| Tag | Content |
|---|
EnhancerAtlas ID | HS108-38893 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:23133230-23134620 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr8:23133683-23133697 | ATGACTCATTCCCC | - | 6.2 | | JUN(var.2) | MA0489.1 | chr8:23133678-23133692 | GGAAGATGACTCAT | + | 6.77 |
|
| | 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 |
| GH08I023275 | chr8 | 23133402 | 23134120 |
|
Enhancer Sequence | CTCCTGCCTC AACCTCCTGA GTAGCTGGGA TTACAGGCAC CCACCAACAC GCCCGGCTAA 60
TTTGTATTTT TAGGGGAGAC AGGGTTTCAC CGTGTTGGCC AGGCTGCTCT CGAATTCCTG 120
ACCTCAGGTA ATATCCTTGC CTCGGCCTCC CAAAGTGTTG GGATTACAGG CATGAGCCAC 180
CATGCCGGGC CATAAATCTG CATTTGGAGG TAGTGTCCAA ATTTCTGCAA AGTCATTTCA 240
TTGTAAGGAG ACCTTCACAG GAGATCCCCT CACTCCATCT GAGTTCCCAT GACTCTGCCC 300
TTTAAGAAGA GGCTAGAACT CTGGAGAGGT TGAGGTCTCC TGGGAACTGA GGGACAACAA 360
AAGTGTCAGA GATTTGGGGG GTGTGGCGGG GACTCTCCTG GCTGGCATGG CACACACACA 420
CAGGCTAATC AGGTAGAGCG AGAACTAGGG AAGATGACTC ATTCCCCTCT CCCACCAGCC 480
CCTGCGCCTC CGCACCCTCC CCTCTCTCCC ACTTTCCCTC TCTAGTTTTG GCCCTTTCTC 540
CACCATCTCT GCCTTTCTCT GCCCTTTTAT CACTCCCACC GCCTTGGCTC CAGAATGGTC 600
TTCACTTCTG GAAACAGCTG TGGCTTATAA GAGTTTCTTA GTTGATTTTC TTGGATTTTT 660
TAGGTTAAAA AAAAAAAAAA TCAAAGGTCG GGTGTGGTGT CTCATGCCTG TAATACCTGC 720
ACTTTGGGAG GCTGAGGCGG GAGGATGGCT TGAGCCAGGA GTTCAGGACC AGCTTGGGCA 780
ACATAGTGAG ACCCCCGTCT CTACAAAAAA TACAAAAATT AGTCTGGTGT GGTGGTGTGC 840
ATCTGTAGTT CCAGTTACCG GAGGCAGGAG GATGGCTTGA GCCCAGGAGT CCAGGTTACA 900
GTGAGCTACG ATCATGTCAC TGCACTCCAG GCTGGGTGAC AGAGGGAGAC TTTGTCTCAA 960
AAACAAACAA CAAACAAACA CAAAAACCAC CAAAAACACA AATATTCTGC AAACAATGAG 1020
AAGTTGATCA CCTCAAATGT CTAAACTTTC CAGTTTTTAT GTCTTTTTGT CAATTTGCTT 1080
TTGTTAATAC CTCTTTAAAA AAAGGTAAAC ACTAGAGGCA TGGGTACATA GCCTTGACTT 1140
GTCCTGAAGT GAATATGGTT CCTCTGTGCT TCTCCATTTA GCCGTGTGTG GTGTTTTGAT 1200
CATTTTATTT AGATCCTTAA ATGAATTTGC GTAGAGTTGT TCTAACTGTG AGTTGGGTAA 1260
AGAACATATA ATAATGTTTC GCTTTTTGAA ACATTCTCTC TGTCACCCAG GGTGGAGTGT 1320
GCAGTGGCGC AGTCTCGGCT CACTGCAAAC TCTGTCTCTT GGGTTCAAGC GATTCTCGTG 1380
CCTCAATCTC 1390
|
