| Tag | Content |
|---|
EnhancerAtlas ID | HS059-34455 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr4:4441990-4443240 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr4:4442535-4442550 | ACAGCTGAGTCATAA | - | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTAATGGCTC ATATAGTGGA CATTTTTTCT AAGCAATTTG TATGGATAAA TTTATTTAAT 60
TTCGAATATC CCCATCAGGT AGGTACTAGT ATTAACAACC TTTTAACAAA GGAGGAAACT 120
GAGGTGTAGA GAAGTTAGGA AACTTGCCCA GGTCACAGTC AGCAAATGGC TGGGCTGGGA 180
CATGACCTCA GGGAACCTAG CTCTGAAGCC CATGCTCGTA ACAACTGCTC CATGTGGGGT 240
ATATTCTACC CATCCTGGGC TGTGGGAAAG GACTTCTGTG GTCGAATCAG TCTGAGAAAG 300
CTGAGTCAAA GCTAGAAAGG TGTTTCACTA TATAAGTTTT CAGAGCCTTT AATATGCTCA 360
AATACATTTT GAATTTCCAA AAAGGATGGT ATTTGCAAAT AACCTGATTG CAGACACTCT 420
CTTCACAGAG TTTTTTGAGA GCAGTTTTCT CAAAAAGACT ATTTAGGAAA TGGTCCTCTA 480
CAAAATTTAA CAAAAAATTT TTTCAAAAGT CACTGTTATC AATCTTTTTA ATTGTTCTGG 540
TTACTACAGC TGAGTCATAA AACTTAGTGC CTTGAAACAG TGAGATTTAT TACTGATCAC 600
TGCTTCTGGG GTCAGGAATT TGGGAACACC TTGGCTGGGT GGTTCTGGCT CTGTGTGTCT 660
CAGGAGGGTG CAGTTAGAAG GCAACTAGGG CTGCAGTCAT CTGAAGGGCT GACCAGGGCT 720
GGAGGGTTCA CTTCCAAGGA GGCCACACAC ATGGCTAGCA AGTTGGTGCT TGCTGGGAGC 780
CTCATTTCTT CTTCATGGAG CTGCATGAGT GTGTTACTGG TGCATGGCAG CTGGCTGCCT 840
GCAGGGCTGG CAGTCTTAAA GACTTTGGTG GAAGCTTCAG TGCCTTTCAT GACCTAGCCT 900
TAGAAGTCAG AAATCATAAT TCTGGCCATA TTCTACTGCC CAACACATTC ACGATGGTCC 960
ACTGGAGTTC AAGGGGAAGA AACACAGACT CCAATTTGCT TTCTCAATGG AGCAGTAACA 1020
TCACTTTTTA AGAAGAGCAT GTGGTATGGG ATCTATTTGG GGGCAGCTTT CTTTGGAAAA 1080
TATAATCTGC TATTCTAAGT ATCACAAATA TGCACAAAGG TAAAGTTATA AGGATATTCA 1140
CCACAAAACT GCTTATAACA ACAACAAAAT GACTTAAATG TTCATGATAA TGTACCTCAT 1200
TTACAGTTGG AAGATATAAT GAAAGAGAAG ATTCTACTTG CAATAGCCAA 1250
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