Tag | Content |
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EnhancerAtlas ID | HS018-21133 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr7:25901550-25902960 |
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) |
NFYA | MA0060.3 | chr7:25901798-25901809 | AGCCAATCAGA | + | 6.32 | NFYB | MA0502.1 | chr7:25901793-25901808 | ACACCAGCCAATCAG | + | 6.75 | ZNF263 | MA0528.1 | chr7:25902227-25902248 | GGAGGAAGGGCACGAGGAAGA | + | 6.14 | ZNF263 | MA0528.1 | chr7:25902224-25902245 | GGAGGAGGAAGGGCACGAGGA | + | 6.1 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00611 | chr7:25900935-25902267 | Adipose_Nuclei | SE_29953 | chr7:25892520-25903534 | Fetal_Muscle | SE_46258 | chr7:25900804-25902075 | Osteoblasts |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I025860 | chr7 | 25899650 | 25902682 |
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Enhancer Sequence | CCAGATCTTT GCATTTTAAA ATTGATGAAA ATAAGACATG ATTTACAAAA AACAAAATAT 60 ATTGAGAGTG AAAATGTGAC AAAAGTGAGC CCCTCGGACC ACACATGCAA CCAATTACTG 120 AGAAAATAAA TAGATGTATA TGGTGTGGCG CTTTTGGAAG AAGAAAAACC GAAGCACGAA 180 ACATAATCAT TGAATTGATC TGGGGGTACT CACTCATTTC ATAAAGCTAA CACTTGCTTG 240 AAAACACCAG CCAATCAGAA GCGTTTCCGG AAGACACTCT ACACCTCTCC GCCTCTTCAT 300 AAATATTTAA ACCGCTTCTT TCTAGATTTG TCATTTAAAT CTACTAGGGA ATGTGCCTCA 360 AGGGCTCATC TTTCACTGGG TCGCTCACAC AGAGGTGGGG CGAGAGGGAG GAGGCGCATT 420 AGCCCTGCGC TCTCATTTGC TTAAACGGCC TTCTTACGTC ATCGTAAGCC TAAGCCAATC 480 CGTGAAGTGC ACTTTGACAA GCTACCCGCC CCTAATTTGT CCTTTCACCG CCAGCCTAAG 540 CCAATAGTGT GGCTGCATGT AAATGAGAAA CCGCGAGCAT CTCCCCCCGC CCCCGGCTCC 600 GCCCAATTTC CCACCTCTTC CCGGAGCGCA CAGACGCCAG CTGAGTGGGA GGGGCCTAGC 660 TGCGGGCGGA GCACGGAGGA GGAAGGGCAC GAGGAAGAGG CGGAGCGGGC CGAGGCGCGC 720 GGAGCTGGGT TTGCTGAGTG CTTCCTTCCT CGGCCCCACC TCCCGCCGGG CAGGATGCCG 780 TTTGATCATT GGCTGGTTTA ATAAAGAGGG CGTGTTTATT TTGCATAAAT AGTGGGCGGG 840 CACCCAGGGC TGCTTTGTAA CTCGAGAACC CGGTGTCCCG CCTGTCTCCC GGGGGGTATG 900 GGCGGGTCTC CCGCCAGCCT CGCCAGACTG AGCCAAGGGC CTGAAGGAAA TAAATGGCTT 960 TCTGAAAAAA TTCGTCTTAA TTCGCCCTTT TGAGAGAATT CTGTTTCTAA ATGCATTTTT 1020 TTCGTTGGTT CTTACAAGTC GTTAAGAGTT GTAACATGAA ATAAGTAGAG ATCACCAATC 1080 TATCCGCCCC CAAATTAATT TTATTTTAAT CTGTGTAAGG GCCACTGCTC CTGGCTGGCC 1140 GTGTGTGAAG CAAAATTTTT GTGCAATAAA AATTATTCCT TCACTAGAAT TCATTTTTTC 1200 CTTTGCTATG AATTCCCTGT CTTCCTAATT TTCCACTAGC AGAGCTAGGG AGAGCCGAGT 1260 TGCACTGAAG CAGAGAAAGG ATGGAAAATT CTTTCGAGCT AAGCATTTAT GAATTGCTTA 1320 TGAATGATGT ATGTGTTAAA ATTGTTTCCA ACAGTAAAAT GCCCCAGGGA TACTCGGTTG 1380 ACAGTTTTTT AATAAGAGAA TTCTTCTTGT 1410
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