| Tag | Content |
|---|
EnhancerAtlas ID | HS159-04013 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr22:38637870-38640540 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr22:38638851-38638866 | AAGGTCAAGAGATCA | + | 6.93 | | ZNF263 | MA0528.1 | chr22:38638626-38638647 | GAAGGAAGGGTGAGAGGGGAA | + | 6.51 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_01704 | chr22:38639075-38640594 | Aorta | | SE_03118 | chr22:38639115-38639831 | Bladder | | SE_03229 | chr22:38639320-38639891 | Brain_Angular_Gyrus | | SE_04072 | chr22:38638377-38640649 | Brain_Anterior_Caudate | | SE_04952 | chr22:38638113-38640525 | Brain_Cingulate_Gyrus | | SE_06393 | chr22:38625983-38648153 | Brain_Hippocampus_Middle | | SE_07869 | chr22:38638766-38640785 | Brain_Inferior_Temporal_Lobe | | SE_08820 | chr22:38639402-38639765 | Brain_Mid_Frontal_Lobe | | SE_24434 | chr22:38639121-38640160 | Colon_Crypt_2 | | SE_26802 | chr22:38639040-38639793 | Esophagus | | SE_27733 | chr22:38638363-38638937 | Fetal_Intestine | | SE_27733 | chr22:38639079-38640130 | Fetal_Intestine | | SE_36672 | chr22:38638998-38639883 | HMEC | | SE_37347 | chr22:38633913-38640545 | HSMMtube | | SE_40787 | chr22:38638947-38640136 | Left_Ventricle | | SE_44907 | chr22:38639025-38639933 | NHLF | | SE_46738 | chr22:38639106-38639953 | Ovary | | SE_50292 | chr22:38638399-38640461 | Sigmoid_Colon | | SE_52132 | chr22:38639045-38639761 | Skeletal_Muscle_Myoblast | | SE_52414 | chr22:38638931-38640491 | Small_Intestine | | SE_53822 | chr22:38638978-38639880 | Spleen | | SE_56252 | chr22:38638947-38639783 | u87 | | SE_63907 | chr22:38639031-38639915 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 38640204 | 38640501 | | chr22 | 38638055 | 38638105 | | chr22 | 38638976 | 38639857 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I038242 | chr22 | 38638461 | 38640963 |
|
Enhancer Sequence | CAGAGCGAGA CTCCGTCTCA AAAAAAAAAA AAAAAAAAAA AAAGAACGAG ACCTGTCTCT 60
TAAACAAAGC CCTTCCATAG TAGGAAGTCA CCATGTAACA TCATATAAAA CTGAAAAACA 120
AACAACAACA AAAACCAGTA CAAGCATATT TTAGGTCATT CTAGGAAGAA AACAGCTGAA 180
AGAGTTGAAA GTACAGTGAA CTTCAGAGTG AGGAGTTAGG GGAGTTTCGT GTTTCAACCA 240
TATGCCTATA TTACTTTAAT AAATGTAATT TTTTTTAGTG TTTTTTAAAA GCAGAATTTT 300
GTTAACAAAG AAAAAAAGCA GGGCCAGGCT TGGTGGCTCA CGCCTGTAAT CCCAGCACTT 360
TGGGAGGCCA AGGCGGGCGG ATTGCCTGAG CTCAGGAGTT CAAGACCAGC CTAGGCAACA 420
CGGTGAAACC CCGTCTCTAC TAAAATACAA AAAAAAAAAA AAAATTAGCC GGGCGTGAAG 480
GCGTGTGCCT GTAGTCCCAG CTACTCGAGA GGCTGAGGCA GGAGAATTGC TTGAACCCAG 540
GAGGAGGAGG TTGCAGTGAG CCAAGATTGC ACCATTGCAC TCCAGCCTGG GCGACAGAGC 600
GAGACTCCGT CTCTAAAAAA AAAAGAAAAA AAGCAAATGA CCGTAGTGCT CAGCTCTGAG 660
CAGGTCCTCA GGAAGGGCTG GCTGGATCTG CAGAGTTCTC CAGCCCAGGT GAATCCCACT 720
CCCTCCTGGG CCCTCCTGGC CCCTCTTGGG CACTGAGAAG GAAGGGTGAG AGGGGAAATA 780
CAAGGATCGG GGGGGACTGC CCCATCACTG ACTCTGCAGA GGCAGCTGCA AGAGAGGGGC 840
TAGGACCCAG AGCAGTGGTG CAGGGACAAG GCAAGGAGCA GGCCCCGCTG CCTCTGATGC 900
TAAAAGCTGG TGAACTTGGC CAGGCACGGT GGCTCACATC TGTAATCCCA CCACTTTGGG 960
AGGCCAAGGC GGGCAGATCA CAAGGTCAAG AGATCAAGAC CATCCTGGCC AACATGGTGA 1020
AACCCCGTCT CTACTAAAAA TACAAAAATT AGCTGGGCGT GGTAGCACAC GCCTGTAGTC 1080
CCAGCTACTC GGGAGGCTGA GGCAGGGGAA TCACTTGAAC CTAGGAGGTG GAGAATGCAG 1140
TGAGCTGAGA TTGCCCCACT GCACTCCAGC CTGGCAACGG TCTCAAAAAA AAAAAAAAAA 1200
AAAAGCTGGT GAACTCGGGG GCAGCCTGAA CTTCACTGCA GCTGCTGTAC TGTTTGTAAA 1260
CTCCCTGGGA GAGGCCAGGC CAAAGGGATA ATCGCGTTGC TAGGAGATGT GCTTCACAGG 1320
GTGGCCGACT TCCTGGAGGA CCTCTCCCCG GGCAGGGAGG CAGGTCAGGG CAGGCGGGGC 1380
CTGAACAAAG AGGCTTCTGG AGTGAGGGGT GCCCGCCAGC CATCTGCTGC CGCCTCTGGG 1440
GCACGGAGTG AGAGTGAAGC GGAGGCTCCC CTGGCTGTGT GCCCCGCCTT CTGCCATGCG 1500
CCTGTCTTTG GGGTCCCGCC GAGAAGAGAG CCCACACTTG TCCCCCGACC ACACAGGAGA 1560
GGCCACCTTG GCAGGGAACA GCTTTGTGCT TCTGAAGGAA CAGGTGGGCA GAGGCTGCCC 1620
CTGGGTACCC ATGCGAGGCT GGCAGCTGAA TGGAAGTGGA TTCTCAGCCC CACACTTCGC 1680
CAATTCCAGC CTTTATGGTG CCCCAGGGAC CCAGAGGTTT CCCTGGAGAC TTGGCTGCTT 1740
CCAGAAATAT CAGACACCAG AGCCCCAGTT AAGCCCTGAG CAGGTCCCCA TCTGGCCTCA 1800
GTATTCTCAT CTGGAAGGAC AGGATGGAAC GCCAGCCTGC GAGGAGGGAG CATGGGATGT 1860
TACTGAGGCC CCACATGGAG GAATGCAAGG CACAGGGCAG GGGTTTGATT AAGTCCCTTA 1920
TTCATCCAAA AGGGAGGAAG TAGGCATCTC CCATGGGCCC GGCTCTGTCT GGGCATGGCT 1980
GCACCCCATC CTGCTCTGGC AGGGCTAATC ATGCTCAGGA AGATGGAACA CGAAGCAAGG 2040
GAGCTGCAGA CTGTGGTGGG GCCGAGGACC TGGATGGGTG CTGGGAGTGA GAGTGGCGGG 2100
GAACAGACGG ATGGAAAGGA GGGACCCCAC GCAGAGCAGA AGAGCTTCCC AGGCCGGGGA 2160
CACAGCACGT ATCAAGCCCT TGAGGCTGGG AAGCACCTGC CTGATGTGGC CGCAGTTGGG 2220
GGTGGGAAGG CAGAAATATG AAAGGCTGGG GTGCAATGGG CTCCTGTTGG GCGCCTCCAT 2280
TTTCTTGCCA AACCTAAAGG CATTTCCTGT GCCCTATGAG TTCTCAGGGA TACACAAGTT 2340
TCAACGTGGA GAGGAAGAGA GACTCCAGCT GCTTGGGGGA TGAGCATGCT TCACTCCAAT 2400
ATCCACAGAG TGCAGGCCTG GGGCAGCACC CTCCCAGGTC AAGGAAACAG ACAACTTCTG 2460
GGCATGGCCA GAGCTGCTCT GCCTGAGATT AGGAAAACCA CATCCGGTCA CTTTACCTAA 2520
AACCAGCAGC ACAGGTGTGG GTAGGAGACA GGAAACCTCA CACTCTGAGA ATAGCATGGG 2580
TATCAATGTA GGGGTCTTTT TTTTTTTTTG AGACAGAGTT TCGCTCTTGT TGCCCAGGCT 2640
GGAGTGCAAT GGCACGACCT CAGCTCACCA 2670
|
