| Tag | Content |
|---|
EnhancerAtlas ID | HS191-01951 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr1:110303050-110304110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:110303111-110303126 | TGCCCTTTGACCCCA | - | 6.87 | | Nr2f6 | MA0677.1 | chr1:110303111-110303125 | TGCCCTTTGACCCC | - | 6.46 | | RREB1 | MA0073.1 | chr1:110303800-110303820 | GGTAGGTGGGTGGGTGGTTG | - | 6.04 | | Rxra | MA0512.2 | chr1:110303111-110303125 | TGCCCTTTGACCCC | - | 6.73 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23201 | chr1:110303121-110309396 | Colon_Crypt_1 | | SE_23812 | chr1:110303183-110309257 | Colon_Crypt_2 | | SE_50503 | chr1:110303762-110309389 | Sigmoid_Colon | | SE_52808 | chr1:110303471-110310714 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 110303861 | 110303996 | | chr1 | 110303474 | 110303853 |
|
Enhancer Sequence | TTACCTTCAC AAGGCCCCTT CCACCCAGGC TTCTTGTGGT AGGGAGATGC AGCCTGCCTC 60
CTGCCCTTTG ACCCCACCCC CCTGCCCAGG GCCCAGCTCT TCTCCCTGTG TTCGCACTGC 120
CAGCATATTC AGGGGACTCT GGCATCATGA GCAAACTCCA TCCTCCTCTT GCTCTGCCTG 180
CTGGGCCTAA AAGAAGCCTC TTCCCAGCCT CCACCCTACA GAGAAGCTGA GTCCTCCTGG 240
CCTCTCCTCG GCTGGCTAGG GGAGCTCTGC CTCTGCTGCC CTGTGGGACC TGCTGCCCTG 300
TGGGACCTGC AGACCATCGC CCCAGCTCCC TCCCTGCTTG TTCTCCATTG GAGCCACTAA 360
CAAGTGGTGG CCAGGACAGG ATGGCTTCTA CCCCAGAGCT CCAGCCTGAC CCTCTGCCTG 420
CTCTCCCCAC CACGCCCTTG TAGCCTGTGC TTCGCCTTCA CCTTGGTGTC GACAGCCCTT 480
CAGGCACCTA AATCTTGCAG TGCCTGCATC ATCCTCCCTG GTAGAGCCAG AGACTCCATT 540
CTAGCCTTGG AGCAGCCTCG GAGCTGCTCA CAGTCACCCT GGAGGCTTGG GCCCAGGTGC 600
CTCCCCTCTC CAACAGTGGC CCTCTCAATC CCCCACAGGG CCCAAAGATC CCAAAGATCC 660
CACACACTCC TGCCTCCAGC CATGCAAGGT CTTGGGCAAT GGAGCAGTGC CCTGGGGACT 720
CGGGCAGCAG GGGGTTGGGA GACAGGGGAG GGTAGGTGGG TGGGTGGTTG TAGGTGCTTC 780
TTATCCCATC CTGCTGCTAC TTCTTCCTGT CTGGGGACAG GACACTCACC CGCTCAACCT 840
CCAGCCAGGC CTGCTCTGTT CAATCTGACC ACCCCTCCCC GTCCCTGACA CTGAGCAGAT 900
GCTCTGGCAG GCTTGTTGGA TCTGAGTCCA TGCGACATGG TTGGGACAGG CTGTTGGCTT 960
CTGGGGCAGG GACTTGTGTG AAGTGTCCAT GTTCTGGCAG GGCGGTGGGC ACATGGGAAC 1020
ACTTGGGTTT AGTTGGACAC TGCCCGGGGG CTGCAGAGGT 1060
|
