| Tag | Content |
|---|
EnhancerAtlas ID | HS059-01065 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:31974170-31975420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:31975003-31975018 | TGACCTTTGGACTCT | - | 7.38 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23348 | chr1:31974366-31975429 | Colon_Crypt_1 | | SE_25647 | chr1:31971291-31977703 | DND41 | | SE_28118 | chr1:31974167-31975646 | Fetal_Intestine | | SE_61646 | chr1:31944906-31977293 | Toledo |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 31974605 | 31974694 | | chr1 | 31974848 | 31975071 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I031507 | chr1 | 31973241 | 31978522 |
|
Enhancer Sequence | AAGCCTGGAT TTTCTCAGCT CCTCTCAAAC ATTTGAGAGA TCTGATGATA CGTGGCCTGC 60
AGAACAACAA GGCAACAAAT AATTCAACAA ATTAGTCTAG CATGTCAGGC ACTGTGATCT 120
GCTGGAACGG GACTTCCTCA GTGGCTTTCC CCTTTGGACA GACATTGACT TTCCAGTTTG 180
TTGTAAGACT TACCTGGCCC ATTTCACTCA TTTGTGTTAC CTGCTTGACC TCTAGGTAAT 240
TGAGTTTTCA ACTGCTGCCT TATAGCAATT ATTGAAGACA ACAGCCCCAC TTACAGAGGA 300
GGAATCTGAG CCCTTACTTG TAGGCACATC AGACCTGGCC AGGCTGGGCA GGGGCCATGG 360
AGGGATGGGT CCCAGCCAGT ATACACCCGT GTGCCCCTGG GAGTGTCCTT CCGGGTCTTT 420
CAGTGCCTTC CAGATAAGGG GGTGGGATAG GCCAGCCTGC TGTCTTTTCT GACCCCCTTT 480
CCTATGTCAC ACAGGAGTTC TGCTCAGAGC CGCCCCTCTT CCCCTGCACC CTCTATGTCC 540
CATGTGCGAT GCCTTTGACA GGCTCTTCTT GGAGGATGTG CGGCTGCCCG AGCTGGATGT 600
AGGCGATTGG CTGGTCTTCC CCTCCATGGG TGCCTACATG TCCTCCATGA GCTCCAGCTT 660
CAATGGCTTC CTGCCTGCCA CCATCTGCTA CACCATGGGC CCCCAGCTCA GGTGCCTAGG 720
GGTTGGGGTT GAAGAGGAAG CAGGAAACCT CACACTCATT TGAGCTTGGG GTGGGAACTG 780
GCCCCAGGGA ATCTCCCTTC CCCTGTTGAC TCACTGAAGT CAAAGTGTCC ATCTGACCTT 840
TGGACTCTCA TCTGCCTCTG GCCCCCCTCC CAGGGAGGTG GAGAATTGCA AAGAGATCCC 900
CAGGCCCTCT AGCCACTGGC TGGCCCTACT CCTGCTTCAG ACGCCCACTG TCCCAGCTCT 960
GCCTCCAGGC CCCAGCTCTG CTGCTGTGTG TGCAGCCTCA GGGCTGTAGG CAAAGGCCTT 1020
GACACCCACC CTGTACCCCA TGTCCTTTCC CCATGAGCCT TCTGGAGGCA GAGCCTTAAC 1080
CCAGAGCCAG CTAGGCTGGA GGGCTTTAAG ACACTCTGGT AGGTAGGCCC CTGGGAACTG 1140
TTGGGAGTTG GGATGGCAGG GAGGAGGCAG AGGTTTGGGT AACTATGAAA TCCTATGCAG 1200
ACCTTCCAAA AATATCTTGC TGTCATTTTG GGTCAGTTCT TTCCTTTTCT 1250
|
