Tag | Content |
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EnhancerAtlas ID | HS098-41999 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr4:40183660-40184860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr4:40184515-40184530 | TGAACTTCTGACCTC | - | 6.38 | RARA | MA0729.1 | chr4:40184512-40184530 | TCTTGAACTTCTGACCTC | - | 6.88 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_10329 | chr4:40183428-40184364 | CD19_Primary | SE_10959 | chr4:40182771-40190307 | CD20 | SE_32473 | chr4:40181985-40184311 | GM12878 | SE_58296 | chr4:40151405-40268478 | Ly1 | SE_58875 | chr4:40171449-40215497 | Ly3 | SE_59742 | chr4:40174017-40209426 | Ly4 | SE_60449 | chr4:40179676-40229305 | DHL6 | SE_61039 | chr4:40177894-40211343 | HBL1 | SE_61530 | chr4:40179190-40208524 | Toledo | SE_62215 | chr4:40173915-40268314 | Tonsil |
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| Number: 2 | ID | Chromosome | Start | End |
GH04I040178 | chr4 | 40179658 | 40184163 | GH04I040182 | chr4 | 40184510 | 40189251 |
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Enhancer Sequence | ACTTAGCCAC ATGACTACAT TCAGCTGAAA AGAAGATTGG GAAAAATAAC CTTTATTATT 60 GGCTACAGTG CTCAGTTGAA AATTATGTTC TGTTGCTAAG GAAACGGATT TTGGGGGATA 120 GTCAGCAGTC TCTAACACAA CTAACAGTGT TTTACCTTGC ATACAGTAAA GGCTTTTCAG 180 GCTGATACAA GAACATGCGC AGAGACAGGA AAAGGTGTTC ATGTGCTTCG AACAGGACAT 240 GGGTGAAAGA TCAGGCTAGA AAGAGAGGCA GATGCCACGT TAGGAAAGGC TTTGAGGGTC 300 AGGCTGAGAA GTTTCCTTTT GTCCTGTAGG CAGTAGGGAG CCAAATAGAT CCTTGTATTT 360 GGTATAAATC CTTCCAGGGA TGTAAGCTAA TTGCTTGTCT GAGTTCATTT TATTTATTTA 420 TTTATTTTGA GACAGGGTCT CACTTTGTCA CCCAGGCTGG AGTGCAGTGG CGGGAACACA 480 GCTCACTGCA GTCTCCACCT CCCAGGCTCA AGCGATCCTC CCACCTCAGT GCCCAAGAAG 540 CTGAGACTAC AGGTGCACGC CACCATGCCG GGCTAAAATT TTTTTTTTGT AGAGACGAGG 600 TTTCGCCATG TTGCCCAGGC TGGTCCATTT AATATATATA TACATATGTA TAGAGAGACA 660 GAGTCTTGTT CTGTTGCCCA GACTGGAGTG CAGTGGCTGG ATCTCAGCTC AATGGAACCT 720 CTGCCTCCCA GGTTCAAGCG ATTCTCCTGT CTCAGCCTCC CAAGTAGCTG GGATTACAGG 780 CACCTGTCAC CACGCCCAGC TAATGTTTGC ATTTTTAGTA GAGACGGGGT TTCACCATGT 840 TGGCCAGGCT GGTCTTGAAC TTCTGACCTC AGGTGATCTG CCCACCTCAG CCTCCCAATG 900 TGCTGGGATT ACAGACATGA GCCACCATGC GTGGCCCCAT TTAATATTTT TTAATATAAA 960 AATTGTGTAA GTTCCAACAT TTAGAAAATA GAGGAATGTA TAAAACCAAC CATGTTACCC 1020 TAAGACAATT CCTGTTAGTG GTTTGGCTTT GCTTCCTCAT AGTCTTTGGA AACACTGTTG 1080 TAGTCATAAT GCACAGATAC AATCCCAAGT CCTGTTTCTC TTTTTGCACG TAACCTTGTA 1140 TCATGAGCAT CTCCTTATGT GGTCACATGA TCTTCCCAAA TACTATTTTC AAATGACCGT 1200
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