| Tag | Content |
|---|
EnhancerAtlas ID | HS053-02449 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:145713260-145714690 |
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 | AAGATGGCAA TGAAGTTAGG CCTTCATAGT TGTTTGTGGG CTCTGGGGAG CTGGTGACTA 60
AAGAATACGG TGGGTGAATT AAGGTGGGGA ATGGGCTGAG GAGATCTGGC TTCCAGTCCT 120
GGCTCCGCAC TAGGTAGCTG TGGAATGTTG ACAAGGTCGT GTCCCTTCTC TAGGCGTGTT 180
TCCTAAGGGA CTGGTGCAGC GGGATGGGAG GGGCGCAGGG TAGGGACCGC TTCCAAGGAG 240
AGAGAGGACA GGCGGGAGGG GCTGATGCAG CTGGTCACTC CGCTGGAGTG GCCAGACTTC 300
GCGGTGCCTA GGGCCGAGTT GAAGAAGAGC ATGTAAGTCT GTTGTGGGCC CCTCACCAGC 360
GCTGGGGGGC AGCGAGGTCA CTGGGCAAGG ATGCTCTGGG AAGTGACCTT GGTGCCCGGG 420
AGGGGAGCAC CCTGTTGTGA TGCAGGCGGG GCAGCGCGGA GCCGGCGGCG CTGATTTCGC 480
ACTCTGGCCG CTAGAGGGCG CTGCCTTTCA GCCAAAGCCG AGTGACCCCC TACCTGCCCC 540
GCGTTGGCCC GCGTCACTCC AGCCATGGGC CATCCAGCGA GCATGGGGGC TAGCCAGGGA 600
AAGTCTAAAC TAGGAGGGGA GATGAGGGGG TGCAAAGTTG GGCCTGGTGG GTCCTGGGGA 660
CGCAGCATGT ACTAGAGCGG CACCTGGCCC TCAACAGAGG GGAGAGCGGG TGGTCGTGAG 720
AAGTCTGGGA ATTTTCCGGG CCCACTACAC GCCAGGGGCG GGTCTCCCCT CTTAAAACGT 780
TGTGAGCCCC AGCGCGGGCA GGGGGGAGGG TGCCCGTGGA GTTGGCATCC TCATCTTTGA 840
TGGTCCCCGG GGCTCCTGAG CTGCGCTGGT GGCCCCAGGG CTCGGTGCCT CTCTCAGGCG 900
ACAGCTCACA GACGGCGGGA AACTCTTCCC TCCCGCACCT TCGGAGGCGG TCCTGGAGTC 960
TTGTGGACTC CTGGGTTCAA ATCCAAGCTT TGTGTGACCA GCACATTGCT GGACCTCACT 1020
CAGCCTCACA TTCCTCTTGT GTTTAAAACT ACCTCATAGG AATGTGGTGA CGGTTAGATG 1080
ACACATAAAG CTTTGCCAGA GGTTTTCTGG GGAGGGTGGG GACAAGAGGG CAAGGAAGAG 1140
TCTCCATTTC CTCTGCCACC GGAGCCCGGA TCTAACCTCT CAGAGGAGCT GGAAGGTCAG 1200
CTCTGAGCTC CACAAATACC TCTGTATACA GATCTCCCAC GACACTGAAA AAGATGCCCA 1260
GAAAGATCTC ATTTGCAGCT GTGAAGGGGC TTCTTTTTCA ATCTCCACAA CCCCAACTGC 1320
CTTAAAGTAG AACCAGACTT GTTAGTAGAC AGAGGTTTGG GCTGGGGGGC CCTTGAAGCT 1380
CTTGTCTGAG ATCTCAGGCT TCCTGCTCAA CACACCAAAG CAGGTGCCTG 1430
|
