| Tag | Content |
|---|
EnhancerAtlas ID | HS182-05995 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr13:99830640-99831630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr13:99831227-99831241 | AGTCCCCTGGGACC | + | 6.08 |
| | | 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 |
| GH13I099178 | chr13 | 99830701 | 99831738 |
| Enhancer Sequence | CCATTGTATG TTTCTGCTGC ATTTTGCTTA TTTATTCATC TGTTGATAGA CACTTGTAAT 60
CGTTGGTCAG TTCCTTTTGA ACCAGGAGAC CCATTAAGGA TTTTCTGATA TTTCTCCAAT 120
ATGGCAAGGG CCTAGGAGAA TACGAAATGA TTTGCAGAAG GCAAAGGAAA GAAATTCAGC 180
CAATATACAG ACTCATGTGC CTGCACAGTC CCTAAATGTC ACTCATACAG TGAGGGATGG 240
CTTTGTGCGT TCCCCATGAC AGTTACTAAG TTATTGCCTC TCACTCCAAA CCCAGGCTTC 300
TCTGCTTGGC TTTGTGATGT TGGGCTGAGA CTCTGCAAAC CACAAGTTGG GTTCTACCAT 360
TTTGGGGTGC TACAGGAAGC TGAGGAAGAA GGAGGGGCTC GTGACCTCCT TGCTGCTTGG 420
GGCCCCTTTG AGCAATACCC CAGGGACACT CCACCCAGCA AATGCAGCTG CTTTCTGCAG 480
CAGCAGCTGA ATCCAGATGC CAGTGCTTGC AACACCAGCA GAGCCAGTTT CACCACTCCC 540
AGCCCGCCAC CAGCTGGCCA GCGCGTCCTT CTCAGAGGTC TGGTCCCAGT CCCCTGGGAC 600
CACTCCTCTA AGTTTCAAGG TTTTGTTTTT GTTTTTGTTT GAGACAGAGT CTCACTTTTT 660
TTGCCCATGC TGGAGTGCAG TGGCATGATC TTGGCTCACT GCAACCTCCA CCTCCCAGAT 720
TCAAGCGATT CTCCTGCCTC AGCCTCCCAG GTAGCTGGGA TTAGAGGCAT GCACCGCCAC 780
ATCCTGCTAA TTTTTGTATT TTTAGTAGAG ATTAGGTATC ACCATGTTGG CCAGGCTGGT 840
CTCGAACTCC TGACCTCAAG TGATCCATCA TCCCCCACCT CGGCCTCCCA GAGTGCTGGG 900
ATTACAGGCT GAGCCACCAC ACTTGGCCAA GTTTCAAGGT TTTAATCATT GGACCTGCTT 960
CCCTCCGTTT GCCCAGCCTG AGAGGTGGTA 990
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