| Tag | Content |
|---|
EnhancerAtlas ID | HS042-18590 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr17:3288930-3290580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr17:3290106-3290119 | AAGAGGTCAAGGG | + | 6.14 | | PLAG1 | MA0163.1 | chr17:3289737-3289751 | CCCCCGTGCGCCCC | - | 6.51 |
|
| | 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 |
| GH17I003386 | chr17 | 3289388 | 3289823 |
|
Enhancer Sequence | AACACCTTTG TGGTAGAGCC AGGATTCAAA GCAGGTCTGA CCTACACCAA AGTCTGAGAG 60
TTACCCACTA CGCTAGAACA CTCTTCTGAG ATTCCGTTTC TTCATAAAAT TAAGATTATT 120
GGATGAGCAA CGTGATTTTC AATCCATTTA GCAAGCAGAA ATTTGTATAT TTATAAACAT 180
ATATTAAAAT GTATATCTGG AACCTCAACA TGCAGGAAGT CTACCCGGAG TTCTAGAATT 240
TCGGCCGGCT GCCTCCTCCC TCCCCTCGGC ATTCCCACCT GTCAGTCCAC TCCATGGCTC 300
CGACCAACCT CACATCTGCC CCCGTGTTCC TCCTCCTCGG CCTGGTGGAC GGAACAGACG 360
CCCACCCGCT GCTGTTCCTG CTCTGCCTTG GCATCTATCT GCTCAACGCC CTGAGCAACC 420
TGAGCATGGT GGCGCTGGTG AGATCCGACG GGGCCCTCCG CTCCCCCATG TATTACTTCT 480
TGGGTCACCT GAGCCTCGTG GACGTCTGCT TTACCACCGT CACGGTCCCC AGGCTGCTGG 540
CCGGCCTGCT CCACCCGGGC CAGGCCATAT CCTTCCAGGC GTGCTTTGCC GAGATGTACT 600
TCTTCGTGGC TCTGGGCATC ACCGAGAGCT ACCTCCTGGC GGCCATGTCC TACGACCGCC 660
CGACGGCGGC GTGCCGGCCC CTGCGCTACG GCGCGCTGGT GACGCCATGG CGCTGCGCCT 720
CGCTGGTGCG TGCGTCGTGG GCCGTGACGC ACCTGCACTC GCTGCTGCAC ACGCTGCTCC 780
TCTCCGCGCT CTCCTACCCC TACCCCACCC CCGTGCGCCC CTTCTTTTGC GACATGACGG 840
TGATGCTGAG CTTGGCGACC TCGGACACGT CCGCCGCGGA GACGGCCATC TTCTCCGAGG 900
GCCTGGCCGT GGTGTTGGCC CCGCTGCTCC TCGTGTTCCT TTTCCTACGC GCGCATCCTG 960
GTCGCGGTGC TCGGCTTGCC GGCGGCCGGC GCCGCGCCTT CTCCACCTGC GGGGCCCACC 1020
TAGTGGCGGT GGCGGTGGCG CTTTTCTTTG GCTCTGTCCT CTCCGTGTAT TTCCCGCCGT 1080
CGTCTGCCTA CTCAGCCCGC TACGACCGCC TGGCCAGCGT GGTCTACGCT GTCATCACGC 1140
CGACCTTGAA CCCTTTCATC AACAGCCTTC GCAACAAAGA GGTCAAGGGC GCCCTGAAAA 1200
GGGGGCTCAG ATGGAGGGCT GCACCCCAAG AGGCGTGAGG GCAAATCTGG CTCACTGGCA 1260
TTTTCATGAT AACAGTTACA GAAAAAAAAA CCTTGTTTTT TGGCTTTCTA AAGCACTATT 1320
AATTTCGATC TACCCTGTCT TATTTCTGTT AAATAAGAAA TTAGACCCGA AGTAAATATG 1380
ACAAAGTGTT TACTGTAGTG ATAGATACAT AGTAGGTTGA ATTCGTGTGT TATCTGAATG 1440
TGTGAGATAG ATTCTACTTT TAAATTTTGG GTAAATGAAA AGACAGCAAA TGGAGGTAGA 1500
CAAATAGTTT GTGAAGAGGG AGAAGAAAGA GTGTGACTAG CAGGAACCCG GTGGGTGGAC 1560
GGGAAGCCTG TGAAGCAATG GATAATTTTT TTTTTTTTTT GAGATAGTGC CTCCCTCTGG 1620
CGCCCACGCT GAGTGCAGTG GTGCCATCTC 1650
|
