| Tag | Content |
|---|
EnhancerAtlas ID | HS098-47334 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:179793020-179794340 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr5:179794158-179794173 | AGGTCACGCAGCCCT | + | 6.37 | | KLF4 | MA0039.3 | chr5:179793530-179793541 | GCAGGGTGTGG | - | 6.62 | | MAX | MA0058.3 | chr5:179793419-179793429 | ACCACGTGCT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 179793346 | 179793679 | | chr5 | 179793724 | 179793803 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH05I180366 | chr5 | 179793361 | 179793510 | | GH05I180367 | chr5 | 179794321 | 179794470 |
|
Enhancer Sequence | TCTTCCGGGT ATGCCTGTAA TTCATGATGT GGATTTTAAA GTAAAGACTC TTATGACCAT 60
GATACCAGTA TCACAGCAAA CAAAACTCAT AATACCTTAA TAGTATCTAA CACTCACTTC 120
CTATTCCTAC TTCCTCGATT GTCTCAAAAA CATCTTTTTA CAGCTTGTTG GTTCAAATCA 180
GTGTACAAAC AGTATCCACA CATGGCTAGT GTGTTTCTAA GACTTGTAAA ATACGGAATC 240
CATGAGAACT TTCACAACTT CCCCATGCCA TTCGCTCTCC CATCTTGGGG TGGTCTGAGA 300
GTAGCAAGTG TTTTTACAGC CTGCAAACCC TCTGTAACTG TGCTCCCGTG AATGTCCATT 360
TCCTGCCTGG CCCGGAGCAG GCACTGAGAC TGTGTGGGCA CCACGTGCTG CTGGAAAAGC 420
AGCAGCCCCA GGGCCCGGAG CCCAGAGTGG CCGGAGATGT GAAGACAAGG GAGGGATGTG 480
TAGAAATGCC GGTGCCCACA AGAGGCGGCT GCAGGGTGTG GACAGTCCTG GCTCCATAGT 540
TGGGCTGGCC AGGGCCGAGC CTTGACTCCC TGCGGCTTCG AGCCTCTGGC ATTCTCCTCT 600
TGCATCAGAC GGAGGCAGCT GGCACTCTCA TACACTGCTG GGGAGAGTAT CCATGGGTAC 660
AACTTTCTTT TTTGTTTGTT TGATTTTTTT GAGACGGAGT CTCACTCTGT CATCCAGCCT 720
GGAGTGCAGT GGCGCGATCT CAGCTCACTG CAATTTCTGC CTCCCAGGCT CAAGAGATTC 780
TCATGCTGGG ATTACAGGCA TGCACCATCA TGCCTGGCTA ATTTTTGTAT TTTTAGTAGA 840
GACGGGGTTT CGCTATGTTG GCCAAGCTGG TCTCGAACTC CTGGCCTCAA GTGATTGTCC 900
CACCTCGGCC TCCCAAAGTG CTGGGGGTAC AACTTTCTAG AGAGAAATTT GGTAGTATAT 960
ATGAACGACC TTAAAATGTC TATTTTCTGA CGCATTATTC TAATGGGATA ATGAACAACT 1020
GGGCAAAAAA TATTTGAGAT GTTCACCTGG TGCTGTTTAT ACTTAGCAAA CGTTGAAAAT 1080
AACCCACATC CCTCAATAGG GACGGGTTAC GTGAAGAATG GAACATGCCC ACCAGGAAAG 1140
GTCACGCAGC CCTGAGACTC AGACACAGGT TATATTGCTA AGCAGAAGAA GAGGGCTACA 1200
GCAACGTTGT TGTATTGCAT AATCCTCATT GTGCTCTTGC TTTATTTTTA ACAGCTTTAC 1260
TGAGATATAA TTCACTTACA TACAATTCAC CCGCTTAATG TGTATAAAAT AGGGAGTGTT 1320
|
