| Tag | Content |
|---|
EnhancerAtlas ID | HS044-01928 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr10:100086060-100087200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr10:100086870-100086888 | GGAAGGGGGGAAGGTATG | + | 6.44 | | EWSR1-FLI1 | MA0149.1 | chr10:100086897-100086915 | CCTCTCTTCCTTGCTTCC | - | 6.54 | | ZNF263 | MA0528.1 | chr10:100086648-100086669 | AGAGGAGGGGTGAGAGGAGTA | + | 6.45 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAGTAATTTA GCCAAGGTCA CACAGCCAGG AAGTGGCAGA GCTTGCATTT GAACCCAGAT 60
TGTCTGACTA AAGCTTGCAC TTTTAGCCTC TTCCCAGTCA CATCTTGTCT GTCTCTGTAG 120
TGCTAGTGGA AGGTTGTCCA TCTGTCTTTC AGGCATCTGC AGTCCCTAGG GTGTGATAGG 180
ACAGCGTCAA AAAACAGTTC AAGAGTGCCA AGCAATCCCA CCACCTCAAT ATATTGATTT 240
CTCCTCTGGA AAGAGACAGG AGAGAAAGAC GAGTTCTGCC TGGTGGCATA AATTAGCTCT 300
GTGCCCTTGG GGCTTTGTCT CACCGTGCTG CTGCCTTGCC ATTCAGGTGG CAGGCCTGCC 360
TGCAGCAGAG CTGTTGCTAG AGGGATTCGC GGCCGGCACA TAGCAAGTGC CGGGACAGCA 420
GCTTCCACAT TGAGCCTGGA CAAATGGCAG AACACAGCAG AGGGCAACGC AATTTACAAG 480
GAATCTTAGC AACCAGGCAA GGGGCAATAA ACCAGAAAAT CGCTGGGGAA ACTCAGCGGA 540
GCATGAGCTA AACGAATTGC AGGATTTGTG AACCAATTTA CACCCATCAG AGGAGGGGTG 600
AGAGGAGTAC CGGGTGGCTC CGAAAGCCGT GGCTGGAGAA CTGCCAGGCT GTCACCCGTG 660
TCAGACTTGT TGAAGGGCAG TGAGGACAGA GAGTCCTTGC CGAGGGACCG CTGGACAGTG 720
GTCTCTGGGG ACATTATGAG AGGACCTTCA GCTGCCCTCT CTGCAAGGGA CCTGGGGTGC 780
CTCATCCCGC TGTGGAGAGA TGGATGTCAG GGAAGGGGGG AAGGTATGGA TGGAGGGCCT 840
CTCTTCCTTG CTTCCAGGGA ACTGGTAAAA GACAGATGAA ATGTTCTTGA CCAGAAATGA 900
AGCCCACCTT TGGTTTCCAT TCCAAGGAGT AAATCTCCCG GGAAGTGAAC ACCGTTTCTC 960
ACATGAGGCA CCCCGATGGG AGGTGGGAAG AGTCTGGTGA GGATGTGGAA AACAAGCAAA 1020
GGAGTGAGCA GCACCTTCTC CTCCGGGTGA CAGTGGCACA TGTCTGTGCA GAAGCACACT 1080
CCCATCCTGG GAGAGCTTTG GGAGGGACAG ATTCAGCTGT CCGTGGACCT GTGCAGTGGG 1140
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