Tag | Content |
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EnhancerAtlas ID | HS095-15226 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr19:41701170-41702900 |
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 | AGATGCCGGA GCGCTTTCAA GGTGCTGGGG ATTGGTGGGC AAGCCCTCGA ATAATAGAAA 60 CAGTTCTCTG TATTACAACA GAAAGCAGGA GGCCCATGCT GGGTGCTGCC AGGAACTCAG 120 TAGTAACTAA GACAGCACCG GTGCTGCTTC CCCAGCGCAC CTAGGCCAGT GGGGAAACAG 180 ACTCACCACA CAGTCCCAGC CCAGAGTGGT CAGGGCCAAG ATGGGGAAGC ACGGGGAGAA 240 AGGTCAGGGT GGGATGGGGA GGGGTCAGGG CAAGAGGGGT CAGGGCCAGG CTGAGGGAAG 300 CCCTGGGACT GTAGGAATTT AGAGGAGGTA CCTGACCCGG CATGTTTGGT GAGGGAGCTT 360 CAGGAAGTCT TCCTGGAAGA GAGGCTGTCG GAGCTGAGAC TCATAAGATG AGTGGGGAGG 420 GTGTTCCAGG CAGAAAGACC AGCACCTACA AAAGCATGAC TTTGAGAGAA GCATTCATCC 480 ATTCAACTGA TGAATTTTCA GACTGGGCAC GCTGGCTCAT GCCTGTAATC CCAGCACTTT 540 GGAAGGCTGA ATGGGGAGGA TGACTTGAGC CTAGGCATTT GTGACAAGCC TGGGCAACAT 600 GGTGAGACCC TGCCTCCACA AAACAAACAA ACAAACAAAA AATCATTATA CCTGGTACCA 660 TGGGTACCAG GTACATAGAA ATGACTCAGG CAGATATGGT GTCCTCTCCT ACTGTGGGAG 720 AGGCGGGCTT ATACTGCAGT AAGACAATAG AGGGAGGGAA TATAATCCTA AAATGAGAGG 780 TACAGATTTG AGAGCAAACA CAGGGCACAG GCATATGTAC GAGGGTAAAG AGGGAATCAG 840 GGAAGGCTTC TCAGAGAAGG TGACATTTAA GCCGGGACAT GAAGGATGAA CGAGTTAGTT 900 CACCAAGGAT GGGATGGAAA GGGGTGAGAG TGATGGAGGC AGAGGGAACT GCAGGATCAT 960 AGGCCTAGAC AGGGGATCCT GACGCCCTTG AGGAAGTGAG AGAAGACCAG CGCAGTCGTA 1020 GTGGGTTAAG TAACAAAGCT GAGAAGCCAG GGAAATCCCT GGTCATGCAG GGCCTGTGAG 1080 TCACGTCAGA GTGTTTGGGC TTTTGTTTTT CCTGGGAGCA GTCGATTTTA AGCAGGGAAC 1140 AGCTGTATTC AGAGTTGGGA AGATCCTGTG GTTGCTGCCT GAAGGGGATG AAACTGGAGG 1200 CTAGGAGCCC AGGGTGATAG GGAGGATCCA GGGTGATGGG GAGGCTGGGA GGTCCGCGGT 1260 GATGGACCAG GGCTGGGGCC AGGGGATGGG GAGGAAGGAG TAATTGGGAG AGGCCTGGGG 1320 CTCTGGCCGA GGAATGGATG GTGGGCTGAA ACAGGGAGAG GAGAGATGCT TAGGCCACTT 1380 TGGAACACAG TAGGGCAAGG ACAGGAGACA CCCAAGGGGA AGTGCCCAAG AGACCACGAC 1440 AGGCTGGCAT TGGACAGGGA AGGTCTGTCT GGAGCAGGTG TCTTGGATAA GGGAGGAAAA 1500 TGGTGCAGTT CCATCCTCCT CCCTCTCTGT TCAACCTCTA AACTACATGG GGCACAGGAC 1560 CCAGTGGGAC TCCATAAATG ATGGGATGGG TGGATGGAAG GAAGGAAGGA GGAAACAACT 1620 CTTCATTCAT CCTGGTTATT TACAGAACAG GCCAGGTGCG GTGCTCACGC TTGCCATTCT 1680 AGCACTTTGG GAGGCTGAGG TGGGTGGATT ACCTCAGGTC AGGAGTTCAA 1730
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