| Tag | Content |
|---|
EnhancerAtlas ID | HS141-18395 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr9:296830-298070 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr9:297687-297701 | ATGAGTCATCTTTA | - | 6.28 | | SPI1 | MA0080.4 | chr9:297785-297799 | TAAATGGGGAAGTA | + | 6.03 | | SPI1 | MA0080.4 | chr9:297514-297528 | TACTTCCCCATTTT | - | 6.72 | | SPIC | MA0687.1 | chr9:297785-297799 | TAAATGGGGAAGTA | + | 6.55 | | SPIC | MA0687.1 | chr9:297514-297528 | TACTTCCCCATTTT | - | 7.06 | | ZNF263 | MA0528.1 | chr9:297103-297124 | AGAGAAGGGAAAGGAGAAAGA | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09184 | chr9:292782-299959 | CD14 | | SE_11443 | chr9:294987-300989 | CD20 | | SE_18623 | chr9:295399-299432 | CD4p_CD25-_Il17-_PMAstim_Th |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 297200 | 298000 | | chr9 | 297155 | 297330 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I000295 | chr9 | 295885 | 298620 |
|
Enhancer Sequence | TGCATAGACT CCCTCCCCAC AAATCCAAAC CCACTAAGAC TCTCCAGGCT CTGTTAACAC 60
ACACCAGCCT GGTTCAGCTT GGATGCCCTC CTCACACCAT GTGGGTTCTG ATTTTCCATG 120
CCAGGCAGTC CATCTTAAAT GGATGCATCC TCACCGTGTT TGGGCTTCAA CTTCCTATTC 180
TGGACCTCCT CGGCTACTCC CTACCCCAAG GCATGGAGGG CTGCCTTGTT CTGATGCACC 240
TTATGATTTT AGCACCAAAT TGTACAGGAA GGGAGAGAAG GGAAAGGAGA AAGAAGATGT 300
GAAAGGAAAG AGAGGGTAGG GAAGAGGAAA AAGAAGATGA GGAACACGTA TTATTTTCTA 360
ATCCTCACAA TAGGTCCTCA AAATGAGCAA CATTTCCCCC TATTTCATAC TTGAGGAAGC 420
TGTGACTCAG AGAGACTAAG GCACTTGCCC AAGGTCTCTT AGTACATTAA GGAGCCAGCG 480
TCTGCACCCA GTTCCTTCTG ACTCTAGAGC CTGGATTCTG CTGGCTGCAC CACACTGTCT 540
TTAAAGAGAA CACTCTCAAA ACGCGCTTGG TCTTTGGATT GTCTCAAATG TGTTAGAATA 600
GTGTTTTAAG AAAAGGAATG CAGATCTCCT GGGAAGCAAT AGGTCGAGTT CATTTCATGA 660
GAATCATTTT TCTAGCCATT GGCCTACTTC CCCATTTTTC TCCTGTCTGC ATCTAGGTGC 720
AACAGGAACT TGGCTTTATT TGACTCCATT GCCAGGGTGG GGTAATGAAG CTGGGACTCT 780
CTTGTAGCCA GCGGCAGTGA GCCAGCAGTC TCACTGCCTA CCCAGTGATG GTTCCTTCTG 840
TGGCCAGCAC TTCTGGAATG AGTCATCTTT ACATGTTTGC CAACCCTTGT CCTCTCCTCC 900
CCAGCCAGGT TCACCCTTGC TGCTGTCAAG GAGCTTTGAG ACTTTCTGAG ATTTTTAAAT 960
GGGGAAGTAG ATGTTAAACC TAGTATGAGG AAGAGAGGGA AAGTTTGCTC TGGTTTCAAA 1020
CACACAGTCA TAGAAGATGC TAGTCTTAAT GCTTTCCATA GCAAAAACCC TGAAGGCTTA 1080
GAGTGTACAC ATTGTGAACT GAACTTTTAA CATTATTGTG TAACTCATTT GTTAATGCCT 1140
ATTTGTCATT GACTGTGGGG TCCATGTGAA AAACTCCCAC AAACACTCTA ACAAAATGGA 1200
AGACAGAAAA GAAAGCAAGC ATCATTTGTG TACAATAGCC 1240
|
