| Tag | Content |
|---|
EnhancerAtlas ID | HS003-30791 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr22:19678640-19679960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr22:19678779-19678792 | TTCCAGAATCTTC | + | 6.16 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 19679200 | 19679849 | | chr22 | 19679104 | 19679921 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I019691 | chr22 | 19678730 | 19680090 |
|
Enhancer Sequence | CTCCTAGTCC TGCCCGGCCC TGCAGGCTCC TCCTTGTGTC CGTCATTCCG TATCTGTACC 60
TCCTTCTACA AGAGAGCCCT AACTTCTAAC AGCATCACTA TGTCTATCAT CTATTTAGCC 120
CTCCAAACAC ACAAGACACT TCCAGAATCT TCTTATTCTC CAGAGGAAAA TGTTTCATCA 180
AAACACCAGA GGCAGCCAGC ATTTTGACAA GAAAACACAA CAAACTTCAT TTCTTTGGAA 240
ATTTGATCTA GGAAAATGTG TCTCTCTCAT TTTGCTAATG GATGTCTGTT TATCAGTCAG 300
AGACCATGAA ACGACTCCTT ATTTTGAATA TCAGATTTTC TTCTTATTCT CAAACCTCAA 360
AACAGCTTGG TAATAATTTA TTTGGAAATT ATCCGAAAGG TAAAAATAAA AACAGAAGCA 420
AGTAATATGC CTTGTTACTG CTCCTTAATT AGGTAAGAGC CTCATTTCTT GGGCTGCTGG 480
GATGTAAATT CTGCATAAAA TGGCTGGCTT TCTTTTTAAG GCTTTGCAGC AGTGTTAACA 540
TTCGGCTGCC AACTAAGTCG ATTTTAATCG CCTTTACAGG AACCTTCACT TTTTCTGTTT 600
GTTCCATTCC ACTCTTTCCT CAGTGGATAA TCCCGCATGT TAAGATTCCT GTGCAGCCGA 660
GGGAGGCGGC TTTTGGCCGG GAGCTTGTGC TCTGGGTGTG AGCGTGGCTG TTGGGAACGC 720
CTTCTGCTCA GAATTCCGTG GTCTCAGCAG ATCGTTCAGT CTAGCCACTG GGACGGGGCC 780
GACCGCACAC TGCTGGACCT CTGAGCGGAA GATGTGTGAG GTTAGGAGGG AAGGAATAAA 840
CAAAGTCGCC TTCTTCCCTG CTGACCTGCC TTGGTATGTC ACCATTACTC AGCTCCTTAC 900
AGAACAGGAG CTTCAAGCTT TCACCGGACA GGCTGGCTTC TTCCCGGGAG CCCCCGCCCA 960
AGGTGGGGCC TGGTGGGGTG GGGCCACCAT CGCTGCTGGA AGCTTTAGCT CTTTTCCCTC 1020
AGCTTGGCCT CCTTTGGCAA CTAATTTTTT AACTTTTTCT AATAGGTAAC AGAGTCCCAA 1080
GATTCCAAGT TCCAGGAGCA TGAAAGGACT CACTTGTGGA GATTCCTGCC TGGGGCTCCC 1140
ACCCACCTAA GGAATGCCAT CCTTGTCACC GGCTCACGGG GCAGCTCTTT GGTATCCTTC 1200
CAGGGTGGTG TGTACAAGTA CAGGCACATG GATGCATGGA TGCATGAGCA TTTTTTTCTT 1260
TTGCCGACAT ATTAATACAC CCGGCAGCAC TCTAGGCCCA TTGGCCTGCA ACTTTTCATT 1320
|
