Tag | Content |
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EnhancerAtlas ID | HS010-02536 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr2:135018670-135019670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:135019079-135019097 | CCTTCCTCTCTTCCTTCT | - | 6.68 | Foxq1 | MA0040.1 | chr2:135019557-135019568 | CATTGTTTATT | + | 6.02 | ZNF263 | MA0528.1 | chr2:135019078-135019099 | CCCTTCCTCTCTTCCTTCTTT | - | 6.01 | ZNF263 | MA0528.1 | chr2:135019075-135019096 | CACCCCTTCCTCTCTTCCTTC | - | 6.08 | ZNF263 | MA0528.1 | chr2:135019067-135019088 | CTCTCCCCCACCCCTTCCTCT | - | 6.45 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_10191 | chr2:135013062-135021743 | CD19_Primary | SE_10845 | chr2:134996522-135089684 | CD20 | SE_18527 | chr2:135018107-135020035 | CD4p_CD25-_Il17-_PMAstim_Th | SE_32531 | chr2:135015418-135021216 | GM12878 | SE_58311 | chr2:134974519-135073637 | Ly1 | SE_59645 | chr2:134963734-135083692 | Ly4 | SE_62223 | chr2:134937777-135083863 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I134256 | chr2 | 135014476 | 135021287 |
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Enhancer Sequence | AGAATAAGGG GCTCATTCTT CTACCCCTCA GTCATTAAGA CCCTTTCTTT CATGCAGCAC 60 CACTACTTCA AGTCTGGATT GAGGAGGGAT TGCACGCACA TGTGTGAGGT TGGAGTCTCA 120 ATCTCAATGT GATTGTCATT GCCATGTTCA AACGATGAGG CTTAGAATGT CCCTTGTCTT 180 ACCTGATGGT CATAGCTCTC TATGACCCTC TGCTTCTTCC CAGCTGTGTC CTGGTGCTCT 240 TTTGCTGTCA GAAGTGCTTG AGCAGACCTC TTGCTGCTGT GGACACCCTA AAAAGCTCCG 300 CACCCCCTCA AGTCTACTAA GGCATGGTGG CTCTCTTCTA GGACAAGACT GTTGGGTGGT 360 GGCTGAGCAT TCGCCTGTCT TTGAGCGTCT GCATTTGCTC TCCCCCACCC CTTCCTCTCT 420 TCCTTCTTTG TTTGTAAATA AAGTTGGTTA GAACACAGCC ATGCGCATTC CATTCTGTTT 480 CAGAGAAGTT AGCCTTCCCT CCTTCACAGG AGGGCCCAAA CCCACTGTTA CTCTCATTCT 540 TTATAACACT CAAGCTACTT AGCATCAAGT ATTTGTTGTA TGAGCTGATC ATGTGTCTCT 600 CCCACTTACA ATGTAAGTTC TGAAAGAGGA GGGACTTTGG TCTGTTTTGT TCCCCACTGT 660 GCCCCAGAGC TTAGTACCTT TTGCCTGGCA CATAGTAAGA GCCATGAATG AATAGCAGCA 720 GCCCCTGGTG AAACTCTGTG ATGCTCTGTG TGGTACAGTT ACAGCTGGGA CTCATTTGAA 780 AATCACAGTA ATGTTTTTAG TGAAGCAGGA AATGAGAAGA AATTCCCTAT GGGCTCTGCA 840 TCTAAGAGGC TCCAAGTAGC TCTTATGCAT GATCCTAACA TGGGAACCAT TGTTTATTCT 900 GGAAGGTAGT TAGTGTTTCT GTTGGGCGGA TGGAACACAT TGTGTTCCTT ACTGATGTGT 960 GACCTTGAAC AAGTCACCGA TCATCTTAAA GCTTACTTCC 1000
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