| Tag | Content |
|---|
EnhancerAtlas ID | HS095-19388 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr22:19678680-19679950 |
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 | CGTCATTCCG TATCTGTACC TCCTTCTACA AGAGAGCCCT AACTTCTAAC AGCATCACTA 60
TGTCTATCAT CTATTTAGCC CTCCAAACAC ACAAGACACT TCCAGAATCT TCTTATTCTC 120
CAGAGGAAAA TGTTTCATCA AAACACCAGA GGCAGCCAGC ATTTTGACAA GAAAACACAA 180
CAAACTTCAT TTCTTTGGAA ATTTGATCTA GGAAAATGTG TCTCTCTCAT TTTGCTAATG 240
GATGTCTGTT TATCAGTCAG AGACCATGAA ACGACTCCTT ATTTTGAATA TCAGATTTTC 300
TTCTTATTCT CAAACCTCAA AACAGCTTGG TAATAATTTA TTTGGAAATT ATCCGAAAGG 360
TAAAAATAAA AACAGAAGCA AGTAATATGC CTTGTTACTG CTCCTTAATT AGGTAAGAGC 420
CTCATTTCTT GGGCTGCTGG GATGTAAATT CTGCATAAAA TGGCTGGCTT TCTTTTTAAG 480
GCTTTGCAGC AGTGTTAACA TTCGGCTGCC AACTAAGTCG ATTTTAATCG CCTTTACAGG 540
AACCTTCACT TTTTCTGTTT GTTCCATTCC ACTCTTTCCT CAGTGGATAA TCCCGCATGT 600
TAAGATTCCT GTGCAGCCGA GGGAGGCGGC TTTTGGCCGG GAGCTTGTGC TCTGGGTGTG 660
AGCGTGGCTG TTGGGAACGC CTTCTGCTCA GAATTCCGTG GTCTCAGCAG ATCGTTCAGT 720
CTAGCCACTG GGACGGGGCC GACCGCACAC TGCTGGACCT CTGAGCGGAA GATGTGTGAG 780
GTTAGGAGGG AAGGAATAAA CAAAGTCGCC TTCTTCCCTG CTGACCTGCC TTGGTATGTC 840
ACCATTACTC AGCTCCTTAC AGAACAGGAG CTTCAAGCTT TCACCGGACA GGCTGGCTTC 900
TTCCCGGGAG CCCCCGCCCA AGGTGGGGCC TGGTGGGGTG GGGCCACCAT CGCTGCTGGA 960
AGCTTTAGCT CTTTTCCCTC AGCTTGGCCT CCTTTGGCAA CTAATTTTTT AACTTTTTCT 1020
AATAGGTAAC AGAGTCCCAA GATTCCAAGT TCCAGGAGCA TGAAAGGACT CACTTGTGGA 1080
GATTCCTGCC TGGGGCTCCC ACCCACCTAA GGAATGCCAT CCTTGTCACC GGCTCACGGG 1140
GCAGCTCTTT GGTATCCTTC CAGGGTGGTG TGTACAAGTA CAGGCACATG GATGCATGGA 1200
TGCATGAGCA TTTTTTTCTT TTGCCGACAT ATTAATACAC CCGGCAGCAC TCTAGGCCCA 1260
TTGGCCTGCA 1270
|
