| Tag | Content |
|---|
EnhancerAtlas ID | HS184-32242 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chrX:49391530-49392540 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chrX:49391598-49391613 | TGGCCTTTGCTCTCT | - | 6.5 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGTCCAATT ACCGGCATCC TCAGCTCACT CCTGGGGTGG GGGCTTTGAG GCAGGTGAAT 60
AAACGCCTTG GCCTTTGCTC TCTGCATGAT CTTCAGGGTC AGGACCTGGG ACGGGCGATC 120
CCTCTGGGGT CATGAGTATG AAATAACGGG AGGTGGGGAT GGAATGGTCC ACTGGGGAGT 180
AGGGAGGTGG AGAAGGAACG GTTTGCAAGG CATTTGCACA GAAGCTTCCT TGATCGCACC 240
ACTAGGGGGC CTACGGAAGG AGGGGACAAC AAATCAAGGA TGGAAACATC CTGCCAGGCG 300
ATACCACTGC GGTAGGCAGA GACAGAACAG TCAGCTCTGG GAGGCACCAC TGGGTAGGGG 360
GCTTGGATCA AACCATTGTG TGTGTTGGGG GGACTCGAAG GGCCGCTTCC ACCCCATGCA 420
AGTGGTTGCA GCCCAAGACT CTGAAGAAGG CAGGAATCAC GCTACCTTGA CTGTCCGTAG 480
CTCACACCCA CCCTCTCGTT TCCCATCCCA GGCAGGCACC AGCTAGCATG ACAGGCCTCC 540
ACCTCTCCTC GGGTCCAGTC CCAGCTCCTT GGGCACCGCC TTCTTTGGCT TTTTGACTTT 600
GAAACTGTGG CTTGCGCTTG CAGGGGCACG TGATTGGATC CAAGCAGAAG GGAGCGGGCT 660
GCAAGGCTCG TTCTCGGATC TGACTGGTCA ACGCGAGCTT TCATTTCTCC TAAGCTTTTT 720
CTGCGCGCAA AAGGGGCAAA CTCCCGCACC TCAACTCGGT CGCGCGCCGA CCTCCAATTG 780
GCCGCTGGTT CGGCGCAGGC GCAATGGTTG CTTGGCCAGA GTTCCGGGCT GCGGTTCCTG 840
GGAATTTTGG GATGAGAAGA GAGATTCGAA TCCTGTCTCG GTGCCTCGAG ACTGACATTT 900
GTCAAAGGGG CCAAAGATAG TAAATCCTGT AGTAGAATTC ACGGAGATCA CTGGCTTGTA 960
ACAGCGTTCT GCCTCTTAGT GCACGGGTGA TGGGGGTTGA CTTCATGTAT 1010
|
