Tag | Content |
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EnhancerAtlas ID | HS176-23813 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr20:25117020-25118280 |
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 | CTGTGAGGGC TGTGCCCTCT TGAATGGATT AATTCTGTTA TCATGAGAAT GGGTTTGTTA 60 TCTCAGTAGT GGATTCATTA TAAAAGAACA AGTTTGATCC TCCCTCTCTC TGTCTCTCTC 120 CCTCCCCCTC CCTCCTTTTG CCCTTCCACC ATGGGATGAT GCAGCAAGAA GGCCCTTGAC 180 AGATGCTGGG ACCCTAATCT TGGACTTCCC AGCCTCCAGA ACCATGAGCC AATAAATTTC 240 TGTTCATTAT AAATTGCCCA GTCTATGGAA TTCTGTTATA GCAGCACAAA GCAGACTAAC 300 AGGGCTGCAG TCAGATGTCA GCCTGGGCTG CATCATTTGA AGGCTCTGCT GTGGCCAGGG 360 GATCCACTGC CAAGGCAGCC CTCACTGGCT GCCGAGCTGG TGCTGGCTGC TGGCAGGAGG 420 CCTTAGCATC TCTCTGTGTG GGCCTCCCCA GGGCTGCTTG GGCGTCCTTT TGGCATGTGG 480 CTGGCTTCCC CCAGCATGAG TCACCCAAGA GAGCAAGGCG GGAGCTGTAG TGCCTTTTCT 540 GACCCATCAA CATTCTGCTG GACACAGAGG CCAGCCCTGA TTGAATGTGG AAAGGACTGC 600 ATGAGAGTGT GGCTCGAGGA GGCCAGAACC ATTGGCAGCC ACCTGGGAGA CTTGGCGATC 660 ACAGAGAGAG GGAGACAAGA CATTGTATGG AAACTGTGAG TGGCTGTGTC AAGCTCATAA 720 TATTCCATAA ACATGGGTGG GGAAGATAAG GATGAATGAT TAGCAAGGAA AGGAGAAAAA 780 ATAAAAAGCA AACCTTGTGC TTCCACTGGA CAGTGGTACC TGAAACTTTT TCTTTTCTCA 840 CCTTCCTTGT TATTTTAAAT GATTTTAAAT AATATCAGTA ATGCATGCAT GTATCTTCAC 900 AATAAGAATG TCCAACAAAG CTCTCCTTAA CCAAACCACC TTGAATGCCA CCCCTCCCCA 960 GAGGTCATCA CTGTAATCAT GCTGAGTCAC ATCCCAGGAC TTGCCTTCAC AGCTTTCCTT 1020 GTATATTGCA GTGTTTGTGT GTGTGTGTGT GTAGGAAATG AATTTCATTT CATGAAAAAT 1080 GTAATTCCAT TTTGTATTTT TTTACATAAA TTGTATCATA TCATATCATT GCTCTTAGAA 1140 TTTTTTCCAC TTAATTGATA CGTCTTGGAC ATCATTGTGT GCAGATACGT AAGTCGATCT 1200 CATTCTTTTT GACCACTGCA TGGCATTCCA CAGTGTGGCT GCACCATGAT CGTAACCATT 1260
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