Tag | Content |
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EnhancerAtlas ID | HS147-03376 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:159859080-159860260 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:159859911-159859922 | AGTGACTCATC | + | 6.02 | JUN(var.2) | MA0489.1 | chr1:159859907-159859921 | AGGAAGTGACTCAT | + | 7.12 | JUND | MA0491.1 | chr1:159859911-159859922 | AGTGACTCATC | + | 6.32 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_09609 | chr1:159858814-159861449 | CD14 | SE_10984 | chr1:159858996-159860585 | CD20 | SE_13325 | chr1:159859276-159860543 | CD34_Primary_RO01536 | SE_27216 | chr1:159859144-159860561 | Esophagus | SE_34829 | chr1:159857787-159861747 | HeLa | SE_42315 | chr1:159858956-159860649 | Lung | SE_53483 | chr1:159859123-159860615 | Spleen |
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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: 1 | ID | Chromosome | Start | End |
GH01I159888 | chr1 | 159858757 | 159861789 |
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Enhancer Sequence | AAGAAAGCTG CTTCTGGGTG AGGCAGGTAC ATGCCAATTT GACAGGTACA TGCCAATAAG 60 ACACAGACAT CTGAGACAGG AAGTGAAACC TCATCTAATA AAACTAATGT GTGTGTGTTG 120 GGGGAGGGTG GTCCAGGAGA TGGACAGAAT GAGTGAGTAG ATTTGCAGCT TAGCCAAGAT 180 CTTGTGTTTC ACAAAGCAAC GTGGCCCTAA ACAGCCTAGG ATCTGGAGTG ACCAGCAGTG 240 ATCCGAATCT AAGACAGCAG TTTATACTGC TTTCAGCATC CCTGAAAAAT AACCAGCCAC 300 TTGTCCTCCA ACGTGTTTTC AGGACTAGAT GGCTCCAAGA AGGAACCCTT CCTCCCTTCC 360 TCTGGCTCCA GGAGTGGCTG CAGGGCTCTA GCCACATCTG GCCACTTGAT GCCACGGCTG 420 ACCAGACATG CTCAGTAAGG GGCCGCAGTC CGACACAGCT CCCGGGGTGT GTGCTAGATG 480 TGCCTCTCCA GCTTGTGACA CAGGTAGGAT TTTCTGGGAA TTAGGGCTTT TAGTGGGTGG 540 AGCCAGGGCA GGGAGAACGG TTGTAGAGGG TGAAGCACTA ACACAAGAGT TAAACCACTG 600 AGCACAGTGT TGGCTCATGG CACATGGTTG AGCTAGGCCT AAGTCCCACA GGATGGGCTC 660 AAGCCTGGGG GCAGCTCTAG TCAGGAAGTG GGGTTGAGCT AATCCCAAAG GAACCCAGGG 720 AGCCCCTGTG AATTTCTTCC TATGGCCTTA GAGTCTGGGA GGAAGCCAGG GGGCTAATTA 780 GGCATCTGGT CAGTTTCCCT TTGCTTCAGA TTCTTAATGC AGCCGAAAGG AAGTGACTCA 840 TCTGGATCAC TTCCCTTTAG GGAGGGTACT AATGGGGACT TAGAGAGGAC TCACTAAGCA 900 CCTCCTCTCT ACCAGTCCCT TAGCTCACAC AGCCAGCTAG AAGTAAGGAA GGACAATGAA 960 GCTGAGAATA AAGGACAGTG GCAATAATAG ATACAACAAT GGGAGAAACA AGAGAGGCCA 1020 GGATGGAGAA GAAAGAAAGA ACTATCAAAC AAAAAGGGGA AAACGAATAG GAAAGAAGTG 1080 GGGATTGGAC TGACAGAATG AAACCAGGTG GGTTTACCCA TCTCCCTACA AAGATCCTTA 1140 GCAAAAGGAT GAGGACTGGA CATAGAAGGG CAGGGGACGG 1180
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