Tag | Content |
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EnhancerAtlas ID | HS095-00632 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:27920840-27924100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr1:27920853-27920865 | GGCAGTGATTTG | - | 6.04 | RREB1 | MA0073.1 | chr1:27921979-27921999 | TGATTGTGTGTGTGTTGGGG | - | 6.51 | RREB1 | MA0073.1 | chr1:27922341-27922361 | GGTGGTTGTGTGTTTGGGGG | - | 6.82 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_00861 | chr1:27914193-27931151 | Adrenal_Gland | SE_01588 | chr1:27912079-27922411 | Aorta | SE_03939 | chr1:27919012-27929651 | Brain_Anterior_Caudate | SE_05814 | chr1:27913859-27923243 | Brain_Hippocampus_Middle | SE_05814 | chr1:27923258-27933300 | Brain_Hippocampus_Middle | SE_07770 | chr1:27919197-27930846 | Brain_Inferior_Temporal_Lobe | SE_20210 | chr1:27921675-27923269 | CD56 | SE_25377 | chr1:27923108-27931282 | DND41 | SE_26518 | chr1:27909071-27932559 | Esophagus | SE_29557 | chr1:27915462-27922531 | Fetal_Muscle | SE_29557 | chr1:27923567-27931291 | Fetal_Muscle | SE_31394 | chr1:27920375-27921463 | Gastric | SE_33503 | chr1:27915499-27922187 | H2171 | SE_33503 | chr1:27922582-27931429 | H2171 | SE_40593 | chr1:27913008-27932820 | Left_Ventricle | SE_42106 | chr1:27919078-27932390 | Lung | SE_46630 | chr1:27920673-27921977 | Ovary | SE_46630 | chr1:27922137-27923402 | Ovary | SE_46630 | chr1:27923435-27923898 | Ovary | SE_48058 | chr1:27919076-27931233 | Psoas_Muscle | SE_51091 | chr1:27913567-27922874 | Skeletal_Muscle | SE_54056 | chr1:27911548-27931728 | Spleen | SE_54527 | chr1:27912777-27922283 | Stomach_Smooth_Muscle | SE_54527 | chr1:27922429-27929632 | Stomach_Smooth_Muscle | SE_62470 | chr1:27916580-27996594 | Tonsil | SE_65253 | chr1:27915143-27922215 | Pancreatic_islets | SE_65253 | chr1:27922257-27931723 | Pancreatic_islets | SE_68682 | chr1:27918827-27923822 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I027588 | chr1 | 27914885 | 27923473 |
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Enhancer Sequence | GTTGGGGGAG GGAGGCAGTG ATTTGGCAAG CACTTGAAAA AGTGTGGGCT GGGGGCAACT 60 CCCCCTGTCC CTCTCTCCCA CATACATGCC AGAGCCAGGG CAGGGCTGGG TACTGAGAGT 120 TCCTGGCTGA AAGACCAGGA TGACCAGGTG CCAAGGGGCT CTGCCCCCAC CCCAAAGAGG 180 CCCCAAACCT TTAAGCCCAG GCCAGGGTGC CCAGAGCACA GGGTCTTGGG TGGGGCAGCT 240 TTGAACCAGA TGTCCAGCCT CACTGTCCAG GAATGAAAGG CCTGGGGCGG TGAAGGGGTG 300 GAGATGCCTC CCCAGGCAGA GGAGGCTCTG GGAAGAGCGG GAGGCCTGGG CAGCAGAGAG 360 AGAGAGAGCG AGAGCACACA AGAGTGAGCA ATGTGTGTGA CAGGCTGAGG CTGTCTAGGG 420 GAACAAGGTG GGGGAGAGGG TGTGCTGGAA TGTGCCAACG GTGGGAGTGA GGGCTGCAGA 480 AGGATTAGGC GGGGTATGTG ACAGGGTGCC GTGGGGTGCA GGCGGAGCAC AGAATGGGTG 540 CAGGGTTGTG ACTAGCTGAG GCTGTCTTTG TGTACAGGTG TGGTATCGGG GTGTTTGGAG 600 AGGTGTAGGG GTGTCCCTGG GCCCTTAGGT GGCTGAGGAA AAGTACCGGA GCTGAGACTG 660 TCTGGGAAGC GGTGGGGCCG GGCCATTAGG ACTGCCTGTC GAGGAGGTGC CGGGATCCAG 720 GAGGCAGTGT GCACAAGTTT CAGGAGGTAT TAGAAGCTTC GGGGCCTGAT CTGTTAGAGA 780 TATACTAGAA CCGAAGCCAT GTCTGTGTGT TTGAGGCAAA TGTTGTGGCT ACAGAGGGTG 840 TTCTTGTTTG AGTGGGTGTT TGAAGCAGTG AGTGTATGTG TGTTGTAGGG GGAGGCTGTA 900 TGTTTGGAAA GGTATAGGGG ATGATACCGG TGTTTGGGGA AGTGCTGAGC TATAGCTGGG 960 AGAAACGTTG GGGGCTGTGG GCAGAGTGTG TGTGTCTGGG GAGGTGTCAG GGCTTTGAGG 1020 GTATGAGTCA GTGGGAAGGT AGCAGGGCTG TAGCTGGGTC CTGGGTGTAT CTGGCAGTGT 1080 TGGGGTTGGA TAGGGGGTTG ATATGCTGAG GGTGTGATAG CTGTGTGTGT GTGTGTGTGT 1140 GATTGTGTGT GTGTTGGGGT GTTTAGGGAT GTATTGGGGG GTCATAAAAA TGTGGGTTTT 1200 GGTTAAGTAC TAGGGCTGTG AACATGTGCC TGGAAAGGTG TTGTGGTTGG TGGAGGATGC 1260 ACTGTGGTTT TGGGGAGGAG CTGGGGAGTG TCTCTGGAAA GGTTATTGGG ATTTTAATTG 1320 GGTACCTGCA AGGGTCTGGG GAGGCGTTAG AGACCTGAGG TCCCTCCATA CGTGGGAAGG 1380 GAAGAATGGG TCTCTGATAT CAGAGATGTG CCACAGGCTA TCGTCCGTGC ATGCACAGGT 1440 ATGAGGGCTG TAACCAGGTT CCTGGTGTCA GGGAGGTGTT GCAGGTTGTG GGTAAGCATG 1500 TGGTGGTTGT GTGTTTGGGG GTATGTGCAT GTGAGGTAGC TGGATGTCGG GGGGTATCTG 1560 TATGTAGAGT GTGTGTGTGG AAGTGTGTGG GCTGGGTGTT GTAGGTGGAG CAGTTGTGTT 1620 TTAGAGGTGT TAGAGCTGTG AGTGTGTATG TGGGGCAGTT GTCTATTTAG AAGGTGTTGG 1680 GAGCTGTAAC TGAGTCCCTG GACCCCAGAG AGGTGATGGG GCTGCAGGGT TTGTGTGTGT 1740 TAGGGGGGAT GCCCCTCTGG GAGAATGAAG GGCAGCATCC TGGCCTTTGC TCCGGGGCCT 1800 AACTGGGGGC TACCCGCTAG AACCCCTATG GTATGGGGTG CCTGTGCGGG GGTGTTGAGA 1860 CAGGCAGTCC ATCTGTCTCA GCCTGTGCCC AGGCCCAAGG AGCAGAGCTG CCTCCTCGCT 1920 CCCTGGGGGG CAGCAGCGGA TCCAAGCCCA CCCATCTGCC TTCAGATGGT CGAGGCAGGA 1980 GCCTCCACAA AGCTGCCTGG AGGGCAGCAC TGCGTTTGAA GAGACACAGG CTGGGGGTGG 2040 GGGAACTGCA CAGCAAACAG TCCTCACGGA GGCTCCTTTA AAAACCACTG ACGCCAGAAG 2100 AGAGGAAGAG GGAGGACAGG GGCGGGTATG TCTGTCCTTG TGCATCTGTG TGGGTCAGTG 2160 CCCAACTTCC AGGCCGGGGG CCCCTTCCCA CGTGCTTGTG CTGGATGTTC CTGTTCAGGT 2220 AGCACTCAGG CCTTGGAAAA CACTGCTCCA ATCCAGGCAA CAGGCTCCCA GCCTCACACC 2280 TGAACTACAC CCTCATATCT GCATAGTCCC TACACTCACA CGCACTCATA CACCTTCCCA 2340 CATGCATGCC TGCCACTGCA CGCTCACACA TGCAGTTTGC CCCATGCCCT TAAACCTTCA 2400 TATATGTACC CCCATCACAC ATACCCCACC CTGCAAAACC CACAGTTACA CACACCCATC 2460 TTACACACAC ACCTATCACA TAAACGTGCA TCCACACATA CATACCTGAC AAGTCACTCT 2520 CACACACACA CCCACACACT CCACACACCT TGGAGCTCCC TGTCACACCC GTACCCTATC 2580 TCACATACAC CCAGTCTCTC TCACACTCCA TGAGGACACT CGCCATCCCT TCTACCTGCA 2640 CATGCAAGCA CATGTTTATA CACATATGCC TCACCACCTT TGAGACAGCT CCCCACTACC 2700 CAAGCCACTG GGCATTTCTC TGTGTCCAGG TCAGGCCCTG AAGCTTTCCA GAAGGGCTCT 2760 CACCGACTGA GAGGACCTTC TGCCTCCCCA CCTTGCCAGC CGGGTTAGAG TATGGGGGTG 2820 GGGGGCAGGT GGCAGGGGGA GGTTCTGTGT GCTCTGGTGT GACTGCCACT GTATGTAGGA 2880 GGGTGTCCCA TGACAGGGCC TGTGAGTCAA CACCTGTACA GGGAAGGAAG CACAGGTGCG 2940 TGTTCACCAG CTATGTTCGT GAGATGCAGA ATGAGTGTGA GGGTGGAGAT TTACATGTCA 3000 CAAATTTGTG TGTGTGTGTG TGTGTGACAG TGTGAGAGTG TGTGTGTGAG AGAGAGAGAG 3060 AGAGAGACGC AGGGCCTGTG TAGACAGGTG TGACCGTGGG GGCTGCGTTT ATACGAGGGG 3120 CATCCCCCGG GTGAATGTGA GGGGGTGTTT CCCAAGACAA GAGAGGTGCA CATGTGCATC 3180 TGGTGCAGGG GTCAGGGCTG CAGGCCTCTC AGCAACCCCC TCCCCCTATG AAAAGAGGAG 3240 CAGGGAGCAA GGGGCTCTGG 3260
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