| Tag | Content |
|---|
EnhancerAtlas ID | HS080-00413 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:18975520-18977740 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr1:18976337-18976352 | ACTGCTGTGTCATTC | - | 6.2 | | Nfe2l2 | MA0150.2 | chr1:18976339-18976354 | TGCTGTGTCATTCTG | - | 6.95 | | ZNF263 | MA0528.1 | chr1:18976624-18976645 | GGAGGAGGGTGAGGGGAAGAA | + | 7.84 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH01I018649 | chr1 | 18976241 | 18976390 | | GH01I018652 | chr1 | 18976454 | 18976529 | | GH01I018650 | chr1 | 18976581 | 18976730 |
|
Enhancer Sequence | GTTCATTCAA GGGAACTTGG AATTCCTCTG CAGGCTGAGA TTACAAAGGG TGGAGTCAGA 60
CTCAAACAGG CCTTAGAGGT CATCTGGCCA TTTTACAGAT GGAAAAGCTC AGGTCCAGAG 120
GGAGTGACAT GAGTGAGGCC AATGGAGGGG AAGGCCACTC TGGTCTGCTG ACAGTTATGT 180
GCGGGTACAG GAGCAAAACG GACTGGTGGA AGCTTTGCTC CCAGGAATTA GGAAGGCATG 240
GGATAAGGAC AGCCATGGGA ATGAGGCCTT TCCCCATGCT GGCAGTTCAT CGCCCTTCGT 300
GTTTAATGTG ACACATGCCT TAAAGTTCTG ATTCACAGAG GGGGAGACTG AGGCACAGAG 360
AGTTGATTAG CCCAAGGAAG TAAGGGGAGG AGGGTCCCCT TCTAACAGGC TCTGCAGGAC 420
TCTGACACCT TTGCCCTAAG AAGCCTGAAG GGCAGCAAGA ATCTCCTCTT CTTACCCCAT 480
CTGGACAATT GCAGCCCCCA TCCCCCTCCC CCGTTCTTCA TAAACCCCAG ATTCTCAGGT 540
CCAGGGGAGA CTGTGGTTCA AGCCATTGCC ACACCCACCC CACCCCGCTA TCACCCACAC 600
TCCCAGCACC CATAAGCACC TACTGGGATC TCAAGCCCTG CTAGATGCCA CAAACTTGGC 660
CTGCTGAAGG GTTAGTCTGT CCACCATCCG GGGAACTGTC CTTTCAACAG CAAGGGAAAA 720
TAAAGCCCAG AGGGAAAAGA ATCACAGATT GTGGTTAGGG TTGGAATTCA GATCCTCATG 780
TAAATGGCCC CATGCAGAGG CCCTAGCCTG AGCACTAACT GCTGTGTCAT TCTGGAAGAG 840
CCGCTTCATG TCTCTGGCCC CTGGTCCTTT TGTCTGAACA ATGGCAAGGC AGGATCCACC 900
TAGTGGTTTT CAAACTGTGT TCCATGGAGT CCTGGGATTC TCAGCCTCAG GGGCCATCCT 960
TTGAGCTGTA ATACTCTGGG CGTGTGTTTA GTGGAGGGGA AGCAGTGAAA AAACAGCCTG 1020
TTTCCCCATG GATAGAGGAA ACTCCGGGGA GGCAGGGCTT TGTCCTGGGA AGAGCAAGGA 1080
CCACTTCCCA TCCAAGGCTA CTCTGGAGGA GGGTGAGGGG AAGAAGCTCT GTATACTCCT 1140
GGAATCAGAG CCCTCAGGCT GTGGTTATTG GTCTTCAGAG ATAAGGTGAT AACTGCTTAT 1200
CTGGTGACAA ATGATTATCC TCCTCTTCTA TTCCTCTGAT TAGGGAACTT TCTCTCCTGG 1260
CTGGGAGGTC TCTTTGGAAA AAGGGCAGGG CTGGTCAAGA GACACTGACA TCTGCCTCTT 1320
CAGTCCCTGC CCGGCTTGCT GTGTGACCAG AAAGCAGTTA CACACTCTGT GCTTCATTTT 1380
GGGGCCTGGT GGAGCAGCTG GCTTGCAATG CCATCCTGGG ATGGTGCTGG AAGGAGGATT 1440
CAATGCAGCC TGTGGGGGAT GGAAGGAGCA GGAGGGCAGA GGGCGGAGGA CAGAGGGCTG 1500
TGCCCCGGAG TCACCCAGGT GCTTTTGCAA GACATACACA CCTGGGTACT TTCTTGATTT 1560
GGGACATCTG AGTACAGTGG CTTTGGAGCA ATCTGTCCCG ATCATTCTGA TGGCCTCCCC 1620
AGCAAGAGCC ACTGGTCTCA TGCAACACCT TTTTTTATAG ATGGAGAAAC TGAAGCCCAA 1680
AGAAGGGAAG AGAATTGTTA CCTGTTGCAT AGCAAACGGA GAGGAGTCAG AAGAGAGACC 1740
CAGTCCCCAA AGTATTATGC CAGGCACCAT GAAGGGAACA TTCTTCCAAA GTTTCTGGGT 1800
CCCTCAGCTT TTGTTACGGT CACCTGTCCC TACTGAGGGT CCCATCTGCC AGGGTACCAT 1860
GCTGGGAACA ATGGGGCTGG CAGGGCAAGA CCTCTGCTTT GTCCTACTGT CCCCAACTCC 1920
TGCTTGTGCC ATGGATGGTC TCCCAGACAC TCACTGTCAT CTCAGCTCTG GGCTCTGAGC 1980
CCTTATATCC ACAGGCAGCT TCAGTGCACG GAAGGACCCC TGGACTTGGA ATCAGTAAGA 2040
CCCAGGTTCC TCCCCATTGC TGCCCCCACC ATGTCCCCTG AGCTGTGGCT TCCCCTCTCT 2100
CAGCCTTAGT TTTCTCATCC AGACAATGGG AGCAAATGAA TTAAAACACA GAAAAGCTAT 2160
GTGGCACATA GGAAGTACAT GCTTAAAATG AGATGAAAGA CCTGAAAGTG ATTTGTGTGA 2220
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