Tag | Content |
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EnhancerAtlas ID | HS044-12684 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr8:38237180-38238960 |
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 | AAGCTTCTGT ATAACAACTG AGAGGATGTT GCCATTTAGG TAGGTTAAAT GTAGTTCAAC 60 TGGTTTGAGT CCACCATATT ACAATGTTAA CAGGCCTTCT TGGTATTAGA GAACAGTTTC 120 AATATCAATG TGATAGGTTA AAGTTTGGAT TACTCCAACT GCTATAATAA AAACAAAAGG 180 TCACACACAC ATTTAATCCA ATATGAAATA AAATAGGCTC TACTTAACAC CAATGTATGT 240 TCTGTAAATT TGTCAGGATT TAAACCTTAG AATAGTAATT ATTTCAAATT GTACAAGTAG 300 TTACAGTTGA ATATATTAGT TACTGTAGTT TCCTGAGAGT CAACTGAAGT TTCAATCAAA 360 AAACGAACAA ACAAAACAAC AACAAAAAAA CCCTGGCATC TCAATGAGAC TCTAAGAACT 420 GCATGCCTAC TTCACAGATC ATTGCACTGT GCTGAACTGG CATCTGGAGA TTGTATTGAG 480 CCAGCTACAT GAAGGCAAAG AGAAGAGATG GGGAAAAGAG AGTTTATTTA AAAAAGAAAA 540 TACTATTCTT AACACACTCA TCACTTAACA CGCTCATCAC CTATAAGCAA GAGCTATCAG 600 AAATACTATT TAAAAATACA TACATTTCTA ATTTTTCAAC ATTCAAAATA CAGCAAGCCG 660 ATAATCTACC ACAAGCAGAG CTTCCTACCC CTTTCACCCG GACACAGCGC TTTGCCAAGA 720 GCACAGGCCC AAGTAAAATA ACCGATGCAA TTTCCTTGTT TACTTAAAGA ATTGCAGAAA 780 ACATGTTGAC TGCTTCTGAG GCTTCCGAAA CAAACGAATT TTCAATACGT AAAAGACTTC 840 ACGATCATGT TTGATATGTA AGCGTAGTAA TGATTCCTTC AGCTAGTAAA AATCTAGTTT 900 TAAATTGATT AAATGGGTTA AATTTACACT GCAGCTCATT AGCATACCTT GTTTGCAACC 960 AGAAGGAAGA GGGTAAAGAG AGGGAGAAAA GCATCAAAAA GGTAGTGATG GAAAACATCA 1020 CTACCTCCTT TGGCGGTTAT GAATAATTTA AAATGACCCA AGACGTAAGG GGAAAAGAGT 1080 TCATGAATAG AAAGAAAGGG GGCTAACAGT CTGAATTGGC CCCTTCCAGA TTCATACTGA 1140 TGTCGGAGAG GAAAAGGAAT TTATTTACAC TGCAGTGCCT TGGCAGCAAA CATGGCTGCC 1200 CCTGCCCCCT TTAAATCGAA ATAATCTTCA CTCCCTCCCC AAAACCATCA AATTATGGCC 1260 ATGTCTCTCC CTGCCTCCCT TCCATAACAC AAACACATCG CCTTCTCCCT CAAAACAGTA 1320 AAACCCACAC CTCCCCATTT CACAACAATC ACAATCCCAT AACCACCAGC TTCTCTATTC 1380 TCTAGCCTTG AAAGAAAGAC ACAGAATACA CACAAATACA GGAACAAAAG GCCTCCCTTC 1440 CTAACACTTT AACGACCTCC ATCCCCTTCT CTTCCTCCCA CTCTGACGCT AAGTCGATCG 1500 TTCTCATCCC TGTCATCATT CAGTTAATTT CCTTCCCTAG CCCAATCCTG TCTTCCAGTT 1560 TCCTGCGTCT ATTTCCCATT CTCCTATTGC AGCCTGCCTC ATCCCCTTTC CTAATCCACC 1620 TTTTCCTTCA CTTCCATTCC TCATTTCTCC CTTCATTCCC ATAAAATGCC CCATTTCTCC 1680 AGCAAATTTA TCCCCTTCTC CCAGACTCTT CTGGTTCCTA CACTCCATCC CCAAATCTCC 1740 CTATTTATCA GTCCACCCAG GTCTGTAATC TCCATGCAAC 1780
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