| Tag | Content |
|---|
EnhancerAtlas ID | HS110-01847 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr17:27481450-27483620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:27482491-27482509 | GGGAGGGAGGGAGGAAGT | + | 6.29 | | NR2C2 | MA0504.1 | chr17:27482564-27482579 | CGGGGGCAAAGGGCA | + | 6.54 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_03450 | chr17:27480460-27484485 | Brain_Angular_Gyrus | | SE_03910 | chr17:27480341-27484877 | Brain_Anterior_Caudate | | SE_04884 | chr17:27475155-27487900 | Brain_Cingulate_Gyrus | | SE_05843 | chr17:27474727-27488125 | Brain_Hippocampus_Middle | | SE_07476 | chr17:27480023-27487637 | Brain_Hippocampus_Middle_150 | | SE_07806 | chr17:27479971-27488254 | Brain_Inferior_Temporal_Lobe | | SE_08959 | chr17:27481799-27482199 | Brain_Mid_Frontal_Lobe | | SE_08959 | chr17:27482421-27482682 | Brain_Mid_Frontal_Lobe | | SE_08959 | chr17:27482686-27482929 | Brain_Mid_Frontal_Lobe | | SE_08959 | chr17:27482931-27483429 | Brain_Mid_Frontal_Lobe | | SE_09987 | chr17:27480834-27483584 | CD14 | | SE_19008 | chr17:27480940-27483656 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19489 | chr17:27480816-27483655 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_28031 | chr17:27480548-27484527 | Fetal_Intestine | | SE_28952 | chr17:27480565-27484674 | Fetal_Intestine_Large | | SE_30293 | chr17:27482624-27483845 | Fetal_Muscle | | SE_32448 | chr17:27481182-27484607 | Gastric | | SE_33834 | chr17:27476050-27486414 | HCC1954 | | SE_34898 | chr17:27480281-27487189 | HeLa | | SE_40250 | chr17:27481492-27483279 | K562 | | SE_41080 | chr17:27481161-27484677 | Left_Ventricle | | SE_42354 | chr17:27480302-27484734 | Lung | | SE_47275 | chr17:27471944-27488173 | Panc1 | | SE_49086 | chr17:27481013-27484627 | Right_Atrium | | SE_50708 | chr17:27480542-27484757 | Sigmoid_Colon | | SE_51291 | chr17:27481312-27484287 | Skeletal_Muscle | | SE_52472 | chr17:27480528-27488119 | Small_Intestine | | SE_53778 | chr17:27480424-27487753 | Spleen | | SE_65361 | chr17:27480507-27484732 | Pancreatic_islets | | SE_66834 | chr17:27481366-27483585 | Jurkat | | SE_68762 | chr17:27481424-27484531 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I029153 | chr17 | 27480398 | 27488021 |
|
Enhancer Sequence | TCCTGAGGCC AGAATCTCAG GCTGCCAGGG CAATCGGGGC TCTGCCAGGC AAAGCCAAGT 60
GCTAAGGGGA ATAGGGATGT TTGCTGGTCA CCGATTCCAG GAAGACAGGC CACAGCAGTC 120
CCCCCAGGCT TCTCAGGCAG GGGGCCCAGT TTCCCTCTTG CCTCTGTTGA TCTTGAGGCA 180
TGGCCAAGTG AGTGGGGACT CGACCCAGCC TGTGCCCGTG TCCTTTAGGG AACATAGGTG 240
CCTGCTGAGA GGAGGCAGGG CTGTGCCAGG CTCAGCACAT GCTGGGTTCC CCCCATGCCT 300
GAAGTGCCAG GCACACTAGC TCCCACAGCC TGGACAGCTC TGGGGAGGGC GAGGCAGAAG 360
ATGCCAGCCC AGCCGGGGAG GAAATCTTTT ACTGCTCTGA GCCCAGTGCT TCTGCAATCA 420
GCTCCACAAC CAAAGCAGTC CACACATGAG GGAGGGGCAG GGGCATGAGG GAAGGGCCCC 480
CAGCAGGAAG AACTAACCAC ACAAGGAGAT GGTATCAGAC CCTTCCCCTC GCCATGTCCC 540
TGGAAGGTTC TACTGGAATC TCTAGATACT TTCCCCTTGA TGTGTTGGGG CCGGGCATGA 600
AACTGGGTGT CACGGAGAGT CATGACAGTC TCACGCTGCC TGACGGTGCT GTCACTGCCT 660
GGCCTCTAGC CCATGCCACC CAGGGCTGAG ATAGATCTTC CTGCACACGT CTTCTGTCCT 720
TGCAGAAGCA CAGGCTCCAT CATCACAGGG TGCTATCTTC AGCCTTTCTT CTCCACAGAA 780
CCAGGCTCAG GGGCTGACAG GGAGCAGTGT TCATCAAGGT GTCCTGACGT CCCACCCTGA 840
TTGCAACAAG GCTCTGGGGA CATCCACATC TGGCCTTTCC TACAGCACAG AGCTCTGCCT 900
CCTCCCCACC ACACATGCAG CCCTCTTCTG CCCCAGGGCC GGGGCAGCCT CAGTCCTGCT 960
GCCAGAGAAG AGCTCCATGG GAAGAACCTG CCGCCCTGTG TGGACCCTGC TTGCCCCAGG 1020
GCCTGGCAGT GAGAGGTGCT GGGGAGGGAG GGAGGAAGTG AGTCAGCTCC CTGCAGAAAT 1080
CTGAGTGGGA GGGAGGAGCC AGCAGAAATG AGATCGGGGG CAAAGGGCAC AGGAGCCAGA 1140
AAGGTCACTA AGAGAGGGAA CCAGGCCCCG AAGGTGTTGC GGGACCCACA GAGTACAAGA 1200
CAGATACAGG TGATGAATTC GGCAGGGCCA CCTCCAACCG AGGCTGGGTG GCCCCAGTAG 1260
GCCAGAGAAC CTGGGTCCAG AGGCCTGGCC CCACCTGAGG ATGGAATCCG AGGCGGCTCC 1320
CCTCCCTGAC TCATGTTCAC ACCAGAGGTA GCAAGGCCTT GTGGGACATG GCCAGCCTCA 1380
TTCTCTCCTC AGAGATGGAG TCTCTGGGCT CCAAGGCCTC CCACTCCCTC TCCTGAGCCC 1440
TACAGCTCCA GAAGCCCAGG TTCCCCATGA CCTGGCCTAG TAGGGACATG CTAAGGTCCT 1500
ACAGACAAGT CACCTAGGCC AGTCAGAGCG GGAAGGTTCC AGGAACCAAA ACTGTCTCCC 1560
AGAGGGGATG GGAGCTGAGC CTGGGCCCCA GGAGCAGAGC AACTGGGGCT GCCTTAGCAC 1620
CCACTCTCTC CTCCCTGGTA GGGACATGTG GGAGCTGTCC CCAGGCTCCA GCTGGAATCC 1680
ATTGCTGTGA CTGGGTAAGA TCCTTGCTGT GAAAATTCCC ATCCTGCTGA CATTCCAGTA 1740
TGAAGGCAGT TCAGGGAGAG CAGCGGAAGG GAAGAGGAAG CCCCACTGGG CCACATTCCA 1800
GCCCCTCAGA GACCTACAGC CAGTGAGACA GGCGCATTCC TCCAAGGTCT GAGACAGACA 1860
CTGCGTAGCC CCCATGTAAT CCTGAATCTT CTTCTCACCC AAGCCTGGCA CCTTCATGTG 1920
GGCTCCTGTG TGGGGGCAGG AGGCAGCCTG TCCCCAGGAC CTCCCTTCCC AGGCTCCTGC 1980
TCCTGGATGC CCACAGAGCT GCCTCTCCTC CAGTCCTGTG AGAGATGCCA GGCCCCAGGC 2040
ATGCAAGAAA CAGTCCATGG GTGGAGATGG GACACGCTAA GGTCCTAGAG ACAAGTCACC 2100
AAGGTCAGTT AGAGCAGGAG GGGTCCAGGA CCCAAAACTG AGCTAAAGTT TTGGTTCTGG 2160
TCTGGAAGAC 2170
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