Tag | Content |
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EnhancerAtlas ID | HS113-31502 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr6:29960190-29962020 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr6:29961762-29961773 | GCAGGGTGTGG | - | 6.62 | 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 | TACATATTTA TTATTTTACT CACCCAGCAT GTGGTACTTT GTTATGGTAG CCCTAGCAAA 60 TTAAAACAGA AATATTACCT TTTCTACTCT GTCCTATGTA TGAACATGAG ACTTTTTAAG 120 AATATGAATT ACCTGGGATT CCAAAACATA GAGTGAGTCA ATGGAAAATA GATGATACAG 180 GGTCATTTCC AAGCCTTTGT GGGTCTCCTG GCCACCACAC AAACATGGAT GTGTTCCCAT 240 TTCTTTTCAG TTTCACACAG TGCAAAAGTT GTGGACATAG AATCACAAAC TGTGTTTAAT 300 TTATTTGAGA CATTGAGTGA GCTAGTTTTG CCCTAATTTT ATAGAAAGAT GATGAACAAT 360 CATAATTACT AAACCAAAGA GGCTTTTTGG CAGGGGATGG CAGGTACTAT GTTTTCTCCT 420 CCTTTTAAAG TGCATTTTCC TAAAGAGTCT TGTCTAGGAG TAAATGTCAT CACTTTGCTT 480 TTTTCCTCCG CATTGATCAC TTGGTCCTCC CTGCATTTCA GTAAGGTTGC TAGAATGGAG 540 GCATTTGTCC ATGATTCACA GATGAATCAG AGGCCCTATG AGTAGAGAGC TTCTCCTGAA 600 GTCACACAGC TCGTGAGTGG TGGAGCAATG ACAGGCACAT GACTCTCCAG GTCCCTAGTC 660 CAGTTTTCTG GGTGCCATGA GAATTACAGC CTTTGGTTCC TTTTACATGT AGTTCATTTC 720 TGAACCTGAG AAGGAGAATG CACCTCAGGT GACTAACAGT TTTTGCTCTT CTGTACTTGT 780 CTGAGAATGA CCCCAAAAGA TTTTTAAAGG CCAATTCTTT GGCTACCAAC CCTATTTTGC 840 CCAGGCATGG ACATGGAGCA GGTGAACACT GCCTTTACCT GTGACATGCC TGAAGATTCT 900 GAGACCTACG TGAATCAGGT AAGCTCCATA CACAGAGGGA CACCCACTCT CCCACCCACT 960 TATTTTCTGT ATCTTTTCAC ACTTCACTTC TTCATTCCTC CCTCTGGCTG TCTTCCCTCT 1020 TTGGGGTCTT CTAGTCCTAA CCTCTGTCTC CTTCCAGGTG ACTAGAGCAG GCTGGTTTGG 1080 AACAGGGCTT GTGTCGGATG AGAATTGTGC CAGGATCCTC AGTGATGGGC AGCATCACTT 1140 TAAGTTCAGT GTTAGGAGCT ACCTGCTGAG ACAGACGTCT CCTCCACAGT GAGTGCTGAT 1200 TTCATGAAAC CCTTAGTTCC TCCCTATTCC TTACTGTGTC TTCAATCCCA TCATGTAGGT 1260 CATGGGCACT TAACGCATAA TGAACAATTG ACTGCTTCAT GCCCCCTGGC CGTTGATGCT 1320 GTGTTGGGAC GTTTTGCTGC CCTCTATGTG GGGTCTGTGC CTTTTCTCAT ATTACATCTC 1380 TTCCACCACA CCCAAGTCCA TCCTCTGAAC CCAGGCAGTA CACCAGCATC TGCATGTGTG 1440 CTGTGTGTTC CTGCCTTGCT TTGTCCTTTC ATGCCTTATT CTCACTGTGC CATGTCTCCT 1500 TCTCAGTTGA ACAGATGCAG TAGGAGACTC GCTCATTCTG GAATGTGACC ATCTGCCCTT 1560 CAGGAGAGGA CAGCAGGGTG TGGGTGAAGG AGACCCTGCT GCCCCCACAC CTGACAGCCT 1620 CCACCACCCC CTGGCTTTCC TCTTCTGCAT CAGCACCACT CCCGAACCAT CATTCCTGAT 1680 CGTCAGAATT TTTAATGTAA CTAAACATGA AACACAAGTG CATCTGCATT ATGTGTGGGT 1740 GCTCTCTCCC TTTATTGTAT TTGGGGTAAG ATTATTTTAG GGCATGGTCC AGGGTAAATT 1800 CCTGTAAGGC CTGGATGCCC TGCTGTGAGG 1830
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