| Tag | Content |
|---|
EnhancerAtlas ID | HS184-10858 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr14:105478270-105480040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr14:105478697-105478716 | CAGCCTGCAGAGGGCGCAG | + | 6.07 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 105478634 | 105479061 | | chr14 | 105479319 | 105479787 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I105012 | chr14 | 105478701 | 105478850 |
|
Enhancer Sequence | TCCTGCAGAA ACCAAGGAAG ACACCACTTA GCACACGGCA GACTCTCTGC GGACAGCGCC 60
CCTTGGATTT CGTCTGACTG CCCTCACTGT ACGCAAGGAG CAGCGACTCC GTAACTGGCA 120
GGGACTTGAC AGAGCTGTAA CTCCCTAACA GAGCTGAGAC GTGGAGCCCA GTGGGAGACC 180
CCCACCCCCA GATCAGCTGC CATCCTGCCT AAGCCAGGCA CAGTCACGTT GTTAGAAACG 240
ACAAACCTCT CAACTGTACC ACGACAGTGT TTTATAGCAA AAAAGATAAA TGAACTAAAA 300
ATAGGAGAAA TATATAAGAG AAATGTAAGT GTTCGAGAGC TTGGCTGAAA ATCTGTTTCA 360
AAAATCTAAC TGTGGTGTGT ACAAAAGAAG AGACCCTGGG GTAACATGAG ATTAATGTGA 420
ACCGTGCCAG CCTGCAGAGG GCGCAGGGCG GGGGCCGGAC AGGGCCGGGC ACACACACGT 480
ACCATTCTGA CTTCCCTCAG GATCCTGCCT CGGACAAAGT CACTTCTGCG TTCAGAAGAG 540
TTAGTGCCTT CCCCCTCAAT GCTTTCACTA AAAGCCTCTA TATGTCGCAG ACAGCCGGGC 600
TGGAAAGCTG TGCCACCAGG AACGCGCAGG GGAAGGACTG CAGGGCTGTA TGCTCATCCC 660
ATGCAGCGAG TGGTCTGTGT TTCGTGCACA ATTCTCCAAG GGACACAGGG TCTCCTGGCC 720
GAGCCTATGT GGCCCTGGAC AGTCCCTTGC TCCCACACCC GCCCATGCTG CCTGCCTTAG 780
GGATCACACC CATTCCTTGG CTCCCCCCAC CCGCCCCACC AGTTCATTTC TCCCAAGGTG 840
CACAGGCTCT GCCTGGCTGC TTTCTACTTG ACATCTCTCA GGTCAATGCC CTCCACTCGA 900
GAGCTCTGAC CAGCCCGTAC AACCATGGCC TCAGGGGCCA CCTCCCCTCT CATCTCAACT 960
CCTTTCTCTT CAAAGGAACC AAAACATGGC AGGGTATGTG TGTGTCCGGG GCAGGGGGGG 1020
TGGGTTCCTC ACCAGTGTGT TGTGGCAGCC CAGAGCTGGC CAAGGCAGTG TTTCTCGGCG 1080
TATGCCTCAG CACTGGCGCT GTTGGTTGAA GATGCAGATT CCTGGATCTT ACCCCAGACC 1140
TGGGCAACTC CGGGATGGCA CCTAAGGCTC AGCCTTGCTG GGCAGGTTCC ACTAAGACGC 1200
ACAGCACAGA TGCACTAGAT GGACATTGGC CATGTCTACT CTCAGAAGTA CAAGTCTGTG 1260
CAAACTGTTT TTTTTTTTTT TTAACTGATT CTAAATTGGG ACATCTCTGG GGCACTAAAG 1320
GCAGAGCAGA CAGGAGGGTG GGCTCTGGCT TTTGACAGAT GCCATTCTGA GCCAGTGCCG 1380
CCTGCGGGGA GCTGGGAGGA TGACAGCTGG CTCAGGGCCA TACTGGCCGG CAGAGTCTGA 1440
CAGGACAAGC ATCTCACGCA TGATTAAGTT TCTCTCTTCT CATGCTTGTA ATGTAGTGAA 1500
ATATTATTTC AAATAATTCA AGTTATGCAT AAATAGGGTT ACAATCTTTT GAATATGCAA 1560
ACTTTGGAAC TTCTTTTTCT CTTAGTCAAT CTGATGGCTC CCTGTGACCA GGGTATACCC 1620
AGGTGCTCTT GGAAAGCTGG CGTATGGGAG GCACATGCTG TCTCTGCTCG GGGTCTGGAG 1680
ACCAAGGATG GGAAGTTTTG CAGTGCGGGA GAACTGGCTG CCAAACATAC CCCTTCCCAG 1740
GAGCCCCTCT GGAGGCTCCC ACCTGCTGGT 1770
|
