| Tag | Content |
|---|
EnhancerAtlas ID | HS059-30387 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr22:29351650-29353150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Twist2 | MA0633.1 | chr22:29351652-29351662 | ACCATATGTT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 29351757 | 29351953 | | chr22 | 29352046 | 29352325 | | chr22 | 29352473 | 29352647 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I028955 | chr22 | 29351881 | 29352070 |
| Enhancer Sequence | AAACCATATG TTTTGGGAGG CTGAGGTGGG AGGATCACCT GAGCCCAGGA GTTCAAGACC 60
AACCTGGGCA ACATAGCGAG ACCCTGTCTC TATTAAAAAA AAAAAAAAGA GCCAGGCATG 120
GTGGCTCGTG CCTGTGGTTC CAGCTACTTG GGAGGCCTAG GTGGGATGAT CACTTGAACC 180
CAGGAGGTCC GGGCTGCAGT GAGCCAGGTT CACATCACTG TACTCTGGCC TAGATGACAG 240
AGTGAGACCT TGTCTCAAAA GAAAACCACA TCAGTAAGCC ATCTTCTCGT TTGCCTCACT 300
AACATCCTGT TGAGGTGTCC CACAAACCAA ACAGGATGTG GGGGTGCGGA GGATTATCCC 360
CTCTAGGAGC AAGTTGCCCC ATCTGGTTGA GGGAGAGGTG GTTCTGTCAC CAGTAGAGCA 420
TGTTGAGTGC TGCAGAGATG GCTGGCGACG GGGATGTCTG GCCTGGCAGA TGTCACCTTC 480
AAGGAGGGAG TGTGCTCATT GCAGGCTGCT TTCTGGGATG GGAGTAGGCT AGTAATGTGA 540
TGTGTGGGGC CTTCCCTGAA ATAGAAGGCA CTGGACAGGC ATGTAGTATG GATAAGGTAG 600
AGAGGGTGAT GGATAGTTTT GGCTTTCCTT GTGAGGTGGG CATGCTGGTG GCATGTTTTA 660
GATTTTCCGA ATGGCCTTTG TTTCCATTTC CTTTTTTTTT TTTTTTTTTT TTTTTAAAGC 720
TGCATCCTTT TGCATCGAAT GAAACCCCAT CAAGGGCATC TCCTAACTCT TCTTCCATTC 780
TCTTGTCCAG GGCTGGTGTT TTTTGTGTGT TTGTGACTGA CAATGCAGCA TGGAGAATTT 840
GGAGAAGCTA GTTTTGCCTT TTCTCCTACA GGAAGAGGGA CTCGTCTGCA AAGAAAGGGG 900
TCTGCCTTTC AGTCCTTTGA AGCCACCTGG TCTGACAAAG ACAGTTTCCC TGTCCCTTTT 960
TGGACCTTGA GCTGAGCAAA AAATTACTTA GTTGCTGAAA GCAGGTCAGT GTAGAGGACT 1020
TCCTCTACTC CTGCTTTGAC TTCATCTGCA AGAGAGCTGA GAACTGAGTG AGGCATTTCT 1080
GCTTCTTGAG ACTTCTCTTG GTGTGGCAGG GCTTCCTGTC CAGGAGGGGC TCCATTGCCT 1140
CATGCCCTGG GTATAAACAG TCCCAGAGGG CTTTGGAATC AGCCTGGGTC AATTCTGGAG 1200
GAAAAATAAG GCCTAATAAG CATGGCTCTT TTCCCAAAAT GTAGCCACAG GGGTCTAAGC 1260
AGCTGATTGT GGGGTCCAGG GCCACCAGGA GTCTTGGCTG GCCTAGCATA TCTTGATTTG 1320
TTAAGAAGGT GGATATGAAT TCAGTCTAGA GAAGATAACG TGCCTATTGT GCAGAATGCA 1380
GGGCTTTTTG TTCAAGGCTG TCTCCATTTG GAAGTAGAAT GACAAAGCAG TGTAGATTTA 1440
CACAGAGCAT CTCTGAGTCT GTTACAACCC TTAAGTTTTA TGGTTTCGAG CCAGGACAGT 1500
|
| |
|
|
|
