Tag | Content |
---|
EnhancerAtlas ID | HS110-00298 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr1:201986440-201988760 |
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 | Stat4 | MA0518.1 | chr1:201986574-201986588 | CCATTTCTTGGAAA | - | 6.27 | Zfx | MA0146.2 | chr1:201988564-201988578 | GAGGCCGAGGCGGG | - | 6.01 |
|
| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:201983954-201986869 | Colon_Crypt_1 | SE_23058 | chr1:201986872-201988608 | Colon_Crypt_1 | SE_23723 | chr1:201986197-201986763 | Colon_Crypt_2 | SE_23723 | chr1:201986912-201988613 | Colon_Crypt_2 | SE_24689 | chr1:201983940-201986805 | Colon_Crypt_3 | 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 | chr1:201986352-201986765 | LNCaP | SE_41626 | chr1:201986861-201988608 | LNCaP | SE_43434 | chr1:201986069-201986790 | MCF-7 | SE_43434 | chr1:201986862-201988630 | MCF-7 | SE_47796 | chr1:201986464-201986785 | Pancreas | SE_47796 | chr1:201986886-201988593 | Pancreas | SE_50066 | chr1:201978058-201988672 | Sigmoid_Colon | SE_52354 | chr1:201976011-201988714 | Small_Intestine | SE_56834 | chr1:201983957-201986837 | VACO_400 | 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 201987200 | 201988600 | chr1 | 201987611 | 201988279 | chr1 | 201986905 | 201988549 |
|
Enhancer Sequence | ATTTGGAAAA AGGCTTTTAC TTACATTTCC CTTCTGAAGT GTGAGCCAGT TAGACAAAGG 60 GGATGCGGGC CAGGGCGTAG GTCTAGCCTC AGAAGCTGGG GAAGCTTTCA CAGCTACTTA 120 GTCTAAAAAT GACCCCATTT CTTGGAAATT ATGCATTAGA CTCTGGTCTA GTTTCCCTAG 180 CCACAATATC TCGGGGTCCT TGCACCCTTA AAAGAGGTGA CCCAGCTGGG CGCGGTAGTT 240 CACGCCTGTA ATCCTCGTAC TTTGGGAAGC CAAGGCGGGA GGATCACGAG GTCAGAAGAT 300 CGAGGCCATC ATGGCCAACA CGGTGAAACC CCGTCTCTAC TAAACATACA AAAATTAGCT 360 GGGCATGCTG GCACGCGCCT GTAGTCCGAG CTACTCAGGA GGCTGAGGCA GGAGAATCAC 420 TTGAACCCAG GAGGCGGAGG TTGCAGTGAG CTAAGATCAT GCCACTGCAC TCCAGCCTGG 480 TGACACAGGG AGACTCTGTC TCAAAAAAAA GAAGAGAGGT GACCCAGTGT GGCCTGAAGT 540 CACCTAGCCA AGAAGTGGGG GAGGGGCCTC TAGAGCCCGG GACATGCTTG TTCAGCCTCC 600 CTTGACTCCC AGCCTCTTCA GCTTCTAAAG GAGATCCTAG CAGGGAGGAG GGCTGGGAAT 660 ATGGCGCTCA GCCCCTTCAC CCTCTTCTGG AGGGCTGGGG GCAGGTGCTG CCCGCTGCGT 720 GCTGACCTTT GCCCTGCCAT TTGCAGTTTA TGAGGCGCTT TCCTCATCCC ATTATCTCAT 780 TTGATCCGCC CCACAGCTCG CTGAGGAGAC CAGGTGTCCC CATTTTACTG ACAAGGCTAG 840 TGGTGGGCTG AAGTCACTGA CTGGGTGAGA GCGGGGCCAG CTCACAGCAT GCCTGCCTCC 900 ACGCTGCAGC TCAGTGAGAC CACCTGGGCA GGTGGCCTCT GCAGGGCAGC GCCTGGGACA 960 GCCTGGAAGA CGGCAGCTCT GGGAGGGACG CCTTTCTCCC CAACAGTTCT CTGCCCTCTC 1020 ACCCCTCAGG ATGCTGCAGA GTCCTGGCAC GGGCCCCTGG GCTGGCCTCC GTGCTGCCCT 1080 CTCTGTCGGG CACCAGTCAC CCTTACCCCG ACTCTCACCA GCCCAGGGGC CTCCTAGCAG 1140 GAGACGGCCC GGTCTCTCGC CCACCAGAGT CTGCATCCCC TCAGGTGTGT CCTGGGCTGG 1200 GGAGTGGGGG TGGGGAGGAA GCCACAGGGC CGGGCTGTTT ATATCCCGCC CTGCCGGAGC 1260 TGCTGGTCAC CTCTTATCTG CTTCTGTGGG ATTGGGTGTG TCGCTGAGCA GGTCAGAGGG 1320 AGGTCACCCC TCCCGTCGTG TTTGGGTGTG CCTGAGGAGG GGCTGGGGTT GGCCCCCTGG 1380 GACAGTTCCT GGCTTATCCC ACAGCCCCAC CTGTCCCACC AATTCTGGGG AAGTCTGGCT 1440 TCTCCTGGGG GAAGTGGGTG AAGGGGTTGC ATTTCTGAGG AGTCTGGTTT CAATCTGCTC 1500 TCTCTCTCTG CTGTTGTCTG TTTACACATC TCTCTCTCTC GCCGGGCTGT GAGCACCTCT 1560 GGGCAAGTGC TGGGGCTTAC TCACCTCAGC ACCTTGCACA GCGCCTGGCA CAGAGGAGGT 1620 GCTCGATAAA TATTTGCTAA ATGGCCCCGT GACTCTCCCT GCCCTGGCCA CTACCTCCCC 1680 CACACACCAC ACACATTCAT ACACACTCAT GGGAACCAAA GTCACACACA CTCACACTCA 1740 CAAAGATAAA TATTCACAAG CCCTCACTCA CATGCCCCTG CACGCACTGC AGACGCTGCC 1800 TGCTCTCACA CACTCGCATG GACCGTATTC ACAACCTCAC ACACTTGCAC ACACCAGCGC 1860 ACGCAACACA CTCCCACCTC ACAGTCTCAC ATAGCCACAC CCAGGCCTGC CTGCACGACT 1920 CACCTCCTCC CTCGGGGTCC TTCTATGAAG CATTTCCTGA CCTCCTCTTT GGCCCTTTTC 1980 CCCCACCAGA TGGGTTCAGC CCTTGCCTCC AGTCAGGACA GGCCTGGTAA TTTGCAGAGC 2040 CCAGTGCAAA GTGAAAGCCT GGGCCCTTGT TAAAGAATTA TTAGGCTGGG CGCAGTGGCT 2100 CATGCCAGTA ATCCCACACT TTGGGAGGCC GAGGCGGGTG GATCGCCTGA GGTCAGGAGT 2160 TTGAGACCAG CCTGACCAAC ATGGCGAAAC CCCATCTCTA CTAAAAATAC AAAATTAGCT 2220 GGGCGTGGTG GTGTGCGCCT GTAATCCTAG CTACTCTGGA GGTTGAGGCA GAAGAATCGC 2280 TTGAACCTGG GAGGCGGAGG TTGCCGTGAA CCAAGATCAT 2320
|