| Tag | Content |
|---|
EnhancerAtlas ID | HS138-26150 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr3:23670380-23671600 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr3:23671313-23671324 | AGTGACTCATG | + | 6.14 |
| | | 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 |
| GH03I023629 | chr3 | 23671091 | 23671330 |
| Enhancer Sequence | GGTACAAACT CTGGTGGCCT TTTTGCAACC ATGGGAGAAA GCCCAGAGAA ATCTCAGCGT 60
TACCAATGGT GTCAGTTTAA GTTCTTCAGG AAGCAAATGC CTAGATAGGA GTAAATGGGC 120
AAAGATCTGA TTAGGGGATA TGCCTGTATA AGGGAAAATA GGGAGGGGGC CAAATAAGAC 180
TAGGAGAGCC ACCAGATTTT GATGATGTCT TACTCTATCC AACTGAAGAA GAGAGGGAGA 240
GAAGATTGGG TGAAGGCATC TTAGACTGCT GTATAGTCTA AGGCAAGTTC AGCAAAGCCA 300
TCCAGGAGTC TTCAAGCCAA ACGTGACTGT CAGAGGAGTC CCAGGTCTTC CAGGAGTGGA 360
TTGGCCTTGG TATCCCTGCC GCATAAACCA CTGGTTGGGA GCCACCCATG GAATGCATGG 420
CTTTTGCACA AACATTGCAA TAGATTTTAA AGCGCAATGG CTGACGCCCT TGGTCAGTTA 480
TGCTCCCTGT AGCTGGAAGT CTGTGAGGCC ACAACACCAT TACTGAACCA CAGCCAAAAA 540
CCAACTTCCT CTGGACTACT TGCTATCAGA GAAAAATAAG CTCCTAATTG TCTGTACCCT 600
TGTCCCATTT TCTATAACTT GCTGCTGAAC GCATTCCTAC CAGAAACACC CTTCACCCTG 660
GGTAAGCCTA GCCTCCCACC AATTCAGGCT TCTCTTTTTC TTATCCTCTC TCTTGTCTCT 720
GTTCTTCACT TTCCCCCTCC AATTTCTCAT GCAGAGCAGA GTAATTCTGT CTCTTTGATA 780
CTTGAACTCC TGCCAACACT CAGCTCTCAA GGTCCCACCT TCAACCCCAA GTTGAAGTGG 840
CTTATCAAGT TGTTTTTCCA AAACAAACAC TATTCTCTCC TTAAGAGGAA TTCTGGTGCC 900
AGGTGGTAAG ATAAAAATTT CAGGGCCAGA CACAGTGACT CATGCCTGTA ATCCCAGCAC 960
TTTGGAAGAC TGACTCAAGA GGATTGTTTG AGGCCAGGAA TCCAAGACCC CATCTCTACA 1020
AAAAAATAAA ATAAAAGAAT TAGCCAGGCA TGGTGGTGCA CACCTGTGTT CCCAGCTACT 1080
TGGGAGACTG ACGCAGGAGA ATAACCTGAG CCCAGGAGGT CAAGGCTGCA GTAACCTGTC 1140
TTGGCCCACT GTACTCCAGC CTAAGTGATA GAGTAAGACC CTGTACTAAA AATAAGAGCC 1200
AATGATAGGG AAAGAAAGAA 1220
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