| Tag | Content |
|---|
EnhancerAtlas ID | HS108-10688 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr12:120925160-120927520 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr12:120925512-120925522 | GCACGTGACC | - | 6.02 | | Nr5a2 | MA0505.1 | chr12:120926506-120926521 | GAGTTCAAGGCCAGC | + | 8.25 | | SOX10 | MA0442.2 | chr12:120925715-120925726 | AAAACAAAGGA | + | 6.32 | | Sox3 | MA0514.1 | chr12:120925715-120925725 | AAAACAAAGG | - | 6.02 | | Zfx | MA0146.2 | chr12:120926474-120926488 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 120925357 | 120925694 | | chr12 | 120925758 | 120926255 | | chr12 | 120926851 | 120927294 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH12I120487 | chr12 | 120925285 | 120926472 | | GH12I120488 | chr12 | 120926786 | 120926862 | | GH12I120489 | chr12 | 120926961 | 120927110 |
|
Enhancer Sequence | TCTCGGCTCA TTACACATGT GCAGTATTTA CTGGGTTCAC ACCATTCTCC TGCCTCAGCC 60
TCCCGAGTAG CTGGGACTAC AGGCGCCCAC CACCACACCC GGCTAATTTT GTTTTTGTAT 120
TTTTAGTAGA GACGGGGTTT CACCGTGTTA GTCAGGATGG TCTCAATCTA AAACAGGAGA 180
ATCATTTATT GAGTGCACTC AGGCCCAGCT GACTCAACGT CCAAAAGACT GGGCCCGGAA 240
GAAAGACAGC ACTTGACTTC TATACACACT TCACAAAAGG GGGTGGGCTA GCTTGAAGCA 300
AGCTTACAGT GGCATGAAAG CAGGGATATA GAGGCAGGAC AAACTCAGGA TTGCACGTGA 360
CCGTTGCCAA GCAACCCAGA TGTCCGTTAT CTAGGTTTGC CCAGGCACAG ACTTATCCCA 420
TAACCTTCAC TATGGCGCCC AGGTGGCCGT AACTCAGGCC AGCTCAGAGG CTCATGACCT 480
TCACTCCACT GCTTAGATAA AACAATACTT GAAGTCACTG GTTACAGAGA ATAGGAATCT 540
ATAAACTCAT TCCATAAAAC AAAGGAAAAT TTGTTTTTCT TCTCCCTATG TTGAGGGAGT 600
ACTGGGAGAA TCTCCAGAGC ACATTAGATA ATATTATGAA GAATTTTCCT GGGTCTGGCC 660
TGTGCCTATT GCTGCCTCTG GGACAAGTCA CCCTCATACA GAAAAACTTA TTTCTCTTTC 720
TTTTTAATTT TGCTTTTCTT TAATTTCCCA CCTCAACAGA GCCACTGGTG GCCGCAGAAG 780
ACAGTCCACG TGTCTTAACC AGACTTACAA GACTCCAAAG GTCTGGCTTC TCCCCACCCC 840
TACTCCCTGT CTTGTCTCTC CCACACTCCC CCAACAGCTT CTCTGGAGCC AAGTCAGCCA 900
GCCTCCTTCC AGCTTCAGGC CTTTGAACAT GCTGTTCTTT CCACCTAAAA AGCTCCCTGC 960
ACTTCCCCCA GCCTAGTTCC CTGCTTGTAT AGATTGTTCC TCTAATGTGA CTCCTGGAAA 1020
AGCCTTCCTT GCCTCTCCGG CTAGAGCAGA GCCCCCATTA ACAGCTCTCA CACCAGCCTA 1080
TCTTTCTCCT CCACTGCATT TGTCACATCC TGTGATCCTG TGTGCATCCT GTTCAATGTC 1140
TGTCTCCACA CATAAAATCT AAACTCCAAA AGGATAGGAA CTGTGTCTGA CTCGCTTCCT 1200
TTCATGTCCC TTGTGCCTAG ATGGGTGCCT TGTATCAAGC AGGTGCTCAA CAAATGTCTG 1260
CTGAAAAAAT GATGCAGGGT GCGGTGGTTC ACGCAGGTAA TCCCAGCACT TTGGGAGGCC 1320
GAGGCGGGTG GATCACCTGA GGTCGGGAGT TCAAGGCCAG CCTGACCAAC ATGGAGAAAC 1380
CCCATGTCAA CTAAAAATAC AAAAAATTAG CCCGATGTGG TGGTGCATGC CGGTAATCCC 1440
ACCTACTGAG GAGGCTGAGA CAGGAGGATT GCTTGAACCC AGGAGGCGGA GGTTGTGGTG 1500
AGCCAAGATC ATGCCATTGC ACTCCAGCCT GGGCAACAAG AACGAAACTC TGTCTCAAAA 1560
AAAGAAAAAA GAGAAAAAAA GGACTAAGTG ACTAAAAGAC AGGGTAGGAA CTCAAGGCTC 1620
ATCCTCTACA TGGCCAAAGC ACTTAGGCAG GAAAATTAAG TAAGTAATAG AGCTTCTCTG 1680
GGGCAGGTGC CAAAGGAAGT CCATCTCTGT ACCTAGCACC TAGCTCCGGG CCTGGCCCAT 1740
AGTAAACGCT CAGAGAATAT TGCTAGCTGA ATAAGCATTA CTTCCATCTA CACGTACTCC 1800
GCCCTCAGTG GTGATCTCAT CCAGTCCCAT TGCTTTAAAT GTCACCTATA AGCTGATGAC 1860
TCTCCAAATT ATAGCTCAAG GCTGGCCCTC TTCCCAGAAC TCATATATCC AACTGCATAT 1920
TTGACATCTC CACTTGGAAT ATCTAATAGG CATCTCAAAC TTAACATGGC CAAAGCAGAA 1980
CTTCTTGTTT CCTCTGCCAG ACTTCCCCAT CTCAATCTAT TCTTCTCATT GTTCAGCTCA 2040
CAAGTCTGGA GTCATCCTTG ACTGCCTCTG GTTCCCTCCT ATTCTGCATC CAATTGCTCA 2100
GCAAATCTGT CAGCTCTACC TTCAGAATAC ATCTGGAATC TGGCCATCTC TGCCCTATCT 2160
CTGCTACCAC CTCCTTGTCC AAGCCACCAT TCCTTCTTAC CTGGACTGCT GCAATAGCCT 2220
CTAACTGCTC CCACCTCTCT CGCTGCTCCC ATCAGCTTCC CCACCTTCCA TCCTCATGCA 2280
GTAGCCAGGT CATCAAGTCT TGGCTCAAAT GGTGCCTTCT CAGAGAGGTC TTCCTAGAAA 2340
ACTCTTTAAA ACAAGACCCC 2360
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