| Tag | Content |
|---|
EnhancerAtlas ID | HS146-01321 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:223917700-223919610 |
| | Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
| SE_00224 | chr1:223917623-223923297 | Adipose_Nuclei | | SE_01908 | chr1:223918292-223919960 | Aorta | | SE_02306 | chr1:223918166-223920027 | Astrocytes | | SE_04026 | chr1:223918327-223919959 | Brain_Anterior_Caudate | | SE_05036 | chr1:223918296-223919826 | Brain_Cingulate_Gyrus | | SE_05972 | chr1:223918153-223920025 | Brain_Hippocampus_Middle | | SE_07159 | chr1:223918575-223919801 | Brain_Hippocampus_Middle_150 | | SE_09681 | chr1:223912826-223918041 | CD14 | | SE_09681 | chr1:223918139-223920041 | CD14 | | SE_23408 | chr1:223918840-223919937 | Colon_Crypt_1 | | SE_24051 | chr1:223918949-223919614 | Colon_Crypt_2 | | SE_25230 | chr1:223918779-223919775 | Colon_Crypt_3 | | SE_26209 | chr1:223918227-223919614 | Duodenum_Smooth_Muscle | | SE_26925 | chr1:223918492-223919864 | Esophagus | | SE_31491 | chr1:223918204-223920043 | Gastric | | SE_37129 | chr1:223917375-223920072 | HSMMtube | | SE_38254 | chr1:223917692-223922239 | HUVEC | | SE_38957 | chr1:223918328-223919928 | IMR90 | | SE_41495 | chr1:223918394-223920179 | Left_Ventricle | | SE_42269 | chr1:223918111-223920107 | Lung | | SE_44530 | chr1:223917549-223919989 | NHDF-Ad | | SE_44904 | chr1:223918045-223919953 | NHLF | | SE_45872 | chr1:223917531-223920254 | Osteoblasts | | SE_49408 | chr1:223918777-223919926 | Right_Atrium | | SE_50365 | chr1:223918695-223919952 | Sigmoid_Colon | | SE_51879 | chr1:223918137-223919804 | Skeletal_Muscle_Myoblast | | SE_53249 | chr1:223918717-223919906 | Small_Intestine | | SE_55958 | chr1:223918085-223920003 | u87 | | SE_63671 | chr1:223918137-223919937 | HSMM | | SE_65644 | chr1:223918515-223920092 | Pancreatic_islets | | SE_67677 | chr1:223918085-223920003 | u87 | | SE_68376 | chr1:223892363-223922876 | TC32 |
|
| | 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 |
| GH01I223730 | chr1 | 223917704 | 223922480 |
|
Enhancer Sequence | TCCCAAAAAA CCAAAAAAAA AAAAAAAAAA AAAAAAACGA AAACCTGAAA TCAGTTGAAA 60
AGTGTGCCTG GGTTGAGATA AGAAGTTGTT AGAGACCAAG GTTTTTATTA TGTAGATGAA 120
GTCTCACAGA GGGCCACTCT CAAAGGCAAT AGATGGCAAA TGTTTTCTAT TCAGACCTTT 180
AAAAGGTGCT ACTAGATGCT CAGCTAATCT CTTCAGGATC AGAAAAAGAC CTGAAGGGAA 240
GGTGATTCTC TACATCAAGC TTGTCCAACC CTCGTGCTGC CCAGGATGGC TTTGAATGTG 300
GCCCAACACA AATTTGTGAA CTTTCTCAAA ATATTATGAG ATTTTTTTTT TTTTTAGCTC 360
ATCATCTATC ATTAGTGTCA GTGTATTTTA TGTGTGGCCC AAGACAATTC TTCTTCTTCC 420
AGTGTGGCCC AGGGAAGCCA AAAGATTGGA CACCCCTGCT ATAGAATGTA GATTTTCCCA 480
CAAGAGACAG CTTTCAGAGA CATTTCAAAA TCTGTCAGAA AAATATATTT TGGGCTAAAA 540
TACTTTGATT TCTTTCAGGG CCTGCTATCT GTCATGTGAT GCTCTACTAG AGTGTGGTTG 600
GAATTTGGTA TCTTATTGCT AGGAAGAGTC TGTTTTGTGA GTCTTAAGAT CTCTGTTTTC 660
AGTTAAGGCT GGTCAGCTGT GCCTGAATTC CTAAAGGAGG AGGATAAAAT GAGGCATGAC 720
GGACCTCCCT TCCCATCGTG GCCTGAACTT GTTTTTCAGG TTTACCTTGG AATCCCCTTG 780
ACTAAGGGGG CACCCATTCA GTTAGTTAAG GGGCTTAGAC TTTGATTTTT AGTTTACAGT 840
AGGCTGAGGT GTATTAAATG CATTTTCGAC TTGCAATATT TTCAACTTCT GATGGATTTG 900
TTCAGATGTA ACCCCGTTGT AAGTTAAGGA GCATGTATAC TTGTATCTAA TCCACTTTGG 960
GCATTGCTGC CAGAAAACCT GTCCTCAGGG AGCTATGGAA GTAGTGGAGG CAAATTATTA 1020
AATGGATGGA TTAATTCCAA GTTCAGATCA TGTTGGGAGT CAGCTGGGAG TCAGTGTGAG 1080
GATCTGGGAG GGGAACAGTA AGGGGTTAAG AGAGATACCC CAAAGGATGA TTAAGGAGGG 1140
AGAGTTGGAA GGAAGGTTTC CCACAAAGAG GAAGCAGGGA GTGATTCATT CTGAAAAAGG 1200
CAAATATTTT ATTATGCTTG GAGGGTCTGG TGCAGAAGGG GAAAGGAAGA GAAGGAAGTT 1260
TGGCTTAAAT TCCCTTAGGA GCCAGTTCAG ATTCCTAAGC TGGCCCGGAC ATCCAACCCA 1320
ATCCGCCTAG CCCCAGCCCT CTCCAGTTCC CAATGCCCAG CCCCACAATG CCCGTCCTGC 1380
TGCCTGCCTG TTCTGGACTC TGCACTTGAC CTTCCCTCTC CCTGAAAGTG CCCCTGCTCT 1440
TCCTCACCCA GCTCCCCGCT CTAAGCCTTC CTCGCCCACC CCAGCCCTCC TACAGTCCCA 1500
GTCTGCCCTG TTCAGACTCA AAGCCTCATG CTCACCACCA TCATCCACAA CCAGTTTCCA 1560
CGTCTGTCTC CTGCCGGCTG TGAGCTCACT GCCTCAGAAC CAGCGCCAGT CTCCTCTAGA 1620
CTGAGTACAG GCCTGGCACG GAGCCAGGAA TGCACCAACA AGGAGCCTGA GACTAGATTG 1680
GAGGGGAAAG AGACATGTCC TCCAGAGTTG ACTTACGCGA GGACAGAGGT GTGCAGAGGC 1740
ACGGCAAGCT GGGCCCCAGG CGAGAAGCAT GGAGTGAGGG ATGTGGAGGC AGCGGAAGGC 1800
ATCTGGGAGT CTGGGCTGCC CCGTAGCAGC TCTGTGTTCT GCCTGCTCTT CCTCCAAGAT 1860
GAGCTCCCTT GGCCAGTGTG TGAAACGTGT GTGTGAGTGT GTCACCGGTA 1910
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