Tag | Content |
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EnhancerAtlas ID | HS105-68027 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr6:16635590-16636870 |
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 | TATAAATGCA TTTGAATCAT CCCAAAACCA TCCCCCGCTC CACCCTAGTC TGTGGAAAAA 60 CTGTCTTCCA TGAAACCAGT CCCTGGTGCC AAAAAGGTTA GGGACCACTG GTCTAGAGAG 120 AAGGAGCTCT TCTTACACAC TGCCCAGAAA CTGAGGATGT GACAGAAGTT CAACGAGAGC 180 TAACTAAACA ACTAAGTAGC AACCTGACAA GGGCTCAGAC AGCTCCAACT AAACCTACAC 240 TGCTGCTGCC GCTTACAAAA GCTCATTCAT ATGTGTGAGT TCAGGCAAAA ACACAGTCGT 300 TATCTGATTC TTTAGGCAGG ACATTGACCA GATAAATAAA TATGTCTGAA TCTGCAGAGA 360 AATAATTTCA AAAGGGCTTC AGAAGGAGAA GGAAAATCCA CTGTAGCCAG AAGCATCCAA 420 AAGCATCCTG AAAACATGAG TGGAGGAAGG CTGAGCAGGT GTGGGCTGGG GAGGCAGGCA 480 ACCCCGCACA GCAGCCAGCA CAAACACAAA GCGACGACGC CCACTGTGCT GGGGAAGCAC 540 AGGCAGCACA GTCCGTGCAA GGGAAACGCG GCTCCCTACA AGGTGTTTTC AAGGTTCCGG 600 TTTCCCCAGA GCACAACCCT AACCTCAGGC AGTGCACAGT TCTCCCAATA AAAGTCACTC 660 GCCCGTGGAG ATCACCGAAC ACCTGAATTG ACACCACGGG CACTTCCAAC CTGTGTTCCT 720 GACCACCCTC CCCATGACCT GCCTCCCTTA CATCATTTCT GTTTTCCTTT CCCATGGTCC 780 TGTGACTTCT CTTACTCTTT CAAATGCAAA ATGTCACAGC TGAAGGGAAG GAACCTCCAA 840 GGATGATCTG GGCTACTGCT TTCTTCTTCA TAGGGGAGGA AACTGAGATT CCAGAGAGGT 900 TGGTAACTTT CCCAAGGTTA CAAAATTAGC AGTGCAGCCG GAACTGAAAC CTACATTGTG 960 TGACCACTCT CCTCCTCCCA AAGCAATTTA GTTTCCAACT GGACCTCATC TGCCTACTTG 1020 TTTCTCCCCC AGCCCCCAGG CAGCCCTTCA CTGTGGCTGC TGAGTCATCA GGATGAGCTT 1080 TGTTCTCAAG CAAGCCACTG GGACAGGCCC TCATGTCTTG AGTAGGACAA AGTATATTTG 1140 GCCACTCCCC ACTTTGTGGT CACCCTGCTC TGCCTGATGC ATGGGCACCT TCTGCCCATG 1200 ACAACTGTCA TTCGCCCTGA ATAGTCTATG CCATCACACC TCCTTATGGC TACTAACATA 1260 AAAGGTAAGT GACTAATAAA 1280
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