| Tag | Content |
|---|
EnhancerAtlas ID | HS007-06253 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr16:21567530-21568960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr16:21567828-21567843 | TGAACTCTTGACCTC | - | 7.64 | | Nr5a2 | MA0505.1 | chr16:21567820-21567835 | GCTGGCCTTGAACTC | - | 8.25 | | RARA | MA0729.1 | chr16:21567825-21567843 | CCTTGAACTCTTGACCTC | - | 7.63 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_37289 | chr16:21565664-21569639 | HSMMtube |
|
| | 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 |
| GH16I021556 | chr16 | 21567476 | 21569066 |
|
Enhancer Sequence | GTTCCAGTGA TTCTCCTGCC TCAGCCTCCT GAGTTGCTGG GACTACAGAC AAGTGTTACC 60
ACACCCCACT AAATTTTGTT TTTGTTTTTG TTTCTTTGAG ATGGAGCCTT GCTCTGTCAC 120
CTGGGCTGGA GTGCAATGGC CAGATCTTGG CTCACTGCAA CCTCCACCTC CTGAGCTCAA 180
GCGATTCTCT CACCTCTGCT TCCCGAGTAG CTGGGATTAT AAGCACCCAC CAGCATGCCC 240
AGCTAATTTT TGTATTTTTA GTAGAGGCAG GGTTTCACCA TGTTGGCCAG GCTGGCCTTG 300
AACTCTTGAC CTCAGGGGAT CTGCTGCTTC AGCCTCCCAA AATGCTGGGA TTACAAGCAT 360
AAGCCACTGT GCCAAGCCTA AAGTGACTTT TCGTAATGAC AATACAATGT CAGGATATTC 420
TCCTTAATCA AAAAAAAAAA AAAAAAGGCA AGCCCAATTC ACGAAAAGGG GTCTTTAAGC 480
TGCCAGCCCC CATCCCCCAG ACTCTGCTAT CGGCAGGGCT GGTCCACCGG GCAGCACTGG 540
CCACTGTTGC CTCAGCGTTC TGTGCAAGCA GGTGCGTCAG AACCGGCTCA TGGAGATATA 600
ATTGAACGAT TGCCTCAGCG CGTGCCAGAC TCTCCAAACA TAATAACAGA TGACGTTTGG 660
GGTCGGCTCC AGGCGGTGAC GTGCTGGCCC CAGAGAATAT TGTCTCTGCT ATTACAACAG 720
ATGCTGTTAA TAGCTATCTA TTTGTAGTTC GGGGCTTTTA CCAAGATGAG CAGGCTTTTG 780
GCAGGCACGG GTTGTTTGAA GGCTTAAAAT TAGTACAAGA GAAGTTTGAG ATGTTCTAAT 840
TACTGGAAAT TTCAAATAAC ACGATGCCGC AAGGGACCGG TCTGCTTCCG GTGCCACTCT 900
CGGGGGTAAT GCACGTTCCC AAGCTGTAAA TGGGGAAGGC TGAGGGCTTC TGTGTGCCAC 960
CTCCCCAGGC AGGCAGGGGC CGCAGCCACT GCAAGCCCCT GCCCACAGAA CTCGGCGATG 1020
ACGGAACCTA GACTGCTCCC TGGAAGTTAG CCTCTGAGAC CATCACATAT TGGCACTGGT 1080
TTGAAAGCCA GGCAAATGTG GGCTCCAATC CTGGCTTCAC ACGGTGGGGC TTTGCAAGTT 1140
GTTTTATAGG TCTGTGGCCC AGACTAGACA TTTGTAAAAG GATAATGATG CCTATGGCAA 1200
GGATTGAGTA CTGTGATGCT TACAAAGTAC CTCCCTAACA GTCCCTGGCA TGCAGTGAGA 1260
GCTCAAATAA TGGTAGCCAC TTACTATTAT TATGACTGGT GTTATTGTTA TTATTAAAAT 1320
TACTGTCATC GCCCAGGCAC GGTGGCTCAC ACCTGTAATC CCAGCACTTT GGGAGGCTGA 1380
GGCGGGCAGA TCACTTGAGG TCAGACGTTT GAGACCAGCC TGGGCAACAT 1430
|
