Tag | Content |
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EnhancerAtlas ID | HS176-02516 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:156895800-156896990 |
Target genes | Number: 24 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:156896349-156896369 | CTCCACCCCACCCCCCACCT | + | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 156896077 | 156896303 | chr1 | 156895882 | 156896378 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I156926 | chr1 | 156895977 | 156896091 | GH01I156927 | chr1 | 156896900 | 156898011 |
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Enhancer Sequence | CAGGCTGAAA GGTTGAACAA AATAAGAAAT CATGGGAGCA AATTTTTACA TAGCGTCATT 60 TCTAGCCATT AGTTCAGTTT TTGCTGTGAC TTAGAAAAGG ACCTCCATTC TTACAGCACT 120 GTTAGAGAAG CAACTGCCAT GTGGAGGCTC ATGTTGTAGT TATCTCTTGC TGTGTGACAA 180 ATTAACCCCA AGATTCAGTG GCTTAAAAGG ACATACATTT ATGATCTCAT AGCTGCTGTG 240 AGATGACCTG GGGGTGGGCT AGCTGAGTGC TCTGGCTCAG GGTTTGAGGT TGCGGTACAG 300 CTGCTGACTG TGGCTGCACT TACCTCAAGG ATCAACTGTG GTGGAGAATC TGCCTCCAGG 360 CTCACTTATG TGGCTGCCTG GGCCTCTCCA CAGGCTGCCT GAGTGTCCTT ACCACATGGC 420 AGCTGGCCAG CTGAGAGAGT GCCAGAGAGC ACTCAAGACG GAAGCCACCG CCTTTGTAGC 480 CTAAACCTGG AGGTGCTGTC CCATCTCTTC TGCCATGTTC TGTTCATTAG AAGTGAGTCA 540 CTTATTTCCC TCCACCCCAC CCCCCACCTC TTCTTTTTTT TTTGGAGACA GAGTCTTGCT 600 ATGTCGCCCA GACTAGAGTG CAGTGGCACA ATCTTGGCTC ACTGCAACCT CCGCCTCCTG 660 GATTCAAGTG ATTCTTCTGC CTCAGCCTCC CAAGTAGCTG GGATTACAGG TGCACGCCAC 720 CATGTCCCGC TAATTTTTTG TATTTTTAGT AAAGACGGGG TTTCACCCTG TTGCCCAGGC 780 TGGTCTCGAA CTCCTGAGCT CAGGCAATCT GCCCGCCTTG GCCTCAAAAA GTGCTGGGAT 840 TACAGGCGTG AGCCACTGTG CCTGGCCAGA AGTGAGTCAC TTCTAATGTG AAGTCCACAC 900 TCAAGGGGAA GGAATGACAC AGGGGCATGA GTTCCAGGAG GTGGGGACCA CTGAAGGCCA 960 TCTTAGGGGC TACCCTACCA TGGGTCACCA ACTTTGGGGA GCAGTCCCTT CACAATGGGC 1020 ACATCTGTGA ATTTTTAGTC TGGGGAATTG TCACATATAT TTCCTATATT GGGGGGGCAA 1080 TCCTTTGACT CTACTTCCTA GCTGCTTCCC AGAGACGCAC ACTTCCTCTC TGTTCCCTTC 1140 CCTTACCTGG CCTCAGTGGT ACCTTCTGGT TCTCAGATCT CCCCTGCCCT 1190
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