| Tag | Content |
|---|
EnhancerAtlas ID | HS059-40826 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr6:106439700-106441000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE41 | MA0636.1 | chr6:106440481-106440491 | GTCACGTGAC | + | 6.02 | | BHLHE41 | MA0636.1 | chr6:106440481-106440491 | GTCACGTGAC | - | 6.02 | | IRF1 | MA0050.2 | chr6:106440390-106440411 | GTGCAGAAAGTGAAAGTGGGA | - | 6.48 | | KLF5 | MA0599.1 | chr6:106440453-106440463 | GGGGCGGGGC | - | 6.02 | | TCF3 | MA0522.2 | chr6:106440185-106440195 | AACACCTGCT | + | 6.02 | | USF1 | MA0093.2 | chr6:106440480-106440491 | GGTCACGTGAC | - | 6.14 | | USF2 | MA0526.2 | chr6:106440477-106440493 | CCCGGTCACGTGACGC | + | 6.4 |
|
| | 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 |
| GH06I105991 | chr6 | 106439475 | 106446468 |
|
Enhancer Sequence | TGGAATGGTT TCTTTCTATA GGTGAACTTA TTTAGGACTA TGGAAGAATG TTTTAGTCAG 60
TGACCAGCCG CGATAATGAC TGATAAGGGC GGTTAGTGAT AAGCGATAAG GACAGGTACA 120
GACATAGGAC CGCTGGCTGG GCTCATCCAG AGCTGGCGCG CAGCCCTCTC CCTGCACTCG 180
TACTGAACTG AGTCCAGTCC AGTCCCCCAC AGGTTAGAGG TGAGACGGAA GCCATCGTGA 240
GTTTGTTTTT TCAGCGAGTG CCGTTTCCTA GGTTGGATGA CAAGCCAGCT TTGGTGGCCC 300
TTCGCTCTCG CTACCCTAAT AAACTACCTG GAGCAAGTCC TTCTTCAGAA ACAAATCACC 360
ACGTCAGCGC TCGGAGGGTG AAGCCCCTAC TACTTTCTAC TTTTGGTTGT GATGCTGGAG 420
GCCCTTACAA TTTCGCAGAA CGTTTTGTGG ACGCGCGAGC TCAGTGTTGC CCTTGCAATG 480
GGGAAAACAC CTGCTTTCCG GGTCCTCGTC CTCCCGGGAG CGCGGACCCT GAACAGCCCC 540
CGTCCGACCT CCCCGGCTCA TCACCCCCTT CCAGAAACGC ATGGAGCTCT TTTTCTTTGG 600
ACTGCCTCTT TTTTGTACTG GCCATCTCAA AATCAAACAA AACAAAAAAC AAAAGAAAAC 660
AAAACAATAT CACTCAGGTG TGAAGCCCCA GTGCAGAAAG TGAAAGTGGG ACTAATCCCG 720
GCTGCTGCAG CACCGCCGAG TGAGCGCCAG GGAGGGGCGG GGCTCCAGGG CACGGCGCCC 780
GGTCACGTGA CGCGCGTCCG CCCAATCCCA GCGGGCCCTC GCCGCGCGCA GAGCTGGGCC 840
TGGGTAGCTC TTCTCTCTCA ATGAAAGCTA TATTTTGGGC TGTTACCACC TAAACGCCAT 900
GTGGAAACAA TGCACCTCCC TCCACTTCAG GTCCCCCTTG CCTGTAAACC TCGAGAGCTG 960
GACGTCCCTT AGCCTGGGAG TTCCTGGACA CTGTGCACAA TCACTCGTCA ACCGCTACCT 1020
ACTAGGTAGG CGGGAAAGAG CTTTGCTTTC TAGGCGTGTG TCTCCAGATG GGCCCAGGAA 1080
AGATAGGGCC TCAGTTCTCT CTGGTTTGTT TGCTGGGGAG GGAGTTAGAG CTGTAAGCCT 1140
CCTTCCTCCA AAAGGATGGT TGGAGGGAGT CCGAAACCTT TGGGTCCCAA GACATGACCT 1200
AAGGAGTCCC GCTGTCGCCA CTCTTCCCGG TTTGGTAGAG GGGGCCCGTG AGTGGCATTT 1260
AGCTCTCGCA AAACTGGGCA GATAGACGCA CATGTCGACC 1300
|
