| Tag | Content |
|---|
EnhancerAtlas ID | HS184-18001 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr20:31693610-31694280 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr20:31694172-31694193 | CTTTTCTTTCTTTTTTTTTTT | + | 6.41 |
|
| | 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 |
| GH20I033105 | chr20 | 31693101 | 31693785 | | GH20I033106 | chr20 | 31694001 | 31694150 |
|
Enhancer Sequence | GGTCAGGGGC TGGGCTGGGC TGACCTGGGA GGGAAGAGAC GGAGCGTCTT GCCTGGCTTA 60
ATCACTAAGA GTGGTGTGAA CTTGGGGGCG AGTCTTTTAA TCATACTGAA GTGCAATTCA 120
CCATTTTCAA AATGAGAGCT TGGACAAGGT CCATAGTCCC CAAAGTGAGC TCCGTAAAGC 180
AGTCCCACAA AATACCCTGC AAAAAGCGTT CCATGGCCGA GCAAGTTTGG GAAGTGCTGA 240
AGATACTCCT GCAGGGTAGA TTCACAATGT CCTTAGCTTT TTGAAAAGTC CTGCTGGAAT 300
AGAGAAGTCT GTTAAATTTC ACTTAATTTA CTTCCCCCAT CCACTCTTTC CTACCCCACT 360
TCTTTTTCTC TCTTCCTGCT CTCTTTCTAG AACAGTAATT AGCAGGTTTA CTTAGGCTCT 420
GACAATCTGA AAACAAACAG CACATCCCAC GGCAGAGTCA ATGGCTAGGG CTCCACGTGC 480
ACTTTCCATT ACTTCACTCG GCAAACATTT GCCATCTCCT CTATGACTGG GCGAAGGGCT 540
GGGTGATGCT GGGGACACAG CTCTTTTCTT TCTTTTTTTT TTTTTTGAGA TGGAGTCTCA 600
CTCTGTGGCC CAGGCTAGAG TACAGTGGCA CGATCTCGGC TCACTGCAAC CTCTGCCTCC 660
CAGGTTCAAG 670
|
