| Tag | Content |
|---|
EnhancerAtlas ID | HS037-33068 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr6:41516600-41517800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr6:41517471-41517492 | GGGGGAGGGTGGAGGGGAGAA | + | 7.34 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27953 | chr6:41514239-41519382 | Fetal_Intestine | | SE_28956 | chr6:41512876-41517548 | Fetal_Intestine_Large | | SE_28956 | chr6:41517637-41519404 | Fetal_Intestine_Large | | SE_31492 | chr6:41512748-41521399 | Gastric | | SE_65317 | chr6:41514517-41518063 | Pancreatic_islets |
|
| | 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 |
| GH06I041549 | chr6 | 41517638 | 41521927 |
|
Enhancer Sequence | GCCTCGGGGT TTTGGGGCTC TGTTACCTGG TGGCTGGAGG GAGGATACTG GGGCTCTGCT 60
CTTGGTACCT GGACAGCTTG TTGGCTCCCA TGGTGCCCTT TCGATCTGAA ACTCAAAAAA 120
CTGTGAGTTG GGGGAGTCAC TCACACTCTA GTCAGTGGGG CAAGGTGGCA AGGGGAAGAG 180
GTGGTTTTGT GGTTGCCCCC TCTCAGCCTC CACACCCAGG GCCAGGGTGA GCGCTGAATC 240
TCTCCTGCGG GACGGGACCC TCAGGACCCA CTTTATCCTG GCTCCAGCCT TGCTACTAAG 300
TTTGGGAGAC CATGGGAGCC TTCTCTCCTG GCACCAAGGG CTGGGCGCCT GGGTGGAGTT 360
TTCTGTCCTT CTCCCTGTCC TGGACAGGTT TCCCAGGAGT TACGGAGTTG GGGAACCCCT 420
GAGCCCTGGA GAGAGAAAGA CCTGACCCCA GTGCTGGAGA ACGCCAGGGC CAGAGCATTT 480
GCAAAGGGTC CCACTTGCAA AGGGACCTGC TCCTGTCCCT TTCTGTGTAG GGATCTTCCT 540
CACACCTAGA CGCCCCCAGC CCCCTTCCTC TGCCTTTAGA GCCGAAAACT TCCGTTCTGG 600
CTGTAGGCAG GTAGGTCCCT TCTTGCCAGG AATGTGCATA TCCTGCTGGG CCCCTACCCC 660
AAACATACCT CTTCCTTGGT GGGAGGGAAG CAGAGGGACT GGGAGAGGAA GGCTTGCTTT 720
TGATCCAGTA ATTCCCCCAA ATGTTTGCTG AGCCCCTACT CTGCCTGGGC AGGTCCCAGG 780
CTGAGTACTG GGGTACCCAA GCAGTGAAGG CTGGGGTCTG CTGTCTGGAC CTCAGATTGT 840
TGGGGTAGGA GAGACAGATA TCACATGGTG GGGGGGAGGG TGGAGGGGAG AAGAATGGGA 900
ACAGGGTGTC TGTTTCAGAG GAGAGTTGTG AGGTGCAAGG GGAGGGAAGG GTTGTCTCCC 960
CAGGAAGCCT TCCCTGCATC TTAACCCTTC CTACCCCACT GCCTTGGCGG TTTCCTGTCT 1020
CTCCAGCCAC AGTGCAAGCC CCCCAGTCCC ATCCTAAGCA GGCACAATGT CTTTATTTTT 1080
TGAATAGCCT AAACTGTGTG AAATAATAAT TTCTTCCATC CAAGAAACTC CTCACAGTTT 1140
CCCTTCTCAC AGATCTTACC ACGCTCCAGC TTCCCTAGAC CAAGGCAGGG CAGGTACTAT 1200
|
