Tag | Content |
---|
EnhancerAtlas ID | HS176-39586 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr8:38237370-38238960 |
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 |
|
| 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATTTAATCCA ATATGAAATA AAATAGGCTC TACTTAACAC CAATGTATGT TCTGTAAATT 60 TGTCAGGATT TAAACCTTAG AATAGTAATT ATTTCAAATT GTACAAGTAG TTACAGTTGA 120 ATATATTAGT TACTGTAGTT TCCTGAGAGT CAACTGAAGT TTCAATCAAA AAACGAACAA 180 ACAAAACAAC AACAAAAAAA CCCTGGCATC TCAATGAGAC TCTAAGAACT GCATGCCTAC 240 TTCACAGATC ATTGCACTGT GCTGAACTGG CATCTGGAGA TTGTATTGAG CCAGCTACAT 300 GAAGGCAAAG AGAAGAGATG GGGAAAAGAG AGTTTATTTA AAAAAGAAAA TACTATTCTT 360 AACACACTCA TCACTTAACA CGCTCATCAC CTATAAGCAA GAGCTATCAG AAATACTATT 420 TAAAAATACA TACATTTCTA ATTTTTCAAC ATTCAAAATA CAGCAAGCCG ATAATCTACC 480 ACAAGCAGAG CTTCCTACCC CTTTCACCCG GACACAGCGC TTTGCCAAGA GCACAGGCCC 540 AAGTAAAATA ACCGATGCAA TTTCCTTGTT TACTTAAAGA ATTGCAGAAA ACATGTTGAC 600 TGCTTCTGAG GCTTCCGAAA CAAACGAATT TTCAATACGT AAAAGACTTC ACGATCATGT 660 TTGATATGTA AGCGTAGTAA TGATTCCTTC AGCTAGTAAA AATCTAGTTT TAAATTGATT 720 AAATGGGTTA AATTTACACT GCAGCTCATT AGCATACCTT GTTTGCAACC AGAAGGAAGA 780 GGGTAAAGAG AGGGAGAAAA GCATCAAAAA GGTAGTGATG GAAAACATCA CTACCTCCTT 840 TGGCGGTTAT GAATAATTTA AAATGACCCA AGACGTAAGG GGAAAAGAGT TCATGAATAG 900 AAAGAAAGGG GGCTAACAGT CTGAATTGGC CCCTTCCAGA TTCATACTGA TGTCGGAGAG 960 GAAAAGGAAT TTATTTACAC TGCAGTGCCT TGGCAGCAAA CATGGCTGCC CCTGCCCCCT 1020 TTAAATCGAA ATAATCTTCA CTCCCTCCCC AAAACCATCA AATTATGGCC ATGTCTCTCC 1080 CTGCCTCCCT TCCATAACAC AAACACATCG CCTTCTCCCT CAAAACAGTA AAACCCACAC 1140 CTCCCCATTT CACAACAATC ACAATCCCAT AACCACCAGC TTCTCTATTC TCTAGCCTTG 1200 AAAGAAAGAC ACAGAATACA CACAAATACA GGAACAAAAG GCCTCCCTTC CTAACACTTT 1260 AACGACCTCC ATCCCCTTCT CTTCCTCCCA CTCTGACGCT AAGTCGATCG TTCTCATCCC 1320 TGTCATCATT CAGTTAATTT CCTTCCCTAG CCCAATCCTG TCTTCCAGTT TCCTGCGTCT 1380 ATTTCCCATT CTCCTATTGC AGCCTGCCTC ATCCCCTTTC CTAATCCACC TTTTCCTTCA 1440 CTTCCATTCC TCATTTCTCC CTTCATTCCC ATAAAATGCC CCATTTCTCC AGCAAATTTA 1500 TCCCCTTCTC CCAGACTCTT CTGGTTCCTA CACTCCATCC CCAAATCTCC CTATTTATCA 1560 GTCCACCCAG GTCTGTAATC TCCATGCAAC 1590
|