| Tag | Content |
|---|
EnhancerAtlas ID | HS060-04040 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr10:70815560-70817030 |
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09172 | chr10:70810273-70818670 | CD14 | | SE_53458 | chr10:70815507-70818363 | Spleen | | SE_56698 | chr10:70815789-70818683 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 70815943 | 70816217 | | chr10 | 70816608 | 70816807 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I069055 | chr10 | 70815322 | 70818956 |
|
Enhancer Sequence | GCATGATTTT GGCTCACTGC AACCTCTGCC TCCTGGGTTC ATGCCATTCT CCTGCTTCAG 60
CTTCCCAAGT AGCTGAGACT ACAGTTGCCC GCCACCACAC CTGGCTAATT TTTTGTATTT 120
TTAGTAGAGA TGGGGTTTCA CCGTGTTAGC CAGGATGGTC TCAATCTCCT GACCTCGTGA 180
TCCACCCACC TCGGCCTCTC AAAGTGCTGG GATTACAGGC GTGAGCCACT GCACCCGGCT 240
ATGTTAGATG TATTTTAAGA CAGCATTCTG AGAAGGGGGT CTGTAGGCTG GCCAGATGGC 300
CAAAAGGGCC CCTGATCAAA GCAAAGATCT TCGGAAGGTA AAGAACATTC AGAGGAGGCT 360
CCTTGTCCCC AGAGAAGGCA GAGTGGTATG TAGTGGACAC AGTAACTCCC TCTCTCTTCC 420
TGTGTGGCCT GCAGGCAAAG GTCACACCGC TCACGGTCAG GGCTGTCTCA CTTCCGTTTG 480
GGGTGAGAGC ACCCCCTCAC TTACTCGTTT CTCATTTTTT GGCAGAAGTG CCCCTTGGCC 540
TCCCATGGCA GCCCTGGGGG AGGGCAATAG GGCTTTTTTC CAGCCTTGTT AACCCAAGGG 600
GGAGGGGGCA ACCCAAACAG TGAGGGAATG AGAAGAGCTT GGACTGGAGG AGAGCAGTTG 660
TTCCTTGAGC CTCGACAGGT AGATGCTGAC CGCCAGCTCC TTGCTGCCCC TCACAATTCC 720
TTCCTGCCCT GATTGCTAGT GTTCCCGCCA GAGGAGGGAC CTGGGAGACC CACTGATGCC 780
TGCTGGCGCT CCTTTAGAGC CCTTCTGCAG CTCGGCAGAC GCTTGGCCCC TGTGATCCAA 840
GCCTGCCCCA GGCACAGTCC CCCACCCTCA GGGAGCTCAC AGTCTGGCCA GGGGATCTGA 900
GCCAAGAACT CAGAGTAGGA AGAGGTTTGC AGCTGGGGCC TGGTACAGGT GTGTAGAGCA 960
AACCAGAAAC AAATGGGTTA ACTTCAGATG ATGTTTCTAC TCTCTCACAC CCACCCTGGG 1020
TTGTCTGGTG CGTGGCTGAG CTGAGTCTTA AAGGCTAGAT AGAGTCTTAG CTGCCCAACT 1080
CACAGCAGTA CCCTTTGGAT CCACCTGCCC CTGTGGGTGG GCACACATGC TGTGTGGGGC 1140
GTGCACAACA GTGACCAGTT GGCGAGAGGT GGTGGTGTCA CCACAGGGGA ACTTGACCTC 1200
CTGGCCCAGC AGCCTAAAAC AGAGGTTGAT TAAAGCAAAA AGAATCATAG TTGTGGATGG 1260
CTGGAGACCT GGGTGTCTGA GGAGATGTCT GAGGTGCGAG TGAGAGGTGC CTGAAGTAAA 1320
CGACAGACCC AGGAAGTGTC TGCCGTGCTG CTCGGAGCCA CGGAACAGGG CCCTTAGACT 1380
GGATCTTTTT TCCCTTGGAG TCCGGGAACT CTTTCAGCCC TCTGGCGAAA GCTGCAGAAC 1440
CATCTCCTCA GGAAAATACA CATGTATCAT 1470
|
