Tag | Content |
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EnhancerAtlas ID | HS031-19672 |
Organism | Homo sapiens |
Tissue/cell | Denditric_cell |
Coordinate | chr6:16635610-16636980 |
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) |
MAFF | MA0495.3 | chr6:16636646-16636661 | CTGCTGAGTCATCAG | + | 6.16 | MAFF | MA0495.3 | chr6:16636646-16636661 | CTGCTGAGTCATCAG | - | 6.1 | NFE2L1 | MA0089.2 | chr6:16636645-16636660 | GCTGCTGAGTCATCA | - | 6.42 | Nfe2l2 | MA0150.2 | chr6:16636647-16636662 | TGCTGAGTCATCAGG | - | 6.36 |
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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 |
GH06I016635 | chr6 | 16635702 | 16637201 |
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Enhancer Sequence | CCCAAAACCA TCCCCCGCTC CACCCTAGTC TGTGGAAAAA CTGTCTTCCA TGAAACCAGT 60 CCCTGGTGCC AAAAAGGTTA GGGACCACTG GTCTAGAGAG AAGGAGCTCT TCTTACACAC 120 TGCCCAGAAA CTGAGGATGT GACAGAAGTT CAACGAGAGC TAACTAAACA ACTAAGTAGC 180 AACCTGACAA GGGCTCAGAC AGCTCCAACT AAACCTACAC TGCTGCTGCC GCTTACAAAA 240 GCTCATTCAT ATGTGTGAGT TCAGGCAAAA ACACAGTCGT TATCTGATTC TTTAGGCAGG 300 ACATTGACCA GATAAATAAA TATGTCTGAA TCTGCAGAGA AATAATTTCA AAAGGGCTTC 360 AGAAGGAGAA GGAAAATCCA CTGTAGCCAG AAGCATCCAA AAGCATCCTG AAAACATGAG 420 TGGAGGAAGG CTGAGCAGGT GTGGGCTGGG GAGGCAGGCA ACCCCGCACA GCAGCCAGCA 480 CAAACACAAA GCGACGACGC CCACTGTGCT GGGGAAGCAC AGGCAGCACA GTCCGTGCAA 540 GGGAAACGCG GCTCCCTACA AGGTGTTTTC AAGGTTCCGG TTTCCCCAGA GCACAACCCT 600 AACCTCAGGC AGTGCACAGT TCTCCCAATA AAAGTCACTC GCCCGTGGAG ATCACCGAAC 660 ACCTGAATTG ACACCACGGG CACTTCCAAC CTGTGTTCCT GACCACCCTC CCCATGACCT 720 GCCTCCCTTA CATCATTTCT GTTTTCCTTT CCCATGGTCC TGTGACTTCT CTTACTCTTT 780 CAAATGCAAA ATGTCACAGC TGAAGGGAAG GAACCTCCAA GGATGATCTG GGCTACTGCT 840 TTCTTCTTCA TAGGGGAGGA AACTGAGATT CCAGAGAGGT TGGTAACTTT CCCAAGGTTA 900 CAAAATTAGC AGTGCAGCCG GAACTGAAAC CTACATTGTG TGACCACTCT CCTCCTCCCA 960 AAGCAATTTA GTTTCCAACT GGACCTCATC TGCCTACTTG TTTCTCCCCC AGCCCCCAGG 1020 CAGCCCTTCA CTGTGGCTGC TGAGTCATCA GGATGAGCTT TGTTCTCAAG CAAGCCACTG 1080 GGACAGGCCC TCATGTCTTG AGTAGGACAA AGTATATTTG GCCACTCCCC ACTTTGTGGT 1140 CACCCTGCTC TGCCTGATGC ATGGGCACCT TCTGCCCATG ACAACTGTCA TTCGCCCTGA 1200 ATAGTCTATG CCATCACACC TCCTTATGGC TACTAACATA AAAGGTAAGT GACTAATAAA 1260 TGGTATCATG AATTAATATG AAACCTTTTA TACAGACAAA TATTTGATTC CTCAGTTATA 1320 TTTTCTTGGG ATCTTTTCTT CCCAGGTCAT AGCAGTGCTG TTTCAACAGG 1370
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