| Tag | Content |
|---|
EnhancerAtlas ID | HS184-11956 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:1950010-1950840 |
Target genes | | Number: 29 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr16:1950740-1950760 | CCACAAACCAGCCACAGACA | + | 6.44 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH16I001900 | chr16 | 1950241 | 1950410 | | GH16I001901 | chr16 | 1950481 | 1950630 |
|
Enhancer Sequence | TGCTTGAACC TGGGAGGCAG AGGCTGAAGT AAACCGAGAT CGCACCACTG CACTCCAGCC 60
TGGGCAATAG AGTGAGACCC TGTTTCAAAA AAAAGAAAAC GAAGGAAAGA AAGGGTAAAG 120
CACCTTTGGT CCAAAGAGGA TCTCAGGGAA TCACAGGAGG GTTGTTTTGC CATTTTGGGG 180
GGGCCTGAGC CCTGGAGGCC AGTGAGCACC AGAACACCGG GCGGGGCAGC AGCCGGCTGT 240
GCTGCTGGCT GGAAGCACCA GGTGAGGCTG CAACCCACGT GTGCACTGAA AGCTCCTGGC 300
TGGCAAACGC ACACTCTCAT GACTGACTGT GAACCATTCC TGACAGTTGT GATGTGTTCC 360
TGATTGCACT GTGTTGTTCT TAGTCGCTTT GTAAATAGAA CCTGTGTGTG CGTGCTGTGC 420
AGGTGAACAT AGATGGTGCC TGTCCCTGCG GAGAGCAAAA GAATTAAACC TCGGAGTTTG 480
AGAGACATGC TCTTCTCCAG AACGCAGCCC CGGCGGCAAC CCCAGGCGGC CGAAGGGACA 540
TGGCAGCAGC AGGCTGGGCT GACCACAAAT ATTTGCACAG GTGAACACTT TAGAAAAGGA 600
AGTCAAATGT AGCATGCGGG TGGCTGGGGA GGAGAGGATG AGCCTCATGG AGCCCCACAC 660
CCTGAGCTTT TGCAGGGAGC AGCCACAGCC TGTGTTCACA CACAGACCCA GCAGCCAGCC 720
CCTGTTCACC CCACAAACCA GCCACAGACA GGCCAAGGTC ACCCGTGGCC TTGTGGCGTG 780
GAGCCCGGGG TTAATTCAGA CCCAATGGCC AGGCACAGTG GCTCACGCCT 830
|
