Tag | Content |
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EnhancerAtlas ID | HS077-00986 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr1:203965340-203967100 |
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 | chr1:203966232-203966250 | CCTTCCCTCCCCCCTCCC | - | 6.02 | EWSR1-FLI1 | MA0149.1 | chr1:203966228-203966246 | TCTTCCTTCCCTCCCCCC | - | 6.32 | TBP | MA0108.2 | chr1:203966558-203966573 | CTATAAAAAGCCCTG | + | 6.42 | ZNF263 | MA0528.1 | chr1:203965794-203965815 | GGAGAAGGAGAAGCAGGATGG | + | 6.09 | ZNF263 | MA0528.1 | chr1:203966646-203966667 | CATTCCACCCCTTCCTCCTTT | - | 6.17 | ZNF263 | MA0528.1 | chr1:203966228-203966249 | TCTTCCTTCCCTCCCCCCTCC | - | 6.32 | ZNF263 | MA0528.1 | chr1:203966224-203966245 | CTTCTCTTCCTTCCCTCCCCC | - | 6.38 | ZNF263 | MA0528.1 | chr1:203966231-203966252 | TCCTTCCCTCCCCCCTCCCCT | - | 7.1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 203966600 | 203966906 | chr1 | 203965600 | 203966600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I203996 | chr1 | 203965194 | 203966596 |
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Enhancer Sequence | AGCCAAAAGC GCTGCTGGAT GGGGAGGGTG CAGGCGGGGC TTTTCTTGCA CCATCCTGGC 60 GCCTGACTGG GTCAAGTTAC TGGAGGCAGT CTGGATTTGA ATGTGCAAAT AAACAGAGGT 120 TGCTTTGATC CTTGAGGCTG ACAGGGAGGG GGAAGAAAAC GGAGTGCCCT GGTCAGAGAA 180 GTGCATGCTG GGCACTTGAA AGAGGGTTTG GGGGATGTGG AGCATGAGCT TGTCCTTATT 240 CCTTTGACTG GACCAAAAAC CTAATTTGTT AAAAAAAAAA AAAAATAGAG AGATCTTGAA 300 AGAGTCAGGG ACCCACATCA GACATTTCAG ACCTCCTCTG GGAACCAAAT ATTCCAATGG 360 CCTTTCTGCC TTGTCACCAG GAGGGGAGTG GGTTGCTTGA AGCCCACCCT CCCTCAAGGC 420 TCTCTTGCCT TTGGGACATC TTGGGTGCCA CTTGGGAGAA GGAGAAGCAG GATGGAACTA 480 TGAGGTGTGT GTGGTTCGGG GTGGGGCTGT AGGTTGGGAG GGGGTAGGGC CTATTGTCTC 540 CCTGGGCACC AATCCACAGC CACAGGCAGG CTTAGAGACG GAGAGACAAA GGAGGGAATG 600 GGAGAGCACA AAGGGAGCGG GAATGAAATG GTAAGTAAAG GCAAACAAAA GTGAGCCGGG 660 GGAGACAAAA GCTGGGAACA ATATTCCCCA GGCAATAGGC TCGGGAACAA TAGGGACACT 720 GACAGCCCCA CAAAGACACC AGTGTCTCCA AGTAGACGTT ATCTCAGGCA GTGGTTGGCA 780 GCCCCACTCT GGCTGCAGCT ATTTTCAGTG CCGCTTTTGT GCCATGCTGA ACAATATTCC 840 TTGCATGGCT GCTGATAGAA AGATGAGAAG GTTTCTGTTT GATTCTTCTC TTCCTTCCCT 900 CCCCCCTCCC CTTTTTCCAG CCCCCACCAG CTCCAGGCAG TCTGAGCTCA AGTCTCTGGC 960 CTGGTTAGGG GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTTG 1020 GGAAGAGACC AAGTGGGGAG GGTCTCTATC TGGGCTTCCA GTTGCCCTCA ATCTTATCAG 1080 GGCCTCCATG GAGGGAAGCT AGTAGAGTGG AGATTAGGGC TGGGCCAGTG GGGCTGAGAA 1140 CTGAGGTGTG CGAGGAGGAT CATCAGGGCA GTGGATTCTG CCCTTGCCCC AAATCACAAG 1200 ACCAGCCTGA GTGAGTGACT ATAAAAAGCC CTGCTTAGCA AAGGTTTTGC CTGTTGCTTG 1260 GCTATTCACA TACATAATAG CCAAGGCCAT AAGGGGTCCA CCCTGTCATT CCACCCCTTC 1320 CTCCTTTGTG CCCACAAGTG TTCCCCACTC TACCCCCATA GCCACTGCTT TCTCCCATTC 1380 TTGTTTGTAG TTTTACCAGC CCCTTGACTA GCTCCCAACT TCCCTCCCCA CCTCCGCCAC 1440 TGCCAGATGA ACCTAAGAGA TCGGGGAAAC TAGTCCTAGC TTGGGAAAAG ACTGGTATGC 1500 ACTGGCCCTT CCTTAGGCCT GATGGCCACT CCCACAGGGG TGTCCATGAT CTTCATCCAC 1560 AGTGCTGCTA TTCCCCACCA AGTATCTCCC CTGTGTTCCT CCCTAGAGGA ACTCTGACCC 1620 TAGAACATTG AGTCAGAGGT GTCCTTTCCC AGGGCCCCCT TGTGCATACG GCTGGTGTAC 1680 TCTTAGTTTT CTCAGTATCT TAGCCCACTA TGGCTGCCCC CGTGGGCTTA GATAAACTTT 1740 ACAGTTTTTC GTCTAGCTGG 1760
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