Tag | Content |
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EnhancerAtlas ID | HS182-19938 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:65609420-65610420 |
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) |
Klf1 | MA0493.1 | chr7:65609501-65609512 | AGGGTGTGGCT | - | 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH07I066144 | chr7 | 65609462 | 65618599 |
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Enhancer Sequence | TCTCAAAAAG GAATTTACCC ATTTCTAAGA GATGACCACA CAAGATGATT TTGTGTGTTT 60 TAATTTTTTA GTTTTAGAGA TAGGGTGTGG CTCTGTCGCC CAGGCTGGAG TGCAGGCTAA 120 AGCGATCCTC CTGCCTCACC TCCTTGTCCT CTGCCTTCCG TAGCTGGGAC TACAGGTAGC 180 TGGGACTACA GGCGCAACCC ATCATGCCCA GCTAATTTAT TTTAATTTTT TTGTAAGGTT 240 TTTTAATGTC GCCCAGGCTG ATTGGGAATG CCTGGCCTCA AGGGATCCTC CCACCTGGCC 300 TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCACACCT GGCCTAAGGT GATTTTGTTA 360 GTTGGTACTT TCTATAATTT GGATGAAGAA AGCATTATTT TCTTCACATT TTCCAGATAG 420 GAATTACCGT CCTGGGCCGG GCACGGTGGC TCACGCCTAT ATCTTACCAC TTTGGGAGGT 480 CGAGGCAGGT GGATCCCCTG AGGTCGAGGG TTTGAGACCA GCCAGGCCAA CATGATGAAA 540 CCCCATCTCT GCTAAAAAAA TACCAAAAAT TTACTGGGTG GGTGTGGTTG CGAGCATCTG 600 TGATCCCAGT TACTTGGGAG GCTGAGGCAG AAGAATCACT TGAACCCTGG AGGCGGAGGC 660 TACAGTGAGC CAAGATCGTG CCACTGCACA CCAGCCTAGG CAATAAGAGG AAAACTCTGT 720 CTCAAAAAAA AAGGAAAAAA GAAAATGACC CCCCTGTTTT TAAAATGGCA TATGCCCTGC 780 TGCTTTGTTT CCTACAATCA TGCCTCTGAT ACCCATTCGT ACCGTGGGCT GGGAGTCACT 840 CACATACACG CTCCTGTTCC CATTCTCTCG ATTTACAGTT GAAGGAACTG AGGGCCACAC 900 TCCAGTGGTT CTCCCATTTT TTATCTGGCA AATTATTCTC TGTGCAGCTC AGTCAGGACT 960 CAGGACTTAG GGCTATGCGA GTTGTCAACG CTGTACTTTC 1000
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