Tag | Content |
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EnhancerAtlas ID | HS080-30033 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr6:1348490-1349440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr6:1348586-1348597 | AGAGATAAGAA | - | 6.32 | Gata1 | MA0035.3 | chr6:1348586-1348597 | AGAGATAAGAA | - | 6.32 | Gata4 | MA0482.1 | chr6:1348585-1348596 | AAGAGATAAGA | - | 6.02 | NEUROD2 | MA0668.1 | chr6:1348753-1348763 | GCCATATGGT | + | 6.02 |
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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 |
GH06I001348 | chr6 | 1349001 | 1349190 |
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Enhancer Sequence | GATGAGCTCC AGGCAACATG ATAAAAACAT CATTGTCCTG AATATAGCAC CATTTGCTTA 60 ATCAAAAGGA AAAGGGTAGG TGAGCTTGGA TGAAAAAGAG ATAAGAAACA GGGGCAAGAA 120 AAGCAACATG CAAGAGTAAT AGCCCAGAAC CCCCAAACAA ATGTGCCAGG CCACACATCT 180 GTCCTGGAGC TTGGGAGACA GTGGGTACCC CTGTGTGTAT CACACTCCCA CACACACCTG 240 CTAAGGATGA AGGTTTAGAG ACAGCCATAT GGTCGGGAAG TGTTACTACT CATATTAACT 300 GTTTAGGGAA TCAGGGGGAA GCAGAGAGAG AGTTCAAGAA GTTGACCAAA GACCACCAGC 360 CAGGTGCAGC AGAAACCTGC TGTGTCCGTG CTAAGACTGC TATAGGGTCC TCTAGGATCT 420 CTCCCTGAAT TTGCAGGTCA TTCAGCACAG GAAGGACACT GAAGTAGCAA CAGCAAGGCA 480 TGAGTCAGAT AGTAGAGGGC TTTGGGCTTC TCCTTATGCC TCCACTCAAG AGTAAAGAGC 540 TCTTCAAAGT CTTGGGTGAC TAAACATTTT AGAGTGGCCA CTTGAGGCTG AATACACAGG 600 ACAATAGAAT GTCTCTTAAG AATCCAAAAG GACTTCCACA ACACAGCAGT GAGCCTGCCT 660 GCAAAGCTCT CCCTGCCCTT TCATCACATC CTGAAGGCTT GTGCTTGGCA GGAAGCAATG 720 GCTGTAGGAG GCCCTGCCAA TTGTTTCAGC CATCACCGCT TTATCATAAG CACAGCTGCA 780 TGTTTTGGCA TCCACTGAAC AACTCTTCTC TCTTGAGTCT AAAAAATAGT CCTAGGAAAC 840 ATGGAGAGCC AGTGCAACAT TTAATTTTTT AAACTATGAA ATAGTTTGGT TCACATGAAA 900 AAGAATACTA ATGTATCTCT GCTGTGACTA TGAAAGTATA TTTATACGGC 950
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