Tag | Content |
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EnhancerAtlas ID | HS050-06001 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:223920000-223922560 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr1:223922394-223922411 | TGGCACACCATGTACCA | - | 6.01 | Gata4 | MA0482.1 | chr1:223920574-223920585 | TCTTATCTCCC | + | 6.62 | Nr5a2 | MA0505.1 | chr1:223921780-223921795 | GACCTCAAGGCCAGC | + | 6.22 | USF2 | MA0526.2 | chr1:223921349-223921365 | CCAGGTCACGTGAGTC | + | 6.03 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_00224 | chr1:223917623-223923297 | Adipose_Nuclei | SE_01908 | chr1:223920427-223922082 | Aorta | SE_02306 | chr1:223920308-223921944 | Astrocytes | SE_04026 | chr1:223920429-223923012 | Brain_Anterior_Caudate | SE_05036 | chr1:223920530-223922321 | Brain_Cingulate_Gyrus | SE_05972 | chr1:223920132-223922577 | Brain_Hippocampus_Middle | SE_07159 | chr1:223920244-223923166 | Brain_Hippocampus_Middle_150 | SE_07996 | chr1:223920284-223922259 | Brain_Inferior_Temporal_Lobe | SE_09681 | chr1:223920277-223921825 | CD14 | SE_19702 | chr1:223921073-223922029 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23408 | chr1:223920555-223922971 | Colon_Crypt_1 | SE_24051 | chr1:223920713-223921438 | Colon_Crypt_2 | SE_24051 | chr1:223921499-223922031 | Colon_Crypt_2 | SE_24051 | chr1:223922112-223922463 | Colon_Crypt_2 | SE_25230 | chr1:223920636-223922879 | Colon_Crypt_3 | SE_26209 | chr1:223920732-223921934 | Duodenum_Smooth_Muscle | SE_26925 | chr1:223921184-223922005 | Esophagus | SE_31491 | chr1:223920239-223923646 | Gastric | SE_33950 | chr1:223920559-223921591 | HCC1954 | SE_38254 | chr1:223917692-223922239 | HUVEC | SE_41495 | chr1:223920316-223922995 | Left_Ventricle | SE_42269 | chr1:223920225-223923100 | Lung | SE_45872 | chr1:223920277-223921720 | Osteoblasts | SE_49408 | chr1:223920327-223922010 | Right_Atrium | SE_50365 | chr1:223920440-223922961 | Sigmoid_Colon | SE_53249 | chr1:223920551-223922027 | Small_Intestine | SE_65644 | chr1:223920306-223922506 | Pancreatic_islets | SE_68376 | chr1:223892363-223922876 | TC32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 223921475 | 223921876 | chr1 | 223922041 | 223922091 | chr1 | 223922066 | 223922385 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I223730 | chr1 | 223917704 | 223922480 |
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Enhancer Sequence | TAAAGGAATA AAAGAAAATC TACTTCATAG AGCAGCCCTG AGGGCTGATG ATTGCCCATT 60 TTTATGGTTA TTTCTTGATT ATATGCTAAA CTTCTTGATT ATATGCTAAA CAAGGGGTGG 120 ATTATTCATG CCTCCTCTTT TTAGATCACG TAGGGTAACT TCCTGATGTT GCCATGGCAT 180 CTGTAAACTG TCATGGCTCT GGTGGGAGTG TAGCAGTGAG GACGAGCAGA GGTCACTCTT 240 GTCACCATCT TGGTTTTGGT AGGTTTTGGC CGGCTTCTTT ACTGCAACTG TTTTATCAGC 300 AAGGTCTTTA TGACCTGTAT CTTGTGCCGA CTTCCTATCT CATCCTGTGA CTTAGAATGC 360 CTTAACTGTC TGGGAATGCA GCCCAGTAGG TCTCAGCCTC ATTTTACTCA GCTCTTATTC 420 AAGATGGAGT TGCTCTAGTT CACACGCCTC TGACACATGT TCAGAAATAA TGGTGATTTT 480 CTTCTACAGG TGGGGACGTT AGCATTATAA TGACATGGTA AAGTTCTGAA GGTAACAAGG 540 GGTTGCCTGT TCCAGTTTCT GCCAGTTTTG GGGGTCTTAT CTCCCTCTGG TATCTGGGCA 600 GAGGTCAAGA AGCTCTGGCA CCATCAGGGG CCAGCTTGTT TCTTTAAGCA GCTGTGCCTA 660 CAAATAAAGG GACTAAAGAA AACAATAAGA AAACCCAGTT ATTTCCTGGG GGTTGCTCTG 720 GTATCCAGCG TGTTTTACTT CACCAAGCGC AATTCTTCCC AGTGCAGGCA CTGGGTGTAA 780 CTGTGACAGC CAGCACCAAC CTGCCCACAC ACCTCCTGTC CTGCAGGACT GTCAGCAGCC 840 TCTGCACTAT AGTGTGACAG AGCCACAGGT AGCTCAGGTG TGCCTCAGCC CAGCCTCTCC 900 TGCACTCCCC CTCCCCTGGC TCCCCAACTC TGCCTCACTT CTGTTTGTGA AGGAAAGACA 960 GCAGTAGCGG AAGGGAAAGA AGGAGAAAAT GCAGAGCAAA TATTATGCTT TCCTCTTGGA 1020 AAACCTCCAG GAGCTGCAAA TATTAGTAAT CCAGCTGCAT CCCACCCCCC AGGATGGGCT 1080 GGGCCTGTCA CACAGCCAAC CTTCAGGATG CAGACACCCA GGCTGGGGAG CACAGCTCTG 1140 GAAATTTACT GACATGGCCC TGAATGAATT TATCTTTTCA GTAGAAGGCC CTGGAGTTTA 1200 AAGGAGTCAT TCATAAGGTC TGTCTGGGAG TGCCTTGTCC TCAGAGGAGG GTCTGGGTGG 1260 GTTGGAGTGG AAGGAAGGGC TGGCTACCTG GTGTGCTCTC CGTGGGTCCC CAAGAAAGGC 1320 AGCCCTGCTG GGGGCAGTGA AGCCCTTATC CAGGTCACGT GAGTCTTGGA AGGGGAAGGC 1380 TGCTGTGCTT AACGATTCAA AAACACAAAT CAAACCTCCT TTCCCAAACA AATTAGAAGG 1440 TGTGGAGGAA GCTTGAATTC AGAGAGGATT TCCCAGAGAC CCATAGGCAA AAGTGGCTTA 1500 ACTGAGCCCA GTGGGTGTCC CAGAATGGGC CAGAGAGAAT GACACTAAAA AGTCTTTGAA 1560 CAAATGAGCA AATGAATACA GGAATGCTCA TCTGCCATAG GCACAAACGT GGTAAACGTT 1620 CCCTGAGAGA ACTGACAGCC CAGGGGTGCA GGGAGAGAAA CGGTCCCAAC TGCAGACTGG 1680 GTCCCAACTG CAGACTCGGT CCCAACTGCA GACTCAGGAG GAGGGAGGCT GTTAAGGGGC 1740 CGTCTTTCCT TCTGTTATGT GAGGAGAAAA GCAGGGAAGG GACCTCAAGG CCAGCCTCTC 1800 CCAGGAGCTG CTGTTCTCAG CCCCGGGATC CAGCGCTACA GGGAAGTGCA GGGGAGGCTC 1860 CACAGTCCCG GCTGGAGACC CGGTCAGGCC TGGGTGGCCA CTCTTCTTTG TAGTGGCCAC 1920 CCTCGTGTCA CCAGCAAATG CTTTTGTATC TACACCCTTC TCAGTGCTCC CCCTCTTTTA 1980 AAAAATGTAC TTTCTTTTTT TAAAAAGAGT TGGGTCTTGC CTTGTCACCT ATGCTGGAGT 2040 GCAGTGTTGC TGTCACAGCT CACTGCAAAC TCCACCTCCT GGGCTCAACC CATCCTCCCA 2100 CCTCAGCCTC CCAGGTAGCT GGGACCACAG GCACACACCA GGACACCTCG CCCAGTGCTC 2160 ACTATTTACC TTTATTTCTT CCTTATTCGG ACACCCCTTG CTTCCAAAGA AGAGTTTCGG 2220 AAGGCTCAAG ACGGTGAGAC AGACACCTTA TGCACTGCTT CACTCTCCCC CGCAGCTCCC 2280 CTCCCTCCTC ACTGACCCCC GGCCACAACC CTCTCTCCTT GCCCCTCACC AGCCGGCACC 2340 CTTGGCAACC CTGGCACCCT TTCGAGGACA AGACTGCCAA ATGTGGCCAA GGTCTGGCAC 2400 ACCATGTACC AATCGAAACT CCACTTCCCT TGAGTTTCAG TTTCCACGCC TATAAAATTA 2460 GCAAATGAAA AGAGCAAACA CTTGGAGACA CTGTTCTCAA TGCTTTGCAT ATTTTTTTCA 2520 TTTAATTCTC AGTGCCATGA GACAGTCTAT TATTATTAAA 2560
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