| Tag | Content |
|---|
EnhancerAtlas ID | HS187-23567 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr8:21867240-21868310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr8:21867847-21867858 | CGCGCAGGCGC | - | 6.14 | | NRF1 | MA0506.1 | chr8:21867786-21867797 | GCGCCTGCGCA | + | 6.62 |
|
| | 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 |
| GH08I022009 | chr8 | 21867112 | 21868911 |
|
Enhancer Sequence | TGCCTCCACA TCCTACCCCC GGCCTTTGCT GGTCTGCAGA ACCCTCTCTT CTCAGTCTAA 60
ATTTACATGC CCTTTGCTCG CCTACGCTTT TCTAGACCCC AAATCGGACC TAATCCTTCT 120
CAAGTCTCCC CTTACTGTGC CCATTCCTAA GAGCCTTAGG GCCCACCTAC TCTTCTGTTT 180
GGAGTGTTCC TAACCCCAAC CCCTGCCTGT CCCAGTAGCC AAAGTGTGCT TCTTACGAGC 240
TGGGCCCAGA CCATGGTGTC ATGACCAGCG ACAAGGATGT GCAGTTTCTG GGGAGTGTAC 300
AGTAAGGGGA GCGGTGGAAT TAATTTGGGT GAAGCCCCTG CAGAGAGACG CCAGACTGGT 360
TTATGCAGGT TAACCCTCAC ATCGCTGCCA TAGCTCGCTA CGACAATGAA AAGAGCAAAA 420
GCTATTGACA CCATCCCGCC TGCACCCTGC GAAAGAAAGG GAGAGTTTGC ACCCCACCTG 480
GCCTGACCTC CCCGACAGCG CTGCAGCCCC GGAAGTAATT TCGCGAGTTT CTTCCGCCGG 540
AAGGTGGCGC CTGCGCACTC AGGTGTCCAC GGCCTCTGTT CCGGCTCTCC CCCAGCTTTC 600
GCCGCCGCGC GCAGGCGCAG TCCAGACTCG GTCCTGGCCG GGGGTTCTAG TGTTGCCGCT 660
GGAAGAGCGA GGTCTTAATT GCTTTGCGGG AGCGTTCCTG GGGAAGTCCA GAGCTGGGTT 720
CCTGCGGCCC TTGGGCCCCC ACGGCGCCGT GTGCCTGGCA GAGGTTCGAG TTCACACGCA 780
CCGTGGCTTG CAGCAGGCAG CCGCAGTGCT AATCAGCGGC GCTGTTCCCG GGCTGGGTGC 840
AGCTGCTAAG GACAAGGCCC CTGCTCCGAA GAACGCGGTG GCTCGGGGAT ACCCTGAAAG 900
GGACGGCCAT GGCGCACATG GGATGCCCTA GGGTTCGTGG GAGGGCATGC AGGCGCAGCC 960
CCCGCAGGGG TTGGCCTGCC AGAGAAGGCA GGGGAGAGCA CTCGGGGCTG CACAAATGGT 1020
GTGGCCGGAG GGAAGGTGCA GCCTTGTGTG TGTCTGGATG AGGGCTGGGC 1070
|
