| Tag | Content |
|---|
EnhancerAtlas ID | HS051-14286 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:41194790-41195940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr19:41195439-41195457 | GCTTGCTTCCCCCCTTCC | - | 6.44 | | PLAG1 | MA0163.1 | chr19:41195645-41195659 | GGGGACAAAGGGGG | + | 6.08 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATTAATACAA CCTCAGTCAC ACACTCAGAC ATGGTTCTGC ATACGCAACC ACTGTCATAC 60
ACAATACTGT CACACAACCC CAGTCACACA GATACAATGT GACTTCAGAC ACAATGGCAG 120
TCACACAGGC AGAGTTGCAC AGACAGGTGT GTGTCACTCA CGTATATAAA ATCAGGTAGA 180
GACACAACTA TAAACATTGT CAGTCACTGG GAGGGTCACA CATGCACATG GAGCCATAGA 240
CAACTCCACT CACACACAGT CACAACTCCA CCCACGTCCT GTCAGTCACA CGCATGCCCA 300
CCCCCAGACT CAACACATAC TGTCACATAC CCAGTTATAG TTACCGAGGC ATACAAACAC 360
AGGGTCACAA AAGACACAAT CACAGACAAC CACAGTCACA ACCATGCACA CCTCCAAACA 420
CAGACAGACT AAAAAGTACA GGATTCTGCA CAGTGAGCAG CTGTCACACA CACATACACA 480
GTCACACAGA TACTAGGGTC ACAGACACAA TCATAGACAC CACCACAAGC ACACACACAC 540
GACACAGGAT TCCTCAGTCA CCAGCTGCAG CGTACGCGTG CACACACACA CACACATACA 600
CAGCCACAGT CACACAAACA CAGGGCACAC TCCTAGCCAC CTCCCCATCG CTTGCTTCCC 660
CCCTTCCCCC CAGGTACCAC ACACAAAGCC GCCGTCACCG TCACCGCAGA CACTGCAGAC 720
AGACAGGGCT GCACCCGGTC CCTGGGGAGC CGCCCCCAGC CCAGCCTGTA TCCTGGAGCC 780
TGAGGGCCAG GTCCAGGAGG GGGAAGCGGT GCATTGTCTG CGGGTGGGGC CACTCTTGGA 840
CAGCTGGGCA GCCCTGGGGA CAAAGGGGGT GGCCTAGGGA TCCTGTGCCC TGGGACCCAT 900
GACCAAGCCA GGGGGTGGAG GGATTGGGGG TTGCCTGAAA TTGTCCTTAT TTTATTCAGG 960
CTGGGGTGGG GTGGAGTCCC AGGCACAGGG ACCTTGTTTT GAGAAGTGGC TGTGCCTGGG 1020
ACTCCGCCCA AGGATTGGGG GGATGCTGTG CCCAGGGTGC CTCTGAGACC TGGGGGCAGG 1080
CTGTGCTTGG AGTCCCCCTA GGCCTTGGCG TGGTGGGAAC GCTGTACCCA GTGACCCCAT 1140
CCTCGAGACC 1150
|
