| Tag | Content |
|---|
EnhancerAtlas ID | HS184-24848 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr5:138897160-138898140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | + | 6.02 | | NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | - | 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 |
| GH05I139517 | chr5 | 138896810 | 138898710 |
|
Enhancer Sequence | TAAATAAATT TCCTTCCTCC AGCTGCAGGG CAAAAAATGG GTTGAAGAGC CGGACTGGTG 60
GTAACTGGTG TGGCCATCCA GCCTGGAGTC GATGTTGGCA TGAATGAAGA CACAGGCAGT 120
TGGGACAGAG AGAAGCGAGT GGGATGTGGA GGTGACCCGA TGAAATACTG GCCCGGAGAT 180
ATGAGGCATG AGGCGGGGAG CACGAGGGTG TCGAAGGGCC AAAATGTGGT AAGAGAAGCC 240
GGAGGAGTGT GAGGACAGGT GGAAGGGATC CAATGTGGGA TCTAAGGGGT CTGAGACCAC 300
CGTGGCCGCG GGAGGCAGGA GAAGGTACCG CAGAGCTCCC GGTGATGTGT CAGGAGGCCC 360
TACACTCGCG CGTGCACTGG CTCGCAGTTT GGACAGAGAC CCTACAGGCC AGGCCGCAGC 420
TGCGCCCAGA CCACCCCCAG CGGGTGAAGA CTGCCGCGGC GGCGCAGTTC CCGGCATGCC 480
TCCGGCCGGT GACTTCATCC GGCCCGGGGC CAAGGCCCGG CCTCCGCTAG AGGGCGCTGC 540
TCTCAGCAGC CGCGCCGCCC GGATGGACTC GCGCCAGAGT AGGACAAGAG AGGCAGGCGG 600
CGGCTGCTCC GTGCGGCTCC CACGCCTCTC GGGCGGCAGG TCCTGCCTCG GACCTGGGAC 660
CACTGGCTGG CGCCTGTGGC TCACATCTCC ACGCCTTTGC CCGCTCCTCC CAGGAGCCCG 720
AGTCAGAAAC CTGTGCTTCA CCCTCGAGAG CGCTGCCATC CTCCCCCTCA ACCAGACGGG 780
CATGGCGTCT GGTTGTCCGT CCTGTCTTCT CATCGTCTCA GAGCCCTTCC CTGACCCCTA 840
CCCTCTCTCA GACCAACAGG ATGATGACAG GAAGAGGATC CAGGACCAAC TCCTAGCGGT 900
GACCTTGAGA AAACAATCTC ATACCCCAGT TTCCCTTACA ATGCAATGGA AATAATACTA 960
ACAACCCTGG AAGAGTGTTG 980
|
