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EnhancerAtlas ID | HS060-00471 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr1:19809200-19810680 | | Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
SE_00361 | chr1:19809437-19814097 | Adipose_Nuclei | SE_05833 | chr1:19809415-19814660 | Brain_Hippocampus_Middle | SE_07251 | chr1:19809878-19813806 | Brain_Hippocampus_Middle_150 | SE_08066 | chr1:19810039-19812101 | Brain_Inferior_Temporal_Lobe | SE_09593 | chr1:19800551-19814880 | CD14 | SE_10714 | chr1:19810121-19812101 | CD19_Primary | SE_12250 | chr1:19809554-19811992 | CD3 | SE_13780 | chr1:19807880-19812155 | CD34_Primary_RO01536 | SE_14589 | chr1:19805927-19813842 | CD4_Memory_Primary_7pool | SE_15716 | chr1:19808924-19813542 | CD4_Memory_Primary_8pool | SE_16772 | chr1:19809545-19813671 | CD4_Naive_Primary_8pool | SE_17553 | chr1:19800597-19813835 | CD4p_CD25-_CD45RAp_Naive | SE_18042 | chr1:19800983-19815154 | CD4p_CD25-_CD45ROp_Memory | SE_18410 | chr1:19800356-19813842 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19269 | chr1:19807023-19813813 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21264 | chr1:19809185-19813813 | CD8_Memory_7pool | SE_22220 | chr1:19808875-19813514 | CD8_Naive_8pool | SE_22607 | chr1:19800179-19812105 | CD8_primiary | SE_23237 | chr1:19809727-19812082 | Colon_Crypt_1 | SE_23924 | chr1:19809819-19810235 | Colon_Crypt_2 | SE_23924 | chr1:19810326-19812909 | Colon_Crypt_2 | SE_25786 | chr1:19807925-19812120 | Duodenum_Smooth_Muscle | SE_26537 | chr1:19809645-19813747 | Esophagus | SE_29645 | chr1:19807678-19809869 | Fetal_Muscle | SE_29645 | chr1:19810019-19812110 | Fetal_Muscle | SE_31447 | chr1:19809641-19813820 | Gastric | SE_41031 | chr1:19809848-19813795 | Left_Ventricle | SE_42185 | chr1:19809630-19813906 | Lung | SE_45720 | chr1:19809467-19812112 | Osteoblasts | SE_47234 | chr1:19806707-19812108 | Panc1 | SE_48688 | chr1:19810445-19812119 | Right_Atrium | SE_50058 | chr1:19801658-19813904 | Sigmoid_Colon | SE_51211 | chr1:19809538-19814893 | Skeletal_Muscle | SE_52345 | chr1:19809239-19813811 | Small_Intestine | SE_53453 | chr1:19809712-19813831 | Spleen | SE_54550 | chr1:19809530-19813805 | Stomach_Smooth_Muscle | SE_62519 | chr1:19761354-19815005 | Tonsil | SE_65446 | chr1:19809727-19812059 | Pancreatic_islets |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAGTCACTA TTTCCCTCAA TGGATAACAG AGATCTAGCT GTATTCTCTA CCATCAAATC 60 TACTGAAAAT GAAAAACATG GTGATCTGAA TTCATTTACC TACAATGCAA CCTCACACCA 120 CCACTTCTGT CCTACGCCAA CCATCTACAC CGGCTTAATG GTCAGAGTAT TCAAATAGGG 180 GATAAACGTA ACAATAAGCA GTCAGAAATT ACAAGGCTAA GGGATACTAA GAACAAGTGA 240 CTGAGAGAAT GAATATGAAA TCCAAGCAGG TAAGTTCATG GACACAGACA CATGCCAAAG 300 AGAACATTCC AAGTGGTTTC TTCCAACGCC AGGTGCTGTT CTAGGCCCCA CGGATACAGC 360 TGCGGAAAAC ACAAGACACA AATCTCTGCC CTCCAAGAGC TCATTCTGGC CCATGCTAAA 420 TATGCCTGTA TCACCATACA GCTATTTCAC TATAAACATG ATTTCCTATA CAAAGGATCT 480 AAAATACAAT ACATGGGCAA TAAATACTGC TCCTCCCCCC TTGCCATGTT TGAATATCCC 540 ATTTTATGTT TTTCAAACGG TATCATTAAA CCTTCTGACA TACAAGCAGC TTGGTACAAT 600 GGGAAGAACA GTTTAGAGCC TGCCAGATGG GCTTCCACTG ACCAACAGTG GTTCCTCCAC 660 TGGCTGAGCA ACACCCTGAA TAAGTCACTC CACCTCCTGA GCCTCAGCTG CCTCATCTAT 720 AAAATGGGGA CAGCCCCAGA AGGGCTTCCT GTGGATGAAA ACAGCTTGTA CAGGTGAAGC 780 ACACCACAGT GACTGGCAGA CAGTTCCTCC ACCCTTTCCA GCCTTTTCAG ATGAGAGCTG 840 AGTACAAGAC TCCTGAGAAG CTTCAGGTGT CATGTGCTCC TCCTGGGGGA CTGAGGCACT 900 TTCCCATCAC CTGGCGAGAA TCGCTGCTTC CTGCCTTATA CTTTGTCCTG AGTGCACACT 960 CAGGAAACTT CAGCCCACTT TCAAAGTCCT CACCCACCAC TGCCCTGGAG AAGTCGTTCT 1020 CCATCAAGGC CTGGGGCCAG GCCCACCTCC CCAAACAAGG AGTTTTCAGC CAAAGTTACT 1080 GGACAAATCC GAAGGCCTTA AAAGTGGCAT TGCCCATGTT TTTAATCAGC ATACAGGAAG 1140 GCATCAAAAG AAAGCTTAAC CCATCTCAAC TACTCACCCT CGTTCAGCAG CAACATCCCT 1200 TGACTAAACA AGGAACCATG GTCCTCAAAA CACTTTGAGG CCCAAAGTCC ACATACAAAC 1260 ATGCTCCAAA AATCCCTTGA TCCTGTCAGG AAGAAGTTCT CTGGCCCTTC CAACCTAAGT 1320 GCTGGGCCTG TCCTGCAGAA GGGTCAAGTG GCAGGAGGGC AGGTCTATCT GTGGGGGCCT 1380 ATGTGAAACC CCAGGTTCCT CAAAAGTCTG GATAGCATCT GCCTTCTTTA CCAAAACAAA 1440 CACCACGAGC GGAGCCAGCA CTCTCCCTAG GCGTTCTGCT 1480
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