| Tag | Content |
|---|
EnhancerAtlas ID | HS191-06888 | Organism | Homo sapiens | Tissue/cell | Trophoblast | Coordinate | chr11:47628240-47629710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF2 | MA0596.1 | chr11:47628751-47628761 | ATGGGGTGAT | + | 6.02 |
| | | 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 |
| GH11I047606 | chr11 | 47628274 | 47630193 |
| Enhancer Sequence | TTCATCCCAT GCCCACATGC CCTTCCTTCC AAATCCAACT TTCTCCTTTG GTTCCTGTCT 60
CATCAACAGC ACCAGGGGAG TCTTTCCCCA TCAGAAGGAA GGTTGGGGGA GCAGCTCCCT 120
GGCAGCTTTT TCTTCCAGCT GAGAGGAAAC TGTCATTGAT GAATGTGAAG AGTTTATCAG 180
CCACTCAGCG ACTAGCTGGG CGAGACTGTA GTTACCAGGA CAGGGCAGTC TCCAGCTCAG 240
TGCCTGCTGC TCTCAGAGCA CGTCAGGCAG TCAGATGTGT GCTTCCCTGG GGACACGACT 300
TCCACGAGCT CATCTAGCAG TCTCACCCTC AACACCTGGT TTCCTCCAAT TTGGCAGTGT 360
GCTGTGGTGT AAAGCTTGCA GGATGTGGAC TCCAATATAC CCAGGTTTGC ATTCTAGTTT 420
TGCTATTTAC TAGCAAGTCA CTTAAATCTT TATCTCTGAG CTTCCATTTC TCTCACTTAA 480
AAAGTGAGAA AAAGTGGCTA TTATCAGGCT CATGGGGTGA TTGAGCTGAC ATATGTATGT 540
ACCTGTGCAT GGAAGGTTTC AAACACACCA GCTTCTGTGC TCAGCTTAGC TTCATGGAGT 600
CTCACGTGTC ACATGTTCTG GGTGAACTGT TGTTTTTTTC CCTTTCTATT AAAACTGTTT 660
CTTTTGGACA GGGTGTAATG TATGTCTTTG CCCAGTGAAC CTTCCTTGGA TGAGCCATGC 720
ATCCCACTAG AAAACAGTCC AGCTCTGAGA AGAGTGTGGG GGCGGAGGAC AGGAAACAGA 780
ACAGAACAGC AGAATGTATG TGGTTCTGGG GCTGACCCTG GACCTCTACC CCTTCAGATG 840
GGCCTGTGAC TCAGGCCTGG CTAGCGTCTC CCAGACACAC CAAATGCTTT ACAGATGGGT 900
GTGTGTTTCA AGCCAGAGTC CTCCTGGGGA TTTTTGCTGG AGCTCTCCAA AGTGATTTTG 960
CTCTTTCTCT GGAATCACAA GCTCTAAGAA GCCATGTGAG TGGAGCTGCC AGCTGGCATC 1020
TTGTTGCCAT GTGGAGAGCC CGTCGGAGAG GGAAACCAGC CGAGGGGTGG GAAGACCGAA 1080
TCCCGATGCC CTTGTTTGAA CCCCCAGATT CACCACTGGC CATTTTTATT ACTTGAGCCA 1140
ATGTAGCCAG TTTGAGTTGG GCTTCTGGGC ATCTAACTAA CTGTTGAGCA TACAATGTTG 1200
ATCCTTTCAT TATTATAATA AAACCACGAG TTCCCTCCTC TCATTAAGAT TCATACTTCA 1260
CTCTTCGTTA AAATCTGTGC TCCGATCATC ATGCAGAAAA ATACTGGGAC GCAATGCATG 1320
TGCGTGCCAT ATTAGAAATT CCAGATTTGC AGACCCATAT CAGAATCTGG GCTTTGCTAT 1380
TTACCACCAG TCTTGGGCAA ATCAATGAAC CCTTCTGAGT CTCACTTTTC CACTACTAAA 1440
ATGGGAGCAG TATTTAGCTT ATATGGCTGT 1470
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