| Tag | Content |
|---|
EnhancerAtlas ID | HS047-18331 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:10159220-10160410 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr2:10160316-10160331 | CCACGTGGGTGGGCG | - | 6.35 | | Gata4 | MA0482.1 | chr2:10159987-10159998 | GGGAGATAAGA | - | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_00309 | chr2:10156361-10160432 | Adipose_Nuclei | | SE_54265 | chr2:10159289-10160122 | Spleen | | SE_65434 | chr2:10159487-10160791 | 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 |
| GH02I010016 | chr2 | 10156362 | 10160791 |
|
Enhancer Sequence | GATTCTCTGT TGTTGGGCAT TTAGGTTATT TTCAAGTTCT AACTAATCCT GCAATAAGCA 60
TCTTGTTCTC CCTTGTTCTG GTTACTCTCT TAAGTTAGAT TCCCAGAAAT GGGATAATTG 120
TTTCCGAAGA TATTTGGGAA CATCTGGGAA GTTCCTGATC TGTATTGCCA AATGACTTTT 180
CTAGAAGGTT GTACAAATTT ACATTCCCGC TACACGTACT CTCTTATGTT GTAATACATG 240
TTTACATGCC TTTTCCCCCA CAAATTATGC CCTATCCACC TTCCTGTCCC CGGTGCCTGC 300
ACAGGCAGCT GCCCAGCAGC GTCCCTTGCA TCACACATGC CCATACTTGC ACCATACGTG 360
ACCGTACTTT CACAGAGGAG AAGGAATATC CAGGGTCAGG GGGAACATCC CTGACAGACA 420
CTCCTGGAAC CAAGACGTGG ACAAGTGTGG ATGGACACTT GGGTCTCTGA ACTCTTTCTA 480
GAACACCTGG CATGGAGATG AGATGGCCAT CAGAGACCTG TCAGTTCTGT TTTCTCGCTT 540
GGCGGCAGGG AAGCTGAGAT CTAGGTGGGG CAAGTGGGTT CCACACGGCA CAGTTCGTCC 600
ATGTCAGTGC AGTGGCTGCT TCTCGGGGTA CGGCCAAGCC GGGGTCTTGC AGCCTCAGCT 660
CCCAGCAGGA CCCGCCCAGC CAGGGTCCTC AACCCTAGGC TGACATCTTG GCCTCACTGG 720
CGTCACAGCT CAGCCCTCAC CCTGCGACTC TGTGCACGTG GGGAGTGGGG AGATAAGAGC 780
TAGAGGCAGA CCTCCTAAGA GGAAGGAAAA CGATGTGGAC TTGGGGGAGG AAGGATCTGC 840
CTTCCCTTTC TTCAGCGAGA GCTTCCTCTT CTCATAATAC AGGGAGGACC TCAAGATGGC 900
TGTCTCCCCC TTTAGAGATG CTGTGTCCCA GCAAAGGGGC ACCTAGAACA GGAATTCTCA 960
ACCTCCCAGG ACAACGGGTG GCCGCTGAGA ACCCGGGAGA CCTGGGGCAA GCGTCTCAGG 1020
CTTTCCTCAG CTGCTCCACC TGGAAACCGG GACGGGCAGG ACCGCCTCTC GAGGCTGCTG 1080
TGAGCGTCCA GTTAGACCAC GTGGGTGGGC GAGGGGCTTG TGCCTTGCCC CAAGGGGAAG 1140
CTCAACACAC ACCTTTATAT AGGACACATT CAAGGAGGCC AAGTTCACCA 1190
|
