Tag | Content |
---|
EnhancerAtlas ID | HS073-04654 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr15:67376600-67379220 |
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 |
|
| 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH15I067079 | chr15 | 67371574 | 67387927 |
|
Enhancer Sequence | AGTAGAGACG GGGTTTCTTT GTGTTAGCCA GGATGGTCTC CATCTCCTGA CCTCGTGATC 60 TGCCTGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCCACCGT GCCTGGCCAG 120 TCTCAGATTT TCATGATAGC CCTCTGAACT CTCCTTGGCT TCTTGCCTTT GGCTGTTTTC 180 TCAATGCATA TATTTTCCTG GGGGACAAAT CTAAGTTTTC ATCTGATGCT CTGCCTTCAG 240 AGGGGAACCA TTCCTTAATG ACCTATTTAA TTGTATTATC ATTGTTGTTT AATTCATCAC 300 ATATTTACTG AGCTTCTTTT GTTGGTGGTG GTGCCATCAG ACACAGTGGT CCAGGAGCTG 360 CAATGCGTTG CTGATGAGGA TGGTCACACA TAGCTCTGCC CTCATGGAGC GTCCCAGGGT 420 GAAATGAGAC CTCCCCTGAG AACCGACTCC CAGGGTAGGG GAAATCAGTC TGCAGGCAAA 480 GAGGAATTCA AATTTAGCCT GAAGCACAGG TTTTCTGTGC TTCTAGGCAC CGGCTGCATT 540 CCAACCGTAG TGCCATAAAA ATACAGGAAG GAAGGGAAAC GTGTTCACAG GTTGGTTAGA 600 GATGTGGAAA CCAACAATCA GCTCTCTCTT ATCCGTAAGA AACTAGAATC TACTGCTGGC 660 TTCAGTCCCT CAGACCTGCT GCTCAACAGA GTGCCCTTTC AAACCTGGGT TAGACTCTGT 720 GCTAATGGCT TTTTTCATGA ACCTCAGACA GCCGGAAAGT ATATTCTTTG AGGATTATGA 780 TCGACTAGGA TGCTCGGGAA TCTTTAAAGA GAAGCACTAT CTTGGCTATA TTTGCCCTCA 840 GTTGTTTTAA GGCCAGTGAG GAGACTGAGC ATTTCAGAGG TGAAGCATTT AGAGGATGGC 900 CTCTGAAAGC ATACGGCTCA GTAAACAACT GACCCATCCT TTGTCACCGT TTTTGTCCAG 960 CGGCTGTCAC CATAGGGGCT CCTCTGGTGT GGAGGAGAGA GAATTAGAGG CAGCAGGCCT 1020 GGGTTCTAGG TCTGCCTCAT TGTGAACCAG CTTCAGGACC TTGGGTGAGT CACTTTTCTG 1080 CCCTGGCCCC TGGCTTCCTC TTCTATAAAC TGAAGGTGTT GGCTTAGCAG GATTTTAAAG 1140 TTTCTTCCAC CTTAAAAACT CTGATTCCTG CACTTGCATT CAAAGAAATG ACTCTATTAC 1200 TCATTTGAAT AGTTTCAGAA TCACTGTATA GTCAACTCTG GACTAGAAAT GGGGGCCTGC 1260 AGTTGAGGAC AGGATGGAAA GAGGTTTGGG GTTCAGGGTG GGCTGTGAGG GCTAGGATTC 1320 TTGATTCCTC ATGATTTGCA ATTGGTTGTT GGTGTTACCA TGGAAGGTTC TCAACCATGG 1380 CTGCTTTTAA AAATTTTGAT GCTCAGACCA CCCCTGGAGA CCAGTGAATT TCAAATTTCT 1440 ACAGGCCGGC CTGGGGAAAT CCATGTTTTT TAACTTTCCT AGGTGATTCC GGTATGTGGC 1500 CGGGATTGAG AATCACAGCC ATAGATGCTT ATGTAAAGCT GTGTTCAGTG TTACAGGCAT 1560 CTGTTCTGGG TGGAAAGTGA TAGTGGTTGG TCAAAAAAAA AGCGTGCACA CACACACACA 1620 CACACACACA CACACACATA CACAGAGAAC AGCTCTAGGT TCTGGAAGTG TGTTGATTTG 1680 GTCACCACAA GTGCTGGTGG TGAGTAGTTG CCCTGAGGTT TGGAGTTCCA GTTCCCTCCT 1740 ATCTCTGGGT CAGTGGTTTC TCAACATCTT TGAAGTAGTG AAACCATCTG TAGTTGGTTA 1800 TTTCTGCTCA GAAACTCACA GTACAAAGTG GGGGGTGGTG CAGGGGGGTG GAGCTGGAAT 1860 GGATTAAACA GGCCCTTACA AATGCCCACA CTTTTTTCAT GAAACTAAGT TAGAGGCCTT 1920 AGCCAACTCC AGCATACCTT AGTGTCAGTT CTTTGGCATT GCCCCGGTGG ATTCTAGGGG 1980 CTGTGAAGGC TGTAGGGGTG TGTGTTACTC CCTGCTGCTT TGGTGAGAGA GTGTCCCTGT 2040 CTTTGGCTGA GAGCATCCTG TCCTGCCACT TCATCAGCAG TAGCATCTAA ACAGCCCTTG 2100 AAGGGAATCA GTATCTACAG CCTAAGAAAT CTGATGGGAC ACATCTCTCT GCATTAAAAT 2160 ATTAACAGAA AAGGTCAAAC TGGGAAGGGG CAGCTAAGTT GGAATATCTC ATTCAGGTAA 2220 AGGGATGGGC TTGTGGATCC TTAATTGGTG TGAAATGCGC CCTAGGAGGG GAGACTATAT 2280 CAGTGCTGAA AGCCCTTGAG GGCTTTCACA GATGAAGGGG GATGGTATGA GAAGCTTTAC 2340 AAATAACAAG GTTTGAGATG CAGTTGTAGA CACATGCCAG ATGTAGGTTG CTATTTTCTC 2400 AGCTCAATGA GGAATCTGTC AAGGCACTCT TAGAAATGGA AAATATAGTT CCTGCCCTCA 2460 GGAACTATAG TGTCACGTGA TAGCAGTGAA GACCTTCTAT GTCCTGGCCA CACAGTGAGG 2520 ATCAGAAGAC AGAGCATGGA GAGTGGAATG GGACACATGG ATCAAGGAAC GTGGACCTGA 2580 GCAAGCAAAA GCAAGTCACT CGGGTCCCAC TATCACATTG 2620
|