| Tag | Content |
|---|
EnhancerAtlas ID | HS047-05826 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr11:44322460-44324110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr11:44322574-44322589 | AATTTCAAGGTCACT | + | 6.12 | | PLAG1 | MA0163.1 | chr11:44323331-44323345 | TCCCCTTGGGCCTC | - | 6.31 | | TFAP2C | MA0524.2 | chr11:44322490-44322502 | CGCCCCAGGGCA | + | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTAAGCTACC AAACCCTGGT GGCGCCTGCA CGCCCCAGGG CAAGCCAGCC TGACCTTCTC 60
CTCAGAGCCT GAGTCAGGGC TTTCCCCATC TCAGGGCCCA TCCCACTGAA CTGGAATTTC 120
AAGGTCACTT GTCTGTCTCT GCCTCTGGAC CTGAAGGCAG GGGCTGCATC CAGAGCTTCC 180
CAGAATACCC CACAAGGCTT GGCATAGTGA CAGGCAAAGT TTGGTGAGCC TTGCGTAAAT 240
GGAATCAAGC CTCTCAGTCC CCTTTGTCTG TGAAATAAGA CATGTGGGCC AGGAGATGAC 300
TGCCATCTCT TCCAACCTTG AGTGAGACCC CCCAACATGT CACCATGACC CATTGTGTGT 360
GTGCTGCAGG GTCAGGGGAG GTACCAGTTT CCTCGATGTA ACCAAAGGCC CTCAGGGCCT 420
GGTGGACAGT CCTACACAGT GGGAGGAGTT GGTCATCTGG CCTCAGCTGA CCCTGGCTTG 480
TGGTTTTCAA GAACTTAGGA AAAGAAAACC CAGCTTGGGG AGCTGGGCAG AGAGCAGGAG 540
TCCCAGCCTG GTGGGGCTGC ATTAGAGTCA GGTCCCTGCA ATCCCACCAG GGATTCCACG 600
GGTGCTCTCC TGCTGTCCTC TAATGCCCAG GAGCTCATGG CGGGGTCTGC TTTACTTCTA 660
AGGAGACTGA GGCAGAACTG CAAGCATCTG CCCTATTTGA TGCACAGAGA GAGTGCAACT 720
TACTGGACTT ATTGCAGGAG TCGCATCCAA CAAGAGAGCG GGTGAGTGGA TTGGATTCCC 780
CAACACTTTC TGCCTTTCCA CCCATTGTAG TGGAAGGAGG AGAACTCGGT GGGTTCCTGC 840
CCTCCTACTA ACCTGGCTGT GGGGGTCCAT TTCCCCTTGG GCCTCAGTTT GCTCATGTGC 900
TAAATGGGGT CAGCAGTGGG CACAGACAGT GCCAAGGACA CGTCTCTTCC GCAGTGAGCC 960
ACACGGGACA GAGGGTATAT TCCAGAGCTG GTGGCTTGTC AGACGGCCTC GCCGCAGTGT 1020
GGGTGGGCTG GATGGACCAT GTTCGAGGGC CCCAGGATGA CGCGGGGGGT GGTTGGGCCC 1080
CACCGGGGAC TTGCCACAGG GAGATTCTGC CTGCCACTCG GTGAGTCAGC TGCTCCTGGG 1140
AGCCATGACC AGGGGCAGGA AGGCCACAGG CCATGATGCA AGGGCGCTTA GTCATTCTCC 1200
CTGGGGGCGC CTCTGGAGGC AGAGGCTATG CCACCCACAG ACCCAGAGAA GCTCCAGAGC 1260
CGTGCACACG GGTACTCACC CTTGCACACC TGAGGCTCGC ACACTGGGGG ACACAGACAC 1320
AAGTGCCAGA GGACAGACAT GCCTTTCACC GGACTACACA CAAACCCTCG GCCTCGCCCT 1380
GAAACACTCA GATAGCAGGA CGTGGACCCA GAGAGAATGG GCACGGCACA CACCGCTCAC 1440
ATTCATGCTG TGCACACGCT CACACAAACA CCTAAGCTGG CTCCTGGGTG CACTTAACCA 1500
TGTGGGGGCA ACACTGCAGG AGACACCAGT TCTTCATTCA TTCTTCCAGC CAGCGAACAT 1560
TTGTTAAGCC CAACTGTACA AAACACTTGG AAGGACATAA GCCGTAACAC AGGAGGCAGG 1620
GACTTGGCAT GTTCTACCTC CTAGGAGAAG 1650
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