| Tag | Content |
|---|
EnhancerAtlas ID | HS034-17411 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:160106040-160106960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:160106423-160106444 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 |
|
| | 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 |
| GH02I159248 | chr2 | 160105445 | 160107579 |
|
Enhancer Sequence | TTTATACATG TCTTAGGACA CCCTGTGTTT CAGACAGTCT TCTTGAGGAT GTCTGAAAAC 60
ATCCTTGGAA GCTAGAGATA GTGCGTCCCT CCCTGTGGGA GGGCAGATGT TTCCTGACTA 120
CTATAATGTC TTGCCTCTTG GGGGCTATTT GCTTAGCCCC CTCATAAGAC TGGGGGTTTC 180
CCAAGCTCAG GGCTCCTCAG CTGTGACATA AACATAAACC ACCACCATGA AACTTACTTA 240
AGAGGGAAAG GGGAGGCTGG GTACAGTGGC TCATGCCTGT AACCCCAGCA CTTTGGGAGG 300
ATTAGGCAGG TGGATCACTT GAGGTCAGAA TTTCAAGACC AGCCTGGCCA ACATGGCAAA 360
ACCCCATCTC TATTAAAAAT ACAAAAAAAA AAAAGAAAGA AAGAAAAAAA ATAGCTGGAT 420
GTGTTGGCAC ATGCCTGTAA TCCCAGCTAC TCGGGAGGCT AAGGCAGGAA CTTCACTTGA 480
ACCCAGGAGG CGGAGGTTGC AGTGAGCTGA GATGGCGCCA CTGCATTCCA GCCTGGGCGA 540
CACAGTGAGA CTCTGCCTCA AAAAAAAAAA AAAAAAAAGA AGGGAAGGGA AAACAATCAG 600
AACCTGAAGT GCAAGTGTCT GCTGTGTCAC GAGTAATAAA CCGTTTGAGT CAGTCAGGGC 660
TCATTGCCCA CATTCATGTG AATGTGGCAA GTTACCCTAG CAGCTTCCTG CCACCAAAGG 720
GCTGCTTTCC TCTGACTTCC TTCCAATGGG ATATGCTGAA ATGAAACTGA GGATTTTTAA 780
AACAATTTTT TTTAAAGTGT CACAAACAAA TCAATGATTT CTTTACATGT TGAATATGAT 840
TTTGCAAAAA TATTTATAAC TTAAAAAGAT TCCCTCAAAT TCTTTATGAA ATCACCATCC 900
AGTTTCAAGA GAAAGCTATT 920
|
