Tag | Content |
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EnhancerAtlas ID | HS098-47825 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:16635510-16637200 |
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 | CTGATTCTAC ATTATGGTGA GTTGCATAAT TATTTCATTA TATATTACAA CATAATAATA 60 TAAATAAAGT GCACAATGAA TATAAATGCA TTTGAATCAT CCCAAAACCA TCCCCCGCTC 120 CACCCTAGTC TGTGGAAAAA CTGTCTTCCA TGAAACCAGT CCCTGGTGCC AAAAAGGTTA 180 GGGACCACTG GTCTAGAGAG AAGGAGCTCT TCTTACACAC TGCCCAGAAA CTGAGGATGT 240 GACAGAAGTT CAACGAGAGC TAACTAAACA ACTAAGTAGC AACCTGACAA GGGCTCAGAC 300 AGCTCCAACT AAACCTACAC TGCTGCTGCC GCTTACAAAA GCTCATTCAT ATGTGTGAGT 360 TCAGGCAAAA ACACAGTCGT TATCTGATTC TTTAGGCAGG ACATTGACCA GATAAATAAA 420 TATGTCTGAA TCTGCAGAGA AATAATTTCA AAAGGGCTTC AGAAGGAGAA GGAAAATCCA 480 CTGTAGCCAG AAGCATCCAA AAGCATCCTG AAAACATGAG TGGAGGAAGG CTGAGCAGGT 540 GTGGGCTGGG GAGGCAGGCA ACCCCGCACA GCAGCCAGCA CAAACACAAA GCGACGACGC 600 CCACTGTGCT GGGGAAGCAC AGGCAGCACA GTCCGTGCAA GGGAAACGCG GCTCCCTACA 660 AGGTGTTTTC AAGGTTCCGG TTTCCCCAGA GCACAACCCT AACCTCAGGC AGTGCACAGT 720 TCTCCCAATA AAAGTCACTC GCCCGTGGAG ATCACCGAAC ACCTGAATTG ACACCACGGG 780 CACTTCCAAC CTGTGTTCCT GACCACCCTC CCCATGACCT GCCTCCCTTA CATCATTTCT 840 GTTTTCCTTT CCCATGGTCC TGTGACTTCT CTTACTCTTT CAAATGCAAA ATGTCACAGC 900 TGAAGGGAAG GAACCTCCAA GGATGATCTG GGCTACTGCT TTCTTCTTCA TAGGGGAGGA 960 AACTGAGATT CCAGAGAGGT TGGTAACTTT CCCAAGGTTA CAAAATTAGC AGTGCAGCCG 1020 GAACTGAAAC CTACATTGTG TGACCACTCT CCTCCTCCCA AAGCAATTTA GTTTCCAACT 1080 GGACCTCATC TGCCTACTTG TTTCTCCCCC AGCCCCCAGG CAGCCCTTCA CTGTGGCTGC 1140 TGAGTCATCA GGATGAGCTT TGTTCTCAAG CAAGCCACTG GGACAGGCCC TCATGTCTTG 1200 AGTAGGACAA AGTATATTTG GCCACTCCCC ACTTTGTGGT CACCCTGCTC TGCCTGATGC 1260 ATGGGCACCT TCTGCCCATG ACAACTGTCA TTCGCCCTGA ATAGTCTATG CCATCACACC 1320 TCCTTATGGC TACTAACATA AAAGGTAAGT GACTAATAAA TGGTATCATG AATTAATATG 1380 AAACCTTTTA TACAGACAAA TATTTGATTC CTCAGTTATA TTTTCTTGGG ATCTTTTCTT 1440 CCCAGGTCAT AGCAGTGCTG TTTCAACAGG AAATGTCATA GCTTGAATGC CAGGTGCACT 1500 TTAAAAAATA ATCTAAACTA AATTAGCTTT TACACCTAAC GACGGCCTGG GAATAATAAA 1560 GGAACTCTTT GAAAAAGGAA GAAAGTGGAG AAATAGGAAC ACTTTTACAC TGTTGGTGGG 1620 CCTGCAAACT AGTTCAACCA TTGTGGAAGA CAGTGTGGCG ATTCCTCAAG GATCTAGAAC 1680 TAGAAATACC 1690
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