| Tag | Content |
|---|
EnhancerAtlas ID | HS088-35485 | Organism | Homo sapiens | Tissue/cell | HeLa-S3 | Coordinate | chr22:41982920-41984380 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr22:41983892-41983907 | GATTAAAAATTAACT | + | 6.21 | | Zfx | MA0146.2 | chr22:41983031-41983045 | GAGGCCGAGGCGGG | - | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 41983447 | 41984096 | | chr22 | 41983691 | 41984236 |
| Enhancer Sequence | AGACCAGCCT GGCCAACATG GTGAAACTCT GTTTCTACTA AAAATTAAAA AAAAAAAAAA 60
AAAAAAATTG GCCATGCGCG GTGGCTCACG CCTGTAATCC CAGCACTTTG GGAGGCCGAG 120
GCGGGTGGAT CACAAGGTCA GGGGATTGAG ACCATCCTGG CTAACATGGT GAAACCCTGT 180
CTCTACTAAA AAATACAAAA AAATTAGCCG GGCGTGGTGG CACGCGCCTG TAGTCCCAGC 240
TACTCGGGAG GGCTGAGGCA GGAGAATGGC GTGAACTTGG GAGGCAGAGC TTGCAGTGAG 300
CTGAGATCAC GCCACTGCAC TCCAGCCTGG GCGACAGAGC GAGACTCCGT CTCAAAAAAA 360
AAAAGAAAAA AAAATTAGCT GGGCGTGGTG GCAAGCGCCT GTAATCCCAG CTACTCAGGA 420
GGCTGAGGCA GGAGAATCCC TTGAACCCGG GAGGTGGAGG TTGCAGTGAA CCGAGATCAT 480
GCCATCGCAC TCCAGCCTGG GGGACAAGAA TGAGATTTCA TCTCCAAAAA AAAAAAAAAA 540
AAAAGATATT AGCCAGGCAT GGTGGCACTT GCCTGTAGTC CCAGCTACCA GCTACTCCAG 600
AAGCTGAGGC GGGAGAATCA CTTGAGCCCA GGAGTTCGAG GCTGCAGTGA GCTGTGATAG 660
CGCCACTGCA CTCCAGACTG AGTGACAGAG TGAGACCCCG GTCTCTAACA ACAACAACAA 720
CAAAATAGCA TCACAATCAA GTTGATTTTT GAGGAGCCAA AGAACAATAA CAAAAATAGC 780
CTCACAAAAC AATGCTTAAT ATTTGCTCTG GGCAAATAGA TCCAGATAAA GGCCTGGAGG 840
GAAGCCACAC CACAGTAACC ACATTAACTT GGGGAGCCGG CCAGGCTCCC CAAGTGCGGT 900
CAGAGTGGAC TTTACCCTTC TCTGTTACGT TTCCATTCTT TACCAGGAGA GTGTGCTCAT 960
GAAAATGTGT ACGATTAAAA ATTAACTTTC AAAAGGCACT AAGCACAGAG GCTGGCCCGT 1020
AGACAAATTA ATAGGCTGTT CTTATTCAGG TTGTTATGTT TGTGGAGCAA AAGGTCAGAG 1080
GGAGGAGTCA GAACTGTGCC TAGGCCCTGC CACTTTTGTT CCAGTTCTTT TATTCATTTA 1140
TTTGTTTGTT TGAGACGGAG TTTCACTCTT GTTGCCCAGG CTGGAGTGCA ATGGCACAAT 1200
CTTGGCTCAC TGCAACCTCC ACCTCCTGGG TTCAATCGAT TCTCCTGCCT CTGCCTCCCC 1260
AGTAGCTGGG ACTACAGGCA CACGACACCA CGCCCATCTA CTTTTTGTTT TGTTTTGTTT 1320
TGAGACTGAG TCTCCCTCTG TCGCCCAGGC TGTAGTGCAA TGGCACATTC TCGGCTCACT 1380
GCAACTTCTG CCTCTCGGGT TCAAGTGATT CTCCTGCCTC AGCCTCCCGA CTAGCTAGGA 1440
TTACAGGTGC ATGCCACCAC 1460
|
| |
|
|
|
