| Tag | Content |
|---|
EnhancerAtlas ID | HS042-08293 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr11:76504040-76505360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:76505039-76505060 | TCCTCCCCCTCTCTCACCTCC | - | 6.92 | | ZNF263 | MA0528.1 | chr11:76505042-76505063 | TCCCCCTCTCTCACCTCCTTC | - | 7.26 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_00254 | chr11:76503160-76520678 | Adipose_Nuclei | | SE_26826 | chr11:76503864-76505597 | Esophagus | | SE_57060 | chr11:76503862-76504558 | VACO_400 |
|
| | 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 |
| GH11I076793 | chr11 | 76504060 | 76505493 |
|
Enhancer Sequence | TGTGTGTCCA GCACTAGCAG AGAGTGAGGA CTGGCCCTGA CTGTCACTGT CGTCACTTCC 60
CACTGCAAAT GCCCAGCCCC GGGCATAGGC CCGGCACAGA GCAGGAACCC CGGGAGAGGT 120
GTCTACTGTG CAGGGCTGAG CAAGGAACCT AGTTCAGTGC CCTGGGAGCA TCTGCAGACA 180
GTTACCTAGG TAACTCCTGC CCCTTTACAT CAGATGCCTC TTTACATCGG CTGTTACTAC 240
CATTGCCTCA GTTCTGTATC TTCTGGCTGC TGGGTGATGA CTGCCCTGTG CCTGTGCACA 300
GCCCTTCACA GTTGGCAGTA AGGGTTAATC AACTTAGGTG AAGAGGGCAG GGCAGAAATT 360
GCCACCCTGT AGTGCAGAGG ACAAGGCTGA GGCTTAAAGA GGGGCAGCGA GAGGTCCCCT 420
CTGGCGGGAT AGCATTTGGG TCGTATTTTG AGCTGCTGGT TACATAAGTG GGAGCTCATA 480
TGAGGCCATT TGGCATTTCA CGGACCCCTT GTATAATCAC CTCTGGGAAT CAAAGGGTAA 540
TCTCAGGGCC TTTGTGCTGT TTGTTTAAAC CCCAGGAAGG GTGGGTATGA ATGAGCAGAT 600
CAGCTTAGCA GGGGAGGTGG GGCCTTTGGT GGTAATGAGC CCTGCGGTGA GGAGCTCGCC 660
CAGGGGAACA AAAGGGGCCT GAAGCAACTT AATATTTTCC TTTTGGTTCC AGACATTGGA 720
ACACTCTGTC CTGCCTCAGC TGGGACCATG CCCAGGATGC ACCTGGGCTG GATTTAATCC 780
TGAAATTGGC CTCTACAAAA GAAAGGGGTG GGAGAGGAGG GTCCCACATG GGGAGGGGGG 840
CAGGGGAGAA GAGTCCCACT TTTCCCTGCC CCTGGGCAAA GCCAGAGTGC AGATCAAGTG 900
GCTAGCCCTT TAAAGTTTCA TGCAGGGCTG GTAATGCAAT CCTGCTGCTC CCTCCCACCC 960
ACCTTCCAGT CTGGAAGGTG GGCAGGTCCC TGGCCCATCT CCTCCCCCTC TCTCACCTCC 1020
TTCCTGAAGT CCAGAGGGAG GGATGGGCAG GAGGGCAGGG GCCCAGAGCA GGGCCACCCA 1080
GATGAAGAGC CTGGCTAGAA GGAAGCTTAG TGCCTTCTGT CTCCCAGGCT GCTGAGGGGC 1140
CACTGTGCAG GGCCGGGGTG ACGACAGACT ATCCAATTGG TCTAGTTAGA AGCTCCCACT 1200
GCCCAACCCT CTCCTTCTCA TGCTGGCACC ACTGAGCACC ACCATCCCAG GAGCTACAGT 1260
GGACGTGAAC ACAGGCTTTG AATCCAACAG CAGTGGGTGG TGTGACCATT AGATGTGACA 1320
|
