Tag | Content |
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EnhancerAtlas ID | HS149-00674 |
Organism | Homo sapiens |
Tissue/cell | NKC |
Coordinate | chr2:42331680-42334080 |
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 | TCCCCGTTTT ACAGATTAAA AATCTGAGTT TAGAGAGACT AATTAACTTG CCCGAGGACA 60 CCCAGCTAAT AGGGGAGAAG TTTGAACCCA CGGATCTGAT TCCAGAGGTC ATGTGTTAAA 120 CCTGTGCTGT ACAATAAACT CTGCCAGTCT CTCTGATCAG AGATGGAAAG GACTCTATTG 180 CAGTCTTCAG CCATCCTTCA CAGTGAGGAA GACCTTCCTG TTACACTCAC CTGCCTTTAG 240 TCGACCTGAG TGATTGCATT CACATTGAAT TCGATGGCTT TCCTGAGGGA CCCAGGCAAC 300 CTATACTGAG GAAGAAACTA TCCATAGGAA CCGGATTCCA AATGAACTAG ATGCAAGTCA 360 CCAAGGCCAG AGTCAGTCCT GGGCCAGCCT TTCCAGTATG ATTTCAGGAC CACAGGGCAG 420 CGCCACTGGC ATTTTTGCCA AAAATCAACC ATAAAAGAAC CATTGTGCTT AACACCAAAC 480 ACATTTAATC CAAAAGTGTG CTTCCATTTA TGCATGTCAC TGCTACCTCA CCTTGGTCCA 540 TGGTCCAAGG TGACTCAAAT ATGTATTTTA TCTGGTACAC CTAGCGTTTT TTTAAAAACG 600 AATTAATTAC CAAAAATTTT AAATTGGAAG ATTATACCGA AATATCTGGA TTTGTAAACA 660 GTTTCCCCAA AACTAAAAAT CTGGCCACAC TGACCTGTAT TCTGCAGTCT ACCACAGGCT 720 CCACCATCCC ATCCTGTCTC TTTCTCTCAC CAACTGCTTG GCCCACCCCT CCTCTCACAC 780 CAAAATGCAA ATATTCCCTA AACAGGTAAC TATTGAATCT AACTAGTCAC ATCGCAGCAT 840 GGAGATCTTA TTCTGAGAGC TGGTTAAGGG AAATTAATTG AGGTAAATTA CGGAGAGAAA 900 GCATTGCTCC GCCAGACAGC GTCAGGCCAT GGCCAGAGCA CAGCAGAAAA GATTTCTACA 960 GTTCTATAAA ACCACAAGAC GAGAAGTTGG TGTTTAAACA GCTGTTATGA AACTAGGGTG 1020 TGTGACAGAA ACATCACCTG TTTCCCAAGA GCTCATCCTC TCACTTAATT CAGCAAACAC 1080 CAAGCTTTTC TTAGCATCCT GGGCCCCCTT CCCTGCAACT CTTCTTTGGC AGTGCCTTGG 1140 GTGATAGTCA GAGGCAAAGT CTGGAGGTGA TTAGATGGCT GCCGACTTAG GCTATAAGCG 1200 AGTCCAAAGG AATGGATCTG GCTTTTGATC AGGACAAAGC TACGTCCAGA GGAGAAGCTG 1260 AGTGAAGAGG AGGCACCAGT GATAAACTTG GGTTTGAGCA GCCAGGATGG AAGCACGATC 1320 TCATTCACCA AGATGGTGAG CAGCTGTGTT CTCTGAAACA CAGACCACGT GAGCAAAAAT 1380 TGTCTTCCCC CAATTTGGAG GCTCCTCCCG CCAAAGCAGT TTAATGGGCA GGCAGAGAGG 1440 AGGCAGAGTG AGGGAAGGTT TTATATGGAA ATGTGGGAAT GAATGAAAAG GCCTTACTTA 1500 AAAGGATCTA TCTGATAGCC CTTGGGACAG CCTCAACCAT CCCCAAATGC CTCTCTGGGG 1560 GGTGGGGAGG CATTCAGCTC TGTGGATATT TGAACTCCGA CTGTTTTTGA AAGTCGCCCA 1620 TGTGACAAAT GTGTCAACAG AGCCCCGGAT GTGCCCTCTG GGGTGGGGAG GAGGGTGGAT 1680 GTGATCAAGT ACATTTCAGG CTTTCAGAGA AACAGGAAAT TCAGTAATCA GAGAGCAAAA 1740 AATCTATTCA ATCTCTTTTA AAGCCAGTGA ATAATGTAGC AGAGTCAGAA TTGTCACAAC 1800 CGCTGGGTGC AGCTTTGGAA AAGATGAAAG ATGAGAGAAT AGGAGAGGAG GAGGAGAGGC 1860 CCCTGCAGCT GGGATCACTC AGAGACACTC TCCTAACCTT CTCCTTCACC ATCTGGTGGG 1920 AAGAAGGAGC CCCTGAAACT TCTCCTCGAC CCCAACACTC ACCGCCTCGC CACCATCATC 1980 TGCCTTGCAT CCAAAGAAGC TCATCTCATC GTGCCTTTGC CCCTATTGAC ATCGGTCCTA 2040 AGAGCTGCTT GGTTCCCAGC TCACCTAATC TCAGCCCACG AATCCCCAGG AGGCTACGTA 2100 TTTTCCCTAT CCCGGGGCTT TCTTCCACCC TCCCCAACTC CTGAAACTCA TCCTCCATGC 2160 CCTCTGGAGT CCACGATCCA TGATTAGCAA AATCTGTTTT ATCCTCAATC TATTCTCTCA 2220 ACATCTGCCT CACTTCTTTC CCTAAGGGGC ACCTGATTGT CCCCTGAGCT CACTGCTTTT 2280 TCCAACACCT TCTCAAGCAG GGGCTATTTT GTTCTCTCAC AGGCTTCTCA CTGAGAGGTG 2340 ACATAGGTGT CCTTCTTACT CCTCATGGTC ACTTTCAGAA ATATCTCCCT CCTCCTCTGC 2400
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