Tag | Content |
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EnhancerAtlas ID | HS051-00695 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr1:36834260-36835980 |
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 | GTCAGACAGT TAAAGAAAAG CTGAAGAATG ATTCTAGATT AAAGGAGACT AAAGACATAC 60 AACAAAGAAA TACAATGGGT GATCTGGGAG AAAAAAGGTA TAAAAGACAT GATTGGACAA 120 CTGGTAAAAT CTGAATATAG ACTGTTTATT AGATAATAGT ATTGTATCAG TTAAATTTCC 180 TGAACTTGCA AATTGCATTG TGGTTCTACA GGAGAATGCC CTTGTTCTTA GGTGATACAT 240 ACTCAAGTGT TTTGGGGTGA AGGGTCATGA AGTCTGTAAC TTACTCTCAG GTCCCCCGAG 300 GCAGAGGAGA AAATCCAGCC TGCTCGAATA GCTCCCAAGA CCTGATTCAC AGGTTCAGAG 360 GGACCTGTGG CTTGTGGGTA CACAGCCCAC AGTGGCAGAA CTTGCAGTCT CATATATGTT 420 GGGCAGAGCC AGCCTGGCAT GAACAGGAAT TCAGTCTTTT ATGGCCCCCT CTCTTCAACA 480 CTGTGCTATT ATCAAAGAAT TGGTTGGGGG GGCGGGGCCT CCATGCAATC TCCAGGCCTG 540 CCACCTGGTG GTGTCTTTCT GTAGTGCAGC TTCACAGGGT TTTTCTGCAC CAGGTGCAGG 600 ATGGTGGGGC CCTGCTCTCC TCAGGCTGAT CAGGAAGGAT GCACTCCATG GGAAGAGCTC 660 ACCTCAGCCA CCTGTGTAAG TGGGGCTGGG CAATCAGATC CCAGGAGGCT GCCGTCTCTC 720 TGCCTGCTGT GGAGGTCCTC CAAGGGCTCC ATGCTCTTCA GGAAGAACCC CAATTCCTCA 780 GTGAGCCTAA GCAGACCTAG AATACTTCTC CAGCCTCACT GCCTTTATAT GCACCCTAAA 840 TCCAGCCACA CCAAATGACA CAATCCCGAG TATGCCATGA ACACCCCTGC CCCGCCCAAC 900 TCTCCCTGGT TGGCACATCC TTCTCCCTTG GTCCTCACTG AAATGTCACC TGCTGCAGAA 960 AGTCTTCACA GAAGGCCTCC TGCCAAAGCT GGCTGCTCCT CCTCCAACCC CCAGAGCACC 1020 TGAGTACACC TCCGTCCCCT CCCACTGTGC TGCAACCATT GGTTTATCTG TCTGACTCCC 1080 CCATCTCAGG CTGTGGGCTC CCTTGAGGGA GCAACTCCAA TCCACCGCTG CCTCCCTGCA 1140 CCCAGCCCAC TGCCTGGCGC AAAGCTGGAA GAGAACACAG TGTGGGGCTG TTTGCTGGGC 1200 ATCTATAAGG CACCATGGTC CCTGCTGGGG CAGGAGACAG AGGCAGTTGA ATAAAGAGGT 1260 ACAAGGTGTG ATTCACAGGA AAACTCTGTC CAAGGAGGGG CCAGTGGCTG GAGTGGGACC 1320 CTGAAGAAAG TACAGATGGT CAGACTAGCC AGTATCTGCC AAGTCATGGC TGGAGACAGG 1380 GTGCCACAGC TGTAGGTAAC TGGGGCTGCA CTGGATAGTC TGTCCAGGAA AAGTCCCATG 1440 TCAGAAATGC ATGAGGCAGA ATGGGGACTA GGCTGGCTGA TTACCGGGGG TTTTGCTTAG 1500 ACAGCATTTG CTGCTGGAGA GCAACCCCTA CTGAAGAATT AAAACTGTTC ATAACATGCC 1560 TGCAGCTGTG CAGAAGCCCT CACTGATGAA GGGATGGACC AGGCCCTGTG CGGGAGAATC 1620 CCCCAAATCC AGCCAAACGA TCTGCTTTCC TGCGGCAAGA TGTGGGGAGT GTGTGAGTGG 1680 CAGCCTGGCC TGTCCCTTCA CACTGGTGAC AGGTCCTCCA 1720
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