| Tag | Content |
|---|
EnhancerAtlas ID | HS051-21556 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr5:399510-400650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr5:400318-400329 | ATGACCTTGAC | - | 6.32 | | Esrrg | MA0643.1 | chr5:400318-400328 | ATGACCTTGA | - | 6.02 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_03106 | chr5:398350-400772 | Bladder | | SE_33646 | chr5:398082-403165 | H2171 | | SE_37211 | chr5:398140-402343 | HSMMtube | | SE_39288 | chr5:398312-402511 | IMR90 | | SE_44252 | chr5:398057-402542 | NHDF-Ad | | SE_44785 | chr5:398068-402100 | NHLF | | SE_45637 | chr5:398228-402500 | Osteoblasts | | SE_58626 | chr5:366707-441100 | Ly1 | | SE_59696 | chr5:390329-441740 | Ly4 | | SE_67033 | chr5:398082-403165 | H2171 |
|
| | 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 |
| GH05I000397 | chr5 | 397821 | 402401 |
|
Enhancer Sequence | CTCAGAAAGC GGGTCCTGGT TTTAAAAGCA TAAGTTTTGT TCTCTAGAAA ATGACATCAA 60
CTTTAGACGT CAGATTGCCT GTCCAGCACA GCCATTTGCC CTCCAGTCAC AGAGACAGCG 120
GGTGCTGCCC TGATCACTGG AGGGTGCCTG GTGCTGCTGC TCACCGCCGC CCTCACAGAC 180
GCTCACTGTT GCCGTCCCAT CTTTCGCAGG AGGAAACCAA GGCCCAGAGA GGTGAATTAA 240
CTCGCCAAGG GTTCGCAGCA AAGGTGAGGG CGGAGGCGGC GTCAGCACTG GCTGGTCTCT 300
CAGCCAGAAG GGGGCCCAGG ACACCGGGTT AACCGAGCGG GGCTGCAGTG GGCGTCAGGA 360
GGGACTGCCT GGGGGCCGCC ATCTGCCTGC TCTTCTAGGG CCCCGGGGCT TCAGTCAGCC 420
TCCCACTCTG TGGCCATCCG GCCAGCTGCA TTCTCAAGAA CTGTTTTCAA ATGTCGGAGC 480
TGCTCCGTGG AAGAGAGTCA AGCCTGCGTT TACTGTTTGT GGGATCTATA AACAGCCAGT 540
TATTCAGCTC CCCAAGCAAG AGCGCTGCCT CGCACGCACG CAAGCCCCAT GGAGCGGCCC 600
CTGTGAGTGA TCTGCCTCCA GGAGGCCGGG CCAGCTGCCC CGACGCCCGC CCGGTGCCCG 660
CTCGCGTGAC TAGCCGCCGT GTTGTGGCTC CGTAACCGTG GCAACGGCTC TCAGGGGAGC 720
ACAATACTCC CAACTTCCCT TTACTCCGAG GAGGGGCAGC CAGGGGGATG TGGAGGGTTG 780
TTCCTTTTTC CCTCATTTTC CCTCTGCCAT GACCTTGACA AAAATAATCT TTGAAGTACT 840
TGCCGGCTAT TTTTTCTGCC CTGGAACTGG AAGAGATCAG GATATTTAAA GGGTTTGACA 900
GAGGAAGTTC CGGCTTTCTC AGAACGTTTG CCCCATTCCC TGCGGTCCCT GGGGGAGAGC 960
GTGGCTCCAG CCCTCACCTG CCTCGGCCCT CACCTGCCCC GACCTCCGTT GTCCTTGCGA 1020
AGTGGCAGGT GCGCCGTTTC CTGACGTTCA GTAACAGCAC ATGGATGTGA TCTTTTTCCC 1080
CTTAAAAAAA GTAGAGCCTT AACCTTAGAG CCAAATCCTT TTTCCGTTTG GAAAAGTGAT 1140
|
