Tag | Content |
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EnhancerAtlas ID | HS098-04633 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:203640810-203644020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr1:203643926-203643936 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:203643926-203643936 | GGCACGTGCC | - | 6.02 | Myod1 | MA0499.1 | chr1:203642872-203642885 | AGCAGCTGCCCCT | + | 6.18 | RFX5 | MA0510.2 | chr1:203641599-203641615 | CTTTGCCATAGCAACC | + | 6.15 | RFX5 | MA0510.2 | chr1:203641599-203641615 | CTTTGCCATAGCAACC | - | 6.32 | Stat4 | MA0518.1 | chr1:203642667-203642681 | CTTCCAGGAAATAA | + | 6.57 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_00067 | chr1:203629585-203648819 | Adipose_Nuclei | SE_02128 | chr1:203640353-203643870 | Aorta | SE_12116 | chr1:203640923-203646594 | CD3 | SE_13787 | chr1:203639960-203647614 | CD34_Primary_RO01536 | SE_14468 | chr1:203640936-203646834 | CD4_Memory_Primary_7pool | SE_18521 | chr1:203639600-203646936 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19166 | chr1:203639152-203646704 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20327 | chr1:203640357-203646733 | CD56 | SE_22546 | chr1:203639536-203646747 | CD8_primiary | SE_25804 | chr1:203639346-203646040 | Duodenum_Smooth_Muscle | SE_26726 | chr1:203640282-203641476 | Esophagus | SE_26726 | chr1:203641519-203646078 | Esophagus | SE_29679 | chr1:203639748-203645291 | Fetal_Muscle | SE_36167 | chr1:203641378-203643905 | HMEC | SE_39762 | chr1:203639598-203643774 | Jurkat | SE_40816 | chr1:203640451-203643887 | Left_Ventricle | SE_42264 | chr1:203640417-203643863 | Lung | SE_44861 | chr1:203640389-203643779 | NHLF | SE_45901 | chr1:203638689-203645287 | Osteoblasts | SE_48668 | chr1:203640299-203643783 | Right_Atrium | SE_53094 | chr1:203640491-203643860 | Small_Intestine | SE_54514 | chr1:203628856-203647840 | Stomach_Smooth_Muscle | SE_66630 | chr1:203639598-203643774 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 203643182 | 203643803 | chr1 | 203641153 | 203643812 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I203669 | chr1 | 203638729 | 203646707 |
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Enhancer Sequence | TCAGCATCTG AACCTTGCAT GCTGACTCTG TGATGCTGAC TAAGGGTCCT CACCACCTTG 60 ACTAAAATCT TGGGTCTTGC TATGCAGAAG TAGCCCTTCA CCCCAAAGCT AAGGAGAAAG 120 GATTGGATGA AAGTTCTCTG TAGAAGTGGA GGAAACACGT GTCTCCTCAG AGGTACCTCT 180 AGAGGTTGTT CTCTGCAACC CTCCAGCTAG AGTGAGCAGG CTCCTTGCCT GGGTGGCACT 240 GCTACCCACA GAGGGGATGG GGGCTTCGAA GCTCTCCTCC CACGACACCT GGTGAATCCT 300 CCATGTCTTC CTCCCTTGAT AGTGGCAGCT GGTGGGGGCT GGGGGGAGGG AGGAGTGCTG 360 CTGTTAGAGC AAGAAGACAA AGTGGCTTTG TCTCTTATCC GTAATATAAG TGCAGGGAGG 420 TGAGAAGACC CTGGGGTTTG GCGTTTCTCC TTGAGGAGCT GAGCCAGAGG CAGGGCTTTG 480 GTTCCTAAGT GATTAGAGGC CTGCATGGCC AGAGGCCGCA CCTTCCCTTT TGGAAAGGAG 540 CTCACCCACA CTCCTTGCTT CCATCTTCCC CTTCCTGGCT CAAGTCATAG GCTCTATTTT 600 CTGGCTATCC TGTTTTTGTT CCTGAGTAAG TTGCGGTGGC TCTTTTTTTT TTTTTTTTTT 660 TTTTTTTTTT TTTTAAAGCT GATTTAGGGG GTTGGGAAAA GAAAACTTTA AAAGTAAAAT 720 AATAAAAAAC AGACCACTCT GTCATTACAG GCACATAAAT AGCTTTACCG TCGCTGGGCT 780 GCACACTCGC TTTGCCATAG CAACCTAAAG CGACTGTTTA TAACAGCTTG TCAACTGGCC 840 TGGAAACCAG CAGCTGCTGC TGGCCGCCCT GGCCTCGGAG CAGTGGGCAG GCGCTCCCTG 900 AGAGGTGTTA TGGAGGCGGT GAGCCTGGTG CTTCTTCTGG AACCGTGGGG GATGGCAGGG 960 GAACGGCAGC CTGGGTTCCA GAGGCAACCA GGGGCAGTAA TGTTTTGGGA GCCAAAGTGA 1020 GCAGCGAATG TCTTTTGTTT TTGTTTTCCC CTCATCTGTG TATGGGCCCC AGCATCGCTC 1080 ATCTCCTGTG GAGATAGAAG ACAGGGCTGG GAGGGGATTT GCTCCACTGG AACCTGAAAG 1140 GGGCCTGGGT GTCCCTCTGA ACCTCACGAG GTGGCTTGTT TTAACTTTTC GAATAGACCT 1200 TGGCTTCTGT TGTAGCCTGT TGAGTGACAT CCTCTCAAGT CTGTTTTCTC AAAGACTAAA 1260 AAAATGTGGG CTTTTTCAGG GCTCTGTCTG GGAAAGGGGG CTGCCCAGAG ATAAATGGAA 1320 GCAGAGATCA GCAACCTGGA AGGACTAGCA GAGGGAGAGG GAAGAGTGAA GGAGACACAT 1380 GGCAAGATCT TCCTGTGCCT TCCCATGTCA GCCTGGAGCT GAAGGGGTTC ATGGGAATGC 1440 TTTGGAACCT CGCAACATTT TCAAAGTGTG GTCCCCAGAC CAGATGCATC AGCTCACCCT 1500 GTTAAGGAAC TTGTTAGGAG TGCACCTTCC CAGGCCCCAC CTCCGTTCTT GTGCACCAGA 1560 AACTCAGGAG TTGGCAGGGA GGGGCCCAAT AGGTTTGCCC CAGTTCTCCA GAGGATCCTA 1620 GTGCTCACTC TGGGTTTGAG AACCACAGCT CTAAAACATT ACTCAAGTGC AAGGAAGCAT 1680 GATCAGTTCG CTTTCCAAAG GCCTAGGCTG ACTGAATGGA TCCTGTCTGT GCAATATGTG 1740 AACAAGGAAG AATAAAACAG GCGCAGAGGG GTGGCAGGTT ATTAGCGATC ATTCCTGGCC 1800 ACCTTTTTTA ATAAGCACTG TCTTTTCAGC ATGGAGCCCT CGCTGATTTG CCTGTGACTT 1860 CCAGGAAATA AGCCCAGAGA AGGCTGGAAT AGGTAAAGCG GGGATGGGAG GTTCTCTGTA 1920 CTCTGTACAG GTGAGACTGT CAGAGTGGAG AAAGGGAATG GGAGCAGCCA GGCCTGATGA 1980 CCAGTATGGG ACATGCTGAC TAGTATCTGG GCCACACAGG AATGTTGTTT TAAGTCCTCT 2040 CCTGCTGAGC GTCTGGGGAC AGAGCAGCTG CCCCTGGTGC TCCCTTTTGG TGGATGAGAT 2100 GTGGCCTCCT CAGTCTGTGG CCAGGCAACT TCTTCCCCCT TGTCCTGAGG ACTCCACCAG 2160 ATCCTGAGGC CTGGGAACAA CCAGGTCCCG ACCCGGTAGC CCAGGGAGAT GACCCCTCTC 2220 CATAAGCATG ACATGATTCT GCTGAAATTC GTTTCTAAAA ATAACCTAGG ATCCGATCCA 2280 GCTGCTAAAA AGCCCCTTTG TTCCCTTGAA ACCAAAATAT GGAAAGCCAC AGCAGCCCCA 2340 AGAAAGACAG TCTGTGTAGT CCAAGAGAGT GCATATACGA AATACTTGAA TGCTGCTGCC 2400 GGAGGGCTGC GTCCTGTCTG TGGCCTAGAA GCTTCCTGCC GCAGCTCTGA GGAGTGAGTA 2460 GCAGTTATCG TTGCTAACCC TTATCCTGAG TGAACGGGGT CAGGAGAGGC TGCCAGTACC 2520 CCTTTTGTTA AACAGACCTT CCAGATGGCA TTGTCACTTC CACCTGAAGG TGGCTCTTGT 2580 CCTCCTTAAA CAACTGAAGG AAATGGTGAG CGCTGCTGTT TCATCCTCTA CATTTTTTTG 2640 AGCTCTAGCT TGCTGTGAAC ACCCCTACCT CCACCCCATA CATCCTCTGA GTCACTGGAG 2700 GACACAGAGG TGACCCAGGC CAGTGTGACT CACACAATTT GAAAGAGGTT GGCTTTCCCA 2760 AGGCTCTGGG CCTAAGGGAC TGCCCTTTCT CATCTTGATA ATTTTTTTTG AGATGGAGTT 2820 TTACTCTGTT ACCCAGGCTG GAATGCAGTG GCACGATCTC AGCTCACTGC AACCTCTGCC 2880 TCCAAGGTTC AAGTGATTCT CCTGTCTCAG CCTTCTGTGC AGCTGGGATC ACAGGCGTGC 2940 AACACCACAC CTGGCTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT CTGAGATGGG 3000 GTCTCACTGT GTCTCCCAGG CTGGAGTGCA ATGGCACAGT CTTGGCTCAC TGCAACCTCC 3060 ATCTCCCGGG TTCAAGCAAC TCTTCTGCCT CAGCCTCCTG AGTAGCTGGG ACTACAGGCA 3120 CGTGCCACCA CACCTGGCTA ATTTTTTGTA TTTTTAGTAG AGACGGGGTT TCACCATGTT 3180 AGCCAGGATG GAATTTTTAT ATTTTTAGTA 3210
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