Tag | Content |
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EnhancerAtlas ID | HS127-26598 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr6:29960000-29961510 |
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) |
NFAT5 | MA0606.1 | chr6:29960349-29960359 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr6:29960349-29960359 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr6:29960349-29960359 | AATGGAAAAT | - | 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 |
GH06I029993 | chr6 | 29960781 | 29960850 |
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Enhancer Sequence | TATCCACTAC CAAGGATGAT CCACGCTGTT ATGAGACGAA TTGTGTCCCT CCCCAACCGA 60 AATTCATATG TTGGAGTCCT ATGTTGAGAA GACAGAAGTG GCCATCTACA AGCCAAGGAG 120 AGAGGCCTCA GGAAAAAGCA ACCCTGCAGC ACCTTGACCT GCACCTGTAG CCTCCAGAAC 180 TGTGAGACAA TACATATTTA TTATTTTACT CACCCAGCAT GTGGTACTTT GTTATGGTAG 240 CCCTAGCAAA TTAAAACAGA AATATTACCT TTTCTACTCT GTCCTATGTA TGAACATGAG 300 ACTTTTTAAG AATATGAATT ACCTGGGATT CCAAAACATA GAGTGAGTCA ATGGAAAATA 360 GATGATACAG GGTCATTTCC AAGCCTTTGT GGGTCTCCTG GCCACCACAC AAACATGGAT 420 GTGTTCCCAT TTCTTTTCAG TTTCACACAG TGCAAAAGTT GTGGACATAG AATCACAAAC 480 TGTGTTTAAT TTATTTGAGA CATTGAGTGA GCTAGTTTTG CCCTAATTTT ATAGAAAGAT 540 GATGAACAAT CATAATTACT AAACCAAAGA GGCTTTTTGG CAGGGGATGG CAGGTACTAT 600 GTTTTCTCCT CCTTTTAAAG TGCATTTTCC TAAAGAGTCT TGTCTAGGAG TAAATGTCAT 660 CACTTTGCTT TTTTCCTCCG CATTGATCAC TTGGTCCTCC CTGCATTTCA GTAAGGTTGC 720 TAGAATGGAG GCATTTGTCC ATGATTCACA GATGAATCAG AGGCCCTATG AGTAGAGAGC 780 TTCTCCTGAA GTCACACAGC TCGTGAGTGG TGGAGCAATG ACAGGCACAT GACTCTCCAG 840 GTCCCTAGTC CAGTTTTCTG GGTGCCATGA GAATTACAGC CTTTGGTTCC TTTTACATGT 900 AGTTCATTTC TGAACCTGAG AAGGAGAATG CACCTCAGGT GACTAACAGT TTTTGCTCTT 960 CTGTACTTGT CTGAGAATGA CCCCAAAAGA TTTTTAAAGG CCAATTCTTT GGCTACCAAC 1020 CCTATTTTGC CCAGGCATGG ACATGGAGCA GGTGAACACT GCCTTTACCT GTGACATGCC 1080 TGAAGATTCT GAGACCTACG TGAATCAGGT AAGCTCCATA CACAGAGGGA CACCCACTCT 1140 CCCACCCACT TATTTTCTGT ATCTTTTCAC ACTTCACTTC TTCATTCCTC CCTCTGGCTG 1200 TCTTCCCTCT TTGGGGTCTT CTAGTCCTAA CCTCTGTCTC CTTCCAGGTG ACTAGAGCAG 1260 GCTGGTTTGG AACAGGGCTT GTGTCGGATG AGAATTGTGC CAGGATCCTC AGTGATGGGC 1320 AGCATCACTT TAAGTTCAGT GTTAGGAGCT ACCTGCTGAG ACAGACGTCT CCTCCACAGT 1380 GAGTGCTGAT TTCATGAAAC CCTTAGTTCC TCCCTATTCC TTACTGTGTC TTCAATCCCA 1440 TCATGTAGGT CATGGGCACT TAACGCATAA TGAACAATTG ACTGCTTCAT GCCCCCTGGC 1500 CGTTGATGCT 1510
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