Tag | Content |
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EnhancerAtlas ID | HS010-01420 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr14:50437050-50438370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr14:50437171-50437191 | GCTGGGTGGTTGGTGTAGGG | - | 6.04 |
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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 | chr14:50436994-50437488 | 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_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 | CCCCAGGACA GAGGGAGGTC CAGTTTGAGC TTTATTACAA ATCCTGTAGG TCGGCTTTAG 60 ATTATAGACA TGGCTTCCTC AGGCAAGGCT GCCCACTTGA GGGAAACAAT TTTGTTGGCT 120 GGCTGGGTGG TTGGTGTAGG GCTCACATTT GGGAGTTCAC TCCTTTCTCT CCCTTTGTCT 180 GAAACGATCA GCACCTTGTT GTGCCTGTTC ACTAGCAGTA CTCGGCACAC AATCGTTTGT 240 TGTGCTGACT CTCCAGTTGC TCGCAATGTG AGGTGGATTT GTTCTACTTC TTCCTTGTGT 300 ATTCTTGGTG AAGGCCGATA ATTTGCTACT TAGTTAACAG ACATGTTATA GGGCTGGAGC 360 CTGAGATAAG GTCAGGAGGA GAAACATCCC GCTTAGCTTG ACAAAGAGCT TGGTTTAAGG 420 CTGGAGAGCT GACTGTGCAA TTGTCTGAGC TGCTTTTCTT GGAAATGGCT CTCTTGGCTG 480 AGCTCCAGAA ATATAATCAA AAGTGGCCTG AAATCACAAG TTTTGCTGCT TGCATTCTTA 540 GTTTCACAAT TTAAGGATTT GGCTGGTGCC TGTCCTGAAA GTGTGGAATT GTCTACTGTT 600 TGCTACACAT GACGTTGAGT GAGTGTGTGT CTATGTGTGT ACACACACAT GCATGTGCAG 660 GACACAGGGA TTGTCTGCGT GGGCATGTTT TACAGTCCAG CTGTTTGTAC CTTCAGGGAG 720 GCAGTGATTA AAGAGCAGTG TATGGCAGGT TTTCTTTGAT TTCAAGAATC ACATATTTGG 780 TTTTGTAGTT AGTGTCTTTG GAGAAGAGTG ATGGAGACTC TTGCATAGAA GTGCAACTGA 840 TTGCTTAGGT GCAGTGGTTT TGCCTTTCTT AAGAACTCCG CCTCAAAAAT ATGGAGATAA 900 TTTACTTAGA AGAAGGCAAT GTGCCGCTTT TTGGAGAAGC AGGTGTACCT GACCTTGCCC 960 TGGGGGAAGT GAAGACCTGA GTTTGAGGAA GTCAAGCTTG AGGCTGTCAG AAGCAGTTAT 1020 TTATATCTGA GTGATGTGTA TGAAAGCCAA AGCCTTTCAT TCCACCACCG TCACGGAACT 1080 AGTTTAGAGA AGAGGAAGGG CGTGCATTTT GCCTTGTTAA ATATCTACTG CACTAAGAAC 1140 TTCTGGTGTG GTTCAGATTT CTGGTAATCT GTACCCAGGC TCTATTGTCT AAAAAGGAGT 1200 GCTTAGACAC TCTTCTTTCA ACCTACTTTG TGGATAAAAC AGCTCACTTC CAGTTGATTG 1260 ATAGACTGTC AACTGATTGT TGCTTCCTTT CACCAGATGC CCCTCGTGTG GGCAGCCTCG 1320
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