| Tag | Content |
|---|
EnhancerAtlas ID | HS069-03578 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr17:34295920-34298330 |
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 | chr17:34296687-34296706 | TAACCACTGGGTGGCGCTG | + | 6.26 | | Nr2f6(var.2) | MA0728.1 | chr17:34297772-34297787 | TGAACTCCTGACCTC | - | 6.22 | | TCF7L2 | MA0523.1 | chr17:34297538-34297552 | TCTCTTTGAACTTT | - | 6.08 |
|
| | 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 |
| GH17I035969 | chr17 | 34296408 | 34298172 |
|
Enhancer Sequence | ACATCTGTCC ATTTTTGTGT AGTCACCCAA GTTCTCAGTT ATATTTTAAA TTTTTGTCTA 60
GAGTTGATGG CTTTGACTTG CAGAATGGTC CATTTGTTAA GTGTGTGAGG GGCTCAGTTT 120
CCCATGCTGG AAGCGACAGG TTTAATATGA ACTTTAATCA TCAGATTCTT ATTAATTTTT 180
TTTTTCCAGA GGGAGTCTTG TTCTATTGCC CAGGATGGAG TGCAATGGCA CGATCTCGGC 240
TCACTGCAAC CTCCGCCTCC CAGGCTCAAG CGATTCTCCT GCCTCAGCCT CCCAAGTAGC 300
TAGGATTACA GGCACCCACC ACCATGCCCA GCTAATTTTT GTATTTTTAG TGGAGACAGG 360
GTTTCACCAT GTTGTATACA TGTTGGTCAG GCTGGTCTCA AACTCCTGAC CTCAGATGAA 420
CCACCCACCT CTGCCTCCCA AAGAAAATTG TTCTTCTTGG TGGGTCCTAT CAAACAGTAC 480
AAAGGTGTTT TGTGTACTCC TCGCCATCAC TTTTACTCTG CTCTATTCTT CGATATAGAA 540
CCTGATTGTG CGTGGTCTCT CTTCCCACTT TTAGTGGGAA GGAAAGCTCC TTGAAAGCAC 600
TGTGCCCTCA CTGTGTACTG AATACCTCAG CTCTCTTCAA AAGGGGAGAA TACAAGGAGA 660
GGTGGGAAGG TGGAAGGTGT GCACACCAGG AAGGGGCTAT CTCAGCAACT AGGCTTATGT 720
ACGAGCCAGC CCAATGAGCT CACAGAGAGA TAAGTCATTG TGGCTTTTAA CCACTGGGTG 780
GCGCTGCTCA CTAATTTTCC TAAAATCATG TCAAGACAGC AATTGCTTTT CAGCAACTCA 840
ATCCAGAACT CCAAGACCTA AATCCACACT CCAGGACCTG GCTTAAACTG CCATCTCGGT 900
GGAGACACAT CCCTGCACTG ATCCCCTCAC TCACAGCCAA GGGGCCCTAT CACATTGACT 960
TCCAACCCCT GCCCCCATGC CTAAGTGTGA AATTCATGAT TAGATATTTA GTGAGGCCCC 1020
CCAGGTACAA AGGGCCCTGG ATGGGAACAG GGTAAATTCG AAGACGTGGC CCCTGCCCTG 1080
AGACAGGCTT TTTGAACTGG CTTAAGATAA GCAGTAGATG TAATGGGTTA ACCTCCCTCC 1140
TGTGCATCCA GAGTGGTGTT GGTTATGCAT CATCCTAGGA GAACTGAGAA AGCAGTCACA 1200
AGTTGTCTGT GTTCTGTGGC TCGGATGAGA AACCTCACGC ATATGATCTG GAGGGGACAG 1260
GGAGGATTCC TTGTTTTTTT TTTTTTTCTT TGGAGACAGA GTTTCAAGTG CAGTGGTGCA 1320
ATCTTGGCTC ACGGCAAGCT CCACCTCCTG GCTAAATAGA GATGGAGAAC TTAAGAGACT 1380
TCATAGGAAG ATTACATTTG CTGTAGCAAG TTGACTGAAA CTGATGTTAA GAGTCCTGAC 1440
CAGTTAGACA TTAACCATAT TTATGACTAC CTTCTCATGG TAATTAGTTA TCTGCAGTCT 1500
CCTGGAATTC CCTGCAAAAG ACAATTCTGC CAACATTGAA GAGGTGCCAC ATTATGAAAA 1560
AAAAAAATGT ATCTTTGAAA ACTGCAGTAA AGCAAAAAAT TACTATGGTT TTTTACTATC 1620
TCTTTGAACT TTTTTTTTTT TTTTTTTTGA GACAGAGTTT CACTCTTGTT GCCCAGGCTA 1680
CTGGAGTGCA ATGATGCGAC CGTGGCTCAC CGCAACCTCC ACCTCCCGGG TTCAAGCAAT 1740
TCTTCTGCCT CAGCCTCCTG AGTAGCTGGG ATTAGAGGCA TGTGCCACCA CGCCTGGCTA 1800
ATTTTGTATT TTTAGTAGAG AGAGGTTTTC TCCATGTTGG TCAGGCTGGT CTTGAACTCC 1860
TGACCTCAGG TGATCTGCCC ACTTCGGCTT CCCAAAGCTC TGGAATTACA GGTGTGAACC 1920
ACTGCGCCCG GCTAAGACTC ATTTTTTGAT CAGAATGCAA GGGAGGAGCG AGGGGGAAGT 1980
TCTGAGTGTG TGCTAGGGGT GGAAATAACT GTTTCTTGAT TCAAGTGACT TCTTGATTCT 2040
TTTGCTCATT ACATGATTCC TTTTCCATCA GCATTTGTGT TGTAGTTGTG GGAACCGATA 2100
AGTGTCACCT GACTCTGTCT TGCCTCTTCC AGCAAGAACT TGCAAGACAG AAGCAGCGTT 2160
TCTCTGGCAA GGGAACCCAT AAGCACCCAA TCTCTGCTGT GAGCCAGGTC CAATACTAGG 2220
CACTTTACTT ATGTTAACCA GTGTAATTCT CCCAATAACC TGTAATTGTT GGTGTTTCCA 2280
TCTCCATTTT TTTTTTTTTT CGAGACGGAG TCTCGGTCTG TCACCCAGGC TGGAGTGCAG 2340
TGACATGATC TCGGCTTGCT GCAAGCTCCA CCACCTGGGT TCAAGGGATT CTCCTGCCTC 2400
AGCCTCCTGA 2410
|
