Tag | Content |
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EnhancerAtlas ID | HS052-00986 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:36834310-36836080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr1:36834767-36834778 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr1:36834768-36834778 | GGGGCGGGGC | - | 6.02 | MAFG | MA0659.1 | chr1:36835749-36835770 | GTTTTGCTTAGACAGCATTTG | - | 6.16 | MAFK | MA0496.2 | chr1:36835750-36835769 | TTTTGCTTAGACAGCATTT | - | 6.36 | MAFK | MA0496.2 | chr1:36835750-36835769 | TTTTGCTTAGACAGCATTT | + | 6.44 | SP1 | MA0079.4 | chr1:36834766-36834781 | GGGGGGCGGGGCCTC | - | 6.52 | SP3 | MA0746.2 | chr1:36834766-36834779 | GGGGGGCGGGGCC | - | 6.11 | SP4 | MA0685.1 | chr1:36834764-36834781 | TGGGGGGGCGGGGCCTC | - | 6.48 | ZNF740 | MA0753.2 | chr1:36834762-36834775 | GTTGGGGGGGCGG | - | 6.27 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00264 | chr1:36830417-36836190 | Adipose_Nuclei | SE_04744 | chr1:36834192-36835611 | Brain_Anterior_Caudate | SE_06364 | chr1:36834212-36836470 | Brain_Hippocampus_Middle | SE_08563 | chr1:36833979-36836143 | Brain_Inferior_Temporal_Lobe | SE_09252 | chr1:36830385-36842613 | CD14 | SE_11159 | chr1:36829411-36836756 | CD20 | SE_13460 | chr1:36834212-36834720 | CD34_Primary_RO01536 | SE_14627 | chr1:36834052-36836571 | CD4_Memory_Primary_7pool | SE_18215 | chr1:36830641-36835788 | CD4p_CD25-_CD45ROp_Memory | SE_18903 | chr1:36830547-36835076 | CD4p_CD25-_Il17-_PMAstim_Th | SE_24109 | chr1:36834425-36834766 | Colon_Crypt_2 | SE_26702 | chr1:36834464-36835879 | Esophagus | SE_28867 | chr1:36832956-36835062 | Fetal_Intestine_Large | SE_31812 | chr1:36835092-36835735 | Gastric | SE_34522 | chr1:36834836-36835921 | HCT-116 | SE_38175 | chr1:36833999-36834841 | HUVEC | SE_50223 | chr1:36834311-36836130 | Sigmoid_Colon | SE_52539 | chr1:36834367-36835842 | Small_Intestine | SE_55982 | chr1:36834818-36835897 | u87 | SE_60634 | chr1:36834487-36864245 | DHL6 | SE_62579 | chr1:36814176-36867515 | Tonsil | SE_65601 | chr1:36834744-36835707 | Pancreatic_islets | SE_67689 | chr1:36834818-36835897 | u87 | SE_69005 | chr1:36834440-36836184 | 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 |
GH01I036365 | chr1 | 36830737 | 36836194 |
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Enhancer Sequence | AAAGACATAC AACAAAGAAA TACAATGGGT GATCTGGGAG AAAAAAGGTA TAAAAGACAT 60 GATTGGACAA CTGGTAAAAT CTGAATATAG ACTGTTTATT AGATAATAGT ATTGTATCAG 120 TTAAATTTCC TGAACTTGCA AATTGCATTG TGGTTCTACA GGAGAATGCC CTTGTTCTTA 180 GGTGATACAT ACTCAAGTGT TTTGGGGTGA AGGGTCATGA AGTCTGTAAC TTACTCTCAG 240 GTCCCCCGAG GCAGAGGAGA AAATCCAGCC TGCTCGAATA GCTCCCAAGA CCTGATTCAC 300 AGGTTCAGAG GGACCTGTGG CTTGTGGGTA CACAGCCCAC AGTGGCAGAA CTTGCAGTCT 360 CATATATGTT GGGCAGAGCC AGCCTGGCAT GAACAGGAAT TCAGTCTTTT ATGGCCCCCT 420 CTCTTCAACA CTGTGCTATT ATCAAAGAAT TGGTTGGGGG GGCGGGGCCT CCATGCAATC 480 TCCAGGCCTG CCACCTGGTG GTGTCTTTCT GTAGTGCAGC TTCACAGGGT TTTTCTGCAC 540 CAGGTGCAGG ATGGTGGGGC CCTGCTCTCC TCAGGCTGAT CAGGAAGGAT GCACTCCATG 600 GGAAGAGCTC ACCTCAGCCA CCTGTGTAAG TGGGGCTGGG CAATCAGATC CCAGGAGGCT 660 GCCGTCTCTC TGCCTGCTGT GGAGGTCCTC CAAGGGCTCC ATGCTCTTCA GGAAGAACCC 720 CAATTCCTCA GTGAGCCTAA GCAGACCTAG AATACTTCTC CAGCCTCACT GCCTTTATAT 780 GCACCCTAAA TCCAGCCACA CCAAATGACA CAATCCCGAG TATGCCATGA ACACCCCTGC 840 CCCGCCCAAC TCTCCCTGGT TGGCACATCC TTCTCCCTTG GTCCTCACTG AAATGTCACC 900 TGCTGCAGAA AGTCTTCACA GAAGGCCTCC TGCCAAAGCT GGCTGCTCCT CCTCCAACCC 960 CCAGAGCACC TGAGTACACC TCCGTCCCCT CCCACTGTGC TGCAACCATT GGTTTATCTG 1020 TCTGACTCCC CCATCTCAGG CTGTGGGCTC CCTTGAGGGA GCAACTCCAA TCCACCGCTG 1080 CCTCCCTGCA CCCAGCCCAC TGCCTGGCGC AAAGCTGGAA GAGAACACAG TGTGGGGCTG 1140 TTTGCTGGGC ATCTATAAGG CACCATGGTC CCTGCTGGGG CAGGAGACAG AGGCAGTTGA 1200 ATAAAGAGGT ACAAGGTGTG ATTCACAGGA AAACTCTGTC CAAGGAGGGG CCAGTGGCTG 1260 GAGTGGGACC CTGAAGAAAG TACAGATGGT CAGACTAGCC AGTATCTGCC AAGTCATGGC 1320 TGGAGACAGG GTGCCACAGC TGTAGGTAAC TGGGGCTGCA CTGGATAGTC TGTCCAGGAA 1380 AAGTCCCATG TCAGAAATGC ATGAGGCAGA ATGGGGACTA GGCTGGCTGA TTACCGGGGG 1440 TTTTGCTTAG ACAGCATTTG CTGCTGGAGA GCAACCCCTA CTGAAGAATT AAAACTGTTC 1500 ATAACATGCC TGCAGCTGTG CAGAAGCCCT CACTGATGAA GGGATGGACC AGGCCCTGTG 1560 CGGGAGAATC CCCCAAATCC AGCCAAACGA TCTGCTTTCC TGCGGCAAGA TGTGGGGAGT 1620 GTGTGAGTGG CAGCCTGGCC TGTCCCTTCA CACTGGTGAC AGGTCCTCCA GGCCACTCCA 1680 GGTTTGTGGT GTGAAAGTCC TTCTGCTGGT CAGAAAAATT CCAACCACTT GCGCTTCTCT 1740 GAAAAGAGAA CTTCTGGCCT AACCATGCAT 1770
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