| Tag | Content |
|---|
EnhancerAtlas ID | HS176-23709 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr20:11176410-11177320 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIA | MA0670.1 | chr20:11176535-11176545 | ACTTGGCACC | - | 6.02 | | TBXT | MA0009.2 | chr20:11176485-11176501 | TCACACACATGTGCGA | + | 6.74 | | TBXT | MA0009.2 | chr20:11176485-11176501 | TCACACACATGTGCGA | - | 6.82 | | ZNF740 | MA0753.2 | chr20:11176815-11176828 | CCGCCCCCCCCCC | + | 6.64 |
|
| | 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 |
| GH20I011195 | chr20 | 11175658 | 11177760 |
|
Enhancer Sequence | CACACACACA CACTCTATAC TTCTATAGAG TATACACACT CTATATTTCT CTGTCTTTCT 60
GTCTCTGTCT CTCTCTCACA CACATGTGCG AGCACACACA CACACAATCA CAGTGCTAGG 120
ATTTAACTTG GCACCTTGGC TTACAATTTG CCTCTCACTG GAGTTTCTGG AGTTTGGTGC 180
CAGTTCAAGA GCATGATCTG TTTGACATGA ATTCTACAGC CCTCTCTTCA TTTCCTCCTA 240
ACTGGATAGC TTCAGTTTGC CGATGATTAA TGAGTCTGGA AGGTGAGCGA CAGTTATCTT 300
AAGGGCTCTC AAAAGTTTAT TTCAGAGACT AGCCAAACTC TCCTGCTACA TTAACTGCAG 360
CGAAGTTTCC TGTTTAACAG CCCATGGAAA ATAACTGCCT GACCCCCGCC CCCCCCCCAA 420
ACCAAGCTGC CATGAGCGCA GCTCTGTTTA TTGGCCAACA GTGTGCATGT TCTCTCTATC 480
GCTTCCTTTC AGGCAGACGA ACATTTTACC TATGAGAAGT AGGAAGTCCA TTGTGAGGCT 540
GGTCCAATAC TGGACCTCAT TTGGATGTGG AGGATTTCTG AAATTGGAAA GTCAGGACTG 600
ATCTGGAAAA TGTGCTTACA GATAGTGGAA CAGGAAAATG ATTCGCTCCC CAAGGCCAGT 660
TCCTCCTCCT CTGCTGGGTG GAAAAGGTGG GAGGAAGGGA CAGGGTGTTC TGCCTGTGAT 720
TGGAATTCCC CTGTAGAGTC ATAGAGGATG AGCAAGCCTT TGGTTTTCCT TTTTCATATT 780
TTATTTTGCA CCTACAATAA TAAGCATGCA GAGAGGAGAC AGAGAGGCCT AAATGAGTTT 840
TTTTCCTTTC TAAATAATGA CCAGCTCTGT ATCAATCTGA AGGCTACTGA GGGATGCTGG 900
TGGCTGGATG 910
|
