| Tag | Content |
|---|
EnhancerAtlas ID | HS048-33080 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr6:161789640-161790790 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr6:161790578-161790589 | GATTGTGCAAT | - | 6.32 |
| | | 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 |
| GH06I161368 | chr6 | 161789833 | 161791340 |
| Enhancer Sequence | AAGACAGTGG GAGAAGCCAC CCAGCCCCCC TCCCCTCACT GCAGTGGCTC ACCTGCCCTC 60
CACTTGCCTG CTTCCCCTGG CACCAGCACT GCAACTCCAC TCCCAGCTGC CCACCCGCCC 120
TTCTGCCCTG GGCCATCGCT GCTGCCTGGC CGGTTCTCCC TTCCCCAACC TGCCGAAAGT 180
GCTTTCAAGA AGGACACCAG GAGGCCACGG CTGCCAAAGC TCATGCCCTT TCTTTGTCAT 240
TGTCTCCAAC TGTCCCACTG CACCTAACAT GTGGGAAAGG GTCACCAAGA AGGCCCTTGG 300
AGTTCCTGCC CTTCTCAGCA TCACAGCTCT TCCTGTGCTT CCTATCCTCA CCCAGCGGAT 360
CCACGGGGAG GGAGGGGAGT CCCAGACCCA GTGACTGCTG CCACTGCTGC CAGCCCCAGG 420
GACCTGGGGG GCAGGAGAAG CAGCTCTATG ACACCCCGGG AGTGGGCGGT GCCCAGGCCA 480
CTGGTTTAGA CCTTTGACTG CCACTTCCGA GAGGGGATTT CTACCAGGAG GAGCACATCT 540
TTGCTTTGCA TCCTTCATGA GTGTCTTAAT GCTGATGTTT AAATCCTTCT GGAGTGATCT 600
CAAGCAGTGG CTGGGTGCCC ACAGGTTCAA GATCACCAAA GCGATTCTAA AAATGATCCC 660
AAGGCTTGTG TCCAGACTCT GGAGATTGGG ATTCAGTAGG TCTGTGGCGG GGTACAGAAA 720
TTAGAATCCC TAAAAATGCC CTAAGGGGTT GCGAGGGGCG GGAGGTTTGG GAACCATTCA 780
TCCTCTGGAG GGCGATTCTC CCTTTGCGCC TGAAGAGGAA CATGGTGAGC TGGGTAACTT 840
ACCCTCTGTT CCCGCCTTAG TCATCAAGCT CTAAAGCAAT GCCTGCTTAT TGTGTTGCCA 900
GGAGGGGAAG GTTTTGTTGT GATTCAGCAT CACCGCCCGA TTGTGCAATA AAGTGTGGCT 960
CTCACGGGGC AGTGTAACTG TTAGGTAATT GCATAGAATT CTGTGCCTGT CTACTGCTCA 1020
CCCGTGGCAG GAGGAATTGC ATGCATGCAT GTGTGTACGC ACGCGTGGTG GAGGTGGGGG 1080
TGGAACAGGA CAAGTCTCTC TCCTAATATA CTTCATGGCT GAAAATAGCG ATTTCATAAA 1140
TATATATATG 1150
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