| Tag | Content |
|---|
EnhancerAtlas ID | HS139-47039 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr6:39207060-39208400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr6:39207610-39207631 | GGAGGCGGGTGGGGAAGGGAG | + | 6.27 | | ZNF263 | MA0528.1 | chr6:39207627-39207648 | GGAGGAGGATGAGGAGAATGC | + | 6.38 | | ZNF263 | MA0528.1 | chr6:39207624-39207645 | AAGGGAGGAGGATGAGGAGAA | + | 6.8 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_23358 | chr6:39208075-39208885 | Colon_Crypt_1 | | SE_27719 | chr6:39207230-39208365 | Fetal_Intestine |
|
| | 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 |
| GH06I039239 | chr6 | 39207231 | 39208885 |
|
Enhancer Sequence | AAATAAGCTT ATGCATTCTG CCCAGGTTTT AAGTAGGCAA GTAATCTGAT TGTTGTAGCA 60
CTTCCAAGAA TTCACAAAGG CAGCTCGTCC TTCAGGAGGT GGTAGCAATA GTTCAGGGGC 120
GAGATGACGG GGACCAGAAG GAAGGTAGGA GCAGTAGCAG TGGGAAGCAG GGACGATTCA 180
GGAGATGTTA GGGGAGTTAG CAGCTTTGTG ATCTAGGGCC CTGCCCCTGT CTTCAGAGCC 240
CTGCTACTTT ATGCTGCTGT CTGCAGAACC TGCTGCATTC TGGAGTTGGC ACCAATACTA 300
ATCTGCCTTT CCTACCCCAT TGCCTGAACA CTTTGCTCCC ACATGGAGCC CCTCCCCCAG 360
CCTGCCTCCC CTGACCTCCC TTGCCGCCTG GCTGCATTAA GCAGCTCCAG CAGGCCTCAT 420
ACAGACCCAC TGTTTAATGC CTATGGCATC CTCATCTGGC CTGGATCTGG CTGCTCCTGA 480
GGGACACCAA GATCCCAGAG ACAATTGGCC ACTTGTCCAC TGAATGGGAG AGGGGCCTGA 540
GGATTGGTTG GGAGGCGGGT GGGGAAGGGA GGAGGATGAG GAGAATGCCA AGGGGAAGGA 600
GCAACCAGGA TTCCTGGGAT TTCTGCCTCC CGAGCCAATG TCCAAGAAGG AGCTGGGCAA 660
TAAACAGAAC TTGAACACAC ACGGGACTTT GGCCATGCAG TCCTAAGACG TGTTCTGGAG 720
TGACAGCTCA CAAGGCACTG GGGATCCACT GGCTTGGAGT CCCCTGTGTT ATTATGGGGC 780
CCATGACACT TAAGTTACTA TTGATCTAAC GTTATGAGCG CCTTCCTCCT CAAACCAGCC 840
ACCTTAATGT TATCCTTCTG TCAGGGACCC AAGCTGGCCC AGCCTGGAAA AAAACCACTG 900
ATTCATGTCC AGCTGAAGGA CATTACTGAA GGTGAAGATA TTGGGGTGGA TGGTCTTCCT 960
CTTCCCTCCC ACTGTTTTTT ACTAGTCTGG GCAAGGAAGG GACCAGTTAT AAAGTGATAC 1020
CATGATCTGA GTCACTGTTA CTGCCTGCTT CTTCAATGCC AGGCATTGAG CTCAGCACTT 1080
TATAATGTTA CTGCATTTAA CCTCACGACT AGCCTCTATG CAGGCCTTGT AATCATCCGC 1140
ATTTTGCATG TGAGGAAACA GGTTCAGAGG GGGTAAGTAG CTTGCCCTAC CTAGTGTGCA 1200
TGGAAGCCAG AACTGAGACC CAGGCTGGTT TGATGGCACT TAGACAGGGT GAGGCCCCAG 1260
GGAACTTTAC TCCTCAAGCA CCCAACCCAT ACCCCTCCGG AGCCAGGCTT TTACCTGCTG 1320
GGGCATGACA GAGCTGGCCC 1340
|
