| Tag | Content |
|---|
EnhancerAtlas ID | HS051-13414 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:3104000-3105050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:3104038-3104053 | TGAACTCCTGACCTC | - | 6.22 | | RREB1 | MA0073.1 | chr19:3104481-3104501 | TGCTTGTGGTTGTGTGGGGG | - | 6.53 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_23423 | chr19:3103917-3107079 | Colon_Crypt_1 | | SE_24036 | chr19:3104073-3105341 | Colon_Crypt_2 | | SE_24788 | chr19:3104029-3105420 | Colon_Crypt_3 | | SE_28165 | chr19:3103547-3105073 | Fetal_Intestine | | SE_29126 | chr19:3103616-3109250 | Fetal_Intestine_Large | | SE_43312 | chr19:3103939-3107073 | Lung | | SE_52730 | chr19:3103568-3105569 | Small_Intestine | | SE_65597 | chr19:3094596-3105081 | Pancreatic_islets |
|
| | 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 |
| GH19I003103 | chr19 | 3103558 | 3104883 |
|
Enhancer Sequence | GTAGAGACGG GGTTTCACCA TGTTGGCTAG GCTGGTCTTG AACTCCTGAC CTCAAATGAT 60
CCACCTGCCT CGGCCTCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCG CCCGGCTTTG 120
AATCTTGAGC ATCGGATGAG CCCCCAGCTC CTGCTGTCAG GGCTGCGCCC TCTTGTGGCG 180
CTTGGAGCCT CCTTTTCTTC CGTTTTCCTT TCCCACCGGG GAAAAGGAAG CTGGGGCACG 240
GACTTCGTTC CTCCTGGTTG GCCTCTCCAG ATCTTGGCCA GCGGGTCCAG TCGGGAGGGT 300
GGTTTTCTCC TCTGGAAGCT GGCTCAGTGG GAGCAGTGGG CGGACTCTGG CCCCTCCTAG 360
TGGTGGCGTG CTGAGTGTAC CTGAGGATGT ACCTCCTGCA GGCTCCCTAG CGTCTGGGGT 420
CCACTGTGGG GCGGCCTGTG GCAGGCCCAC CAGGAACCAT GCTTGCACAG GCAAAGCACC 480
TTGCTTGTGG TTGTGTGGGG GGCTCCCTCA GGTGTGGGAG ATGTGGGCCC CATTCTCCCA 540
GGAGCCATGG CTGGTGACAT GCAGTCAGGT CCATCCTGAC GGGCACTGGA GTGCGGGGGA 600
CCCAATGGGG ACATGAGGGA TCCAGCACTG TGGACCAGGG CCAGGTTCAT TTGGTTCGCT 660
CAGGAAACAT GTACACAGCG CCTTCTGCAT AGGGGCTAGG GATGCAGGTG GGCAGGGCAG 720
CCACAGCCCC TGCGCTCAGG AAGCTGGCGA GGCAGGCTGC AGACGGGCAC TGCCACACCT 780
CACTGAGGAG GGAATGGCAG AGCCACCCTC AAAGGGCCTG TGCTGTGGGG GTGCTGGGCG 840
CTTCCTGAAC GCCGGGCTCT TGGATTTCTG CAGTGGGGGT TCTCCGGGCG TTTGGGAAGG 900
GGAAGGACCT GATGGAAGGG GTAGTTTATA TTTAACTCTG GTGCTGAAGC AAGGGTCGCA 960
CACAGCTGCC AGTGCCCACG ACGGCCTCCT GGGAGGCTGA GCTCACCAGC TCCAGACCCA 1020
GTCTGAGGCA GGAACCTGGG GGTCTCACAG 1050
|
