Tag | Content |
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EnhancerAtlas ID | HS003-03470 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:206722360-206725490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr1:206723310-206723323 | TGCAGCTGTCTCC | + | 6.24 | Myog | MA0500.1 | chr1:206723309-206723320 | CTGCAGCTGTC | - | 6.62 | NFAT5 | MA0606.1 | chr1:206722649-206722659 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:206722649-206722659 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:206722649-206722659 | ATTTTCCATT | + | 6.02 | NFYA | MA0060.3 | chr1:206725435-206725446 | AGCCAATCAGA | + | 6.32 | Stat6 | MA0520.1 | chr1:206725005-206725020 | ATTTCTCTAGAAATC | - | 6.48 | Tcf12 | MA0521.1 | chr1:206723309-206723320 | CTGCAGCTGTC | - | 6.14 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_11917 | chr1:206724465-206726413 | CD3 | SE_14503 | chr1:206723756-206726196 | CD4_Memory_Primary_7pool | SE_16490 | chr1:206724410-206725962 | CD4_Naive_Primary_8pool | SE_16959 | chr1:206724682-206726215 | CD4p_CD225int_CD127p_Tmem | SE_17411 | chr1:206724289-206760065 | CD4p_CD25-_CD45RAp_Naive | SE_17843 | chr1:206723887-206758306 | CD4p_CD25-_CD45ROp_Memory | SE_18269 | chr1:206723684-206769868 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19128 | chr1:206724239-206727389 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20034 | chr1:206723900-206726386 | CD56 | SE_20823 | chr1:206724369-206726312 | CD8_Memory_7pool | SE_22080 | chr1:206724399-206726390 | CD8_Naive_8pool | SE_22390 | chr1:206723695-206743626 | CD8_primiary | SE_31229 | chr1:206724792-206726343 | Fetal_Thymus | SE_39708 | chr1:206724385-206725772 | Jurkat | SE_53552 | chr1:206724778-206725653 | Spleen | SE_55221 | chr1:206724799-206726079 | Thymus | SE_62534 | chr1:206724532-206763666 | Tonsil | SE_65624 | chr1:206724203-206725339 | Pancreatic_islets | SE_66615 | chr1:206724385-206725772 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I206550 | chr1 | 206724171 | 206726307 |
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Enhancer Sequence | TTTTTGTATT TTTAGTAGAG ACAGGGTTTC ACTATGTTGG CCAGGCTGGT CTCGAACTCC 60 TGACCTCAGG TGATCCACCC ACCTTGGCCT CTCAAAGTGC TGAGATTACA GGTGTGAGCC 120 ACCATGCCTG GCCTGTGCTT CATTTTGGAT CATTGCTATT GCTGTGTCTT CAAGTTTGTT 180 AATCTTTTCT TCTGCAAAGT CTAATCTGCC ATTAATCCCC ATCTAGTATA TTTCCCATCA 240 AAGGCATTGT AAATTTCAAC TCTAGTGGTT TGATGTGGAT CTTTTAAATA TTTTCCATTT 300 CTCCTACTTA ACTTTTTGAA TAAATAGCAT ATACTTATTC AGACATTTCT CTGGGCTCCT 360 CACAGCCTAT CCCCTTCTAC CCTAGAAGCA GTGGGCTGCC TGAGACACCA GAATTAGTGT 420 CTTTGACCAA TGCTAATATC TGTGTCAGTT GTGGTCAGTA GTCGAGACAG AGTCTCACTA 480 AGTTGCCCAG GCTGGTCTTG AACTCCTGGC CTCAAGTGAT CCTCCCACTT TAGGCTCCCA 540 AAGTCCTGGG ATTACAAGCA TTAGCCACTG CACCCAGCCC TGTGGAAATA TTCCTGAGTT 600 TTGTTCTAGG ACCCAGTTAA ATTACTTAGA AGTTCGATCC TTTTTAAGGT TTTAAGAGCC 660 TCTTTAAGAT TTGTCAGGAT TGGAATAGTC CTCAGTCTAG GGCTAATTAT TTCCCACCAC 720 TAAGGTAAGA CTCTCTGTGT ACTCTACTCA GTGCCTAATA AATCATGAGG TTTTCTGGTA 780 TGGCTTGTAG GAACAGGCAC TATTCCTGCC CTGTATGAGG GCAGACACTG TTACCTGTAA 840 TCCTTTTGGG CGGTTCTTTC TCTAGCCTTG GGTCATTTCT TCCCATGCAC ACACCGATCA 900 GTAAGCACGC AGGTGAATAC TATAGGGGCC TTTCTGCAGT TCTCTCTCTC TGCAGCTGTC 960 TCCATTCAGT TACTCTGTCC TGTGAACTCG GGCTGCCTTT GTCTCCCTAG ACTCGAGCAG 1020 CATCTCCTCA GCTTCAGGGG GTTTTCCAGG CTCCACCTTA GTACCCGCTC TGCACCACAT 1080 CTGGGAGTAA ACTGGGAGTA AATCTAGGGA TCAACTCATT TGTTTCCTGT GTCTCGGGGA 1140 TTGCTATTCC TCATTACCTG ATAGCCAGTA TTTTAAAAAC CACTGTTTCA TTAGTTGTAT 1200 CCATTTTTTT GGTTGTTTTA ATCAGGAGGA TATATCTGAA TCCTATTCCC TCATCTTTGC 1260 CAGAAGCAGA ACTCCCCCAG GCACTGTTCT AATCCTGATT CGTACTAGTT CATTTAATAC 1320 CCAGCCTTAC GCATTGGGTA AATGCCTTGA GGGCAGGGAT CCTATCTTTT GCCATTTAGT 1380 CTTCCTCATA ATGCACTGGG CCTTGCACAT AGTAGGTGCT GAAGAAGTCC TTCATTTTAT 1440 TCGATTTTGA ACTTGGATTT GTGGAGGTTT TTTGCATTCA GAATGCTGGT TCTCCCACTT 1500 ATTATGACAC TAGGAAAGTA CATAACCTCT CTTAGCTATT ACATGGGGAC ACCAGTGTGG 1560 TTGTTGTGGC AACTGTATAA AAGCACTTGT AAACTCCATG GAGCATGAAC CTTGTTTGTT 1620 TACCAGTGTG TTCCCAGCAC CTACCACAAG GAATATATAT AATAGGACTG GCAAATAACA 1680 TAGTTTCCCT TGCCCCTATG GTGTTTTAGA GCCTTCAGCC CAGCAGGCTG CTTGCCCTCT 1740 GTAGACACAT TATCCTCAAG ATAGCTATGG GTGTGAACAA TGCTGCTCTC AGCATCTTAA 1800 AATATGGTAA CGCTCCAAAA TGGGGATTTT GTGTTGTACC CTGAGCACAC AGGCACAAAT 1860 CCATGTGCCT GCCCTGCTAC CCAGTCCTAA GGCTGCTGAC AGCCCCTTTC TGCCATCTTG 1920 GAGCAAGTTT AGCGCTCCCA GCTCTAAAAT CTGGCTTTCT ATAGCTTAAT AACTTTATGA 1980 TCTAGCAATC AATTGATATT GACAGAATCT TTTGTTATTC TGTGGCCACC AGAAATGAGA 2040 GGAACTCACC ACCTTTAGTT GACATGGCAG GAATGTCAGG AAAGTCAGAA ACTAGGGTCC 2100 CACATCTAAT CTTTCCTGGT AGATGTGAGG GTGGGGAGCA GAATACATTA GACCCCACCT 2160 AGTCCCTCAG TCAGTATTTC CTTAGCTTCC AAACCCCAAA TTTGGCACTG ATTTCTTCTA 2220 TTCTGACTCC TTCCCTTGAT AAGAAGCTAA TGGCTGCTCC CAGGGGATTC TAGAGGTGCC 2280 AGATGCACAC CAGCCCACCT ATATCTGCCA AGAGAAGGAG CCAGTCCCCC GCTCCCTCCA 2340 CGTTACCCTG AGCGGACATC CTTCATTCTT ACCCTGGCTA GGCCGTCCCA TCTGGGACAG 2400 CTTTCTCCAT GGCTCCTTCA CAGACTCCTG CCACACTTTA GAAGCCAGAA GTGCTGGCCA 2460 AAGCTGTCAG TGATTCCTTT GCACTGGACA GCCGCCCTCA CAGGAGCCTC TCCAAGGCCT 2520 ATCTGACCAG CCCCAGATGG GCCCAGCCCA CGCCAATGTA TTTCTGATTA GGCAGAATGG 2580 AAATGCTTCC CAAAAAGGAG GCACCTGAAG TCCTGGCCAC AAGGAGGGAC AGAGCTCTGG 2640 TGCATATTTC TCTAGAAATC CTTAAACCCT GGAGACATTT CTCTGGGCTC TTCACAGCCT 2700 ATCCCCTTTT ACCCTAGAAG CAGTGGGCTT CCTGAGATGA CCCCCAGGTG GGCTAGGCTA 2760 GCCCTGAGGC GAGAGGCAAG ACCCTCCTTG CTAGATGTAG CAGTGCAATA GTTGTTCACA 2820 TCTCACCCTG GTGACCATGC TGCCCGGGAT GTTGGAGGAT TGGCCCTGCC CAGAGAGGGG 2880 CACATCAGGG AGACGGCTGT TGATCAGAAA TAGCTTTTGT CACTCTGTAT TCTCACTAGG 2940 GAGGAAAATT AGAAGACAGA GCCCTTGGGC CTGACTCAGA CCCTGACATG AGTTCTTGAG 3000 GGTGTGGACA ACTGGGGTAA CTCAGCTATC TTCAGTAGGT TCAGTGTCAA GGCCTATCGA 3060 AGCTGTTAGC CTGGCAGCCA ATCAGAAGTG TGGTGTGGGT TAGCACCGCT GAGAAAGTGA 3120 CTGTAGGGTG 3130
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