| Tag | Content |
|---|
EnhancerAtlas ID | HS060-17127 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:11176440-11178770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr19:11178462-11178472 | TCTAATTAAA | + | 6.02 | | HNF4G | MA0484.1 | chr19:11177226-11177241 | TGACCTTTGCTCTCC | - | 6.09 | | Myod1 | MA0499.1 | chr19:11177194-11177207 | GGTGACAGCTGCT | - | 6.41 | | Myog | MA0500.1 | chr19:11177197-11177208 | GACAGCTGCTG | + | 6.14 | | Spz1 | MA0111.1 | chr19:11178654-11178665 | GCTGTTACCCT | - | 6.62 | | Tcf12 | MA0521.1 | chr19:11177197-11177208 | GACAGCTGCTG | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 11176719 | 11176769 | | chr19 | 11177357 | 11177435 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I011064 | chr19 | 11175225 | 11176754 | | GH19I011067 | chr19 | 11177735 | 11177992 |
|
Enhancer Sequence | ACAGGATTTT GCCACGTTGC CCAGGCTGGT CTCAAACCCC TGGGCTCAAG CAGTCTGTCC 60
ACGTTGGCCT CCCACAGTGC TGGGATTACA GATGTGAGCC ACCACTCCCA GCCAGAATTT 120
ATTTTAACGT TTATGGAAAA CCAACTCACC AAACCTATGA TTTCATGGTT TTCAGAATGA 180
GGCCAATTTA AAAATAAGTG CCTTAGTCTG GGGGTGTTGG CCCATATCCA TAATCCCAGC 240
ACTTTGGGAG GCTGAGGCAG GAAGATTGTG AAGATTGCTT GAGGCCAGGA ATTTGAGACC 300
ATCCTAGACG ACATAGAGAC CCCCCATCTC AACAACAAAA ATAAAAAAAT TAGCCAGGCA 360
CAGTGGTACA CATCTGTAGT CCTAGCTACT TGGGAGGCTG AGGCAGGAGG ATCACTTGAG 420
CCCAGGAGTT CGAGGCTGCA GTGAGCTGTG ATCCCACCAG CGCACTCCAG CCTAGGAGAC 480
AGAGGAAGAC CCTGTCTCAA AAAAAAATTT TTTAAGGAAA ATTTTTTAAG AAAAAAAATG 540
AGGGGAGCCT ACAGAAATAA CTTTGAGTGT CCACCTGTGC AAAACCCATG TCATGGGGAC 600
ACAGGGACAT GTTAGCTGTG GTGCAGATGA GTGGTCCGGG CTGCAGGCCT GTCTGACTCA 660
GGTCTCAGAC ATCGGCTTTG GCCTGAGGGC CTGGAACCAG CTTGGTCCCC ATATGGCAGT 720
GGCCCCAAGC CAGGGGCCTT CACCTGTGTG ACCTGGTGAC AGCTGCTGGC TGGCTGCTGC 780
CCTTCCTGAC CTTTGCTCTC CACACCTGCC CCTCTCGCAG GCCTTTCCTC TGTCTTTCAG 840
TCCCGCTGGC CAGTGCCCTT CTCCCAACAA CCCCAAGGGC TGGGGGACTT CATTCCTGTT 900
TCCCAGATGA CACAAGTGGA GCTCGGGGAG GTTGAGCCAG TGGCCTAAGG CTACACAGAT 960
CTGAGCTTGG GTTTGGGGGA CATGAGACTC CTCAGGGGCT GCCACCTGCT CTGGGGTCTG 1020
GAGCAAGGAC CCTGAGACTT GAAAGTTGAA ATGGCGCCTG GAACCAGGTG GTGGACTAAG 1080
CAATGGCGGG CAGGTCGGTG TGTCCCCAGG AGTCAGGAGA GGCTGCCACA AGACAGGAGT 1140
GAGCAGGACC TTAAAGCTGA AACGCCGGAT GGTCAGGGCA TGATGGGACC TGACACGGCC 1200
TGGACTAGGA GGGGGTGGGA AGAATAATAC GGGACATCAT ATGTGGCAGG GGGTCATGCG 1260
CTTTCCCATC CAGCCATCTA GGCTGGCTCT CCTAGATTCT TTTTGTTTTG TTTTGAGACA 1320
GAGTCTCGCC CTGTTGCGCA GCTGGAGTAC AGTGGCACCA TAGCCTCTCG AGTAGCTGGG 1380
ACGACAGGCG CGCACCCACA CCCAGCTAAT TTTTGTATTT TCAGTAGAGA CGTGGTTTTG 1440
CCATGTTGGC CAGGCTGGTG TCAAACTCCT GACCTCAGGT GATCCGCCTG CCCCATCCTC 1500
CCAAAGTGCT GGGATTACAG GCATGAGCCA CCAGGCCCGG CCTCTCCTAG AGTCTTGCTT 1560
CCATCAAGTC ATGGAGTCTC CTTTTCCTTC CCTGGAGTTT GAGTGTACTT GGGACTCACT 1620
GGTAACCAAC AGAGTTCAAT GGAAGTGACA TCATGTAACT ACTAAGAGTA GGTCACAGAA 1680
AGCACAGCTT CCGCCTTGCT TGCTCGCTCA CTCTTGAATC ACCAGCTGCC ATGTAACAGC 1740
CTGACTTCCT GGAGCCTGCC ATTTTGTGAG GAGGCCCAAC CAAGCCCATG CTATAAGGCC 1800
ACCAAGACCA CGGGAAGAGA AAGCAATGGC TGCCCCAGCC CTAGCCCTCA GCTGTCACCA 1860
GCTGCATCAG AGACCCTGAG CCCGTACCGC CGAGCTGAGC CCTTCCCACA TTCCTGACCC 1920
TTAGAAACCA CAAGAGCTAA TAAACACATT GTTTTAAGCC ACTAAGCTGT TAGGCAGCAA 1980
CAGTACTGGA ACATCATAAA ATAATTTTTT AAATGACAGG GATCTAATTA AACGTGGAAG 2040
GATCTTGAGA ACATTGTTGA GGATAGAACA GCAGGCTGCA CAGTGAAGCA AATGTCCAGC 2100
AAGATGGACA CACACTGGAT CCTGGATATG TGTTCTGGAC CATGTCACTA GTACATCACA 2160
TTTAGAGAAA GCTGTGTCAG GACCCACCCC AAACACAAAA CAGCCTGAAC TGCTGCTGTT 2220
ACCCTTGGCA GTGGGGGAGG GAAGGGTGGC GTTAAGAGAT TCCCCAAGAT GGTGAGGTCA 2280
CCTGGCCATT TTATTTTTTA TTTTTATTTT TTATTTTTGT ATATATATAT 2330
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