Tag | Content |
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EnhancerAtlas ID | HS092-18295 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr15:67376610-67379240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE40 | MA0464.2 | chr15:67379071-67379081 | GTCACGTGAT | - | 6.02 | NFAT5 | MA0606.1 | chr15:67379034-67379044 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr15:67379034-67379044 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr15:67379034-67379044 | AATGGAAAAT | - | 6.02 | TFEB | MA0692.1 | chr15:67379071-67379081 | GTCACGTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_09181 | chr15:67372130-67380269 | CD14 | SE_10181 | chr15:67376562-67379350 | CD19_Primary | SE_10875 | chr15:67354078-67404812 | CD20 | SE_11885 | chr15:67376608-67378831 | CD3 | SE_14469 | chr15:67372591-67378218 | CD4_Memory_Primary_7pool | SE_17822 | chr15:67372009-67379559 | CD4p_CD25-_CD45ROp_Memory | SE_18371 | chr15:67372540-67379321 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19163 | chr15:67376577-67379271 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20091 | chr15:67376576-67379361 | CD56 | SE_22489 | chr15:67377194-67379335 | CD8_primiary | SE_26536 | chr15:67378292-67379034 | Esophagus | SE_27694 | chr15:67378179-67381111 | Fetal_Intestine | SE_28551 | chr15:67377637-67381892 | Fetal_Intestine_Large | SE_31411 | chr15:67378417-67379301 | Gastric | SE_32497 | chr15:67372219-67380062 | GM12878 | SE_35858 | chr15:67377384-67379023 | HMEC | SE_37941 | chr15:67376611-67378556 | HUVEC | SE_42172 | chr15:67378222-67378979 | Lung | SE_44149 | chr15:67376922-67379302 | NHDF-Ad | SE_44749 | chr15:67376828-67379034 | NHLF | SE_45534 | chr15:67371483-67404480 | Osteoblasts | SE_47100 | chr15:67357928-67475420 | Panc1 | SE_47566 | chr15:67376879-67377148 | Pancreas | SE_50064 | chr15:67376548-67379341 | Sigmoid_Colon | SE_52344 | chr15:67377942-67379331 | Small_Intestine | SE_53518 | chr15:67376640-67379175 | Spleen | SE_58377 | chr15:67342858-67447290 | Ly1 | SE_59897 | chr15:67354926-67408793 | Ly4 | SE_60508 | chr15:67357006-67428179 | DHL6 | SE_61631 | chr15:67357404-67427415 | Toledo | SE_62286 | chr15:67356723-67443338 | 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 |
GH15I067079 | chr15 | 67371574 | 67387927 |
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Enhancer Sequence | GGGTTTCTTT GTGTTAGCCA GGATGGTCTC CATCTCCTGA CCTCGTGATC TGCCTGCCTC 60 GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCCACCGT GCCTGGCCAG TCTCAGATTT 120 TCATGATAGC CCTCTGAACT CTCCTTGGCT TCTTGCCTTT GGCTGTTTTC TCAATGCATA 180 TATTTTCCTG GGGGACAAAT CTAAGTTTTC ATCTGATGCT CTGCCTTCAG AGGGGAACCA 240 TTCCTTAATG ACCTATTTAA TTGTATTATC ATTGTTGTTT AATTCATCAC ATATTTACTG 300 AGCTTCTTTT GTTGGTGGTG GTGCCATCAG ACACAGTGGT CCAGGAGCTG CAATGCGTTG 360 CTGATGAGGA TGGTCACACA TAGCTCTGCC CTCATGGAGC GTCCCAGGGT GAAATGAGAC 420 CTCCCCTGAG AACCGACTCC CAGGGTAGGG GAAATCAGTC TGCAGGCAAA GAGGAATTCA 480 AATTTAGCCT GAAGCACAGG TTTTCTGTGC TTCTAGGCAC CGGCTGCATT CCAACCGTAG 540 TGCCATAAAA ATACAGGAAG GAAGGGAAAC GTGTTCACAG GTTGGTTAGA GATGTGGAAA 600 CCAACAATCA GCTCTCTCTT ATCCGTAAGA AACTAGAATC TACTGCTGGC TTCAGTCCCT 660 CAGACCTGCT GCTCAACAGA GTGCCCTTTC AAACCTGGGT TAGACTCTGT GCTAATGGCT 720 TTTTTCATGA ACCTCAGACA GCCGGAAAGT ATATTCTTTG AGGATTATGA TCGACTAGGA 780 TGCTCGGGAA TCTTTAAAGA GAAGCACTAT CTTGGCTATA TTTGCCCTCA GTTGTTTTAA 840 GGCCAGTGAG GAGACTGAGC ATTTCAGAGG TGAAGCATTT AGAGGATGGC CTCTGAAAGC 900 ATACGGCTCA GTAAACAACT GACCCATCCT TTGTCACCGT TTTTGTCCAG CGGCTGTCAC 960 CATAGGGGCT CCTCTGGTGT GGAGGAGAGA GAATTAGAGG CAGCAGGCCT GGGTTCTAGG 1020 TCTGCCTCAT TGTGAACCAG CTTCAGGACC TTGGGTGAGT CACTTTTCTG CCCTGGCCCC 1080 TGGCTTCCTC TTCTATAAAC TGAAGGTGTT GGCTTAGCAG GATTTTAAAG TTTCTTCCAC 1140 CTTAAAAACT CTGATTCCTG CACTTGCATT CAAAGAAATG ACTCTATTAC TCATTTGAAT 1200 AGTTTCAGAA TCACTGTATA GTCAACTCTG GACTAGAAAT GGGGGCCTGC AGTTGAGGAC 1260 AGGATGGAAA GAGGTTTGGG GTTCAGGGTG GGCTGTGAGG GCTAGGATTC TTGATTCCTC 1320 ATGATTTGCA ATTGGTTGTT GGTGTTACCA TGGAAGGTTC TCAACCATGG CTGCTTTTAA 1380 AAATTTTGAT GCTCAGACCA CCCCTGGAGA CCAGTGAATT TCAAATTTCT ACAGGCCGGC 1440 CTGGGGAAAT CCATGTTTTT TAACTTTCCT AGGTGATTCC GGTATGTGGC CGGGATTGAG 1500 AATCACAGCC ATAGATGCTT ATGTAAAGCT GTGTTCAGTG TTACAGGCAT CTGTTCTGGG 1560 TGGAAAGTGA TAGTGGTTGG TCAAAAAAAA AGCGTGCACA CACACACACA CACACACACA 1620 CACACACATA CACAGAGAAC AGCTCTAGGT TCTGGAAGTG TGTTGATTTG GTCACCACAA 1680 GTGCTGGTGG TGAGTAGTTG CCCTGAGGTT TGGAGTTCCA GTTCCCTCCT ATCTCTGGGT 1740 CAGTGGTTTC TCAACATCTT TGAAGTAGTG AAACCATCTG TAGTTGGTTA TTTCTGCTCA 1800 GAAACTCACA GTACAAAGTG GGGGGTGGTG CAGGGGGGTG GAGCTGGAAT GGATTAAACA 1860 GGCCCTTACA AATGCCCACA CTTTTTTCAT GAAACTAAGT TAGAGGCCTT AGCCAACTCC 1920 AGCATACCTT AGTGTCAGTT CTTTGGCATT GCCCCGGTGG ATTCTAGGGG CTGTGAAGGC 1980 TGTAGGGGTG TGTGTTACTC CCTGCTGCTT TGGTGAGAGA GTGTCCCTGT CTTTGGCTGA 2040 GAGCATCCTG TCCTGCCACT TCATCAGCAG TAGCATCTAA ACAGCCCTTG AAGGGAATCA 2100 GTATCTACAG CCTAAGAAAT CTGATGGGAC ACATCTCTCT GCATTAAAAT ATTAACAGAA 2160 AAGGTCAAAC TGGGAAGGGG CAGCTAAGTT GGAATATCTC ATTCAGGTAA AGGGATGGGC 2220 TTGTGGATCC TTAATTGGTG TGAAATGCGC CCTAGGAGGG GAGACTATAT CAGTGCTGAA 2280 AGCCCTTGAG GGCTTTCACA GATGAAGGGG GATGGTATGA GAAGCTTTAC AAATAACAAG 2340 GTTTGAGATG CAGTTGTAGA CACATGCCAG ATGTAGGTTG CTATTTTCTC AGCTCAATGA 2400 GGAATCTGTC AAGGCACTCT TAGAAATGGA AAATATAGTT CCTGCCCTCA GGAACTATAG 2460 TGTCACGTGA TAGCAGTGAA GACCTTCTAT GTCCTGGCCA CACAGTGAGG ATCAGAAGAC 2520 AGAGCATGGA GAGTGGAATG GGACACATGG ATCAAGGAAC GTGGACCTGA GCAAGCAAAA 2580 GCAAGTCACT CGGGTCCCAC TATCACATTG CATATCTTCT CCTTTTTTTT 2630
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