Tag | Content |
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EnhancerAtlas ID | HS051-10691 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr16:68786040-68789130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIL3 | MA0025.1 | chr16:68787553-68787564 | TTATGTAACCT | + | 6.14 | Nr2f6(var.2) | MA0728.1 | chr16:68786073-68786088 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_23322 | chr16:68786073-68787147 | Colon_Crypt_1 | SE_23322 | chr16:68787368-68787838 | Colon_Crypt_1 | SE_23322 | chr16:68787899-68789733 | Colon_Crypt_1 | SE_24253 | chr16:68786090-68786429 | Colon_Crypt_2 | SE_24253 | chr16:68786596-68787062 | Colon_Crypt_2 | SE_24253 | chr16:68788032-68788811 | Colon_Crypt_2 | SE_27219 | chr16:68786047-68787223 | Esophagus | SE_27219 | chr16:68787264-68787859 | Esophagus | SE_27219 | chr16:68787861-68792041 | Esophagus | SE_27849 | chr16:68785764-68791708 | Fetal_Intestine | SE_28787 | chr16:68785690-68791659 | Fetal_Intestine_Large | SE_31536 | chr16:68786448-68786964 | Gastric | SE_31536 | chr16:68787957-68791247 | Gastric | SE_36063 | chr16:68786065-68787329 | HMEC | SE_36063 | chr16:68787373-68792875 | HMEC | SE_41715 | chr16:68788101-68788695 | LNCaP | SE_47710 | chr16:68788043-68788799 | Pancreas | SE_50611 | chr16:68786027-68789777 | Sigmoid_Colon | SE_52716 | chr16:68785875-68787188 | Small_Intestine | SE_52716 | chr16:68787232-68791878 | Small_Intestine | SE_55574 | chr16:68786520-68786933 | Thymus | SE_55574 | chr16:68788037-68788442 | Thymus | SE_55574 | chr16:68788642-68789105 | Thymus | SE_57149 | chr16:68786526-68787152 | VACO_400 | SE_57149 | chr16:68788029-68789670 | VACO_400 | SE_57852 | chr16:68788247-68789174 | VACO_503 | SE_64463 | chr16:68786079-68787849 | NHEK | SE_64463 | chr16:68788023-68792031 | NHEK | SE_65496 | chr16:68786507-68790288 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 68786306 | 68786901 | chr16 | 68788311 | 68788711 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I068750 | chr16 | 68783950 | 68792784 |
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Enhancer Sequence | GACTGGGTTT CACCATGTTG GCCAGGTTGG TCTTGAACTC CTGACCTCAG GTGATCCACC 60 CGCCTTGGCC TCCCAAAGTG CTGCGATTAC AGGCGTGAGC CACCACACCC AATCTGGACC 120 CCCTATTTAT GATAGTAAAC CCTGCCCTCA GCCCTCCCCA CCTCTTTTAC TTAATTTTCT 180 TCTAGTACTT TTCACTGTCT AACATGCTAT GTATTTCACT TATTTCTCCT GTTCACTGCG 240 GGTCTCCTCC CACTAGAACA GAAGCCTCAG GAGGCCAGGG ATTTTTAATG TCTTTTGTTT 300 TGTACTTGGG CTGAATTGCA GTTAGAATAG TGCTTGGTAC ATAATAAGGG CTCAGTAAGT 360 ATCCGAAGGA ATGAATGAAT GAGAGGTTTC AGAGTGTATT TAATACAGAC AGGACTAAAC 420 AGATCTCTCT AGAGGATATT TCACTGTAGT TGTTTTTTTC TTTTTTTAAA GACAGGGCTT 480 TATGTATTAG CCACAGAGAA GGGAGGAGGG GTGTTCTCAG GGCGTGTGCC TCTGGTTGGC 540 ACTCCCCAGT TTCTCTGAGC TCTGCACACC CCTGATGTAA CCTTACCTAA TTGTCTTGTC 600 ACAAAACAGC TTGCAGTCTG GAGTCTAAAG GTCAGATGAG CCATTTCTAC CCCACACTTC 660 TGAGTGTAAG GAAGCACCAG ATCAAAATCT AGGCAGATAT CTGAGCCCGC CAGAGCCATC 720 TGTTTGGTTT CCTATTGTGT GGGTAACACC TTCCTTGAGC AAGGCTCTCA GATACACCCA 780 ACACCTGCCC CCTGGGTATC TCAGCATCCT TCAGACCCAT GAATTGTTCA AGAACCGATG 840 TCTGTTCTTC CAGTTTTTGG CAGTGCAGAG GAGCCTGGAA AGAGCTTGAT GAGAGACGCA 900 AAAAGCTCAA AGACAAAAAT GCAAGGCCGG CCAGGCGTGG TGGCTCACGC CTGTAATCCC 960 AGCACTTCGG GAGGCCGAGG CACAAAAATC TCTTGAACCT GGGAGGTGGA GGTTGCAGTA 1020 AGCTGAGATC GCGCCACTGC ACTCCAGCCT GGGCGACAAA GCGAGACTCA GTCTCAAAAA 1080 AAAAAAAAAA AAAAAGCAAG GCCTGCTTAA TCAGATCTCG GCCAAGATAA AAATCTCATG 1140 GCTTCAAAAT CCATCTGATC AATAAATATT CATGAGAGAG TACTGTAGGG CAACATCTTG 1200 TAAATCTTTT TTTTTTCTTA TTTTCTTGAG AGGGAGTCTC CCTCTGTCAC CCAGGCTGGA 1260 GGGCAGTGGT GCAATCTTGG CTCACTGCAA CCTCTGCCTC CCAGGTTCAA GCGATTCTCC 1320 TGCCTCAGCC TCCTGAGTAG CTAATTTTTA GCCACCATGC CCGGCTAATT TTTGTATTTT 1380 TAATAGACAC GGGGTTTCAC CGTGTTACCC AGGATGGTCT CAATATCCTG ACCTCGTGAT 1440 CTGCCCTCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCG CGCCCGGCAC 1500 ATCTTACAAA TCTTTATGTA ACCTAGACTG TCCTGCCTTC AGCAGGGTAA TGGCTTAATG 1560 GGTAGTGTGG CTAGATTTAG CAAATAACAA TACAGGACTA TCAGTTACAT TTGACTTTCA 1620 GATAAACGAT GGCTAATATT TAGCATAAGT ATGTCCCATG CAATATTTGA GACATACTTA 1680 AAAAAAAATT ATTTGGCAGG GGCAGGGCAC GGTGGCCGAC TGTAATCCCA GTACTTTGGG 1740 AGGCTGAGGC AGGCGGATCA TGAGGTCAGC AGATCGAGAC CATCCTGGCT AACATGGTGA 1800 AACCCCATCT CTACTAAAAA TACAAAAAAA AATTGGCCAG GCGTAGTGGC AGGCGCCTAT 1860 AGTCCCAGCT ACTTGGGAGG CTGAGGCAGG AGAATGGCTT GAACCTGGGA GGTGGAGCTT 1920 GCAGTGAGCC AAGTGAGCCA TTGTACTCCA GCCTGGGTGA CAGAGCGAGA TTCTGTCTCA 1980 AAAAAAAAAA AAAAAAATTA TTCGGCAGGG CACAGTGGCT CATGCCTGTA ATCCCAGCAC 2040 TTTGGAATGT TGAGGTGGGA GGATCCCTTG AGACCAGCCT GGGCAACATA GGGAGACCCT 2100 GTCTCTACAA AAGATTTTTA AAAATTAGCC AGGCCTGGTG GCATGAGCTG GCAGACCCAG 2160 CTACCTGGGA GGCTAAGGTG GGAGGATCAC CTGAGACCAC AGAGGTCAAG GCTGCAGTGA 2220 GCTGTGACTG CCTCCCTGCA CTCCAGCCTG GGCGACAGAG TGAGACACTG TCTCAAGAAA 2280 AAAGAAAAGT ATTTGTTGTT GTACTCTGTA TTGTGATCAT AAGCAACAGT GTATTGAGCG 2340 GTGCTTTCTG TATGTTGAAC TCTTCCCGTA TGCCATCTCC TGTAACCCTC ATGCACACAG 2400 GTGTGTCATG CACACAGGAA GTGGGAGAGC CTGGCCGTAT GTCTGGTGGC TGTTGGACTC 2460 CAAAGTCTGT GCTCTTTATA GCAGGAAAAG GCAACTCACA GAACAGTCTG TGAGCAGCCA 2520 GGTGAAAGGG ATGGATCATT CCTTCTCTGA AGGTCTCAGG TGACAGAGGT ATTTGTCTGT 2580 CCATTCACTT AATGAATTTG TGCTGAGCAC CTGCCAAGCC CTCTGCTAGG CATTGGGGAT 2640 GCAGCGGGGC CCAAACAGAG AAAAAGCCCT GTCCTCATGG AATTTCTCTT CTAATTGGAG 2700 GGGACAGGTA GATGGTGATG TATGGAAGAA AGAATAAAAC TCAGCAGGAA GGGTGATAAA 2760 AACTATGCAT TGGGGTGGAG AAATTTAGGG GCAGTCATCA CTAAGAAGGA TGGCATTTGT 2820 GTAAAGAAGA AGAAGTGAGG TGCTCAATAG ATGTTAGAAC TGGACTGTGT CAGCTGGGTG 2880 TGGTGGTTTA TGACTGTAAT CCCAAGCCAA GGCAGGTAGA TCTCTTGAGC CCAGGAGTTC 2940 AAGACCAGCC TGGGCATGAT AGAACCCCGC CTCTACAAAA AATCCAAAAA TTAGCCAGGT 3000 GTAGTGGCAT ATGCTTGTAG TCCCAGCTAC TTGGGAGCTG GGGTGAGAGG ATCACTTGAG 3060 CCTGGGAGGT TGAAGCTGCC TGGGAGGTTT 3090
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