| Tag | Content |
|---|
EnhancerAtlas ID | HS139-53242 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr8:42162790-42163860 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr8:42163641-42163651 | GACACGTGCC | + | 6.02 | | NR3C1 | MA0113.3 | chr8:42163809-42163826 | AAGGACATTGTGTTCTT | + | 6.24 | | NR3C1 | MA0113.3 | chr8:42163809-42163826 | AAGGACATTGTGTTCTT | - | 6.41 | | NR3C2 | MA0727.1 | chr8:42163809-42163826 | AAGGACATTGTGTTCTT | - | 6.39 | | NR3C2 | MA0727.1 | chr8:42163809-42163826 | AAGGACATTGTGTTCTT | + | 6 | | Npas2 | MA0626.1 | chr8:42163641-42163651 | GACACGTGCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26990 | chr8:42162285-42164496 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 42163245 | 42163764 | | chr8 | 42163516 | 42163784 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I042305 | chr8 | 42162761 | 42162910 |
|
Enhancer Sequence | AGGGTAAGTG ACCTCCTGGG ACTGGGAAAG CCTCAGGTGG GCGTGCCGGG AAGTGGCCTG 60
GGAGGAAAGG AGCACACTCT GCATATTTGT GTGTATTTGC ATTTCCTTGC CTGTGCTTTG 120
ATTCTCTGGG AATGCTGTTT GATTTGAAAC AAAATTGAGC AAAAAAGTTG TTGCAGATTG 180
AGGCAAGTTT AAATGGATTA CATTGTTAGT TGCTCAAGTT GCAGGAATCT GATAAGGAAA 240
ATAATGTTTG CCTTCCTACC TCCACCCCTA GCCTCTGGGA CTAGCGCTTC TTGGAAGTCG 300
ACTTTTTGTT TTCCATTTGC TTTAAGAGCC TCGCCTCTCG ACTCTAAATG GAAACCAGTG 360
GTCAGTTGGT TGTGGATGTG GCTGGGAAGA GGCACTGGGA GCTGGCCTCT GCTGCCAAGC 420
CTGGTCCAGC CTATAGTTTC CCCAGAGCTC TTTGTGGCCT CCTCAGTGGC CACCCGGCTC 480
AGACGTGGTG TTGACTGCCC CACAAGCTTG ACATTGTGGT CTTTACCCAC CCACTCTATG 540
TGTTCAGCTG GGGTGGTGAG CACAGGCTCA GCTGAGTGGA ATACAGTGAA TGAGTTCTTA 600
GATCACCTAA TCCCTTCCCA TACAGCTGCC CTTAGCACCT AGGCCTGGCC TGTGACTACC 660
ACAGGGCTCG CCCTTGTTCC AGTTCACCCT CACTCCTGTC AGTGGTGCTC AGATTTGAGA 720
ACTGAGGGCA TTTACTGAGA AGAGGCTGGC CCGGTCCTTC CTGTTTCAAG TCTGGGTTTA 780
GCTGTCTTGA GGGCTGGTGC CTGTTCTGTT CATTCAGCTT CCCTCTGATG ATGCGTGGCA 840
GAGTGTGGGA GGACACGTGC CTAGCATTTT TACAATATGC CTTTTCTTTT AGCCCTGAAT 900
CTACCGTGTC GAGGGCATTC TTTTGTGTAT CTGGTGGCTC TTAGGAGTTT GGGATCTAAT 960
AGTACCTGGG AATTCAGAAA TACCTCTGCT CTAACACCAG GCAGTCAGAA TCCTCGTAGA 1020
AGGACATTGT GTTCTTATAA CCCTCAGCTT TCTCCTTCCT TTTGTTTTAG 1070
|
