| Tag | Content |
|---|
EnhancerAtlas ID | HS108-11974 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:39672530-39673870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr14:39673210-39673222 | TGTCAGGGGGTG | + | 6.22 | | NFE2L1 | MA0089.2 | chr14:39673311-39673326 | GCATGACTCAGCAGA | + | 7.23 | | Nfe2l2 | MA0150.2 | chr14:39673309-39673324 | CTGCATGACTCAGCA | + | 7.41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr14 | 39673628 | 39673859 | | chr14 | 39673031 | 39673603 | | chr14 | 39672861 | 39673002 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I039203 | chr14 | 39672488 | 39674045 |
|
Enhancer Sequence | TTAACTGGAG ATCATCATGG CGGATGGGAG GCAGAACTAG ACTGCAGCTC TGACTCTGAT 60
GGACAGAGCA GTGTGTGGAG GCTCACGTCA TGAATTTTAG CTTCAGATCA ACTGCAATAA 120
CAGACCACCA ATCCTGAGAG GACCCACAGA CCCTCTGAGG GAAGCAGACT GCTCCTGCAG 180
GACCTTGGAG ACACCCCAAA TATTGTGAGA GCCCCAATTG CGGAAGTGGG AAAGCGAGAT 240
CCTCCTCTCC CGAACACACA CCCCCTCTGG AGAAACTGAA GGACTGTTTG CAGGAGAAGT 300
TTTTGATCTT ACCTGGAGCT GATTCAATTT AGACAGCCCA ACAAAATACA GGTGTAGAGG 360
AAGCAGTAGG AAAGGCCCTG GGAACTTGCT GGGTCCCCAG CAGGCCATTC CTGCCTGGCA 420
CCACAGGGAT CTATCAGGAG AGTGGGCAGA AGAGTGAGGG AAAACACCAC AGGGAGAAGG 480
AAATCTCCAG CTGAACTTTG TGACAATTTG AACCTGGTGA GAAGCCTCCT GGCCAGAACT 540
CAGGGGAGGA TGCATATCAG TGTGCAGACT CCACAGACTG GGGTAGAACT AAAGCCCTTT 600
TATGTTGCAG CTGGGAGGAG GGTAGCCTGG GGCAAGTTCT CAAGCCCAGC CCACCCACTG 660
TCCAGAAACA GACTTGACGC TGTCAGGGGG TGCATGGTGG GTGTGGGACC AGCTCTTTAG 720
TTTGTGTGGG AGGTGGATGA GGCCTGTGAC TGCCAGCTTT CCCCCACTTC CCTGACAACC 780
TGCATGACTC AGCAGAGGCA TCTATAATCC TCCTAGGTAC ACAACTCCAT TGACCTGGGA 840
ACCTTACCCC ATCCCCCACA GCAGCCACAG CAAGACCCGC CCAAGGATAG TCTGAGCTCA 900
GACATGCCTA GCCCTGCCCC CACCTGATGG GCCTTCCTTA TCCACTCTGG TAGCTGAAGA 960
CAAAGGGCAT ATAATCTTGG GACTTCAAGG GCCCCACCCA CCACTGGTTC CTCTCCATAC 1020
TACCATAGTT GATGCTCTCT GGAAAGCATC ACCTCCCAGC AGGAGGCCAA CTAGCACAAA 1080
AATAGAGCAT TTAAACCACC AAAGCTAAGA ACCCTCACAG AGCCCATTGC GCTCCCCTGC 1140
CACCTCCACC AGAACAGGTG CTGGTATCCA TGTCTGAGAG ATCCATAGAC AGTTCACATC 1200
ACAGGGCTCT GTGCAGACAA CTCCCAGTAC CAGCCCAGAG CTGGGTAGAC GTGCTGGGTG 1260
GCTCGATCCA GAAGAAAGAC AACAATCACT GCAGTCTGGC TCACAGGAAG CCACATCCAT 1320
AGGAAAAGGG AAGACTCAAG 1340
|
