Tag | Content |
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EnhancerAtlas ID | HS101-20864 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr19:4082920-4085290 |
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) |
EWSR1-FLI1 | MA0149.1 | chr19:4084376-4084394 | TCTTCCTCCCTCCCTCCC | - | 6.36 | HSF1 | MA0486.2 | chr19:4084568-4084581 | TTCTAGAAGCTTC | + | 6.28 | MYCN | MA0104.4 | chr19:4084542-4084554 | GGCCACGTGGCC | + | 7.22 | MYCN | MA0104.4 | chr19:4084542-4084554 | GGCCACGTGGCC | - | 7.22 | Myod1 | MA0499.1 | chr19:4084615-4084628 | TGCAGCTGTCCCC | + | 7.12 | ZNF263 | MA0528.1 | chr19:4084371-4084392 | CCCCTTCTTCCTCCCTCCCTC | - | 6.14 | ZNF263 | MA0528.1 | chr19:4084310-4084331 | GGAAGAGGAGCGGAGGGAGGG | + | 6.48 |
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| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_00903 | chr19:4083864-4084455 | Adrenal_Gland | SE_02962 | chr19:4083523-4085082 | Bladder | SE_12453 | chr19:4083727-4085036 | CD3 | SE_19502 | chr19:4083630-4085257 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20194 | chr19:4083237-4085170 | CD56 | SE_22707 | chr19:4083615-4085191 | CD8_primiary | SE_23073 | chr19:4083139-4085071 | Colon_Crypt_1 | SE_23728 | chr19:4083583-4084973 | Colon_Crypt_2 | SE_24683 | chr19:4082893-4083451 | Colon_Crypt_3 | SE_24683 | chr19:4083592-4085030 | Colon_Crypt_3 | SE_26575 | chr19:4082693-4085061 | Esophagus | SE_27700 | chr19:4083659-4085066 | Fetal_Intestine | SE_28696 | chr19:4083692-4085120 | Fetal_Intestine_Large | SE_31428 | chr19:4083442-4085057 | Gastric | SE_42412 | chr19:4083527-4084881 | Lung | SE_50061 | chr19:4082762-4085231 | Sigmoid_Colon | SE_53358 | chr19:4083688-4084969 | Spleen | SE_55380 | chr19:4083851-4084635 | Thymus | SE_58113 | chr19:4083508-4084948 | VACO_9m | SE_62529 | chr19:4051126-4090382 | Tonsil | SE_65287 | chr19:4083611-4084987 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I004082 | chr19 | 4082946 | 4085145 |
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Enhancer Sequence | CATGGCCATA TTTTGAACCT CGTTGCTCCC AGCCCGCGCC CCCAGCCAGG CTGGGCCTCT 60 CCAAGGGCCC CTGTCACCCA GTCCTGCCAC CCAGCCTTTG CTGACACCGT TGCCCATGTT 120 GGCCCCGCCA CTGTTGGGAA TGTCCTCTCC AGCCCTCAGC TGTGGATTCC CCTCCTTCCC 180 AGGACTTCTC CTCTAGGTGC TGGCTAAATT TGCCTTTAGC CCTTAGGGCG GCTATAAATT 240 CTAATTTCTG GGCCCGAGCG AGCGCCGTGG GGAGGCTGCA GGCTCCCCAG CGATGGACAG 300 GGGCTCTTAT CTTTTAGGAT CCCACAGAGC ACTGCAGAAA AGCCCCAAAT ATTTGTGGGT 360 CACGAAGGCA GTGTCCTGTC AGGGGAGACA GCAGGATGGT GGGACCACAG GATCGTCCAT 420 GTCTTCCCTG GGGGAGGTTC GAGTCACCTT CAGAAGGTCA CCTAACTTGC AGGGACTCCG 480 CTGCCGCAGA GGTTGTGTGG GGAGAGGCAA ACCTGGTCAG CCTATTTTGT GGGGTGCAAA 540 CAGAAGGGAT GTGGGCCTCC TCGGAAGTCT GCAGAGAGGA TTCGCTCCTC CGTGGACGCT 600 TCTCTCTTTT CTTGAGCCTG TGATGAGTTC CTTTGCAAAT AGGGAAACTG AGGCTCTCAG 660 AGGGGATTCT ATCTTCCCCA AGGTCACAGG CCCAAGGACA GCAGAAATAT CGTCAGGCCT 720 GTGGTCCTGA TGTTCAAACA GGAGGCCCTG GCTGGCCGCA GCGACTCACG CCTATAATCC 780 CAGCACACTG GGATCAGAAG GATTGCTTGG GGCCAGGAGT TCCAGGAGTT TCAGGCCAGC 840 CTGGGCAATA CGGTGAGACC CCATCTCTAC GAGAAAGTTT CAAAAAATGA GCTGGGCATG 900 GTGGCGCGCG CCTGCAGTCC CAGTTACTCA GGAGGCTGAG GCAGGAGGAT CGCTGGAACC 960 TGGGAGGCGG AGGCTGAAGT GAGCTATGAT GGCGCGCCAC TGCCCTCCAG CCTGGGCAAC 1020 AGAGTGAGAC CCTGCCTCAA ACAAAAACGT AAACAAAACA GGAGGCCCTG CTCTCCTGAG 1080 GGGCTGGTGG TGAGTCACTG GTAGATGGGA GAGAGCTGGG GTCAGGGTCC CAGCTGGGGG 1140 GGTGGGTCCT CACCTGTGCT ACCCTCCAGG GGGCCTCTCT CCAGGCCTCT GTCCCTCCCC 1200 TGGGAAGCCT GGCAGAAACC TGAGACTGGG CCTCCAGTTC CAGGTCGCCA CTGGGCCCAG 1260 GCCTCTCCTG TCCGCCTGCC AGGGACTGCG GAACAGGTAA CTCCTGCGCC ACCCTAAACC 1320 CACCTGGCCT GTTGCTCCAG GTGCGGCCTG GAGGCCCCGG GGCCTGCACA CCTGGTCAGC 1380 TCAGAGGCCA GGAAGAGGAG CGGAGGGAGG GGTGGGGCCG CCGGCCGCTG CTGGTTTCGT 1440 TTTGAGCCGG GCCCCTTCTT CCTCCCTCCC TCCCACTCCT CGCCAGACCC CTGCATTCTG 1500 GGAAAGGCTG TGACAACTTC CTCTGAACTC TCCTTAACCT GCCCTGGAGC CCAGGGCCTC 1560 CAGGAGGCTG AGTTCCGCCT GCGGGACCTG AGGCTTCCTG CAGGTCACAC ACCTCCACCC 1620 CTGGCCACGT GGCCCTAGAC CGCCCACCTT CTAGAAGCTT CTTTATGTGC TGCCCCATCA 1680 TGTCCCCACC CCGGGTGCAG CTGTCCCCTG CCTGCACCCC CTCCACCCTG TGTCCCAGAC 1740 TCTGCACACA GGAAACCGCC CTGGCCCCAG GGAGGGCTGC CTGAGACCCC CGCCTCCAAC 1800 CTGCACTGGG GACATCTGGG CTGGATGGTC CTCGGGAGGT GGGGCTGCCT TGGGCACTGC 1860 AGGGTGCTGG GTGACATCTC TGGCCTCCAT CCATTCCATG GCAGGGGCAC CCCCTGTCTC 1920 GACAACCACA GACGTCTGGG AGTTTCCAAG CCTCCCCTGG GTGGGGGGAC AGAATTGTTC 1980 CTGCTAAGAT CCAGTGGATT AAAAGACATC TGTGAGGGGA CAGAAATGAC TGAGTTTTGT 2040 GCCGGCCGGT CAGGCAGTCC CTGGCAGACA AAATTCCCAA GTATTTGCAT CCAAAAAAAC 2100 AAAACAAAAC AAAACAAAAC AAAACCACCC AGCGTGGTGG CTCACACCTG TCATCCTAGC 2160 ACTTTGGGAG GCCAAGGCGG TCAGATCATT GAAGTCAGGG GTTCGAGACC AGCCTGGCCA 2220 ACATGGTGAA ACCCTGTCTC TACTAAAAAT ACAAAAATTA GCCGGGTGTG GTGGCACATG 2280 CCTGTAATCC CAGCTACTCG GGAGACTGAG GCAGGAGAAT CGCTTGAACC CGGGAGGTGG 2340 AGGTTGTGGT GAGCCGAGAT CACGCCACTG 2370
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