Tag | Content |
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EnhancerAtlas ID | HS012-25841 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr8:145038930-145041350 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr8:145040223-145040235 | TGCCCCCTGGCA | - | 6.62 | KLF4 | MA0039.3 | chr8:145039873-145039884 | CCACACCCTCC | + | 6.32 | RREB1 | MA0073.1 | chr8:145039159-145039179 | CCCCCACCCCCCCGCCCACC | + | 6.13 | RREB1 | MA0073.1 | chr8:145039149-145039169 | CCCCAACCAACCCCCACCCC | + | 7.4 | RREB1 | MA0073.1 | chr8:145039148-145039168 | CCCCCAACCAACCCCCACCC | + | 9.78 | RUNX1 | MA0002.2 | chr8:145041231-145041242 | AAACCACAGAC | - | 6.62 | ZNF263 | MA0528.1 | chr8:145040343-145040364 | CCTCACGCCCCTTCCTCCTTC | - | 6.42 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_02906 | chr8:145040086-145040764 | Bladder | SE_09260 | chr8:145034556-145040156 | CD14 | SE_12121 | chr8:145039150-145040900 | CD3 | SE_14847 | chr8:145039197-145041588 | CD4_Memory_Primary_7pool | SE_16928 | chr8:145039798-145041337 | CD4p_CD225int_CD127p_Tmem | SE_17383 | chr8:145034326-145054098 | CD4p_CD25-_CD45RAp_Naive | SE_17884 | chr8:145039216-145041514 | CD4p_CD25-_CD45ROp_Memory | SE_18961 | chr8:145039229-145042264 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19196 | chr8:145039718-145041365 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23034 | chr8:145039553-145040644 | CD8_primiary | SE_23735 | chr8:145039917-145040401 | Colon_Crypt_2 | SE_31395 | chr8:145039839-145041000 | Gastric | SE_37176 | chr8:145039935-145042270 | HSMMtube | SE_44278 | chr8:145040057-145041129 | NHDF-Ad | SE_46680 | chr8:145039958-145041197 | Ovary | SE_50057 | chr8:145039713-145041288 | Sigmoid_Colon | SE_52367 | chr8:145039878-145041226 | Small_Intestine | SE_55146 | chr8:145040283-145041253 | Thymus | SE_61753 | chr8:145002108-145053930 | Toledo | SE_62528 | chr8:145001740-145054046 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 145040615 | 145041072 | chr8 | 145040786 | 145041230 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I143964 | chr8 | 145038538 | 145042092 |
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Enhancer Sequence | TCTTAGGCCT ATCCTGTGCC TGCTCTGTTA GCTTCCCAGG TAGCCACTCG TTTAGCAAGA 60 AAGAAGAGAA AGAGATGCAC TTTCAAAAGG TCAAAAGACA CATTCATTTG AAAAACAGAG 120 CAGAATAAAA ATCATAAAAG CCACAACCAG AGACCTTTAC TGCAGCTACC TCCTTCTGCT 180 CCTGCAGACC CACACTTCCA GCCCTGACCA GCCCCACTCC CCCAACCAAC CCCCACCCCC 240 CCGCCCACCC TGGTGTGCCC CTGTGGATGG CCTTCCCCAC CCTCACCGTC CCACTTGGCC 300 CCAGCCCACC TGACACACCA GCCTGCCCAA GAGCACCCAG ACTCACACCA GCCACCCTGA 360 TGCCGTCCTG GGGCCTTCCT TTCCTGCAGC ACTGGCCCTG GGTCTGCCGC TACTCCTGGA 420 GCCACACAGG GACACAAAGT GATCCCCATC CCATTCCTGG TCCTGGGTCT CCTCTGCCTC 480 CAGGAAGAAG CAGCAACAGT CCTGCCAAGA GCTGACCACC AGCTGGGAGG ACTCTTCTGC 540 AGCTAACCAG GACCCAAATC CTGGAGAGCA GGCCCCACAG GCTGATGTCC CAAGTCCTAC 600 AGGATCCTGT CTTCCCAGCT GGCACCCTCC TTCCACCGTC TGAACGCGTG TTCCCAACTC 660 CCCTTCCACT GGGCCTACAG ATGACCCGGC CCATGCCCCA TTTTGGGTCC CTGACCTCAT 720 GACCCACGGC CCCTGCTCTC CCAGCCCCGC ATCTCCCTAC CCACTGTGGG TCTGTGGGCA 780 TCACCCATGA CCCCAGCGGT GGGAGATCTG GGCACCTGGT CCCACTAGCA TCGCCCTTCC 840 CAGCCTCCTC CAGTCCCTTC TTGAGGTACC TGGCCCCTGG CCCCTCTGCT GCCAGCTCCT 900 CTTGGGCCTC ACTGGGGAAA CTGAGGCCAC AGGGCACCAC TGCCCACACC CTCCCAACAG 960 CCCAACCCTG GGAAAATCTC CAGGGCCCTC AGTGGTGAGC AGCAGTCTGG ACTGGCCACT 1020 GATGATGTGT GGCTGGGTAA ATGTGAGCGA CCACTCAGTA CTCACCCTGG GCCAGGTGAT 1080 GCCCATGCCC CCTGTGACCA TGCAGGTCCC TCAGGCCAAG GCCCAGGGAA CTCCTTCCCC 1140 AGGGAACTCG GGCCAGCATC CAGCTGAGGC TGTGACCTGC TGCGGCCTAG CCTCCATGTC 1200 ACCGCTCTGT CCTGGAGAGG GTTCTCCCTC CCTGCCACCC TGCTGGACCC ACCATAGCCT 1260 GGCACCAGCA GGGCCTCCTG AGCACTTCCC ACATGCCCCC TGGCACCTCC AATCCGACGA 1320 CACCCCAAGC AGTCCCGCTG AGGTCCCAAC ACCCCTCATC ACCTGGTCCC AGCACCATCC 1380 AGGCCTCACC CTGCTCCCAA CGTGGCCCTG CTTCCTCACG CCCCTTCCTC CTTCGCAGAC 1440 CCAACAGGCC CCCATGGCTG CACAGCTGCC CACTGCTCTG CTTCCCGGCT GCCTCTTCTC 1500 ATAGGCACCT AAGCTCTGGA GGACCCCAGG CTCAGAGCTC TGGCCCGAGG CCTGCCCTAG 1560 TGATGGCCTC CCAGCCTGGC CTCCCCACCT CAGCCCAGCA TTTCCTGCAC CTCAGTGTCT 1620 GCACACGCAT ACCTATCTCA CAGGCATCTC TGATTTTATG CACCCAAGGC TAAGCGCTGG 1680 CTCTTCCGCC CTCTCTGCCG CAGGCACATC CTCTCCACCC CAGGCTGCTC TCTACCTCCA 1740 CAGCCACCAC GGGGGACTCC TCAGCCGCTC CTTGGGAGGC ACCAGGCCAG GATCTTGCAG 1800 GGGTCCAGCC AGCTCCAAGT CCACCTATCC CTCCCACCCA ACGCTTGTTT CAAGCCACAC 1860 CTGCCACAGG ACAGGGCGGG GCTCGGCTGG GGGGGTACAA AAGTGAAGCA ACACATAGTC 1920 CCCGCGTCAG GAAGCTGGAT TCTGCCACAG GACAGGGCAG GGCTCGGCTC GGGGGCACAG 1980 AAGTGAAGCA ATACACAGCC CCTGCGTCAG GAAGCCGGAT TGGTGGAAGG GGAGATGTTT 2040 ACAATCATCC CTGTAACCCA CAAGCCCACG GCCAGACCCT ATGAGCGTGA CACCAAGCAT 2100 GACATCGAGC CTCCTTGAAC ATCTCGACCT CAGCCCCAAG CAAATTCCAC AAAGATTAAC 2160 GACAGAGATG TTTAAAAAAA TGCAGCAGTG CTGGAAGCAA CTCTCAGCAG ATGTTTTTCT 2220 AAAAGAAGGC CATTTTAAGC ATAGCATAAA ATCCAGAAAT CATAAAAGAC TGGTGAGTGT 2280 TAAAAATTGA TATGGCTAAA GAAACCACAG ACAGAATTAG GCCAGGCGCG GTGGCTCACG 2340 CCTGTAATCC CAGCACTTTG GGAGGCCGAG GTGGGCAGAT CACGAGGTCA GGAGATCGAG 2400 ACTGTCCTGG CTAACACGGT 2420
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