| Tag | Content |
|---|
EnhancerAtlas ID | HS003-47612 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr9:128136000-128137570 |
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 | chr9:128137171-128137190 | GGGTGACATCTTGTGGCCA | - | 6.09 | | Foxd3 | MA0041.1 | chr9:128136152-128136164 | AAACAAACAAAC | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 128136410 | 128137140 | | chr9 | 128136627 | 128137500 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I125374 | chr9 | 128136680 | 128137462 |
|
Enhancer Sequence | TTAGCTGGGC GTGTTGGTGA ATGCCTATAA TCCCAGCTAC TCGAGAGGCT GAGGCAGGAG 60
AATCACTTGA ACCCGGGAGG CGTAGGTTGC AGTGAGCCAA GATCACGCCA TTGCACTCCA 120
GCCCGGGCAA CAAGAGCAAA ACTCCACCTC AAAAACAAAC AAACAAAAAA ATTCATCAAG 180
TCTGAGCAGA TTCCTCTTCT GCCTAAAATC TTCTCTTTTC TACCTGGGTT CTGTCCTGCC 240
TTTTCAGCCA CATGCCTCTG GTCCTTCTCC TTCCCCTCCA GCCAGCCCCA CTCCAGCCAC 300
TGAGAACTAT CACCTTTCCC AAAGTGCTGC CCTTTGCCGG CCTCTAAGCC TTTGCTGATG 360
CCCAGATCTG ACTGCCTCCC CCACAGTCCT TCCTCCTGCC TCAGATGGCC CTTCTGGAGG 420
AAAACCCCAG GTGCCCCCTC CTGCCTCCCT CCTCAGTGAG GCCTCACCCC CATCCCTCCC 480
TCTCCAGAGC AGTGTCTCCC TGGAGCCTGT GCTCCTAGGG GAGGGCATGC CTCCAAATGG 540
CAGGTGTCCC TAATGTTTGC AGATGGGGAT GGATGAGAGG CAGAAAGTAG CCCTTCAGGG 600
CGGGGATTCC ACCATCTTTT CCTTCCAAAT TCAGGCCCTG CTGGGACAGG AACTATCCCT 660
GTCGTGGTCC AGGGCCAGGT AGTTCTTCAC GTCCTCTGGG AAGACAGAGT GCCCCAAAGC 720
CCTTGATCTC CAGTGGGTAG AATTAGGTGG GGCAGAGGCT GTGCCACACC AGGTCACACC 780
TCTCCTGTGT CTGCTCCCAC CCCACCAAGC ACAGGGCCGG GATGAGGATG CCTGGAGCCC 840
AGCTCAGTGC CTGCCTGGGT TGCAGCCCTG ATCACACCAA AGTGTCTTGT CTGTTTGCAG 900
CCCTTTATCT GGCTAGCAGG GTTTAATTTT ACTCTGGGAA GGTGGGATTT TTGTCCCTAT 960
TTACTTATTA TTTTCGAATT TATTATCTTT AGGTGGCATC TACAAATCGG CGTCCTCTGA 1020
GGGCAACAGC GCCCCGTTCT GCTAGAAATC CCGAGATTTG CAGCCACTGC AGCACGCTGC 1080
CTCTGCGGCT TCTCCGCACC ATCCCCGACC CCTTCCCCCG CGAGTCTGCC GTCGGCCAGT 1140
TTCCTCCCAG GCCCCGGCTT TGCTGTTCCT TGGGTGACAT CTTGTGGCCA AGGACAGGTA 1200
CAAACCATTG GCTGAAAAGG AGGAGCAAAG GCAGCCCTCA GCCCTCTCTG GAGGAGCCTT 1260
GGGGCGCCTT CGAGGATGCC CAGGAGGGCA GGGGGCTCCT GAACAGGGAA TCGGCTCTCA 1320
GACCCCGAAT GGGCTTGCAC CAAGCCCTTC ATGAGACAGC TGTGGCTGGA GCCCAGAATT 1380
CACCCAGGCC CCCCGAGGCA GACACACCAG GTTCCTCTCT GCCCACCCTG CGTTGTGGCA 1440
AATAATCATT ATTCCCGATA TAAAGCTTTT CTCTAGCAGC CCAACGACAA GGTTATTATT 1500
CCAATCTTAC AGATGCAGCA ACAGCCCTGA GCCACAGCCA GTGACCTGAG CCCAGCCCAC 1560
AGGTGCCAAC 1570
|
