Tag | Content |
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EnhancerAtlas ID | HS047-27440 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr5:131835720-131837280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr5:131837047-131837066 | CAGCACCCCCTGCTGGCTA | - | 7.03 | GSC | MA0648.1 | chr5:131836989-131836999 | GGGGATTAGC | - | 6.02 |
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| Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
SE_00037 | chr5:131820679-131837440 | Adipose_Nuclei | SE_04124 | chr5:131835240-131837326 | Brain_Anterior_Caudate | SE_06435 | chr5:131828999-131837748 | Brain_Hippocampus_Middle | SE_10340 | chr5:131835704-131837777 | CD19_Primary | SE_10915 | chr5:131818633-131838738 | CD20 | SE_13479 | chr5:131836174-131839047 | CD34_Primary_RO01536 | SE_17370 | chr5:131818848-131837330 | CD4p_CD25-_CD45RAp_Naive | SE_17764 | chr5:131818558-131837415 | CD4p_CD25-_CD45ROp_Memory | SE_18258 | chr5:131818792-131837424 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19103 | chr5:131836302-131837314 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19972 | chr5:131828783-131837777 | CD56 | SE_22284 | chr5:131818534-131837164 | CD8_primiary | SE_23079 | chr5:131830842-131839811 | Colon_Crypt_1 | SE_23750 | chr5:131835068-131838981 | Colon_Crypt_2 | SE_25340 | chr5:131835682-131838025 | DND41 | SE_25784 | chr5:131828604-131839493 | Duodenum_Smooth_Muscle | SE_26597 | chr5:131834716-131837077 | Esophagus | SE_27629 | chr5:131830752-131839506 | Fetal_Intestine | SE_28559 | chr5:131830527-131839276 | Fetal_Intestine_Large | SE_31393 | chr5:131829777-131839489 | Gastric | SE_39368 | chr5:131835375-131836017 | Jurkat | SE_39368 | chr5:131836085-131837612 | Jurkat | SE_40726 | chr5:131829734-131835879 | Left_Ventricle | SE_40726 | chr5:131836212-131838737 | Left_Ventricle | SE_42103 | chr5:131829574-131839460 | Lung | SE_44054 | chr5:131830691-131837759 | MM1S | SE_47919 | chr5:131836298-131837089 | Pancreas | SE_48659 | chr5:131835953-131838663 | Right_Atrium | SE_50051 | chr5:131828811-131839642 | Sigmoid_Colon | SE_52336 | chr5:131828839-131839793 | Small_Intestine | SE_53285 | chr5:131829513-131839339 | Spleen | SE_54554 | chr5:131829395-131838583 | Stomach_Smooth_Muscle | SE_61818 | chr5:131790756-131837647 | Toledo | SE_62219 | chr5:131721125-131837948 | Tonsil | SE_65342 | chr5:131835327-131838706 | Pancreatic_islets | SE_66244 | chr5:131835375-131836017 | Jurkat | SE_66244 | chr5:131836085-131837612 | Jurkat | SE_67186 | chr5:131830691-131837759 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 131836369 | 131837068 | chr5 | 131835833 | 131835962 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I132493 | chr5 | 131828971 | 131839447 |
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Enhancer Sequence | TGCTCTGATT GCAGTGCCAG ACGTATGTCA TACCTCGAGT AAGAGGCAAA GAGGCAGAGA 60 TGCTGGGAGT ATGGAGACGG AGCAGGTTAT CTCAGTCATT GTTCACAGAT GGCTACTCTG 120 AGGAGGGGAC AGTTCAGCAA AGCCTCAAAG GATGAGTCAA AGGTTAATAG GCTAATAGTA 180 GGGGAGGGCA TTCCAGAACG TGAAAACAGC CCAAGGAAAG GCTTGGCAGC TCAGAAGTGC 240 AGAACGGATC TCGCTTTTGG TGTGGCCTGG AGTAGCTGCC CCAGAAGCTG AGGCTGGACC 300 AACCAGTAGG GGCCACACTC TGAAGAGCCT GGATGCTGTG CTCAAGAGTG GACTCTATCC 360 TGGTAGACAG AGGCCGCTCA GGGCTGGACT GATGTTGCCT TCCTTTCTGG AGCCAAGGCC 420 CAGACCAGGG TCTATCATCA GGTGTCTGTT GAATTAAATG CTAGGGCAGG TCTTGTGAGG 480 GCCACTGGTG GCCTGACCTA TGCTTTAGAA AACTTTCTGT GGCTGCTACA GAGGATTACG 540 CCTGTGGCAC ACCAGGGCAA GACTAGGGTG AGATAGTTTC CTAAAGGCAC AACATTTAAG 600 GAGGTACTCG CTCTCAGGGG CCAACCCTAT ACTTGGGTGA GTCTGACGGT GAGTAGCTCC 660 TTAAAGGTTT CACCCTAAGC ACCTGCCCTG CCTGCTTGCT CCACCCTATC TGGTCCCTTC 720 TGCACACTGG AGGCTGGGAG GTAGACTAGA GGCAGCTCAA GTGATCCAGG CATATTAGGG 780 CTGTGGCCAC AGGGGATAGA GATAGGCCTA GTTGAGAGCA GAATCAGATG ACAGGATTTG 840 CCAGGACATG AGACTGGCTG GAGCAGGACC CATCCCCCCT CCCTGGGTGC CCCATTCTGG 900 GAGAAGTGTA GGAGACCCCC CACTCTGCCT AGGAGTCTAT ATGTCCACAG CCAGGGCCAA 960 AACAAGATCT TAGGCCTTGG CTTCTGTCCT AGGTTATGAG TCTAGGGAAC CAAGGACACT 1020 AAGCTAAAGA GAGTAGGGCA GCAGGTGAAA AAGCCACAGG CTGCCCCAGG AAGGCCCAGG 1080 CCACTGGAGA CCACAGCTAG AACCTACAAC CATGTCCCGA GACTGCTCGG CCTTGCCCTT 1140 TGGATGCTTG GGCACAGCAG GAAGGAAGTG ATAAGGGTGC CTCCACTGCT GGATGGGGCG 1200 TGTCTGTCAG TCCATCTTCC CCCCGCTGTC TGCCCAGCAA GACCAGGGGC CACCCCCAGG 1260 TGCTCCCCAG GGGATTAGCA GCTTGGTTCC CCAGCCCACA CCCCTAGAAG CTCTGACCCT 1320 ATGGCAACAG CACCCCCTGC TGGCTAATAT GGAAAACCAA CCCCTTTCCC TCCTCTAGCA 1380 GGCGGAAGTT TAGGGGTCTT GGAGAAAGAG AAGGGTGCAG GCACAATGCT GCGGGAAAGG 1440 GTGGGGGCAG GAATTCAGGA TGGACTTTGG CTATGGCAGA TAAGCAGGTG CCACCTGGTA 1500 AACAGAGCAC CTATTTCCTG ATCAGTAGCC TTTGAACAGA TGCCAGAGAG GCCAGGACAC 1560
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