| Tag | Content |
|---|
EnhancerAtlas ID | HS113-00092 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:3587150-3589460 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:3587261-3587282 | AAAGAAAAAGAAAAAGTGAGG | - | 6.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I003671 | chr1 | 3587953 | 3592317 |
|
Enhancer Sequence | ACCTGGAAGG CGGAGGTTGC AGTGAGCTGA GATCGTACCA CTGCACTCCA GCCTGGGTGA 60
CAGAGCGAGA CTCTATCTCA AAAAAAATAA AATAAAATAA AAAAGATAGG AAAAGAAAAA 120
GAAAAAGTGA GGAGAAATGA GGAGGAAGTC GAGCAATTTA ACCCCAAATG GTGCTTCTCC 180
AGCAGTCACT CTGTTCCTGT CCTGACCTGA CCTGCTGGGC CCCGCCCGCT CAAACCAAAT 240
CATGGATTCT GTCATCGCTT CTTCACGGAG CACCTACTGT GTGCCAGGCG GGTGCTGGGG 300
CTGCAGCGCA GAGAGCAGTC AGGGCTTGGT GGTCTGGCCC GCAAAGAGTC AGCATGTGAA 360
TGTCTCTCCA TGCGATGGGT GCTGGGAGGG AGGAGCCCTG GCAGGTCTGG GGAAGACCAG 420
CGTCTCTTAA ATGGGGGTGC GCGGGCCCTG AGGAGTGAGG CTTCCTGACA GCCGTCCCTC 480
GTGGGTGCCA TGCTGGTCAG AGTGGGGTCT GGCTGCACAG CCTCCCTCAG GGCTGGGCTG 540
GAAGCACAGG TCGGCTGGCA CCTGTCCAGG TTTCAGGGTT CCAGGGCTCC AGCTGGAACT 600
GCCTCAGGGA TGGCAGGGGT GGGCCTGTCC CTGGAGAGGC GTGGGGTGTG GGAGCTGGGA 660
GCGTGACGGG AAGCAGCCCC CTCAGACCTG GAGTAGCATG GAGCCTAGGA TCCATTGTGA 720
CCTTGGTGGT CCTGTACCCT GTCCAGCTCC AGTTGCTGTT CCTGCCTCTC CCTGACCTAC 780
TGGCTGCCCA GGCTGCCCCT TGGCCGAGCT CCACCATGGC CAGTGCCCCT CCATTCGCTT 840
GTGAGTCCCA CAAGATCACA GCCCTGCCCA GGGCCTAGGC AGCTCTTGGG CTGACCCAGC 900
CATCGTCGGG AGCCCCCTTC GTGACGGGGG CAAAGGCTGG ATCGTTGTCT GCCCTGCAGG 960
AGCCGGGGCC TCCAGAGGAC GGGCTGCCTG GCGGGAAGGT GGAGCTCACC GGAGCCCAGC 1020
CTAAGCCAGC TGTGGTGCTT CTGAGATGTG CGGCCCTGGG CAGGCTGCTC GCCCTCTCGG 1080
GGCCTCTGGG AACACCTGGG GACTTCCCGC TGGGTTCCTC TGAGGATTGA ATGAGCTTGA 1140
AAATATGGAG GATTTGGCAC AGGGAATGCT GGGCAGCAAT ATCAGAAAGG CAACCCTGAG 1200
AGCCAGCGGA CAGCCACTCT GAGGAACAGC AGTGGCTGCC TCTGGAAGGA GTGAGGGGTG 1260
GGTGGACCCC CGTGATCGCT GCACGGGGGA GGTCACGGGG CTGAGCGGCC ACCACTGTGC 1320
AGGGGAGGTC ACAGGGCTGA GCGGCTGACT CCAGAACAGG AAGGGAACAC GCCAGGAGGG 1380
AGGATTGCTC ACTGAGTCAG GGCGGGACTC AGAGGGACGC ATGACAAGTT CAGGGAGTTG 1440
ACAGCTGTCT GGAAGGGCAC GTCTGCTCAG ACCGCAGGGT AGGGAGTGGT CAGCAGGGAG 1500
ACATGTCCAC TGGTGCAGCG GGCGTGTCCC AGACCCCTTA GAGAAAAGCC CAGAGCCAGG 1560
GGTGAGGGGT ATGTGTAGGG TGGGGACATC TCAGAGTGGA GCATCCCCAC CAAGGGTGTC 1620
CAGAGGAGGG TGGCCAGGTG GGGACAGCAG CTTGAGAAGG GTCATTCTCT CTTGGTTGGA 1680
GGAGTGGAAG TGCTTCTCTG GGGAAAGAAA GAAGATTCTG GAGGACAGCA CAGGCACTTC 1740
CAACATGGGC GCTGGCCGCA CAAAGGCTAG TGACACCCGG TGTGATCCCT TGGGGTAGAA 1800
AGGGGGTGTG AGAGGAGGAT CGGAGGGGGC AGAGGACAGG GATGTGTCTG TGCAGAACGA 1860
GGCTGTGGCA GCTCCAGCGA AGGCGGCTGC GGCCCCATCA GTCACCTGCC CTGCTGAGGG 1920
CAGCGCTGTA CTCATCACCT GTGAACACAG GTATCGACTC AGACACCCAC TCTGGCCATA 1980
AGCTCCGCTC TGTCCCAGCC CTGGACCCCT CACCCCCTAT CCTTGGCAGT CGGTCCTCTG 2040
GGTCTTCTTC CTGTGCCCAC TGTGCTGGTC TGAACCTCCC TTAGTGACAG ATCTGCTCCT 2100
ACCACCCCCG CCAGGGTCGC CCTTCCTCTA ACAGGTGGGC TCCTGGCAGG AAACATCACC 2160
AAGCTCAGCG CCCCAGTTCC CTGACAGGGC CCCACTTCCC TCCTGCCGCC AACCTCGTCC 2220
CCCCAAGGGC CATGTCCCTG CCCACCCCTT CCACCCCTTT CTTAGAGGAA GCTCAGCCCA 2280
TCAGGCCGCT CATGCTTCTG ACCCCACCTC 2310
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