| Tag | Content |
|---|
EnhancerAtlas ID | HS051-23296 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:31565760-31566850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:31566522-31566541 | GCCTGCCCCCTGGTGGTCA | - | 7.28 | | EWSR1-FLI1 | MA0149.1 | chr6:31566619-31566637 | CCTTGCTTGCCTCCTTCT | - | 6.16 | | HNF4G | MA0484.1 | chr6:31566134-31566149 | TGAACTTTGAACTCC | - | 7.08 | | Hnf4a | MA0114.3 | chr6:31566132-31566148 | CTTGAACTTTGAACTC | - | 6.65 | | Nr5a2 | MA0505.1 | chr6:31566126-31566141 | CGTGGCCTTGAACTT | - | 7.11 | | Rxra | MA0512.2 | chr6:31566134-31566148 | TGAACTTTGAACTC | - | 6.72 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH06I031598 | chr6 | 31566041 | 31566378 | | GH06I031599 | chr6 | 31566421 | 31566610 |
|
Enhancer Sequence | TCTTAAACAC CTGGCCTTAA GTGATCCACC CGCCTTGGCC TCCCAAAGTG CTGGGATTAC 60
AGGTGTGAGC CACCACACCT GACCTAATAT ATGTTTTTTC CTTTGTATCT GTGTTTCTAG 120
CTCTGTGTCA CAGTACTTTT GTAGACTGTC CAGTTCCCAC CCATCACTGA AGTAATTCAG 180
AGCTTTCTTT TGGAGAAGCA GTCATCTCAT GGTTAAGAAT GCTGGTTTGG AATGAGTCTA 240
GGTTCAAATG TCAGCTCCCC CGCAATCCCC ACAATTATGT TATACAACCT TTTTTTTTTT 300
GAGACAGGGT CTCACTCTGT CAACCATTCT GGAGTGCAGC GGTGTGATCA TATGATCATA 360
GCTCCCCGTG GCCTTGAACT TTGAACTCCT GAGCTCAAGT GACCCTCCCA CGTCAGCCTC 420
CAGAGTATTT GGGACTACAG ACACACATCA TCACGTTTGG CTCACTTATT TTTATTTTTT 480
GTACAGACAG AGTCTCACCG TGTTGCCCAG GCTGATCTAA AACTCCTGGC CTAAAGCAAT 540
CCTCCCACTT CGGCCTCCCA AAGTGCTGGG ATTACAGGTG TGAGCCACTG TGCCCAGTCT 600
AATCTTGAAC AAATTATTTT ACCTCCCTAA GCTACCGGAA CAACCACACA TGCCACACAA 660
CCTGGGAAGG ACCAACTCAG CCATTCTCCA GCAGCGAAGT GGCTGCCACC CCAGGGATAT 720
CTAACTAGAG GATGTGGGAT GGAGGCGTCA TGGCAAGGCA AGGCCTGCCC CCTGGTGGTC 780
AGAGAGCATG GGAGGCCCGA GCTACCAATG GTGGCTTTTC TCAACTGGGC CTTGATTCCA 840
GCTTCTGCCC GATCCCCTAC CTTGCTTGCC TCCTTCTATC AACACCCCAT TCACACCCCA 900
AAGGATCAAT ATAGGAAAAA TTGTCTCTAC TATCTCAGCT GTAAGAAGCC CACGGTTTGG 960
GGAGGGAGAA GAGGTCACCA CCAGTGGGGA CGTGGAATAA GTAACTGGCT GGGGATAAAA 1020
CTCCACTCTT CCGGCCGGGA GCAGTGGCCC ACGCCTGTAA TCCCAGCACT TTGGGTGGCC 1080
GAGGTGGGCA 1090
|
