Tag | Content |
---|
EnhancerAtlas ID | HS059-00100 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:2573380-2575610 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr1:2574921-2574932 | GCTTCCCGCCC | - | 6.02 | INSM1 | MA0155.1 | chr1:2574927-2574939 | CGCCCCCTGCCA | - | 6.07 | KLF5 | MA0599.1 | chr1:2574671-2574681 | GGGGCGGGGC | - | 6.02 | NRF1 | MA0506.1 | chr1:2574631-2574642 | CGCGCAGGCGC | - | 6.14 | PPARG | MA0066.1 | chr1:2575050-2575070 | CTAGGTCCCGATAACCCAAT | + | 6.2 | ZNF740 | MA0753.2 | chr1:2573940-2573953 | CTGCCCCCCCCAC | + | 7.34 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 2574343 | 2574764 | chr1 | 2574810 | 2575479 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I002640 | chr1 | 2572379 | 2575568 |
|
Enhancer Sequence | AAAAGCCCGG CCGCCCCTGC CCTGCAGAGG TCCTCTGCAC AGCCAGCTTC TGCTGGCTCC 60 CTGGGGATGG CGGGGCCCTG GGCTGCACAG GAGCTGCCCG CTGCTTCTGG AGGGGCTGGC 120 TGACCATGGG CAAGGGCAGG AAGGGGGACC CAGGGTAGAG GACCCCTCCC TGCAATTCCC 180 ACTGCCCTGG AACCTGCCAA AGTGCTGTTC CGACCCTTGG CCCAAGGCCT GGCATCCTTG 240 CCCACTGCTC TTCTCCCTGG GCCTCGGATC AGGGACCTGG ATTTACCTCC TCATGGTCCC 300 CTCCTGGCAG CCCTACCGCC CCACCGGCTG GGCCCAGGTT CCCTTGACTG GGTGACCACA 360 CCGGCCTCCT CCCTCGGTCC CTCTGGGCCA AGTCACCTCT CCATCGGGCC CTCTGAGGGG 420 GCTGCTGCCC AGCCCTTCCA CTCTGCCCAC CTTCTGAAGG CTGCTCCAGG CCTCTGAGCA 480 CGTGCACCCT AGCCCCTCTC CCTGGGGCTG CTGGACGGAG GGCACAGCCT GTGCTGTGGG 540 CTGCTGCTGG CCAGGCCTGC CTGCCCCCCC CACTCCTCCC GGGCACTTTC CTGAGCCCAC 600 CCAGGCCCAA TCGCCTCATC TCTGACCCAG TTTTTTCACA GAGTCAACCA CGACCAGAAA 660 TCCGCTCGCC TCGCTGGGCT CCTCCTCCGC TCAAGAATCT GCAGGGGTTC CCCGCTGCCT 720 GAGGAACACG CCAAGGTGCA GGCCCCGCCT TTCTCGCTGG CGCTGCCTCT CTTCCAGCAG 780 CCCGGCGGTC CTCGACGCTA CCTCCCCCGG GGGGCGCAGC GCACCCAGGA CCCCGCCAGG 840 CTTGGCCGCA CGGGGCGAAG CCGAGGCCCA CGCCCGGGGT CCGTGCAGGG AGCGAGGGGG 900 TCCCACGGCC CCGGCTTTGC TGCTGGGCTC CCGCAGGGCA CAGTGTGGCC TCTTCTGCCA 960 GCTGTGAGCG GCGCTGAGCA GGGCAGGGGC TCGAAACCCC GTCCCTCGCC TGCGGTGCGG 1020 CCCGCGGGAC CGCCCCTCTC CGGGCGGAGG CACCTGACCC CGACCCGTAG TTCACGGCCC 1080 GGGGTGGTAG TGAAGCCTCG GCCCGCGCAG GACCCGCACA TTTGGGCCGG GTCCATGGCA 1140 GCAGGAGGGC GAGGCCCCGA GCAGCTGTCG GACCCCGGGA GCCCCCAGGC CGCCCCAGTG 1200 GGGAAGGGCG CTCAATCCGA CCCCAGACTC CCCTGAGCCC GCGGCTCGGG CCGCGCAGGC 1260 GCAGTGCCAC CCGGAGGGGG CCGCCTGCCG AGGGGCGGGG CGCAGGAAGC GGGGCGAAAC 1320 CACTGTTGGC TCATTTCCGG GTGGGTCCCC GTCTCCAGGC AACCATTTCG CGTCCTGCAG 1380 ATTCTTGCCT GTGCCGGGAG CCGCCTCCTG GCGCCGCAGC CCAGCCGTAT TCTGCAGCCT 1440 CGGAGACCCG CGTCCAGCCC CGCCTCCGGG CTCGGTGACC CCCGTTCAGG AGACCCCATC 1500 TAGCCGCCTC CTCTGGGCTC CGGGACCATG GCCCCAGCCA GGCTTCCCGC CCCCTGCCAG 1560 GCCCTGCTCC CACCTCGAAG ACCCCAGCAC AGACCCCTCC TCCTGGCTTG GAAACGCCCA 1620 GTCCCTCTGG GAGCTCTGAG ACCCCACCCC GCCCAGCCCG GCCGCCTCCT CTAGGTCCCG 1680 ATAACCCAAT CTCAGCGTTG CTCTTCAGCT CGGGGGGGGC AGCGGCGCCC CCTCTGCAGC 1740 ACCGAACTGC CCCTTACACT GGTGTAGCCC CGACTCCGCC ATGAGCTCCC TGTTCTTCCT 1800 AGTGTGGTTT CTGTTTTCCT AAGTGGCCCC GGAGTGCTAG AACCCGCTGG TGTCAGGAAG 1860 CATTAAGGAG GTGAAATCCT GCCCAGGCCC CACTGGGGTG TAGTTCTGCC TCTGGGACCC 1920 CAAAGCCTGC TGTGCTCTTG GCCTCCCAGC CTGCCTTGTC CCCACGTGCC TTCTCCCGGC 1980 CTGCCATGGG TTTGGGGTGG GCTTCCTGCC GGGCAAGGTG CCCCTGGCTG GCTCAGTCTG 2040 GCCCTGAGGG CAAGGTCCTC TTCCCTCTCT TGCACCCAAG TCACCTGTGG CTTATACTTC 2100 CCATACAAAG AGGCTGAGAG GTCGGTGGGG TTGTAGGGCT AAGGTGGCCA GAGACCGTCT 2160 TCCTGGGCCA GAAGTGGGTG CCTCCCACCC CACCCCAAAC CTAACTGAAA TCAACCCAAC 2220 CGCAGAGAGT 2230
|