| Tag | Content |
|---|
EnhancerAtlas ID | HS095-08923 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr14:39672650-39674020 |
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 | CAGACCACCA ATCCTGAGAG GACCCACAGA CCCTCTGAGG GAAGCAGACT GCTCCTGCAG 60
GACCTTGGAG ACACCCCAAA TATTGTGAGA GCCCCAATTG CGGAAGTGGG AAAGCGAGAT 120
CCTCCTCTCC CGAACACACA CCCCCTCTGG AGAAACTGAA GGACTGTTTG CAGGAGAAGT 180
TTTTGATCTT ACCTGGAGCT GATTCAATTT AGACAGCCCA ACAAAATACA GGTGTAGAGG 240
AAGCAGTAGG AAAGGCCCTG GGAACTTGCT GGGTCCCCAG CAGGCCATTC CTGCCTGGCA 300
CCACAGGGAT CTATCAGGAG AGTGGGCAGA AGAGTGAGGG AAAACACCAC AGGGAGAAGG 360
AAATCTCCAG CTGAACTTTG TGACAATTTG AACCTGGTGA GAAGCCTCCT GGCCAGAACT 420
CAGGGGAGGA TGCATATCAG TGTGCAGACT CCACAGACTG GGGTAGAACT AAAGCCCTTT 480
TATGTTGCAG CTGGGAGGAG GGTAGCCTGG GGCAAGTTCT CAAGCCCAGC CCACCCACTG 540
TCCAGAAACA GACTTGACGC TGTCAGGGGG TGCATGGTGG GTGTGGGACC AGCTCTTTAG 600
TTTGTGTGGG AGGTGGATGA GGCCTGTGAC TGCCAGCTTT CCCCCACTTC CCTGACAACC 660
TGCATGACTC AGCAGAGGCA TCTATAATCC TCCTAGGTAC ACAACTCCAT TGACCTGGGA 720
ACCTTACCCC ATCCCCCACA GCAGCCACAG CAAGACCCGC CCAAGGATAG TCTGAGCTCA 780
GACATGCCTA GCCCTGCCCC CACCTGATGG GCCTTCCTTA TCCACTCTGG TAGCTGAAGA 840
CAAAGGGCAT ATAATCTTGG GACTTCAAGG GCCCCACCCA CCACTGGTTC CTCTCCATAC 900
TACCATAGTT GATGCTCTCT GGAAAGCATC ACCTCCCAGC AGGAGGCCAA CTAGCACAAA 960
AATAGAGCAT TTAAACCACC AAAGCTAAGA ACCCTCACAG AGCCCATTGC GCTCCCCTGC 1020
CACCTCCACC AGAACAGGTG CTGGTATCCA TGTCTGAGAG ATCCATAGAC AGTTCACATC 1080
ACAGGGCTCT GTGCAGACAA CTCCCAGTAC CAGCCCAGAG CTGGGTAGAC GTGCTGGGTG 1140
GCTCGATCCA GAAGAAAGAC AACAATCACT GCAGTCTGGC TCACAGGAAG CCACATCCAT 1200
AGGAAAAGGG AAGACTCAAG GGACAAAAGA ATCTGAACAA CAGCCTTCAG CCTTAGACCC 1260
TCCCTCTGAT AGAGCCTATC CAAATGAGAA GGAACCAGAA AACCAACTCT GGTAATATGA 1320
CAAAAAAAGG CTCTGTAACA CCCCCCAAAT AATCACAGTA GCTCACCAGC 1370
|
