| Tag | Content |
|---|
EnhancerAtlas ID | HS146-05677 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr16:12049250-12050340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF13 | MA0657.1 | chr16:12049437-12049455 | GTGGCACGCCCCTTTATT | + | 7.14 | | POU4F2 | MA0683.1 | chr16:12049914-12049930 | GTCATTAATCATGCAT | - | 6.46 |
|
| | 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 |
| GH16I011955 | chr16 | 12048908 | 12050918 |
|
Enhancer Sequence | AGAGACTATC TTTGGATAAG AAATTTGCCA TTCTGGCCAG GCGTGGTGGC TCACGCCTGT 60
AATCCCAGCA CTTTGGGAGG CTGAGGCAGG TGGATCATAA GGTCAGAAGA TCGAAACCAC 120
CCTGGCCAAC ATGGTGAAAC CCTGTCTCTA CTAAAAATAC AAAAAAACCT AAAAATAGCC 180
AGGCATGGTG GCACGCCCCT TTATTCCCAG CTAGCTACTT GGGTGGCTGA GGCAGGAGAA 240
TTGCTTGAAC CTGAGAGGCA GAGGTTGCAG TGAGCTGAGA TCGTACCACT GGACTCCAAC 300
CTGGGTGACA GAGCAAGACA CTGTCTCAAA AAAAAAAAAA GAAAAGAAAA AAGAAATTTG 360
CCACTCCTCC TCCCACCTCT TGCAGATAGT GGCAATGGAA AGTTACCCAA TGATGCTTCT 420
TGGGAAGCCT TCCACTGGGA GGATGCTTGG AGAGAAACGT TTAATCCCAC TCCACGTATC 480
CCCTCTGGAA CTTGACTCTC GTTTTGCAAA CAGGAAAAAA CCGGTCACCC ACTTAGATGA 540
CTCAGCCAGC CCCAGGCCTC CTCTGGTCCA CTGCAGAGTT CCCGAAGACC CAAATGTTTT 600
GCCTCAGCCA CACGTTTTCA CTTATTTTTG ATTCATTCCA AAGGCAGGCA GGAAATTGCC 660
GCCAGTCATT AATCATGCAT GAATCTTTCC TCTGCGCCTC TTCCATGAAC AAGACCCATG 720
TTGATGGGCA CCTCCCTCTT GTGATCTTAC CTTGATGGGC TCTGACAGCA GGTCGTAGGT 780
GTCTCTCTCT ATTTCACAGC ACAGGTCACC AACACTCAGG CAGGGAAACT GAATTGCTCA 840
AGCCCTGTAA GTGGGAGAAC CAAGCCTTGA ACCTGGCTCT GTGGGCTCTT AGTGGAAAGC 900
CCACAGGGTG GGTTAAAGGC CTGGTTCCCA CATTGCACTA AAAAATGAAC ACTCTCTGGA 960
GTCCCGCTCT CAGTAGCCAT CTGGATGAGA AATGATCTCT TGCCGGGAGC AGTGGCTCAC 1020
GCCTGTAATT TCAGCGCTTT GGGAGGCTGA GGCGGGCAGA TCACCTGAGG TCAGGAGTTT 1080
GAGACCAGCC 1090
|
