| Tag | Content |
|---|
EnhancerAtlas ID | HS192-00882 |
Organism | Homo sapiens |
Tissue/cell | U2OS |
Coordinate | chr1:145713200-145715520 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:145713744-145713763 | TGGCCGCTAGAGGGCGCTG | + | 7.3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I145720 | chr1 | 145713284 | 145714909 |
|
Enhancer Sequence | TCATAAAGTG TCAAGGGGCA GCACAGGAGA AATTCTGGAT GAGGGATGTG GAAAGGCTGC 60
AAGATGGCAA TGAAGTTAGG CCTTCATAGT TGTTTGTGGG CTCTGGGGAG CTGGTGACTA 120
AAGAATACGG TGGGTGAATT AAGGTGGGGA ATGGGCTGAG GAGATCTGGC TTCCAGTCCT 180
GGCTCCGCAC TAGGTAGCTG TGGAATGTTG ACAAGGTCGT GTCCCTTCTC TAGGCGTGTT 240
TCCTAAGGGA CTGGTGCAGC GGGATGGGAG GGGCGCAGGG TAGGGACCGC TTCCAAGGAG 300
AGAGAGGACA GGCGGGAGGG GCTGATGCAG CTGGTCACTC CGCTGGAGTG GCCAGACTTC 360
GCGGTGCCTA GGGCCGAGTT GAAGAAGAGC ATGTAAGTCT GTTGTGGGCC CCTCACCAGC 420
GCTGGGGGGC AGCGAGGTCA CTGGGCAAGG ATGCTCTGGG AAGTGACCTT GGTGCCCGGG 480
AGGGGAGCAC CCTGTTGTGA TGCAGGCGGG GCAGCGCGGA GCCGGCGGCG CTGATTTCGC 540
ACTCTGGCCG CTAGAGGGCG CTGCCTTTCA GCCAAAGCCG AGTGACCCCC TACCTGCCCC 600
GCGTTGGCCC GCGTCACTCC AGCCATGGGC CATCCAGCGA GCATGGGGGC TAGCCAGGGA 660
AAGTCTAAAC TAGGAGGGGA GATGAGGGGG TGCAAAGTTG GGCCTGGTGG GTCCTGGGGA 720
CGCAGCATGT ACTAGAGCGG CACCTGGCCC TCAACAGAGG GGAGAGCGGG TGGTCGTGAG 780
AAGTCTGGGA ATTTTCCGGG CCCACTACAC GCCAGGGGCG GGTCTCCCCT CTTAAAACGT 840
TGTGAGCCCC AGCGCGGGCA GGGGGGAGGG TGCCCGTGGA GTTGGCATCC TCATCTTTGA 900
TGGTCCCCGG GGCTCCTGAG CTGCGCTGGT GGCCCCAGGG CTCGGTGCCT CTCTCAGGCG 960
ACAGCTCACA GACGGCGGGA AACTCTTCCC TCCCGCACCT TCGGAGGCGG TCCTGGAGTC 1020
TTGTGGACTC CTGGGTTCAA ATCCAAGCTT TGTGTGACCA GCACATTGCT GGACCTCACT 1080
CAGCCTCACA TTCCTCTTGT GTTTAAAACT ACCTCATAGG AATGTGGTGA CGGTTAGATG 1140
ACACATAAAG CTTTGCCAGA GGTTTTCTGG GGAGGGTGGG GACAAGAGGG CAAGGAAGAG 1200
TCTCCATTTC CTCTGCCACC GGAGCCCGGA TCTAACCTCT CAGAGGAGCT GGAAGGTCAG 1260
CTCTGAGCTC CACAAATACC TCTGTATACA GATCTCCCAC GACACTGAAA AAGATGCCCA 1320
GAAAGATCTC ATTTGCAGCT GTGAAGGGGC TTCTTTTTCA ATCTCCACAA CCCCAACTGC 1380
CTTAAAGTAG AACCAGACTT GTTAGTAGAC AGAGGTTTGG GCTGGGGGGC CCTTGAAGCT 1440
CTTGTCTGAG ATCTCAGGCT TCCTGCTCAA CACACCAAAG CAGGTGCCTG ACATAAAGGC 1500
GCCATGGACC TCTTTGGTGG TCTGGGAAGG CATATGGAGT CCCTTCTCAG AACAACATTT 1560
AAAAATTAAT AAGATACATG GGATAATAAA GGGAACAAAT TATGACAAGA CAGTTGTCAA 1620
AACATTAGAA GAATGTGTGG TAGAGCAGTA CACATGCTTC TTTAGATTTG ACATCAGCCT 1680
AATAACTGTT GTAATTCTGT AGTAGTGCTG AGCGTTAAGG ACATTTGGAG AAATCTATAA 1740
AAACTGTAAT GAGATTTGAA AATATTTGTG TTTTCTATTG ATGGCAAATT CTATTGTGGT 1800
TCATTGTCTA CATTCATAAC TGAAGCAAGT GCTGACTTTC AATTAAAGAT TAGTGAAAAT 1860
AAAGATGTAT TTTTCCCCCC AATTCACAAA TCCCATGAAT AAATCTATTC ACGGACCTCC 1920
AAGAGGTCCA TGACGTGAAC CACCTAGGAC ATGAACTTCC CCCGGAGGTG CCTCACAGGG 1980
CCAGCTCCAA GCCCCGTGGC ACCTCCCGGC TTGTCTCAGG CCAATCCTTG AAGAGCTCCA 2040
GCAGATCTAA ACTTTGGTAA CTTTCCTCTG GTAATTTGAG GAATTCCTCC ATTTGAGGAA 2100
TGTCAGAATG GGGCCAGGAT TCCTGAATGC CCATGGAAGA AAAGCGAGCA TGCTGGTCTG 2160
GCGGGCAGAA ATAACCTTCT CCCCAGGCTC CAGAGGGCAG AGGACATTTC CCTCCAAAAG 2220
GCAAGTTTCT CAGGGACCTC ATGAGAAGCC TGTCCTCACC TGAGCAGTTC TGTCAACCAT 2280
CCCATCCCTT CACCTGGACC CCAGGTCCCC AGCAGGCCTT 2320
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