| Tag | Content |
|---|
EnhancerAtlas ID | HS197-03500 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr11:13181570-13182890 |
Target genes | |
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 | AACCAAGGGA TGAATTTGCT GCTTCAGGCC AGTGTGTCCA GCCAGAGCTT CTGGGTAGCG 60
ACTTTTTCTT CCATTCAAAA CTTGGGTTGG AACTGGAGAG TAATTCTTCT AATAATCTAC 120
ACCCACTGGC AGCTATTTTC CTTGAATATA AACTCCTTCT TGCATGTTAC AAATATTCCA 180
AAAAATCTGC CCATAGTTGC AAACAACTCC CTTCCCTTAG AAACTATTAC AGATTTAAAT 240
AAGTAATCAC TCCAGAAAGT AGATAATTCA TCCCATTTTC CATTTGTGAC CCACCTTGCA 300
GCTGTCCCCC TGACATGCCT TAGTTGTTTT CTGTCACAAC CCTATTGTTT GGGAAAATAT 360
TCTCATCTGG TTACACGACT GTTGAAACTT GCCTGTAAAA TGATGAGCCA CTTGCGGCAA 420
TGCCACAGCC TAGGGAATTA GTTGCTATTA AAATCGTGTT CAAACCAGGG CGTTGCCAAG 480
GTGCCGACGT CTTGGGAAGC TGCCTGGAGG GCTTTGGCTC TCTAACAAAG ACTTGAAGAT 540
GGCAGAATCT CAGTGGGGTT TCTAAATCAT GGACAGGCAG ACAATTTGAG GCCACAATCG 600
CCTGGAGACC ACTCTAAAAG CCTTAGTGAG TGAAACCTCC TGGGTTTTAA AAGCTTTTAA 660
TTCACAAGAG CCAGATGTGG CCAATGTGGG CAGGTAAAGT AGGGAAGCTT TGAGCTGAGA 720
ACCAAAGCCA GAAAAAAGAA AGGTGAAGAA AAGCATGTCA TTGACCCATT TTTCACTTTC 780
TCCATCATAT GCAGCTATTC ATAAACCCAG AACACTTATC CAAATAGCAA TTAATACACA 840
GACTAGCATG TTCCTGCTTG TACCTGAAAG TTGTAAATGG CAGTAAAGTC AGCCGTGTGT 900
AAATGGTGTA GTGACGTGTG TGAGACATAC CAGCACAAGA CATGCCCACA CTTTTCATTT 960
TTTGTCAAGT CTGGATTAGC CTGAGAGAGG GGACTGTAGG CGTGAATCAT ACAGCCAAGG 1020
ACCTGGAGTC TCTCCTTTTG TGTTAGTGTG GGATGTATCA GAATAATGGT CCTCGCAGCA 1080
GGCTGGTGCT TCCAGTGGCA TTTTTCTCAG GCTAATGTTA AAGTTAATTT GCATTCCCTG 1140
ATCCCACCCA GACTCTTCTT TCCAGGGTCA GTGAGGTGGA AGGGGGAGTG GGTTGAAGCT 1200
GTCAAGAAGC TCTGTAGACT TGTCCTTGTA TAAGTGGTCT TCACATTTTT CTTTTACTGT 1260
CATACTTTCT AAAAGAATTT TGAAAACCTA TATGCATTTG CACATTTTTA AGTTGACATC 1320
|
