Tag | Content |
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EnhancerAtlas ID | HS108-29770 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:197121060-197122240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr3:197121579-197121590 | GATGAGTCACC | - | 6.32 | JUND | MA0491.1 | chr3:197121579-197121590 | GATGAGTCACC | - | 6.62 |
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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 |
GH03I197392 | chr3 | 197119359 | 197123101 |
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Enhancer Sequence | TCTACTAAAA ATACAAAAAA TTAGCTGGGC ATGGTGATGG GCACCTGTAA TCCGAGCTAC 60 TCAGGAGGCT GAGGCAACAG AATCGCTTGA ACCTGGGCGG CGGAGCTTGC AGTGAGCTGA 120 GGTTGCGCCA CTGCACTCCA ACCTGGGCCA CAAGAGTGAA ACTCCGTCTC AAAGAAAAAA 180 GGTCTATTTT TAAAAACTAC TAACTGAGAA AGAAGTAAGA GCCTTGAAGA AACAGAAAGA 240 AGGAACCTGA GCATGCCACG GCAGGAGAGG ATGAGAACGG CATGGAGAAG GGGGAGGCGC 300 AAGCAGCTGG AAGCCCACGG CGGAATGGGC CGGTGCTCGG AGAGCTGTTC GGATGGCACG 360 GGAGCTGATT GTCTTGACGT TAAGTTCCTC GGTGAGGAGA GAACAGAAGT TAATGGCACC 420 CACCGGGCCT GGGTGGAGCC TCAGCACCAC CAAAGAAAGC AGATTCTGCA TTTGGAAAGC 480 CTAGGCCCTC TCCTTGAACC TGGTTCTCAA GGTTTCGGTG ATGAGTCACC TCGTTCCCCC 540 TCACCAGCTT CTGTCTTTAG CCACAGCACT GACGTGTCTG AACCCGCACG CACCTCCTGA 600 GCTGGAGCAC CCGTCATCTT CACACCACAG ATGACTAACC ATGGCCTGCT CACAGTCTCC 660 TCATTATCAC GGAATGAAAA TGCTACATGC CTGAAAGCTG AGGTTTTGGG AACAGGATGA 720 GAAGAGCTGC GGAAGGAATG GAGATGCAGG TGGCAATGAG CTAAGCTTTT GACAGGCCCT 780 CGCAGTCCTC GGGAGCAGGG GCCAAGTGAC CACAGATCCA GAGAGAGTGC TCTCCTTGGC 840 AGGGCCGCAT GAAATCTCAT TCATTACAGC CTCCGATTAG GTTCCCAGGC TCATTAAAAT 900 CTGTGTGCCA TTCACTGTTT CTCTTGGATC AGACTGGATT CTACTGTGCA GAGAATTGCC 960 AGGGCTTCCA AGTGTCCAGT GCAGGCCAGA TAGCATCTCT TGGCTTCACT TCTTCCTGAA 1020 GTTTCTCCCT GTGCTTCTGT GTGCTCACTG CCAAGAACAC AAGTCAGCAT TCAGGCCCAC 1080 GGCTGCCAGC TGAAACAAGG GCTTCTGACC CAGACAAAGC CCGCAGATAA AGTCCAAAGC 1140 ACTTGAGCTA AACTTACTCT AAAAACTATG GCAGTACAGG 1180
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