Tag | Content |
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EnhancerAtlas ID | HS039-00693 |
Organism | Homo sapiens |
Tissue/cell | ESC_NPC |
Coordinate | chr1:204606240-204607560 |
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 | AAAATTCCCT TTACTGTGCG GTATGTTGGA ATTTTTCATA ATAAAGTATT GGGGGGAAAA 60 TCCCCAAATG GTTTGAATGT GAAGCCAGGA CTGAGAACTA TTACTTCTGA AGGAAAAATC 120 CATAAAGCAA ATGAGCTTCT TTCCTCTGCC GTCCACATGT GAAAGAACAT CCCTACTTTC 180 TCATCAAACC AATCAGATCT AGCCCAATGC TTTCTAGCCC AATGCTTCCC AGCCCTTCTC 240 AAGCCAGGGC ACATATAGAT GAGTGTATTT GTACAGTGCA CCAGGGGAGA GGGTGGTGGC 300 TGCTGGCAGC CAGAGGGAGC GGCTCAGGGA GACGCTTGGT TGCCCCAGGC CCCACAGGGC 360 TGCCCTGAGT GCCAAGGGCT GTGCCTGGAG TCCACTGTCC ACAGCCAGAC CAGCTGACCA 420 GCTCTGCTCT GTGCAGATGC CCCTGAGTCT CCCAGTTCTA AACCACAGCT CAGCATTCTT 480 AGCAAGGATT AAATCCTTTC CCAGACCAGA GTCTGCCTAT TGCAGCACGT GACGTGTGTG 540 TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TTTGGGGGCA GTCGCTGAGA 600 GGGTGGTAGA GAGGACTCCT CTGCGGGAAG GCCCCGACCC CCGGGCCTCA TCTGTATGCT 660 CCTCCACACC CTGCTCACCC TGTGGGGGAG TGCCATGGCA ACACCGTGCT CTTTAAACAC 720 AGGAGTTTGT GCTCCCATCG CAAAGCAGCA TTAGGCAATT TAATTAAGGA GCTGGCAGCA 780 GACAAACTTT GTGAGTTAAA GGCATTTTAT TAAATCCCAT TGTATTATGC AGCTCAATTC 840 CCCCAGGAGC TGCGGAGCTG GGGGAGGACA GAGGAGAATG TACTAGGGTT TTCTTTTCCT 900 TTCCTTGCTT TTCTTCTGGT CTCCCTCCCG CCTCGTGAAA GCATTCACTG AGCGTAGGGG 960 GACCCCAACA GTGATTGCCT GCTCTCACCC ACCCACCCCC CGCCCCGAAC ATCAGGCCTT 1020 GGCATGAGGC CTGCAGGCAG AGGCCTGGGG AATATAATCA CCAGCACTGA TCTCACGCAC 1080 TACTGTTCGC AGAGCCAGAG CGCTGTCATG GTGATCTGGG GCCAGGCCTC CGACCTGCTT 1140 TAGTGTTCAC AACAGGACTC GGCTCTGTGA TTTTGTGCAC CATTTCATTG AATCCCCCCG 1200 CACCGTTGGA GTCAGAACTA CTGGCACCCT TATTTTACAG GCAAGGAAAC TGAGGCTTAC 1260 AGATGTGAAG TAACTTGCCC AAGGTCTTCC TTTTTTTTTT TTTTTTTTTT TTTTTTTGAG 1320
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