| Tag | Content |
|---|
EnhancerAtlas ID | HS101-02716 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:151342920-151345110 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:151343993-151344014 | GGGGCAGGGAGAGAGAGAGAG | + | 6.32 | | ZNF263 | MA0528.1 | chr1:151343987-151344008 | GGAGGTGGGGCAGGGAGAGAG | + | 6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTGGAAGTC CTCAGGCTGG TTTCTACCCC TGGGTGTGCC CCACTTCCTT TATCTGTAAA 60
GTAAGGTGTT TGGCCCAACT CTGGAGAGCC CAGAGGCCTG CCCACCAGAG AGATAGGGAG 120
CAACCCTCCC TATCTCTGAA GTCTGGCAAG AGGGGCCATG CTAATCTCCA GGATGTAAGT 180
CAGCAGATGT GCAGTAGGGC TGGGACATCA CAGCTACCAG CACCCCAGCA TCAGAGTTTG 240
GGGCCTGCTG GGGAGCAGGG GTTAAAGAAT ACCCAGAGGG GGTGGCAGGC TGAAAGAAAC 300
CCTGGAGTGG AGTCCACAGG CCTGGGCCCT GTCTCCTGCC TTGTCCTGTG GCCAGTCCAG 360
CCTCTGCCTT CACAGCTGGG CCGCAAGTGG GGAGCCAGGA GTAGGCAGAG TGGGGCCTCC 420
ACTGGGGCCT GGGACTCCCA CTCGCAGCAG CCAAGAGACT TAGGAAGCTG AGAGGCAGCA 480
ACAGCGTTCA GAGTCTGGAA ACCTGGTTTC AAGTCCCAGT TTTGACGCCC CGTTTCTCCA 540
TTTTCTCCTC TTCATTTACG AAAAGTGGGC AATAATGATA TTCTACCTAC TTTGCTAGGT 600
AGATATGGAG GACAAATAAG ACAATGTATT CCAAAGGCCT TTCATAAAAA TGAATTAGGC 660
CGGGTGCGGT GGCTCATGCC TGTAATCCCA GCACTTTGGG AGGCTGAGGC GGAAAGATCA 720
CCTAAGGTCA GGAGTTTGAG ACCAGCCTCA CTAACATGGC AAAACCCTGT CTCTATTAAA 780
AATACAAAAA TTACCCTGTA TTAAAAATTA GCCTGTATTA AAAAATACAG GCATACACCT 840
GTAATCCCAG CTACTTGGGA GGCTGAGGCA GGAGAATCAC TTGAACCTGG GAGGTGGAGG 900
CTGCAGTAAG CCGAAATCAC GCCACTGCAG TCACTCCAGC CTGGGCAACA AGAGTGAAAT 960
TCTGACTAAA AAAAAAAAAA AATAATGAAT TACTGTGTAA ATATGGGAAG GGCTGTGCCA 1020
GAGGAGAGGA GAATGCCAGG GAGTGCTCGA TGCCCAGCGA GAGGGCTGGA GGTGGGGCAG 1080
GGAGAGAGAG AGAGGTCCAG TTCACAGGAG TTAAGGAGAC TGGTTCTGTT ACACAATCTT 1140
GCTAAGTCGG GGCTTGGCAC CAGATGACAG GGGGTGGGGA AGGAGGTTGC TGGATACAGA 1200
AGGGAAAGGA GATTTTAAAA CTCCAAGACC TCAAGACAGA GATACAAAAA ATACAAAGCT 1260
AGGGAGAAGC TGAGAGGGAA GTAAAAGTGC AGAGATGGAG CTGCCCGCTC TGCAGCCTCG 1320
GCCCACCCCA CACCCCAGCA ACCCCAGCCC CAGCATTTCT TAGGGTCAGG CCTGGCATGC 1380
CACTGCAGCC CCAGGGAGCA TCATTCCTCT TTCTGGGGAA TACCCCCATC TGAAACATCT 1440
CAAGCAAGGT CTCGGAGCAG CTTTGGGTTT GGGATGGACT CATGGAAAGC TCAAGTGGGT 1500
TTTCCATGTC AGGCTGGCTG CTGGGCATTC TGCCAGCTCG GCATTCTGCC AGCTCAAGAG 1560
CCAGCCCCGA GCGGGGAAGG ACCTCCCAAC CAAACCTCAG TTCCTTCTTA GCCTGTCACC 1620
CAGAAGCCTA CAGATGGAGG AATAGCAGGG CCAAGGGGGA TTTAGGGGTG GGGGAGGCAT 1680
TGAAACAGGT CCCCAGTGAA AGAGTGTGGG GGTCTCTGAT TTCCCTCCCA GAGAGCTTTG 1740
CTGTGTGGAG TAGCTAGAGA GTGACCTGGG CACAGAAAGG CTTTGGACTC CCTACCTCGC 1800
TGGAGTACAA AGTTGGCCCA TGGCTGAAAT CAGGATCACC TCTCTACTAT GTGAGGGCCA 1860
GGGACCTAGT GGTGTTTTCT AAGAGCGCCC ATCTGATTTT CCCAGCTGCA GAAAGGCACC 1920
CTGGTCCCAG CCTCTGCTGG ATGGAGCCAA GTCAGGGCCC AGGATCCCAT CTCCCAGCAG 1980
TGCCTCTGCC CGTCTTCCTC AGAAAGTTTG GCTGAGCTGG GAAATGCAGT GGGGTGGTGG 2040
GGGAGGGGGT GTGCAGACTG GGGACAATGA AGCAGAGTCC ACTACTCCCT CCCCAGCTCC 2100
CCACTCAGGT TTTCTAGCAT TTTCTGGAGG AGGGCCTTCC AAATTAGGGG CAGACAGAGC 2160
AGGCAATGGG TGATTGGAAA CCCCTCTCCT 2190
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