| Tag | Content |
|---|
EnhancerAtlas ID | HS092-23322 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:1597310-1598630 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr2:1597794-1597808 | GAGGCCTGGGCCCC | - | 6.42 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_47254 | chr2:1594860-1599976 | Panc1 | | SE_57913 | chr2:1597243-1597568 | VACO_9m | | SE_69031 | chr2:1597964-1599411 | H9 |
|
| | 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 |
| GH02I001590 | chr2 | 1593940 | 1598822 |
|
Enhancer Sequence | CAAACCCACT GGGCCTTGGT CTTGGACTTC AGCCCCCAGA GCAGAGAGAC GAGTGTCTGC 60
AGCTTGTAAG CCCCATCTGC TGTGGTTGTC ACAGCTGCCG AGTGACCAAG GCAGGTGACA 120
GAGGAAGCTG GATTCGCTGC ACATCTGCTC CGTCCAGGCC TCTCACGATG CCTACAGCAT 180
CCCTGTCCTC TGGGAAGAGC CCTTGCTGTG AGGAAGAGCC CTGACACTCC AGCATGTGCT 240
TTGCATAAAA GCTGCTGTCA TCTTACAGAC TCCACAAGTG ACCAGCCCAG CCGCAGGCAC 300
TGACTCAGGC CGCCAGGTTG CTGCCCCTCC CTGGGGCTGT GAGCAGGCAT CTGGCCACAG 360
AGAATCCTGG ACTTGCTGCC AAGAGCCAGA TGTCGCCTGC TGGGACCCGC CAGGAGTCCT 420
GTTCCCAGCC GAGCAGAGGG GCCTGGCGGA GAGGCCCAAG CCAATGGCGG GGAGAAGCAG 480
AGACGAGGCC TGGGCCCCAC TCCCATCTCT GTTCCTTTGA ACTGAGGTTT TGTCACTGAC 540
AATAAGGGTT CTGACTCACA CATCTGCTTA AGTTGTGGTT CGGGCACTTA ACGTTTCATC 600
TGAAGTTTCC TGAACGTCAG CCAAAGGCCA TCAGCTCGGC ATCTAGAGCC TTTCAGGTCC 660
GTAGGAATCC ACAGATACAA GTTGTAGAGA AAGGAGGTCC AAAGAGATAA AGTGTCAAAC 720
GACATCATAG TAAATGGCCT CAAACAAAAA CCTCCAAAGA CTGTTTTCCC ACCACAGCAC 780
ACCGACTCAT AATGAACAAG GAGAGAGGGA ATTTTGCTGA GCTTGGTGCT TCAGGAACGC 840
CTAGAAAAGG AAGAGGCTTC TACCGCTGGT GCTTGAACCG AGGGGCAGCT CCTGCAGACA 900
GGCCCTGAGG GCTGGCTGCC ACGGAAACAA CAACCGGGCT GAGCTGAGAC CTGAGACACG 960
AGGTCCCCTT GCTCCACGAG CACCTGGGGA CCCGCCCCTG CACACCCCAG TGCTCCTGGG 1020
CTGGAAGCCG CATCTCTCCA ACCTCTGCCT TCGTCTTTTA TTCTCATCCT CAAACGAGGC 1080
CTTCTGGCCC GCCTCCCTCC CACGGCCACC CCAGCCCCTT CTCATTCTGC TCTTCGCGAA 1140
GCCGCCAGAA GGTCCTTTAA ACTGTGAGCG CTTCAGCACA GTGGGATCCT CCCAGGCCTG 1200
TGACACAGCA CCCGGTACGC GCAGCACACA GGCCCAGCCT CAGGCCCTGC ACCAGGCTCT 1260
GCTGCCCCCT GGTCTCCCAC CCCGCAGGCT AGCGTCCACT TCTCTCCAAG ACCTCAGCTC 1320
|
