Tag | Content |
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EnhancerAtlas ID | HS081-01624 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:201986510-201988730 |
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 |
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| 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 |
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| 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 |
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Enhancer Sequence | CAGGGCGTAG GTCTAGCCTC AGAAGCTGGG GAAGCTTTCA CAGCTACTTA GTCTAAAAAT 60 GACCCCATTT CTTGGAAATT ATGCATTAGA CTCTGGTCTA GTTTCCCTAG CCACAATATC 120 TCGGGGTCCT TGCACCCTTA AAAGAGGTGA CCCAGCTGGG CGCGGTAGTT CACGCCTGTA 180 ATCCTCGTAC TTTGGGAAGC CAAGGCGGGA GGATCACGAG GTCAGAAGAT CGAGGCCATC 240 ATGGCCAACA CGGTGAAACC CCGTCTCTAC TAAACATACA AAAATTAGCT GGGCATGCTG 300 GCACGCGCCT GTAGTCCGAG CTACTCAGGA GGCTGAGGCA GGAGAATCAC TTGAACCCAG 360 GAGGCGGAGG TTGCAGTGAG CTAAGATCAT GCCACTGCAC TCCAGCCTGG TGACACAGGG 420 AGACTCTGTC TCAAAAAAAA GAAGAGAGGT GACCCAGTGT GGCCTGAAGT CACCTAGCCA 480 AGAAGTGGGG GAGGGGCCTC TAGAGCCCGG GACATGCTTG TTCAGCCTCC CTTGACTCCC 540 AGCCTCTTCA GCTTCTAAAG GAGATCCTAG CAGGGAGGAG GGCTGGGAAT ATGGCGCTCA 600 GCCCCTTCAC CCTCTTCTGG AGGGCTGGGG GCAGGTGCTG CCCGCTGCGT GCTGACCTTT 660 GCCCTGCCAT TTGCAGTTTA TGAGGCGCTT TCCTCATCCC ATTATCTCAT TTGATCCGCC 720 CCACAGCTCG CTGAGGAGAC CAGGTGTCCC CATTTTACTG ACAAGGCTAG TGGTGGGCTG 780 AAGTCACTGA CTGGGTGAGA GCGGGGCCAG CTCACAGCAT GCCTGCCTCC ACGCTGCAGC 840 TCAGTGAGAC CACCTGGGCA GGTGGCCTCT GCAGGGCAGC GCCTGGGACA GCCTGGAAGA 900 CGGCAGCTCT GGGAGGGACG CCTTTCTCCC CAACAGTTCT CTGCCCTCTC ACCCCTCAGG 960 ATGCTGCAGA GTCCTGGCAC GGGCCCCTGG GCTGGCCTCC GTGCTGCCCT CTCTGTCGGG 1020 CACCAGTCAC CCTTACCCCG ACTCTCACCA GCCCAGGGGC CTCCTAGCAG GAGACGGCCC 1080 GGTCTCTCGC CCACCAGAGT CTGCATCCCC TCAGGTGTGT CCTGGGCTGG GGAGTGGGGG 1140 TGGGGAGGAA GCCACAGGGC CGGGCTGTTT ATATCCCGCC CTGCCGGAGC TGCTGGTCAC 1200 CTCTTATCTG CTTCTGTGGG ATTGGGTGTG TCGCTGAGCA GGTCAGAGGG AGGTCACCCC 1260 TCCCGTCGTG TTTGGGTGTG CCTGAGGAGG GGCTGGGGTT GGCCCCCTGG GACAGTTCCT 1320 GGCTTATCCC ACAGCCCCAC CTGTCCCACC AATTCTGGGG AAGTCTGGCT TCTCCTGGGG 1380 GAAGTGGGTG AAGGGGTTGC ATTTCTGAGG AGTCTGGTTT CAATCTGCTC TCTCTCTCTG 1440 CTGTTGTCTG TTTACACATC TCTCTCTCTC GCCGGGCTGT GAGCACCTCT GGGCAAGTGC 1500 TGGGGCTTAC TCACCTCAGC ACCTTGCACA GCGCCTGGCA CAGAGGAGGT GCTCGATAAA 1560 TATTTGCTAA ATGGCCCCGT GACTCTCCCT GCCCTGGCCA CTACCTCCCC CACACACCAC 1620 ACACATTCAT ACACACTCAT GGGAACCAAA GTCACACACA CTCACACTCA CAAAGATAAA 1680 TATTCACAAG CCCTCACTCA CATGCCCCTG CACGCACTGC AGACGCTGCC TGCTCTCACA 1740 CACTCGCATG GACCGTATTC ACAACCTCAC ACACTTGCAC ACACCAGCGC ACGCAACACA 1800 CTCCCACCTC ACAGTCTCAC ATAGCCACAC CCAGGCCTGC CTGCACGACT CACCTCCTCC 1860 CTCGGGGTCC TTCTATGAAG CATTTCCTGA CCTCCTCTTT GGCCCTTTTC CCCCACCAGA 1920 TGGGTTCAGC CCTTGCCTCC AGTCAGGACA GGCCTGGTAA TTTGCAGAGC CCAGTGCAAA 1980 GTGAAAGCCT GGGCCCTTGT TAAAGAATTA TTAGGCTGGG CGCAGTGGCT CATGCCAGTA 2040 ATCCCACACT TTGGGAGGCC GAGGCGGGTG GATCGCCTGA GGTCAGGAGT TTGAGACCAG 2100 CCTGACCAAC ATGGCGAAAC CCCATCTCTA CTAAAAATAC AAAATTAGCT GGGCGTGGTG 2160 GTGTGCGCCT GTAATCCTAG CTACTCTGGA GGTTGAGGCA GAAGAATCGC TTGAACCTGG 2220
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