Tag | Content |
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EnhancerAtlas ID | HS055-02592 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr14:71247420-71249930 |
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 | chr14:71249642-71249660 | CCTTCCTTCCCTGCTACC | - | 6.77 | EWSR1-FLI1 | MA0149.1 | chr14:71249638-71249656 | CTTTCCTTCCTTCCCTGC | - | 7.24 | Foxa2 | MA0047.2 | chr14:71248901-71248913 | TGTTTACATAGC | + | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_36405 | chr14:71247656-71254025 | HMEC |
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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: 2 | ID | Chromosome | Start | End |
GH14I070780 | chr14 | 71247318 | 71247844 | GH14I070781 | chr14 | 71247857 | 71250079 |
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Enhancer Sequence | GCCACTTTCC TTACTAAAGA ACATCTCCTT AAACACCTGC CTCCCCTGAA TTTTCTCATC 60 GTATCAGCTC AAACTGACTG AGAAGAGCTG CCAGATCTCC GTCATACCTC TGAAGTACCC 120 AGCTACATAC CAGATAAAAA TAACCAAAAA AGAGGAAGCC TATCAGATGC TCGATGGTTT 180 TGTCAACAGA AAGCAGTTCT TTCTTGGCAG GTGGCCATGG GGTGCAGCCG CCGCACAGGC 240 TCTCCAGGGC CTTGTATCCC CAAGCTCTGC TAGCAGAGTT CCCTTAGCAG GCATGGAAGG 300 TTGCATTTTC AAAGTGGTCC ATCATCTCCC ATCCTCTGTG CTTTTCCCCA GTGTGATCTT 360 GACACTTTTC CCACTGAGAG GTGGGTCTGT GTCCTCTCCA CTTGAAGCTG AGTGGTCTTG 420 AGACTCACTT TAACAGAATG CAGAAGAAAT GACAATGCCC GACTTCTAAG CTAGATCAGA 480 AAAGATGCTA CAGCTTCCCC ATGTTCACTG GAACACTTGG GTCTGCAGCC TTGAGCCACT 540 ATGTAAGGCC AAGAGCCCTA AGAGAGCCAT GCTCATGGAC AGACTGCACA TGGGCACTCC 600 CATCAGCAGT CCTGGCCTCC AGCTTCTCCC AGCTCAGGCA CTGAGCCATG TGTGTGAACA 660 ACCTTCAGAT GGTTCCTGCC TCCATCTGCA GCCTCCCCTA GCCTTCAAGT CTTCCCAGGT 720 GAGGCCCCAG ACATTGACAA GCCATCCCTA ATGAGCTCTT TCCAAATTCC TGACCCAAGT 780 CTCCATGAGC TTAATAAAAT GTTCTTGTTT GGGGTCGTTT GTTCTGAAGA AATAGTAATG 840 GAAACAGTAG GTGATACACT GTGAGTCTAG TCTCATATCT GCTGCTGCTC TTGAATTTTT 900 TAAAAAGGAA AAACTACCTT TTACTGAGCA TTTACTTTGT GCCAGGCATT ATGCTAAGGG 960 TTTACACACA TAACTTCATT TAATCCTCAT TATAATGCCA TGAGTAAATA CTAGAATTAT 1020 CCCCATTTTA CAGAGGAGGA AATGGGCTCA GGGTCGAGGA CTTTGCCCAA AGCCAGGTCT 1080 GCCTGATTCA GAGCCCACAA CTGTACCAGC CCACAACTGT ACCAGCCCAG GTTCTCTGGC 1140 CACTTAGAAA GAGGAGCTGT TTCACATGGA AGACTCAACT TCTTGGGAGC ATGGCTTTCC 1200 TAGTCAACAT TCCAGGTCTG GGAATTGCCT AAAGAACCCA GGTGATGGGA CATGGCATCA 1260 GTGAACACTT GGCTCTGTCT GAGCTGGGGC AGGCCGCCTT CCCTGGGAGG TCATAGCTAT 1320 GGCCTACCTG CCCTATTACC AACTCTTGAA TCCTACCCCT TCTTTGAGGC CTAATTGTTC 1380 CATCAAGGCC TCCCAGGGAA TTCTGCCTTC TCCAGACCCC ATCTCATGTA TCTTGACACG 1440 CTGCCCCCTA CTACATCACA CTGTTCTGGT TGTTTAGGAT GTGTTTACAT AGCACAACTC 1500 CTAAGGATGG AAAGAATGCA GTGGAAGTGA CCTCTATGTT ATGTATATAA TAAATTGACC 1560 GTATTTCTTA CAGCATGTAT GCAATAGCAG GCACGTCAAT TTCTTATGAG GACATTTGGG 1620 TAATAAAATT ACCCACATCG GTTGAGAATC ATGATCTATA CAAAAAGAAA ACATTCCAGG 1680 CTCTGTGACC TGCACTTCAC CCCAGGCATT GCAGAGGAGA AAGGATTTGA GGGCAGAGGA 1740 GGAAGCGGTA CAAGCCACCA CAGATACCAC CTTCATCCCA TCACCTTGCA GGCAAGGAAG 1800 TCCCAACCAC AAAGGCTCGA AACACTGGGA GTTGCCATTG TGAACCACAA GTCCTTAATA 1860 GCCCTGGAAA GCTATGAAAC ACCAATTAAA GTTTCCTATG AATCACTTTT CAACCTCTCC 1920 ATGTAAGAGC AGGGAGGAAC CAACCTCAAG TACCTCCTCA GGCCAAGACT AGCTTTGCTC 1980 TGACTCACTG TCTTTCAGTC TATGATATGG ATGCTTTTCT AATTCCTTCC TCCCACCTCC 2040 ATGTCCATTG CATGGGGAAG ATGAGACTTC CTAGCATCTT CCTAGTCTAC CTCTGAATAT 2100 TACTCTACAA ATCCTGTTCC CCATGAGACA GAGTTGAGGA TCTCACCATG GTAGGGAAAA 2160 TTCAAAACTA TACAAATTCT CTAGATGTTA CACCTCAGTT TCCAGGTGAA AGCCAGTCCT 2220 TTCCTTCCTT CCCTGCTACC TGGAAGGTGG GCATAACAGG CATACCCAGA AACTGCTGGG 2280 AAAACGCTCA AATGCCGTGT TCTCTGCCTT CAGTGAATGC CCATGTAAGG AAAAGTCTTA 2340 GAATATCTTA TTTTTCCTCA GTGGGGTCAC TTTTACTCTT CCTGGAAGGT CATTATCCCA 2400 GTCTCTCCAC CAATATACTA CACATCAAAT CAAGCATCAA AATGCTTGTA AGAAACCTAA 2460 AATTGGCCAG ATTCATGGTC CATGCAACTA GAGTCAAGCA TATAAAGCCA 2510
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