| Tag | Content |
|---|
EnhancerAtlas ID | HS037-41528 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chrX:19880600-19881900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEOX1 | MA0661.1 | chrX:19880998-19881008 | GTTAATTAGC | - | 6.02 | | RREB1 | MA0073.1 | chrX:19881820-19881840 | ACACCCAACACCCCCCAACC | + | 6.98 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09810 | chrX:19879669-19890537 | CD14 | | SE_11771 | chrX:19879266-19891591 | CD20 | | SE_32590 | chrX:19879867-19886294 | GM12878 | | SE_58605 | chrX:19810059-19915925 | Ly1 | | SE_60015 | chrX:19844904-19906955 | Ly4 | | SE_60833 | chrX:19844705-19907071 | DHL6 |
|
| | 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 |
| GH0XI019862 | chrX | 19880532 | 19886365 |
|
Enhancer Sequence | ACCATTCTTC CACTCAAGCT TCACTATAAG TTTGGTGTTT GTTCTTGCTT CAATTTTAGC 60
AGAATTCATG TTGCTCTGAT AGGGGCTCTT TCCAAACTGG TGTCTTATCT TTCTTAGTGC 120
CTCAAACTAG ATACTATTCA GACATGTTAC AGCCAAGTTA GTGTGAGTTT ATTTTGGTGC 180
AAAAAAAAAA AAATTTAAAT CCATGAATAG TTTTTTCATA ATACCCATTT TCCATGAACT 240
TGTTGAAGTC TCCTCATATA GCTCTGTATT ACTTGGCTTT GATCCTTATC CTAAAAGAGG 300
TCAGCTCACA ATTGAAGTAT CCAAATGAAA AACAAGCACT CCAGGGATGG TGGATCAGCA 360
TTTGAAAGAC TAATCAGAGT CCATTTGCAC CAGAGTTGGT TAATTAGCAT GATGAAAACA 420
AGCAGTGGCC CTCTGCTCTA GGAATTGGGT GAAAATATTG TGCCACCATC TCCATCCTCA 480
GAAGAACCGC ACAAAAGAAT CTAGAAATAA CAGCAGTCTG CCCCCTTCAG AGAAGAGGCC 540
CAGGACTGTC AGGGGCCATT GTCAACCACT AAAGGAGGAC CCTGTCCCCT CCCTGGGGGT 600
TAGCTGAATC CCGGCACTGG AATACAGTGG CATCTGCCTT GAATGTCTCT TTCCCAAAAG 660
GGGCCCGGCC AGAGGGCTCA AGCTTTGCTG AGCTTACAAA ACAGACTGCA GTGTGCTCTC 720
TTTTTTTTTT AAAGAGACAG GGTCTTGCTC TGTTGCCCAG GCTGGAGTAC AGTGACAGGA 780
TCATAGCTCA CTACAGCCTT GAACTCCTGA GCTCAAGTAA TCCTTCCACC TCAGCCTCCC 840
AAGTAACAGG GACTATAGGT ATGTGCCACC ACGCCCAGCT AAAGCAGGGC TCTCTTCATG 900
CCTGCTTACT AACAAGTGTC TGAATGAGTG GCCAAAACGT GTCTGAGACT TGCTTTCACT 960
GTAACATACC TCCCAGTCAT GGGACCGTGG GAAAGGATGC ACAAAGCTCC CACGTACTAT 1020
TTCTCAAAAG AACTTGTCAG TTCTTCAAAG TCCAAACCAG TTTAAGTTCA CAACAGATTA 1080
TTTGTTAGAA TTCTTGAGAA CACATTTAAG GCTCTGTGAG CCTGTACCAG ACCGGTTTAC 1140
ATTCTCCAGA GCAGAGCCCT CCTGGGACGG GGTCCCCAGC TGGGCTGCTG CTCTCTCCAG 1200
AGAGAGTTGT TTGGACAGTG ACACCCAACA CCCCCCAACC TCCCTCGGGA CACCAAGTGG 1260
CCACAATGAA CCCCTGAGGC TTTTAGTGGC AAGAGTGCAC 1300
|
