| Tag | Content |
|---|
EnhancerAtlas ID | HS150-01248 | Organism | Homo sapiens | Tissue/cell | NT2-D1 | Coordinate | chr1:205106980-205108080 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Pou2f3 | MA0627.1 | chr1:205107952-205107968 | GGTTATTTGCATAAAA | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 205107000 | 205107835 | | chr1 | 205107779 | 205107829 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I205137 | chr1 | 205106957 | 205107726 |
| Enhancer Sequence | AATATATGAG GATGTTACAT CTACTCCTTT GCCAGTATCT ATAATTTTTA AAAATTGTAA 60
GCAAATCCTG CTCAGTAAAA TGTCTTAGAC TAACCATCGT GTTTCTCTAT GGTCCCAGCT 120
TAGAACCTGG AGCAGTTCCC CTTATTTTCA GAGCCAGTGG CTTCACATTG AGCCTGACAT 180
TTGCCTCTTA AACTCCTGCT TCCACACATA GAAAGGCTCT GAGTTAGCCT TTACCTAGAT 240
GCTTGAGGGT CTTTGTGATT CATGGGGAAG CCATGCTGAG AAAATAAGGG ACGAAGGAAA 300
GAGAGAGGAA ATAGAAGCCA AGGCAGTCTT CATAGGTTGA AAAATACTCC AGAGATTTAG 360
AAATGTCCTT CCCAGAGACC AAGTTGTGGC CTCTCTGTGT CAGGCCCCAA TCTGTCAATC 420
TTCTTTCACG ACCTTGCCTC CCAGTAGTGC CAGAAGGGTG GCTGTGGAGG TCAAGGAGCC 480
CAAGAGGTGA ACTGTAGCGA CCATGTGTCA CCTGGCACCT GTCCTGAATT TAGGTCCCTT 540
TTCTAACTGC TGCTTGATTA CTTTTCAGGA GTTATATCTC CTCCAATGAA TGTAATTTTT 600
AGTGAGCAGG CAAATTTAGG TGCCTGCCTC CCATCATGGA ATCTGAAGGG GACAGATCCT 660
TCCAGTTCTG AACCAGTAAA GCTAGAAGAT GGGCCTGGGA CCTATGCTGG GCCAGTCGAG 720
AAAACGCGCC CTGGCTGCTA ACTCATGAGG GAGTAAAGAT GGTTCATCAT AGCCTTAGAC 780
AGGCCTTTGC AAAAGCTTGC AAAGCTGCTC TGGTTCTAAG GGAGGAGACC ACCCCTCATA 840
TTGTCTTGTG CCCAATTTCT GCCTCCAAAG AAAGAAGAAG TAAAAACTAA AAGGCAGAAA 900
TGAAATCCAC AAGCAGACAG CCTGGCGCCA CACCCTGGGC CTGGCAGTTA AAGATCGACC 960
CCTGACCTAA TTGGTTATTT GCATAAAAAA GGCACTGTGA AGATCCTGTC CTGTTCAGTT 1020
CCTTTCTAAT TACCGGTGTA TGCAGCCCCC AGTCACGTAC CCCCTGCTTG CTCAATCGAT 1080
CACGACCCTC TCACGTGGAC 1100
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