| Tag | Content |
|---|
EnhancerAtlas ID | HS047-10173 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr14:65120690-65122210 |
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 | TGTGTGTTCT CTGAACAAGC TTCTTGAAAG CAGGATCTGT GTTTTATTCA CCCTTATATC 60
CCCAAAGCCT GGCAATGCCT GACTTGGAGT AGGCAGGAAT TTTGTCAGTA ATGTACTGAG 120
CATTCACAAC ATGTGTCAGA CACTCTTCCA GGGCTGATAC GCATAGTAAC TCTTAATTCT 180
CATAATCACC TAATGCGGTT GGTTATATTA TCATTTCCAT TTTTTAGATT ACAAAATGGG 240
GCATGAAGAG GTTGAGTAAC TTGCTGGAGG TTATGAAGTA AGAGCTGAGA TTTAGACCAG 300
GGCTGTTTTG TTCTAGAGCC CACGACCATC CTCTACCACA TCTGCAGTGT TTGTAGAACT 360
GAATTAAAGA TGAGTGAGTA GATCTGTCAA ACTTGTGCCA GGGAAAGCCC ATAAGCTTAC 420
ACCAGACACA GCTAGAAAGA CATTGAGGAA GTCCTGGAAA CCACCAGTGT GTTTTTAGGT 480
GACTCATGGA GGCAAGAGAG CAAGTTGCAA TGTCTCCGAG GGTAGTTGGT TTAGGAAAGG 540
ATGAAATATG TCAGAAAAAT CTATGTACAT AAATAAAACC AAGCAGCTGT GTTCACATTA 600
AGATCCAAAC GGAAACCCAG CTGAAGTAGG AGCCGTTGGA TCTGTCCCAC CAACCTGTTG 660
TGAGCATGAG CTAGGTAAAT ATTTGGCTGA TACAAGGTCC ATCACAGGTT AATAGCTCTG 720
GTCATTACCA AGCCTGGTTA TGCTGGAATT GCATGTAGTC TCAACTGGAC ACTCATGTTT 780
AAGCACAATT TAAAAAATCA CCAAGGGAAA CCAGGAAGCA ACACTTCTAT TTGGGAAGTC 840
AACTAATGGA AAGTTTTCTA AAATAAGTAA CACAGCTTCA GCTTCAGCAA TGGGATTTGT 900
GACATCCCTC CCGTGTCACA GTTAATGTCT ACCTTGTTTA ATACCACATA ATAGTACTTT 960
TAGCCTTCAG AACCTTGAAA CTGCATAACT ACTGGAACAG TTTAAAAAGA ATGAGAACAT 1020
AATGATTTCA TACAGCCCAT ACGTTTCCCA AATAAGTAAA GGGAAGCTGA CTTACGGCAA 1080
TGAGAGGCGG TGTGGTAACC CGGAGAAACT AGGCTGTCGG TGGGACACAT GGGTGTGAAT 1140
CAGCTCTGCT ACTTACATGC TCTGTGTGTC TCCGCAGGAC ACTTAACCTC TTTGAGCCTT 1200
ACTTTCGTCA TCTGGAAATC AAGAGGGTTG CCCTAGATAA TTCTAAGGAC CGGCCCAGCT 1260
GAAGGTTTGT GAGTGCATGA GAAGCCTGCG GTGGGTAAGG TTATGGTGTC AGCTTCCACG 1320
TGGTCTGCGT ATACAGTGAA GCCCACGTGC CCTGCTCCAT TTGGAGAGGC AGCTTGGCCA 1380
AGGTGTAGAA TTGGAATCAT CTGCATTGGA AGCTGCCTTT TGAAAGTGCT AGCAGTGTGC 1440
CCCAAGCGCT TGTTTTCTGA TGGAGCTGAT CTGCCCTGCC CAAGCACTAA CTGGGAAGCT 1500
CTTACCCTTA TTTTCCCTTT 1520
|
