| Tag | Content |
|---|
EnhancerAtlas ID | HS108-11705 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:21046550-21047870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ATF3 | MA0605.2 | chr14:21046706-21046718 | GATGACGTCACT | - | 6.11 | | ATF3 | MA0605.2 | chr14:21046706-21046718 | GATGACGTCACT | + | 6.14 | | FOXH1 | MA0479.1 | chr14:21047855-21047866 | TGTGGATTGGG | - | 6.14 | | JDP2(var.2) | MA0656.1 | chr14:21046706-21046718 | GATGACGTCACT | + | 6.07 | | NR2C2 | MA0504.1 | chr14:21047538-21047553 | TGCCCTTTGACCCTG | - | 6.81 | | Nr2f6 | MA0677.1 | chr14:21047538-21047552 | TGCCCTTTGACCCT | - | 6.43 | | Rxra | MA0512.2 | chr14:21047538-21047552 | TGCCCTTTGACCCT | - | 6.41 | | ZNF263 | MA0528.1 | chr14:21047333-21047354 | CCCACCTCATATTCCTCCTCT | - | 6.18 |
|
| | 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 |
| GH14I020577 | chr14 | 21045898 | 21047747 |
|
Enhancer Sequence | TGTAAATGGT AAACAATTTA CATGGTTTGC ATGTGAGTAA AGTTCCTCCC AGCAGGAGAC 60
TTTCCAGAGC TGGGGCACAG TGGGGACACC ATTCAGAAGG GGATCAGGCT AGAGAACTAC 120
CAGAGGGAAA GGGAAATCAG AGAGGGCGAT TGTGTGGATG ACGTCACTCA GCAAAACAAA 180
GTAGGCCCCC ATGTTCCACA AGCCCTGCAT TAGTGTGTGG ACTGCTCCCA CAGGGCCTGA 240
AACCAAGACA CATTGAATAT CGGCCTTTAA ATGAAAGTCT TATAATTGGC CTGGCTCCAG 300
AAATCTGTCC AACTTGTCAC TGTATACCCA AACAGTGAGT GTGAATGCAA GACACACAGA 360
AAAGAACACA TAAAATTGAA CAGTGCAAAG CCTAAAAGGA AAATAGAATA CAAAAGTCAT 420
GGCAGTGTGC AAAAGGGAGA TGTGTATTGA GGGCACAATC TAGTCAAGAG AAGAGAGCAT 480
GGAAGTTGGA TGAGGAAGGG ATGTAAACGG AAAAAAGGGG AAAGGTAGCA TTAGCTGGAT 540
GTGGTGGTGC ACGCCTGTGG TCCCAGCTAC TTGAAGGGCT GAGGTGGGAG GATCACCTGA 600
GCACGGGGGT CGAGCCTGCG ATGAGCTGTG TTCGCGCCAC TGCAGTCCAA CCTGGGTGGC 660
AAAGTGAGAC CCTGTCTCAA AAAAATAAAA GAAAAGAAAG AAGAAGGTGA AAGGTATAAA 720
GAAGGGGGAA GTGATCACAC TTTGTGTGGG CAGGGTCAAG GGTTTATCTT CCCAACCCTG 780
CCTCCCACCT CATATTCCTC CTCTAACAGG CATCTGTTTC CTGTACCCAG GAGAGATCTC 840
CGAAGGGACA TTTAACATGA CAGGTCAGAC AGCTCAGCCC ACATTCTCAC AGAGAACATG 900
GGGTTCCTGG AACAGCCTGA GCTGGGGAGG ACGAGGGGAA CACATGCATA GCAGCAGAGC 960
CCGGAAGCTT GGCCAGCCGT TGTGACCGTG CCCTTTGACC CTGTGTGAGA CAAACCTCAG 1020
GACCTGTTCA AGCCTCCAGT GAGGACGCCT CCTCAAAGAC CACCTCGGCC AGAGTTGACT 1080
GGGGCAAGTC TCTTACCTAA AGAAGGTTTA AGAGGAGAGG GGAGTGTCAA CAAGGAGGCA 1140
AAGCAGCCAA ATGTGCAGAG GGCCTGGAAA CTAGAACGGG GCTTAGCTCA CATTGCTCTC 1200
CTCAAAGACA GCAAATGCAT CAATTTGCTT TCCTGGGAGG ACTGCATGAG AACATCCCCT 1260
TCCTGTACCT ATGCCCCCAC TATGTTCTAT TTTTAATCTT ATTTGTGTGG ATTGGGTAGG 1320
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