| Tag | Content |
|---|
EnhancerAtlas ID | HS060-30224 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:106093930-106094760 |
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 | chr6:106094434-106094449 | TTATGACTCAGCTTT | + | 6.06 |
|
| | 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 |
| GH06I105643 | chr6 | 106091392 | 106097419 |
|
Enhancer Sequence | AGAGATCATC TGCATTCCTG TTACCTAGTC AAGTGTCCTG GATAAATCAC AAAAACATCG 60
AAGTCTTAGG TCACGTCACC AAGTCTCACG TTCCAAGAAC TGTCAAGAGA TTGCTTATGT 120
AGCCACAGGC CAGACAGACA GGGGCTTTGT GAGACTATCC CTCAGGGGTG CTGGGGGTGT 180
TTGCATTGTT AGCCTGGAAA AAGCTAGCCA GACCAACATA GTCACAGCAA TTGAAAATCC 240
TGAAGGCCCA TCTATGACCA AATGTATTAA TAAATAAAAA GACCTATAAG AAACCTTCCC 300
ACCAGCATTA ACCACACCAA AAGCAAGTCA AACCCAGGCT TCTCATAACT GGTTCTTGTT 360
CCAACACAAG AGTGAGAAGA GCATCTTGCT GCGGCCAACG GTTACTATAG CTCTCCTTTT 420
GTAGAAAGCC ACCGTCTTCG AAGAGCTTAC TAGGTGTCTC CACTAAAGAA CAAAAAACAT 480
GGGTAAGACT GGTTTCCTCT CAAGTTATGA CTCAGCTTTG ATCACCACAC TTCCACTTGA 540
GCCTATTAAC GTTCAGTGGA CAGAATGTCA CTCTTTTTCA ATCAGCTGCT ACAGCAAACA 600
ATAGCCTTGC TGCATTTCAG TCATATAGAA AGCCACAGAA TATTTCCTTT TGACTCTCTT 660
CTCTCCACAT CAGACCCACA GTCAGGCTCA TGCTGAGGTC TATCTTCTCA CAATCTACTA 720
GAAAGTGGCC TGCCTCTACA TGCTTACCCT GCTAAAATGA GAAGCAAGAA ATAAACAACT 780
TCATGTTAAT TATAAATAGG AGGCACTGGA TATTAAACCT GCCCATAGAA 830
|
