Tag | Content |
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EnhancerAtlas ID | HS018-13682 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr2:233367150-233368640 |
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) |
CREB1 | MA0018.3 | chr2:233367868-233367880 | CGTGACGTCACC | + | 6.32 | CREB1 | MA0018.3 | chr2:233367868-233367880 | CGTGACGTCACC | - | 6.32 | ZNF263 | MA0528.1 | chr2:233367188-233367209 | CCCTTCCCCCTATCCTGCCCC | - | 6.04 | ZNF263 | MA0528.1 | chr2:233367630-233367651 | GGAGGAGAGGGGGGCGGGGAG | + | 7.08 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I232500 | chr2 | 233365404 | 233368709 |
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Enhancer Sequence | TTTTTTCCTT TCCCTTGCTG GTGTCCTTGA CAAGGCTTCC CTTCCCCCTA TCCTGCCCCT 60 TCCCCAACCC CAGCTGTAAT GCTCCTCAGG GGCCCAGAAA CCTGGCTGGG GAGGGGCTGA 120 GGCTATGGGC TCGGCTTCTC TAAGGCTGAG AGGGTCCCCC TGGGGCCTGC AGCACCCCCA 180 GCCAGACCCA GGACTGTGTG TGCGCACGCG TGTGTGCAGG TGTTGCTTGG AGACTCCTGT 240 GCCCTTGCGT GCATGTATGT GTCCCTGGGC ACCACGGCGT GCATATCTGA AGTATGCTCC 300 TGCTGACACA CACCTGCGTG CGCACAGGCC CCCGTGTGCA CACGTGTGTG CATGCTTGGG 360 TGTCAATGTT CACGCGTGTG TGCGTGCGTC CTCACCGTGC ATGCGCCCAC AGAAAATACC 420 ACCGAAGTAA GAGACGGAAG AGACGGGAGG TTGGGGGGAG TGGAGCGGGG TGGTGTTGGG 480 GGAGGAGAGG GGGGCGGGGA GGCAAGATCA GACGACAAAG AAAGGGAAGG CAGAGGCGGG 540 GGCGGGAGGG AGGTTTATCC GTAGGAGTCA GCCCAGTTGG GTCAAACTAA GGACCCAGTG 600 CAGACCCCGA GGCCCAGAGA CACAGGTGTG CGCACAAACA CGCACTCTGC GGAAGGCCGG 660 GGCGGGCCTG GCCGCTGCGG GACTCCTGGC CCGGCGCCCT TGACGTCAGC GGCTGGGCCG 720 TGACGTCACC TCACCGCCCC CGCCGCGCTC CCGCCCCCGC CCGCGGGCAC TCAGTCTCCG 780 CTAATGGCAG GCGACGGGGA ATGGCACATC TGTCTTGCCG GGAATTAGTT CATTGAATCA 840 GGCGGCCCGA GCTGCGGCAG CGACCTTAGC CCTGGCCCCA GGGAGGGGTC TGGGCGGGCG 900 GCGTGGGGGA GGTTCAGGCT GGAGGGCTGA GTGCGGGGAC GGGAGGAGGG GACTCACCTG 960 GACTCGCGAG GGGGACTGAG CGCTCTCCAA ATATAGGTCA ATGTCCCGCT CAGCCTCCCT 1020 CCCCCAGCAC CGTGAGGACC GAGGCCTGGG GCCTGGCGCC CGCCTGGTGG ACCTCGGGGG 1080 CAGGCTGGGG ACCGGGCCCC TGCGGGACGC GGCGCGGCAG GACGCTCCCC GCGCCTTTCT 1140 TTCTGCACCT GCCCCTCGGG GTGGGTCCCC CTCTTTACCC TCGCTTCCCC CCGCGGGTGC 1200 CGATAAAGGC GGCTAATTCC CGAGCCCGGG GAGGGAGGGG GCGACTGTTC CAGTCAACAC 1260 TTCCCCGCGC TCTTCCCCGA CCCTCCCAGA GCGTTCCCGC TGCTCAGGGC GAGGAGCAGC 1320 TGCGGCCAGT TTGTCCTAGC GGTTTAGGAG GCAGGGAGGT TTCCTCCAGC CTGGAGCTCT 1380 GGCTCGGGCC CTCGGGCCCC AACACCTTCC CGCTGAGACC GCGGGCGTTG TCCCTGGGTC 1440 TCTCTGCCTC CATTTCCCCC ACCTCCATTC TGGTTACCCC TTCCCCCCAC 1490
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