Tag | Content |
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EnhancerAtlas ID | HS073-01297 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr1:211508780-211510210 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr1:211508854-211508867 | AGATAATTAATTA | - | 6.62 | NFIA | MA0670.1 | chr1:211509663-211509673 | ACTTGGCACC | - | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_11018 | chr1:211497674-211531751 | CD20 | SE_18741 | chr1:211499006-211512184 | CD4p_CD25-_Il17-_PMAstim_Th | SE_50866 | chr1:211507885-211511963 | Sigmoid_Colon | SE_58653 | chr1:211499387-211528047 | Ly1 | SE_59878 | chr1:211498570-211518290 | Ly4 | SE_62650 | chr1:211498824-211528354 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I211334 | chr1 | 211507979 | 211511416 |
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Enhancer Sequence | CGTCTGCACC TTGAAAAATA TAAGACACAA TTCCAGCACT GCTTTCTTCG TGCTGGGGAA 60 GACTATTATT GAACAGATAA TTAATTACAT AAACAATTAT TTACATTCCC GGCAAGTGCT 120 GTTAAGGAGA AGTACAGGTG GTTAAAGGGC ATGTCATAAG TGGGGGGGAC CCTAACTTGA 180 TGGAGGAGGC ACACAGAGGC ATGGCTGCAT ATGTGAGGCT TCATCTGGGC TTGTATGTGT 240 TTAGCTCAGC AAGAGGTGGG GAGAGAGGAA AAGATGTTTC CGGAAGAGAC AACAGCTTGA 300 GGAAAGGGAG ACCCAGCCTT AGGGTGAAGG CTGTAAGGGG GAAAGGTTCT CTGTTCATAT 360 GAGGAGTGGC AAAAAGACCA GGAATCCAGG AGAGGTGGAG GACAGGTGGG GAGATTGGCC 420 TAATTCAGAG GTCACCTCTG CCGCCACCCT GGCAGGGAAG GGGCAGAGCA GGGGCCCCAT 480 GCAGGGAGAT TTGCAGGTGT GGTGGCAGGA AGTAGAGGTG GTCTGGTCTG ATGATCTCTG 540 TTTTTTTTTG CTGTGCAGTA AGGAAGTAGA GTTTCCTGGT GAGACTGGAG GGAGTGGTCA 600 AGGTTTGTGG AGGAGAGAAA GGTTTAAAAT CAACATTGAA CAGAGTGAGC TGAGAAGGAA 660 CAGCTGGCTT TGTGCTATGT TATTGTGTTG GCATGATGAA GTCTCTGGAA AAGGACTCTG 720 GCAAATGGGA TTTTAGATCT CTAGCACCTT GTACAATGCC TGGCACCTAA ATGAGGGCCC 780 CATAAATGTT GATTGCATTG AATTATTGGC TGGCTACCTA TATACATTTT TCTCAGCATT 840 TCCCCTTTCT CAGGTGCCTG CTACCCTTGG GCTAAAGCTT CCCACTTGGC ACCTCACCCA 900 GAGGCTAGCT CACATTAGTG TGTCAGAGGG AGCGCTGCTC AGGCTTTACT CTTCCGGTCC 960 TAGTTGGCTA CACTGTCCCC TCACCCCTTA CAGTGACTCC CCAACTCCTA CCCCAGGTCA 1020 GCCATCATGA GCCAGCCTTG CACTCTCCAG CTGGGACTGG TAGAATTTCA GGACTTACAA 1080 ACAGGTGAAA TGAAAAGGTT TAGGCAGTGA GAAGCGTGCT TAGCAGGAGA GAGGCTGCTC 1140 TGCTTGCTGG AGAATAGCTG TTACAGTCAT TCTGTAAGTA TTTACTAAGC ACCTGTCATG 1200 TGCACTGTTT TGTTTGTCTG TTTGTTTTTG TTCTGTTTTG AGACGGAGTC TTGCTCTGTC 1260 ATCCAGGCTG GAGTGCAGTG GTGTGATCTT GGCTCACTGT AACCTCCACC TCCCTGGTTC 1320 AAGTGATTCT TATGCCTCAG CCTCCTGAGT AGCTGAGATT ACAGGCGTAT GCCACCATGC 1380 CCAGCTAATT TTTGTCTTTT TGGTAGAGAC GGGTTTCACC ATGTCGGCCA 1430
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