| Tag | Content |
|---|
EnhancerAtlas ID | HS145-04592 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr11:76474570-76475400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr11:76475356-76475367 | TCTGATTGGTT | - | 6.62 | | Nfe2l2 | MA0150.2 | chr11:76475287-76475302 | CACCATGATTCAGCA | + | 6.82 | | Nkx2-5(var.2) | MA0503.1 | chr11:76475244-76475255 | CTTGAGTGCCT | - | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_26826 | chr11:76473940-76476097 | Esophagus | | SE_33832 | chr11:76474085-76476157 | HCC1954 | | SE_34932 | chr11:76474172-76475929 | HeLa |
|
| | 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 |
| GH11I076763 | chr11 | 76474293 | 76475698 |
|
Enhancer Sequence | TGAATGAATA GCCAGGTCCA CAGGAATACT TTGGTAACAA GATGCTTACT GCTTCAAAGG 60
AAGCCCATTT TCCTAAAGGT TGGAGGTGAC AGACCCAGGC TGAGGCAGGC ATAGCTGGCC 120
CAAGATCTCC TTCTGACATG GGAGGTGGAA TCCACTGGAG AAGCCGCTGC TACCCAGAAC 180
CTTCCCATAC GTGCCTGGGC TCCAAACTGG GAGCTGGCGG ATTCCCCAGG CCTGGAAACC 240
CCCAGTAGGG TTGTCTGACT CCACCCACAC CCCACAAGGC TGGTCATTCT CAACCCTGTT 300
TCTTGGAAGG AGAAACTGGC TCATGATCAG ACGTTCTGGA ATTCACTACA GGAAGTGGCC 360
ATTGAGTGAG AGGAAAGGCC CCTGGTTAAA TGAGCCAAGA ATTCTGCATT TTGATTCCCA 420
CTCCAACATT TAAAGCCATG GGATGCAGGC TCAGACGGAC CTGGGTTCAA CTCCAGTTCT 480
GCTGTTTAAG AGCTGCCTGG TTTCTGGAAA GTTACTTACT TCACTGAGCC CTGGTTTCCT 540
CTTTTGGGAA AGGGATTATA GTATCTGCCT CAACAGGTTC TTGTGAGGAT TCTAAGAGGA 600
ACCTGTAGGG CTGATACTCA GCTGGCATGC AGATTCTAAC TTACTGCTTG GTAAACAGCC 660
ATGACTCAGA GCCCCTTGAG TGCCTCTGCC ATGCAACCCA GCATCCCCCA ACCTTCCCAC 720
CATGATTCAG CAACCAAGGG GTTAATATCT AGCCCCTCAG AAGGTCCTCA AGATCCTGGC 780
AACCCTTCTG ATTGGTTGCT GCCCATACTG AACTAAATGG GTGCCAATAA 830
|
