Tag | Content |
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EnhancerAtlas ID | HS018-01997 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:208003910-208006510 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr1:208004251-208004261 | GGTGCCAAGT | + | 6.02 | NFKB1 | MA0105.4 | chr1:208005402-208005415 | AGGGGATTCCCCA | - | 6.71 | NFKB1 | MA0105.4 | chr1:208005402-208005415 | AGGGGATTCCCCA | + | 6.82 | RARA(var.2) | MA0730.1 | chr1:208005268-208005285 | TGACCTCTGTGTGACCA | - | 6.3 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_01610 | chr1:208003718-208006602 | Aorta | SE_02940 | chr1:208003945-208006074 | Bladder | SE_03907 | chr1:208003545-208007521 | Brain_Anterior_Caudate | SE_06993 | chr1:208003570-208005482 | Brain_Hippocampus_Middle_150 | SE_08580 | chr1:207991706-208006704 | Brain_Inferior_Temporal_Lobe | SE_09440 | chr1:208003916-208007804 | CD14 | SE_10475 | chr1:208004630-208006320 | CD19_Primary | SE_11488 | chr1:207992533-208010277 | CD20 | SE_12401 | chr1:208004637-208006256 | CD3 | SE_13353 | chr1:208004754-208006344 | CD34_Primary_RO01536 | SE_14644 | chr1:208004273-208007930 | CD4_Memory_Primary_7pool | SE_17929 | chr1:208003706-208007813 | CD4p_CD25-_CD45ROp_Memory | SE_18828 | chr1:207994794-208013240 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20606 | chr1:208004352-208006469 | CD56 | SE_24155 | chr1:208004812-208005329 | Colon_Crypt_2 | SE_25829 | chr1:208003915-208006434 | Duodenum_Smooth_Muscle | SE_26666 | chr1:208003798-208005871 | Esophagus | SE_41597 | chr1:208003977-208004826 | LNCaP | SE_42138 | chr1:208003616-208008639 | Lung | SE_48593 | chr1:208003701-208006541 | Right_Atrium | SE_49524 | chr1:208003918-208005343 | Right_Ventricle | SE_50299 | chr1:208003929-208006142 | Sigmoid_Colon | SE_52485 | chr1:208003912-208006536 | Small_Intestine | SE_53314 | chr1:208003646-208008432 | Spleen | SE_54764 | chr1:207991828-208013085 | Stomach_Smooth_Muscle | SE_59011 | chr1:207980241-208007571 | Ly3 | SE_61319 | chr1:207994376-208006461 | HBL1 | SE_62794 | chr1:207980098-208006634 | Tonsil | SE_65312 | chr1:208003968-208004591 | Pancreatic_islets | SE_65312 | chr1:208004839-208005692 | Pancreatic_islets | SE_65312 | chr1:208005804-208008071 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I207830 | chr1 | 208003920 | 208007544 |
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Enhancer Sequence | TCTAAGTATA TATAATCACA AAAAGTATGA GAATGTGCTC GATGTTGGGG TGGGGACAGA 60 AATGGTACTC ATAGAGTAGA AGTCTGATGG CATTCATGGG GAAAAGGCTC CTAAGGAGCA 120 GTGCCATTAA TAGTTGCAGA CCAACAGCAG TGATCATGGT GTGGTCAGAC CTCAGCCATG 180 AAGACCACAC TGTGCCAGTC TCCTGGAGGA ACTACCCCAG AGCCACTGAG GAGCTTTCCC 240 CCAACCCAAG AGACCATGAC ACTTCCACCC ATGTCACTGA GCTGAAGCGA AACAAGGCCC 300 AGCAGTGACA ACGAACACTC CAAGGACACA ATGCAGTGCC AGGTGCCAAG TGAAAATCCG 360 AGAGGCAAGG GCTGGGGACA GCCTGTGCTG GAGGGTAGGT TCTGGCAGAG GTGAAATGCA 420 GACACACACT CAGAATGCCG CCACAGACAG GGAGCCGGAG CCAGGCGGCA GAGAGTGAGT 480 GACCTGGCAG ACGCTGGCCA AGAACACAGG GCTCCCCGAC CCTCAGGGTA AAGGAAGACA 540 AGCAAAGGCC AAGTTGAGTG CTGAATTCAC AGCACAAATG GAAGTGAACC CCAGCACCAA 600 CAGGGACTCC CGTGTGAAAT ACGCCCAAGG GCTGCACAGA GAGGGGCATG TTTGCATGGG 660 GGAAGGTCAG GCCTGCAACA GCAGATATTG TGACTAGGAT GCTCTGTTTG TAAGTAGATG 720 CTTTTTCCTG GACAGACACA GTCAGTCTGT CTCTCAGGCC AGAAATCCAG GCTCCAAAAT 780 GTCCTGCCCA AGCTGGCTCC CATCACCTCT TGGGAAAGTG AAACAGGCCA AAACATCTAT 840 CTTGTCTTAG GCCGCTAATC ATTAAATCTA AGCTCCCACC CCAGAGGGCT CACAACTCAG 900 CCATAAGCAA AACCCAGACT GGCAATAGCA CTGGCACCTG CTATCCTGAC TATGGGCTGG 960 GGCTGAGTGA ATGTGGCCAC TCTGCTAACC ACTGGTCACA GCTCCTGCTG CCTAAAATAC 1020 AGGAGGACAA AGTCTTCTTG GGACTGAGGG AGTAACCCAA TGTGCCTCTT GGCTGGCTGC 1080 TCAAAATCTT GGCCCTGCCA ATGGATGGAA ATAATTTCCA GAGAGACAGA GTGTGGTTGG 1140 GCCATGTGAG AGGGACTTGA GGAGAACATT ACTCCATTCC TCAACAGCGG AACCTGTAGC 1200 CTGTGCCAGG CCAGACATGG CCGGGATTGA GGGGTCTTGG CCAGACTCCC TCCAGGCACA 1260 GGTTGGTGCC CTCAGACGCT GCTGCTGCTC TTGTGGGCAG GAGGAGATGT CTCTAGGGTA 1320 GGAAGAACCT AGGCCTCTGA TGATTTATGG GTCTGTGCTG ACCTCTGTGT GACCACATGG 1380 GTTTAGCACC ATGTGACTTA AAAATGGAGT CGCTTTCCTG CCTCACAACA AACTTCTGCT 1440 CTACTTAACT GAGTCAGATC TAGACAGCAG GAATCATAAA CACAAGTGGG GCAGGGGATT 1500 CCCCAAACAC TTCTGACTTG AACTTTCATT TCCATACTGC CTTATCCCCC AAGCAGGGGC 1560 ACGTCCGTAC CTGCAGCCTA GGACAGAGGA GAAAAGAGAC CAGGGCCATT ATGCATGGCC 1620 TGGGTGCAGG TCCGAGCTTT CAGCAAAGTG CCAGCTTTGC CAGGAGCAGG GACAAAACTT 1680 CCAGGGCCGA GACTCTCATT CAGGGGTGGG AGAGGAGCTG GGGACTGTCT AAAACATAAC 1740 AGTTAATATT TGGGATACGT TTTCATAATG TGAAACCATA CCAAAAGTAA AGTTCCACAA 1800 AACCTTTGAT GATGTGAATA CTTCCTCTGC ACTGGGAGGG GATGTTGACC AGAATCTTTG 1860 GGGGTGGGAG GCAGTCCTGT GGTTGATTTA TTTACTGAAG GTAGGTGTTG GAATTACACT 1920 CTTTTAGAGG GTTCAGCTCT CTGAAACCCC CTGGGACCAC TGGACAGCCA TTATTCTCAG 1980 GCTAGGATTT GACATAGGCC TCCGAGGCCA ATGTTCTTTC TCCAAAAGCA GCACAGCAAC 2040 AACAGCTCTG CCTTAAAAGA CAGAAGATTA CACTTAGAAG ATTTCTCCAA CGCCACATAC 2100 TTTGGAGGTG AGAGGAGTAC CCCATCACTC TCCCTCTGAA AACTTCAAAA CCTTCAGAGG 2160 CCAGGGTGAA TATTTAGAAA GCAGGCGGGT CCAACAGAAA GAACGGCCAT TGATCTATTC 2220 CAAAAAAATA ATGTGTTTGG GGCCCATGTG TCAGGTACAG CGCGAGGCAC TTTTTAAGGA 2280 GCTCCACCCT TGGCTGGCAG GAACTCCCTC GGTCAGCAGA GGCTGGTAAA CTAAGAAAGC 2340 AAGATGCTAG GAGGACAGCT GGCTCCTTAA TCCCACCCTG GCCCCCCAAA CAAGACAGCT 2400 CAAGTCTTGC CGGCCCTGGA GGCCCAGGCA CTTGGACATC ACTTGCTCTA TGCCTTTCTT 2460 GGGAGGCAGA GCTTAGTGGG GGTTGAGGAG AGATCTACAG GCTGAGTGCG CTCATGACAC 2520 AATCAAGAAG TTTCTGGGGC CAGGTGCGGT GGCTCACGCC TGTAATTCCA GCACTTTGGG 2580 AGGCCAAAAG AAGCCAAGGC 2600
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