Tag | Content |
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EnhancerAtlas ID | HS012-15519 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr19:33807110-33808290 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_23205 | chr19:33807290-33808548 | Colon_Crypt_1 | SE_23808 | chr19:33807307-33807856 | Colon_Crypt_2 | SE_23808 | chr19:33807877-33808251 | Colon_Crypt_2 | SE_24807 | chr19:33807275-33808732 | Colon_Crypt_3 | SE_27669 | chr19:33806391-33808979 | Fetal_Intestine | SE_28569 | chr19:33806150-33808989 | Fetal_Intestine_Large | SE_50571 | chr19:33806572-33808704 | Sigmoid_Colon | SE_52944 | chr19:33806866-33808848 | Small_Intestine | SE_56753 | chr19:33807362-33807766 | VACO_400 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 33807400 | 33807737 | chr19 | 33807341 | 33808220 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I033315 | chr19 | 33806478 | 33809626 |
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Enhancer Sequence | GCTGGAGTGC AGTGAAGTAG CCGATCTCGG CTCACTGCAA CCTCTGCCTC CCAGGTTCAA 60 GCGATTCTCC TGCCTCAGCC TCCCGAGTAG CTAGGATTAC AGGCACACAC CACCATGTCT 120 GGCTAATTTT TGTGTTTTTA GTAGAGATGG GTTTCGCCAT GTTGACCAGG CTGGTCTCGA 180 ACTCCTGACC TCACGTGATC CACCCACCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCAT 240 GAGCACTGCA CCTGGCCAAC AGTACCTTAT TTTTATTGCT GGCCCTGAAG AAACCTATAC 300 AGTACTCAGA TACAGTAAAG TTTTTCATAC AACACGAGCT CATTTCTCTC AAACATGGAC 360 TGGGGTTTCC TGTCGTGTTG ATTTAGCAGT TCGGGGACTG TAGGTGCGGC AGGATTGTCC 420 CATCCCACCT CTCTAATTAG TCTCGTCTCT ACCATTTTCA GTCAAAATTC CAAAGGTCAC 480 TTGGAAGGCA CATAGCCCAC GAAACTGTCC AGACACTCCC TTTTGGCCAA ATAACCCTCC 540 ACAGCCCAGA TTCCAGTGCA GAGCCCTGGG AACCAGGGGC ATGCTGTTTC CAATCCTCAT 600 CTGCTTAGCC AACAGGGAGA GGTAACAATG AACAAATTGA GTTTCAACCA GCATATCTTT 660 AGAACCCAAT TTTTGTTATA ATTGATTAGA AAATCTAGCT TACATTCCAA ATGCACTCTT 720 TTTTTTTCTT TTCTTAATCT TAGTCAAGGT GCAATAACAG TTAAACGAAA ACCAGCATGA 780 GTCAGGTTCC TATAAAACTG TCTGCTCTCA GAGTTCAGCA TTTTTCTAGA GCAGGAACAT 840 TTGCCGGCAG TCAGCATAGA ACGGGGTTAT TCTGGCCTCT TACTTTTCTA GGGGAACTCA 900 TCATAAGACA AGCAGCTCAC GTGGAATCTG ACACTGACAT GGAATGCACA CACTGGGTGG 960 ACATTGATGG AGTTCTTGGG TCTCACTCTG TTGCCCAGGC TGGAGTGCAG TGGTGTGATT 1020 TTGGCTCACT GCAACCTTTG CCTTCTGGGT TCAAGAGACT CTTATGCCTC AGCCACCCCA 1080 TAGCTGGGAT TACAGGCACC CGCCACCATG TCTGGATAAT TTTTATATTT TTAATAGAGA 1140 CGGGGTTTCA CCATGTTGGC CAGGCTGGTC TGAACTCCCA 1180
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