| Tag | Content |
|---|
EnhancerAtlas ID | HS191-39736 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr9:131926120-131927220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr9:131926327-131926339 | TGCCAGGGGGCA | + | 6.62 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_26914 | chr9:131925600-131927318 | Esophagus | | SE_27869 | chr9:131926168-131927163 | Fetal_Intestine | | SE_30321 | chr9:131925792-131927372 | Fetal_Muscle | | SE_31776 | chr9:131925609-131927314 | Gastric | | SE_34379 | chr9:131925753-131927407 | HCT-116 | | SE_42081 | chr9:131925740-131927299 | LNCaP | | SE_43197 | chr9:131925818-131927233 | Lung | | SE_46983 | chr9:131926080-131926439 | Ovary | | SE_47992 | chr9:131926032-131927087 | Pancreas | | SE_50677 | chr9:131925646-131927330 | Sigmoid_Colon | | SE_53874 | chr9:131926668-131927241 | Spleen |
|
| | 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 |
| GH09I129163 | chr9 | 131925742 | 131927610 |
|
Enhancer Sequence | TAGGTGAAAG GTTCACCCCA CGTCTAGACA CGGTCTCTGG TTGGCTGCCA GTCAGGCTGT 60
GGTGCTGCTA ATGCACAGCA GTGGCGGCTG TCACCGTGCC CTGCAAGGTG CTGCTCACGG 120
ATGCCTGAAC TCAACCCTCT CTACGCCTGT GCCCAGGTCC CTGCCGAGGA TGGGAGGGAG 180
AGGCCAGGCA GAGCCAGGGC ACCAGAGTGC CAGGGGGCAG GGTAGCAGGG GGACCAAGAA 240
CCTGTCTCAG GGAGGTGGGG AGGTGGCAGG AGACAGGACT GCACCTGAGT CGAAGCTTCA 300
AACACGCTCC ACTGTCTCAG ACTTCACTCA ACACAAACTC AACGATAAAA TGATGTTGAA 360
TTTCAAGACA GCAGAGCATT AGACTCCAAG CATGGGCTCA TTTGAACATG GGGCCCTGTG 420
TGACTGCACG ATCCCTGGCC AGTGGCCTTC TTGTTCTGGC CGCAGAGAAA ACCTAAGAAG 480
AGGCCAAGGA GAGGTAACGA ATAAGCCCTG ATGACATCAT GTGAGCCTCT GGATCCAGCT 540
ACGCCTGAGC CGAAACACCC ATGGACTTCC CTGTTTCTGT GCCAGGAAAT AAATCCGCTC 600
TTTGCTTCAG CCAGCTTTAG CTGAGTTTCT GAGGCCTGAA CAATATGGGA CCCTGAGAGG 660
AGAGGATCCA AGGCCCAGGA ATCTCGACAC CCGAATCCCT TTCTTGGCTT AAAGAATCTT 720
GGAGCTGTCC ATCAACTTGG AATGTCTGCA GGTTGCCTAG AGGTCTCACT GCCCCTCCCC 780
ACATGGATCT GTCCTGTTCT GGGGCCACGT CCTTTATCTG TCTTAGGCCT GGATTTCTTT 840
TTATGAACAA AGGGAAGCTT TATTCCCCAG TCTTCCCAGT TCTCCCCAGG CTGTTTGATG 900
TGGGTGTTAA AGGAGACACT GGACTTCCAC ACTGGGGGTG TGTGTGTGTG TGTGTGTGTG 960
TGTGTACTGG ATTTCCACTC TGTGGTGTGT GTGTGTGTGT GTGTATGTGT GTGTGTGTGT 1020
GTAGTGGCCT GGAGGGTGCC AGGGAGCTGG GAGGACAGCA GGAAGGATGC ATGGAATGTT 1080
TAAGAAACAT CAGGAAGGCC 1100
|
