| Tag | Content |
|---|
EnhancerAtlas ID | HS184-16761 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:121310300-121311210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr2:121310999-121311016 | GTAAGCTCCGCCCACTC | + | 6.02 | | SP8 | MA0747.1 | chr2:121310710-121310722 | GACACGCCCACT | + | 6.37 |
|
| | 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 |
| GH02I120550 | chr2 | 121308041 | 121311056 |
|
Enhancer Sequence | CAAAGTCCAG TCAGGCAAAC TCTTGCCCTT GTTTCCATTA AACACATATC TTCATCTTTT 60
TCGTACTTTT AATAATAGCA GGAAGTAAAT CTGGCCATGT AATGTGAGAA AGGTAATAGT 120
CCCAGGTCAG GAAATCCTGT TGCTTGGAGT CTCTTGGGAA TGTTAACTTT CCCACTCTCA 180
CCCTACCGGG ATCCTGACCT CCTGCACAGT TGGCTTCCTC AGGCAAAACT GGGCCAGAAA 240
TTCTGGGCCG TTGGCCAGAG TCAGACCTTC GTCCTCTGGT AGCGTCCGCT GGAAAAGAGG 300
AGGCGAGAGT CACCAGGAGG CTGGCCCCAC TCGCAGGCCC TGCCCTCTGC CGGTGGGTCC 360
TATGGATGAC ACGAGGCCGC ACTGGGCTGG AGAAGAAGAG AAGCTCCTGA GACACGCCCA 420
CTCTGCAGAG GGAGGCAACC GCACAGGTAA TCCATCCTCT CTAGGCTTTT CTGTTCCCGT 480
GCAGTAAGTG AAGTGAAGCA AGGTGAAGAA GTGAAGTGAG CATTCAGGAC ATGAATTGGC 540
ACGTGGTCGG TGCTAGAGGA GCTGGCAAGG TAGACTCTGG TCTCTTCTGT GGTGCTGAAG 600
CTGGGGAAAT AAGGAACAAT CTCATCCACA GGCCAGGCCT CCGGCGTGCT CGGGAGCTAC 660
TGACGGAAAC TCCTAGGGAA CTTCCCTTGT GGAAAGAACG TAAGCTCCGC CCACTCGGGC 720
AGCTGAGGCC ATTGATTCGT TCACTCATTC GCTGGACTAT TTCTCCAGCC CATGATCTTA 780
TTTTATAACA AGTACAACAT TCATTCATTT TTACACATAA TTACCTCACT TATTCCATGG 840
AAGAACCCTG CAAGTTTGAT GGTTGTAGCA TGCAATTATC GATGGTTGCT CATGCAATTA 900
TTCATTCCTT 910
|
