| Tag | Content |
|---|
EnhancerAtlas ID | HS161-08762 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr2:43436150-43438600 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr2:43436583-43436594 | GGGCGGGAAGC | + | 6.02 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_00296 | chr2:43437036-43438790 | Adipose_Nuclei | | SE_02969 | chr2:43437301-43438552 | Bladder | | SE_09435 | chr2:43435994-43442184 | CD14 | | SE_13297 | chr2:43437195-43438199 | CD34_Primary_RO01480 | | SE_13409 | chr2:43436855-43438842 | CD34_Primary_RO01536 | | SE_14384 | chr2:43437082-43438015 | CD4_Memory_Primary_7pool | | SE_23059 | chr2:43435636-43436863 | Colon_Crypt_1 | | SE_23059 | chr2:43437029-43438580 | Colon_Crypt_1 | | SE_23724 | chr2:43437108-43438529 | Colon_Crypt_2 | | SE_24685 | chr2:43437071-43438522 | Colon_Crypt_3 | | SE_25333 | chr2:43435716-43436820 | DND41 | | SE_25333 | chr2:43437248-43438244 | DND41 | | SE_26557 | chr2:43435567-43436848 | Esophagus | | SE_26557 | chr2:43436992-43438585 | Esophagus | | SE_27617 | chr2:43437101-43438574 | Fetal_Intestine | | SE_28536 | chr2:43437132-43438609 | Fetal_Intestine_Large | | SE_30898 | chr2:43437035-43438523 | Fetal_Thymus | | SE_31392 | chr2:43437058-43438494 | Gastric | | SE_42201 | chr2:43437107-43438599 | Lung | | SE_49954 | chr2:43435662-43436925 | RPMI-8402 | | SE_49954 | chr2:43437061-43437837 | RPMI-8402 | | SE_49954 | chr2:43437929-43439181 | RPMI-8402 | | SE_50052 | chr2:43437129-43438588 | Sigmoid_Colon | | SE_52337 | chr2:43437228-43438505 | Small_Intestine | | SE_53288 | chr2:43437488-43438534 | Spleen | | SE_54937 | chr2:43437479-43438753 | Stomach_Smooth_Muscle | | SE_55103 | chr2:43437454-43438410 | Thymus | | SE_61450 | chr2:43354337-43468354 | Toledo | | SE_62203 | chr2:43354169-43468733 | Tonsil | | SE_65350 | chr2:43437314-43438678 | Pancreatic_islets | | SE_68698 | chr2:43437173-43438588 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I043208 | chr2 | 43435568 | 43436925 | | GH02I043209 | chr2 | 43437114 | 43439109 |
|
Enhancer Sequence | TTTTCCTCAC TGTTAAAATG GGAGAATATG CTTGCCCCAG CTCTACCCCG AAAGTGGAGC 60
AGCAGCAGTT GACATTTTTG ACTGCAAAAT GTGTGCCAGG CACGGAGCCA AGCCCATCAC 120
ACCCAGCGTC GCAGAAATTC TCTCAGTAAC CTTGTGTGGA AGACACAATG GCGATTTCCA 180
TCTTGCAGGT GAGGAAACTG AGGCTCAGCT GGGTCTGTCA GTACCCTAAA GTCATATAGC 240
TGAGTGATTC CAGAGCTCCT ACTCTCAACA TTGCACTTTA TTGTTCCAAG TAAAAGATTG 300
CATTCAATCC TGTTCAGTTA CTCAGTCATC TAGCATTTAG ATGGCACCAA CTGCATGCAG 360
CCACTGAGTA AGCCACAGCC TTGATTTAAG TATCTTGTGG CCGCCCAGCT GGCACTATGT 420
TGGGGAAGGT GGGGGGCGGG AAGCAGGAGA GTTGCTGCTC CCCAAGAGCC TGGAGGTGTG 480
GGGAAATGGG GCTCAGCCAC GGGAGATTGT GAATACAGGT TCTGCCACCA GCCACTTCTA 540
GGCGTGGCTG CATAACCGTG GATGATTCAC TTAACCTCTG TCTGCTGGGG TTCTGGCTCC 600
CATGATGGTT AGAACACCAC CTTCTAGGAT TGGTTCAAGG ATGGCATGGC ATAATAAGAA 660
CACTTTGAGG GAGGGGGTTT GACAGAGTAT ACTCCATAAA TTATGGCCAC TGTTATTATT 720
ATTATTATTG AGATGGAGTC TCAGTCTATC ACCCAGGCTG GAGTGCAGTG GCGCAATCTC 780
AGCTCACTGC AACCTCCGGC TCCCAGGTTC AAGTGATTCT CCTGCTTCGG CCTCCCTAGT 840
AGCTGGGATT ACAGGCGCGT GCCACCACGC CCAGCTAGTT TTTGTATTTT TAGTAGAGAC 900
AGGGTTTTGC CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACTCAGGTGA TCCTCCCGCC 960
TCAGCCTCCC AAAGTGCTGA GATTACAGGT GTGAGCCACT GCACCTGGCC ATGGCCATTA 1020
TTCTTAAAAC GAGCAACTGG AGAACAGGGG ACTATTGAGC TTGGCCAGAT GTCCAGCTAT 1080
GTATCCACAG GGGCCTCAGG AGTTTTCAGA GTGGGGAGCA AGGCCTCTGG CCTGGAGCAG 1140
ACAGGGCTGC TTCCTAGAAG AGGAAGCCTC AGGTGCCAGG CTGAAGGGCT GGAAACTGGG 1200
AGCTGGTGGG AAGGAAGGTG TCTGGGCCAG GATGTGGAGT GGGGCAGGGA GGAGGTGCGC 1260
CTTTGAGTGT ATGTGAGAGA GACAGAGACA GCTGGCCCTG AGGCCACCGT ACAGGTGTGA 1320
ACAGGTGAGC CGTGAACCCC ATGCTGATTC TTTGCAGGGC AAGGGGCTCC TATGCCAGGG 1380
AGAGGCCTCT GGGACACAGG AGCGCTGTGG GGTAGGGAAG CCTGCACGCC TCACACGTGG 1440
GGGATGCATG GCCTGCAACT GACCAGAAGA AGCCCAGTTA GGCCCTGGCT GGGCTCTCCT 1500
TTGGTGCTAT CCCTTGGGCC AGTATCAAGA GCTGCAGATG TGCACGCCTA TGGAGCTCTT 1560
GGGAGCCTCA GCCCTCACGC CCCCATCATC ACCCCCCAGC CAGCCCACGG GGCCTCAGGT 1620
GGCGGGAAGG CAGGACCGCA GGGCCTGTGG CAGGGCAGGG AAAGGCACGG AATGGTGTTT 1680
ACATTTTCCC TCCTTCCCTG CTGGCCTGGC GGTTACACCA CTGCGGTTTG TTGGCCCCAG 1740
GGAGCGCCTC CCTTACATAA CGCCTGACAT AACTGCCCTA AAACACACGC ATGGCAACTC 1800
CCACATAGCA CCACACATGC TGTCATGCCG GCTCACCCCC CCACACTCAC ACACACTCAC 1860
AGAGCCACAC CACAGCCTCA CGCACTCACA CACACACACC CCTTCCCACA CACGCTGTCA 1920
TCCCAATGCT GTCATTTCAG AAAGGATTTC TTTTGCTCCC ACCACCCATC ACACAGGCAG 1980
GGCCTCCCCG ACGTGGCTTC AGTGCCTCTG GTTCCTCAGG CCCCAGGAGC CCTGAGCCCA 2040
CTGGGACTGC TCCAGGCCTC GCCTGGGTCT CCCAGGTGGC AGCCTCAGAC TGTGGTGCCA 2100
GCCTAGGCAG TGGACGACAA CAGGGGGACT TGAGAACAGG GCAGGGAGTC GGAGAAAGAC 2160
CAGAGTCCAG GCTGGAGCCC CTGAGATGTG GACTCCAGAA ACTCAGAACA GGCAGTGGGG 2220
AGGGACAGAC AGGGAGGGAC GCGGCCTCCG AGGTATTATA CTTAGTGCAA CATGTTACTA 2280
CGAGGGCAGG CTTCAAGCAT TTAATGCATG ATGGGCCAGG CGCAGTGGCT AACGCCTATA 2340
ATCCCAGCAC TTTGGCAGGC CGGAGGATGG CTTGAGCTCA GGAGTTCGAC ACCAGCCTGG 2400
ACAACATAGC GAGACCCCCT GTCTATAAAA AATAAAATAA TACTATAAAT 2450
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