Tag | Content |
---|
EnhancerAtlas ID | HS060-24481 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:53840160-53841770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr3:53840794-53840809 | GGTTAATATTTAATT | - | 6.11 | MEF2C | MA0497.1 | chr3:53840649-53840664 | TAACCAAAAATAGCC | + | 6.07 | ZNF263 | MA0528.1 | chr3:53840260-53840281 | TGCCTTCCCTCCTCCTCCCTC | - | 6.01 | ZNF263 | MA0528.1 | chr3:53840160-53840181 | CCTCATCTACCCTCCTCCTCC | - | 6.07 | ZNF263 | MA0528.1 | chr3:53840240-53840261 | TCCTCCCCCTTCCTCTCCCTT | - | 6.11 | ZNF263 | MA0528.1 | chr3:53840238-53840259 | CCTCCTCCCCCTTCCTCTCCC | - | 6.21 | ZNF263 | MA0528.1 | chr3:53840235-53840256 | TTCCCTCCTCCCCCTTCCTCT | - | 6.33 | ZNF263 | MA0528.1 | chr3:53840172-53840193 | TCCTCCTCCTTCTTTTCCCTC | - | 6.34 | ZNF263 | MA0528.1 | chr3:53840234-53840255 | CTTCCCTCCTCCCCCTTCCTC | - | 6.46 | ZNF263 | MA0528.1 | chr3:53840176-53840197 | CCTCCTTCTTTTCCCTCCCCC | - | 7.05 | ZNF263 | MA0528.1 | chr3:53840211-53840232 | CTCCCTCCTCCCTCCTCCCTC | - | 7.13 | ZNF263 | MA0528.1 | chr3:53840254-53840275 | CTCCCTTGCCTTCCCTCCTCC | - | 7.1 | ZNF263 | MA0528.1 | chr3:53840187-53840208 | TCCCTCCCCCTCTCCTCCCTC | - | 7.32 | ZNF263 | MA0528.1 | chr3:53840204-53840225 | CCTCCTCCTCCCTCCTCCCTC | - | 7.32 | ZNF263 | MA0528.1 | chr3:53840184-53840205 | TTTTCCCTCCCCCTCTCCTCC | - | 7.53 | ZNF263 | MA0528.1 | chr3:53840208-53840229 | CTCCTCCCTCCTCCCTCCTCC | - | 7.81 | ZNF263 | MA0528.1 | chr3:53840197-53840218 | TCTCCTCCCTCCTCCTCCCTC | - | 7.87 | ZNF263 | MA0528.1 | chr3:53840201-53840222 | CTCCCTCCTCCTCCCTCCTCC | - | 8.04 | ZNF263 | MA0528.1 | chr3:53840194-53840215 | CCCTCTCCTCCCTCCTCCTCC | - | 9.49 | ZNF263 | MA0528.1 | chr3:53840191-53840212 | TCCCCCTCTCCTCCCTCCTCC | - | 9.98 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65337 | chr3:53836445-53843559 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 53840192 | 53840232 | chr3 | 53840360 | 53841163 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I053804 | chr3 | 53838172 | 53842050 |
|
Enhancer Sequence | CCTCATCTAC CCTCCTCCTC CTTCTTTTCC CTCCCCCTCT CCTCCCTCCT CCTCCCTCCT 60 CCCTCCTCCC TCATCTTCCC TCCTCCCCCT TCCTCTCCCT TGCCTTCCCT CCTCCTCCCT 120 CACTTTCTCT GCTTCTCCCT CATCTTCCTG TCAAGTCTGT CAGTGCCCTC TGCTCACGGG 180 GCAGGTTCTG GACTTGTTGG TCCCCTTCAC TCTGGGGCCA GGAAACCCAT CCCACCTAGA 240 GGGGCTGGGG CTGGGGCTGG CTGCTTCCAC CTGCTTTCCC TCTGCAGCGG TGGGTGGCAG 300 GAGCTGGCGG ATCTGGGTCA TCCTGAGCAA GGAACTCCAG CTGGGGGAAG AGGTGCAGCC 360 CTGGCCCCTT CCAGCCCTTG GCTGAACAGT TTCATTTTGG ACATGTGGGC ATTTTGCTGA 420 TGGTTAAGGA CTATCCATTT CTGGAATTTC TGAGGAATGA AGCATATTTT TGAACAGGAC 480 TCTAATCAGT AACCAAAAAT AGCCGTGACA CATCGGCTTC TGAGTCTGCC AACTGCATAT 540 ACTATAAAGA GCACCACTGG GAGGTGCCCA GGGCCCTCTG CCTCACTCCA ACTGTCACAG 600 CCCCACTGGG GAGTGTGACC AGACCCATTT CCATGGTTAA TATTTAATTC CTCAGCCCTG 660 AACACATGCA GCTAAATGAA GTCACTCCTT TCCCATAAAT ACTAGATGAA GCAGATGCAG 720 GTGAGGCCGG GTGATGGCCC TCGCCCTTGT GAGTTCCACT GCCTTCCTCG GGCCTCGGCC 780 TTTGTCTACT GCCTACTTGG CCAAGCAAGC AAGCACATGA ATCCCACCAG CCACAGTGCC 840 AGAGAGGAGC TGAGTGGGCA GGAGTGGCTG TGCTCTTGAT TCATAAGGTG GTTTTGCTTT 900 GCTGCCCCGC AGCTCAGACC TTGGACAGGA AGAACATTTC CCTCCTCCAC CTGTGTTCTC 960 AGCTGCAGGG GGATTCCCTC CTCCTCCAGA GAGTGTTGTG CAGAGCACAT GAGATGGTGG 1020 GGATCCCTGG AGCATTTTAG AAATGGAAAA GCACCACATA CAGGAGAGGG ACCGCTGCTC 1080 TCCTTTCCCA GCCCCCAGCC CGGCCATTCG ATCTGGAAAC CTATGCTCCA CAGCACAGTT 1140 GGCCCCTGGG TGGTGCGTGG AGGGAAGGCT TTCTGATGAG GCAGCCGTGT GTGTCCCATG 1200 TAGGCAACTG AACCAGGAGG CCCCACAGTG CGCACTGGGC ACGAGAGACC AGGACTGGCT 1260 GTCTCGTTCC TCTCTGCTGG GCAGTGCCTA GCCAAGGACT CAGCCCGGTC TCTTGTGTGC 1320 AGCCCCAGTG TGCCTGGGAG TCCTCCCCTG GCTAGGCCCT GGGCTTTCCA ATAGCGGAAT 1380 GAGGGGCATG TGGAGTTTTG CCAGGGCTGA GAAAGGAGGC CCTGTGATCC GAGAAAAGCA 1440 GCGGTCAAGA TAGGAGCCAT AGAAATGCCT TGTAAACGAT AGGTGTGCTC TCGACAGAGG 1500 CCCCTGCAAG GGGTAGGAGG TTTCTGGGAG GAGGCTGCTG GCTGTGTCTT AGGGCCCCAG 1560 AATTCAGACT GATCTCCCGG GCCTGGTGCC CTGTGAAGCT GGGAGCTGTG 1610
|