| Tag | Content |
|---|
EnhancerAtlas ID | HS042-04109 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:230864350-230865220 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:230864918-230864933 | TGCCCTTTGACCCCC | - | 7.16 | | Nr2f6 | MA0677.1 | chr1:230864918-230864932 | TGCCCTTTGACCCC | - | 6.46 | | Rxra | MA0512.2 | chr1:230864918-230864932 | TGCCCTTTGACCCC | - | 6.73 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32194 | chr1:230864487-230865515 | Gastric |
|
| | 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 |
| GH01I230728 | chr1 | 230864231 | 230865816 |
|
Enhancer Sequence | CGATAATAAA ATGCTGCCAC TTACTGAGAA CTTTTGAGGT ATGGGTCACC CTTTTAAGCT 60
TTTGCATCTA CGGCCTCATT TTCATGCTTT GTAACAGTGT CCACAGCAGC ATACAGAGAA 120
GGGGAGAAAA GGTTTGTGTG TACTCTTTGC ACCATAGCTC TTTCAGCACA TGCATTAGTT 180
TTGCTCTTGC CTCACATCCT CTTTTACTAA TGCCAGGAAA CACATCCAAC ACAACCTTAT 240
ACTCCCTGCA ATCCCTGTCT CATGGGAGTA GAGAATCCTC ATAGTGAGGA TTGAATTAGT 300
TAACATATGA AAGCATTTGG AGCAGAGCCT GCCAGGCAGT GAGCCCTGGG AGAGCATTAG 360
TTGCTATATC ACTCGTGAAA AGCCTTCCGG AAATGTGGTT GTCCACTAGG AGACTGAGCA 420
AAGACAGTCA GGTACCCATG CAGTTAACTC AGTCAGGCTA ACAGCAAACA GAACTTCAAA 480
GGCCACCTGA CCCTCTCCCC TGACCCAGAA AGCCTGAGGC ACCTGCCTGG TGCAGTTTCT 540
CCACCATCTG CCATGCAGGG CACCACCATG CCCTTTGACC CCCACCTTCC ACTCTCTCTC 600
TGGACTTTCA TCCGCACTCA GCAACAGCCT GTTGGCGCCA AACAGCCTCC AGCCCTAATT 660
GCTCTTCCTA GCTCCCGGGC AGTGTTCCCA ACACCTAGTA GCCACTGTAA GGACAAATGC 720
AACTTAAAAA CAAGAGGCTT AATTCTCCCG GTTGAAAATG GGGGAAGAGG TTTCCCTCCC 780
TCTCTTATTC TCAGAGCATT TACCTTAGAA AACTTGTAAT TATAAGCACT TTCTCCTCTC 840
TTTCAAATGT ATATAACATT TTTGTGAAGA 870
|
