| Tag | Content |
|---|
EnhancerAtlas ID | HS051-19053 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:13393680-13395050 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2B | MA0660.1 | chr3:13394885-13394897 | ACTATTAATAGC | + | 6.02 | | NFE2L1 | MA0089.2 | chr3:13394407-13394422 | GAGTGACTCAGCTAT | + | 6.06 | | RREB1 | MA0073.1 | chr3:13393932-13393952 | CCCCAACCCACCAGGCCCCA | + | 6.23 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_25550 | chr3:13381546-13397526 | DND41 | | SE_60521 | chr3:13346467-13410905 | DHL6 | | SE_68786 | chr3:13393302-13396458 | H9 |
|
| | 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 |
| GH03I013351 | chr3 | 13393475 | 13395873 |
|
Enhancer Sequence | CATGCTGAAG GACAAGGGCA AGGCCATTAG ATCCAGGAGG ACATGATTAG GCTGCCCCTC 60
GGGAAGAACA GGCCCAAAAG CCCTAGGGCC TGGCCTTGCT CCTGGCCACA AGCCCCTGGT 120
GCTCCTGAGC CCAGCAGAAT GGCCACAGAC CCTTTGAGGT CTCCCTTCAG CCTCCTGAGG 180
TGGAATGAGT TGCTGGCTCC TCCACTCCAG ACTGAGGAGA GGGTTGGGAG CAATCCAGCT 240
TAGAAGACGC CACCCCAACC CACCAGGCCC CAGTGGTGGG CAACTCACAC ACACGCCCTG 300
CCTTGCAGGA CCTCACAGCA AAGGGTCAGC TTCAGAGCAT GTGGCCGCTG GCCAGGCCAG 360
GCATCGGGGG AGGGTCCCCT GGAAGTGTGG CCAAGGCTGG CTCAGGAGAG GACAATGACA 420
GCCCTCATCC CCTAGGGTGG CACATGACCC ACTGAGCTCT GCTTCCCACC ATGTGTCACA 480
CAAAGGAGCC ACCCAGATCT GAGGCCCCCA GGAATCACGT GTTTGAGCAC CTCCTCAGGG 540
CCACAGGTGT GCCAGGCACT CGGGGTGCAG CAACTGCCGG CAGGGAGAGG CGACTCCAAT 600
GCACGGATGG AAGAGCAAGA GTGAGTCAAT GACAGGAAGG TGTGCATTGT GGGTGACAAG 660
GACAAGGAAG GTGTCTGCAA GGGAGAGCAG CTCTCAGGGG AACACAGACT GCAAGGGGAG 720
GAAGCCTGAG TGACTCAGCT ATGGGGGGTG GGGGGACATC AGGGCAGGGA GGAAGTGCAA 780
AGTCATGGGG ATAACATGTC AGGGTGCTCA GGCATCAGGC AGGAGGCCGT GACGCCCCCT 840
CACTCCCAAT CAAGGGAATC CTGGTGCCAG TGAGGACTGA GCCATCAGGT ATAGGCACAG 900
GTGTGCCCCT TCAGTGACCC CCTCCCTCCA GGCCAGCCTC CCCAGTGCTG CCCCCACGGG 960
ACCCCAGCCT CTTTCAAAGT TTGCTCCCAA GAGGACAATA GAAGTGCCTC ATCCTGGCAT 1020
TTAGGGACCA TGGGAATACA GTTACAGTCC CACCTTCTCC TTCCAGCCTG TACCTGCTGC 1080
CTCCACCTTA TTCAAGACCT AAGTTTCCTT GTGGCTGTAC CCCCCATGAG GTGGCTGTCA 1140
TCCAGGAAGG GCTATTCTTG AGAAGCCCTT CCCATTCCCA CCTCCAATGT ACCTATTGGT 1200
CCCCTACTAT TAATAGCAGT GCCTCTCCTG GGGCCTCCAA GAGGCTGGGG TGGGGGAGTG 1260
GTGGTCAAGC AGACAGTGAC TCAGGACACT GTGATACCCG GTGGAATTTA AGCAGAAGTA 1320
GGAGGCTTGC CCCGCTACCC ATAGCCCACC CACCACTGGG CCCTGGGAGA 1370
|
