| Tag | Content |
|---|
EnhancerAtlas ID | HS088-05165 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:207871220-207872530 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:207872413-207872432 | CTCTGCCACCTGCTGGCCT | - | 6.62 | | Gfi1b | MA0483.1 | chr1:207872377-207872388 | GGCTGTGATTT | - | 6.02 |
|
| | 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 |
| GH01I207698 | chr1 | 207872301 | 207872450 |
|
Enhancer Sequence | GAGTATGAGC TTGCCTGACC TGCTGGACAT TGAAATTGGG GTTAGGAATT AGTCCAAAAA 60
GGGGAGATTT GATGTGGCTT AAAAAAAGAC AGACAGACAG ACACACACAC ACACACACAC 120
AATCAGAGAG ATGAACTTTT GAAAGTATAT ATAGGAAGAA AGGAAAGACA CATATGGAAC 180
TAATAACATG AGATATGAAG AGGACACTGG GCCATATATT AACTGGCAAA TTCAAAGACA 240
AGTATAATTA CTTGTTATTA ATATATAGGT AACACAGTAA GTTTAAAAAA TCCTATTTTC 300
AAAATTTTAG AATTTCAAAA CAGCAAATAG AATATGAGTA ATTTAAGAGT CTCAGAAAAA 360
ATTGCAAGTA ACAAAAAACT TATTCTAAAG AGCTAGGATC ATTTAAGAAT CATTTCAGTA 420
AATTCTTTAA ACCATCAGTA ATGAAATTTG TAATAGGACT GAAAGTGTAA AAATCAGCAT 480
TTTAAAAAAA TCCAGTCATA TATCGTCTGG CTAGTCATGG GCTCTGGGCT CTGAGCTGGG 540
GTTCTGATGG CTGCTGTTAA TATTTCCAGC AAGGTCATTA CCTTGTTTAT GTCCACCTAG 600
TGCTCTTCAC AGGGTGCACA TCTCTACACG GGAGCTGACC AGCATGGGCA ACAAAGCACC 660
TGATCCCAAA ATGTAACACA GAATCTTGGC AGGCTCCAAA AGCCAGCACC CAGTAAGAGT 720
TAGGAGGGCA TCGGGGCCCA ACAGACATTG AGAATTTTCA ACAATTGCGT ACAAAAATTA 780
TGTCCTCTCT TCTTTCCTTT TTCCCCTAGA ATATTCGTGC TTACTCTTCA GCAGCCCAAA 840
TTGCCCTTTT GAGCCTTCTT CACGCCATCA CAGATGTGGA GATGAAAGGA CAATCTCTGT 900
TCTCTCGCCA GCTATTTCCC ACTTTACCAC TCCAAACTGG GAGCTGTTTT ACTTGCTGTT 960
CCAGGGTCAG AGTTACGAAG GCATTGCATT AGAAGACTGG GTTTCTAATA ATGACAATGA 1020
GTAATCAGTG AAACTCCAAG CCTGGGTCCT GGGTCAAGGA GATGGTGGCT ATTTTGTGAC 1080
CACCTTTTTC AATTCAAGCA GGACTATCAT GTGACCAAGC TACTGCATTT TGCCACTCTA 1140
TATTGCTCCC TTCTGGAGGC TGTGATTTTT CCAGAATAAC GTAGCCTGTG CAACTCTGCC 1200
ACCTGCTGGC CTCAGGTCCT CAAAATCCTG AAATTGGGGC TGGGCCTTAG ATTGTGAACT 1260
AAGTGTCCTC TTGGCTGAAA CAGCTCGCTA TTCACTCCTA TTTTCTTCTT 1310
|
