Tag | Content |
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EnhancerAtlas ID | HS095-18393 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr20:25117030-25118200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr20:25117514-25117525 | CATGAGTCACC | - | 6.62 | FOSL2 | MA0478.1 | chr20:25117515-25117526 | ATGAGTCACCC | - | 6.14 | JUNB | MA0490.1 | chr20:25117515-25117526 | ATGAGTCACCC | - | 6.32 | JUND | MA0491.1 | chr20:25117514-25117525 | CATGAGTCACC | - | 6.02 | NFE2L1 | MA0089.2 | chr20:25117997-25118012 | CATGCTGAGTCACAT | - | 6.03 | ZNF263 | MA0528.1 | chr20:25117137-25117158 | CTCCCTCCCCCTCCCTCCTTT | - | 7.06 | ZNF263 | MA0528.1 | chr20:25117133-25117154 | CTCTCTCCCTCCCCCTCCCTC | - | 7.53 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 25117918 | 25118069 | chr20 | 25117283 | 25117752 |
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| Number: 2 | ID | Chromosome | Start | End |
GH20I025136 | chr20 | 25116932 | 25117871 | GH20I025137 | chr20 | 25117881 | 25118030 |
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Enhancer Sequence | TGTGCCCTCT TGAATGGATT AATTCTGTTA TCATGAGAAT GGGTTTGTTA TCTCAGTAGT 60 GGATTCATTA TAAAAGAACA AGTTTGATCC TCCCTCTCTC TGTCTCTCTC CCTCCCCCTC 120 CCTCCTTTTG CCCTTCCACC ATGGGATGAT GCAGCAAGAA GGCCCTTGAC AGATGCTGGG 180 ACCCTAATCT TGGACTTCCC AGCCTCCAGA ACCATGAGCC AATAAATTTC TGTTCATTAT 240 AAATTGCCCA GTCTATGGAA TTCTGTTATA GCAGCACAAA GCAGACTAAC AGGGCTGCAG 300 TCAGATGTCA GCCTGGGCTG CATCATTTGA AGGCTCTGCT GTGGCCAGGG GATCCACTGC 360 CAAGGCAGCC CTCACTGGCT GCCGAGCTGG TGCTGGCTGC TGGCAGGAGG CCTTAGCATC 420 TCTCTGTGTG GGCCTCCCCA GGGCTGCTTG GGCGTCCTTT TGGCATGTGG CTGGCTTCCC 480 CCAGCATGAG TCACCCAAGA GAGCAAGGCG GGAGCTGTAG TGCCTTTTCT GACCCATCAA 540 CATTCTGCTG GACACAGAGG CCAGCCCTGA TTGAATGTGG AAAGGACTGC ATGAGAGTGT 600 GGCTCGAGGA GGCCAGAACC ATTGGCAGCC ACCTGGGAGA CTTGGCGATC ACAGAGAGAG 660 GGAGACAAGA CATTGTATGG AAACTGTGAG TGGCTGTGTC AAGCTCATAA TATTCCATAA 720 ACATGGGTGG GGAAGATAAG GATGAATGAT TAGCAAGGAA AGGAGAAAAA ATAAAAAGCA 780 AACCTTGTGC TTCCACTGGA CAGTGGTACC TGAAACTTTT TCTTTTCTCA CCTTCCTTGT 840 TATTTTAAAT GATTTTAAAT AATATCAGTA ATGCATGCAT GTATCTTCAC AATAAGAATG 900 TCCAACAAAG CTCTCCTTAA CCAAACCACC TTGAATGCCA CCCCTCCCCA GAGGTCATCA 960 CTGTAATCAT GCTGAGTCAC ATCCCAGGAC TTGCCTTCAC AGCTTTCCTT GTATATTGCA 1020 GTGTTTGTGT GTGTGTGTGT GTAGGAAATG AATTTCATTT CATGAAAAAT GTAATTCCAT 1080 TTTGTATTTT TTTACATAAA TTGTATCATA TCATATCATT GCTCTTAGAA TTTTTTCCAC 1140 TTAATTGATA CGTCTTGGAC ATCATTGTGT 1170
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