Tag | Content |
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EnhancerAtlas ID | HS177-01780 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr1:204606330-204607560 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr1:204606903-204606914 | CCACACCCTGC | + | 6.62 | LMX1B | MA0703.2 | chr1:204606996-204607007 | AATTTAATTAA | + | 6.32 | NFYA | MA0060.3 | chr1:204606426-204606437 | AACCAATCAGA | + | 6.62 | RREB1 | MA0073.1 | chr1:204607225-204607245 | CACCCACCCACCCCCCGCCC | + | 7.01 | RREB1 | MA0073.1 | chr1:204606808-204606828 | TGTGTGTGTGTGTTTGGGGG | - | 7.55 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 204606879 | 204606993 | chr1 | 204606530 | 204607469 | chr1 | 204606613 | 204606768 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I204637 | chr1 | 204606312 | 204608312 |
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Enhancer Sequence | CTGAGAACTA TTACTTCTGA AGGAAAAATC CATAAAGCAA ATGAGCTTCT TTCCTCTGCC 60 GTCCACATGT GAAAGAACAT CCCTACTTTC TCATCAAACC AATCAGATCT AGCCCAATGC 120 TTTCTAGCCC AATGCTTCCC AGCCCTTCTC AAGCCAGGGC ACATATAGAT GAGTGTATTT 180 GTACAGTGCA CCAGGGGAGA GGGTGGTGGC TGCTGGCAGC CAGAGGGAGC GGCTCAGGGA 240 GACGCTTGGT TGCCCCAGGC CCCACAGGGC TGCCCTGAGT GCCAAGGGCT GTGCCTGGAG 300 TCCACTGTCC ACAGCCAGAC CAGCTGACCA GCTCTGCTCT GTGCAGATGC CCCTGAGTCT 360 CCCAGTTCTA AACCACAGCT CAGCATTCTT AGCAAGGATT AAATCCTTTC CCAGACCAGA 420 GTCTGCCTAT TGCAGCACGT GACGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 480 TGTGTGTGTG TTTGGGGGCA GTCGCTGAGA GGGTGGTAGA GAGGACTCCT CTGCGGGAAG 540 GCCCCGACCC CCGGGCCTCA TCTGTATGCT CCTCCACACC CTGCTCACCC TGTGGGGGAG 600 TGCCATGGCA ACACCGTGCT CTTTAAACAC AGGAGTTTGT GCTCCCATCG CAAAGCAGCA 660 TTAGGCAATT TAATTAAGGA GCTGGCAGCA GACAAACTTT GTGAGTTAAA GGCATTTTAT 720 TAAATCCCAT TGTATTATGC AGCTCAATTC CCCCAGGAGC TGCGGAGCTG GGGGAGGACA 780 GAGGAGAATG TACTAGGGTT TTCTTTTCCT TTCCTTGCTT TTCTTCTGGT CTCCCTCCCG 840 CCTCGTGAAA GCATTCACTG AGCGTAGGGG GACCCCAACA GTGATTGCCT GCTCTCACCC 900 ACCCACCCCC CGCCCCGAAC ATCAGGCCTT GGCATGAGGC CTGCAGGCAG AGGCCTGGGG 960 AATATAATCA CCAGCACTGA TCTCACGCAC TACTGTTCGC AGAGCCAGAG CGCTGTCATG 1020 GTGATCTGGG GCCAGGCCTC CGACCTGCTT TAGTGTTCAC AACAGGACTC GGCTCTGTGA 1080 TTTTGTGCAC CATTTCATTG AATCCCCCCG CACCGTTGGA GTCAGAACTA CTGGCACCCT 1140 TATTTTACAG GCAAGGAAAC TGAGGCTTAC AGATGTGAAG TAACTTGCCC AAGGTCTTCC 1200 TTTTTTTTTT TTTTTTTTTT TTTTTTTGAG 1230
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