| Tag | Content |
|---|
EnhancerAtlas ID | HS184-10793 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr14:102947910-102949080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr14:102948878-102948893 | TCACCTTTGACCTCC | - | 6.58 | | Nr2f6 | MA0677.1 | chr14:102948878-102948892 | TCACCTTTGACCTC | - | 6.59 | | RREB1 | MA0073.1 | chr14:102948194-102948214 | CCCCCAGCCACCCACCTCCC | + | 6.94 | | Rxra | MA0512.2 | chr14:102948878-102948892 | TCACCTTTGACCTC | - | 6.65 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_07774 | chr14:102947499-102948610 | Brain_Inferior_Temporal_Lobe |
|
| | 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 |
| GH14I102481 | chr14 | 102948221 | 102948390 |
|
Enhancer Sequence | AGCCTGGGCA ACAGAGTGAG CCTCCATCTG TAAAAGAAAG AAAACAGAGT CACATGTGAA 60
AATCAGTAGG TTGACATGTC AGTGGGTTCT ATAAGATGTG CTATAAGAAA CATGTCTCTC 120
CTGCCAATTT TGCCCTCTCT GGAGAGTTCC TTTCAGTTCT TTTCGCTGCC TGTCTCTGAA 180
TGCTGCTTCG GGAGCTGTGT TTGGTCCCCT GACTTCAGGT GTTTCTGGTT GACTCTCTGC 240
GGGAAGAGAA GCATGCAGAG CTCTTGCATC CCCCGTCCCC CATTCCCCCA GCCACCCACC 300
TCCCTTCCTA CTTCCACCCT GCCAGAGCTG CAGTGCTTCC TGGGCACGGG CCTTGCTGTG 360
AGGACAGAGG AGCTCTTCAC AGCGGAGGCA GGGGATGAAT CACACCTGCA GTTCCTTGTC 420
TGTGTGACTC TTTGTTTTCC CTGGACTTGA TAATCATCTT GTTTGCTCAT CTAGTTTTTT 480
TTCTTTTTTT TTTTGAGACA GAGCCTTGCT CTGTTGCCCA GGCTGGCGTG CAATGGTGCG 540
ATCAATCTCT GCTCACTGCA ACCTCCAACT CCTGGGTCCA AGTGATTCTT CTGCCTCAGC 600
CTCCCGAGTA GCTGGGCTTA ACAGGCGTGT GCCACCACAC CCAGCTAATT TTTTGTATTT 660
TTAATAGAGA CAGGGTTTCA CCACATTGGC CAGCCTGGTC TCAAACTCCT GACCTCAGGT 720
GAGCCACCTG CCTTGGCCTC CCAAAGTGCT GGGATTACAG GCATGAGCCA CTACACCCAG 780
CCTGCTCATC TAGTTTTCTA AGTGCAGTTC CACACATTCA ATCCCAAACT CTCTGCCAGT 840
TGTCTCACAC ATTAGGAATG TGTCCTCTCC ATTTCTTCCC CCTGCAGAGA TCTCTCCTGC 900
ACCCTCTTGG CCAGCTCCAG TCTGGCCTCG TTCCTCTCTC TACCCGGGAC CCAGCTGTTG 960
TCCTAGCGTC ACCTTTGACC TCCCCTCATG TTAGAGCCCC TTTCTCCCGG ATCCCGGGTC 1020
TTCCTCTCTC TGTGTCTGTG TTTGTTTGGG TGGAGTTTAT CTTCCAGTCG GTTCCCAAGG 1080
AAGGGTTCAT GGTTGGTGAC TTTTTGGAGG TATTGCATGT CTGAAAAGTC TTTCATCTGT 1140
GTTCACCCTT GACCTTGCTG GATATAGCAG 1170
|
