Tag | Content |
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EnhancerAtlas ID | HS109-06901 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr14:50437550-50438430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr14:50438381-50438401 | TGGTGGGGGTTGTGGTAGGG | - | 6.06 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_10422 | chr14:50436293-50440675 | CD19_Primary | SE_11322 | chr14:50434928-50450149 | CD20 | SE_12397 | chr14:50436611-50440674 | CD3 | SE_14517 | chr14:50436253-50440629 | CD4_Memory_Primary_7pool | SE_18008 | chr14:50436287-50441310 | CD4p_CD25-_CD45ROp_Memory | SE_18398 | chr14:50435547-50450215 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19249 | chr14:50436647-50441600 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23843 | chr14:50436755-50438200 | Colon_Crypt_2 | SE_23843 | chr14:50438225-50438549 | Colon_Crypt_2 | SE_26110 | chr14:50436618-50440695 | Duodenum_Smooth_Muscle | SE_26864 | chr14:50435814-50440863 | Esophagus | SE_27688 | chr14:50435832-50440503 | Fetal_Intestine | SE_28581 | chr14:50435682-50440551 | Fetal_Intestine_Large | SE_31801 | chr14:50436632-50440413 | Gastric | SE_33888 | chr14:50436450-50440724 | HCC1954 | SE_34928 | chr14:50437713-50440512 | HeLa | SE_37039 | chr14:50436659-50444504 | HSMMtube | SE_39133 | chr14:50436864-50440961 | IMR90 | SE_43300 | chr14:50436836-50440506 | Lung | SE_44190 | chr14:50436790-50440625 | NHDF-Ad | SE_44956 | chr14:50437912-50440562 | NHLF | SE_47176 | chr14:50432303-50449980 | Panc1 | SE_50518 | chr14:50436606-50441475 | Sigmoid_Colon | SE_52447 | chr14:50436726-50440446 | Small_Intestine | SE_55597 | chr14:50436738-50439895 | Thymus | SE_56500 | chr14:50438313-50439782 | u87 | SE_58661 | chr14:50425951-50447448 | Ly1 | SE_60380 | chr14:50426505-50445615 | Ly4 | SE_60743 | chr14:50425923-50445269 | DHL6 | SE_61099 | chr14:50426023-50471480 | HBL1 | SE_62298 | chr14:50396222-50471436 | Tonsil |
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| 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 |
GH14I049969 | chr14 | 50435787 | 50451256 |
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Enhancer Sequence | AAGTGGCCTG AAATCACAAG TTTTGCTGCT TGCATTCTTA GTTTCACAAT TTAAGGATTT 60 GGCTGGTGCC TGTCCTGAAA GTGTGGAATT GTCTACTGTT TGCTACACAT GACGTTGAGT 120 GAGTGTGTGT CTATGTGTGT ACACACACAT GCATGTGCAG GACACAGGGA TTGTCTGCGT 180 GGGCATGTTT TACAGTCCAG CTGTTTGTAC CTTCAGGGAG GCAGTGATTA AAGAGCAGTG 240 TATGGCAGGT TTTCTTTGAT TTCAAGAATC ACATATTTGG TTTTGTAGTT AGTGTCTTTG 300 GAGAAGAGTG ATGGAGACTC TTGCATAGAA GTGCAACTGA TTGCTTAGGT GCAGTGGTTT 360 TGCCTTTCTT AAGAACTCCG CCTCAAAAAT ATGGAGATAA TTTACTTAGA AGAAGGCAAT 420 GTGCCGCTTT TTGGAGAAGC AGGTGTACCT GACCTTGCCC TGGGGGAAGT GAAGACCTGA 480 GTTTGAGGAA GTCAAGCTTG AGGCTGTCAG AAGCAGTTAT TTATATCTGA GTGATGTGTA 540 TGAAAGCCAA AGCCTTTCAT TCCACCACCG TCACGGAACT AGTTTAGAGA AGAGGAAGGG 600 CGTGCATTTT GCCTTGTTAA ATATCTACTG CACTAAGAAC TTCTGGTGTG GTTCAGATTT 660 CTGGTAATCT GTACCCAGGC TCTATTGTCT AAAAAGGAGT GCTTAGACAC TCTTCTTTCA 720 ACCTACTTTG TGGATAAAAC AGCTCACTTC CAGTTGATTG ATAGACTGTC AACTGATTGT 780 TGCTTCCTTT CACCAGATGC CCCTCGTGTG GGCAGCCTCG TGTGTGTGTG GTGGTGGGGG 840 TTGTGGTAGG GACCTTGCAA TATCTCTAAG CTCAAAATAA 880
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