| Tag | Content |
|---|
EnhancerAtlas ID | HS052-24739 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr22:28205780-28207360 |
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: 2 | Chromosome | Start | End |
| chr22 | 28206046 | 28206443 | | chr22 | 28206447 | 28207160 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I027809 | chr22 | 28205675 | 28207444 |
|
Enhancer Sequence | CAGCCTCCCA TCTCTGAGCA CTCACCATAA GATGGACTCC TTTCCATAGG TTATTTCTAA 60
TTCTCGCACC AATTGTACTG CAGGAATAGA TGTGTGCCCA TTTTATGGAC GGGAACCTAG 120
AGGCAGGACA CCACTTTGAG AAGGAGCTTG GGGAGAGTTC CTCCAAAAGA AGATCCCACA 180
CTTATTGCCC AAAGGGCTCA GGAAGGAAAC GAACGGAACC CCCAGGGAAC CCTCAGACAC 240
CCCACCTCCC ACCCCCACCA TCAGTCACAC TGTCTAAGGG ATTGTAAAGT GGACGACAAT 300
GGGGCTGATG GGCTTTGAAT GGCCCTTCCC ACCCAACTAG GAAACAGAGC CCAGAGGCAG 360
TGAGTAATGT GCTTATTTGA TCAGATTCTT GGAAACGTTC ACAAATCATC ACCATTCGCC 420
CTGTGACAGT GTTACCAGCT CTTCCTTTAA TTGTTGTTGT GTGCATAGCA GGAAGGCAGT 480
GCAGTCTGGA GGTGAACAGG GTCGGCCTCA GGCTCGACTG CACATAGTCC CTTTACCTCC 540
TTGAGCCTCA GTTTCCCCAT TTGTCAAATG AGGAGGATAA TCTTCTCTGG AGTTGTCAGG 600
GGGGTGAACA AGCACAGAGC ATTTAGCACG TAGTTAACAC TCAATAAACG GCAGCTACTA 660
CATGGAGCCA GGCCCCTGCA GGGCGGGTGG CTCCCTGCGG GGCAGCCCTG AATTGATGAG 720
GTGCCTGCTC TCTTTGGTCT CCCCTCAGAC CCTGGCTGCA TGGTCCTGAG ACTCCTGGCT 780
CCGGTCCGGT CCGGAGGCCT TGTCACGCCA AGGCCCTGCC AGCAAGGAAA AGGAGCGCTG 840
AGTAGAGAGA GGACTCACCC CGGGTTCTCT GGGCCAGGCC CCAGCTGTGC AGGCCCCACC 900
CTCTCTTGGC CACCTCCACC CCAGCTGAGG CTTAGCCGCC AGCCTCCGAC ATTTGCCACC 960
CGGCCACCTG GTGAGCTCCA GGCAGGCTGC AGGCGCCAGC TGCCCCCACC TCTGGCTCCG 1020
ATGAGCTCAT CTGGGTTTCC AAACTTCCAA AGCGGCCAGG AATGTTTGCT CAAATGTTCC 1080
GAGCCCAGAG AGCGTTAAGA GCAAACCAGT GCCCTCCGCC CCCCTTCCCT GAGCAGAAAG 1140
CAATCTGCTA TAACTCAGAC AGGCCGGCCT CACCAAGCCC AGGAGATGGA TGCAGCGTTT 1200
TGGAATCTAT ATCACCCAAA AGGAAAATGC CTCTTAAATC ACAGGGAGCT GGGAGAGAGC 1260
GGGAGCAGGA GGCACCGGGA CCCAGTGATG TTCCAGAGGT CAGGCCTGGA GGAGGGGAGT 1320
ATCACCAGGC ATGGAGTCAC CCTGGTCATC AGTGTGTCTG CTGCACCTTC TTGGCTCAGG 1380
TGGAGAGAGG GAGGCCTGGG GACGCTCCCC TAACTTGAAT GCTTGCTGGG TGTGCACACA 1440
CACGTACATG CACTCATGCA CACCTGTGTC CACATGCACA CACACATGCA CAAAGTGCCC 1500
ACACTGATTC AGCCCACTCC CAGGTCTGTT GAAATCTCTG CCCATTTTAT CCCTCCCTTC 1560
CTGGCCCTGG CCACCGCTCT 1580
|
