Tag | Content |
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EnhancerAtlas ID | HS104-03825 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:154404380-154406640 |
| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00437 | chr1:154403931-154408447 | Adipose_Nuclei | SE_06653 | chr1:154406381-154408124 | Brain_Hippocampus_Middle | SE_09189 | chr1:154398672-154408855 | CD14 | SE_14719 | chr1:154404065-154406200 | CD4_Memory_Primary_7pool | SE_17632 | chr1:154404159-154407544 | CD4p_CD25-_CD45RAp_Naive | SE_18405 | chr1:154399517-154407766 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19165 | chr1:154402693-154406528 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_24531 | chr1:154405908-154406164 | Colon_Crypt_2 | SE_26130 | chr1:154403236-154408131 | Duodenum_Smooth_Muscle | SE_26877 | chr1:154404909-154408834 | Esophagus | SE_32086 | chr1:154405170-154405757 | Gastric | SE_36673 | chr1:154402794-154406528 | HMEC | SE_41139 | chr1:154403000-154404975 | Left_Ventricle | SE_41139 | chr1:154404983-154406220 | Left_Ventricle | SE_41139 | chr1:154406358-154407850 | Left_Ventricle | SE_41647 | chr1:154405094-154405908 | LNCaP | SE_42431 | chr1:154403426-154404945 | Lung | SE_42431 | chr1:154404999-154407895 | Lung | SE_44716 | chr1:154402429-154408017 | NHDF-Ad | SE_48261 | chr1:154404078-154406393 | Psoas_Muscle | SE_48261 | chr1:154406400-154407797 | Psoas_Muscle | SE_48934 | chr1:154404044-154404956 | Right_Atrium | SE_48934 | chr1:154405011-154406384 | Right_Atrium | SE_51380 | chr1:154404969-154406160 | Skeletal_Muscle | SE_52880 | chr1:154404061-154404906 | Small_Intestine | SE_52880 | chr1:154405284-154406259 | Small_Intestine | SE_54278 | chr1:154404054-154404758 | Spleen | SE_54278 | chr1:154405144-154405803 | Spleen | SE_54618 | chr1:154399097-154409137 | Stomach_Smooth_Muscle | SE_62668 | chr1:154357227-154415486 | Tonsil | SE_64458 | chr1:154402184-154407649 | NHEK | SE_65390 | chr1:154404574-154407875 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 154405619 | 154406249 | chr1 | 154405181 | 154405498 | chr1 | 154405027 | 154406213 | chr1 | 154405122 | 154406194 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154429 | chr1 | 154402030 | 154407873 |
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Enhancer Sequence | TTTAAAATTT CTGAAGTGAT TATTTATGGA ATTTCCCATT TAATATTTTT GGACCGCAGT 60 TGACCACAGG TAGCCGAAAT CTTGGAAAGC AAAACCTCAG ATAAGGCAGG ACTACTGTAT 120 CAGAAAGCCA GAGCAGTGAC TTCAATAGGG TGGTTCAGCT CCCACTTGGG TCTGTTTCCA 180 TAGAGTTACT GGGCTGCCTG GCAGTCATGT TTTTGTTCTG TCCTCTATGA TGAAAAGTGC 240 GGATTACCAT CTGTGAATGA TGCAGCTGCC ATTAGCACTG TCAGCTCATG CCCCAAGCCT 300 GGATAGCTTC ACAGCCCAGC AAAGGATACA CCTTGTTTGT ACCTCAAAGG CTTGTACCAT 360 AGATAGGATT AGCCAGGATA GAGACTGTGG CTGGCAGCTT CCCAGGCCAG CCTGTGGAAA 420 GCTCTGTCAT TTCTGACACT TCAACTGAAA TACTTTTTTT TTTTTTTTTT TGAGATGGAG 480 TTTCGCTCTG TCGCCCAGGC TGGAGTGCAG TGGTGGGATC TCGGCTCACT GCAATCTCCG 540 CCTCCCGGGC TCAAGCGATT CTCCTGCCTC AGCCTCCTGA GTAGCTGGGA TTACAGGCGC 600 ACACCACCAC GCCTGGCTAA TCTTTGTATT TTTAGTAGAG ATGAGGTTTC ACCATGTTAG 660 CGGGGCTGGT CTCGAACTTC TGACCTAGGG TGATCCGCCT GTCTCGGCCT CCCAAAGTGC 720 TGGGATTACA GGCGTGAGCC ACCGCGCCCG GCTTGACTGG AATACTTTCC ATGTTGACAG 780 CGGGAGTGGG AGAGAGTACA GTGCTTGTCC TCCCGAGCAG CCTCGTGCCT TTGCTTCCAT 840 CTGCTTTGAA GAGTCAGCAT GACCACTGGG CGCCTTTGAA GTGAGGAAAG AGCAGGGGAA 900 GTGGCTTCGA GAGCCTCAGG GGCCCCAGCC CCCACTGAGG CCCCACCCAG ACCTCAGGCC 960 ACTGCAGGGC CTGGAAGAGA CAGGCCCCTG GAAAGGGATT ACTGGGAGCT CTGCTTTTTC 1020 TCTTGTGTGT CTGCTTTCAC ACCCTTGCCC AACTGCAGCA CTGCTCCCTC CTTCTTCCAC 1080 AGGCAGGGGT GAGCTCAGCC TCTGCCTTGG ACCAGGCGCA GTGCTGGGGC AGTGGGAGGA 1140 AGCGGGCCAA CAAGACTGAG CCCCGGCCCT CTGACCCCAC CTGGGCACAC ACGTAAAGCA 1200 GTCGGTGACC CTGCCTTCGT GGCTGGGTGG AAGCCTGGGT GGTGTTGGGG GAAGGAGGAA 1260 AGGGGCTTTA ACTCAGCCTG GAAAGGTTGG GTTTGTCCCA TGTGCTGGAT TCAGCAGGAG 1320 CCCAGGGTTC GAACCCAAGT CAGAGGTGGC AGACTCGTCA CCCCAGCTGG AGGGTGAGTG 1380 GTTGACGTGG CCTCACATGC CCACATGTGT CATAAGAGGG TGAAGCCTCA GGTTTCCAGG 1440 CCAGGTGGGA TGGTGGCTGA CTCACCTCGA ATGTCTTCAG TTACCCAGAA TTCTTTTCTG 1500 GACTCACCTG CCAGAACCCC TCTAGCACTT TTTGTGTCTC TGGAGTGGCA TTTCTGCTGG 1560 GTGTCTAGTC ATCTGAGGAC AGATCTTTTT TGTTAGTGCC TTGAAGGCAG GGTGGGGCCT 1620 CTCTTGATTC ATTTCTATAT CCCCTACAGT GCCAAGAGCA CAGGCCCAGC GGGAGACCAG 1680 AGCTGGCCAG CCGACCATTG CCTGAGTGAC TAGCTGAGCC CTCCAGCCTA GCTCCCCTCA 1740 CCCCTCGTGC CAGGCGCTAG GCTACATGTT TATATATATT TGTAAATCCA GCTAGTTTCC 1800 TCATCTCTAG ATTTTACATT TATTGCTCAA TTTTTTTTTT TTGAGATGGA GTCTCTGTCG 1860 CCCAGGCTGG AGTGCAGTCT CTGTCACTGC AACATCTGCC TCCTGGGTTC AAGTGATTCT 1920 TCTGCTTCAG CCTCCTGAGT AACTGGGACT ACAGGCATGC GCCACCACGC CAGGCTAATT 1980 TTTTATTTTA TTTTTTGTAT TTTTAGTAGA GACAGGGTTT CACCATATTG GCTAGGCTGG 2040 TCTCGAACTC CTGACCTCAT GATCTGCCTG CGTTGCCCTC CCAAAGTGCT AGAATTACAG 2100 GCGTGAGCCA CCGCGCCCGG CCTTATTTCT CAGTCTTAAC AGAACCAGCC ACGTGTGATT 2160 GTTCATGCCT GTAATCCCAG CACTTTGGGA GGCTGAGGCG GGCAGATCAC CTGAGGTCAG 2220 CAGTTCGAGA CCAGCCTGGG CAACATGGTG AAACCCCATC 2260
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