| Tag | Content |
|---|
EnhancerAtlas ID | HS047-01114 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr1:41798240-41799420 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr1:41799185-41799196 | AGCCAATCAGA | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCAGCCTGGG TGACAGAGCA AGACTCTGCC TCCAAAATAA ATAAATAAAT AAATAAACCA 60
GTCAAACTGG ATTGGGGCCC ACCTTAGGGC CTAATTTTAA TGTAATCACC TCTTTAAATG 120
CCCCATGTCC AGATACAGTC ACATTCTGAG GAACTAGGGG TTAGGGCTTC AACAAATGAT 180
TTTTGGGGCT GGGCATGGTG GCTCACACCT GTAATCCCAG CACTTTGGGA GACCGAGGCT 240
GGCAGATCAA CTGAGGTCAG GAGTTCGAGA CCAGCCTGGC CAACATGGTG AAACCCCATC 300
TCTACCAAAA AAACATACAA AAATTAGCTG GGCGTGGTGG TGCACACTTG TAGTCCCAGC 360
TACTGAGGAG GCTGAGGCAG AAGAATTGCT TGAACTTGGG AGATGGAGGT TGCAGTGAGC 420
CAAGATTGTG CCACTGCACT CCAGCCTGGG TGACAGAGCA AGACTCTGTC TCAAAAAAAA 480
AAAAAGAAAA AAAAAAATTT TGGGGGGGGT CGTAATTCAG CCCATAGCGC CACCTTCCTT 540
CTCTGCATCT TTCTGCATGT TGCTGTTCTC TCTGCCTGAA ACACTGTCCA CATTTTCTCT 600
TCTTCTCCCA AGAAGTTCTC CTACTCATCA TCTAAAACCT AGACAGAGCG TCACCACCTC 660
CAGGAAGGCT TCCTAGCTAG ACTGCTGCCT CCTCTGGGCT CTCACAGCCC ACTGTGTTGA 720
CCTATATCAT GACATGTATC ACACTCTAAG AACTGTCATT TGCTGGGGTG GATGCCTGTT 780
GTTTTGATCT GTACAGCATC CCATTCCCCC TCTGATAACA GCATCTTCTT CTCTTTGAAG 840
AAGTGACGCC CCCTCACCCC CTCCACTCCT GTGACTGTGG CTCAGATGAC TCAGTAAATT 900
ACAGTTGCTG CTTCTTGCCG CAGGAATGAG CATGTGATGA AGCAGAGCCA ATCAGAGTCC 960
TTCCCTGAGA TTTTTATCTA CAAATGTTGG GCAGGAAAAT GCTGATCTTT CCTCTGGGGT 1020
CCAGAATGAC GTAAACTTGG AGCTTTGTGT GGTCATGGCC CAGATTTGTC CTGCCAGGAA 1080
GGACGTCTAT CTGCAGGGGA AAGAATCAGG CCCACGCCCA AGGGAAGCAC CTATGAAGAG 1140
CTGGTCACTC TATGTAAATT TTAAGCTTTT CATATATAAT 1180
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