Tag | Content |
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EnhancerAtlas ID | HS095-18108 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr20:4565230-4566680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr20:4566579-4566597 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:4566583-4566601 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:4566587-4566605 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:4566591-4566609 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:4566595-4566613 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:4566599-4566617 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:4566603-4566621 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:4566611-4566629 | GGAAGGAAGGAGAGAGAG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr20:4566607-4566625 | GGAAGGAAGGAAGGAGAG | + | 8.99 | EWSR1-FLI1 | MA0149.1 | chr20:4566575-4566593 | AGAAGGAAGGAAGGAAGG | + | 9.09 | TEAD1 | MA0090.2 | chr20:4566248-4566258 | CACATTCCAT | + | 6.02 | ZNF263 | MA0528.1 | chr20:4566608-4566629 | GAAGGAAGGAAGGAGAGAGAG | + | 6.04 | ZNF263 | MA0528.1 | chr20:4566612-4566633 | GAAGGAAGGAGAGAGAGAAAA | + | 6.39 | ZNF263 | MA0528.1 | chr20:4566604-4566625 | GAAGGAAGGAAGGAAGGAGAG | + | 6.76 | ZNF263 | MA0528.1 | chr20:4566573-4566594 | GGAGAAGGAAGGAAGGAAGGA | + | 6.93 | ZNF263 | MA0528.1 | chr20:4566576-4566597 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr20:4566580-4566601 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr20:4566584-4566605 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr20:4566588-4566609 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr20:4566592-4566613 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr20:4566596-4566617 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr20:4566600-4566621 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 |
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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 |
GH20I004584 | chr20 | 4565089 | 4566346 |
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Enhancer Sequence | TTAATAGCCC CAGGCATGAC CCTCAACAAG AGAGGGGCAG AGATGATAAA TACTCCAGGT 60 TCCTCATCTC TCAGGTGGGC ACCACCAAGT TCCCAGCATG ACTGAGCCTC AGCTGCCCAC 120 TAATCTGCTC CTTAGTCATC CTGTAGGGCT GCCTTCCCTT CCCTGTCTCA CTTCCCCACT 180 CCCCCACCAG AAACTTCTAA GATCATCTCC CAAATAAACT ACTTATACTC AGATTCTTAT 240 CTCAGGGTTT GCTTATAGGA GATCCCAACC TAAGATAAGT CCTTGACCAG GTGGCAGTGG 300 GGCTACAGAG AAGCCTCCAA TGTAAGACAT ATCAGAGGTT GGTGATGTTT CTTATGGGAA 360 GCCATGAGAC AGCTGGGACT ATGGTTTCTT GTACTTTCAA CCAGCGAAGG GGCCACCCAA 420 GATCCACAAG AGATCTAGGT TGATGGACAC TCAAGGAAAA TGAGCCTGGT TTGTTACCAA 480 GACACCCTAG TCCCAAATTC CATTGTGGAG TCCCCAGCCC TTGTAAATTA GGCTAGATCA 540 TAGCAGCCAC AGGAACTCAT CTTGTTTCTT TACTCAAACA CACACACTAA AGGCATAGTG 600 GTTGTTGTAG TAGTTATTTA GTTCTGAGTA ACATATTACT GCAAACTTAG TGGCTTAAAA 660 CAACAGTAAG CTTTATTATT TTCACAGTTT CTGTGACTCA GAATTCTGAA GCAACTTAGA 720 TGGGTGGTTC TGTCTCAGGG TATTTTATGA GGTTACATCA GATTTCAGCT GGGGCTGACT 780 CATCTGAAGG CTCAACTGGA GGGTCCATTT CCAAGGTGGC TCACTCACTG GATGGCAAGT 840 TGGTGCTGAC TCTTGCTGGA GAGCCTCAGC CCCTCTCTAT GTGGACTCCT CCCAGGGATA 900 CTTGAGTGCC CTTACGACAT GGCAGCTGGC TTACCTCCGA ATGAGTGATG AGAGAGAGCT 960 AGGTTGAAAC TATCCTTTTG ATGACCTAGC CACAGGAGTC ACATAGCAGC ATTTCCATCA 1020 CATTCCATAG TTAGAGGCCA GTCACTAAAA CAAGCTCACT TTCAAGGGAA AGATAATTAG 1080 TTTACGCCTT TTGAAGGGAA GATTGTCAAA GAATTTGGGG GCATACTTTA AGATCACCAC 1140 AGTTGCCTAA TTGATCCATT TCCCTAGATT CTCACCCTAA TCTTGAACGT GATGATCTTT 1200 CCAATCCTAT GACAAGAAAG AAGCTGGAAG CCGAGGCAGG GGGATTGCTC GAGCCTGGGA 1260 GCTCGAGGCT GCAGTGAACT ATGATGGCAT GACTGCACTC CAGCCTGGGT GACAGAGCAA 1320 GATCCCATGT TAAAAGAAGA AGTGGAGAAG GAAGGAAGGA AGGAAGGAAG GAAGGAAGGA 1380 AGGAAGGAAG GAGAGAGAGA AAAGAAAAGA GAAAAAAGAA GAGAAGAGAA GGAAGCTGGC 1440 TGGAAAAGAT 1450
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