| Tag | Content |
|---|
EnhancerAtlas ID | HS047-24401 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr3:124351550-124352690 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CUX1 | MA0754.1 | chr3:124352439-124352449 | TAATCGATAA | + | 6.02 | | CUX2 | MA0755.1 | chr3:124352439-124352449 | TAATCGATAA | + | 6.02 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27806 | chr3:124352033-124360885 | Fetal_Intestine | | SE_28844 | chr3:124352021-124360652 | Fetal_Intestine_Large | | SE_32154 | chr3:124349692-124351694 | Gastric | | SE_35423 | chr3:124352333-124356676 | HepG2 | | SE_53162 | chr3:124352426-124354504 | Small_Intestine |
|
| | 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 |
| GH03I124628 | chr3 | 124347275 | 124360641 |
|
Enhancer Sequence | GTACTTACAG GGGGCCCTGG AGTTGTCCAT CAGGAGGGCC TTCTGACATG TCTCCTTCCT 60
CAGGTTTTGT CAACTAGGCC ATCTCAAATC TCCATTAGTG TGTTACCTTG AGCCTAAGTG 120
ATTTGGATTC TTTTTATTCT TAAGACATTG GCCAGTTTGA TTTGTGGCTG ATTCAGAAGC 180
TGACTAGCCC CTAAGACTTC CAGCAGACAG AAACCATTTG CCAGATTTGG AGATAGGACC 240
TGGGCCTGAG GGGAGTCATT TGGTCATTAG TTCCCTACCT CTACTAAGGA CTACATTAAA 300
ACCAGCTAGA CCTGTTTAGA TTTAGAATAA AAGAATGAAG ATTGTTTCAT TTTGAAAACA 360
GGACTGTGCT GGGAGATTGT AGCTGTTTTC AAGTCTCTTG AGCAGTGCCA CACATCAAAA 420
GGAATAGATC ATCCAGAGTT ACTCCAGATA ACTATGATGA ACAGATGAAG ATTACAATAG 480
GCAGGGTTTC CGCTCAAAGA AAAAGTTTAA TCTAGGAGTC AGTCAGTGAT TAAATGGGCC 540
TTCATGAAAA CTAATGAACG CCCATACTGG AAGGTTTGAG AGACTGTAGC CAAAGTTAGG 600
CTGGATGAAG CTGAGATTCT GTAACCAAAA GACAGTGGAT ATGTTTTGGT TGGGGAAATG 660
AGATACCTGT TTTATTTGGC ACACAATCCT GCTCTAATCA CTGATGTGGC TAAGAAATTC 720
TTTGTGATGT GTAACTGGAC CCCCTCTTGT TGTGATTTTA TGCTACCTGC CATTTCTCCC 780
TCTGGAAATG GCAGCTAAGC CTGGCGGCAT TTGGGCTATG GTTTCATAGC CCTACAAAAA 840
TGTAAAAGTT AGGCTCTCTC TGACTACTTC CAGCTTTTTC TTTTCTTGCT AATCGATAAG 900
ATAGATAGTT TCTGGTTTTG CTTCTTTTTG GGGGTGTGTG TGTGTGTGTG TGTGTTCCCC 960
ACTGGTGCTC ACTCTCATTT GAAATAAGCA GGTGTATCCA TGTATCAAAA GAGGAAATTG 1020
CGACTGAACA GTTAAGAGTG AGTTGAGAGA GGAACTCTCC TCCTATGTAT TATTTTTGTT 1080
AATGTCAAGT CCAGAACCAC TGGCATGTTT GTGACACAGT AACTAATGCT GCTCTTTTGT 1140
|
