Tag | Content |
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EnhancerAtlas ID | HS105-77458 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:38237390-38238960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr8:38238445-38238463 | TCTCCCTGCCTCCCTTCC | - | 6.38 | FOXA1 | MA0148.4 | chr8:38237933-38237949 | CCTTGTTTACTTAAAG | - | 6.12 | ZNF263 | MA0528.1 | chr8:38238141-38238162 | GAAGGAAGAGGGTAAAGAGAG | + | 6.32 | ZNF263 | MA0528.1 | chr8:38238637-38238658 | TCCATCCCCTTCTCTTCCTCC | - | 6.51 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_07312 | chr8:38237134-38245250 | Brain_Hippocampus_Middle_150 | SE_10139 | chr8:38236601-38241638 | CD14 | SE_10271 | chr8:38237365-38244878 | CD19_Primary | SE_11060 | chr8:38236385-38245465 | CD20 | SE_11965 | chr8:38237226-38241340 | CD3 | SE_13576 | chr8:38236466-38245077 | CD34_Primary_RO01536 | SE_14339 | chr8:38237148-38241360 | CD34_Primary_RO01549 | SE_14429 | chr8:38236678-38245259 | CD4_Memory_Primary_7pool | SE_15452 | chr8:38237129-38241589 | CD4_Memory_Primary_8pool | SE_15986 | chr8:38237291-38241636 | CD4_Naive_Primary_7pool | SE_16361 | chr8:38237166-38245026 | CD4_Naive_Primary_8pool | SE_16907 | chr8:38237053-38245064 | CD4p_CD225int_CD127p_Tmem | SE_17412 | chr8:38236425-38245328 | CD4p_CD25-_CD45RAp_Naive | SE_17853 | chr8:38236359-38245393 | CD4p_CD25-_CD45ROp_Memory | SE_18625 | chr8:38236213-38245134 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19283 | chr8:38236898-38245091 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20206 | chr8:38237077-38244873 | CD56 | SE_20781 | chr8:38236763-38245292 | CD8_Memory_7pool | SE_21505 | chr8:38237501-38245182 | CD8_Naive_7pool | SE_22103 | chr8:38237424-38245100 | CD8_Naive_8pool | SE_22450 | chr8:38236752-38245023 | CD8_primiary | SE_28478 | chr8:38237194-38245208 | Fetal_Intestine | SE_30208 | chr8:38237060-38241321 | Fetal_Muscle | SE_32221 | chr8:38237417-38241186 | Gastric | SE_34843 | chr8:38237461-38241566 | HeLa | SE_38816 | chr8:38237425-38245014 | HUVEC | SE_45040 | chr8:38237738-38245112 | NHLF | SE_45781 | chr8:38236789-38245350 | Osteoblasts | SE_54044 | chr8:38237283-38241293 | Spleen | SE_60820 | chr8:38236786-38245125 | DHL6 | SE_62516 | chr8:38216009-38245243 | Tonsil | SE_63185 | chr8:38236165-38245411 | GLC16 |
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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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Enhancer Sequence | AAATAGGCTC TACTTAACAC CAATGTATGT TCTGTAAATT TGTCAGGATT TAAACCTTAG 60 AATAGTAATT ATTTCAAATT GTACAAGTAG TTACAGTTGA ATATATTAGT TACTGTAGTT 120 TCCTGAGAGT CAACTGAAGT TTCAATCAAA AAACGAACAA ACAAAACAAC AACAAAAAAA 180 CCCTGGCATC TCAATGAGAC TCTAAGAACT GCATGCCTAC TTCACAGATC ATTGCACTGT 240 GCTGAACTGG CATCTGGAGA TTGTATTGAG CCAGCTACAT GAAGGCAAAG AGAAGAGATG 300 GGGAAAAGAG AGTTTATTTA AAAAAGAAAA TACTATTCTT AACACACTCA TCACTTAACA 360 CGCTCATCAC CTATAAGCAA GAGCTATCAG AAATACTATT TAAAAATACA TACATTTCTA 420 ATTTTTCAAC ATTCAAAATA CAGCAAGCCG ATAATCTACC ACAAGCAGAG CTTCCTACCC 480 CTTTCACCCG GACACAGCGC TTTGCCAAGA GCACAGGCCC AAGTAAAATA ACCGATGCAA 540 TTTCCTTGTT TACTTAAAGA ATTGCAGAAA ACATGTTGAC TGCTTCTGAG GCTTCCGAAA 600 CAAACGAATT TTCAATACGT AAAAGACTTC ACGATCATGT TTGATATGTA AGCGTAGTAA 660 TGATTCCTTC AGCTAGTAAA AATCTAGTTT TAAATTGATT AAATGGGTTA AATTTACACT 720 GCAGCTCATT AGCATACCTT GTTTGCAACC AGAAGGAAGA GGGTAAAGAG AGGGAGAAAA 780 GCATCAAAAA GGTAGTGATG GAAAACATCA CTACCTCCTT TGGCGGTTAT GAATAATTTA 840 AAATGACCCA AGACGTAAGG GGAAAAGAGT TCATGAATAG AAAGAAAGGG GGCTAACAGT 900 CTGAATTGGC CCCTTCCAGA TTCATACTGA TGTCGGAGAG GAAAAGGAAT TTATTTACAC 960 TGCAGTGCCT TGGCAGCAAA CATGGCTGCC CCTGCCCCCT TTAAATCGAA ATAATCTTCA 1020 CTCCCTCCCC AAAACCATCA AATTATGGCC ATGTCTCTCC CTGCCTCCCT TCCATAACAC 1080 AAACACATCG CCTTCTCCCT CAAAACAGTA AAACCCACAC CTCCCCATTT CACAACAATC 1140 ACAATCCCAT AACCACCAGC TTCTCTATTC TCTAGCCTTG AAAGAAAGAC ACAGAATACA 1200 CACAAATACA GGAACAAAAG GCCTCCCTTC CTAACACTTT AACGACCTCC ATCCCCTTCT 1260 CTTCCTCCCA CTCTGACGCT AAGTCGATCG TTCTCATCCC TGTCATCATT CAGTTAATTT 1320 CCTTCCCTAG CCCAATCCTG TCTTCCAGTT TCCTGCGTCT ATTTCCCATT CTCCTATTGC 1380 AGCCTGCCTC ATCCCCTTTC CTAATCCACC TTTTCCTTCA CTTCCATTCC TCATTTCTCC 1440 CTTCATTCCC ATAAAATGCC CCATTTCTCC AGCAAATTTA TCCCCTTCTC CCAGACTCTT 1500 CTGGTTCCTA CACTCCATCC CCAAATCTCC CTATTTATCA GTCCACCCAG GTCTGTAATC 1560 TCCATGCAAC 1570
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