Tag | Content |
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EnhancerAtlas ID | HS120-00578 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr1:201986810-201988580 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr1:201988332-201988343 | AGCCACACCCA | + | 6.14 | NR2C2 | MA0504.1 | chr1:201987451-201987466 | TGCCCTCTCACCCCT | - | 6.45 | NR2C2 | MA0504.1 | chr1:201987162-201987177 | TGACCTTTGCCCTGC | - | 6.4 | Nr2f6 | MA0677.1 | chr1:201987162-201987176 | TGACCTTTGCCCTG | - | 6.45 | RARA(var.2) | MA0730.1 | chr1:201987749-201987766 | AGGTCAGAGGGAGGTCA | + | 6.41 | REST | MA0138.2 | chr1:201988024-201988045 | CTCAGCACCTTGCACAGCGCC | + | 7.87 | Rxra | MA0512.2 | chr1:201987162-201987176 | TGACCTTTGCCCTG | - | 6.09 | Zfx | MA0146.2 | chr1:201988564-201988578 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:201986872-201988608 | Colon_Crypt_1 | SE_23723 | chr1:201986912-201988613 | Colon_Crypt_2 | SE_24689 | chr1:201986888-201988638 | Colon_Crypt_3 | SE_25977 | chr1:201976074-201988947 | Duodenum_Smooth_Muscle | SE_26730 | chr1:201985712-201988797 | Esophagus | SE_27624 | chr1:201975812-201989193 | Fetal_Intestine | SE_28545 | chr1:201974530-201989440 | Fetal_Intestine_Large | SE_31432 | chr1:201983938-201989177 | Gastric | SE_33417 | chr1:201986876-201989229 | H2171 | SE_33792 | chr1:201978127-201990221 | HCC1954 | SE_34304 | chr1:201974676-201989923 | HCT-116 | SE_34741 | chr1:201985668-201989981 | HeLa | SE_41626 | chr1:201986861-201988608 | LNCaP | SE_43434 | chr1:201986862-201988630 | MCF-7 | SE_47796 | chr1:201986886-201988593 | Pancreas | SE_50066 | chr1:201978058-201988672 | Sigmoid_Colon | SE_52354 | chr1:201976011-201988714 | Small_Intestine | SE_56834 | chr1:201986879-201988600 | VACO_400 | SE_57376 | chr1:201986910-201988595 | VACO_503 | SE_57945 | chr1:201986912-201988581 | VACO_9m | SE_65333 | chr1:201986253-201989108 | Pancreatic_islets | SE_67013 | chr1:201986876-201989229 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 201987611 | 201988279 | chr1 | 201986905 | 201988549 |
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Enhancer Sequence | GCACGCGCCT GTAGTCCGAG CTACTCAGGA GGCTGAGGCA GGAGAATCAC TTGAACCCAG 60 GAGGCGGAGG TTGCAGTGAG CTAAGATCAT GCCACTGCAC TCCAGCCTGG TGACACAGGG 120 AGACTCTGTC TCAAAAAAAA GAAGAGAGGT GACCCAGTGT GGCCTGAAGT CACCTAGCCA 180 AGAAGTGGGG GAGGGGCCTC TAGAGCCCGG GACATGCTTG TTCAGCCTCC CTTGACTCCC 240 AGCCTCTTCA GCTTCTAAAG GAGATCCTAG CAGGGAGGAG GGCTGGGAAT ATGGCGCTCA 300 GCCCCTTCAC CCTCTTCTGG AGGGCTGGGG GCAGGTGCTG CCCGCTGCGT GCTGACCTTT 360 GCCCTGCCAT TTGCAGTTTA TGAGGCGCTT TCCTCATCCC ATTATCTCAT TTGATCCGCC 420 CCACAGCTCG CTGAGGAGAC CAGGTGTCCC CATTTTACTG ACAAGGCTAG TGGTGGGCTG 480 AAGTCACTGA CTGGGTGAGA GCGGGGCCAG CTCACAGCAT GCCTGCCTCC ACGCTGCAGC 540 TCAGTGAGAC CACCTGGGCA GGTGGCCTCT GCAGGGCAGC GCCTGGGACA GCCTGGAAGA 600 CGGCAGCTCT GGGAGGGACG CCTTTCTCCC CAACAGTTCT CTGCCCTCTC ACCCCTCAGG 660 ATGCTGCAGA GTCCTGGCAC GGGCCCCTGG GCTGGCCTCC GTGCTGCCCT CTCTGTCGGG 720 CACCAGTCAC CCTTACCCCG ACTCTCACCA GCCCAGGGGC CTCCTAGCAG GAGACGGCCC 780 GGTCTCTCGC CCACCAGAGT CTGCATCCCC TCAGGTGTGT CCTGGGCTGG GGAGTGGGGG 840 TGGGGAGGAA GCCACAGGGC CGGGCTGTTT ATATCCCGCC CTGCCGGAGC TGCTGGTCAC 900 CTCTTATCTG CTTCTGTGGG ATTGGGTGTG TCGCTGAGCA GGTCAGAGGG AGGTCACCCC 960 TCCCGTCGTG TTTGGGTGTG CCTGAGGAGG GGCTGGGGTT GGCCCCCTGG GACAGTTCCT 1020 GGCTTATCCC ACAGCCCCAC CTGTCCCACC AATTCTGGGG AAGTCTGGCT TCTCCTGGGG 1080 GAAGTGGGTG AAGGGGTTGC ATTTCTGAGG AGTCTGGTTT CAATCTGCTC TCTCTCTCTG 1140 CTGTTGTCTG TTTACACATC TCTCTCTCTC GCCGGGCTGT GAGCACCTCT GGGCAAGTGC 1200 TGGGGCTTAC TCACCTCAGC ACCTTGCACA GCGCCTGGCA CAGAGGAGGT GCTCGATAAA 1260 TATTTGCTAA ATGGCCCCGT GACTCTCCCT GCCCTGGCCA CTACCTCCCC CACACACCAC 1320 ACACATTCAT ACACACTCAT GGGAACCAAA GTCACACACA CTCACACTCA CAAAGATAAA 1380 TATTCACAAG CCCTCACTCA CATGCCCCTG CACGCACTGC AGACGCTGCC TGCTCTCACA 1440 CACTCGCATG GACCGTATTC ACAACCTCAC ACACTTGCAC ACACCAGCGC ACGCAACACA 1500 CTCCCACCTC ACAGTCTCAC ATAGCCACAC CCAGGCCTGC CTGCACGACT CACCTCCTCC 1560 CTCGGGGTCC TTCTATGAAG CATTTCCTGA CCTCCTCTTT GGCCCTTTTC CCCCACCAGA 1620 TGGGTTCAGC CCTTGCCTCC AGTCAGGACA GGCCTGGTAA TTTGCAGAGC CCAGTGCAAA 1680 GTGAAAGCCT GGGCCCTTGT TAAAGAATTA TTAGGCTGGG CGCAGTGGCT CATGCCAGTA 1740 ATCCCACACT TTGGGAGGCC GAGGCGGGTG 1770
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