| Tag | Content |
|---|
EnhancerAtlas ID | HS176-17931 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr18:42169160-42170370 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr18:42170211-42170224 | CACATTTGCATGT | + | 6 |
| | | 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 |
| GH18I044589 | chr18 | 42169264 | 42170367 |
| Enhancer Sequence | TGCGCCTTAC ACACAGTATT TTCTCAATAA TTATTTATTG AAATATTTTG AAATAAAGTT 60
AGTTGTAGGG GACTGACCTG CAACTAACCA CCTATTCTAT CAACTCAGAG GCCAGATGTT 120
CACAACACTG AATTACGGAG TCAAACATAA CCAGCAAAGG TTCTGAACAG AACAGAACCC 180
AGGCTCAGGA ACTAAAGCAT AGCATGCCAA TATAATATCA ACTTAGAGCA GTTCAGTTAT 240
CTCTCTTCTC TAATGCCTCT CTCCCAAGGC CATGGTAACG AGCTAATAAA ACCAAATATG 300
TAGGGCCCTG AATAAGGCAT CCATTAAACT CTCACATTTA CTAAGTATTC ATTCCTTTCC 360
CTTCTCTCAG CTCTTCATCT TACTCCCAAA GAAACTTGGA CAAGTCACTT CTTCCGGGGC 420
TTTCATGTTT TTTGCTGTAA AAGTAAAGGA TTGGAAAAAA CAGTTATTGC CTAAACTGGT 480
CAAACTCAGC ATCATTAAGA CAGCTTTGGC TGAAAACTTC CAAGGGTGGA CCTGGAAGCC 540
AGTTTCTTTA TAAAGTTCCC CCAGGTGATC CTGCGGCAGC CAGTCCAACT TAGAACTGCC 600
ATCCAGTGTG TTGGAAACAC TAGCCTTTTC CAGCTCTAAC AGGCAATGGT TTCATTTTTC 660
TCTCTGCTTC TCACATGGAA AGTGTTTATT CAATAAATCA GAATATGACT CACTTGGCTG 720
GCATTTTTTG TTCCACCAGA TGAAAACTAT GCCATAATTA GCAGTGAAGG TCTACTCTAT 780
GTGTATGTGT ATGTGCATGT GGGTATATGT GAGAGTGTGT GTGTGTGTTT GTGTGTGTGT 840
GTCTGTGTGT GTGTTGGTGG ACTGGGGTGG AGAAGCGTAA AAAAAGTCGT GCATCCCTCA 900
ATCACTTCCA TTCCTGACTG GCAGAAGTAG ACTTACCAAT AATGACATTA CAGCACAGTG 960
AAGCAGTGAG CTGCTTCCAG AAGGCTGCCC TTAAATAGAG ACAAAGTGAA GATGTCCTTT 1020
ATTCTTCTGC TGTTATTACA TCAACATCAA TCACATTTGC ATGTTGGCCA ATGGCCACTG 1080
TCCTTTTAAG TAAACACCAG AATACTGGTC ATTGTGGGCT CTAAGAATGG GTTGGTAGAA 1140
ACAAAATCAA GACCAGTCCA GAGCTTTGCC ATTAGTTTAA CAGGCAGTAT GACTAGAACC 1200
AAAGCCCATT 1210
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