| Tag | Content |
|---|
EnhancerAtlas ID | HS108-18463 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr18:19314860-19316280 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr18:19315697-19315713 | CACAGTGTAAACAAAG | + | 6 | | RELA | MA0107.1 | chr18:19315340-19315350 | GGAAATTCCC | - | 6.02 |
|
| | 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 |
| GH18I021735 | chr18 | 19315071 | 19316448 |
|
Enhancer Sequence | ACAAGTCAAT AGGAGTTAAT TTTGGTACAC AAAAAATGGA ACTCCATGCA GTTTTTTCAT 60
AATACACATT TTCCATGAAC ATTTTCAAGT CTCCTTGTGT ATTTTCTTTC CTTTTGGGTA 120
AGTACTGAAG AGTGGAATGG CTGGATCATA TGGCAGTGTA TGATTAAGTG TTGATTTTAA 180
GAACTTGCTG GCTGGCAAGG TGGCCAAATA GGAACAGCTC CCGTCTGCAG CTCCCAGCGA 240
GATGGATGCA GAAGGCAGGT GATTTCTGCA TTTCCAACTG AGGTACCTGG TTCATCTCAC 300
TGGGACTGGT TGGACAGTGG GTGCAGCCCA CGGAGGGCAT TGTCTCACTC AGGAAGCACA 360
AGGGGTCAGT GGATCTCCCT CCCCAAGCCA AGGGAAGCTG TGAGAGACTG TACTGGGAGG 420
AACGGGGTAC TCCGGATCAG ATACTGTGCT TTTCCCACAG TCTTCACAAC CAGCAGACCA 480
GGAAATTCCC TCCGGTGCCT ACGCCACCAG GGCCCTGGGT TTCAAGCACA AAACTGGGTG 540
GTCATTTGGG CAGATACTGA GCTAGCTGCA AGGGTTTTTT TTTTTTTTCA TACCCCGGTG 600
GCATCTGGAA CACCAGCAAG ACAGAACCGT TCACTCGCCT GGAAAGGGGG CTGAAGCCAG 660
TGAGCCAAGT GGTCTGGCTC AGCGGGTCCC ATCCCCACAG AGCCCAGCAA GCTAAGATCC 720
ACTGGCTTGA AATTCTCGCT GCTAGCACAG CAGTCTGAGG TTGACCTGAG ATGCTCAAGC 780
TTGGTCGGGG GGAGGGGCAT CCGCCATTGC TGAGGCTTGC GTAGGCAGTT TTACTCTCAC 840
AGTGTAAACA AAGCTGCCGG AAGTTCGAAC TGGGTGGAGG CCCTCTGCAA CTCAGCAATG 900
ACACTGCAGC CAGACTGCCT CTCTAGATTC CTCCTCTCTG GGCAGGGCAT CTCTGAAAAA 960
AAGGCAGCAG CCCCAGTCAG GCACTTATAG ATAAAACCCC CACCTCCCTG GGACAGAGTA 1020
TCTGGGGGAA GGGGCAGTTG TGGGTACAGC TTCAGCTTAC TTAAACGTCC CTGTCTGACA 1080
CCTGTGAAGA GAGCAGTGGA TCTCCCAGCA CAGCGTTCGA GCTCTGATAA GGGACAGACT 1140
GCTTCCTCAA GTGGGTCCTT GACCCCCATG TATCCTAACA GGGAGACACC TCCCAGTAGG 1200
GGCCGACAGA CACCTCATAC AGGAGAGCAC TGGCTGGCAT CTGGCAGGTG CCCCTCTGGG 1260
ATGGAGCTTC CAGAGGAAGG AACAGACAGC AATCTTTGCT GTTCTGCAGC CTCTGCTGGT 1320
GATACCCAGG CAAACAGGGT ATGGAGTGGA CCTCCAGCAA ATGCCAGCAG ACCTGCAGCA 1380
GAGGTTCCTG ACTGTTAGAA GGAAAACTAA CAAACAGAAA 1420
|
