| Tag | Content |
|---|
EnhancerAtlas ID | HS177-14324 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr21:47123930-47125110 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr21:47123992-47124007 | GATGTCAAGAGGTCA | + | 7.08 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AATTACCAAG TAGGGAGTAC AAGGAGAGAC GAGGATCCAG GATGGAGGCT GGCCCTCTGG 60
CTGATGTCAA GAGGTCAGAA GGGAAGACAC GTTTATCTTG AGTTGGGAAG AACAAACTGG 120
TCAGCTGGAG GAAAGCCAAG GGGCACTGCC CAGCCGCTGA GTGGGTGGTG GTGAAGGTCA 180
TATCAGATGC TGGGGATGGC TCCAAGGAGA CTCTGGTGGC AACCCTGAGC AGTGTGGAGT 240
CAGTGGTGGC TGGGAGAAGG GCCATCACTG CTGGGGTGGA GCAGAGCCCT CAGGAATGAG 300
GGGAGTTGAC ATAGTTTGTC TGCAGAAAGG AGTAAGGAAA CATGGTGGTT GGTGGGGGAA 360
CTGGGAACAA GAGCAGGAAG TTTTAAAATG CAGGACATGC TATCCTCTGT TGCTGTGGTC 420
TGCGGGCCAG CTGCAGACTG GGAGGCCGCA GCGTCTGCCC CCATTTTCCT GCTCTCCCCT 480
GGCAGAGGCG CCCCAGGGGG CTCCAGGGGA GTGCTGTCTG CTGCTGGCGG TGGGGGGCGG 540
TGATCGGATA TGGGAAGGAG GGAGACATGG AGACATAAAA CATTGTCTAA GTGAAGGGCA 600
ATCGTATTTG AAGTAATTTG AAGATTGACA GGAAATTCAT AAAGGGAATA TGGAGTTCCG 660
TTTACAACAG CAAGAGATGC CTTGTCCATA GCTTCCTGAC CTCTGGAAGA ACAGAAGTTG 720
CTGCTGGCAG AGTTCCAAAA CATGAAAATG TAAAATGGAA TTGAATAATC TCTCCTAAAT 780
CAATTTTGTG AGCCAAATGA CCTAGAGAGT GATGTGATAC AGTGCAGGTA GACGACACAG 840
GGCGCTGCTG TCTGCTGAAT ACATGATGGC AGTTGATTCT GGAGATAACC AAATACCAGC 900
TTCCCTTTGG TCTCTGGAGC CTGGTTTCTA CCATTAGCCT CCACAGAGCC CATCTTGGGG 960
AGGTGTGCCT CTTTTTTCTG GCTTCGGTGT GCTGATTCCA GAGTCTGTTG TGAGGGTCAC 1020
CTTGCTGGCT GTGAGGAGCT CTCTCTCTGG GCCCAGCCGG AAGGCCCTTG CAGCCTCTTT 1080
TCAGGAGCAC TGGGCTGTTG CTTTCTGTGC AGCATCGTGT GGATGCATCC TCTGAGTGAG 1140
GCTCATTTGC TTATGTGAGT TCCCTTGATC AGCCAGGTTC 1180
|
