Tag | Content |
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EnhancerAtlas ID | HS170-01336 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr15:67376760-67379410 |
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 | TCTTGCCTTT GGCTGTTTTC TCAATGCATA TATTTTCCTG GGGGACAAAT CTAAGTTTTC 60 ATCTGATGCT CTGCCTTCAG AGGGGAACCA TTCCTTAATG ACCTATTTAA TTGTATTATC 120 ATTGTTGTTT AATTCATCAC ATATTTACTG AGCTTCTTTT GTTGGTGGTG GTGCCATCAG 180 ACACAGTGGT CCAGGAGCTG CAATGCGTTG CTGATGAGGA TGGTCACACA TAGCTCTGCC 240 CTCATGGAGC GTCCCAGGGT GAAATGAGAC CTCCCCTGAG AACCGACTCC CAGGGTAGGG 300 GAAATCAGTC TGCAGGCAAA GAGGAATTCA AATTTAGCCT GAAGCACAGG TTTTCTGTGC 360 TTCTAGGCAC CGGCTGCATT CCAACCGTAG TGCCATAAAA ATACAGGAAG GAAGGGAAAC 420 GTGTTCACAG GTTGGTTAGA GATGTGGAAA CCAACAATCA GCTCTCTCTT ATCCGTAAGA 480 AACTAGAATC TACTGCTGGC TTCAGTCCCT CAGACCTGCT GCTCAACAGA GTGCCCTTTC 540 AAACCTGGGT TAGACTCTGT GCTAATGGCT TTTTTCATGA ACCTCAGACA GCCGGAAAGT 600 ATATTCTTTG AGGATTATGA TCGACTAGGA TGCTCGGGAA TCTTTAAAGA GAAGCACTAT 660 CTTGGCTATA TTTGCCCTCA GTTGTTTTAA GGCCAGTGAG GAGACTGAGC ATTTCAGAGG 720 TGAAGCATTT AGAGGATGGC CTCTGAAAGC ATACGGCTCA GTAAACAACT GACCCATCCT 780 TTGTCACCGT TTTTGTCCAG CGGCTGTCAC CATAGGGGCT CCTCTGGTGT GGAGGAGAGA 840 GAATTAGAGG CAGCAGGCCT GGGTTCTAGG TCTGCCTCAT TGTGAACCAG CTTCAGGACC 900 TTGGGTGAGT CACTTTTCTG CCCTGGCCCC TGGCTTCCTC TTCTATAAAC TGAAGGTGTT 960 GGCTTAGCAG GATTTTAAAG TTTCTTCCAC CTTAAAAACT CTGATTCCTG CACTTGCATT 1020 CAAAGAAATG ACTCTATTAC TCATTTGAAT AGTTTCAGAA TCACTGTATA GTCAACTCTG 1080 GACTAGAAAT GGGGGCCTGC AGTTGAGGAC AGGATGGAAA GAGGTTTGGG GTTCAGGGTG 1140 GGCTGTGAGG GCTAGGATTC TTGATTCCTC ATGATTTGCA ATTGGTTGTT GGTGTTACCA 1200 TGGAAGGTTC TCAACCATGG CTGCTTTTAA AAATTTTGAT GCTCAGACCA CCCCTGGAGA 1260 CCAGTGAATT TCAAATTTCT ACAGGCCGGC CTGGGGAAAT CCATGTTTTT TAACTTTCCT 1320 AGGTGATTCC GGTATGTGGC CGGGATTGAG AATCACAGCC ATAGATGCTT ATGTAAAGCT 1380 GTGTTCAGTG TTACAGGCAT CTGTTCTGGG TGGAAAGTGA TAGTGGTTGG TCAAAAAAAA 1440 AGCGTGCACA CACACACACA CACACACACA CACACACATA CACAGAGAAC AGCTCTAGGT 1500 TCTGGAAGTG TGTTGATTTG GTCACCACAA GTGCTGGTGG TGAGTAGTTG CCCTGAGGTT 1560 TGGAGTTCCA GTTCCCTCCT ATCTCTGGGT CAGTGGTTTC TCAACATCTT TGAAGTAGTG 1620 AAACCATCTG TAGTTGGTTA TTTCTGCTCA GAAACTCACA GTACAAAGTG GGGGGTGGTG 1680 CAGGGGGGTG GAGCTGGAAT GGATTAAACA GGCCCTTACA AATGCCCACA CTTTTTTCAT 1740 GAAACTAAGT TAGAGGCCTT AGCCAACTCC AGCATACCTT AGTGTCAGTT CTTTGGCATT 1800 GCCCCGGTGG ATTCTAGGGG CTGTGAAGGC TGTAGGGGTG TGTGTTACTC CCTGCTGCTT 1860 TGGTGAGAGA GTGTCCCTGT CTTTGGCTGA GAGCATCCTG TCCTGCCACT TCATCAGCAG 1920 TAGCATCTAA ACAGCCCTTG AAGGGAATCA GTATCTACAG CCTAAGAAAT CTGATGGGAC 1980 ACATCTCTCT GCATTAAAAT ATTAACAGAA AAGGTCAAAC TGGGAAGGGG CAGCTAAGTT 2040 GGAATATCTC ATTCAGGTAA AGGGATGGGC TTGTGGATCC TTAATTGGTG TGAAATGCGC 2100 CCTAGGAGGG GAGACTATAT CAGTGCTGAA AGCCCTTGAG GGCTTTCACA GATGAAGGGG 2160 GATGGTATGA GAAGCTTTAC AAATAACAAG GTTTGAGATG CAGTTGTAGA CACATGCCAG 2220 ATGTAGGTTG CTATTTTCTC AGCTCAATGA GGAATCTGTC AAGGCACTCT TAGAAATGGA 2280 AAATATAGTT CCTGCCCTCA GGAACTATAG TGTCACGTGA TAGCAGTGAA GACCTTCTAT 2340 GTCCTGGCCA CACAGTGAGG ATCAGAAGAC AGAGCATGGA GAGTGGAATG GGACACATGG 2400 ATCAAGGAAC GTGGACCTGA GCAAGCAAAA GCAAGTCACT CGGGTCCCAC TATCACATTG 2460 CATATCTTCT CCTTTTTTTT TTTTTTTTCT GAGACGGAGT TTCGCTCTTG TTGCCCAGGC 2520 TGGAGTGCAG TGGTGCGATC TCAGCTCACT ACAACCTCCA CCTCCCAGGT TCAAGCGATT 2580 CTCGTGCCTC AGACTCCCAA GTAGCTGGTA TTACAGGCGC CTGCCACCAC ACCTGGCTAA 2640 TTTTTAGTAG 2650
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