Tag | Content |
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EnhancerAtlas ID | HS093-09237 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr14:50437830-50438410 |
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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I049969 | chr14 | 50435787 | 50451256 |
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Enhancer Sequence | TTTTGTAGTT AGTGTCTTTG GAGAAGAGTG ATGGAGACTC TTGCATAGAA GTGCAACTGA 60 TTGCTTAGGT GCAGTGGTTT TGCCTTTCTT AAGAACTCCG CCTCAAAAAT ATGGAGATAA 120 TTTACTTAGA AGAAGGCAAT GTGCCGCTTT TTGGAGAAGC AGGTGTACCT GACCTTGCCC 180 TGGGGGAAGT GAAGACCTGA GTTTGAGGAA GTCAAGCTTG AGGCTGTCAG AAGCAGTTAT 240 TTATATCTGA GTGATGTGTA TGAAAGCCAA AGCCTTTCAT TCCACCACCG TCACGGAACT 300 AGTTTAGAGA AGAGGAAGGG CGTGCATTTT GCCTTGTTAA ATATCTACTG CACTAAGAAC 360 TTCTGGTGTG GTTCAGATTT CTGGTAATCT GTACCCAGGC TCTATTGTCT AAAAAGGAGT 420 GCTTAGACAC TCTTCTTTCA ACCTACTTTG TGGATAAAAC AGCTCACTTC CAGTTGATTG 480 ATAGACTGTC AACTGATTGT TGCTTCCTTT CACCAGATGC CCCTCGTGTG GGCAGCCTCG 540 TGTGTGTGTG GTGGTGGGGG TTGTGGTAGG GACCTTGCAA 580
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