Tag | Content |
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EnhancerAtlas ID | HS098-17190 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr14:50436860-50438540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr14:50437171-50437191 | GCTGGGTGGTTGGTGTAGGG | - | 6.04 | RREB1 | MA0073.1 | chr14:50438381-50438401 | TGGTGGGGGTTGTGGTAGGG | - | 6.06 |
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| Number of super-enhancer constituents: 32 | 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 | chr14:50436994-50437488 | NHLF | 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 | GTTCCCTTGG ACTTACGTGT CTAACGAGGA AGAAAGGCTT CATTCTGGGA CCTTCAGGGT 60 AGCCTGGCTT GCACACTGGA TCTAGGTTCA CGGGTCATGA AAACTACAGT GGCTTTCTTC 120 CCTCCCAAGC CTCCAGCTAC TCCCAATCTG AGCAAATGGC CCCCAGATGG ATTCTATGTT 180 CTGAGTCCGT CCCCAGGACA GAGGGAGGTC CAGTTTGAGC TTTATTACAA ATCCTGTAGG 240 TCGGCTTTAG ATTATAGACA TGGCTTCCTC AGGCAAGGCT GCCCACTTGA GGGAAACAAT 300 TTTGTTGGCT GGCTGGGTGG TTGGTGTAGG GCTCACATTT GGGAGTTCAC TCCTTTCTCT 360 CCCTTTGTCT GAAACGATCA GCACCTTGTT GTGCCTGTTC ACTAGCAGTA CTCGGCACAC 420 AATCGTTTGT TGTGCTGACT CTCCAGTTGC TCGCAATGTG AGGTGGATTT GTTCTACTTC 480 TTCCTTGTGT ATTCTTGGTG AAGGCCGATA ATTTGCTACT TAGTTAACAG ACATGTTATA 540 GGGCTGGAGC CTGAGATAAG GTCAGGAGGA GAAACATCCC GCTTAGCTTG ACAAAGAGCT 600 TGGTTTAAGG CTGGAGAGCT GACTGTGCAA TTGTCTGAGC TGCTTTTCTT GGAAATGGCT 660 CTCTTGGCTG AGCTCCAGAA ATATAATCAA AAGTGGCCTG AAATCACAAG TTTTGCTGCT 720 TGCATTCTTA GTTTCACAAT TTAAGGATTT GGCTGGTGCC TGTCCTGAAA GTGTGGAATT 780 GTCTACTGTT TGCTACACAT GACGTTGAGT GAGTGTGTGT CTATGTGTGT ACACACACAT 840 GCATGTGCAG GACACAGGGA TTGTCTGCGT GGGCATGTTT TACAGTCCAG CTGTTTGTAC 900 CTTCAGGGAG GCAGTGATTA AAGAGCAGTG TATGGCAGGT TTTCTTTGAT TTCAAGAATC 960 ACATATTTGG TTTTGTAGTT AGTGTCTTTG GAGAAGAGTG ATGGAGACTC TTGCATAGAA 1020 GTGCAACTGA TTGCTTAGGT GCAGTGGTTT TGCCTTTCTT AAGAACTCCG CCTCAAAAAT 1080 ATGGAGATAA TTTACTTAGA AGAAGGCAAT GTGCCGCTTT TTGGAGAAGC AGGTGTACCT 1140 GACCTTGCCC TGGGGGAAGT GAAGACCTGA GTTTGAGGAA GTCAAGCTTG AGGCTGTCAG 1200 AAGCAGTTAT TTATATCTGA GTGATGTGTA TGAAAGCCAA AGCCTTTCAT TCCACCACCG 1260 TCACGGAACT AGTTTAGAGA AGAGGAAGGG CGTGCATTTT GCCTTGTTAA ATATCTACTG 1320 CACTAAGAAC TTCTGGTGTG GTTCAGATTT CTGGTAATCT GTACCCAGGC TCTATTGTCT 1380 AAAAAGGAGT GCTTAGACAC TCTTCTTTCA ACCTACTTTG TGGATAAAAC AGCTCACTTC 1440 CAGTTGATTG ATAGACTGTC AACTGATTGT TGCTTCCTTT CACCAGATGC CCCTCGTGTG 1500 GGCAGCCTCG TGTGTGTGTG GTGGTGGGGG TTGTGGTAGG GACCTTGCAA TATCTCTAAG 1560 CTCAAAATAA GGACATTGGA CTCTAAAAAC TACCAAAAAC CATACATCGG AAACTCTTGG 1620 GTTCATCATG ATAATAAATG AAGTCTCACA TAACTAGCTT TCATTTTTAT GCCTCTTGAG 1680
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