| Tag | Content |
|---|
EnhancerAtlas ID | HS098-09432 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:17405110-17406440 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:17405634-17405653 | TGGCCAGCAGGTGGCGCTA | + | 9.81 | | NFE2L1 | MA0089.2 | chr11:17406149-17406164 | AGTGCTGAGTCACAG | - | 6.47 | | Nfe2l2 | MA0150.2 | chr11:17406151-17406166 | TGCTGAGTCACAGTC | - | 6.55 | | Stat6 | MA0520.1 | chr11:17406265-17406280 | CTTTTCCAGAGAAAT | + | 7.58 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_51469 | chr11:17404927-17412296 | Skeletal_Muscle | | SE_65430 | chr11:17405038-17411938 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I017383 | chr11 | 17405181 | 17405350 | | GH11I017384 | chr11 | 17405561 | 17405810 |
|
Enhancer Sequence | GAATGGTCTA AGACACCACC CTTTCTGACC CTGTGTCCTC ATCTACAAAC TCAAAGAAGA 60
ACAGTGCTTC TCTCATAGTC CTGCTGGGCC ACAGTGATAC ATGGTACTTC CCTTCTCCTT 120
TTCAGGGGCC CTGGAGTTGA GACAGCTCTG CACATAGCGT GTGGATGGGC CAGACTGCTT 180
CCTCTGCTGT CACATGATGA CTAAGGGATG CAATCCTGGA GGCAGAATAT CACAAACAAA 240
ATTATCACAG AAGTTCCTGC TGGGCTGAGT AGTGCTCAGG TGAACTTCTT TGTCCAGTTG 300
AGGCCAGTGC CATAGAGAAA GGGTGCCCCC AGATGGAGGT AGCACCATCA GTGGGCAAGA 360
ACACCTTCGC GGAGGAGGGA GGCTTGGTCG AACTGCCTCT CTATGCCTGG AGCTTTCCAG 420
CCCCTCCCTG GGTTATGCCT TAAGGCTGGG GGTCTCCCTC AGAGTTGGTG GAAAACCTAG 480
GACCAGTGGT CCTGATTTTT CTCTGCCGAA GTAAGTCTTC TCTGTGGCCA GCAGGTGGCG 540
CTAAGCCCTC AGTTCTGTGG GCTTCACACT CACCAGCAGC TTAAGGTCCC TGAGGGGTGG 600
AGGAAGGTTA CTCTGGTTTG GGCTCCAAGG ATGGTACTGC CAGCAGGTCC TTAGTGAGTC 660
TGGCCTTTCT CCTTGGCCTT AATGGCAGCC AAGCTGAGTC GCAAGAGCCA GCCTCCTAGG 720
ATCCTGGGCT GACTCTGAGT AGCTTTCACC CCTTCACCCT CAAAACCAGA AATGGGTCAG 780
CTCTGCAAGG AAGGGAATCA GCGCTGGGGA CTGCATGGGT GCTGGGAGAG GGCAGCTTAG 840
AGCTCAGACC AGCAGCGGCA ACTTCCTGGC CCCTTGGCCC TGCCTCTGGA GCCGCCTGAG 900
ACAGACCCTC ACTGATGCCC TGTCTGCAGG CCTCACACTG TAGCAATAAC CCTGGCTTTT 960
TGTCCTGTAC GCCATCCATC CGTTATTCAT TCATTCATTT GTTCATTCAT GTAGCACCTA 1020
CTCCATGTAA GCCAGCCACA GTGCTGAGTC ACAGTCCCTG ACCTCAGGAA GCCATGGACT 1080
TGTGGATGGG GAGACAGACC CCTAAACGTA GGCAAAAGGA GAATGCCCAC AGCACAGCAG 1140
AGGGAAGGGA CCTTCCTTTT CCAGAGAAAT CAGGGAAGGT TTCGAGGAGG CATCACTCAG 1200
CCTGGATTTT TATGGATTTC AACAGACAGA GATGAGGCCT GGGCAGTCCA GGCCAAGGGA 1260
GTAACATAAG CAAGGTCTGG GAGGTAGGAA GCTCAACATT ATGTGTCAGG AGGGATAGGA 1320
CAGCGAGGTA 1330
|
