| Tag | Content |
|---|
EnhancerAtlas ID | HS184-16525 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:86181650-86182630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr2:86182140-86182152 | TTCTGTTTACTT | - | 7.22 | | FOXP2 | MA0593.1 | chr2:86182141-86182152 | TCTGTTTACTT | - | 6.32 | | Gata1 | MA0035.3 | chr2:86182306-86182317 | AGAGATAAGGA | - | 6.02 | | Nkx3-2 | MA0122.3 | chr2:86182326-86182339 | CTTAAGTGGTTAA | - | 6.5 | | ZNF263 | MA0528.1 | chr2:86182592-86182613 | CTTCTCCGCTCCTCCTCCTCC | - | 7.32 |
|
| | 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 |
| GH02I085954 | chr2 | 86182101 | 86184793 |
|
Enhancer Sequence | CTTCCCTCCC AGACAGAGCA ATGCATGCTT GCCACCTTGA TGGTGCAAGC ATCACTAGAT 60
CTGAATTTGA GGTGAGGAAA TTCAAGGCAA CCACAGTACA CGTTGTCCCC CGTCGGACCC 120
AGGGAAAGGC ACTTGAGACA GGAGCAGGCC TGTGGTGCTC TTGGCACAAG GCAAAATGGA 180
GGAACAGGGT GGTGGTGGCA GGGTGCCCTA ACCTGGTCTT GGGGGGTTTA AGAAGTTCCT 240
GTTTTGAAGT GTTTCAATAG CCAGTGAGAG TGAGCCATGG AGAATAAAAA TGTACAAGTA 300
AACAGTCGTT CCACTTATAC ACAGTTAAGG ACTTGTGGGA GGGGGGCAAG TTCCAGTTTT 360
TCAACATAGT TTCTGATTGA AAGTGCCATT GTAACCCTCA TTATGGCCAC CAGCTTAAAT 420
TTGAGGGCTC CCGTTGCCCT GGAATAAACC CCTAGTTTTC AGACTTCCTG GAGCCACCAT 480
CCTTCATCTC TTCTGTTTAC TTTTTTCTCT TCTGTTTAAA TTGGAGGGCC ATTTATGCCC 540
TCCCCTTCTC CTTGCTGAAG TTGTGTACAC AATGACTGGC ACAGAGGTGT TTCTACCTGC 600
ACAGGCTCAT GACATTCTCA CAGTCAGCCC ATAGATCGGT TTCTTCTCTC AATCTCAGAG 660
ATAAGGAAAC TGAGGTCTTA AGTGGTTAAG TCATTTGTCC CAGGTCGCCT GGCAGCAAGT 720
TGTACCCACA GTGCTAGCCA ATGTCTCGCT GACATGTGTG GGCACCACAT GGGCCCATCC 780
ATGGTCAGGG ACTTTTCCTG GCTCTGCCCA TAGCATCCTC ATTCGTCTTG TTTGCTTATA 840
TGTTTCTTAC AACTACCTCA CAGCCTCAAC CATGTCTTTA AAATTATTCA ATTATTCATA 900
GAGCTGGATT TACAAGTCTA GGTCTCCTTC GTCAGGGGTG GCCTTCTCCG CTCCTCCTCC 960
TCCTCTCTGG AGGTGGTTTC 980
|
