| Tag | Content |
|---|
EnhancerAtlas ID | HS108-00074 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:1873890-1876060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:1874294-1874305 | AGAGGGTGTGG | - | 6.02 | | MYC | MA0147.3 | chr1:1874008-1874020 | GGGCACGTGGGG | - | 6.07 | | NR2C2 | MA0504.1 | chr1:1874393-1874408 | TGACCTCTGACCACT | - | 6.05 | | SP1 | MA0079.4 | chr1:1875862-1875877 | ATGGCCACGCCCACG | + | 6.22 | | SP3 | MA0746.2 | chr1:1875864-1875877 | GGCCACGCCCACG | + | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1874601 | 1874908 | | chr1 | 1875848 | 1876000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001942 | chr1 | 1873910 | 1876089 |
|
Enhancer Sequence | CTGCCAGGCA GCCCCTGGGT GCGGGGCCCT GGAGGGGACA TGAGGGGTGG AACCCCTCCC 60
TCCAGGGCTC TGCCCGCCTC CTGCCCAGGG CATCCCCACA TCCTGCAGCT CAAGCACAGG 120
GCACGTGGGG GGCCTGGGAC GGCCACAGGC CTCGGTTATG ACAGCAGCCT CCAACCCAAG 180
ACGAGCCTGA GAGAGCCAAG GTACCCGCCA GTCACCTGGG AGGCCATGCG TCTGTCCGGT 240
CCCTACCTCC GGCTCCCTTA AGCCAACGGC CTCCTCAGGA CCACCTGGAG CCTCCCTGTT 300
CCCACAGTGA AGCCTCCCTC CCCTCCCCCG TCTTGGAGCC TCTGCTAAAC AGTGTTGTGG 360
CCGCCCCGCC ACAGCTGCCC CGGGCAATCC ACGAGGGGGG ACCCAGAGGG TGTGGCAGTG 420
AGAAATCTCC TCCCTCCTGT GCTTCCATGC GACAGTCACC CATGCTGTGG CAGCCTCATC 480
TCCGTCCATC ACAGACCTGC CTCTGACCTC TGACCACTAC CCAGAGGCCA CCCACAGTGC 540
GTCTGGGCAC GCCAGCCTCT GCACCCCTAC TGCTGGGCCC CATGGGAGGC GGGCGCCCGG 600
GTGCTCAGAG ACCGCGCCCT CCCCGTCAGG CAGACGCTGC TCTGCCTTCC GGTTCCCTTA 660
TGGGGCCAGA GTCTATACAA ATGAGCACAC AGCTACACTG AGGTACACAC AACCACAGCC 720
GGAGACCATC CACAGAGCTG GGCCCCACTC AGCCCTCAAT GCCCGACAGA CACGCCTGGG 780
CCCTTTCTGT CAAGTTTCCA AGGCCACTGA GAGGCTGTAG TAGGACGATG CCGGAGGCGA 840
GCAGACTCCA CCGCAGACAC GCCAACACAC GCAGCTGGCT CCCGGGTCAC CGCAGGCTGC 900
ACATTCCCGG CCCATGCCGG GCCCACAGGA GTCCGACAGC AGGAGGACAG GCGCCGCGGG 960
AGCTGTTCCT ACCCAGGTCA CCGGGGAGAG GTGGCTGTGC CTGGGGCCGG TGCCCGGGGC 1020
CTCTGTGTCC GCACACCCTG CTCCTTGGTG CTGGTGGCAC AGGGGCTCCG TCATGGAAAC 1080
CCCGCAGGCC CAGCCTCGCC GTCCCTCTGC GCTTTCCCAC CGGCGTGGCT GTTCAGGGCA 1140
GGCTGCTTGC TCTGATGTCT GGAGCCCTTG CCAAACCCTG CAAGTGGAGG CTTCCTCCTC 1200
CAGGCTCACC CTGCCTGTGT CCACGAGGGG CTGAGGACTC TGGCCGGGCC CAGGCGGGCA 1260
GTGCGTTTCC TGTGGCTGCT GAAAGGATTT GCCCCAAGCT TAGGGGCCCC ACAACACAGA 1320
GGCACATTCA TTCTCTCCAC GTCCTGGAGG TCAGAAGCCA AGACGGAGCT AAGGCCAAGG 1380
TGCGGGCAGG GCCGTGCCCT TGTGGCTCTA CGGGACAGGT TTCTCCTCTC CTTTCACAGC 1440
CTCTAGAAGC TGCAGTGTCC CCGGGCTCGG GGCCCTTCCT CCATCTTGGA AGCCGACAGT 1500
GCAGTGTCTT CAAATCGGCC TGACTCTGAC CCTCCTGCCT CCCTGTGACG CCTCCCGTGA 1560
TGACACTGGC GCCTCCCAGA TGATCCTGGA TCACCCCCCA CCAAGGTCCC TCTCCCCAAC 1620
CATGTCTGCT AAGCCCCCTG CTTGCCACAC AGGATGCCGT TCAGGGCCTG GACAGCAGCC 1680
GTGGCAGCCC CAGGTGCCAT GTCCCCGCTG GCCACTGGGG GGCTCACCGC GTGTGCACAG 1740
GCAGGCAGCG GCTCACCCCG TGTGCGTGGG TCACCCCGTG TGCGTGGACA GGAGGGGGCT 1800
CACCGCGTGT GCACAGGCAG GCAGCGGCTC ACCCCGTGTG CGTGGGTCAC CCCGTGTGCA 1860
TGGACAGGAG GGGGCTCACC GCGTGTGCAC GAGCACAGAG TCCTGGTAGA GCCGGTCATA 1920
CATGCAGATC TTCAGGTCCA CGCTGGGCTT CGGCACCCAG ACCGGCACAT CGATGGCCAC 1980
GCCCACGACC CTGAAATGCA GCTGCATATG GACACAGGAG CTCAGCAACA GGAGTTCCTT 2040
GGGCACAGCA GGCATTGTTG GTGAGCACTG ACACAGCTCC CAGGAGGAAC GTTTCATGGG 2100
CTTGAGTTTT CTAACTCTTT GGGACGGCTG TGGCACTTTT CATATCATAT CATTCAAAAT 2160
ATTCTTTTTT 2170
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