| Tag | Content |
|---|
EnhancerAtlas ID | HS061-01781 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:174143540-174144620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr1:174143928-174143942 | TTTTATCTTATCCC | - | 6.05 | | NR2C2 | MA0504.1 | chr1:174143848-174143863 | TGAGGTCAGAGGGCA | + | 6.95 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGATTCTTCA GAGAAACAGA ACCAATAGGA TAGCTATGTG TAGATACAGA TCTGTTGGAA 60
TTGGCTTACA CAATTATGGA GGCTGAGAAA TCCCGTGATA GGCCGTCTGC AAACTAGGGA 120
ACTAGGGAAA CCAGTAGCTC ATTTCAAGTC CAAAGGCCTG AGAACCAGCA GAGCCAACAT 180
TGTATTAGGT TGGTGCAAAA GTGATTGAGG TTTTTGCAAA ATAACTCTCA ATTCGAGGCT 240
GAAGGCTGAA AAACTAGGGG GCTGCTGATG CAAGTCCTGG AGTCCAAAGG CTGGAGAACC 300
TGAAGTTCTG AGGTCAGAGG GCAAGAAAGA CAAATGTCTG AGCTCCAGAA CAGAGAGTGA 360
GTGAATTTGC CCTTCCTCTG CCTTTTTGTT TTATCTTATC CCCCAGCAGA TTGGATGGTG 420
CCTGCCCACA CTGGGTAAGG GTAGATCGTT CTTACTCAGT CTATTGATTC AAATGGCAGT 480
CTCTTTGGGA AACACCCTCA TAGGCAAATG CGGAAATAAT GCTTTTACTA GCTATCTGGG 540
TATCCCCTAG TTTAGTCAAG TTGACAACTA AAACTAGCTA TCACAGTAAA TTTATGAAGG 600
TGTCAAAGTA TTTATATTAC TAAGATTTTT AAAATATGAA ATAGGATGAA AACCAGGGGG 660
TAAACTTAGT ACAGTTATCA AATTGTTTTT TTCAGCATGA TTGATTTCTA AAAGGCTTTG 720
AATAACCATA GATTTAATTT TCTTGTATAT GACACAGACC AGTAGATTAT GGAATGCTAG 780
ACATTGTTCA GTACAATATT ATATAACTGT AGTTAGAAAT TACTTAGATA CCAGAGTTAT 840
GGTTCTTAAC CACTTGGGTA CCAAGAATTT TTAGAGAGCA TGAACCATGT CGTCTTTTTG 900
TTCTGGATGG CATGAAGTTG GGGTCTGAGC ATAGATATCA TCTTAAAAAG CCTTTCTTGA 960
GACTGTGGTC TCTGTTAGAA ATCTCTCATT TGTGCTTTTA AAGCATTCAG TTTTCCTCTT 1020
TGTTGTCATA CTAATCACAT TGTATTGCAA CTTGCCTGTT TCTGCATTAG ACTACAGGCT 1080
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