Tag | Content |
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EnhancerAtlas ID | HS088-05101 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:206722280-206725490 |
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 | TCTCCTGGGT CCAAGTGATT CTCCTGCCTT GGCCTCCCAA GTAGCTGGGA TTACAGGTGC 60 CTGCCAACGC TCCCAGCTAA TTTTTGTATT TTTAGTAGAG ACAGGGTTTC ACTATGTTGG 120 CCAGGCTGGT CTCGAACTCC TGACCTCAGG TGATCCACCC ACCTTGGCCT CTCAAAGTGC 180 TGAGATTACA GGTGTGAGCC ACCATGCCTG GCCTGTGCTT CATTTTGGAT CATTGCTATT 240 GCTGTGTCTT CAAGTTTGTT AATCTTTTCT TCTGCAAAGT CTAATCTGCC ATTAATCCCC 300 ATCTAGTATA TTTCCCATCA AAGGCATTGT AAATTTCAAC TCTAGTGGTT TGATGTGGAT 360 CTTTTAAATA TTTTCCATTT CTCCTACTTA ACTTTTTGAA TAAATAGCAT ATACTTATTC 420 AGACATTTCT CTGGGCTCCT CACAGCCTAT CCCCTTCTAC CCTAGAAGCA GTGGGCTGCC 480 TGAGACACCA GAATTAGTGT CTTTGACCAA TGCTAATATC TGTGTCAGTT GTGGTCAGTA 540 GTCGAGACAG AGTCTCACTA AGTTGCCCAG GCTGGTCTTG AACTCCTGGC CTCAAGTGAT 600 CCTCCCACTT TAGGCTCCCA AAGTCCTGGG ATTACAAGCA TTAGCCACTG CACCCAGCCC 660 TGTGGAAATA TTCCTGAGTT TTGTTCTAGG ACCCAGTTAA ATTACTTAGA AGTTCGATCC 720 TTTTTAAGGT TTTAAGAGCC TCTTTAAGAT TTGTCAGGAT TGGAATAGTC CTCAGTCTAG 780 GGCTAATTAT TTCCCACCAC TAAGGTAAGA CTCTCTGTGT ACTCTACTCA GTGCCTAATA 840 AATCATGAGG TTTTCTGGTA TGGCTTGTAG GAACAGGCAC TATTCCTGCC CTGTATGAGG 900 GCAGACACTG TTACCTGTAA TCCTTTTGGG CGGTTCTTTC TCTAGCCTTG GGTCATTTCT 960 TCCCATGCAC ACACCGATCA GTAAGCACGC AGGTGAATAC TATAGGGGCC TTTCTGCAGT 1020 TCTCTCTCTC TGCAGCTGTC TCCATTCAGT TACTCTGTCC TGTGAACTCG GGCTGCCTTT 1080 GTCTCCCTAG ACTCGAGCAG CATCTCCTCA GCTTCAGGGG GTTTTCCAGG CTCCACCTTA 1140 GTACCCGCTC TGCACCACAT CTGGGAGTAA ACTGGGAGTA AATCTAGGGA TCAACTCATT 1200 TGTTTCCTGT GTCTCGGGGA TTGCTATTCC TCATTACCTG ATAGCCAGTA TTTTAAAAAC 1260 CACTGTTTCA TTAGTTGTAT CCATTTTTTT GGTTGTTTTA ATCAGGAGGA TATATCTGAA 1320 TCCTATTCCC TCATCTTTGC CAGAAGCAGA ACTCCCCCAG GCACTGTTCT AATCCTGATT 1380 CGTACTAGTT CATTTAATAC CCAGCCTTAC GCATTGGGTA AATGCCTTGA GGGCAGGGAT 1440 CCTATCTTTT GCCATTTAGT CTTCCTCATA ATGCACTGGG CCTTGCACAT AGTAGGTGCT 1500 GAAGAAGTCC TTCATTTTAT TCGATTTTGA ACTTGGATTT GTGGAGGTTT TTTGCATTCA 1560 GAATGCTGGT TCTCCCACTT ATTATGACAC TAGGAAAGTA CATAACCTCT CTTAGCTATT 1620 ACATGGGGAC ACCAGTGTGG TTGTTGTGGC AACTGTATAA AAGCACTTGT AAACTCCATG 1680 GAGCATGAAC CTTGTTTGTT TACCAGTGTG TTCCCAGCAC CTACCACAAG GAATATATAT 1740 AATAGGACTG GCAAATAACA TAGTTTCCCT TGCCCCTATG GTGTTTTAGA GCCTTCAGCC 1800 CAGCAGGCTG CTTGCCCTCT GTAGACACAT TATCCTCAAG ATAGCTATGG GTGTGAACAA 1860 TGCTGCTCTC AGCATCTTAA AATATGGTAA CGCTCCAAAA TGGGGATTTT GTGTTGTACC 1920 CTGAGCACAC AGGCACAAAT CCATGTGCCT GCCCTGCTAC CCAGTCCTAA GGCTGCTGAC 1980 AGCCCCTTTC TGCCATCTTG GAGCAAGTTT AGCGCTCCCA GCTCTAAAAT CTGGCTTTCT 2040 ATAGCTTAAT AACTTTATGA TCTAGCAATC AATTGATATT GACAGAATCT TTTGTTATTC 2100 TGTGGCCACC AGAAATGAGA GGAACTCACC ACCTTTAGTT GACATGGCAG GAATGTCAGG 2160 AAAGTCAGAA ACTAGGGTCC CACATCTAAT CTTTCCTGGT AGATGTGAGG GTGGGGAGCA 2220 GAATACATTA GACCCCACCT AGTCCCTCAG TCAGTATTTC CTTAGCTTCC AAACCCCAAA 2280 TTTGGCACTG ATTTCTTCTA TTCTGACTCC TTCCCTTGAT AAGAAGCTAA TGGCTGCTCC 2340 CAGGGGATTC TAGAGGTGCC AGATGCACAC CAGCCCACCT ATATCTGCCA AGAGAAGGAG 2400 CCAGTCCCCC GCTCCCTCCA CGTTACCCTG AGCGGACATC CTTCATTCTT ACCCTGGCTA 2460 GGCCGTCCCA TCTGGGACAG CTTTCTCCAT GGCTCCTTCA CAGACTCCTG CCACACTTTA 2520 GAAGCCAGAA GTGCTGGCCA AAGCTGTCAG TGATTCCTTT GCACTGGACA GCCGCCCTCA 2580 CAGGAGCCTC TCCAAGGCCT ATCTGACCAG CCCCAGATGG GCCCAGCCCA CGCCAATGTA 2640 TTTCTGATTA GGCAGAATGG AAATGCTTCC CAAAAAGGAG GCACCTGAAG TCCTGGCCAC 2700 AAGGAGGGAC AGAGCTCTGG TGCATATTTC TCTAGAAATC CTTAAACCCT GGAGACATTT 2760 CTCTGGGCTC TTCACAGCCT ATCCCCTTTT ACCCTAGAAG CAGTGGGCTT CCTGAGATGA 2820 CCCCCAGGTG GGCTAGGCTA GCCCTGAGGC GAGAGGCAAG ACCCTCCTTG CTAGATGTAG 2880 CAGTGCAATA GTTGTTCACA TCTCACCCTG GTGACCATGC TGCCCGGGAT GTTGGAGGAT 2940 TGGCCCTGCC CAGAGAGGGG CACATCAGGG AGACGGCTGT TGATCAGAAA TAGCTTTTGT 3000 CACTCTGTAT TCTCACTAGG GAGGAAAATT AGAAGACAGA GCCCTTGGGC CTGACTCAGA 3060 CCCTGACATG AGTTCTTGAG GGTGTGGACA ACTGGGGTAA CTCAGCTATC TTCAGTAGGT 3120 TCAGTGTCAA GGCCTATCGA AGCTGTTAGC CTGGCAGCCA ATCAGAAGTG TGGTGTGGGT 3180 TAGCACCGCT GAGAAAGTGA CTGTAGGGTG 3210
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