| Tag | Content |
|---|
EnhancerAtlas ID | HS184-17695 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr20:2457410-2458530 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr20:2457535-2457554 | TGGTGCCCTCTACTGATAA | - | 6.06 |
| | | 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 |
| GH20I002477 | chr20 | 2457481 | 2457630 |
| Enhancer Sequence | ACAAGAGCAA AACTCTATCT TAAAAAAAAA AAAAATAGAA AAGAAAAAAA ACAGGTACTC 60
TCCAGGACCT GGTGAAAGAG CCACCTGACC CAAGAAAGAG GACCCTTCTC CCTGCAGTGT 120
TGCTCTGGTG CCCTCTACTG ATAAACCTTA TGCCAGCTGG CAAAGGAAAC ACGTAAAGGG 180
CCCAGATCCA TTTTCACAGA CCAGGCAACA CAAGAATTTG AAGCTCAAAC AATAAGTTGA 240
TAATTGGCAC AATTTCACAT ACACACACAG ACGTACTCTA CCACATAGAA AGGCACAATC 300
CTGGACGCAG ATGGGAAAAA GAGGACACCC AGTTTGACTT ACCCTCTAGA GAAGAAACTA 360
TTCTTATGGT AAACACAGAT AAGAGGGGTG TTGACTTTCT GCTTGGATTC CTGGAGTGGT 420
GAGAACTTTT TCTCTTTTGC AAATGTGTCT ACTGTTCGAA AGCTGTGTTT GTGAGAGTCC 480
TCTTTTACAT TCTTGCCTGT CTTCTACATT CAGGCAATCA CCAAGTGCTT TGGAGACAAA 540
CCCTATGAAG TCTATCTTCT CTTTCAGTCC ACTCTGCTGT TGCCATAGCT TGTTATAAAT 600
TTTGCCTGGA CAACTGCAAT ACTTCTGACT TCCCAGATTT TTACTGGTCT CAGTGCTGTT 660
TATCACACTT CCTTTCATTC TCTTAAGTTT CCTCTCGGAT TCTCTGCAAT ATCTCTTCTA 720
GATCTCCAGC CCCATATGAA ATTCCTTTGT CAATATATTC AGCAGAAAAT CTGATTGGAA 780
ATGTTTTCAT ATTCTTACTA GCTATGTCAA GTGTACCTCC AATACTGCAC AATTTATTTA 840
CTCAAAGATT TTTACAGGTT GAGCCTTTCT CTCAAGACAG GTGACCAGAT GCAGTGGCTC 900
ATGCCTGTAA TCCTAACACT TTAGAAGGCC AAGGTGGGAG AATTGCTTGA GCCCAGGAGC 960
TTAAGACCAC CTGGGTAACA TAGTAAAACC TTGTCTCCAT TAAAAAAAAA AAGACAAGCC 1020
ACTTTTAGTG GCCGTGACTT AGGAGAAGGT ACAGGCCCTT CTTCTTTAAC CTAGGTTACA 1080
GGTTACTAGA ACAGACACAG AAGAGAGGAA GCTAAGACAA 1120
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