| Tag | Content |
|---|
EnhancerAtlas ID | HS108-37517 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr7:100221500-100222640 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr7:100222568-100222579 | GAGCCATAAAA | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 100221882 | 100222165 | | chr7 | 100221691 | 100222200 |
| Enhancer Sequence | CTTCTCTACC AAAAAAAAAA AAAAAAAAAA AAATTAGGCA TGGTTGTGCG CGCCTGTAGT 60
CCCAGCTACT CGGGAGGCAG AAGTGGGAGA ATCACTTGAA CCCGACAGGC AGAGGTTACA 120
GTGAGCCGGG ATCGCGCCAC TGCACTCCAG TCTGGGTGAC ATTAAGACAC TGTCTCCAAA 180
AAATAAAGAA AGAAAAATAA ATAAAAATAA AAACTCCCCT TTGCTCACAT CACCTCTCTG 240
CTCAAAAACC TCTCTAATTT CCTTGATGCT AAGACCCTTA ACATCCAAAC TTCTAATCCT 300
GGTGTTCGAG GCTCCCCACA GTTGATCGAT AACACCACAT TTGGTGGTCC CCTCCCCTCT 360
GCCTCTTCAT GGGGCCCCTG TTCTGGCTCT GCTGGTCCAC ACCCCGCTTC CAAGTAAAAC 420
CAGACTGATT TCACTGCCAC ACCCGAATTC TGGTCTCTCC ACCCTGAAAT GTCCTCTTTA 480
CTTTGCATCA ATCCACATCC TGCCTGTTCT TCAAGATCCA AGTCACAGTC TAAAGCCAAG 540
GTCAGCAAAC TTTTTCTGTG AAATGCCAGA TAGTAAATAT TTTAGATTTT GCAGGCCATG 600
CTGCTTTTAT TGCAGCTACT TAACGTTGCT GCTATTACAC AAAAGTAGCC ATAGAGAGCG 660
TGAAAACCAA TAAGCATGGC TGTTTCAATA AAACTTTATT TACAAAAACA GGGAGCAGAG 720
GCTCACGCCT GTAATCCCAG CACCTTGGGA AGCTGAGGTG GGAGAGTCGC TTGAGCCCAG 780
GATTTTGAGA CAAGCCTGGA CAATATAGTG AGATCCCATC TCTACAAAAA ATTTTAAAAA 840
TTAGCGGAGT GTGGTAGTGT GTCCTTGTAG TCCCAGCTAC TCAGGAGGCT GAGGTGAGGT 900
GAGAGGATTG CTTGAGCCCG GGAGGTGGAG GTTGCCGTGA GCCCAGATCA TGCTACTGCA 960
CTCCAGCCTG GGCAACAGAG TGAGACCGTC TCAGAAAAAA AAAAAACAAA AAAACAAGCG 1020
GCAGTTTGAA TTTGGCCAAT GGGCAGTAGT TCACCAACCC CTGGTCTAGA GCCATAAAAT 1080
TCACTGGGTC TGGCCCAATC CTGTATTGCA GGCTCTGAAG TCCTGAGTCC TTCCCTCTCC 1140
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