Tag | Content |
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EnhancerAtlas ID | HS018-00047 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:2427010-2428040 |
Target genes | |
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) |
CREB3 | MA0638.1 | chr1:2427795-2427809 | AGGCCACGTCATCC | + | 6.07 | HSF1 | MA0486.2 | chr1:2427758-2427771 | GAACCTTCCAGAA | - | 6.19 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I002495 | chr1 | 2427256 | 2428289 |
|
Enhancer Sequence | TAGGTGCCCT GCCCCACGGG GAGGCCCCGC ACACTCCTGG GAGCCTGGCC CAACCGGGCC 60 CTTCTCTGCG GTGACCCCAC CAGGACCATC CCTGAGCAGG GCAGGACCTA CCCCCTTCTT 120 GGCCCCTGGA AGCAGTGAAG TGGTAGGGAG TGTGGTGTGC AGGGCAGGCT GGTGGCTGTG 180 GGCAGTGGGG GCAGGGGCGG CTGAGCAGGT GGCTGGAGGG CCCAGGTCCC CACAGCCCTG 240 GATGCTGCCG GGCTGTCGGC TCTCGGTCCT CACCGCCTCC TCTTATGAGG CCCCCAGCCT 300 CATGCCCTCC CCAGGGGGCA ACAAATGCCT GCCATGAAGT GGCTCCCCCT CTTCCCGTCC 360 AGTCAGGCTG AATTCAAGGC CCAGGCCCCC GTGTCGGAGG CCTTCCTCAG CACTGTCTGG 420 GGTCTCTTTG AGGTCTCAAA CCTACAGGCC CAGAAGGAAC TCCCACCCCT CCCGGACCCT 480 GGGCTCCCCC CGTGCCGCCC ACTCCCTCCT ATTGCCGTCT CCCCTCACTT CCATCCCCCA 540 ATGGTTCCTC CGTGCCCCTC GCCTGGGCAC AGCCCCCTCC TGTCTCATCC CGTCCCACGT 600 GCCAGCCGGG CTCTGCCCTT AGCACACATC TGATCCACGT GTGCCGCTGC CACCCGGCCG 660 ACACGGAGGC CCCCTTGGAC CCTGGCCTCC TCTCCACATA GCGATTCTAG GCCAGACCCA 720 GGCCCCGAGC CCAGCTCTCC CCTGCTCAGA ACCTTCCAGA AGCCCCCACA CCTGCCACGC 780 TTGGCAGGCC ACGTCATCCT CCACTGCACA CAGTGCCTAG GGACTTTGCA CCTGCTGGTA 840 GCTCCCAGCC AGCCCACATC CTGCCCAGCA CTCAGGTTTC CGCAGCCCGC GGCCCAGTCT 900 GGCGTCCGTC TCTGATGGTT CGGGGCCTGC TGCGTGAATT AATGAGGCTG CCCGAGCCCT 960 GGAGCCCGTC TCACGGAGCT GGGTGCCAGG CTGGCCCTGG ACGGGAGGGG TTCTGACCCC 1020 CTGCACCTGC 1030
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