| Tag | Content |
|---|
EnhancerAtlas ID | HS108-02867 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:151342460-151345110 |
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 | GTGGACAGAC AGTCCAGCAG GGCCCCGGGA GGGTGGGAGG AGGGCTGATG CAGCCGGGGT 60
CGTGTGGTGT AGTGAATATG ACACGGACTC GGGGCCCAAC CCCAGCCCAC CACTGACTAG 120
CCAGGGGAGC TTGGGCAAAG TACTGAAGCT CCTCGACCTC AATTTCTGCA TCCTCTGTAA 180
AATGGAGATG GTAAGAATTT CACAGTGGGC TTTTACGAGA AGTAAACACG AGGGTGCAGT 240
AGGTGTGCAG CTCTGTGTTT GTCTGGTCGA AGCCCAGGCA CCCTTGGCTG TTCTTGAGGA 300
GCTGCTCTCA GGGAGTGGGG TGGCGCCTGC TCAGCTCCCT TCACCAAGAT GCTTCTATAT 360
CAGGGGGAGG CCACTTCCTG CTTTTCTCTC CCCTGGGTCC TGATCCCAGG CTGCTAGCCA 420
AGGGCTGGAT TACATAACCG AGGGTCTGGG GCTAATACCA ACTGGAAGTC CTCAGGCTGG 480
TTTCTACCCC TGGGTGTGCC CCACTTCCTT TATCTGTAAA GTAAGGTGTT TGGCCCAACT 540
CTGGAGAGCC CAGAGGCCTG CCCACCAGAG AGATAGGGAG CAACCCTCCC TATCTCTGAA 600
GTCTGGCAAG AGGGGCCATG CTAATCTCCA GGATGTAAGT CAGCAGATGT GCAGTAGGGC 660
TGGGACATCA CAGCTACCAG CACCCCAGCA TCAGAGTTTG GGGCCTGCTG GGGAGCAGGG 720
GTTAAAGAAT ACCCAGAGGG GGTGGCAGGC TGAAAGAAAC CCTGGAGTGG AGTCCACAGG 780
CCTGGGCCCT GTCTCCTGCC TTGTCCTGTG GCCAGTCCAG CCTCTGCCTT CACAGCTGGG 840
CCGCAAGTGG GGAGCCAGGA GTAGGCAGAG TGGGGCCTCC ACTGGGGCCT GGGACTCCCA 900
CTCGCAGCAG CCAAGAGACT TAGGAAGCTG AGAGGCAGCA ACAGCGTTCA GAGTCTGGAA 960
ACCTGGTTTC AAGTCCCAGT TTTGACGCCC CGTTTCTCCA TTTTCTCCTC TTCATTTACG 1020
AAAAGTGGGC AATAATGATA TTCTACCTAC TTTGCTAGGT AGATATGGAG GACAAATAAG 1080
ACAATGTATT CCAAAGGCCT TTCATAAAAA TGAATTAGGC CGGGTGCGGT GGCTCATGCC 1140
TGTAATCCCA GCACTTTGGG AGGCTGAGGC GGAAAGATCA CCTAAGGTCA GGAGTTTGAG 1200
ACCAGCCTCA CTAACATGGC AAAACCCTGT CTCTATTAAA AATACAAAAA TTACCCTGTA 1260
TTAAAAATTA GCCTGTATTA AAAAATACAG GCATACACCT GTAATCCCAG CTACTTGGGA 1320
GGCTGAGGCA GGAGAATCAC TTGAACCTGG GAGGTGGAGG CTGCAGTAAG CCGAAATCAC 1380
GCCACTGCAG TCACTCCAGC CTGGGCAACA AGAGTGAAAT TCTGACTAAA AAAAAAAAAA 1440
AATAATGAAT TACTGTGTAA ATATGGGAAG GGCTGTGCCA GAGGAGAGGA GAATGCCAGG 1500
GAGTGCTCGA TGCCCAGCGA GAGGGCTGGA GGTGGGGCAG GGAGAGAGAG AGAGGTCCAG 1560
TTCACAGGAG TTAAGGAGAC TGGTTCTGTT ACACAATCTT GCTAAGTCGG GGCTTGGCAC 1620
CAGATGACAG GGGGTGGGGA AGGAGGTTGC TGGATACAGA AGGGAAAGGA GATTTTAAAA 1680
CTCCAAGACC TCAAGACAGA GATACAAAAA ATACAAAGCT AGGGAGAAGC TGAGAGGGAA 1740
GTAAAAGTGC AGAGATGGAG CTGCCCGCTC TGCAGCCTCG GCCCACCCCA CACCCCAGCA 1800
ACCCCAGCCC CAGCATTTCT TAGGGTCAGG CCTGGCATGC CACTGCAGCC CCAGGGAGCA 1860
TCATTCCTCT TTCTGGGGAA TACCCCCATC TGAAACATCT CAAGCAAGGT CTCGGAGCAG 1920
CTTTGGGTTT GGGATGGACT CATGGAAAGC TCAAGTGGGT TTTCCATGTC AGGCTGGCTG 1980
CTGGGCATTC TGCCAGCTCG GCATTCTGCC AGCTCAAGAG CCAGCCCCGA GCGGGGAAGG 2040
ACCTCCCAAC CAAACCTCAG TTCCTTCTTA GCCTGTCACC CAGAAGCCTA CAGATGGAGG 2100
AATAGCAGGG CCAAGGGGGA TTTAGGGGTG GGGGAGGCAT TGAAACAGGT CCCCAGTGAA 2160
AGAGTGTGGG GGTCTCTGAT TTCCCTCCCA GAGAGCTTTG CTGTGTGGAG TAGCTAGAGA 2220
GTGACCTGGG CACAGAAAGG CTTTGGACTC CCTACCTCGC TGGAGTACAA AGTTGGCCCA 2280
TGGCTGAAAT CAGGATCACC TCTCTACTAT GTGAGGGCCA GGGACCTAGT GGTGTTTTCT 2340
AAGAGCGCCC ATCTGATTTT CCCAGCTGCA GAAAGGCACC CTGGTCCCAG CCTCTGCTGG 2400
ATGGAGCCAA GTCAGGGCCC AGGATCCCAT CTCCCAGCAG TGCCTCTGCC CGTCTTCCTC 2460
AGAAAGTTTG GCTGAGCTGG GAAATGCAGT GGGGTGGTGG GGGAGGGGGT GTGCAGACTG 2520
GGGACAATGA AGCAGAGTCC ACTACTCCCT CCCCAGCTCC CCACTCAGGT TTTCTAGCAT 2580
TTTCTGGAGG AGGGCCTTCC AAATTAGGGG CAGACAGAGC AGGCAATGGG TGATTGGAAA 2640
CCCCTCTCCT 2650
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