| Tag | Content |
|---|
EnhancerAtlas ID | HS098-36609 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr22:28206150-28207630 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_01727 | chr22:28205001-28208024 | Aorta |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I027809 | chr22 | 28205675 | 28207444 |
|
Enhancer Sequence | GCTTATTTGA TCAGATTCTT GGAAACGTTC ACAAATCATC ACCATTCGCC CTGTGACAGT 60
GTTACCAGCT CTTCCTTTAA TTGTTGTTGT GTGCATAGCA GGAAGGCAGT GCAGTCTGGA 120
GGTGAACAGG GTCGGCCTCA GGCTCGACTG CACATAGTCC CTTTACCTCC TTGAGCCTCA 180
GTTTCCCCAT TTGTCAAATG AGGAGGATAA TCTTCTCTGG AGTTGTCAGG GGGGTGAACA 240
AGCACAGAGC ATTTAGCACG TAGTTAACAC TCAATAAACG GCAGCTACTA CATGGAGCCA 300
GGCCCCTGCA GGGCGGGTGG CTCCCTGCGG GGCAGCCCTG AATTGATGAG GTGCCTGCTC 360
TCTTTGGTCT CCCCTCAGAC CCTGGCTGCA TGGTCCTGAG ACTCCTGGCT CCGGTCCGGT 420
CCGGAGGCCT TGTCACGCCA AGGCCCTGCC AGCAAGGAAA AGGAGCGCTG AGTAGAGAGA 480
GGACTCACCC CGGGTTCTCT GGGCCAGGCC CCAGCTGTGC AGGCCCCACC CTCTCTTGGC 540
CACCTCCACC CCAGCTGAGG CTTAGCCGCC AGCCTCCGAC ATTTGCCACC CGGCCACCTG 600
GTGAGCTCCA GGCAGGCTGC AGGCGCCAGC TGCCCCCACC TCTGGCTCCG ATGAGCTCAT 660
CTGGGTTTCC AAACTTCCAA AGCGGCCAGG AATGTTTGCT CAAATGTTCC GAGCCCAGAG 720
AGCGTTAAGA GCAAACCAGT GCCCTCCGCC CCCCTTCCCT GAGCAGAAAG CAATCTGCTA 780
TAACTCAGAC AGGCCGGCCT CACCAAGCCC AGGAGATGGA TGCAGCGTTT TGGAATCTAT 840
ATCACCCAAA AGGAAAATGC CTCTTAAATC ACAGGGAGCT GGGAGAGAGC GGGAGCAGGA 900
GGCACCGGGA CCCAGTGATG TTCCAGAGGT CAGGCCTGGA GGAGGGGAGT ATCACCAGGC 960
ATGGAGTCAC CCTGGTCATC AGTGTGTCTG CTGCACCTTC TTGGCTCAGG TGGAGAGAGG 1020
GAGGCCTGGG GACGCTCCCC TAACTTGAAT GCTTGCTGGG TGTGCACACA CACGTACATG 1080
CACTCATGCA CACCTGTGTC CACATGCACA CACACATGCA CAAAGTGCCC ACACTGATTC 1140
AGCCCACTCC CAGGTCTGTT GAAATCTCTG CCCATTTTAT CCCTCCCTTC CTGGCCCTGG 1200
CCACCGCTCT CCAGACCTGG GCAGCAGCTG GGCTCTAAAC CTGATAAAGT CAGGTCACAG 1260
ACAGCCCTTC ACTCATATCC TTAGAACATT CAGTGGATCT ATCTTTTGAG AATAAAGATC 1320
AAATTCCTCA CTGCAGTGTG CAAGGCCCTG CATGCCCAGC CCGGGTGACC TTGCCATGCC 1380
TGGCCCAGTC CCTCCACCAG AGCTGCACTG GCCCCTACTG TGCCCTTCTC ACCTTCTCCC 1440
ATCACAGGCC CTGGCAGGGG TTGTGCCCAT GGCTGGAGGG 1480
|
