| Tag | Content |
|---|
EnhancerAtlas ID | HS007-09901 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr2:242834330-242835400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr2:242834769-242834782 | TTCTGGAAGGTTC | + | 6.19 | | Nr2f6 | MA0677.1 | chr2:242835046-242835060 | TGACCTGTGACCCC | - | 6.32 | | Rxra | MA0512.2 | chr2:242835046-242835060 | TGACCTGTGACCCC | - | 6.39 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_41854 | chr2:242832519-242835830 | LNCaP | | SE_47509 | chr2:242834250-242835853 | Pancreas | | SE_65768 | chr2:242832233-242835648 | 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 |
| GH02I241890 | chr2 | 242832226 | 242835723 |
|
Enhancer Sequence | GGTCCCCTCC GGTCTGTGCC TCATACAAAC AATGGGTATT CTGCTGAAAT TCACCTCCTG 60
GAGCAAAGAT TTCAGAAATG CCCTCTGTAC ACCAGGTGAA TTGCAAAGGG GCCAGGTGTG 120
AGGAGGGACT CCGGGCTCAG AGCCCTGGGG GCTGGCGTCC CTCTCCTCTC CTGGAAAGCC 180
GGCCCAGCCA TCCCTCTTCC CCTTGCCCCT CTCCTACCCT CCCTGGTCTC CTTCTCTCCC 240
TGTCTCTCTT CTGCACTGGG CGCCTTCCAG CCTTGGGAGC TGGGCCCAGC TTTGCCTGAG 300
GATTAACGAC AAAACAGAGT GAAGATGTGG CTGGCAGACT GCCCGCTGCC CCTGTGGCCG 360
GGACCTCTGC TGTCAATGGG AAGGTGACTG CATCGTTGGA GAGTAATTGG GTCATGAGGC 420
AAGCAGGAGG GGGTGGCTGT TCTGGAAGGT TCTGCAGGGC CAAACTGTGA TGAAGATTGC 480
AGCATGAATA TGCTCTTCCA TCCCCCAAAA GTCCAGTCTG ACACCTCAGT TTATTACGGT 540
GTTGACAGTA ATAGTGTTCT GAGGATATCA TCAGATAAAA TCACTCCTCC GCAGCCTGGG 600
GCTTTGCAAA GATTAGCGAG TGGTTTCTGT TCATGAACTA TCTTCAGGGC TGTTAATCAC 660
CTCCCTCCCT CCCTGCAAAT CCCTGAGTCA CTAGCGGTGA GGGTGGGGCC CAGTGCTGAC 720
CTGTGACCCC AGCCCTGGAC ATCTCCATGG CCAGTGTTGC GAGGGCCCTG GCTGCGCTTC 780
TGCCCACTGA CTGGCAGACC AGGCATCCAG GCACCCGGGC TTTGTGTCAG GTTCCGATCC 840
TTCTTTCTGC ACGTGCTGTC TGTGCAGTAG TTCATGGTCA GCCCCAGAAA TGCACACTTG 900
AGATGGCGTG GGCCTGCGTG GAGTCTGCAC GTGGCACAGC AGGGACCTGG CTACGCGATC 960
CTCTCGTTAG TGCTTTGTTG GGTTACCCAT GACCTGCAAA GCTGGGGCTA ATTTCTTTGT 1020
CTTTGACAAG ACCCGCAAAG CTGGGGCTAA TTTCTTTGTC TTTGACAACT 1070
|
