Tag | Content |
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EnhancerAtlas ID | HS141-00312 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:26613420-26614720 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr1:26614546-26614557 | CCACACCCTGC | + | 6.62 | Myod1 | MA0499.1 | chr1:26613689-26613702 | AGGGACAGCTGCT | - | 7.52 | Myog | MA0500.1 | chr1:26613692-26613703 | GACAGCTGCTG | + | 6.14 | Tcf12 | MA0521.1 | chr1:26613692-26613703 | GACAGCTGCTG | + | 6.02 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_09234 | chr1:26600437-26620418 | CD14 | SE_10276 | chr1:26609716-26620076 | CD19_Primary | SE_11598 | chr1:26601677-26620618 | CD20 | SE_12127 | chr1:26609517-26619068 | CD3 | SE_13098 | chr1:26613251-26615233 | CD34_Primary_RO01480 | SE_14176 | chr1:26610126-26617625 | CD34_Primary_RO01549 | SE_15660 | chr1:26609807-26618647 | CD4_Memory_Primary_8pool | SE_16821 | chr1:26610331-26617967 | CD4_Naive_Primary_8pool | SE_17222 | chr1:26613332-26618016 | CD4p_CD225int_CD127p_Tmem | SE_17706 | chr1:26601754-26619073 | CD4p_CD25-_CD45RAp_Naive | SE_18032 | chr1:26601635-26619607 | CD4p_CD25-_CD45ROp_Memory | SE_18600 | chr1:26600628-26620343 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19301 | chr1:26601729-26619077 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20500 | chr1:26609324-26619072 | CD56 | SE_21239 | chr1:26609862-26619058 | CD8_Memory_7pool | SE_22719 | chr1:26601924-26619047 | CD8_primiary | SE_24040 | chr1:26613586-26613984 | Colon_Crypt_2 | SE_26906 | chr1:26613419-26617713 | Esophagus | SE_31060 | chr1:26610152-26618849 | Fetal_Thymus | SE_31862 | chr1:26613453-26614342 | Gastric | SE_31862 | chr1:26614480-26617883 | Gastric | SE_40404 | chr1:26609226-26616392 | K562 | SE_41449 | chr1:26613365-26617866 | Left_Ventricle | SE_42616 | chr1:26613355-26618804 | Lung | SE_50183 | chr1:26601943-26618863 | Sigmoid_Colon | SE_52659 | chr1:26613372-26618804 | Small_Intestine | SE_53610 | chr1:26609706-26619005 | Spleen | SE_55161 | chr1:26613407-26618780 | Thymus | SE_62762 | chr1:26609498-26620090 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 26613887 | 26614371 | chr1 | 26613470 | 26614562 |
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Enhancer Sequence | CTCAGGTGAT CCGCCCGCCT TGGCATCCCA AAGTGCTGGG ATTACAGGTG TGAGCCACCA 60 CGCCAGGCTG AGGCAGGGGT TATTTAGTTC CATTTTACAC ATGAGGAAAC AGGCCCACAG 120 AGATGAAAAA TGACTCGTCC CAAGCCACTT GGTGAGAGGA GGAACTGGGA AGGGAGCCGG 180 GGCTGACTCT CAAGTCTGTT TCCCCCACCC ATCTGCACCA TCAGGAGAGG GAGGTCAGAA 240 GAGGGACAGA TGGCTCTCAG GGAGGATGTA GGGACAGCTG CTGGCCAGAA CAGATATGGG 300 ACAGACCTTA GGTTGTGCAA CTATTTCTGG GTCACAGACC CCTTTGAGAA GCTGACAAAG 360 CTCTGGCCTC CTCTTCTGAA ACACGTGTGG CGCATACAGC TGTGTTCTGG CTTCAGGGGA 420 GAATACGGAG CGGTGGGGAC AGCCGTGACA GACAACAGAG CAGAAAGGTG GAGGGCAGGT 480 AGATGCTGGC TGGGTACAGA CCAGGGGCCT GTTCTGTCAT CTTTGATGGG ACCTGGCCCC 540 CAAGTAAGTC ATCTGTTTGG GTGTGCCCTA CAACACACCA ATAACTTTTG GGGCCTCAGA 600 GAGGCTGTTT TTCAACAGGA CAAGCAGGCT GCGGCAGGAT GTGGGTCAGG GCTCTGGGGA 660 CCTAATTCCT TTCCTCTCAG TGGTGCAGTG GCTGTACCAG GGAGGTGCAG ATGTGTTTCC 720 TGTTGCTTTT GCAGCAGGTG AAATGGTAGG CCCCAGCTGG CCTTCTCCTC TCCCCTATAT 780 TTCCTACCAT TGAAGGGGCT ATACCTGCCC CCAGCCCCTC CGGGGGCTCC CCACATAGTC 840 CCTGAGATTC CCAGGAAAAA CTCGCCTAAC AGAATGATAC CAAGACACTT TTCTTTTAAC 900 AACTACCTTA AGGACAAATA GGCAAACCTA AAAACAATAG CAGAATAGAT CATCTCATAC 960 AATGCCTGCC TCAACCCTTT TTTTTTTTTT TCCGAGAAAG GGTCTCCCTC TGTCACCCAA 1020 GCTGGAGTAT AGCGGCACAG TCATGATACT GCAACCGTGA CCTCCCGGGT TCAACTTATC 1080 CTCCCACCTC AGCCTCCCAA GTAGCTTGGA CCACAGGCAG GCATCACCAC ACCCTGCTAA 1140 TTAATTTAAA AAAAAATTGT AGAGATGGGG TCTCGCTGTG TTACCAGGGC TCTGTCTTCT 1200 TTATAGATGG GGAAAGTGAG GCCCAGAAAG GTCAGATGAC ATGGCCTGAT CAGACCAGAC 1260 AGAGCCAGGA AGAGCACCAA ATACACCAAC TCCTAATTCA 1300
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