Tag | Content |
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EnhancerAtlas ID | HS052-16818 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr17:73342800-73343970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr17:73343681-73343702 | TCTTCTCCACCCTCCTCACCC | - | 6.12 | ZNF263 | MA0528.1 | chr17:73343158-73343179 | ACTCCTCCCCCTTCCTTCTCC | - | 6.4 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_09177 | chr17:73334036-73349163 | CD14 | SE_10509 | chr17:73334088-73345751 | CD19_Primary | SE_11413 | chr17:73324621-73349939 | CD20 | SE_14041 | chr17:73342974-73344244 | CD34_Primary_RO01536 | SE_18858 | chr17:73341106-73345174 | CD4p_CD25-_Il17-_PMAstim_Th | SE_25706 | chr17:73334095-73345615 | DND41 | SE_54131 | chr17:73342676-73343992 | Spleen | SE_61022 | chr17:73284104-73345918 | HBL1 | SE_62513 | chr17:73287335-73369120 | Tonsil |
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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 |
GH17I075334 | chr17 | 73330718 | 73345080 |
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Enhancer Sequence | TTACCACACC TGGCTAATTT TTGTATTTTT TAGTAGAGAC GGGGTTTCAT CATGTTGGCC 60 AGGCTAGTCT CAAACTCCTA ACCTCAAGTC ACCTTGGCCT CTCAAAGTGC TGGGATTACA 120 GGCATGAGCC ACTGTGCCCA GCCTGCTCTG ACTTTTTGGC TCTGTAAGAA CCACATCAAC 180 AGGCTCCCTC ACTCTCTGGC TCCCAGTGCT ATTAATCAAT GGGGAGGCCT GCAGAAGGTC 240 AGACGAAGGG AGGGTCAGGT CAGGGCATTC ATTCTCCCAG CTCCCACCCT GAGAGTGTCT 300 GTGGACAGTC TTGGACTCTC AATTGAAAGT AAGTCCTTTC CTTCTCCAGG TTTGGGCAAC 360 TCCTCCCCCT TCCTTCTCCC TGTCGTAGGC CTCATGGTGG TAACCTGATT ACCAGCTGTG 420 GACACTGCAT TATCCCTGTG GTTTCTAGAG AAACTTCGCC CACACTGATA GCGGCAGGAG 480 GCAGACAAAT GCCTCACAGG GGCGGGTCTC CAGTGAAACC CCACCTCTAA GCCAAAGACA 540 ACTGAAAGCC TGAAAGCCAC ACTACAGGTC AAATCCATGG ACCGGACTGA GAACCCATCT 600 TCCCATTTGG TAGGCTTTCC TCTGATTGAT CCCCACTCTT CACCTATTTT ACATCTACCT 660 ACCCTTTCCG AATTGATTTT CTACACTGCC ATGCCCATCT TTGAGTGGTG CCTTTGCTTT 720 AGCCTTTCTT TGCATGCCCA CAAACCATTC AGCATGCATG CCCCTGTTCT GAGCCCATAA 780 AAGCCCCCAC CCAGCCACAC TGGGAGAGAA ACCACCAGAC TTCAGGGGTG GGGAACCACT 840 ACCTCCTCCG CTCCTGAAAG CTGTTCACCG CTCAATAAAA TTCTTCTCCA CCCTCCTCAC 900 CCTTAAATTG CCAGTGTAAC CTCATTCTTC TCAGACACAG GACAAGACCT TGGGAACTGC 960 TGAACCTGGG AACAAGCCAT AACACAGGTG AGCTGGGGCA TACCCAGCCC AGCCATGAGC 1020 TGAGCTGGTG CGCAACCAAG ACTTAGCCTG AGTGGGCTGA GTGTGGAGGT CCCCAGCTGG 1080 AGTCAACACC TTGCAAATAG TCTCATTATT AAAATCCTCT CAATTTAAGT GTGTCAGGTG 1140 TTCTCTACCA GGACTCAGAC TGAAATTAGC 1170
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