| Tag | Content |
|---|
EnhancerAtlas ID | HS080-01964 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:118250210-118251680 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr1:118251056-118251066 | GCTAATCCCC | + | 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 |
| GH01I117708 | chr1 | 118250679 | 118251611 |
|
Enhancer Sequence | ACCTGACACA GTAAGTAATC AATCAATATT TGTTGAACTA ATAAATACAT GAAGATGCAC 60
CCCTGCCCTC ATGTTATTGC TTTCTAGGGG AAGAGATAGG TAAGGAAACA AGCATAACAC 120
AAAATTTTGT GATGAAGTAA TTATACACTG GGAGTCCATG GAGCACCTAA CAGTTTTGAG 180
GAGGTCTGAG ATGCTGCTGG AGGAGTTTGT ATTCTAGTTC CTGGCAGGAG ATCTGAAGCA 240
TATTTAAGAA TTAAGTGAAT GGGGGGTGGG AGGTGGAAGA GGAAACTGGA GAGAGTAGGA 300
GGCTCCAGGC AGAAGGATCA GCTTCGTCAA AGACTAAGAA GTGAGACTGC ATGGTCCTCA 360
AATCCCTTCT CTTACTCTTC TGCCTTCTTT CCAATTCCCG TTTGTCCCAG GCTAAGGCCT 420
TGCTTAAGTG ATCTCTGTCA GAAGGATGGA GTGAAAGCAG GAAGAGAGTC CCTTCTGGCT 480
CACAAGCAGG GTGGCCAACC ATCACAGTTT GCCTGGGACT GTCCTGGCTT TAGCACTGAA 540
GGGTTCATGT CCTGGAAAAC CTTTGGTCCC TGGATAAACA GGAAAAGTTG GTCACCCTGC 600
TCAGAGGGTT TGTTCTGGTC ACCCAAGTCA CCTGGAAGGA GAAACAGGGC ATCTGAGTGT 660
CTTGGAATGA TCCCTGGGCT GGGGCCAGGA CACCCGGGTT TAAGTCCCAG CTCTGTCCCA 720
CACCAGCCTT GTAATTCTGA GGAAGTTGTG TCTCTAGCCT CCCTATATTG ACAACATTTG 780
CTTAGTTTCT ATATTCTGTA TGCTCTGGAA ATTGGGGCTT CGATCCTAGA GAGATTTCTA 840
GGGCTAGCTA ATCCCCAGAG TAAGCAAATG GCTCCCCGTG GAGCATGCTT TTGATATGCA 900
AACCAGCCAA TCCAGAGCCT GCACCCCCAA CCCTCTCCTT TATCAAACGC TCACACACCA 960
ATGCAATATC TCCCCTGCCC TAAACCACCC CAGGGCCAAG TCCTGGACAA CTAGGGATCA 1020
CGCCTATAGC CCAGAACCTA CTGAAATTAT CCAAACTACC CAAAGCTGAA CTTACTCAGC 1080
ATAGTTGCAG TACCTTGCCC ATTCCTTCCC ACAGGAACCC CAGTAAAGGC CCTGAGCCAT 1140
GCATACTCTC CTCTCCCCTC CCCACTTCTG CCTCCTGACC GACCCAGCGC TTCCTGGGGT 1200
GGCCTGCGTG GCACGCCGTA CCTCCTGTTC TAGAGGCCTG TGAGTATAAA CTTTTTCCTC 1260
CCTGACAATC ATTTCCATTT CTTACCATGC CTGATTAAAA CAAACTCCAG GTCCATTTTA 1320
TCACACTCCT CCCTGCCGTT ATTGGCCCTC CTGCCTCACG GGGTTGTTGC GAGGGCCTAA 1380
TAAGATAATG TTTATAAAAA TGCTTTGTCA GCTTTCAAGG ATAAGGTATT TTTATGATCA 1440
TTCCTTTCTG CATCATTTAG GTTTGAAAAT 1470
|
