Tag | Content |
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EnhancerAtlas ID | HS047-02987 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:209989000-209990840 |
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 | chr1:209989737-209989755 | GGAAGGATGGGAGGGAAG | + | 6.13 | REL | MA0101.1 | chr1:209989034-209989044 | GGAAATCCCC | - | 6.02 | RREB1 | MA0073.1 | chr1:209990187-209990207 | TGTGTGTGTGTGTATTGGGG | - | 6.29 | ZNF263 | MA0528.1 | chr1:209989734-209989755 | GGAGGAAGGATGGGAGGGAAG | + | 6.81 | ZNF263 | MA0528.1 | chr1:209989731-209989752 | AGAGGAGGAAGGATGGGAGGG | + | 6.9 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27309 | chr1:209987826-209990934 | Esophagus | SE_34153 | chr1:209987800-209991306 | HCC1954 | SE_35823 | chr1:209987333-209991619 | HMEC | SE_64223 | chr1:209987771-209991222 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 209989834 | 209990041 | chr1 | 209989503 | 209989704 | chr1 | 209989141 | 209990065 | chr1 | 209989263 | 209989693 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I209814 | chr1 | 209987498 | 209991386 |
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Enhancer Sequence | AAGTTGTGGC TGCGTATTCT GCCCCTCTCT GTTTGGAAAT CCCCTGCACA GCTTTGCCAG 60 CTACTCAGCT TGGTTCATCA GGGGATTTTT TAAAAATTTA GTTTTTAAGA GTTTTATCCA 120 AGGTCTCAAA GCTGGTAAAT GGTGAGTAGG AAGTTGATTC TGCCCGATCT GTCTGACTCC 180 ATGCCCTTTC TATTAGGTCA TGAAGGGGAA CCTGAGGATT GGAGCTTTGG AATGTTAATC 240 TTACCCAAAG GCCTGAAGTA ATACCCCAGA ATGTGAACAT GTGTGACCAT CTGCCTGTCC 300 TGGGGGTGGG AAGAAGGCAG CATGCTCTAT CCTTGACCCT GATTGAGCCC AGGGGCTGAA 360 TCTGGAGCTT TGGGGCCTGG GAACCTCTCT ACCTGCGTCA ATGTCTGGAG GCCCTGAGAG 420 TTTCGCTCAG GCTCAGAGCA GGCATCGCAA CCTCCCAGTT ACTATTCTGT GCTGTGGCAA 480 GTGCCAGCTT GTCCTCTCTT CCCCACCCAG CCCGGGAAAC CGGCAGCATT TCTAGTTCAG 540 GCCCAGACCC GTCCTGGCAG CCTGGATTCC ACTGCCTAGG CAGGAAGCTC ATCTCAGCCC 600 AGTGACCTTT TCTCTCTGTT TTTTGTCACA GAGGAATTTC CATGCCAGCA GTATGGGGCA 660 ATGGGGGTGG GTGGCCAAAG GTTTCCCCCT TAAGCCACAA GAGCCATGGA GTGGAGGTAA 720 GCTAAGCAAA CAGAGGAGGA AGGATGGGAG GGAAGGATCA GGAAGATTTA GAGAGTCCAT 780 TCCTCAGGCT GCTTCATCCT CAAATTCCAA GGTAAATAAA GGTGTTGGGA AGGATGCACT 840 ATATGTCCAG CTGCCCAGCC CTGAAGATCC TCCCCCTAGA GAACTGAGAC AGGAGTTTTC 900 TCACATTCCC ACATGCAGGA GGGAAAGAGG CTGGGCCTGG GCAGGTCTAG AGAGTTCTGT 960 TCCCCTGCCC CAGGGGAACA CGCCTAGGCT TGCTGACCTC TCAGGTAGGA GTCTGTCAGG 1020 TTGGAAGCTG GGCCTCTCAT TGTGTGTGTG TGTGTGTGTG TGTGTGTGAG AGAGAGAGAC 1080 ACGTGTGTGT GTGTGTGTGT GTGAGAGAGA GAGACACGTG TGTGTGTGTG TGTGTGTGAG 1140 AGAGAGAGAC ACGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 1200 ATTGGGGGAG AGAAGCATAT AGGATAGGGT GGCCAGATTT AGCAAATAAA AATACAAGAT 1260 GCCCAGTTAA ATGTGAATTT CAGATAAACA ATGAATACAT GAATACACTA AACAATTATT 1320 TGTTGTTTAT CTGAAATTCA CATTTAACTG GGGATCCTTG ATTTTACTGG CAATCCCAAT 1380 AAAGGGAGTC GGGGCTTGAG GGAACTGGAC TGAGGCTGGC ACGCCCATTC CTTTGCCTCT 1440 CTGATTTCAG TGAGGTAGGG CTAATTCCCA GACATATACC CCTGCCTTGA CCTGCTCCTA 1500 ACCTTGAAGC CAGAGAATCC CTTAGACATT GGCTTTTCAG GGCATACACG GGCCCCAACC 1560 CACATAGCTA GGGCTCCTTT GACTTCAGTT CTCAAACTCC AGAGACTTTC ATGACAACTG 1620 TTAATGCTCC ATCCTGGAGC CCCTTTGAAG ATGAAAAGCT CTCCTGAGAA GTGGAGTGCT 1680 CTGTTGTTGT AATTAACATA ATTAAAAGCA ATTTGTCTCA TAGTCCCATA GGAAACTGGG 1740 GGACTTCCCT TCTTGTATGA AATCCCCACC ACACTCTCCC AGGAGATGGA CACCACTTCT 1800 AACCCAAGCC TAGCCCCAGT CCCTGTTCCC ACCCCATTCT 1840
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