| Tag | Content |
|---|
EnhancerAtlas ID | HS164-08243 | Organism | Homo sapiens | Tissue/cell | Raji | Coordinate | chr22:22020420-22021800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr22:22021236-22021247 | AACCACTCAAG | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr22:22020881-22020896 | GAGGTCAGGAGTTCA | + | 6.22 | | Zfx | MA0146.2 | chr22:22020857-22020871 | GAGGCCGAGGCGGG | - | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTAAGTTGAG CCGCAGTCGG GAGCGGCGCT CCACTCTGCC TCAGTGAACC GCCTGTCCCG 60
CACTGCGCGC CGCTCGCCTT CCCTCTCAGC TACTCCCCAG AGCACAGCCC AAAGGTCACT 120
TCCTCCCGGA AGCTGCCGCC CTGTCTCCAG TCAGGGTAAT GACCCTCGGG CCGCCGCGCT 180
CTCCCGGGGC CGCGGCTCCG ATGACGTCAG CTGCGGGCTC GAGCGCAGCC CGGTTTTCCT 240
TACTCTGGTT CTGCCCGGAC CGTCCCCCGT CTGTTCGCGA GTTTCGCCCT TGAATGAGTA 300
GTCTCTACCT CTTCCGTACT TCACGTCTCG CTGTGTTCTG GTTCATGCCT ATCAGCCTGC 360
AAACGTGCTG CAGAGCCTTC TAATTTAAAG CAAACCAGGT CGGGCGCAGT GGCTCACCTG 420
TAATCACAGC ACTTTGGGAG GCCGAGGCGG GCGGATCACC TGAGGTCAGG AGTTCAAGAC 480
CAGCCTGGCT AATACGGTGA AACCCCGTCT CTACTAAAAA TACAAAAATT AGCGGGGCGT 540
GGTGACGGGC GCCTGTAATC CTAGCTATTT GGGAGGCTGA GGCAGGGGAA TCGCTTGAAC 600
CCGGGAGGCG GAGGTTGCGG TGAGCCGAGA TCGTGTCACT GCACTCCAGC CTGGGCGACA 660
GAGCGAGACG CTGTCTCAAA AATAATAAAT AAAATTTAAA AATCCACCCG TGCCCCGTGC 720
CCCACGTCCC ACGTTCCCCT CCCGCTGCCG CCGTGTTGTT TCTCTTAAGA ACAAGTGAGA 780
GACTAGTGGC TTCATGCTGT TTTCTGAGTC TCTTGAAACC ACTCAAGTCA GAATTTCGAC 840
CCCAGAACTG TTGGGCTTCT CAACAGTATG TCACACCGTT GACCACTCCC TCTTTCTGAA 900
GCCCTCCTTT GGTATCTGGG ATTTCACCTG CTCTTTGTTT TCTCTCGACT TCAGCGGCCT 960
CTCTTTTCAG GTTCCCAGCG ACTTCTTGTT GCTAAATATA GTATTCAATC CTCAGTCCTC 1020
ATTTTTTTTT TTTTTTTTTT TTGAGACGCA GTTTCGCTCT TGTTGCCCAA GCTAGAGTGC 1080
AATGGTGAGA TCTTGGCTCA CCGCAACCTC CGCTTCCCGG CTTCAAGAGA TTTTCCTGCC 1140
TCAGCCTCCC GAGTAGCTGG GATTACAGGC ATACGCCACC ATGCCCAGCT AATTTTGTAT 1200
TTTTAGTAGA GAAGGGGTTT CTCCATGTTG GTCAGGCTGG TCTCGAACTC CTGACCTCAG 1260
GTGATCCACC TGCCTCGGCC TCCCAAAGTC CTGGGATTAC AGGCGTGAGC CACCGCGTCT 1320
GGGCAGCCTC AGTCCTCATT TTGTTGGGCT TCTCAACAGT ATGTCCCACT GTTGACCACT 1380
|
| |
|
|
|
