAACAG ACTCACCACA CAGTCCCAGC CCAGAGTGGT CAGGGCCAAG 180 ATGGGGAAGC ACGGGGAGAA AGGTCAGGGT GGGATGGGGA GGGGTCAGGG CAAGAGGGGT 240 CAGGGCCAGG CTGAGGGAAG CCCTGGGACT GTAGGAATTT AGAGGAGGTA CCTGACCCGG 300 CATGTTTGGT GAGGGAGCTT CAGGAAGTCT TCCTGGAAGA GAGGCTGTCG GAGCTGAGAC 360 TCATAAGATG AGTGGGGAGG GTGTTCCAGG CAGAAAGACC AGCACCTACA AAAGCATGAC 420 TTTGAGAGAA GCATTCATCC ATTCAACTGA TGAATTTTCA GACTGGGCAC GCTGGCTCAT 480 GCCTGTAATC CCAGCACTTT GGAAGGCTGA ATGGGGAGGA TGACTTGAGC CTAGGCATTT 540 GTGACAAGCC TGGGCAACAT GGTGAGACCC TGCCTCCACA AAACAAACAA ACAAACAAAA 600 AATCATTATA CCTGGTACCA TGGGTACCAG GTACATAGAA ATGACTCAGG CAGATATGGT 660 GTCCTCTCCT ACTGTGGGAG AGGCGGGCTT ATACTGCAGT AAGACAATAG AGGGAGGGAA 720 TATAATCCTA AAATGAGAGG TACAGATTTG AGAGCAAACA CAGGGCACAG GCATATGTAC 780 GAGGGTAAAG AGGGAATCAG GGAAGGCTTC TCAGAGAAGG TGACATTTAA GCCGGGACAT 840 GAAGGATGAA CGAGTTAGTT CACCAAGGAT GGGATGGAAA GGGGTGAGAG TGATGGAGGC 900 AGAGGGAACT GCAGGATCAT AGGCCTAGAC AGGGGATCCT GACGCCCTTG AGGAAGTGAG 960 AGAAGACCAG CGCAGTCGTA GTGGGTTAAG TAACAAAGCT GAGAAGCCAG GGAAATCCCT 1020 GGTCATGCAG GGCCTGTGAG TCACGTCAGA GTGTTTGGGC TTTTGTTTTT CCTGGGAGCA 1080 GTCGATTTTA AGCAGGGAAC AGCTGTATTC AGAGTTGGGA AGATCCTGTG GTTGCTGCCT 1140 GAAGGGGATG AAACTGGAGG CTAGGAGCCC AGGGTGATAG GGAGGATCCA GGGTGATGGG 1200 GAGGCTGGGA GGTCCGCGGT GATGGACCAG GGCTGGGGCC AGGGGATGGG GAGGAAGGAG 1260 TAATTGGGAG AGGCCTGGGG CTCTGGCCGA GGAATGGATG GTGGGCTGAA ACAGGGAGAG 1320 GAGAGATGCT TAGGCCACTT TGGAACACAG TAGGGCAAGG ACAGGAGACA CCCAAGGGGA 1380 AGTGCCCAAG AGACCACGAC AGGCTGGCAT TGGACAGGGA AGGTCTGTCT GGAGCAGGTG 1440 TCTTGGATAA GGGAGGAAAA TGGTGCAGTT CCATCCTCCT CCCTCTCTGT TCAACCTCTA 1500 AACTACATGG GGCACAGGAC CCAGTGGGAC TCCATAAATG ATGGGATGGG TGGATGGAAG 1560 GAAGGAAGGA GGAAACAACT CTTCATTCAT CCTGGTTATT TACAGAACAG GCCAGGTGCG 1620 GTGCTCACGC 1630
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