| Tag | Content |
|---|
EnhancerAtlas ID | HS048-19794 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:16190780-16191790 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr2:16191247-16191263 | ATGCTTTCTGGGAATT | + | 6.02 | | BCL6B | MA0731.1 | chr2:16191248-16191265 | TGCTTTCTGGGAATTAA | + | 7.97 | | RORA(var.2) | MA0072.1 | chr2:16191135-16191149 | TTAAACTAGGTCAG | + | 6.36 | | ZNF263 | MA0528.1 | chr2:16191196-16191217 | TCTTCCTCTCTCCCTGCCTCC | - | 6.02 | | ZNF263 | MA0528.1 | chr2:16191199-16191220 | TCCTCTCTCCCTGCCTCCCTC | - | 6.55 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_05657 | chr2:16190399-16192156 | Brain_Cingulate_Gyrus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 16190856 | 16191000 | | chr2 | 16191000 | 16191693 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I016051 | chr2 | 16191341 | 16191490 |
|
Enhancer Sequence | GAAGGCAGGA GGATAATAGG TGAGTTCCAT CCATCCGTCA GCCATAATGG TCGCGGACAC 60
TCCACGCCTT TTGTCTGCTG GTTTCCCTGA GGATGCAGGC TAGGGACCTG GGGTATTTAC 120
ACTGCCTTTA TGTGTGTGGT TTTTAAATCA GCCCTCTTGT TTACTTCCCA GCCTTTACCC 180
AGGCTGTTTA CTACCTTTGG AGGGGCCAGG CCACTAAGTC AACATGCATT AAGACCCAAC 240
ATCAAAATGT CATAATGCGA ATGAGCAGAA TTCTGAAAGG CCAGGGACAT TGGCTGCTCT 300
GTTGGGTCCT GTTTAGTCTG AGGGTAATGA AGAGCTCACA GATGACCTGA TTTCATTAAA 360
CTAGGTCAGA CTCAGCTGAA AAGCGGCTAT GACTCTCACC CAGTTATATA GCCAGCTCTT 420
CCTCTCTCCC TGCCTCCCTC CGCCCCCACC CCCACCTCGG GGCTTGAATG CTTTCTGGGA 480
ATTAACGCTG AGTTTTGTCA ATACAGTAGC TAAATCTCCA TGGAATAATT GGACCTTTCC 540
CTTCGGCTTC TGTTTGCGCA GTGGCAAGGC CAGGCATGGG AGAGAAGCGG GTGGACTTTA 600
ACGCAGCATG TATGATTCAG TTGTAGCAGT TTGCTTTTGA GCCAGACATT CTGAGTTACA 660
GCATCTTATC TGAGGGCTGT ATTGACGGAA GCAGCTGAAC TGACTCAAAG AGGAGTTATC 720
ATGCAAACAA GGCTTTCAAT GTGTCCAGGC TCACCAGCAA CACACGGGCC CTCTGCATCT 780
TCAGAAGCCT CCTGGTGGGG AGTAGGAAAG GGACCAGGCA GAGGGTGGAG GCAGGAAGGA 840
GTGGTGTCTG AAGGCTGCTG AGGGAGGAGA GGTGGTCCTC CCCCGTCCCT CCTTGCCAGG 900
GAAAGACTGA GTCTGTGGTG GGCATTCCAG GCAGGCAGAA TTCACTTCAT CCATACAGAA 960
GAAAGCATTT CTAACAATTA AAACTGTCTG AAGATTGGAT GGGCTGTCAG 1010
|
