| Tag | Content |
|---|
EnhancerAtlas ID | HS051-04625 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr11:61468530-61469730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr11:61468632-61468644 | CAGTAAACAGAA | + | 6.02 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_23644 | chr11:61462269-61469316 | Colon_Crypt_1 | | SE_23957 | chr11:61468603-61469360 | Colon_Crypt_2 | | SE_25088 | chr11:61465275-61469220 | Colon_Crypt_3 | | SE_27201 | chr11:61461011-61469578 | Esophagus | | SE_29301 | chr11:61465002-61469417 | Fetal_Intestine_Large | | SE_41676 | chr11:61465207-61469249 | LNCaP | | SE_47728 | chr11:61468658-61469276 | Pancreas | | SE_51045 | chr11:61461234-61469434 | Sigmoid_Colon | | SE_63420 | chr11:61457154-61498627 | NCI-H69 | | SE_65661 | chr11:61460755-61471450 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCCAAAGAGG TTGTGACTTG CCCACACCTC TTGAATGGCC AGGCCCCATG TCCAGCCTGG 60
ATTCTCTGAC ACCAAGCCCC ATGTGTTTTC CACTGTGCCC TGCAGTAAAC AGAAGTGCTA 120
ATAAAGAAGC GTGCTAATAC ATAATTAATC CCACCTCCAT CCCTTGGGCC TTTTCTCTCT 180
CAGACGCCCT GAGCACCGCC CAGACGTGAT CTCATGTGTC CTACCAAGGC CCCAGAAGAG 240
CAGAGAGGAG GCTGGGCTCT GAGGGGCCAT GGGGACTAGG AGCCAGCCTC TCCGCTGCCA 300
GGCCCAGCCC TACTGCATGC CTGCTGCCCG CCTCTCCCTC TGCTCTAGGT AGGGAAGCTG 360
CCGAGGCTCG GGCATGTCTC AGGCACCTGC TGTCTTCCTC TGGTCTCGTG GATTGTACGA 420
ACCTGGAGGA GGAAAGCAGC CGGGATTCGA TGAGCCCCCA TGTGGTGGGG ATGTGTGCGC 480
GCAGGGGCCC AAGGCTCTGC TTAAAGGGAA GGAGTATTGC TGAGGCTTGT TCTAGTGCCT 540
TCCTCTAAGG AACCCTCAGT ATATCTTGTT TGTTCTCACA TTCGAGGGAA GTTGGCAAAG 600
GGCAGTTCTG TGTCACAGGG AAGGGGGTGG ATGAGGACCC CGAAAACCTG CCCTTTACCG 660
AGTCTCACCC CCGAGCCTGC TGAGGTCACA CAGCGGCAGT CAGTGGGGGG TTAGGTTTTC 720
TTGTTTTGTT TTTAGAGACA GGGTTTTGCT CTGTCACCCA GGCTTCAATG TAGTTTTGCA 780
ATCACAGCTC ACAGCAGCCT GGAACTCCCC AGCTCAAGTG ATCCTCCTGC TTCAGCCTCC 840
TGAGTAGCTA GGACTACAGG CATGTGCCAC CATGCCCAGA TAAATTTTTT TTTTTTTAAT 900
AAAGACAGGT TCCCCGTATG TTGCCCAAAC TATTCTCAAA CTCCTGGCCT CAAGTAATTC 960
TCCTGCGTCA GCTGCCTGAG TAGCTGGGAC TATAAGCATG CACCACCACA TCTGGCTAAA 1020
TTAAAAAAAA TTTTTTTTGT AAAAATGGGT TCTTACTAGT TTCGAACTCC TGGCCTCAGT 1080
GATCCTCCAG CCTCGGCCTC CCAAAGCATT GGGATTACAG GTGTGAGCCC CCACAGCTAG 1140
CCCATGTTAG GTTCTCTCTC TCTTTCTCTC TCTCTCTGTC TTTAACTCTG ATAATTACAA 1200
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