Tag | Content |
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EnhancerAtlas ID | HS010-00139 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr1:55723510-55724300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr1:55724272-55724282 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:55724272-55724282 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:55724272-55724282 | ATTTTCCATT | + | 6.02 | ZNF263 | MA0528.1 | chr1:55724132-55724153 | TCTCTTTCTCTTTCCTCCCTC | - | 6.24 |
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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 |
GH01I055257 | chr1 | 55723503 | 55726916 |
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Enhancer Sequence | TAAATGACAG GGATCCTTGG TGATAAAATC TGAGGATGAA TACACAAGAT AGATATGTTT 60 TGATAAGGAC AAGAGGAGCA GGAGGCCTGG GCAGAGAACA GAAGTGAAAG CTGAAGCCAT 120 GACAAGCTTT TGCCAGAATC AGAGAGAGAG GGTCAATTTG TTGAAGTCTG GCTTCTCCTG 180 AAGACAAATC ATTGTCCTCC TGTACTCTTG GTGCTTTGGT TAGATCGCAA CACCTGAACC 240 CACACCAGGA CTTGTAGGGG TGAAAATGTG TTTCAGAAAG CATCTATGCA ACCTAGATGC 300 CAGCTGGGGC TCCCCCTCCC TGGGAAGTCT GGTTAACCTC GACCTGAACC CAAACACCAC 360 AGCCTGTGAC GTCACAAGTC CTCTTTGCAA TTTCTCTCTT GCTCTGATCT CTTCCTCCAC 420 CTCACTGCTT TGTGCTCCCT GCCCCAAGTC AATTCTGAGG CAAAGTTCTG CCCTTCCACC 480 AAGTTCTACA AAACCCACAT GCACCAATTC TTTTGTGAGC TTAGTTTGCT GCTGAAGATG 540 GCTGGGGCAG ATGTTGCAGG TTGGGGGTCC CAGCCACAGA GCTTTCTGCC TTCTCCCAGT 600 TCCATTTCCT CCATTTTTCT GGTCTCTTTC TCTTTCCTCC CTCTGGCCCC AACACAAGTG 660 CCTCCCCTGC CTCACATAGG AGAGACATTC CAACCCAACC ACTTAATGTA TTTTGCCAAC 720 TAAGAGAGTT TACTCATCCT AAGGGGAAGT CTGTTTAAAG TGATTTTCCA TTCACATAAC 780 AGGTGTTATT 790
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