| Tag | Content |
|---|
EnhancerAtlas ID | HS176-07624 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr11:76474610-76475360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| 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 | GATGCTTACT GCTTCAAAGG AAGCCCATTT TCCTAAAGGT TGGAGGTGAC AGACCCAGGC 60
TGAGGCAGGC ATAGCTGGCC CAAGATCTCC TTCTGACATG GGAGGTGGAA TCCACTGGAG 120
AAGCCGCTGC TACCCAGAAC CTTCCCATAC GTGCCTGGGC TCCAAACTGG GAGCTGGCGG 180
ATTCCCCAGG CCTGGAAACC CCCAGTAGGG TTGTCTGACT CCACCCACAC CCCACAAGGC 240
TGGTCATTCT CAACCCTGTT TCTTGGAAGG AGAAACTGGC TCATGATCAG ACGTTCTGGA 300
ATTCACTACA GGAAGTGGCC ATTGAGTGAG AGGAAAGGCC CCTGGTTAAA TGAGCCAAGA 360
ATTCTGCATT TTGATTCCCA CTCCAACATT TAAAGCCATG GGATGCAGGC TCAGACGGAC 420
CTGGGTTCAA CTCCAGTTCT GCTGTTTAAG AGCTGCCTGG TTTCTGGAAA GTTACTTACT 480
TCACTGAGCC CTGGTTTCCT CTTTTGGGAA AGGGATTATA GTATCTGCCT CAACAGGTTC 540
TTGTGAGGAT TCTAAGAGGA ACCTGTAGGG CTGATACTCA GCTGGCATGC AGATTCTAAC 600
TTACTGCTTG GTAAACAGCC ATGACTCAGA GCCCCTTGAG TGCCTCTGCC ATGCAACCCA 660
GCATCCCCCA ACCTTCCCAC CATGATTCAG CAACCAAGGG GTTAATATCT AGCCCCTCAG 720
AAGGTCCTCA AGATCCTGGC AACCCTTCTG 750
|
