| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00545 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:18975990-18977780 |
Target genes | |
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 | CTTACCCCAT CTGGACAATT GCAGCCCCCA TCCCCCTCCC CCGTTCTTCA TAAACCCCAG 60
ATTCTCAGGT CCAGGGGAGA CTGTGGTTCA AGCCATTGCC ACACCCACCC CACCCCGCTA 120
TCACCCACAC TCCCAGCACC CATAAGCACC TACTGGGATC TCAAGCCCTG CTAGATGCCA 180
CAAACTTGGC CTGCTGAAGG GTTAGTCTGT CCACCATCCG GGGAACTGTC CTTTCAACAG 240
CAAGGGAAAA TAAAGCCCAG AGGGAAAAGA ATCACAGATT GTGGTTAGGG TTGGAATTCA 300
GATCCTCATG TAAATGGCCC CATGCAGAGG CCCTAGCCTG AGCACTAACT GCTGTGTCAT 360
TCTGGAAGAG CCGCTTCATG TCTCTGGCCC CTGGTCCTTT TGTCTGAACA ATGGCAAGGC 420
AGGATCCACC TAGTGGTTTT CAAACTGTGT TCCATGGAGT CCTGGGATTC TCAGCCTCAG 480
GGGCCATCCT TTGAGCTGTA ATACTCTGGG CGTGTGTTTA GTGGAGGGGA AGCAGTGAAA 540
AAACAGCCTG TTTCCCCATG GATAGAGGAA ACTCCGGGGA GGCAGGGCTT TGTCCTGGGA 600
AGAGCAAGGA CCACTTCCCA TCCAAGGCTA CTCTGGAGGA GGGTGAGGGG AAGAAGCTCT 660
GTATACTCCT GGAATCAGAG CCCTCAGGCT GTGGTTATTG GTCTTCAGAG ATAAGGTGAT 720
AACTGCTTAT CTGGTGACAA ATGATTATCC TCCTCTTCTA TTCCTCTGAT TAGGGAACTT 780
TCTCTCCTGG CTGGGAGGTC TCTTTGGAAA AAGGGCAGGG CTGGTCAAGA GACACTGACA 840
TCTGCCTCTT CAGTCCCTGC CCGGCTTGCT GTGTGACCAG AAAGCAGTTA CACACTCTGT 900
GCTTCATTTT GGGGCCTGGT GGAGCAGCTG GCTTGCAATG CCATCCTGGG ATGGTGCTGG 960
AAGGAGGATT CAATGCAGCC TGTGGGGGAT GGAAGGAGCA GGAGGGCAGA GGGCGGAGGA 1020
CAGAGGGCTG TGCCCCGGAG TCACCCAGGT GCTTTTGCAA GACATACACA CCTGGGTACT 1080
TTCTTGATTT GGGACATCTG AGTACAGTGG CTTTGGAGCA ATCTGTCCCG ATCATTCTGA 1140
TGGCCTCCCC AGCAAGAGCC ACTGGTCTCA TGCAACACCT TTTTTTATAG ATGGAGAAAC 1200
TGAAGCCCAA AGAAGGGAAG AGAATTGTTA CCTGTTGCAT AGCAAACGGA GAGGAGTCAG 1260
AAGAGAGACC CAGTCCCCAA AGTATTATGC CAGGCACCAT GAAGGGAACA TTCTTCCAAA 1320
GTTTCTGGGT CCCTCAGCTT TTGTTACGGT CACCTGTCCC TACTGAGGGT CCCATCTGCC 1380
AGGGTACCAT GCTGGGAACA ATGGGGCTGG CAGGGCAAGA CCTCTGCTTT GTCCTACTGT 1440
CCCCAACTCC TGCTTGTGCC ATGGATGGTC TCCCAGACAC TCACTGTCAT CTCAGCTCTG 1500
GGCTCTGAGC CCTTATATCC ACAGGCAGCT TCAGTGCACG GAAGGACCCC TGGACTTGGA 1560
ATCAGTAAGA CCCAGGTTCC TCCCCATTGC TGCCCCCACC ATGTCCCCTG AGCTGTGGCT 1620
TCCCCTCTCT CAGCCTTAGT TTTCTCATCC AGACAATGGG AGCAAATGAA TTAAAACACA 1680
GAAAAGCTAT GTGGCACATA GGAAGTACAT GCTTAAAATG AGATGAAAGA CCTGAAAGTG 1740
ATTTGTGTGA AATACATGAT CCCTAAAAGT CTATATGCTG AGAATTTCCC 1790
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