| Tag | Content |
|---|
EnhancerAtlas ID | HS040-23674 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr22:19679100-19680150 | 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 | CTCATTTCTT GGGCTGCTGG GATGTAAATT CTGCATAAAA TGGCTGGCTT TCTTTTTAAG 60
GCTTTGCAGC AGTGTTAACA TTCGGCTGCC AACTAAGTCG ATTTTAATCG CCTTTACAGG 120
AACCTTCACT TTTTCTGTTT GTTCCATTCC ACTCTTTCCT CAGTGGATAA TCCCGCATGT 180
TAAGATTCCT GTGCAGCCGA GGGAGGCGGC TTTTGGCCGG GAGCTTGTGC TCTGGGTGTG 240
AGCGTGGCTG TTGGGAACGC CTTCTGCTCA GAATTCCGTG GTCTCAGCAG ATCGTTCAGT 300
CTAGCCACTG GGACGGGGCC GACCGCACAC TGCTGGACCT CTGAGCGGAA GATGTGTGAG 360
GTTAGGAGGG AAGGAATAAA CAAAGTCGCC TTCTTCCCTG CTGACCTGCC TTGGTATGTC 420
ACCATTACTC AGCTCCTTAC AGAACAGGAG CTTCAAGCTT TCACCGGACA GGCTGGCTTC 480
TTCCCGGGAG CCCCCGCCCA AGGTGGGGCC TGGTGGGGTG GGGCCACCAT CGCTGCTGGA 540
AGCTTTAGCT CTTTTCCCTC AGCTTGGCCT CCTTTGGCAA CTAATTTTTT AACTTTTTCT 600
AATAGGTAAC AGAGTCCCAA GATTCCAAGT TCCAGGAGCA TGAAAGGACT CACTTGTGGA 660
GATTCCTGCC TGGGGCTCCC ACCCACCTAA GGAATGCCAT CCTTGTCACC GGCTCACGGG 720
GCAGCTCTTT GGTATCCTTC CAGGGTGGTG TGTACAAGTA CAGGCACATG GATGCATGGA 780
TGCATGAGCA TTTTTTTCTT TTGCCGACAT ATTAATACAC CCGGCAGCAC TCTAGGCCCA 840
TTGGCCTGCA ACTTTTCATT TGATTGATTT TTAATTATTT ACTTTTTTAA AAAATTGTAG 900
TTAAATATAC ATGACATATA TTTACCATTT GAGTCTTTTT TTTTTTTTTG AGATGGAGTC 960
TTGCTCTATC TCCCAGGCTG GAGTGCAGTG GTGTGATCTC GGCTCACTGC AACCTCCACA 1020
GCCTGATCCT GGGTTCAAGG GATTCTCCTG 1050
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