| Tag | Content |
|---|
EnhancerAtlas ID | HS184-17361 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:218375440-218376140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr2:218376018-218376030 | TGCCCCCAGGCA | - | 6.04 | | RUNX1 | MA0002.2 | chr2:218375997-218376008 | GTCTGTGGTTT | + | 6.62 |
|
| | 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 |
| GH02I217510 | chr2 | 218375208 | 218377380 |
|
Enhancer Sequence | GTGTTCTGTT ACAGTTTTCT TCCACCTCAT ATTTGATTTC GGTAGAAGCA TTTTCATCTG 60
CTGGAATGTT TTAATTCCTG TTTTTTTTTT TTAAGTTATT GGCCTTGTAT GAGTGTCGTC 120
TGCCATTTTC TATTCATTTT TAGATGTTTA AATATACAGT TGTAGATAGG CGCAGTCATG 180
GCGTTTGATG ACTGACCATG TTTCTTAGTT CAAGAGCACC CTCTTCTGTT GGCATGGGAA 240
AGTGTAGTTT CTTCACTGAC AGCAGCTTTT GTGGGGGAGG GGTTGGTGTG CCTTCTGAGC 300
TTTGAGATCC ACTTTTGCTT GGTAGGACAC TCTTTCTTCG TTCTTCCCCT CCACTCAGAC 360
GCCTCTGAAG CCCTGCTGCC AAGCGGCCCC CTCTCCTCCA GAAATAGTGC CCTTTCCACA 420
GGCCAGCCCA GCCCCATGGG CAGTCAAACC CTCCCTTTCA TTCGCATCCT GAAGCAGCGC 480
CCTCAGGCTA CCTGGCCTGT GAGTTGTTCA AGCTATTTCT CAGTCAGGTG CGAAGTTCTC 540
TTTCTGGAGG TTATTTTGTC TGTGGTTTTG GACACTAATG CCCCCAGGCA CCGTTCTCCT 600
TTTCCAAACA ATCTTCAGGC TGAGTCTTTG CTCCAGCACT TGCTCTGGAG ACCACCTTGA 660
GCCTGGGAGT TTACTCCCTT ATCTGTAGGT AATTTGAAGT 700
|
