| Tag | Content |
|---|
EnhancerAtlas ID | HS105-20833 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:121351930-121353240 |
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 | TCACGAGGTC AGGAGTTCAA GACCAGCCTG ACCAACATGG TGAAACCCCA TCTCTACTAA 60
TAATAGAAAA ATTAGCTGGG CATGGTGGCA CGTGCCTGTA ATCCTAGCTA CTCAGGAGGC 120
TGAGGCAGGA GAATTGCTTG AACCGGGACC CGGGAGGTGG AGGTAGCAGT GAGCCAAGAT 180
CGCACCACTG CACTCCAGCC TGGGTCCAGC CTGGGCTACA GAGCAAGACT CTGTCTCAAA 240
AAAAAAAAAA AAAAAAAAAA AAGGGACGCA ACCACGGCGG AAGAACAACT GCCAGTCTAA 300
CTGTGCGTGA AGGCTGGCAG TGATGGGGCC GAGACTGGGA ACCGCCCCTT CTCCCTGAGA 360
CTGTTCATAG TGCTGTGGGT CACAGGAGTC ACCTTCAACG TTACCACCAT TGACACCAAG 420
AGACAGACTG AGAGAGTGCA GAAGCTGTGC CCAGGAGGGC AGCTCCCATT CCTGCTGCAT 480
GGCACTGAAG TGCACACAGA CACCAACAAG ATGGTGGAAT TTCTGGAGGC AGTACTGTGC 540
CCTCCGAGAT ACCCCAAGCT GGCAGCTCTG AACCCTGAGT CCAACACAGC TGGGCTGGAC 600
ATATTTGCCA AATTTTCTGC CTACATCAAG AATTCAAACC CAGCACTCAA TGATAATCTG 660
CAGAAGGGAC TCCTGGAAGC CCTGAAGGTT TTAGACAATT ACTTAACATC CCCCCTCCCA 720
AAAGAAGTAG ATGAAACCAG TGCTGAAGAT GAGGGCATCT CGCAGAGGAA GTTTCTGAAT 780
GGCAATGAGC TCACCCTGGC TGACTGCAAC CTGTTGCCAA AGCTACACAT AGTACAGGTG 840
GTGTGTAAGA AGTACCGGGG ATTTAACATC CCTGAGGCCT TCCCGGGAAC GCGTCAGCAC 900
TTGAGCAATG CTTATGCATG GGAAGAACCC GTCTCCACCT GCCCAGATGA TGAAGAGATC 960
CAGCTCGCCT ATGAGCAAGG GGCCAATGCC CTCAAATAAG CCCCTCCTGG GACTCCCTCA 1020
ACCCCCTCCA TTTTCTCCAC AAAAGCCCTG GTGGTTTCCA TATTGCAACC CAATGGACAC 1080
ACTCCAAAAT GGCCAGTGGA CAGGGAATCC TGGAAGACTT GTTCTGGGAT GGTGTGGGGA 1140
AGAGGGGATG AGGGAAATAA ATGGGGGGCT GGGTGAGATT TTTATTGTGG GGTGGGATGG 1200
GCAGGACAAC ATATTTCAGT AATAAAATAG AGAAAAAAAT GAAAAAATAA ATAAACAGCC 1260
GCATCTGTTA AAGAAATAAA GAAAAAATGT AAATACAATT TAAAAATATT 1310
|
