| Tag | Content |
|---|
EnhancerAtlas ID | HS118-07668 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr16:89476440-89478540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr16:89476490-89476504 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_01214 | chr16:89477166-89477942 | Adrenal_Gland | | SE_09347 | chr16:89472243-89478334 | CD14 | | SE_18507 | chr16:89472523-89479900 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_26651 | chr16:89476700-89478024 | Esophagus | | SE_31628 | chr16:89476758-89478120 | Gastric | | SE_41566 | chr16:89477183-89477966 | LNCaP | | SE_45841 | chr16:89476427-89478265 | Osteoblasts | | SE_47910 | chr16:89476440-89477162 | Pancreas | | SE_47910 | chr16:89477378-89477916 | Pancreas | | SE_65322 | chr16:89474227-89478511 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I089405 | chr16 | 89471661 | 89478808 |
|
Enhancer Sequence | TTTTCACGGT GTGAGCCAGG ATGGTCTCGA TCTCCTGACC TCGTGATCCG CCCGCCTCGG 60
CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACCGCGT CCAGCCTCAA TCTAAATTTA 120
AAACACAGTT TGCTGTTCAG CTACAGGGCA GAATTTCACA CGGAGCAGGC ACCTCACAGA 180
TGCCAACCCG GTGGGTACGG CCCTTTGAGT GTCACCTAAA GCCTCATAAC ATCATCACCA 240
AGCCCATCCC CAAAAGCTGT AGTTAGTAAG CCACCAGGAT TTGATATTTA GAAACTTTTC 300
CCACTAACAA AAAACAAGCA AGAATAAATT TTAAACAAAG GCTGACTGTA CCAAGGAAAT 360
GGAGATAATA AACAGAAAAA GACTCATGGA CACTGGTGTT GGGAGTGATG GTCTTAGCCC 420
TCAGACCAGA CTAAGACACC CTGCAGAGCT GAGGCTGTCA GGAACCACGC AGAGCCACGG 480
AAGGGAAACA CCTGCCCCCG GGCTACAAAG GCCACCCTCT GCCCTCTGCT TACTGCTCTG 540
GTTCTGCCCT CCAGACACAA GCAGGTCCCT AAAGCAGTTG CTATCCTGCT GACGTGCTGA 600
CACCATCAGA TATGAACAAG AATCCCAGTT TTATTTTTCC TAATAAATAA ATCATCCATT 660
TAGCAAAACG TCAACGATAC CAAAAGCTAT GAAAGCATCC TTGGATTTAC AAAGAACCCT 720
CGCTTCTCAT TTCCCTTATT TTCCCATGCC CAGGCAGAGA GCCCTCTAAG CCCATGGGAA 780
GCTTAACAGA AGGGGGTGGG GAGTGGCCAA CTGTGGCCAG GGCAAGACAG AAACCACATG 840
TGCGTGAACA CGTGTTCTAC ACAGAGCCTT ATGTACTGGG CCACAGAATA AGCAGAGCTG 900
GGCAGCTCCT GCTGCCAAAG TCAACATGTT CAGGCTGCCC GGCCTCCACA GGCGCTTTCC 960
TGAAAGCTGC CTGCAGAGAG AAGGGTGGCC AGGGCAGGAG GCAGGATCCT GAAGCTGCCT 1020
GCAGAGGGAG GGGCGGCCAG TGCAGGAGGC AGGTTCCTGA AGCTGCCTGC AGAGAGAAGG 1080
GTGGCCAGGG CAGAAGGCAG CAGCACAGGG GCTCGGGCCC ACGCTGGCTG TCCACACCCA 1140
GGGCCACGCC TCCATGACGG TGCCCTCCAC CACATCCCCT CTCGTGTGTG CTGGTGCCAC 1200
CACGGGGGCC CAGGGACCTT TTTGCTCTAC TTCTCTTTCA AACTTGCAGC CCTGTGCCAG 1260
CAGCCAGCAC TGCCTTCAGA ATCCCTGCAC ACAGCGGTGG GAAACCTTGA CTGCACCGGA 1320
AGAGGAGCAG GCTGCCCTGG CTGGGCCAGA CGCTACACAT CTTGCTGTCG AGATGGTCTA 1380
CATTTCTTCC TTTTTTCTTT TTCTTGTAAT CCTTCTGTCA CCTAGAGCTG GAGTGCAGTG 1440
GTGTGATCAT AGCTCACTAC AACCTCTGCC TCCCGAGCTC AAGAGATCCT CCTACCTCAA 1500
CCTCCTGAGT AACCATGACG ACAGGCACAC ACAACCACGC CTGGCTAATT TTTGTATTTT 1560
TTGGAGAGAT GGGGTCTTGC CACGTTGCCC AGGCTGGTCT CGAACTCCTG ACCTCAGGCA 1620
ATCCTCCCAC CTCAGCCTCC CAGAGTGCTG GGATTACGGC CAGTTTACAT TCGGAACCCA 1680
CCACTATCCC CTTGTTGACA GTAAGCACAT CCCAAATCAT TTTTCCCAAT GGACAACACA 1740
AATAAATAAT TAAGATCCTT ATTCTAGAGT GGGGAAAAAA AGAGACTAGA ATTCTCAGCA 1800
GAACTTGAGG AATCCAATGG CCAGTAACGA AGATGCCTCC CAGAGTCTCC TGGCCATGTT 1860
CCATCCCTCC CCTCAGCCAG GTACTGGGGT GAGATGCCTC CCAGAGTCTC CTGGCCGTGC 1920
CCCATCCCTC CCCTCAGCCA GGTACTGGGC TGAGATGCCT CCCAGAGTCT CCTGGCCGTG 1980
CCCCATCCCT CCCCTCAGCC AGGTACTGGG CTGAGATGTC TCCCAGAGTC TCCTGGCCGT 2040
GCCCCATCCC TCCCCTCAGC CAGCTACTGG GCTGAGATGC CTCCCAGAGT CTCCTGGCCG 2100
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