Tag | Content |
---|
EnhancerAtlas ID | HS050-70944 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:136752680-136754990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr9:136753512-136753523 | AAAACAAAGCA | + | 6.02 | TFAP2C | MA0524.2 | chr9:136754673-136754685 | TGCCTTGGGGCA | - | 6.62 | TP53 | MA0106.3 | chr9:136753601-136753619 | GGCAGGCCCAGACATGTC | + | 6.26 | TP53 | MA0106.3 | chr9:136753601-136753619 | GGCAGGCCCAGACATGTC | - | 6.32 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_01082 | chr9:136749245-136753638 | Adrenal_Gland | SE_65284 | chr9:136749035-136756462 | Pancreatic_islets | SE_68854 | chr9:136750296-136756066 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr9 | 136752940 | 136753800 | chr9 | 136754680 | 136754862 | chr9 | 136753303 | 136753756 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I133886 | chr9 | 136751508 | 136756106 |
|
Enhancer Sequence | CACACTGTGC AGCCATCACC ACCGTCACAC ACACATTCCC CACGCGCCTC CCTGGGGACA 60 CCACGGACTC CACTTACCCC CAGCAGAGAC CCTCCCCAAC CCCAGCACCC CAGGGACATC 120 AGAGGCTGAG GGATGAGATC ACAGCAGCCA GGACACAGAC CAGAGGGATG ACGGCCAGCC 180 TGACACGGCG ATCAGCGAGG CCAGGAACCG CCCCTGCCCC TGCCTCTGCC TCCCATCCCC 240 CGCCCCCCAC CCAGGGGCTG CTTTTGCATC TTCAGGGGAG GGAAGGTAAG GCTCCTGCGT 300 GGCCAGCCTC CTCACCACCA GCCCTGAAGG AAAGACGAGG CGCATTCACA GCGACCCTCT 360 TCCACGTAGA GCAACGCAGC GTCCACAGAA GGCAGCCACT CCTCTATGCT CCCCACCAGG 420 AACCCCCAGT TCCCAAGCCC GAGCTTAGGC TGAAGGGTAG ACCCTGCCCA GGAGCACCCC 480 TTGGATGAGC CTTGAGGGCC TTGTGCTAAG GGAAATAAGC CAGTCACAAA GGACAAATAC 540 CACGGGACTC CCTACAGGAG GTCCCCGCAG GACTCTCTTA CATGAGGCCC CTGGAGCCGG 600 CAGACTCACG CAGACAGCAA GCAGAAGTGG GGAGCCAGGG GCCAGGGGAG GCTGGGGTGA 660 GCGCTGAATG GGGGCAGAGT GTCCGCCTGG GCGGATGAAG CAGTTCGGGA GACGGACGGT 720 GGTGACGGCT GCACAGCAAC GTGAGTGTGT TCAGAGCCAC CGACCTGTGC CCTGGAAAAT 780 GGTTAAGAAG CTAAATGCTA TGTTCTGTGT ATTTTACCAC AGTCAATAAA ACAAAACAAA 840 GCAGCAGCTG CATGTGGGGG CCACGCACAC CTGGATCTTC CAGGCCTCCA GCTCTTTTGA 900 ACCCAAGGCC AAACACGGAC AGGCAGGCCC AGACATGTCT GTCCCTACAC CACCGGCCCT 960 GGGTCATGGG GCAGTTTCCA TAGAAACCGC TGTGTCCAGG AGCCACGTCA CTCTCACAGA 1020 TGGACAGACA GACGGATGCA GCTCTGGGAA GGGCTTTTCC AGCTTCCACA TCTCCAAGTC 1080 TCAGCCTCAT CGTGGACACG ATAAGACCAA CGTCCCCCAA ACAGGGTCAG AGCTAGACAA 1140 ACACCAGACT CCACCCCAAT TAGTATCATG AGCCTGAGCC GACTGATCTG TTCCAAAGGG 1200 CGTCATCCCA GCGGCTGGCT GCAAGATACT TAACATTTAA TTTCTAGGTC CAGGGAGGCT 1260 GCCATTAGCA AGATTAATTG TGTGCACACA CAATTTAATT TCCCCCACCT CAGAAACAAA 1320 AGTGACACTT ACCCCAATTA CAGGACGCTG GGCCCTGGCG GACAGCCCGT CATTCGCATT 1380 CGCAAGGAGA CGACACGAAC AGCATGGAAA TGAAGCGCCC CTGCCAGGGG GGCAGGGACA 1440 CCGCGTCCCC GTCCCTGGGG AAGCCTCACT TCTGAGGAGC TCTTTGCTGA GATCAAGATG 1500 GCCTGAGGCA GGTCCGGCAG GGATCTGGAG CTGAGCTGAA AGGGGTCTCA GTGCTGCCTG 1560 CTCTTCCGCC CTCGGGGTGG GAAACCGAGG CCCAGCAAAC CACAGGCTTG GGGTCGGATA 1620 CCAGATGACC CCAGACAAGC TGACCCCCAG GTCTTGGCCT GGGTTCCTCG TCCAGGAAAC 1680 TAGAGTCATC ACAGTGCTCC TCTTACAGCG GGTGCCGAAG GGTGGGGGCT CACGGGCACG 1740 AGCCTAGAAC ATGCCCACGC CTGTGTGGGA GACAGCATGC CCACTCTGGG TGCTAGCTGC 1800 TGGCTTTCTA GACTGGCCTG ACCCCTCCTA AGAGCCTAGG AGTCAAAGGG GTGGGGGAAG 1860 GCGGCCACTG GCACAGTGAT CTGCGGTCCT CGGTTCCCTT CTCTCCCCAA GGCCACCCTG 1920 AGACCCCTGG AAAGACTAAG GGATGCTTGG GAGGGAAAGG CACTGGGTCC AGGGCCTGGG 1980 GGAGCACATA GCTTGCCTTG GGGCAGGTGT GGGCAGCCCA CAGCTCCGCA GCAAGGACCA 2040 CCCCAGTCCC ACACTGCAAC TGCACAAATA CATTAAGCCA GCCGGCCCGT CAGCACCTGC 2100 TTCCTCAGCG ACCGAGTGCG TCATGAAATC CCAGGAAACT CCCCAGGGCA CCCAACGAGG 2160 CTCGGCTGTT TGTTCAGAAG ACATTTCATT TACACACACA CACAAAAAAT TTTTTTCTTC 2220 TCTGTCCCCC GTTAAACCTA ATCAGGCTTC CCCGATGTGA TGGTGTTTTA CTCATGTCTC 2280 AACTGTTAAT GTCGATACAA GGCTGAAGAC 2310
|