| Tag | Content |
|---|
EnhancerAtlas ID | HS101-23463 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:43435670-43438640 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
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 | CTGCATTGGG AAGGGATGGG GGAAAACAGG GGAATAGAGG TACAGCACTC AGGTACAGCC 60
TGTGGACCCC AGGCCAGGCC AGGCTGGAGG TCTTCCAGGA TTGGAAGGCT AACAGGGCAG 120
GTCACCCTGG AGAGACAGGC TCAGCCTCCC CTGAAGGGCC ACAGTGTCTT CCTCCTTTAA 180
GGAGACAAGG TTACTCTGAT GCCCACCTCT TCCTGTAAGG CCTCCTTGAT TAATCCCTCC 240
TTCACAGGGG TAGAAAAATG AGAGTACTAT CTTTCCAAGA GGACACTGCT CTCTTGCTGA 300
TCAGAAACTT TTGTAAGGTC TAGAAAAATA TTTTCCTCCA TTGACTCCAC TGCCTCTATC 360
CACACTGACT GGATGAGAAG CGCTGGCCTG TTGTTAAAGG TTCCAGGCTA GGAATCAGCA 420
ATTTGCAGTT GCAGTCCAAG TCCTGCAGGA ACTTGGGAAA GTGGTTTCTC TGGGCCTCAG 480
TTTTCCTCAC TGTTAAAATG GGAGAATATG CTTGCCCCAG CTCTACCCCG AAAGTGGAGC 540
AGCAGCAGTT GACATTTTTG ACTGCAAAAT GTGTGCCAGG CACGGAGCCA AGCCCATCAC 600
ACCCAGCGTC GCAGAAATTC TCTCAGTAAC CTTGTGTGGA AGACACAATG GCGATTTCCA 660
TCTTGCAGGT GAGGAAACTG AGGCTCAGCT GGGTCTGTCA GTACCCTAAA GTCATATAGC 720
TGAGTGATTC CAGAGCTCCT ACTCTCAACA TTGCACTTTA TTGTTCCAAG TAAAAGATTG 780
CATTCAATCC TGTTCAGTTA CTCAGTCATC TAGCATTTAG ATGGCACCAA CTGCATGCAG 840
CCACTGAGTA AGCCACAGCC TTGATTTAAG TATCTTGTGG CCGCCCAGCT GGCACTATGT 900
TGGGGAAGGT GGGGGGCGGG AAGCAGGAGA GTTGCTGCTC CCCAAGAGCC TGGAGGTGTG 960
GGGAAATGGG GCTCAGCCAC GGGAGATTGT GAATACAGGT TCTGCCACCA GCCACTTCTA 1020
GGCGTGGCTG CATAACCGTG GATGATTCAC TTAACCTCTG TCTGCTGGGG TTCTGGCTCC 1080
CATGATGGTT AGAACACCAC CTTCTAGGAT TGGTTCAAGG ATGGCATGGC ATAATAAGAA 1140
CACTTTGAGG GAGGGGGTTT GACAGAGTAT ACTCCATAAA TTATGGCCAC TGTTATTATT 1200
ATTATTATTG AGATGGAGTC TCAGTCTATC ACCCAGGCTG GAGTGCAGTG GCGCAATCTC 1260
AGCTCACTGC AACCTCCGGC TCCCAGGTTC AAGTGATTCT CCTGCTTCGG CCTCCCTAGT 1320
AGCTGGGATT ACAGGCGCGT GCCACCACGC CCAGCTAGTT TTTGTATTTT TAGTAGAGAC 1380
AGGGTTTTGC CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACTCAGGTGA TCCTCCCGCC 1440
TCAGCCTCCC AAAGTGCTGA GATTACAGGT GTGAGCCACT GCACCTGGCC ATGGCCATTA 1500
TTCTTAAAAC GAGCAACTGG AGAACAGGGG ACTATTGAGC TTGGCCAGAT GTCCAGCTAT 1560
GTATCCACAG GGGCCTCAGG AGTTTTCAGA GTGGGGAGCA AGGCCTCTGG CCTGGAGCAG 1620
ACAGGGCTGC TTCCTAGAAG AGGAAGCCTC AGGTGCCAGG CTGAAGGGCT GGAAACTGGG 1680
AGCTGGTGGG AAGGAAGGTG TCTGGGCCAG GATGTGGAGT GGGGCAGGGA GGAGGTGCGC 1740
CTTTGAGTGT ATGTGAGAGA GACAGAGACA GCTGGCCCTG AGGCCACCGT ACAGGTGTGA 1800
ACAGGTGAGC CGTGAACCCC ATGCTGATTC TTTGCAGGGC AAGGGGCTCC TATGCCAGGG 1860
AGAGGCCTCT GGGACACAGG AGCGCTGTGG GGTAGGGAAG CCTGCACGCC TCACACGTGG 1920
GGGATGCATG GCCTGCAACT GACCAGAAGA AGCCCAGTTA GGCCCTGGCT GGGCTCTCCT 1980
TTGGTGCTAT CCCTTGGGCC AGTATCAAGA GCTGCAGATG TGCACGCCTA TGGAGCTCTT 2040
GGGAGCCTCA GCCCTCACGC CCCCATCATC ACCCCCCAGC CAGCCCACGG GGCCTCAGGT 2100
GGCGGGAAGG CAGGACCGCA GGGCCTGTGG CAGGGCAGGG AAAGGCACGG AATGGTGTTT 2160
ACATTTTCCC TCCTTCCCTG CTGGCCTGGC GGTTACACCA CTGCGGTTTG TTGGCCCCAG 2220
GGAGCGCCTC CCTTACATAA CGCCTGACAT AACTGCCCTA AAACACACGC ATGGCAACTC 2280
CCACATAGCA CCACACATGC TGTCATGCCG GCTCACCCCC CCACACTCAC ACACACTCAC 2340
AGAGCCACAC CACAGCCTCA CGCACTCACA CACACACACC CCTTCCCACA CACGCTGTCA 2400
TCCCAATGCT GTCATTTCAG AAAGGATTTC TTTTGCTCCC ACCACCCATC ACACAGGCAG 2460
GGCCTCCCCG ACGTGGCTTC AGTGCCTCTG GTTCCTCAGG CCCCAGGAGC CCTGAGCCCA 2520
CTGGGACTGC TCCAGGCCTC GCCTGGGTCT CCCAGGTGGC AGCCTCAGAC TGTGGTGCCA 2580
GCCTAGGCAG TGGACGACAA CAGGGGGACT TGAGAACAGG GCAGGGAGTC GGAGAAAGAC 2640
CAGAGTCCAG GCTGGAGCCC CTGAGATGTG GACTCCAGAA ACTCAGAACA GGCAGTGGGG 2700
AGGGACAGAC AGGGAGGGAC GCGGCCTCCG AGGTATTATA CTTAGTGCAA CATGTTACTA 2760
CGAGGGCAGG CTTCAAGCAT TTAATGCATG ATGGGCCAGG CGCAGTGGCT AACGCCTATA 2820
ATCCCAGCAC TTTGGCAGGC CGGAGGATGG CTTGAGCTCA GGAGTTCGAC ACCAGCCTGG 2880
ACAACATAGC GAGACCCCCT GTCTATAAAA AATAAAATAA TACTATAAAT TAGGAAAAAT 2940
GCATGTGACC CTCCCAAGAA ACACGTGAGC 2970
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