Tag | Content |
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EnhancerAtlas ID | HS138-44856 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chrX:71343140-71344410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX5 | MA0510.2 | chrX:71343850-71343866 | TGTTACCAGGGCAACC | + | 6.17 | RFX5 | MA0510.2 | chrX:71343850-71343866 | TGTTACCAGGGCAACC | - | 6.44 | RREB1 | MA0073.1 | chrX:71343666-71343686 | AAACACACCACCCCCACCCC | + | 6.59 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09541 | chrX:71339133-71348160 | CD14 |
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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 |
GH0XI072120 | chrX | 71340401 | 71347550 |
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Enhancer Sequence | GATGAGATGG CATAGATAAT TAATGAGCAG ATAGGGAAGA AAATGCCAAA AGCAGGTCTA 60 CAAGTCTTCC CACGAGGAAG GAGAGCCATT GAGGGGTTTT GTAGAGGAGC AGCAAGGCCA 120 GGTGTGTGAA TTCAAAGGCC CACGGCCCCC ACCCCCAGGC ATGTTGAAGG TGGACCTATT 180 AGAACAGGTA GAGACTAGAG CCTGCTTCAG TAGCTCAGGT GAGAGAGGAG GAAGGGCTGA 240 ACTGTGGGTG GAGAGGTCAT CAATTTGGGG ACACTCTTTC TGGCAAGCCT CACAGCCAAC 300 AGGCCTCATC TGTATGATGC AAGAGGTGAA GGAGACCACA GTCGCTGGAG GCACCCGCCC 360 TTCTCTAGCT TGGTCATGTG AGGAGATCCT ACAAGGCAAG GCTTCCCCAG GCCGTGGGAC 420 CTTCGCCATG AGTTCACCTG CTGACATCTT CCCTTTTAGC CTCTTTCTCA CCCGAACAGC 480 CCACTGCAAG AGCAGAATAA AAAGCCTGGG CCCTACTTTC CCACACAAAC ACACCACCCC 540 CACCCCCCAT CAGGAGAGTT GCTGAGGCGA GGGGCCCCGC TCTACCCCAT GTGTGGCAGG 600 CAGGAAGGGG AGAGGGGACA CAGGGAGCAG GTCAGGGCCT GCTCTCTGTC AAAGGAAATA 660 TCCACCCTCC TAAGCCTTTA AGAAACTGTT TTCTTCCAAG TAGGTCCCGC TGTTACCAGG 720 GCAACCGAGA GCCCTGGTAT TTGTGTTTCT GTCTTTGGAG TCCCTGGGGA GAAGTGGCCT 780 GCCGAGCTTT CCCTAGTCTG GGCAGGATAC AGGAAGTGCT GGCCGGAGGT GGAGCCCACT 840 CCCCACCTCC CATTAAGGGG GTGGTCTCTT GCCTGATTAA TGCCTGTCCT TATCCCCTGG 900 AAGAGTCCAC CCCCACCCTC AGGAGCCACT TCTGGCGGTC AAGGGCACAG GCTTTGGCTC 960 CTATGGACCT GGTTTCTCGG GGGCAGAATT CTGCACCTAC CTTGTGGCAC ATCTCTCTCA 1020 AATGGGTGTC ACCTGCTGTC TGAGGCAGGT ATCCAGGAGG GGCAAGCTCA CATCAGACCA 1080 TGGTACCTGC TGAGGGATCG TCACGCATGC TATGTTTCTT GATCACTTAC TTTGTGCTAG 1140 AACTGGATCT GTGGGTCGGT TCTTGCTCCA GGGAGCTCTA GGGGAAGGCT CAGAACCAAA 1200 CTGGCCATTA AATGTCACAC GGGCTAGTTA GTTCCCAAAG CTCTATGCTG CTCTAGGCTG 1260 GGCTGTGTTG 1270
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