| Tag | Content |
|---|
EnhancerAtlas ID | HS081-03363 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr11:13181830-13182870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr11:13181866-13181879 | TGCAGCTGTCCCC | + | 7.12 | | NFAT5 | MA0606.1 | chr11:13181844-13181854 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr11:13181844-13181854 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr11:13181844-13181854 | ATTTTCCATT | + | 6.02 |
|
| | 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 |
| GH11I013159 | chr11 | 13181514 | 13182931 |
|
Enhancer Sequence | AGATAATTCA TCCCATTTTC CATTTGTGAC CCACCTTGCA GCTGTCCCCC TGACATGCCT 60
TAGTTGTTTT CTGTCACAAC CCTATTGTTT GGGAAAATAT TCTCATCTGG TTACACGACT 120
GTTGAAACTT GCCTGTAAAA TGATGAGCCA CTTGCGGCAA TGCCACAGCC TAGGGAATTA 180
GTTGCTATTA AAATCGTGTT CAAACCAGGG CGTTGCCAAG GTGCCGACGT CTTGGGAAGC 240
TGCCTGGAGG GCTTTGGCTC TCTAACAAAG ACTTGAAGAT GGCAGAATCT CAGTGGGGTT 300
TCTAAATCAT GGACAGGCAG ACAATTTGAG GCCACAATCG CCTGGAGACC ACTCTAAAAG 360
CCTTAGTGAG TGAAACCTCC TGGGTTTTAA AAGCTTTTAA TTCACAAGAG CCAGATGTGG 420
CCAATGTGGG CAGGTAAAGT AGGGAAGCTT TGAGCTGAGA ACCAAAGCCA GAAAAAAGAA 480
AGGTGAAGAA AAGCATGTCA TTGACCCATT TTTCACTTTC TCCATCATAT GCAGCTATTC 540
ATAAACCCAG AACACTTATC CAAATAGCAA TTAATACACA GACTAGCATG TTCCTGCTTG 600
TACCTGAAAG TTGTAAATGG CAGTAAAGTC AGCCGTGTGT AAATGGTGTA GTGACGTGTG 660
TGAGACATAC CAGCACAAGA CATGCCCACA CTTTTCATTT TTTGTCAAGT CTGGATTAGC 720
CTGAGAGAGG GGACTGTAGG CGTGAATCAT ACAGCCAAGG ACCTGGAGTC TCTCCTTTTG 780
TGTTAGTGTG GGATGTATCA GAATAATGGT CCTCGCAGCA GGCTGGTGCT TCCAGTGGCA 840
TTTTTCTCAG GCTAATGTTA AAGTTAATTT GCATTCCCTG ATCCCACCCA GACTCTTCTT 900
TCCAGGGTCA GTGAGGTGGA AGGGGGAGTG GGTTGAAGCT GTCAAGAAGC TCTGTAGACT 960
TGTCCTTGTA TAAGTGGTCT TCACATTTTT CTTTTACTGT CATACTTTCT AAAAGAATTT 1020
TGAAAACCTA TATGCATTTG 1040
|
