Tag | Content |
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EnhancerAtlas ID | HS098-44600 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:42857750-42859210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:42858519-42858537 | GCTCCCTGCCTTCCTCCC | - | 6.29 | EWSR1-FLI1 | MA0149.1 | chr5:42858523-42858541 | CCTGCCTTCCTCCCTCTC | - | 6.33 |
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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 |
GH05I042858 | chr5 | 42858150 | 42859102 |
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Enhancer Sequence | CAATTTTATC CACCTGTTGG AGGTAACTGG AAAGCAGGAA AAAATATAAG ACACATAGGA 60 CATCAGACTG TGCAGGACAA TGATACCTAA AAAAGAGAAA AAACTCAAAA ATAAAAAGAA 120 ACAGAGTATC AGTGAGCCAT GGAACAACTT CAAGCAAGCT AATTATATGT GTTACTAGAT 180 TAACCAGGGT GGGATGGGGG CAGAAAAATA TTTGAAGCAA TAATGGGTAA CACTTTTCCG 240 AATTCTAGAA ACTCAAGATC CAAGAATCTC CTCAATTGAG GGCTCATTAC TCAATAAGTA 300 CAAGAAAAAA AAATAAAAGA GAGACTATCA TTATAGTAAA AGAAATTTAA CTCAGTGGTG 360 GAAATCCATA AACTATTTCC CTTAAAAGAG GTCTGTATGT TAAATAGTTT TGTAAAACCT 420 GTTTTAAATA TATTTGCATT TCTTCTGTAA ATCAGTACTA CAATAGAAAT AGTTTGATTT 480 TGCTTTTAGC AGAACTCAAA ACTAGCTTGG ATATGTCAAT AGATCTCATT GTTCTGCCAA 540 TGTATTATTC ATCAGGGTCA CATGGTCAGG CCAGACCGAG CTTACAAGGC AGCTGGAAAC 600 TCTGCCCAAT TCAATTATCT GTTTCACCAC AGCTACAAAT CATGTACTTC CTTAATGTAT 660 GTGTTTAGGG GCTTGACTCC CATCCCATTC TCCATTTAGA GACACTCAAA GCCAAGGTAG 720 TCTATGACCT CCTGCAAACT TCCCTACCTG CCCTTGACCA GTGGCAGTGG CTCCCTGCCT 780 TCCTCCCTCT CAAGCAGGCC CAGCTAAGTT TCCACTGGCT ATTTTTAAAC TCTGAGTGGC 840 TAAATGAATT AACTCAATTT GTAGAAGAAA AGACAAGGAA GCTGTGTTTT GGCATTTAAT 900 CCACACATCT TTCTTCCATC CAGCTTTTCC ATTAAATAAA ACTGGTACTT TAAACCTCCA 960 CATTTTTTAA AAAAATTGTA CCATTTACAC AGTCATGAAA AAAAAAATCA ACTAGCCTTA 1020 AACTATCAGC ATGCTGACTT TCTGATTACT TGCTAAGAAA CCCCAAAAGA CAAACTACAG 1080 ACACGTTCTT AAAATATTTC CTCAAGAACG TGGGGCACAT TATTCTTGTC ACATCCTGAC 1140 TGCCAGGAGG AGCTACATCC CTCTCCCCAA GTGGAACTGC CAGGAATGAA AGCTAAGAAG 1200 CCCCATTGTC TGCCTGTGGA ACTCGGCACA GTCACTGCTT GGTATTCCTG GGTCCGTGAG 1260 CACAGGCTCA GCTTCCTTGT TTTTTTTAAC AACGTGCCTG TCCATGTATT GTTTGCCAAC 1320 TCTTAGGATC CCTTTCCCTT GCATCTCGGC CTGAGCACTT GTTTATTGTG CACACTAAAA 1380 AGTACGGTCT GTTGAAGAGA AACAAGGCAA TTTCTAAAAG CAAAGTCAGG CTGGAACAGT 1440 CTGTGTTCAA AACATAGAGT 1460
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