Tag | Content |
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EnhancerAtlas ID | HS064-08132 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr2:42331480-42334000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LHX2 | MA0700.1 | chr2:42331717-42331727 | ACTAATTAAC | + | 6.02 | MSC | MA0665.1 | chr2:42332676-42332686 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr2:42332676-42332686 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr2:42332676-42332686 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr2:42332676-42332686 | AACAGCTGTT | - | 6.02 | mix-a | MA0621.1 | chr2:42331717-42331728 | ACTAATTAACT | - | 6.14 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_10312 | chr2:42325221-42336343 | CD19_Primary | SE_11146 | chr2:42323572-42336874 | CD20 | SE_11946 | chr2:42327841-42337002 | CD3 | SE_14693 | chr2:42327772-42338606 | CD4_Memory_Primary_7pool | SE_16102 | chr2:42330639-42336500 | CD4_Naive_Primary_7pool | SE_16740 | chr2:42330928-42334630 | CD4_Naive_Primary_8pool | SE_16987 | chr2:42327433-42336274 | CD4p_CD225int_CD127p_Tmem | SE_17444 | chr2:42325062-42338640 | CD4p_CD25-_CD45RAp_Naive | SE_17811 | chr2:42325303-42338643 | CD4p_CD25-_CD45ROp_Memory | SE_18685 | chr2:42325197-42338156 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19964 | chr2:42327606-42335969 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20190 | chr2:42327806-42336196 | CD56 | SE_21801 | chr2:42328127-42336332 | CD8_Naive_7pool | SE_22420 | chr2:42327613-42337810 | CD8_primiary | SE_30543 | chr2:42332455-42333846 | Fetal_Muscle | SE_43599 | chr2:42327765-42335085 | MM1S | SE_50137 | chr2:42330972-42335286 | Sigmoid_Colon | SE_53105 | chr2:42331604-42335241 | Small_Intestine | SE_53609 | chr2:42330894-42335238 | Spleen | SE_55583 | chr2:42331692-42334918 | Thymus | SE_62313 | chr2:42323195-42370065 | Tonsil | SE_67366 | chr2:42327765-42335085 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 42332532 | 42332812 | chr2 | 42333001 | 42333603 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I042097 | chr2 | 42324141 | 42336955 |
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Enhancer Sequence | CAAAGTACTC AGCACGCCAA GGCATTATAC TTTGACTTAT CATTTTCTGA GCCCCAGCAA 60 AATTTAAAAC ATAGTGAGTG AGTCTTCTAA ACATGAAGTC ACACCCCATT TCTGATGTAG 120 AAGCTTACAC TTTAGGAACT GCTACGGAAG CACTTTGCAA GCGCCATCTC ACTGAATACT 180 ACTTAGAAGG AACTATTAAC TCCCCGTTTT ACAGATTAAA AATCTGAGTT TAGAGAGACT 240 AATTAACTTG CCCGAGGACA CCCAGCTAAT AGGGGAGAAG TTTGAACCCA CGGATCTGAT 300 TCCAGAGGTC ATGTGTTAAA CCTGTGCTGT ACAATAAACT CTGCCAGTCT CTCTGATCAG 360 AGATGGAAAG GACTCTATTG CAGTCTTCAG CCATCCTTCA CAGTGAGGAA GACCTTCCTG 420 TTACACTCAC CTGCCTTTAG TCGACCTGAG TGATTGCATT CACATTGAAT TCGATGGCTT 480 TCCTGAGGGA CCCAGGCAAC CTATACTGAG GAAGAAACTA TCCATAGGAA CCGGATTCCA 540 AATGAACTAG ATGCAAGTCA CCAAGGCCAG AGTCAGTCCT GGGCCAGCCT TTCCAGTATG 600 ATTTCAGGAC CACAGGGCAG CGCCACTGGC ATTTTTGCCA AAAATCAACC ATAAAAGAAC 660 CATTGTGCTT AACACCAAAC ACATTTAATC CAAAAGTGTG CTTCCATTTA TGCATGTCAC 720 TGCTACCTCA CCTTGGTCCA TGGTCCAAGG TGACTCAAAT ATGTATTTTA TCTGGTACAC 780 CTAGCGTTTT TTTAAAAACG AATTAATTAC CAAAAATTTT AAATTGGAAG ATTATACCGA 840 AATATCTGGA TTTGTAAACA GTTTCCCCAA AACTAAAAAT CTGGCCACAC TGACCTGTAT 900 TCTGCAGTCT ACCACAGGCT CCACCATCCC ATCCTGTCTC TTTCTCTCAC CAACTGCTTG 960 GCCCACCCCT CCTCTCACAC CAAAATGCAA ATATTCCCTA AACAGGTAAC TATTGAATCT 1020 AACTAGTCAC ATCGCAGCAT GGAGATCTTA TTCTGAGAGC TGGTTAAGGG AAATTAATTG 1080 AGGTAAATTA CGGAGAGAAA GCATTGCTCC GCCAGACAGC GTCAGGCCAT GGCCAGAGCA 1140 CAGCAGAAAA GATTTCTACA GTTCTATAAA ACCACAAGAC GAGAAGTTGG TGTTTAAACA 1200 GCTGTTATGA AACTAGGGTG TGTGACAGAA ACATCACCTG TTTCCCAAGA GCTCATCCTC 1260 TCACTTAATT CAGCAAACAC CAAGCTTTTC TTAGCATCCT GGGCCCCCTT CCCTGCAACT 1320 CTTCTTTGGC AGTGCCTTGG GTGATAGTCA GAGGCAAAGT CTGGAGGTGA TTAGATGGCT 1380 GCCGACTTAG GCTATAAGCG AGTCCAAAGG AATGGATCTG GCTTTTGATC AGGACAAAGC 1440 TACGTCCAGA GGAGAAGCTG AGTGAAGAGG AGGCACCAGT GATAAACTTG GGTTTGAGCA 1500 GCCAGGATGG AAGCACGATC TCATTCACCA AGATGGTGAG CAGCTGTGTT CTCTGAAACA 1560 CAGACCACGT GAGCAAAAAT TGTCTTCCCC CAATTTGGAG GCTCCTCCCG CCAAAGCAGT 1620 TTAATGGGCA GGCAGAGAGG AGGCAGAGTG AGGGAAGGTT TTATATGGAA ATGTGGGAAT 1680 GAATGAAAAG GCCTTACTTA AAAGGATCTA TCTGATAGCC CTTGGGACAG CCTCAACCAT 1740 CCCCAAATGC CTCTCTGGGG GGTGGGGAGG CATTCAGCTC TGTGGATATT TGAACTCCGA 1800 CTGTTTTTGA AAGTCGCCCA TGTGACAAAT GTGTCAACAG AGCCCCGGAT GTGCCCTCTG 1860 GGGTGGGGAG GAGGGTGGAT GTGATCAAGT ACATTTCAGG CTTTCAGAGA AACAGGAAAT 1920 TCAGTAATCA GAGAGCAAAA AATCTATTCA ATCTCTTTTA AAGCCAGTGA ATAATGTAGC 1980 AGAGTCAGAA TTGTCACAAC CGCTGGGTGC AGCTTTGGAA AAGATGAAAG ATGAGAGAAT 2040 AGGAGAGGAG GAGGAGAGGC CCCTGCAGCT GGGATCACTC AGAGACACTC TCCTAACCTT 2100 CTCCTTCACC ATCTGGTGGG AAGAAGGAGC CCCTGAAACT TCTCCTCGAC CCCAACACTC 2160 ACCGCCTCGC CACCATCATC TGCCTTGCAT CCAAAGAAGC TCATCTCATC GTGCCTTTGC 2220 CCCTATTGAC ATCGGTCCTA AGAGCTGCTT GGTTCCCAGC TCACCTAATC TCAGCCCACG 2280 AATCCCCAGG AGGCTACGTA TTTTCCCTAT CCCGGGGCTT TCTTCCACCC TCCCCAACTC 2340 CTGAAACTCA TCCTCCATGC CCTCTGGAGT CCACGATCCA TGATTAGCAA AATCTGTTTT 2400 ATCCTCAATC TATTCTCTCA ACATCTGCCT CACTTCTTTC CCTAAGGGGC ACCTGATTGT 2460 CCCCTGAGCT CACTGCTTTT TCCAACACCT TCTCAAGCAG GGGCTATTTT GTTCTCTCAC 2520
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