| Tag | Content |
|---|
EnhancerAtlas ID | HS139-34803 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr22:19678660-19680000 |
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 | TGCAGGCTCC TCCTTGTGTC CGTCATTCCG TATCTGTACC TCCTTCTACA AGAGAGCCCT 60
AACTTCTAAC AGCATCACTA TGTCTATCAT CTATTTAGCC CTCCAAACAC ACAAGACACT 120
TCCAGAATCT TCTTATTCTC CAGAGGAAAA TGTTTCATCA AAACACCAGA GGCAGCCAGC 180
ATTTTGACAA GAAAACACAA CAAACTTCAT TTCTTTGGAA ATTTGATCTA GGAAAATGTG 240
TCTCTCTCAT TTTGCTAATG GATGTCTGTT TATCAGTCAG AGACCATGAA ACGACTCCTT 300
ATTTTGAATA TCAGATTTTC TTCTTATTCT CAAACCTCAA AACAGCTTGG TAATAATTTA 360
TTTGGAAATT ATCCGAAAGG TAAAAATAAA AACAGAAGCA AGTAATATGC CTTGTTACTG 420
CTCCTTAATT AGGTAAGAGC CTCATTTCTT GGGCTGCTGG GATGTAAATT CTGCATAAAA 480
TGGCTGGCTT TCTTTTTAAG GCTTTGCAGC AGTGTTAACA TTCGGCTGCC AACTAAGTCG 540
ATTTTAATCG CCTTTACAGG AACCTTCACT TTTTCTGTTT GTTCCATTCC ACTCTTTCCT 600
CAGTGGATAA TCCCGCATGT TAAGATTCCT GTGCAGCCGA GGGAGGCGGC TTTTGGCCGG 660
GAGCTTGTGC TCTGGGTGTG AGCGTGGCTG TTGGGAACGC CTTCTGCTCA GAATTCCGTG 720
GTCTCAGCAG ATCGTTCAGT CTAGCCACTG GGACGGGGCC GACCGCACAC TGCTGGACCT 780
CTGAGCGGAA GATGTGTGAG GTTAGGAGGG AAGGAATAAA CAAAGTCGCC TTCTTCCCTG 840
CTGACCTGCC TTGGTATGTC ACCATTACTC AGCTCCTTAC AGAACAGGAG CTTCAAGCTT 900
TCACCGGACA GGCTGGCTTC TTCCCGGGAG CCCCCGCCCA AGGTGGGGCC TGGTGGGGTG 960
GGGCCACCAT CGCTGCTGGA AGCTTTAGCT CTTTTCCCTC AGCTTGGCCT CCTTTGGCAA 1020
CTAATTTTTT AACTTTTTCT AATAGGTAAC AGAGTCCCAA GATTCCAAGT TCCAGGAGCA 1080
TGAAAGGACT CACTTGTGGA GATTCCTGCC TGGGGCTCCC ACCCACCTAA GGAATGCCAT 1140
CCTTGTCACC GGCTCACGGG GCAGCTCTTT GGTATCCTTC CAGGGTGGTG TGTACAAGTA 1200
CAGGCACATG GATGCATGGA TGCATGAGCA TTTTTTTCTT TTGCCGACAT ATTAATACAC 1260
CCGGCAGCAC TCTAGGCCCA TTGGCCTGCA ACTTTTCATT TGATTGATTT TTAATTATTT 1320
ACTTTTTTAA AAAATTGTAG 1340
|
