| Tag | Content |
|---|
EnhancerAtlas ID | HS175-04798 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr11:76474400-76475880 |
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: 4 | Chromosome | Start | End |
| chr11 | 76474777 | 76474856 | | chr11 | 76474549 | 76475408 | | chr11 | 76475426 | 76475558 | | chr11 | 76475707 | 76475810 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I076763 | chr11 | 76474293 | 76475698 |
|
Enhancer Sequence | TACCTGTTAA GCACCCAACT TCTCCACCAG CCCGGACCCA GGTGAGGCTG GAACCAGGTG 60
AAACAGGACC CAGGTAAGGC TGGACCCAGG TAAGGTGGGA CTCAGGTGGC ACAGGGCATG 120
GGAGGTACTC TCTAAATAGT TGTTCAATGT TAAAGGAATG GATGAACAAA TGAATGAATA 180
GCCAGGTCCA CAGGAATACT TTGGTAACAA GATGCTTACT GCTTCAAAGG AAGCCCATTT 240
TCCTAAAGGT TGGAGGTGAC AGACCCAGGC TGAGGCAGGC ATAGCTGGCC CAAGATCTCC 300
TTCTGACATG GGAGGTGGAA TCCACTGGAG AAGCCGCTGC TACCCAGAAC CTTCCCATAC 360
GTGCCTGGGC TCCAAACTGG GAGCTGGCGG ATTCCCCAGG CCTGGAAACC CCCAGTAGGG 420
TTGTCTGACT CCACCCACAC CCCACAAGGC TGGTCATTCT CAACCCTGTT TCTTGGAAGG 480
AGAAACTGGC TCATGATCAG ACGTTCTGGA ATTCACTACA GGAAGTGGCC ATTGAGTGAG 540
AGGAAAGGCC CCTGGTTAAA TGAGCCAAGA ATTCTGCATT TTGATTCCCA CTCCAACATT 600
TAAAGCCATG GGATGCAGGC TCAGACGGAC CTGGGTTCAA CTCCAGTTCT GCTGTTTAAG 660
AGCTGCCTGG TTTCTGGAAA GTTACTTACT TCACTGAGCC CTGGTTTCCT CTTTTGGGAA 720
AGGGATTATA GTATCTGCCT CAACAGGTTC TTGTGAGGAT TCTAAGAGGA ACCTGTAGGG 780
CTGATACTCA GCTGGCATGC AGATTCTAAC TTACTGCTTG GTAAACAGCC ATGACTCAGA 840
GCCCCTTGAG TGCCTCTGCC ATGCAACCCA GCATCCCCCA ACCTTCCCAC CATGATTCAG 900
CAACCAAGGG GTTAATATCT AGCCCCTCAG AAGGTCCTCA AGATCCTGGC AACCCTTCTG 960
ATTGGTTGCT GCCCATACTG AACTAAATGG GTGCCAATAA ATGCTCTGTA AACTACAAAG 1020
TGCTGGCTAA CCCCAGATCC ACACTTCCAG CTCCAATTTA TCTCCTGGAG GCTCTTCACC 1080
CACCTCCCGG CCCTTCCACC TTCATACTTC ATGCAAATGG CACTCTCACA ACTCCCAAAT 1140
TGAACTGAGT TTCTCCAGTT AAACTCATCC CAGGGACTGC CTCCACCTCT GCCTGGCAGA 1200
CTCCTTCATT ACCCAGTCTC TATCTGGCAG TGCTGTTTCC TCTATGTCCC CTAGCTCTGT 1260
CCCTCCTTCC TGCCCCCACC CACCTGGTGC CTTCATCATT TCTCTGCTAA ATCACAACTA 1320
CCTTCCCACT GGCCTCTGGA CTCCAGTGTG TCCTTCCACA TCATTCTCAC ACTGTAGACA 1380
GAATCACCTT CCAAAAGCGG GGTCTCTCAT TGAGCCCTCA GTGAAACGTC AGCCACCATT 1440
GACATCCCTC AGTAATGATC ATTGGAGGTT TGGTTCCTGG 1480
|
