| Tag | Content |
|---|
EnhancerAtlas ID | HS073-02586 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr11:68822860-68824130 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr11:68822929-68822945 | TTTGTACTTTGACCCG | - | 6.39 | | MEF2C | MA0497.1 | chr11:68823551-68823566 | TTCTATTTTTGTCAA | - | 6.29 | | TFAP2A | MA0003.3 | chr11:68822977-68822988 | TGCCTGAGGCA | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09733 | chr11:68821567-68824186 | CD14 | | SE_54738 | chr11:68815445-68823414 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH11I069054 | chr11 | 68821809 | 68824749 |
|
Enhancer Sequence | CCCAGCGCCT GGCCGCTGCT CTCCTGGTTT ATTGCTGATT CTCTGGAGTG AGCTGCCTTT 60
TCCCCAGACT TTGTACTTTG ACCCGGTGAG CAAGGCACAC TTTCTTGGAC AAGCAAGTGC 120
CTGAGGCAGA GGCTATGTCA GCTCTCCTCC CTCTCCACCA TGCAAACTGA GGCCAGTGTG 180
CCGTCAGCTC TCCTCCCTCT CCACCATGCA AACTGAGGCC AGTGTGCCGT CAGCTCTCCT 240
CCCTCTCCAC CATGCAAACT GAGGCCAGTG TGCCGTCAGC TCTCCTCCCT CTCCACCATG 300
CAAACTGAGC CCAGTGTGCC GTCAGCTCTC CTCCCTCTCC ACCATGCAGA CTGAGCCCAG 360
TGGGCCGTCA GGGGTTGCGC AGGCTGACAG GGCCTCTGGG AACAGTCCAG TGTCTGCAGT 420
GCTGCTGTGA GGAGAGGTCC CAAGTGAATA AGTGAGGCCC AGGTGGTCCC TCCTCAAGGC 480
TCACCCTGCC ACCCCAAAGA GAAGAGGAGA GGAGGTGGGC GTGGGGCAGA AAGGGGTTTC 540
TTATGCACAC AGCAGCTGCT GCATGTTTGA CTCTGGGTTC TGCCTGTGAC GCACGTCCTC 600
CCACAAGCTG GAGGTGGGCC TTTGGTGCTC ACCTAAGCTT CTGAGCCTCG TCAGAGACTT 660
AGTGCCTTTC CAGGGAGGTG CAGGCTACGT TTTCTATTTT TGTCAAACAG TGATTCCAGT 720
GCTGCGGTCT CAGGGGCCCC CACATCCATG CCCATGGTGT TAGATCAGGC CCTGGCTGCA 780
GCCCTCCTCA GCGCCAGCCC TGCCGCTCCT TGGCTGGGCC TTGGGCTCAC GTGGCTTCCT 840
GGTCGCGTGG GGCCTCTGCC CGGCACTGCC CTGTAGTCCC TTGTGGGCAG GGCGGGCTGT 900
GTGCCGACCG AGGGTTGTGG CTGGATGCTG GTGTGTGTGA TTGCAGGCCC CGGGCAGTTT 960
CTCATTTCTT CCTTTGTAGC TTATCATGTG GTTAGCAGGT CTGGGGGTTT TTCAACTGGA 1020
ACTGAAACTG GCAAGAGGTT GTCATTAGCG TTTTTTGAAT GGTTGGTGTG TTTGAGAAGT 1080
GTCAAAAGGT GAGAGAGGGT ACATCAGCAA GCTGTGACCT CTGGGGGCTG TCTTTTATTT 1140
TATTTTATTT ATTTATTTTG AGACACAGTC TCGCTCTGTT GCCCAGGCTG GAGTGCAGTG 1200
GTGCAGTCTT GGCTCACTGC AACCTCCGCC TCCTGGGTTT AGGTGATTCT CCTGCCTCAG 1260
CCTCCCCAGC 1270
|
