| Tag | Content |
|---|
EnhancerAtlas ID | HS003-00088 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:2573400-2575160 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I002640 | chr1 | 2572379 | 2575568 |
|
Enhancer Sequence | CCTGCAGAGG TCCTCTGCAC AGCCAGCTTC TGCTGGCTCC CTGGGGATGG CGGGGCCCTG 60
GGCTGCACAG GAGCTGCCCG CTGCTTCTGG AGGGGCTGGC TGACCATGGG CAAGGGCAGG 120
AAGGGGGACC CAGGGTAGAG GACCCCTCCC TGCAATTCCC ACTGCCCTGG AACCTGCCAA 180
AGTGCTGTTC CGACCCTTGG CCCAAGGCCT GGCATCCTTG CCCACTGCTC TTCTCCCTGG 240
GCCTCGGATC AGGGACCTGG ATTTACCTCC TCATGGTCCC CTCCTGGCAG CCCTACCGCC 300
CCACCGGCTG GGCCCAGGTT CCCTTGACTG GGTGACCACA CCGGCCTCCT CCCTCGGTCC 360
CTCTGGGCCA AGTCACCTCT CCATCGGGCC CTCTGAGGGG GCTGCTGCCC AGCCCTTCCA 420
CTCTGCCCAC CTTCTGAAGG CTGCTCCAGG CCTCTGAGCA CGTGCACCCT AGCCCCTCTC 480
CCTGGGGCTG CTGGACGGAG GGCACAGCCT GTGCTGTGGG CTGCTGCTGG CCAGGCCTGC 540
CTGCCCCCCC CACTCCTCCC GGGCACTTTC CTGAGCCCAC CCAGGCCCAA TCGCCTCATC 600
TCTGACCCAG TTTTTTCACA GAGTCAACCA CGACCAGAAA TCCGCTCGCC TCGCTGGGCT 660
CCTCCTCCGC TCAAGAATCT GCAGGGGTTC CCCGCTGCCT GAGGAACACG CCAAGGTGCA 720
GGCCCCGCCT TTCTCGCTGG CGCTGCCTCT CTTCCAGCAG CCCGGCGGTC CTCGACGCTA 780
CCTCCCCCGG GGGGCGCAGC GCACCCAGGA CCCCGCCAGG CTTGGCCGCA CGGGGCGAAG 840
CCGAGGCCCA CGCCCGGGGT CCGTGCAGGG AGCGAGGGGG TCCCACGGCC CCGGCTTTGC 900
TGCTGGGCTC CCGCAGGGCA CAGTGTGGCC TCTTCTGCCA GCTGTGAGCG GCGCTGAGCA 960
GGGCAGGGGC TCGAAACCCC GTCCCTCGCC TGCGGTGCGG CCCGCGGGAC CGCCCCTCTC 1020
CGGGCGGAGG CACCTGACCC CGACCCGTAG TTCACGGCCC GGGGTGGTAG TGAAGCCTCG 1080
GCCCGCGCAG GACCCGCACA TTTGGGCCGG GTCCATGGCA GCAGGAGGGC GAGGCCCCGA 1140
GCAGCTGTCG GACCCCGGGA GCCCCCAGGC CGCCCCAGTG GGGAAGGGCG CTCAATCCGA 1200
CCCCAGACTC CCCTGAGCCC GCGGCTCGGG CCGCGCAGGC GCAGTGCCAC CCGGAGGGGG 1260
CCGCCTGCCG AGGGGCGGGG CGCAGGAAGC GGGGCGAAAC CACTGTTGGC TCATTTCCGG 1320
GTGGGTCCCC GTCTCCAGGC AACCATTTCG CGTCCTGCAG ATTCTTGCCT GTGCCGGGAG 1380
CCGCCTCCTG GCGCCGCAGC CCAGCCGTAT TCTGCAGCCT CGGAGACCCG CGTCCAGCCC 1440
CGCCTCCGGG CTCGGTGACC CCCGTTCAGG AGACCCCATC TAGCCGCCTC CTCTGGGCTC 1500
CGGGACCATG GCCCCAGCCA GGCTTCCCGC CCCCTGCCAG GCCCTGCTCC CACCTCGAAG 1560
ACCCCAGCAC AGACCCCTCC TCCTGGCTTG GAAACGCCCA GTCCCTCTGG GAGCTCTGAG 1620
ACCCCACCCC GCCCAGCCCG GCCGCCTCCT CTAGGTCCCG ATAACCCAAT CTCAGCGTTG 1680
CTCTTCAGCT CGGGGGGGGC AGCGGCGCCC CCTCTGCAGC ACCGAACTGC CCCTTACACT 1740
GGTGTAGCCC CGACTCCGCC 1760
|
