| Tag | Content |
|---|
EnhancerAtlas ID | HS148-05616 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr14:65120720-65122200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr14:65121167-65121178 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr14:65121167-65121178 | GGTGACTCATG | + | 6.02 | | MYC | MA0147.3 | chr14:65122030-65122042 | GCCCACGTGCCC | + | 6.44 |
|
| | 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 |
| GH14I064653 | chr14 | 65120427 | 65122220 |
|
Enhancer Sequence | CAGGATCTGT GTTTTATTCA CCCTTATATC CCCAAAGCCT GGCAATGCCT GACTTGGAGT 60
AGGCAGGAAT TTTGTCAGTA ATGTACTGAG CATTCACAAC ATGTGTCAGA CACTCTTCCA 120
GGGCTGATAC GCATAGTAAC TCTTAATTCT CATAATCACC TAATGCGGTT GGTTATATTA 180
TCATTTCCAT TTTTTAGATT ACAAAATGGG GCATGAAGAG GTTGAGTAAC TTGCTGGAGG 240
TTATGAAGTA AGAGCTGAGA TTTAGACCAG GGCTGTTTTG TTCTAGAGCC CACGACCATC 300
CTCTACCACA TCTGCAGTGT TTGTAGAACT GAATTAAAGA TGAGTGAGTA GATCTGTCAA 360
ACTTGTGCCA GGGAAAGCCC ATAAGCTTAC ACCAGACACA GCTAGAAAGA CATTGAGGAA 420
GTCCTGGAAA CCACCAGTGT GTTTTTAGGT GACTCATGGA GGCAAGAGAG CAAGTTGCAA 480
TGTCTCCGAG GGTAGTTGGT TTAGGAAAGG ATGAAATATG TCAGAAAAAT CTATGTACAT 540
AAATAAAACC AAGCAGCTGT GTTCACATTA AGATCCAAAC GGAAACCCAG CTGAAGTAGG 600
AGCCGTTGGA TCTGTCCCAC CAACCTGTTG TGAGCATGAG CTAGGTAAAT ATTTGGCTGA 660
TACAAGGTCC ATCACAGGTT AATAGCTCTG GTCATTACCA AGCCTGGTTA TGCTGGAATT 720
GCATGTAGTC TCAACTGGAC ACTCATGTTT AAGCACAATT TAAAAAATCA CCAAGGGAAA 780
CCAGGAAGCA ACACTTCTAT TTGGGAAGTC AACTAATGGA AAGTTTTCTA AAATAAGTAA 840
CACAGCTTCA GCTTCAGCAA TGGGATTTGT GACATCCCTC CCGTGTCACA GTTAATGTCT 900
ACCTTGTTTA ATACCACATA ATAGTACTTT TAGCCTTCAG AACCTTGAAA CTGCATAACT 960
ACTGGAACAG TTTAAAAAGA ATGAGAACAT AATGATTTCA TACAGCCCAT ACGTTTCCCA 1020
AATAAGTAAA GGGAAGCTGA CTTACGGCAA TGAGAGGCGG TGTGGTAACC CGGAGAAACT 1080
AGGCTGTCGG TGGGACACAT GGGTGTGAAT CAGCTCTGCT ACTTACATGC TCTGTGTGTC 1140
TCCGCAGGAC ACTTAACCTC TTTGAGCCTT ACTTTCGTCA TCTGGAAATC AAGAGGGTTG 1200
CCCTAGATAA TTCTAAGGAC CGGCCCAGCT GAAGGTTTGT GAGTGCATGA GAAGCCTGCG 1260
GTGGGTAAGG TTATGGTGTC AGCTTCCACG TGGTCTGCGT ATACAGTGAA GCCCACGTGC 1320
CCTGCTCCAT TTGGAGAGGC AGCTTGGCCA AGGTGTAGAA TTGGAATCAT CTGCATTGGA 1380
AGCTGCCTTT TGAAAGTGCT AGCAGTGTGC CCCAAGCGCT TGTTTTCTGA TGGAGCTGAT 1440
CTGCCCTGCC CAAGCACTAA CTGGGAAGCT CTTACCCTTA 1480
|
