| Tag | Content |
|---|
EnhancerAtlas ID | HS182-00355 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:19798410-19799200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:19799047-19799068 | AGAAGAGGAGGAGAAAGGGAA | + | 6.06 | | ZNF263 | MA0528.1 | chr1:19799053-19799074 | GGAGGAGAAAGGGAAGTGAGG | + | 6.5 | | ZNF263 | MA0528.1 | chr1:19799050-19799071 | AGAGGAGGAGAAAGGGAAGTG | + | 6 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_09593 | chr1:19798183-19799387 | CD14 | | SE_12250 | chr1:19798539-19799214 | CD3 | | SE_17553 | chr1:19780030-19800464 | CD4p_CD25-_CD45RAp_Naive | | SE_18410 | chr1:19788739-19800215 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_22607 | chr1:19798397-19799299 | CD8_primiary | | SE_23237 | chr1:19798668-19799216 | Colon_Crypt_1 | | SE_26537 | chr1:19798669-19799295 | Esophagus | | SE_31447 | chr1:19798627-19799207 | Gastric | | SE_47234 | chr1:19798254-19799184 | Panc1 | | SE_52345 | chr1:19798394-19799308 | Small_Intestine | | SE_62519 | chr1:19761354-19815005 | Tonsil |
|
| | 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 |
| GH01I019471 | chr1 | 19798184 | 19799387 |
|
Enhancer Sequence | TCCTCAACAA CCAATATGCA TCTCACAGAT AGTATGTAAC CAAGATAAAA GTAGGATCCT 60
TGAGGATATT CCCAGGATTC TCCTACGTGC TCTCCATCTG GAATACAGAA AGCTCAGAAA 120
CCATGGGCCA TCAGCACACA GGGAAAACCA GTTCTGTGGC AGGCAAAAGG ACAAGGGTAT 180
TCTAGTTAGA AGGTTGATAA ACGCCTCCAG ATAAAGTTAT TAGAGGAAGG ACAGATGAAA 240
TCAGTGTTTA AGAAAATGCG AGGCCTGTTT CCCAGGAATA TTACCTAGTG CAAAGTAGGA 300
TGAAAAAGTA AGAGAGGTTG TCATGAACTG AGGACATGGA GACCCTACTC ATCTCGAAGG 360
CAGATGTTGC CATCTACAGC CTAGAGCTCT AAACCCTCTG AGGTTAGGGA TCTCTTTCAA 420
CATCTCTGGG TGGCTCAAAC CCTTGGGGCA TGAACTAATA ACCTGTCGGT TATGTAGGCA 480
GGCAGCAGAC TGTGGCCTCT GCTCGTCCCT GGCCGCAGGT GTAACACAGC CAGGGCAAGG 540
AACCAGCTGG TCCTGAGTGT GAACACCAGC TTAGCCAATG ACAGCTTTAT CCTCATACTA 600
TGCTCTATTA TTCCAGAGTC TGCCTGGATG TGTGCAGAGA AGAGGAGGAG AAAGGGAAGT 660
GAGGGGCAGG ACTATGCAGT ACCCAAGGAC TCAAAGGTGA TTCCAGACCC TGACTACCGA 720
TTAGTAGTTA CTATGTAGAG AATGAGGTTC CATTTTAGAT GAAGAGCTGC AACTACTGCG 780
CTTTCATTCT 790
|
