Tag | Content |
---|
EnhancerAtlas ID | HS037-39476 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr9:2199890-2201270 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Sox3 | MA0514.1 | chr9:2199946-2199956 | AAAACAAAGG | - | 6.02 |
| | 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 |
GH09I002200 | chr9 | 2200292 | 2201190 |
| Enhancer Sequence | AAACAAAAAA CAAGTTACTT ACTTAATACT CCCGTTCCAA ATAGGAGAAA TTGGCCAAAA 60 CAAAGGGGTT ACAGGACCCA TGCAAGTCCA AAACCCAGCA GGATAGTCAT TAAATCTTAA 120 AGCTCCAAAA TAATTTCCTT TGACTTCATG TCTTACATCC AGGCCACACC AATGCAAGGG 180 ATAGGCTCTT AAGGCCTTGG GCAGCCCTAC CCCTGTGGCT CTGCAGGGCT CAGCTCCCAT 240 GGTTGCTCTC AAGAGCTGCC ATTGAGTACC TGTGGCTTTT CCAGGTTCCT GGGGTCTGTA 300 GAACAGTTGC CCTCTTCTCA CAGCTCCACT AGGCGGCGCC CCAGTGGGGA CTCTAAGTGG 360 GGGTTCCAAT CCCACATTTC CCCTCTGCAC TGCCCTAGTA GAGGTTGTCC ATAAGGGCTC 420 TGCTCCTGCA GCAAACTTCT GCCTGAACAT CCAGACATTT TCATATATCC TCTGAAATCT 480 AGGCAGAGGC TCCCAAGCCT CAACTCTTGC CCTCTGTGTA CCTGCAGGCT TAACACCACG 540 TGAAAGCCAC CAAGGCTTAT GGCTTGCACC CTCTGGAGCA CCAGCCTGAC ACGTATCTGG 600 TGCCCTTTTA GCCATGGCTG GAGCTGGAGC CCCTGGGATG TAGGCAGCAG TATCCTGATG 660 TGGGGCAGGG AATCAGGGCC CTGGGCCTGG CCTGTGAAAT CGTTCTTCCC TCCTAGGCCT 720 CTTGGCTGCC ACAAAGGTCT CTGAAATGCC TTCAAGACAT TTTCTCCATT GTCTTGGCTA 780 TTAACACTCA TCTCCTCTTT ACTTATGCAA ATTTCTGCAG CTGGTTTGAA TTCCTCCCCA 840 GAAAATGGGT TTTTCTTTTC TACTACACGG TCCCGCTGCA ACTTTTCTAA ACTTTTATGC 900 TCTGCTTCCC TTTTAAATAT AAGTTCCAGT TTCAGATCAT CTCTTTGTGT ACACATATGC 960 ACATATGCTG TCAGAAGCAG CCAAGGCACT TCTTGAATGC CTTGCTGCTT AGAAATGTCT 1020 TCTGCCAGAT ACCCTAAATC ATCTCTCTCA AGTTCAAAGT TCCACAGATC CCCAGATCAG 1080 GGGCCCAAGC CACTAGTCTT TTTGCTACAG TGTGGCAAGA GTGACCTTTA CTTCAGTTCC 1140 CAATGTGTTC CTCAGAGGCT TCATTTGAGA CCACCTCAGC CTGGACTTTA TTTTTTTTAT 1200 TTTTATTTTT ATTTTTTATT TTTGAGAGCG AGTCATGCTC TGTCACCCAA GCTGGAGTGC 1260 AGTGGCGCGA TCTTGGCTCA CTGCAACCTC CGCCTCCTGG GTTCAAGTTA TTCTCCTGTC 1320 TCGCCCTCCT GAGTAGCTGG GACTACAGGT GCGTGCCACC ACACCTGGCT GATTTTTTTT 1380
|
| |
|
|
|