Tag | Content |
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EnhancerAtlas ID | HS047-20347 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:218814990-218818120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr2:218815119-218815132 | AGGAGCAGCTGCT | - | 6.11 | TFAP4 | MA0691.1 | chr2:218816883-218816893 | AACAGCTGAT | + | 6.02 | ZNF263 | MA0528.1 | chr2:218815447-218815468 | TCTCTCTTCTTCTCTTCCTTC | - | 6.54 | ZNF263 | MA0528.1 | chr2:218815450-218815471 | CTCTTCTTCTCTTCCTTCTTC | - | 6.58 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00005 | chr2:218814233-218816533 | Adipose_Nuclei | SE_00005 | chr2:218816981-218819519 | Adipose_Nuclei | SE_00853 | chr2:218814951-218815887 | Adrenal_Gland | SE_00853 | chr2:218816106-218818070 | Adrenal_Gland | SE_01533 | chr2:218815009-218822370 | Aorta | SE_02897 | chr2:218815125-218815667 | Bladder | SE_05795 | chr2:218814846-218820959 | Brain_Hippocampus_Middle | SE_25781 | chr2:218815724-218826606 | Duodenum_Smooth_Muscle | SE_26522 | chr2:218814850-218822390 | Esophagus | SE_31466 | chr2:218817040-218819258 | Gastric | SE_40583 | chr2:218814884-218822626 | Left_Ventricle | SE_42478 | chr2:218814905-218822400 | Lung | SE_46622 | chr2:218815028-218815701 | Ovary | SE_46622 | chr2:218815752-218816065 | Ovary | SE_46622 | chr2:218816451-218818162 | Ovary | SE_47481 | chr2:218816602-218816981 | Pancreas | SE_47481 | chr2:218817712-218818055 | Pancreas | SE_48107 | chr2:218816913-218819250 | Psoas_Muscle | SE_48552 | chr2:218816054-218820597 | Right_Atrium | SE_50265 | chr2:218817096-218820679 | Sigmoid_Colon | SE_51152 | chr2:218816807-218819635 | Skeletal_Muscle | SE_52433 | chr2:218817012-218820775 | Small_Intestine | SE_53299 | chr2:218817566-218820251 | Spleen | SE_54481 | chr2:218814653-218824098 | Stomach_Smooth_Muscle | SE_65278 | chr2:218817776-218819523 | Pancreatic_islets |
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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 |
GH02I217950 | chr2 | 218815123 | 218817843 |
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Enhancer Sequence | AAGTGAACCA CAGCAAATGC CACTGCCCAC GTGCACCTCC ACTGTCTCTC TGCCCCTTCA 60 TCTGTGAACT CCTTGAAGCC TAGGGCCATT TCCCATTCAT CTCTGAATGG CCAAGAGGTA 120 GAAACTACCA GGAGCAGCTG CTAGGAACAG GATAACATCC TGACAAGGCC AGGCCTGTGG 180 GCCCTGGTCA CTGGGGAGCG TGCTGGCCAC ACCCCGAGAG CTGACCTTTA GCCAAGCTGG 240 CTCCTGGGCT GGGGGAGGTG AGGAGGTCTG GCTGGTGGCG GAACACTTGG CTCACATGTG 300 CTGTCCCAGG TAGGCCCTGG TGCTGGCCAG CTGGTTCCCA CTCCCTAGGC CTCCCCTCCT 360 GCCACCATCT AGTAGCCCTA TGGAGACCGA TCCTAGCCAG GCATCCTCGC CCAAAGCCCA 420 GAGCTGTCCA CTGGCCCAGG TCCAAGTCTG GTTCCTCTCT CTCTTCTTCT CTTCCTTCTT 480 CTGTTCCCCT CCCTCCTCTG CTGTCACCCG CACGGCCCTC TTCCTCCTCT GCACTCTTCT 540 GCGCAGCACC TTCCTTCCCC TCCCCTGCTT CAGTTTACCC CTCGGCTCAC TTTCCATCTC 600 CCCGAGCCCA TCCTCCAGGG CTCTGCTCAT GGCCAATCTC CCTGCCCCGG GCTCCGAGGG 660 AAAATCTCCC CGTTGCTGCA CCCTCCTCCG CTCCCTAGAG TTTTTAGTGA TGTAGCACTT 720 TCAGGGTTGG AGAGAGCTGG AAACTTCCCT CCTGAGGACT TCGGATCCAC CCCTATAGAA 780 AATAATCATC ACCTTGCTCC ACTTTGAAAT GGGGAGCTAT CCCTCCAGGG GGAAGGGAAT 840 CACAGAAACC TGGCCCCATC CTACCAGGAG TGGAGAAGAG ATCCCAGGCT TTGGAAGTGC 900 ACCGACCACA TCTGAAGCTG TGTAACCTCG AGCAAGTTAT TTCACTGCTC TGAGTACTGA 960 GTGCAAGATC TGGCCTAGAG CAGCTCTCCA TAAATGTTGG CTCCCCAGAC ATTCTCCTCC 1020 TTCAAAGAAG CCGTCACCAC CCCCATCCCA GAATTACGAT TCATCTCTCT GTCATGTATC 1080 TCCCTGCCTA ATAATGCTCA GATTTAGTGA GTGTTTCCCA ATTGACATAC TGTTCCTAGA 1140 GCTTTGTGGG GATTAACTCA TTCTAATCCT GCCAGCACCC CATTGGGTAT TGACCTTTAT 1200 GAATCCCATT TTACAGAGGA GGAAACTGAA GTTCAGAGAC ATCAGCTATG TTTGCTACTC 1260 CTCTCCTAAC TACAGCAGCT GCAGCAAGCC GGCAGGGCCT CAGGGCCTGG CTGGACCACA 1320 TTCCAGCATA TCAGGGCTCT CCTTGACCTG ACAGGGGCTC GCCCGCCCCT GCCTACACAC 1380 CCCAGGCCCT CAGGGCTCAC TCCCCATCCT CAAGGCGGCT CCCACCACTG GGGGAAACCT 1440 GCTTCCTGGA ACCCTTGGTT TTGCTTCAGG GAACAAATCT CCCCAAAGCT TTATTCAACA 1500 CACACACACA CACAGCCACG CAATCACTGG AAGTCTCCCA TAGTGGTAGC TTCACAGGCT 1560 AGACGTCCCC AGGTTTTTCA GTTTCTGTAC TCTTCCACAT GCCAGGTGCT CAGTGGTTCT 1620 TTCTCTGGTT CTGATCCTTT TCCAGTTGGC TCCATCCCAT CTGTCCCTCA CCCCTTCATT 1680 CCACAAGTAC TTTCTAAGTG CCCGCAGTGG CCCAGGCCCT GTGAGGCCCT CCAGGCAGAA 1740 CATGAACACA GCCAGATGGG CCCCTGCCCT CAAGGAGCAC TTGATCTAGG AGAGGGAGCC 1800 GCTGAAGGAA CAAACACAAA CACACAACAC AAATCGTGCT GAGTGACCTG AAGGGAAAGA 1860 ACAGGCGGCC GGAGGGAGAG ACATTTAGAT CCCAACAGCT GATGGGCACT TAACATGTGC 1920 CAAGCCCTGG TACAGCCCCA GTGCCTGCAT TCACTCATTC CCTCCTCTCC CCATACCTGG 1980 GAGTAGATGT TATTCTAACC CTACTTTGTA CAGTTGAGAG AGCTCAGACG CAAGAGGTGA 2040 AGCCACTTGT CCAAAGTCAA TGATAATGAG ACAGCAAATA AGCAGGGGTG ATAGGACTTG 2100 ATTCCCAAGT TTGTACTCTT AACCACTATG TCATATTGCC TCTAAAAGGC CCAGAGAGGG 2160 TTCATTAAGG CCCACTTCCC AAACCGGTGA CTCTCCCGCG CCACACACAC ACACACACAC 2220 AAAAGCCAGC AGCAGCCTGC CCAGTGCAGA AGTCAGCAGG CCCAGCCTGG TGAGGACATG 2280 GACACCACAC TGTGATCTTA TCCATGTACC CAAATGCAGC ACTGGCTTCA CCAAGATGGC 2340 AGTCCCCAAC CTCCAGACTT TCAGCTTGTT CTCCAACTCG GATGGCGTGG ACACTTGACC 2400 TTTACGCTGG TAGGCTTCAA GGTGGCTGGA GGGACTGGCT AAAACAACAT GAATGGGGCT 2460 GATGAAGACC CCTTCCCAGC AGGGCTTGCT TGAGAAATGG ATCCTGGTCT CATGGATGCG 2520 AACAGGATTG GGGCAAGAAG GGCCCCCAAA TCAGGGAAAC AATCACTCCA AGCCCTCCCC 2580 AAGGCCACCC AATCAAGGCT CACAAAATGT TGAGGATTTA GAGTTGAGCA GCCCAGTCCT 2640 TTCCTTGTAA TGACATGGAA ATGAGGCCCA GGGAGGACAG GTATGGAGTC CCAAAATCAC 2700 CATAGGGAGG AGCTCAATGA CGTCAACCCT AGACAGGGCT CCAGCTCCCA GCCCAGCGCT 2760 CAGGCCTCTG CATCACACTG GTCCCCAGGA GAGGAGATGC TGGCCTGGCC ATCTGGGGAT 2820 GGAAGCAGGA GCCTCACGTC TGTTCCTAAT GTCCATGAGG AGGGAAAGAG CAGCTCGGGC 2880 CCCTGGGGCA GTGAGGGATC TGCAGGGCCC AGATGAAGGA TGCTTGGGCT CCAGGAGCAG 2940 CACAGTCCTG CCCTCCATTA GATGATCCTA GCAGAGGCTG GGGCGGAAGG GGTGGGAGAG 3000 TGCGGGGCAA CAGCTACAGC CCCGCCCTCT GGGTGCTCCT CACCAGGGAC CCCATGGGTG 3060 ACTGTTTTCT TGGAACATTG TGTTCAGGCT GTGAGCCTTG GCTCAAGCAA TCTACCCTGG 3120 CAAATCTCCA 3130
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