| Tag | Content |
|---|
EnhancerAtlas ID | HS154-12493 | Organism | Homo sapiens | Tissue/cell | Osteoblast | Coordinate | chr2:73216490-73217980 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr2:73216984-73216995 | TTTCTGGGAAG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTCTCTGTC TCAGTTTACC TATCTGTAAA AAGGGATAGT AATACCTACA ACACCCCAGG 60
GCTGGTATAA GAATGTATGT AAGTGGTGGG TGTGAGCTTG GCATATAAGA GACCTCAATA 120
AATGAAGCTA TATAATCATG ATGTCACGGG ACCGGATGGG GTGACTGCAC CTTTTTCATC 180
TTTGTATGTC CACCACTTAG GGCTACACTC ACTGGCACAT AGTACACGCT CAATAAACTG 240
GTGACTGAGG AATAAATGCA GGAACCAACA AACATACGAC GGCATGGAAA AGGCAAAGGC 300
TGGGAGTGGG GCTTTGCGGA GGAGAGAAAG ATGGGGTTGG GCTAGGCAGA GGAAAAGGAC 360
TTTCTGGTGG AGAAATGCAT ACAAGTGCAG GCCTGGAGAG AGAAAAGACA AGATGCATGA 420
AACCAGAAAA GGAGTTGGGT TGCAGAGGCC TCTGCTTCCC CAGACAGAGG CCAAAGCCAG 480
CCCCTGTGCT GTCTTTTCTG GGAAGCGTGG GAGGAGCCGT GGCAGGACTC CTGGCCTGAC 540
GGGCCGGGGC AGCCTGCTCT GAGGTCTGGC ACGCCTGGCG GCTCAGCAGC CCACCCTGTG 600
CCCTCAGGCC TGGCTCTGGC CTTAATGTTG TGGGTGGTTG GGGAGGACGC AGAGCCTTGG 660
GAAGGCCTCC AGGGCTGCCA GGCGCCTGCC GCTGTTGGGG CAGGGTGCAG CAAGGCAGAA 720
ACAGCCCAGC CCAGGCTGCG ACTGTGAGAC CCAGGAAGAC AAGGAAGTGC TGGTCCGCCA 780
GCCCCGGGGC AGCGCAGCAT TCCGTGGAGC CAGAGTACTT CCTGGCATGC CCACCCTGGG 840
CTCTCGGGAA CACAGCCTCC ATCTTAAGTC TCAGGCTGAT CCTCAGAGTC CAATCCTTGT 900
CCTCCCAGCT CGCTCGAGGG AAGGCTGGGA GGCAGCCAGG GGCATCACGG CGTGGACACA 960
CTTCAGTGGT ACAGTGGGCA GGGCTGGGGA GCTGCCGGCT CATACTGGGC CCTGCTGCCC 1020
CCGCCACATG AATAGAATTC ATCAAGTCCA GGAGCGAGTG ACTCAGAAAT GGCCTCCCTC 1080
ACCCCCAAAA AAGTGCATTG AGAGAAAGTG TGGGAGGAAG CTGGAGGACA CGCAGACGGG 1140
CAGTAGCAAT GAAGAGGAGG GGGGCTCGGG AGAACTCAGT GAGCACTTCC TACGTGAGGC 1200
CACTCAGCAC ATATTCACAT GAAATATCTT AATGAGATCC CCACAACAAG GCTTTTAGAT 1260
AGACCATGTT GGCCCTTTTC ACAGATAGAG ACAGGTCCAG AGAGGTTAAA CAACTTTGCT 1320
CAAGGATAGA CATCTATTAT GAGGCAAGTA AAGCTAGCAT TTGAACGCAG GGCCTGCTAA 1380
TTCCAAAGCC TTGCTCCTAA CCAGGGTGCT ATGACTTTCC CATTGTCTTC CACCTGAGGG 1440
AGGGATGCTT TAATATCTCC AGGCGTTTGA ACGGCACATC TGCATAGCAA 1490
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