Tag | Content |
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EnhancerAtlas ID | HS051-19647 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:56726600-56728420 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr3:56727785-56727796 | AAAGATAAGAA | - | 6.62 | LMX1B | MA0703.2 | chr3:56728184-56728195 | TTAATTAAATC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr3:56728388-56728403 | GAGGTCAGAAGATCA | + | 6.15 | RARA | MA0729.1 | chr3:56728388-56728406 | GAGGTCAGAAGATCAAGA | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 56726951 | 56727634 | chr3 | 56727841 | 56728091 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I056692 | chr3 | 56726629 | 56730144 |
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Enhancer Sequence | GAGGACCTCT GTGTCTAGCT CAGGGATTGT AAACGCACCA GTCAGCGCCC TGTCAAAACA 60 GACCACTTGG CTCTACCAAT CAGCAGGATG TGGGTGGGGC CAGATAAGAG AATAAAAGCA 120 GGCTGCCCTA GCCAGCAGTG GCAACCTACT CGGGTCCCCT TCCACACTGT GGAAGCTTTG 180 TTCTTTCGCT CTGCAATAAA TCTTGCTACT GCTCACTCTT TGGGTCCACA CTGCTTTTAT 240 GAGCTGTAAC ACTCACTGCG AAGGTCTGCA GCTTCACTCC TGAGCCAGCG AGACCATGAA 300 CCCACCAGAA GGAAAAAACT CCGAACACAG CCGAACATCA GAAGGAACAA ACTCCAGACG 360 TGCCACCTCA AGAGATGTAA CACTCACCGC AAGGGTCCGC GGCTTCATTC TTGAAGTCAG 420 TGAGACCAAG AACCCACCAA TTCCGGACAC ACTAGGGAAG CCTGAAAAAG ACCCTCTTAA 480 TTTGGCAAGA AACCATGTTG AAGTTGATTC CTGGTTAATG ACTGGAAGAA AAACTTCCAT 540 GCAATGAGGA GAAGCAACAA AAGGGAGAAA TTCAATTGAA AAAAAGAATA TAGTTAGCAA 600 TGAACAAGAA GCAAGTGTCC TCTCACCAAC ACAGCTGACT CTGGTAACCA CAAACCTCAG 660 CTAAACCCAG AAGTCAAGAG CTGTCACTTA AGTTTTGTTT CATTTCTGAG TGAAACCCTT 720 CTAAGACTTT ATTACATGCA ATGCCATGGA TTAATGTCAT AGACATAATG TTAAATGAAA 780 GACGTACTGT ATGATCCCAT TTACATGATG TTCAAGGACA GACAAAAATA ATCTATGGTA 840 ATAAAAGAAT TGTGGTTCCC TTGTGGGGGT GAAGATGTAC TGTATGATCC CATTTACATG 900 ACGTTCAAGG ACAGACAAAA ATAATCTATG GTAGTAAAGG AATTGTGGTT CCCTTTTTGG 960 AGTGGGGGTG GTAGGTAATT GACTCAAAGG GGACATGAAG GAACTTTCTG GAATGATGGA 1020 AATGCTCTGT ATCTTGATCT GGGTGGTAGT TATACAGACA GGGGCATACA CATATAAGTA 1080 TTCATTGAAC TGTATGCATA GAGTTGCATT TTATTCTGTG ATGTTATTCT TCAATTAAAT 1140 AAACAAAAAC AAAACTTTTC TATGGATTCT CATTATTCCA GGGACAAAGA TAAGAATTCT 1200 TCATGTGGGC AATGGACCCT TACTGATTCT GACCTTTGCC TGCCTTTCCA TCTTGCACTT 1260 CACTTCCCTA AGCTCCTCCT TGGTTCTTCC TATGTCTGGC ACACTTGCCA AACTCCCTGG 1320 CCATGCAATC AACCTCAGCA CATGATATGT TTCCTGTGTG GGATGTTATT CTTCCCCGTG 1380 CCACCCTCTT CTCCAGTTCC AGTAAGCTAC TGCACTTCCT TTGGCTGAAG CTTCACTTCC 1440 CTGTGTGAAC TTCTTTCATA ATCGGCCCCC CATTCTAGGT CGAGTTCCCC ATTGGATGCT 1500 CTTACAGAAT TTTGCTCCTT TTACTCAGAC CATTTACCTC CCAATTTCCT CAATTTGTAA 1560 TTACTCCCTC ATTTGTGGGA CTATTTAATT AAATCTGTCT CTCTCACTAC AGTCTGTGCC 1620 ATACCATGGA CTGAGGGTCA ATGTCTGGGT TCTGCTTACC ATGGTATCCC CAGGGCTCAC 1680 CACAGTGCCT GGAACACAGT AAGTGTTTAC TAAATATGTT TTTGGGCCGG GCGCAGTGGC 1740 TCACGCCTGT AATCCCAGCA CTTTGGGAGG CCAAGGCAGG TGGATCACGA GGTCAGAAGA 1800 TCAAGACCCT CCTGGCTAAC 1820
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