Tag | Content |
---|
EnhancerAtlas ID | HS098-59091 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:136820460-136822990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr9:136820818-136820838 | CCCCCACACTCCCCCCACGC | + | 6.37 | SOX10 | MA0442.2 | chr9:136821578-136821589 | TGCTTTGTTTT | - | 6.02 | Stat6 | MA0520.1 | chr9:136821714-136821729 | TAGTTCCTGAGAAGT | + | 6.62 | TBP | MA0108.2 | chr9:136821692-136821707 | GTATAAAAAGCACGC | + | 6.26 | ZEB1 | MA0103.3 | chr9:136822120-136822131 | CCCACCTGCCC | + | 6.14 | ZEB1 | MA0103.3 | chr9:136822148-136822159 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr9:136820928-136820949 | CCTACTCCTCCCCACTCCTCC | - | 6.01 | ZNF263 | MA0528.1 | chr9:136820517-136820538 | CCCCACTCCCCACACTCCTCC | - | 6.06 | ZNF263 | MA0528.1 | chr9:136820680-136820701 | TCCTCCCCACCTCCTTTCTCC | - | 6.27 | ZNF263 | MA0528.1 | chr9:136820535-136820556 | TCCCCACCCCCCTGCTTCTCC | - | 6.43 | ZNF263 | MA0528.1 | chr9:136820741-136820762 | CCCTCCCCACCACGCTCCTCC | - | 6.79 | ZNF263 | MA0528.1 | chr9:136820532-136820553 | TCCTCCCCACCCCCCTGCTTC | - | 7.33 | ZNF740 | MA0753.2 | chr9:136820877-136820890 | ACGCCCCCCCCAC | + | 7.12 |
|
| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_01047 | chr9:136820744-136822945 | Adrenal_Gland | SE_11499 | chr9:136813009-136823179 | CD20 | SE_47581 | chr9:136820829-136821633 | Pancreas | SE_47581 | chr9:136821636-136822499 | Pancreas | SE_47581 | chr9:136822517-136822921 | Pancreas | SE_53205 | chr9:136820884-136823003 | Small_Intestine | SE_58888 | chr9:136808664-136846599 | Ly3 | SE_59920 | chr9:136808267-136829110 | Ly4 | SE_60430 | chr9:136808943-136859823 | DHL6 | SE_61238 | chr9:136792252-136860234 | HBL1 | SE_65284 | chr9:136819974-136820724 | Pancreatic_islets | SE_65284 | chr9:136820725-136823047 | Pancreatic_islets | SE_68866 | chr9:136818889-136823005 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr9 | 136820706 | 136822319 | chr9 | 136820918 | 136822600 | chr9 | 136822429 | 136822886 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I133953 | chr9 | 136818975 | 136823072 |
|
Enhancer Sequence | GAAGCTGAGT CGGAAGCACG GTCCCCACAC TCCTCCTTAC TCCCCGCCCA CGCTCCTCCC 60 CACTCCCCAC ACTCCTCCCC ACCCCCCTGC TTCTCCCCAC TCTCCCCATA CTCCCCACTC 120 CCCCTGCCAT GCTGCCCCAA CTCTCCCCAT GCTCCTCAGT CCCTCCAATG CCCCCCAAGC 180 TCCTCCCCAT TCCCCACATG CTCCTCCCCA CTCCCCACGG TCCTCCCCAC CTCCTTTCTC 240 CCCACTCCCC CCATGATCCT CCCCACACCC CCACTCCTCC CCCCTCCCCA CCACGCTCCT 300 CCAACTATCC CCACTCACCC CATGCTGCTC CCCATTCCCC CCAAAGCTCC TCCCCACTCC 360 CCCACACTCC CCCCACGCTG CTTCCCACTC CCCCCACGCT GCTTCCCACT CCCCCCAACG 420 CCCCCCCCAC GTTCCTCCCC ACCCCCCCAC TTGCACTCCA CTCCCACTCC TACTCCTCCC 480 CACTCCTCCC CACAGCTCTG GCCTCCCCCA GCCCGAGGGG AGCCCTCTAA ACCCTCCAGC 540 TCAGGCTGCT CCGTGAAGCT CAGTTCCTGC CGCTTCCGCT CAGCACAAAG GCACGGCCCC 600 TGCTGGAGGC CCCCGCTCCG GGGAGCTCTC AGACGGGCAG CCAGCACCTC ACTGCCCATC 660 TGCTCCTTCC CTGCTTACTC GCAGAGTCAA GACCTGGAGC CCACGGGGCC AGGAGGCACA 720 AAGCACAGCT TCCCAGGTGA CGCTGGACAA GTCGCTGACC CTCCTGGAGC CTCAGTTTCC 780 CCAACCCAGT GGCTCTGAAT GAATTCCCTG GATTCCTGAG AAGGAGGGAG CTTCCTCACT 840 GGTTCACAGG GAGAGAGGGA GGGAAGGGGG TTCTGACAAT TAAAAACAGG TCTGCAAGTC 900 AGGAACTCGA TGATCTCCAG AGGTGCCATG ATCCCCTCGT CTACCCAGCC TCCCCTGGGC 960 CCTGCAGCCC CTCCCTACCC TGTGACCCTC AGCCCAAGCC CCTGGGGAGG GTCTCTGGTT 1020 CTCAGCTGTG GGGTTGGGCC CAGCGGGTCT GGGGGCCTGG TGGGGAAAGG GTGTCTAGGG 1080 TACTCTGTCT TTCTACCTTT CTGAGTTGTT TCTTCTTTTG CTTTGTTTTG TTTCGTTTTG 1140 TTTTTTTTCC AACGAGTAGA CATTACTTTT AGAATTTCTT AAAAAGTTAT CTCAGCTTTG 1200 GGTTGGGTTA GGGAGGAGGG AGTCCTGGGA ATGTATAAAA AGCACGCAGC CAGTTAGTTC 1260 CTGAGAAGTC AGAAAATGCG AAGATCAACT GAGAAGCTGT ACTTTCTGGA AATTCCAGGC 1320 GAACCAGCAC CAGGCCCCTC GGCTGGTGGG CAGAGCACCA GGGGGCGAGG GAGCGGGAGG 1380 GGGATTCCCT GCTGCCAGGC CAACAGCTGG GCCAGCCAAG GTCAGGAATG CTGCAGCTGC 1440 AGCCTCGCCT TCCGCCCCCA CCCAGGCGGG AGCCCAGTGG GAGGGAGGCT GCCCCTGCCA 1500 GGGCCTGGGA CAGAGCCCTC TGTGGGGGAC AGGCCAGGCA GGAAACCCGG CCGTCCTCAA 1560 GCAGGAAAGC TGGGCCAGAG CTGGTACTTC AGCAGGGAGC TGAACTCCAG TCCTGGGCGC 1620 ACCTGTTTGC AGTCACAAAA AGGGCAGACT GCAGCACCCA CCCACCTGCC CAGCTCCCCA 1680 CCCAGCTCCC CACCTGCCCG GGGTACCCAG GACTCTCTCC AACGCCACCA GTGTCTCTCT 1740 GGTTCCTCAC TCTGTGCAAG CCTACCCTCT GGTGCTCTCC CGGTTAGGAT GATCGTCCCT 1800 GCTTTACCAG GTGGGGAAAC TGAGGCTCGG CCTGGCAGTT ACGGGCCTCC CCTGTACCAG 1860 CTGCTGCAGG TCCGGTCTCA TTTCACCAGG GAAGGATGTG TGCCCAGGAC GCTGCTCCCT 1920 GGGATGAAAC GGGTTTGTTT TTTTCTCCCA GTATAGAAAT AACCCTGCCT GGATGAGGGC 1980 AGGGAAGTAG AATAACATGA AACCGACAAG AACTCCCATC CTAAAACACC ACTAACCACT 2040 GAGGGCGTTT TTCTGTCGTC TCTTGACTCT GGGTTTTTAG GGGTTTTTTA TGTGTGTGTG 2100 GTGTTTTCTA CATATTTGAC TACTGGGAAT AATATGGCAT ATTGCGTCCT GGTGCCCCTT 2160 CGCTGACAGC ACAGGTGTCC CAGCTCCCTG CCTCCCCGGC TGCAGGGCAG GGCGAGGAGG 2220 GGAGGCCAGG GACATGCGGG CCTGGTACCT TCCAGGGCAA GAGGGACGTC ATCCCCGTGG 2280 GCAGAGCAGG AAATGGAGGA ATGTTGAGTT CCCTGCACCC GCTGTCACCG TCACAGCTGG 2340 CCCCACCTCA GCCGGGACAC CCTGCCTGGG CCACTCCAAG TGACTGTCAC AACCCGAGAG 2400 CCTATGGCCA AGATGAGCTC CACCAAGTAA AAATGGTGGA GTGTGGGGAA AAGCAAGAGA 2460 GATCAGAGTG TCACTGTATC TGTGTAGAAA GAAGTAGACA TGGAAGACTC CATTTTGTTA 2520 TGTACTAAGA 2530
|