| Tag | Content |
|---|
EnhancerAtlas ID | HS034-08534 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr13:111227690-111228520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr13:111227885-111227897 | GCTGACGTCACC | + | 6.14 | | CREB1 | MA0018.3 | chr13:111227885-111227897 | GCTGACGTCACC | - | 6.14 | | EWSR1-FLI1 | MA0149.1 | chr13:111228302-111228320 | CTCTCCTTCCCTCCCTCC | - | 6.44 | | RREB1 | MA0073.1 | chr13:111228285-111228305 | CCCCAACACAACCACCTCTC | + | 6.26 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_31501 | chr13:111227618-111229200 | Gastric |
|
| | 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 |
| GH13I110574 | chr13 | 111227321 | 111230168 |
|
Enhancer Sequence | TCAACATGAC TCAAAACCAG AATTTGAAGC AATGTATCTG CTGCTACTAA ATTTAAATCT 60
GCTGCTGCTC TTCACAACCT GCAGGAGAAG GAACGCATTT CTTCGCTGGA CAGGATGCCT 120
TCCCCAGGGG CTACCATCTG CCCTTCCAGC CTCTCCCTGA CACACATGGA ACTTCTGGGT 180
GGCTCCCAAA CGCAGGCTGA CGTCACCAGA TGCTGATTCT GATCCTCACC CTTCCACCCC 240
CCATGTCAGC CCTGACCTCA GAGCCTTGTT GCCCAGCAAG CCACTTCATT CTGTGCAGCC 300
TCTGGGGAAG CTCCGTGGTG ACCTCCGCTG GCAGGATCAT CTGGCCCTGG CTCCTTTTTC 360
ATCCTTCATT GGTTAGCAGG TCAGTTTCTC CCGCTGGATG GAGAACTTCT GCAGAGACGG 420
CCAAGCTGAG CCCTCCCCTC ACCGCAGGGA AGAGCTGAGT CAGATGAGAG CAGGGAGGCC 480
AATGTCACTT CCCCAATGTC ACCAAACGTC AAATAGAAAA GTTCACCTGG AAGGAAGCAG 540
TGGGGACAAA ACCACCACAG GGCGACTTGT GGGCTCACAG ACAGAGGCCC CGCTTCCCCA 600
ACACAACCAC CTCTCTCCTT CCCTCCCTCC CACACACCCC AGAGGTCATC ACAGCAGCTG 660
GGCGTCCCGC AGCCCATTTG TCCATCCCCC ACCCGCTCTG GGGGACCTGC TCCTACACAG 720
CAGACCCTGA AACCAACATC ACCTGCGACT TCGTCGTGGC CCAATCTCGC AGTCGCTTTA 780
GCCTTTCAAT CTACTTGTCT TGCACCCTGT TCCCCACTTC CTTCTTTTTG 830
|
