| Tag | Content |
|---|
EnhancerAtlas ID | HS145-15549 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr22:19678870-19680100 | 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 | TTCTTTGGAA ATTTGATCTA GGAAAATGTG TCTCTCTCAT TTTGCTAATG GATGTCTGTT 60
TATCAGTCAG AGACCATGAA ACGACTCCTT ATTTTGAATA TCAGATTTTC TTCTTATTCT 120
CAAACCTCAA AACAGCTTGG TAATAATTTA TTTGGAAATT ATCCGAAAGG TAAAAATAAA 180
AACAGAAGCA AGTAATATGC CTTGTTACTG CTCCTTAATT AGGTAAGAGC CTCATTTCTT 240
GGGCTGCTGG GATGTAAATT CTGCATAAAA TGGCTGGCTT TCTTTTTAAG GCTTTGCAGC 300
AGTGTTAACA TTCGGCTGCC AACTAAGTCG ATTTTAATCG CCTTTACAGG AACCTTCACT 360
TTTTCTGTTT GTTCCATTCC ACTCTTTCCT CAGTGGATAA TCCCGCATGT TAAGATTCCT 420
GTGCAGCCGA GGGAGGCGGC TTTTGGCCGG GAGCTTGTGC TCTGGGTGTG AGCGTGGCTG 480
TTGGGAACGC CTTCTGCTCA GAATTCCGTG GTCTCAGCAG ATCGTTCAGT CTAGCCACTG 540
GGACGGGGCC GACCGCACAC TGCTGGACCT CTGAGCGGAA GATGTGTGAG GTTAGGAGGG 600
AAGGAATAAA CAAAGTCGCC TTCTTCCCTG CTGACCTGCC TTGGTATGTC ACCATTACTC 660
AGCTCCTTAC AGAACAGGAG CTTCAAGCTT TCACCGGACA GGCTGGCTTC TTCCCGGGAG 720
CCCCCGCCCA AGGTGGGGCC TGGTGGGGTG GGGCCACCAT CGCTGCTGGA AGCTTTAGCT 780
CTTTTCCCTC AGCTTGGCCT CCTTTGGCAA CTAATTTTTT AACTTTTTCT AATAGGTAAC 840
AGAGTCCCAA GATTCCAAGT TCCAGGAGCA TGAAAGGACT CACTTGTGGA GATTCCTGCC 900
TGGGGCTCCC ACCCACCTAA GGAATGCCAT CCTTGTCACC GGCTCACGGG GCAGCTCTTT 960
GGTATCCTTC CAGGGTGGTG TGTACAAGTA CAGGCACATG GATGCATGGA TGCATGAGCA 1020
TTTTTTTCTT TTGCCGACAT ATTAATACAC CCGGCAGCAC TCTAGGCCCA TTGGCCTGCA 1080
ACTTTTCATT TGATTGATTT TTAATTATTT ACTTTTTTAA AAAATTGTAG TTAAATATAC 1140
ATGACATATA TTTACCATTT GAGTCTTTTT TTTTTTTTTG AGATGGAGTC TTGCTCTATC 1200
TCCCAGGCTG GAGTGCAGTG GTGTGATCTC 1230
|
| |
|
|
|
