| Tag | Content |
|---|
EnhancerAtlas ID | HS047-08771 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:121351760-121353160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr12:121352016-121352026 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr12:121352016-121352026 | GGCACGTGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr12:121351934-121351949 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27043 | chr12:121352024-121353293 | Esophagus |
|
| | 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 |
| GH12I120914 | chr12 | 121352192 | 121353043 |
|
Enhancer Sequence | AATGACATCT GTTATAAACC CCACAATACA ATGTCATAAC TTTAGCTCTT AAATAGCCAC 60
ATCTGTCAGT GTGCCTATAT GATTAAAAAA AAAAAAAAAA AAAAAGGAAG GCCCAGGTAC 120
GGTGGCTCAC ACCTGTAATC CCAGCACTTT GGGAGGCCCA GGCGGGTGGA TCACGAGGTC 180
AGGAGTTCAA GACCAGCCTG ACCAACATGG TGAAACCCCA TCTCTACTAA TAATAGAAAA 240
ATTAGCTGGG CATGGTGGCA CGTGCCTGTA ATCCTAGCTA CTCAGGAGGC TGAGGCAGGA 300
GAATTGCTTG AACCGGGACC CGGGAGGTGG AGGTAGCAGT GAGCCAAGAT CGCACCACTG 360
CACTCCAGCC TGGGTCCAGC CTGGGCTACA GAGCAAGACT CTGTCTCAAA AAAAAAAAAA 420
AAAAAAAAAA AAGGGACGCA ACCACGGCGG AAGAACAACT GCCAGTCTAA CTGTGCGTGA 480
AGGCTGGCAG TGATGGGGCC GAGACTGGGA ACCGCCCCTT CTCCCTGAGA CTGTTCATAG 540
TGCTGTGGGT CACAGGAGTC ACCTTCAACG TTACCACCAT TGACACCAAG AGACAGACTG 600
AGAGAGTGCA GAAGCTGTGC CCAGGAGGGC AGCTCCCATT CCTGCTGCAT GGCACTGAAG 660
TGCACACAGA CACCAACAAG ATGGTGGAAT TTCTGGAGGC AGTACTGTGC CCTCCGAGAT 720
ACCCCAAGCT GGCAGCTCTG AACCCTGAGT CCAACACAGC TGGGCTGGAC ATATTTGCCA 780
AATTTTCTGC CTACATCAAG AATTCAAACC CAGCACTCAA TGATAATCTG CAGAAGGGAC 840
TCCTGGAAGC CCTGAAGGTT TTAGACAATT ACTTAACATC CCCCCTCCCA AAAGAAGTAG 900
ATGAAACCAG TGCTGAAGAT GAGGGCATCT CGCAGAGGAA GTTTCTGAAT GGCAATGAGC 960
TCACCCTGGC TGACTGCAAC CTGTTGCCAA AGCTACACAT AGTACAGGTG GTGTGTAAGA 1020
AGTACCGGGG ATTTAACATC CCTGAGGCCT TCCCGGGAAC GCGTCAGCAC TTGAGCAATG 1080
CTTATGCATG GGAAGAACCC GTCTCCACCT GCCCAGATGA TGAAGAGATC CAGCTCGCCT 1140
ATGAGCAAGG GGCCAATGCC CTCAAATAAG CCCCTCCTGG GACTCCCTCA ACCCCCTCCA 1200
TTTTCTCCAC AAAAGCCCTG GTGGTTTCCA TATTGCAACC CAATGGACAC ACTCCAAAAT 1260
GGCCAGTGGA CAGGGAATCC TGGAAGACTT GTTCTGGGAT GGTGTGGGGA AGAGGGGATG 1320
AGGGAAATAA ATGGGGGGCT GGGTGAGATT TTTATTGTGG GGTGGGATGG GCAGGACAAC 1380
ATATTTCAGT AATAAAATAG 1400
|
