Tag | Content |
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EnhancerAtlas ID | HS148-02618 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr10:100141910-100143320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr10:100141918-100141936 | CCTGTCTTCCTTCTTTCC | - | 6.95 | EWSR1-FLI1 | MA0149.1 | chr10:100141922-100141940 | TCTTCCTTCTTTCCTTCC | - | 8.23 | FOSL1 | MA0477.1 | chr10:100143206-100143217 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr10:100143206-100143217 | CATGAGTCACC | - | 6.02 | ZNF263 | MA0528.1 | chr10:100141910-100141931 | CCTCTCTCCCTGTCTTCCTTC | - | 6.11 |
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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 |
GH10I098382 | chr10 | 100142250 | 100143982 |
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Enhancer Sequence | CCTCTCTCCC TGTCTTCCTT CTTTCCTTCC AGAAAACCAG CAATATTGAC CAAAAACAAA 60 TTTTCAACAA GATCAAGAAG TTGATGGTCC TGATGCTGAA TGAGGGAGGG GGCTTGGCTA 120 CTTTCGAAAA AGCTTGGGGA TCCAAACATT GTTCTGCACT GTCCTGGTCA CAATGCTTCT 180 AGGGGGCTAG TTTCAATTCT GGGTGCCAGG TTAAAAAGTA TATAGAAAAG ATCACCTTCT 240 GCAGAATACA AAAATGACAA AAACGACAAA AACGATTTCA TCAATAAAAG CCACAGCAGC 300 AGCTCCACCA TGTACTGAAT GCTTATCATG TGCTAGATAC TGGATGGAAA CATGATCTAT 360 TGTTTGATGT GAGCTTTAAA ACAACTCTTT TACAGCTGAG AAATCTGAGT TTACCAACAT 420 TAAGTAATGA GGTGGATCTA TTTGATCCTG TATAAATTTG CCCAGGAAAT GGAGGAAGGG 480 AAGCTTTCCC AGGGAAGATC CTGCCTTATC TGCAGATGGG ACGGCTTGGA CTGTGGCCTT 540 GGCTGCTGGA ACTGGAGAAG CTGGCTGGGA GGGCTGCATT ACCACGGGAA CTCTGGATGG 600 ATTTTCCTGG ACAAGGGTGA CAATTCAACT CTCTTTAGAA TTCTAGAGGT TTATATTGAA 660 AGGTGTTGGT GATGCAACAG ACTTAGCTCA TGGGAGGCAG AAGCCTGAAT GCTCTGGAAT 720 CAGGAAGACC GGGCTCCCAG ACGGCCTCAG TGGAATCCAC TTTGCAGTCA CCCTTGGCTG 780 CTTTTTGCCT GACTGGAGGA TTCTGTGGCT TGAGATGCCC AGCATTGTTC AGGACCGTGG 840 CCTTTGAGGG TGACTCTGTG GATCATGGGG AAATTGGGTC CATTCTTATA GCTTGCCAGG 900 AATGTGACAG CGGTTGACTG GGCCCCACCT GGGCAGTCCT CCAATTGTTG GTAGTGGGGG 960 TCCCAGGCAA GGACAGGGGA TGCTTGGATC AGACTCTTCC ACTGGTTAGA TGGACTGTTT 1020 TTTGTTTTGT TTTGTTTTGA GATGGAGTCT CTGTCGCCCA GGCTGGAGTG CAGTGGCACA 1080 ATCTCGGCTC ACTGCAACCT CTACCTCCTG GGTTCAAGTG ATTCTCTTGC CTCAGCCTCC 1140 CAAGCAGCTG GGATTACAGG CGCCCGCCAC CATGCCTGTC TAATTTTTGT ACTTTTAGTA 1200 GAGATGAGGT TTCACCATGT TGGCCAGGCT GGTCTTGAAT TCCTGACCTC AAAGTGATTT 1260 GCCTGCCTGA ACTTCCCGAA GTCCTGGGAT TACAGGCATG AGTCACCATG CCTGGCCTTT 1320 AAATGGACTG CTTCTTAGCT GATGTAAGAA TTATGAGTAC CCCAGAGAAG TCTATCCCAC 1380 CAACTAACAC AGAGAAAAAA TACAAGCAAA 1410
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