| Tag | Content |
|---|
EnhancerAtlas ID | HS197-09117 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr17:44343480-44345610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB7B | MA0694.1 | chr17:44345146-44345158 | GCGACCACCAAA | + | 6.52 | | ZBTB7C | MA0695.1 | chr17:44345146-44345158 | GCGACCACCAAA | + | 6.37 | | Zfx | MA0146.2 | chr17:44344117-44344131 | GGCGCCCAGGCCTC | + | 6.11 | | Zfx | MA0146.2 | chr17:44344123-44344137 | CAGGCCTCAGCCGC | - | 6.19 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CATACACATT CCAGGATACA TTCTCTGTCA TCTGGAATCT CCTCCCTTCC ACAAACCCAC 60
GCTGTCTTAA GCACTATTTT CCTATTTGTT GTTGACCTAA TCTAGAAAAA AGCGGCCATC 120
ACTCTTTCTC CCCCACTCAG TCCCTCAGTC CCGAAACACC CTTATTCTCC GCACTTGTCA 180
CCCCACCCTC TGCTGCCCCC ACCGCAGCGC GCAAACGCAC ACGAGTTTAA AGTTTAGGCT 240
GTGATGCTAT CCTCGCCCGC AGATCACAGG ACAGACATTC TCGGGGACAA CTTTGCGAGG 300
CCATGTGCTC GTCCCCCTTA GGAAGGAAGA GGGAGAAATC CCTGCGGCTC GGTTTTGTTC 360
CAATGGTCTG CTCAGCGAGT GATTCCCGTT TCCCCAAAGG CTGCCCCTCA TTAGCATGAA 420
CGGGGACGCG GGTGTGGAGA AGGGGTTAGA GGAGAGAAAG CAAGCAAAAG CCCAGGCTCA 480
CTTTTAGAGC CTGGGAACCC TGTCTGCAAA AATGACAGCT AGAGCTTTCT GGCTCCTCTG 540
TTTAATCGTC GGATCATCCC CCGAAGCTCC GGTGGAGAGA AAAAGTAAGA TCGGTGTAGT 600
GCGGAGCCCT GGGAGCGGAG CGGGGATCTG GGGAGGGGGC GCCCAGGCCT CAGCCGCCGG 660
CCGACAACCG GGCCACCTTC CGTGAGGCCG CACACGCTCC CACAGGCCCG CGCCTGGCGC 720
AAGCCGAGAA CCGCGCGTCG CCGCGCCGCG GGCCCGCGAC GGAGGAAGCC CCGAGACGCG 780
CGCGCTCACG GGCCCTACGC TTCCCCGCCG CCCGGCCGCG CGCGCGCGCC GCCGAGGGCC 840
CCGCCGGCCC TGCCCACCCC AACCGGCCGC GCGCCGTTGT GCCGGCCCCC GGCTCGCCGC 900
CCGCGCCGCC GCCGCGCCTC AGCTTCAGAT TCGGCCTCAG TCAGCCGCGC AGGGACGCGG 960
AGCCCGGCGC CGAGCTCTGC GCTTGCGCTT GCCGGGCGGG CATGGACGGG CGAGAGGCGT 1020
TCTGCAAGCG CGAAATCGGT GAGCCCGGCC GCCGCGCCGC CGCCCCGCGA GCCTTTCCGA 1080
GTCCCGGAGA ATCCTGCACG CGAGATCCCA GGGCGCCCGA CCCATGCGGG CCGTTTCGCT 1140
GTTGCTAAAA ACCAACGCCC AGGGACTGGG AGAGGAACTG GGGTTCCCAA ACTGTTTTTT 1200
GGAAGCAGCG ATGAACGGGA TAGTGCATGA CGTGGACGTG CTGGGCGCGG GCATCTGGCT 1260
GGTGACCCTG CTGGTGGATC GGGACGGGCT GTACAAGATG AACCGCCTGT ACCTCACTCA 1320
CCCCCGACGT CTTCTTCTTC CGAGTCCACA TGTTAGTCCT GGACTCCTCC AGCTGCAATA 1380
AACCGTGTCC AGAGTTTAAA CCTGGTATTG AAACTGAGCT GAATGACGCT GCATATGTAC 1440
TTTATACCAC CGTTTGTAAC GTGGGTGCCA CAGCCCGGGC TGTGGGTCGT CCAGTCTTTT 1500
TTTGGGACGG ATGGGGGACA GTATTGTAAC ATGATTAGGA TTTAGACGAC AGGTATTATT 1560
TCCGCCACTG TGATTTAAGC ACCGTCAGCC CCACCCCCAC GGGTGAGAAC GGCAGCTGTT 1620
GGCACAAAGC GGGCTGTCAA TAAATAGATG TTGACAAATG GAGTGAGCGA CCACCAAACA 1680
CCATTGCCAG AAGGGACTGT ACAGAACTGA GTTTAGAAAA GCTGCTTTTT TGGGGGAGTG 1740
TGTGGAGGGT TGGTAGCGGG GAATACCCAC TCCCACATCT TTTTTTTTTT TTTTTTTTTT 1800
TTTTTAGACA GAGTCTCGCT CTGTTGCCCA GGCTGGAGTG CAATGGCGCC ATCTCAGCTC 1860
ACTGCAACCT CCGTCCCCCA GGTTCAAGCC ATTCTCCTGC CCTCAGCCTC CCAAGTAGCT 1920
GGGATTACAG GCTGAGCCAC TGCGCCCAGC CCCACTCCCA CATCTTTCTA GGCATGTGCT 1980
CTGGGAAATC CTGATACAAT GTGATAAGGA CCTTTGTTCT GTAATGTGGG CTGGTTACGT 2040
ATTGCTTTCC CTTCCCCACA CCCCGTGCTA CTTTTTGTAT TTTTAGTACA GATGGGGTTT 2100
CACCATGTTG GCTAGGCTGG TCTCAAACTC 2130
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