Tag | Content |
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EnhancerAtlas ID | HS080-32672 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr7:21519760-21521020 |
Target genes | |
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 | chr7:21520955-21520973 | GGGAGGAAGTAGGGAAGG | + | 6.56 | FOXP2 | MA0593.1 | chr7:21520265-21520276 | TTTGTTTACTT | - | 6.62 | RUNX1 | MA0002.2 | chr7:21519827-21519838 | GTCTGTGGTTT | + | 6.62 | ZNF263 | MA0528.1 | chr7:21520956-21520977 | GGAGGAAGTAGGGAAGGGGAG | + | 6.5 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH07I021480 | chr7 | 21519941 | 21520964 |
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Enhancer Sequence | TGGTACAATG TTGACAGTGT GCTTGTATTT TGTTGAGGAT TTTTGCATCC ATATTCATAA 60 GAGAGATGTC TGTGGTTTTC TTTTTGTATT GTTTTTATCT GATTTTGGTA ATGATAATAC 120 TGGCTTCATA GAATGAATTG GAAAGTATTC CCTCCAAACT GGTATTAATT CTTTAAATGT 180 TTTGTGGAAT TTACCAGTGA AGCTGTCTGT TCTTGGGCTT TTCTTATGGG TAGTTTTAAT 240 TACGAATTCA GTCTAGTTGC TTGTTGTAGG TGTATTCTGA TTGATTATTT GTTCTTGAGT 300 CAGTTTTAGT ATTTTGGTCC GTATTTTTCT AGGAATTTGT CCATCTCCTC TGAGTTACCC 360 AAGTAATTGC CGTAGAATTG TTCATGGTAT TCCTTTGTAA TCCTTTTTGT TTCTATAAGG 420 TTGGTAGTGA TATCTCCTCT TTGATTTCTG ATTCTAATAA TTTGAGTCCT ACTTTCTTGG 480 TCAGTCTAGC TAAAAGTTTG TTAGTTTTGT TTACTTTTCC CAAGAATCTC AATATTTGAC 540 ATTTTTTCTG ACCCTAAGAA GGTTCTTCAC AGCCTCTTTG CTCACTTCTT TCTGGCAAAC 600 TAGCCAACCT GTAGTTAAGC CTTTATTTCC AGTGAATCTC TTAGTCTTCT CCCAATTAAC 660 TGCCTTTTGA AACCATCTCT ACTTTTTTTG AGAGTACCCT TAGGCTTGAA CTTCTTCACA 720 TTGTCTTGCA AATGAAGTCA ATTCCTTTGG GAAGAGATTT GGAGCTCTTT GTTTTATGGT 780 GTGTTTCTGA CTTATGGCTT TTGAACCGGG GGTTGAGACA GTGGCTTTCT TTCTGAGTTA 840 CAACCCTGCT TTAAGAGCTG AGTGCCTGGT TGCTGGGGCA GCAATAGCCT CAGGTCTTCT 900 CAACTGGCCT CTCCTGGCTT AGAACTTTGA CTTTATGAAC TATGAATGGG CCAGGTCAAG 960 GGCAACCTGG ACCCCAGTAT TTTCATCATG CCACATCCAA GGTAGAGTCT ATGTCCCAGG 1020 GCTAAGGACT TGGTTCTGCT ACACTTGCCT GGAACTTAGC AACAGGCAAC CAGGGGTAAG 1080 ATAAGAAATG CAGACATCTT GCCCCTCCTG GGGCCATACT CCTCTGACCG GGAGGTGGGA 1140 AGAGTAGGAA TCATATTCTT AGCTGCACCA GTCTCTAATG TTCCTGTGTG GAAACGGGAG 1200 GAAGTAGGGA AGGGGAGAGT CTTGGTTCAA ATACCACAGA CTCTTACTGT TCTTACCAAT 1260
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