| Tag | Content |
|---|
EnhancerAtlas ID | HS073-12608 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr6:106439660-106440910 |
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 | TGTAAGAACA AATGAATGGG CCAAGCTCAT GTTAGTGATC TGGAATGGTT TCTTTCTATA 60
GGTGAACTTA TTTAGGACTA TGGAAGAATG TTTTAGTCAG TGACCAGCCG CGATAATGAC 120
TGATAAGGGC GGTTAGTGAT AAGCGATAAG GACAGGTACA GACATAGGAC CGCTGGCTGG 180
GCTCATCCAG AGCTGGCGCG CAGCCCTCTC CCTGCACTCG TACTGAACTG AGTCCAGTCC 240
AGTCCCCCAC AGGTTAGAGG TGAGACGGAA GCCATCGTGA GTTTGTTTTT TCAGCGAGTG 300
CCGTTTCCTA GGTTGGATGA CAAGCCAGCT TTGGTGGCCC TTCGCTCTCG CTACCCTAAT 360
AAACTACCTG GAGCAAGTCC TTCTTCAGAA ACAAATCACC ACGTCAGCGC TCGGAGGGTG 420
AAGCCCCTAC TACTTTCTAC TTTTGGTTGT GATGCTGGAG GCCCTTACAA TTTCGCAGAA 480
CGTTTTGTGG ACGCGCGAGC TCAGTGTTGC CCTTGCAATG GGGAAAACAC CTGCTTTCCG 540
GGTCCTCGTC CTCCCGGGAG CGCGGACCCT GAACAGCCCC CGTCCGACCT CCCCGGCTCA 600
TCACCCCCTT CCAGAAACGC ATGGAGCTCT TTTTCTTTGG ACTGCCTCTT TTTTGTACTG 660
GCCATCTCAA AATCAAACAA AACAAAAAAC AAAAGAAAAC AAAACAATAT CACTCAGGTG 720
TGAAGCCCCA GTGCAGAAAG TGAAAGTGGG ACTAATCCCG GCTGCTGCAG CACCGCCGAG 780
TGAGCGCCAG GGAGGGGCGG GGCTCCAGGG CACGGCGCCC GGTCACGTGA CGCGCGTCCG 840
CCCAATCCCA GCGGGCCCTC GCCGCGCGCA GAGCTGGGCC TGGGTAGCTC TTCTCTCTCA 900
ATGAAAGCTA TATTTTGGGC TGTTACCACC TAAACGCCAT GTGGAAACAA TGCACCTCCC 960
TCCACTTCAG GTCCCCCTTG CCTGTAAACC TCGAGAGCTG GACGTCCCTT AGCCTGGGAG 1020
TTCCTGGACA CTGTGCACAA TCACTCGTCA ACCGCTACCT ACTAGGTAGG CGGGAAAGAG 1080
CTTTGCTTTC TAGGCGTGTG TCTCCAGATG GGCCCAGGAA AGATAGGGCC TCAGTTCTCT 1140
CTGGTTTGTT TGCTGGGGAG GGAGTTAGAG CTGTAAGCCT CCTTCCTCCA AAAGGATGGT 1200
TGGAGGGAGT CCGAAACCTT TGGGTCCCAA GACATGACCT AAGGAGTCCC 1250
|
