| Tag | Content |
|---|
EnhancerAtlas ID | HS063-00581 |
Organism | Homo sapiens |
Tissue/cell | GM18505 |
Coordinate | chr1:235094110-235095580 |
| | Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
| SE_01666 | chr1:235092553-235095108 | Aorta | | SE_04136 | chr1:235094714-235095506 | Brain_Anterior_Caudate | | SE_06052 | chr1:235092563-235095925 | Brain_Hippocampus_Middle | | SE_09160 | chr1:235089274-235102029 | CD14 | | SE_13412 | chr1:235092302-235095085 | CD34_Primary_RO01536 | | SE_13412 | chr1:235095208-235096433 | CD34_Primary_RO01536 | | SE_14852 | chr1:235090111-235096258 | CD4_Memory_Primary_7pool | | SE_19577 | chr1:235094887-235096195 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_21117 | chr1:235092380-235094348 | CD8_Memory_7pool | | SE_23314 | chr1:235092463-235096122 | Colon_Crypt_1 | | SE_23955 | chr1:235093106-235095692 | Colon_Crypt_2 | | SE_25800 | chr1:235089687-235101859 | Duodenum_Smooth_Muscle | | SE_26806 | chr1:235093373-235094625 | Esophagus | | SE_27663 | chr1:235089063-235101555 | Fetal_Intestine | | SE_28576 | chr1:235088850-235101396 | Fetal_Intestine_Large | | SE_31572 | chr1:235091850-235096149 | Gastric | | SE_33758 | chr1:235092170-235101690 | HCC1954 | | SE_34767 | chr1:235092103-235099043 | HeLa | | SE_36952 | chr1:235089804-235094553 | HSMMtube | | SE_40307 | chr1:235092364-235094852 | K562 | | SE_41640 | chr1:235093134-235096135 | LNCaP | | SE_42265 | chr1:235093078-235096175 | Lung | | SE_43462 | chr1:235092226-235096141 | MCF-7 | | SE_45558 | chr1:235095403-235101783 | Osteoblasts | | SE_47119 | chr1:235087515-235103374 | Panc1 | | SE_47599 | chr1:235093135-235096097 | Pancreas | | SE_50040 | chr1:235092229-235094403 | RPMI-8402 | | SE_50071 | chr1:235089709-235100691 | Sigmoid_Colon | | SE_51271 | chr1:235092438-235095754 | Skeletal_Muscle | | SE_52352 | chr1:235089712-235101497 | Small_Intestine | | SE_53330 | chr1:235094402-235096188 | Spleen | | SE_54553 | chr1:235090275-235096009 | Stomach_Smooth_Muscle | | SE_56760 | chr1:235093122-235095649 | VACO_400 | | SE_59259 | chr1:235089283-235124733 | Ly3 | | SE_60969 | chr1:235059965-235155853 | HBL1 | | SE_61435 | chr1:234961094-235124239 | Toledo | | SE_62329 | chr1:235047040-235185428 | Tonsil | | SE_65393 | chr1:235092372-235101616 | Pancreatic_islets |
|
| | 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 |
| GH01I234953 | chr1 | 235089124 | 235101946 |
|
Enhancer Sequence | CTCTGGCTGG CCGGCACTAT GCCCAGCAAG GCCACCTCCC GTAAGTGACA CGCCAGGGTC 60
TTGCTGAATC ACAATAAGCT GGGAGCTCTG TGCACCCCCC AAAATGATCT TCCACACAAT 120
GAAAAGCACT CGAAAGAAAT GGTTACAGCT GCTGGGGGCA CCGTCAGCCT TTGAGGGCAG 180
TGAGGTGCCA GGGTGGCAGC CTCTGGGGCA AACAAGTCCC AGATCCACCG CTTCCCAGCT 240
GTGGAAGTTT CCTGCCCCTT TCTGGGCCTC AATTTCCTCG TCTGTGAAAT GGGCATAACC 300
GTGTCACTTC ACCAGGGGGT TGTAATGGGT AAATGCCCCT GCTCTGTGGA TAAGCAGGGG 360
TCTTTTGAGC TATTTCCACC AGAAATGGCA GAAGCACGGC AGGGCAGGAG AAGCACCTGT 420
CTGCGGGTCA GGACAGAAGG CAAAGGTGTC TTTACACACA GAATATGCTA CAGTTCTTTG 480
TCACGCCCTC AACCTCCAGG ACTGTCTGCT TGGCTGTACA GTCTGCTTAC CATATTCCCT 540
CCAAAGTAGG GCCCCAGCCC CGCCCAGCCC CTCATGGACT CCACTCCAGA CCCTCCTCCC 600
AGACAGCCGG GGAAGAGAGG CAGAGCCTGC GGTGTTCCCC TCACTGAGCT GCGGCAGTTC 660
CCCTCTCTTC CTTTCTCTCA GGTGACTCTT TTGACCCCCA AGGATCCCTG AACACTCATG 720
TGCTGTCTCC AGCCTCTCTT GCTTGGAAGA GGAAAGAAAT ATCTCGGGTT CCTTTGTCTT 780
CGGGCCACAC TAGCTCCTCC CTACCCCACT TACTCAGGAC ACACCAGGAG GGTGCAGAAG 840
GACTGGCTGC CCAACGGAAG GAGATTTTAT CACTGATATT GCTTGAACTT ACTGGTGTGT 900
GGCAATTAAA ATGGTTTAAA AGCAGTCTCA CTTGGAGCTG GATTGATTCT TGTCTTTAAA 960
CTCTCTAGGG ACGATGCCGT CCTCACTGCC AGCCCCCAAG GCACACCCAT CCCCGTACCC 1020
TCCTTGCTAC TGCTCATCCA GGACCCCATC TTTACGGGCC TCCCAAGTCA TAGGCGGTCA 1080
CTCTCTTCTC TCCTTGGATG CCCTTAACAC AGAAAATGAT CTGCGCCCTA GTTACCGCCT 1140
CTCCTACAGG AGCCCTCGGG AGACAGGCTT GTCGGGAATC CTCAAAAAGG GTGCTCTCCC 1200
TCTCCCCGGA AGCTCTTCTT GGGCCCTTTG GGAAAGCAAA GAAATAACCC GTCCTCCAAA 1260
TCCCCATGGG CATAAGAGGA GGGTCTTTGA TGCCTCATTT TTCTTCTTGT GTTTTTATTT 1320
TCCCTTTTTG CAGATCTCTG CATTTAATGA GGAAGTGCTG TCAGCAGAAA GGAGAGGAAG 1380
CTTCACCCCG ACCATCCGCA GGACCCACAT CCCTCTCAGC GGGAAGGCAG AATCATTCAT 1440
CTATTGCTCT CCTTGAAGGG CAGCTCCAGA 1470
|
