| Tag | Content |
|---|
EnhancerAtlas ID | HS064-00040 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr1:3588950-3591220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:3590343-3590354 | TGTGGATTGGG | - | 6.14 | | REL | MA0101.1 | chr1:3590388-3590398 | GGGGATTTCC | + | 6.02 | | TFAP2C | MA0524.2 | chr1:3589640-3589652 | TGCCCCCGGGCA | - | 6.02 | | TFAP2C | MA0524.2 | chr1:3589640-3589652 | TGCCCCCGGGCA | + | 6.37 |
|
| | 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 | AGGGGGTGTG AGAGGAGGAT CGGAGGGGGC AGAGGACAGG GATGTGTCTG TGCAGAACGA 60
GGCTGTGGCA GCTCCAGCGA AGGCGGCTGC GGCCCCATCA GTCACCTGCC CTGCTGAGGG 120
CAGCGCTGTA CTCATCACCT GTGAACACAG GTATCGACTC AGACACCCAC TCTGGCCATA 180
AGCTCCGCTC TGTCCCAGCC CTGGACCCCT CACCCCCTAT CCTTGGCAGT CGGTCCTCTG 240
GGTCTTCTTC CTGTGCCCAC TGTGCTGGTC TGAACCTCCC TTAGTGACAG ATCTGCTCCT 300
ACCACCCCCG CCAGGGTCGC CCTTCCTCTA ACAGGTGGGC TCCTGGCAGG AAACATCACC 360
AAGCTCAGCG CCCCAGTTCC CTGACAGGGC CCCACTTCCC TCCTGCCGCC AACCTCGTCC 420
CCCCAAGGGC CATGTCCCTG CCCACCCCTT CCACCCCTTT CTTAGAGGAA GCTCAGCCCA 480
TCAGGCCGCT CATGCTTCTG ACCCCACCTC CAAACCCTCC TGACCCGCTT ACCCCCAGGA 540
GCACCGCCCA CTCCAAGGCG CAAGCAAGCT GGGGCTGGGG TGCAGACTTC TCTTCCACCA 600
CCCACCCTCC TCATACCCAG CCTCTGAGGG CCTCACAGAC ATACATGATT TGCCTCCAGT 660
GGGCCAGGGT TATCTGTTTA CCGCGTTGCA TGCCCCCGGG CATGGAGCTG GCACCGGCTG 720
CCGCTGCAAC TGGGCACTAC CCGTTTCGAG GACGCCTCAT TCCCTGAGAG ACTGAGGATA 780
GGCTGGTGCT CTGCAAAAGG GTGCGGAGAC CACTGTAAAA GTGGGGTGAG ACACGCGTGC 840
TGACCATGAA ATGGAGAGGC ACTCGAAGGA GCCAGGGACC CGGCAGCCAG CAGACCCCAC 900
CTTTCCGCCC CCGTGTGTGC AGTTCTGTCG CTCAGCCTGG TGCCTTTGGG ACCCGGGCCT 960
CATTGGTTCT TCCTCCACTG CCACCACCTG ATACTAAATA ACCGTCGGTC AATGGCAACT 1020
CGATACGGTT TATGGGGCAT CCACGGTGTG CCCAGATAGA GGAGTGCTTT CGCTTTTGAT 1080
ATGCGTAGAG TTACTTCATT CCACCTAGCG CTTCTAGGAG GCACTACAAT TATCTCCATT 1140
TTACAGACAA GGAAACAGAG GCTCAGAATG GGCAAGACAT CTATCTGAGG TCACACAGCT 1200
AGAGCGCGGC AGAGGTGGGC TGCGTGGGCA GAGCAGGAGA GGGAACTGGA GTGTGTGCCC 1260
GGCAGTGCTG GGCTTCAGGG CACGAAGCGG TGGGGCAGGA ATCATGTGTC TTGGTATGAC 1320
CCAAACACAT ATATGACAGC AAGAAGGCCT GGGCAGGCAG CAGAGGACAA GGCGGGCCTC 1380
TTGGATGTCT GGATGTGGAT TGGGCCTCAA TGTACCGGTG AAGATAGATG GACAGGCAGG 1440
GGATTTCCAG AGAGGGGCTT CCCAGGCAGG GTGCGGGGTG TGGCTGTGCG GTGGGAACAC 1500
GGACTGGGGA GGGGATTGCA GCCGGGCCCG TGCCTCCCTT GCTCAGCTCC AGGTCAGGCC 1560
AGGGTAGAGC CAGGCTGCTG GGTTCGACCT CCACCCTGAC CAGCTGTGTG CCCATGGAGG 1620
GCTGGTCTTC CCTCTCTGTG CATGTCTCCT GGTTGGTAAC AGGTGTGTGG CCTCACTGGG 1680
CCGTCGTGGG GTGGCTGGAA TCCCCGGGAA TTAGCCATGC TTTGGTGTTT CTACATTTCA 1740
CTTGGCTGAG TGTGAACTGA CCCAGGAAGC TGGTTGGGGG CACCCCCACC CACGGGGGGT 1800
CGGGCATTTT GGTTTGGTCA TGGCCTCAAA GCTTCTGGGG TGAGGCTCAG GGATTCCCCC 1860
AGACTGTCCT GGGCATCTGC CTCCCCTCCC CTCCCGCTTC CCGTGGGCCA CGGCCCAGGA 1920
GAGAGAGGGC AGCTTGCTCA GGCACCTCCA GCTGTCCGCA TATTTCACAC GGTGCACGCT 1980
ACCCCACCGT GGGAGGCTGT GTTTGTCTTT CATCCCCATG CTGGGCTTCC CCAAACTAGG 2040
GGAGTGGGGC AGCAGGCGTG CCATCTGTGG CGGTGAGGGG GGCTCTCAGC CGCATCCTCC 2100
TCACCAGGCC CTGCGGACAG GCCTTCGTCC CTGCCCCTGA CCTGCTGACG AAGCCGTCCT 2160
GGCAACCCTG TCTGAAGGAC CTGGCCCCAT CGTACCCACA GAGGGAGGCC ACATGGTCCT 2220
TAGCCTCTGT CGGGAGGGGC AGGCAATGCT GGCAGAGGGC CTTGCCCCTG 2270
|
