Tag | Content |
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EnhancerAtlas ID | HS042-03533 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:204606340-204607530 |
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 | TTACTTCTGA AGGAAAAATC CATAAAGCAA ATGAGCTTCT TTCCTCTGCC GTCCACATGT 60 GAAAGAACAT CCCTACTTTC TCATCAAACC AATCAGATCT AGCCCAATGC TTTCTAGCCC 120 AATGCTTCCC AGCCCTTCTC AAGCCAGGGC ACATATAGAT GAGTGTATTT GTACAGTGCA 180 CCAGGGGAGA GGGTGGTGGC TGCTGGCAGC CAGAGGGAGC GGCTCAGGGA GACGCTTGGT 240 TGCCCCAGGC CCCACAGGGC TGCCCTGAGT GCCAAGGGCT GTGCCTGGAG TCCACTGTCC 300 ACAGCCAGAC CAGCTGACCA GCTCTGCTCT GTGCAGATGC CCCTGAGTCT CCCAGTTCTA 360 AACCACAGCT CAGCATTCTT AGCAAGGATT AAATCCTTTC CCAGACCAGA GTCTGCCTAT 420 TGCAGCACGT GACGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 480 TTTGGGGGCA GTCGCTGAGA GGGTGGTAGA GAGGACTCCT CTGCGGGAAG GCCCCGACCC 540 CCGGGCCTCA TCTGTATGCT CCTCCACACC CTGCTCACCC TGTGGGGGAG TGCCATGGCA 600 ACACCGTGCT CTTTAAACAC AGGAGTTTGT GCTCCCATCG CAAAGCAGCA TTAGGCAATT 660 TAATTAAGGA GCTGGCAGCA GACAAACTTT GTGAGTTAAA GGCATTTTAT TAAATCCCAT 720 TGTATTATGC AGCTCAATTC CCCCAGGAGC TGCGGAGCTG GGGGAGGACA GAGGAGAATG 780 TACTAGGGTT TTCTTTTCCT TTCCTTGCTT TTCTTCTGGT CTCCCTCCCG CCTCGTGAAA 840 GCATTCACTG AGCGTAGGGG GACCCCAACA GTGATTGCCT GCTCTCACCC ACCCACCCCC 900 CGCCCCGAAC ATCAGGCCTT GGCATGAGGC CTGCAGGCAG AGGCCTGGGG AATATAATCA 960 CCAGCACTGA TCTCACGCAC TACTGTTCGC AGAGCCAGAG CGCTGTCATG GTGATCTGGG 1020 GCCAGGCCTC CGACCTGCTT TAGTGTTCAC AACAGGACTC GGCTCTGTGA TTTTGTGCAC 1080 CATTTCATTG AATCCCCCCG CACCGTTGGA GTCAGAACTA CTGGCACCCT TATTTTACAG 1140 GCAAGGAAAC TGAGGCTTAC AGATGTGAAG TAACTTGCCC AAGGTCTTCC 1190
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