| Tag | Content |
|---|
EnhancerAtlas ID | HS087-13708 | Organism | Homo sapiens | Tissue/cell | HEK293T | Coordinate | chr22:19678840-19679940 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| | | 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 | ATTTTGACAA GAAAACACAA CAAACTTCAT TTCTTTGGAA ATTTGATCTA GGAAAATGTG 60
TCTCTCTCAT TTTGCTAATG GATGTCTGTT TATCAGTCAG AGACCATGAA ACGACTCCTT 120
ATTTTGAATA TCAGATTTTC TTCTTATTCT CAAACCTCAA AACAGCTTGG TAATAATTTA 180
TTTGGAAATT ATCCGAAAGG TAAAAATAAA AACAGAAGCA AGTAATATGC CTTGTTACTG 240
CTCCTTAATT AGGTAAGAGC CTCATTTCTT GGGCTGCTGG GATGTAAATT CTGCATAAAA 300
TGGCTGGCTT TCTTTTTAAG GCTTTGCAGC AGTGTTAACA TTCGGCTGCC AACTAAGTCG 360
ATTTTAATCG CCTTTACAGG AACCTTCACT TTTTCTGTTT GTTCCATTCC ACTCTTTCCT 420
CAGTGGATAA TCCCGCATGT TAAGATTCCT GTGCAGCCGA GGGAGGCGGC TTTTGGCCGG 480
GAGCTTGTGC TCTGGGTGTG AGCGTGGCTG TTGGGAACGC CTTCTGCTCA GAATTCCGTG 540
GTCTCAGCAG ATCGTTCAGT CTAGCCACTG GGACGGGGCC GACCGCACAC TGCTGGACCT 600
CTGAGCGGAA GATGTGTGAG GTTAGGAGGG AAGGAATAAA CAAAGTCGCC TTCTTCCCTG 660
CTGACCTGCC TTGGTATGTC ACCATTACTC AGCTCCTTAC AGAACAGGAG CTTCAAGCTT 720
TCACCGGACA GGCTGGCTTC TTCCCGGGAG CCCCCGCCCA AGGTGGGGCC TGGTGGGGTG 780
GGGCCACCAT CGCTGCTGGA AGCTTTAGCT CTTTTCCCTC AGCTTGGCCT CCTTTGGCAA 840
CTAATTTTTT AACTTTTTCT AATAGGTAAC AGAGTCCCAA GATTCCAAGT TCCAGGAGCA 900
TGAAAGGACT CACTTGTGGA GATTCCTGCC TGGGGCTCCC ACCCACCTAA GGAATGCCAT 960
CCTTGTCACC GGCTCACGGG GCAGCTCTTT GGTATCCTTC CAGGGTGGTG TGTACAAGTA 1020
CAGGCACATG GATGCATGGA TGCATGAGCA TTTTTTTCTT TTGCCGACAT ATTAATACAC 1080
CCGGCAGCAC TCTAGGCCCA 1100
|
| |
|
|
|
