| Tag | Content |
|---|
EnhancerAtlas ID | HS101-34128 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:1827260-1828680 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr5:1827980-1827991 | GCTTCCCGCCC | - | 6.02 |
|
| | 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 |
| GH05I001827 | chr5 | 1827743 | 1828695 |
|
Enhancer Sequence | TGTAAATGCA CGAAGTCTAA TAACATGAGT GAGTCATAAG AACTCTAAGA ACAGCTTCAT 60
CTCCATGTAG GGGACCTGCT TTCGGGCTGG TCTTGTCAGG AGGTAACAGT AAGAAAGATT 120
CAAACCAGGC AGATCCGGGA TTGAAAACTG ATCCAGCCTC AACTTCCTGG ACTATTTTTT 180
ATCTACCTAA ACTTCTCATG TCTTACAATA ATTACGTTTT CTTTTTTACC TTTCTTTTTG 240
GGGATTTCTG GCACTTTCAT CATTTAGAGG CTCTGGTGGA AGAGCCAGCT AGCTGTTCAC 300
CACTGTGGAG AGGACTTTGA AGGCACGGGG GCCACGCCTG GCATCCCCTG CCCCATCACG 360
CTCCTCGCGT GGAGCTCTGT TTCCCAGCTT GACTTTGTGC CTAGATGAAC CGGCTGAAGG 420
ATGCGTGACT TGACTGCGTA GATGAACCGG CTGGTAGCAC ACTGCGGCTC CTCTTATGGA 480
AACATGCTCC TGGCCCTGTG GCCTGTGGGG CCCCCCCTCC CCGGATGTTC GCATCATCTC 540
GCCAGGTCAG CTCAGCAATG TCGTCTAACA GCCGGGACTG ATGTGGTCTG CATGGCTGAG 600
CCCCCCAGAT CCGAGTGTTG AAACCCTCGG TGGGGTTATG AGGAGGCGGG TATGAAGTGG 660
TATGAGGAGG AGGGTCCCTC AGGAATGGGA TTCGTGCCCT TATAAAAGGG ACTCCAGAGA 720
GCTTCCCGCC CCTTCCACAA AGTGAGGACA CAGCGAGAAG GGGCTGTCCG TGAACTCGGA 780
GCTCTCAGGG GACACGAAAC CTGCCGGAGG CCTGATCCTG CGTGTCCTGG GGCTCTCCGT 840
GGGCATTTCC TGTCTGCGTG GAGAGGCACA GCCGCAGCGG GAGCCGGAGC AGGTGGTGTG 900
CAGGGAGAGG CGGAGCCGCG CGCAGGGAGG GGCGGAGCCG CGCGCAGGGA GGGGCGGAGC 960
CGCGCGCTGG GAGGGGCGGA GCCGCGCGCT GGGAGGGGCG GAGCCGTGTG CAGGAATGAG 1020
AGGGGCGGGA GAGCCCGATT TCACTGCTTG CGCCCTTGGA TGCTGCTTGA GCCCGGTTGT 1080
GGGTTCTCAT TCTGTTAGGC AGATTGGGCT TGGTGTTTAT CCCATTCACT GGATGGAATC 1140
CTGGTGGACT GAGGTCTGGC CCCCGCTTAG GAATGCGGAG ATGGGAGCAG GTTAGTCCTG 1200
TGCTGGCTCC GAGGTCGCCC TGAGGTCGCG CCCTGGGCTG TGGGCTGCCC CAGCTGCTTG 1260
CTTCCAGGAG CACCATTTTC CCTTGCAAAG AAAGGACGCC ACTGTGGTTA TTGCACGTGG 1320
CTGTCGCCAG ACGTTTTCTG AAGCCAGATG AAGTGAGCCC ACTACTTTGG GGAGATCAGT 1380
CAGCTCTGTT TGTCGTCAGA ACATCTGAGC ATTCAAACAA 1420
|
