Tag | Content |
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EnhancerAtlas ID | HS110-03472 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr3:119513560-119514650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr3:119514107-119514118 | GGATGACTCAG | + | 6.32 | JUN(var.2) | MA0489.1 | chr3:119514104-119514118 | AAGGGATGACTCAG | + | 6.33 | JUNB | MA0490.1 | chr3:119514107-119514118 | GGATGACTCAG | + | 6.14 | Nr2f6(var.2) | MA0728.1 | chr3:119513568-119513583 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28530 | chr3:119513306-119516847 | Fetal_Intestine | SE_29517 | chr3:119513320-119516900 | Fetal_Intestine_Large |
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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 |
GH03I119794 | chr3 | 119513178 | 119516613 |
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Enhancer Sequence | GATCACCTGA GGTCAGGAGT TCAAGATTAG CCTGGCCAAC ATGGTGAAAA ACCTGTCTCT 60 ACTGAAAATA CAAAATTAAT CTGGTGTAGT GGCCCATGCC TTGCGGTCCC AGCTACTTGG 120 GAGGCTGAGC CAGGAGAATT GCTTGAACCC AGGAGGCACA GGTTGCAGTG TGCCAAGATC 180 GTGCCTTTGC ACTCCAGCCT GAGTGACAAG ATTGAAACTC TGTCTCAAAA TAAGTAAATT 240 AAATTAAATA ATGTAAAATA AAATAAAATA GGACTGCCCA AATTGTGTAA GCCTCAGAAC 300 CCACGTAAGC TGACTAAAGG GCACCTCTAC TTGCCCATTG ACTAACCTGA ACACCAGATG 360 AAATTGCTCT TCCAAACACC ACTAGCTGGG GAGTTGGCTC TTGGCTGGGG TTGGTCAGTG 420 CACAGGCCAG TAAGGGAGCT GGGCAAGTGC AGAAGTGGAG ACTAGCTGTG TCCCAGACAG 480 CGACTCTCCG GCTGTGACCC TGGAGAGTCC TTTAGCAGGG CAAAGTGCAA CATAGGCAGA 540 CCTTAAGGGA TGACTCAGTA ACAGATAAGC TTTGTGTGCC TGCAGGGGGA TGGGAAGAGG 600 GTGGGGCAGG AGAGGGACAT AAAAGGGCTC TGAGGCATTG TACTGTGAAT TCCTTCAGTC 660 TCCTGCTCTG CTCAGCCAGT CAGCCCTGCC TCCCTTGTTT AGGACCACAC AGCACTGCTG 720 GGTGTCTGCC TTTCCTTGTG ACTCTTCTCT AGCCTCTGCA TGGCCAGCAG CCCTCTTCTT 780 TTCTCCTATT CTCTTAAGAA ACATGCCCAT CACCTGCAGT TTCTCTGGGC TCCCCGTTAA 840 TCTGCCTTCC TCATCTCCTA ATGCTGCCTC CTCCCTCCCA TTGCCGGTGC CTGGAAATAG 900 TCAAGGCTGG GTTCTGTTCT TTTGCTTGAA TTTCTTTCAC TTGGCTTCTT GACTCTTTCT 960 AAACTACAAT CCCCCCATTC TCACTGCCTT AGTTTTCCCT CTCTCTGTGT TTCTCAAACT 1020 ATATCCCACC ACGCCCTGAC AAGGGCTTCT CTCCTGTAGA TCATCCCTTT TCTAGTATTT 1080 TGCTAGAAAT 1090
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