| Tag | Content |
|---|
EnhancerAtlas ID | HS091-06349 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr10:105643850-105645180 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_00621 | chr10:105644321-105651380 | Adipose_Nuclei | | SE_26776 | chr10:105644183-105645170 | Esophagus | | SE_35854 | chr10:105643735-105645552 | HMEC | | SE_41453 | chr10:105644115-105645500 | Left_Ventricle | | SE_64264 | chr10:105643765-105645000 | NHEK |
|
| | 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 |
| GH10I103884 | chr10 | 105644501 | 105644690 |
|
Enhancer Sequence | AAAAAAAAAA AAAAAAAAAA AAAAATCCAC TTATCACTGC TGCTAATCAG AGTGTATATT 60
CAGAGAAACC TGAATCTGTG CTCCCCAGCT GCAATCCTGA AACTTGGCCC AAATCAACTC 120
TCTGCTTGTA TTAATTTTGC CTCAGCTCCT TCCTTTTAGG TCGTCGGCAG TAGTCAAACT 180
GGGGGTTGTG CCTATTAGGG GATAACGAAA CCAATTTTTG TAGGTTGCGA TCAGCAACTT 240
TTTCTTACCA AACTCAAAGA GAGCAGAAAT AGAACGTTAC AGAATATCTT GCATTGTAAT 300
TTGGATACAT ATTAATTCAT GAAACTTAAT TTCATATACA TCTTATGCAT TAGAATTATA 360
TAATTTATTG GGTCATGATG TAAAATGTAT TTCTAACTTT GAGTCAAAGT CAAACTTCTT 420
TACCAAAAGC AAACCCTCTC CAGTTGTCAC AGTTTAAAAC TCCATGGCAG GCGCAGGCAT 480
GGTCTCTCTC TGCCGTATAC CCAGTATCTG GCACACAAAA GGTGCTCCAC AAAGTCACTG 540
AAAGTTGTTT ACAGATGAAA AATGCTTTAG GCTTCAGGAA GGTGCTCGAA GAGGTATTGC 600
GGTGTGAGGC AAAGCACGGT TCAAGGTTTG GTGCACTTCT GTAGCTTTGG GCAAGCCATC 660
CCTAGGCCTG AGTGTTCTCA GCTGTGGTGA AAACCACTTC CAAGGCCCTT TCCAACCCTA 720
AGGTTCAGAG ACTGCTCCTG GGCTAACAAA AATTTGCTAA ATTCTGACCT CTAGTGGCTG 780
TGTCCACTCA TTACTCCTTC CAACTGGGAT TGCTGGCATC TATACTTCCA GGCTGTTTCT 840
TCAACATTCA CTCCATAGAC TTCCTGAACA CCTACTATGT GTGCATTGCT GAGCAAGGAG 900
GAGCAAGTAG AGCTTGGCAG ACCTGGAGCT GCCACTGGAG TCCACCACAC CAGAATTCAA 960
GCCCTGGCTC TACAACTGGG ACAAAGTCAC TCCCGGGAAC AAAACCACTT CCTTCTCAGG 1020
GTGGCTGTGT GGATGAGAGA CCAGGGGGAA CTACTATGAT TTGGTTCATC ATATCCGTAA 1080
TCCAAGAAGA TGAATGTAAC TTAGTTCCTG CTCTAGAAAA GCTTCATCCC TTCCCAAGAA 1140
GAAAAGCCTC TCAAGGAGGA AGAGCTGACC AGCAAGCAAG GATAGGTTTG ATGATGGAGG 1200
GTGAGGGGCT CCAACCACAC AGACCTGCAC ACGGTAGGGA GGAGCAGAGG GAATTTAGTG 1260
CTGCTCAGCT TTTAGTTTCT GCAAGGCCTG GATGCTTGGA CCCAGGGCTC AAGGTGACTT 1320
ACAGGCATCC 1330
|
