Tag | Content |
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EnhancerAtlas ID | HS074-10161 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr22:38710850-38713160 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr22:38712847-38712858 | AAATCACAGCC | + | 6.02 | SP2 | MA0516.2 | chr22:38712596-38712613 | ATAACCCCCACCCCTTT | + | 6.05 | Zfx | MA0146.2 | chr22:38712873-38712887 | CCGGCCGGGGCCTC | + | 6.3 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_01248 | chr22:38708331-38715029 | Adrenal_Gland | SE_02485 | chr22:38708304-38713310 | Astrocytes | SE_04547 | chr22:38708123-38713293 | Brain_Anterior_Caudate | SE_05752 | chr22:38708075-38713340 | Brain_Cingulate_Gyrus | SE_06431 | chr22:38703285-38713337 | Brain_Hippocampus_Middle | SE_07619 | chr22:38708097-38715180 | Brain_Hippocampus_Middle_150 | SE_08599 | chr22:38708236-38713337 | Brain_Inferior_Temporal_Lobe | SE_09054 | chr22:38711150-38711655 | Brain_Mid_Frontal_Lobe | SE_24180 | chr22:38709584-38714935 | Colon_Crypt_2 | SE_26981 | chr22:38708079-38715680 | Esophagus | SE_28309 | chr22:38708475-38715154 | Fetal_Intestine | SE_32216 | chr22:38708241-38715041 | Gastric | SE_32871 | chr22:38710638-38711643 | H1 | SE_32871 | chr22:38712133-38715025 | H1 | SE_34648 | chr22:38704038-38716322 | HeLa | SE_35963 | chr22:38708089-38713318 | HMEC | SE_40787 | chr22:38704155-38715170 | Left_Ventricle | SE_42688 | chr22:38708087-38715695 | Lung | SE_44915 | chr22:38708144-38715036 | NHLF | SE_45934 | chr22:38708162-38713369 | Osteoblasts | SE_49297 | chr22:38708292-38715050 | Right_Atrium | SE_50488 | chr22:38708133-38715075 | Sigmoid_Colon | SE_52414 | chr22:38708184-38713332 | Small_Intestine | SE_53881 | chr22:38705637-38715050 | Spleen | SE_56215 | chr22:38708106-38715579 | u87 | SE_59089 | chr22:38654708-38715012 | Ly3 | SE_64669 | chr22:38708412-38713280 | NHEK | SE_67437 | chr22:38708118-38714885 | MM1S | SE_68731 | chr22:38708137-38716244 | 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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Enhancer Sequence | CCTTCCTCAG GGCCAGGGGG GAGCCCTCTG CTCTGGCCTG GGGCAGAGGA GGGACCCCTC 60 TGCTCTGGCC TGGGGCAAAA GTCCGGACAC CCTGTTCCTG GTCAGCAGAG GAGGAAACTG 120 AAGGCCTGGA GGCAGTGCTG CCGTGGGGAC AGGGACCAGG GACTGCAGTA AACAGGGGGA 180 GGGGTGTTTA CAAGAGGACC AGCATCAAGG ACTAGCAAGA GGGAACTCCT TTCACAGACA 240 GGGTACTCAG GCTCACAGAG GCCATGCCAC CTGTCCCACA CCACCCTGCA GATGGTACAG 300 CCTCGCCGAG GACAGGGCTC CGGCTGTCCC ACCTGGTGGT CTCCCACACT CACAAACAGG 360 GCAAAACAGG AAGACTGCAG AGCAGCTGTG CTGGCACAGA AGATCAGCCC CTTGCCCGTG 420 CCAAGTGCTG CCCCCAACAA CCAGGCCAGC CTGGGAGGGA GATGGATTCC AGGGACAGTG 480 GGCAGATCCC AGGAGAGACA GGGAACCCCG GCACCTGGCT CCCAAGGAGC TCACCAGCCC 540 TCCACCAATA ACCACGAGGC AGGGACCTCC ACCAGAGCTG GCCAAACTCT GGGCTCTCAA 600 TCAAGGGCCG CTGCCCATAT GCTTGGCCTG TCTCAGCTGA GGTGCCACGC TGCCAGGGGA 660 ACACAGTCCA CGTTTGCAGG AAACCCACAC GCCACACATC CCACGTACAC ACACGTCCAG 720 CTTCCCGAGT GTGTACACTC CAACGGAAGA AAGAAAAGCA GGCACACACA GTGAGCCCTG 780 TTGGGGGGTA AGGGGGGGTG TGCACGCAAC CCCCCCCCAA CACCTCAGTC CACTTTCTGC 840 CAACACCAAT TCAGAGACCA CACATGGCAG CCAGGAAACC CGCAGGTTAG GAAAGGAACA 900 TAAATATACC CGCATCCTAT ATTACATAAA TACCCACGCC GGGTTATATA AATACCCGTG 960 CCCTCTGTCT GGGTGTCTTA CATAAATATA CTGCACATGA CCCCCCAGTC TCTCCCCACT 1020 CACCGGCTGT CTGCAGAGAA CGAGAGCGGG AAGGGGCAAG CCCTTCAGGA CCCCCTGACT 1080 GCTATGTGCC AGCCACCCAG ACCCCCAGTC GCTCCCCAAC ACCCCAGGGG TCCAAGGTCC 1140 CTGGGGGAGC CTAGACTGTC CCGGCACCAA TACCCAAAAA GCCTCCCAGA GGAGAGCAGA 1200 AAAGCTTCAT TCAGGAATGG AGAGGCTTTT CAGTTCTTTT GCTGCTTCTC CCATGGGGGA 1260 GGGGGGGAGA TAAACAAAGT GGGGGGAAAA GTGGATATAA AGGTTCAAGA GTTTCAGCAG 1320 GTTAAAAAAA TTAGACAAAC TACCAACCAG CATGGCACAC GGGCAGTGCT TCTTACTCCC 1380 CGAACACCAT CGCCTACCCC TGAGCCGGGG CCCTTGTCCC TCGGACGATT AAAATAAAAA 1440 TTGAAGGGAC ATCATAGAAA CGAAGGCAAA GGAGACCCAA ACACAGGCAT TGCTTGGAAG 1500 CAACTTGAGA CACTTGTGTC CCCTTCTCCT CTCTCCAAAT CCTTCTCCAG GAAGGAGGCT 1560 ATGCCAGGAA GAAAATATGC AAGAAAACTA AGGGAAAAGT TGGGGAGGGG GCTCACCCCA 1620 CTTCGAGTTA GGGTATTAAC AAGAGCTTGG GAATCCTCTA ACGACACCCA GACACTGTTT 1680 TGCGTTCCTT AGAGACTTGC AAGACATCAA TCTCTCACAC AAAAATGGGA GAATCCGATC 1740 CGACAAATAA CCCCCACCCC TTTCTTTCTC TCCACAAAGA AAAACAAATC AGTGGCCTGG 1800 TGACCACACA CCTCTTCACC TTAGGACCCC CAAACGCCCG TCATCCAACG AGCGGGCGCA 1860 GCCTTGCGAA CCCCCAGGTC CGGGCGCCGG GGCCGGGAGA GCAGGGGGCG CCGGTGATTG 1920 TCCGATGAAA CGCTACGCGG GCCCGAATCA ACAGTATCCG GCGCCCAGCA CCCCAAGCCC 1980 CCTCCCTCAG CGTCCCCAAA TCACAGCCGG GGTGGCCGCC TGGCCGGCCG GGGCCTCGGA 2040 GGGCCCAGCG GGGGGAAGCG GAGGCAGGCC GGCCGGGGGG CCTCCCCCGC GAGCCTGCAA 2100 AATAACAGGC CCCCTCCTCC TCGTCCCCAG CCGCGCCTTT GTCCTCGCCG GGCCGAGCGG 2160 GCGGCGCCCG GGCTGCCCCC CCTACACCCC AGCGCGAACG CGCGTGTGTC TGCCCTCCCT 2220 TCCCTCCCTC TCCAGCAAAA ACAAAGAGGC TGAGGGAGCC CGATTCCCCC CAGGTTTGCA 2280 CCCTTCCGCG GGCCCGCGGC CCCCCGATAT 2310
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