| Tag | Content |
|---|
EnhancerAtlas ID | HS042-45311 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr8:38507850-38509330 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr8:38508936-38508947 | GGCCACACCCA | + | 6.62 | | MEF2C | MA0497.1 | chr8:38509235-38509250 | GATCTAGAAATAGAA | + | 6.12 | | PLAG1 | MA0163.1 | chr8:38508421-38508435 | GGGGCCTTCGGGGG | + | 6.82 |
|
| | 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 |
| GH08I038650 | chr8 | 38507537 | 38509759 |
|
Enhancer Sequence | AGGGCTAGAG CATTGAATGC CAGGAGAAGG TAGAGGGTAT GAATGGAAAT GGGATGAGAG 60
CCTAAGCAAG GTTTAATTTA AAACTTCCAG CAAACTGAGA TCAAAAGAAC GTGGCCTTCT 120
AGCCAGTCTT TCCATGGAGA CAACTGAGGA GCCTGGAGTG GGCAAAGGAC CCTCGGGCTT 180
GCGGTGGCCA CGGGCACCCC AGAGGGACGG AGGGCGCCAT ACCGCGGTTG CCATGTTCCT 240
GCATGTGTTT GAAATCTGGG CTGACAAGAA GAGCTGGACA ATTTTGCTCC GTTACGTATT 300
GAATTCTCTT CTCTGTGGTA CAGGATCCCC TTGAAGCGTG ACAGCTGCAA TGACTTCCAG 360
ATGTCCGCCT CCTGTCTCCT AGCCGACTGG GGTGGATGTG GTAAACTCCG CGATGGAAAC 420
CAAAACCCCC ACCAGATGTG CCATGTCAAC GTCAGCCTCG CGCACATCTG GCTTCAATGC 480
CGGCCGCCAG CCCCAGAACA AATGGCGGCT TTCCCGCTGT ATTCAGCTAG TCAGCGTTCC 540
CCGGTTAAAA GGCGCTGGGG CAGGAACGGC CGGGGCCTTC GGGGGCGCGA CGCGGCGACG 600
CCCAGCCTGG GAAGGGGCGC GGGGCCCGTG TTGGCCGCGG TGGGTCCCGG CTCCCTGGAG 660
GCTGAGCCCC GGGCGCTCTT TCCTCGCGGC GCTGCCGTGG GGTGGCCGGG AGGGCAGAAC 720
GAGGGGCTGC GGGACGGTGT TCGGAAGAAA ATCGTGCGAG TTTAAAAACA TCCAAAGTGA 780
GCCGAGCTGG GCCCCAAGCC TCGGCCTCGC GCACTCGCCA GGCCCAGGAG GCGGAGCAGG 840
CGTCGGGACG GCGGCGACCA GAGCCTGCTG GACAAGCGGG GCCGGGTGCC TCAGCCCGGC 900
CTCCTCCTGG CCTCCCTCTC CCCAACTCAC GCATCCACCA GCAGGACCCC CTACAGGGCA 960
GGCGCAGGAG TGAATCTTAG CTGTCATTAC TACTGAGGTG GTATTTTTCT AAATAAAAAA 1020
ATCAGACAAA TGGATATCCT GAAAACAGGA CAGAGCGTGT GAAACCTGGA CTCAGGGAAG 1080
GATGGTGGCC ACACCCAGGC CCGCTTGTCC ACGGCAGCCG GCAGGAGCGG GCACTATCAT 1140
GTTTACGAGC TGCCCTTCTA CCTACCCACG AAGTCTCATT TAGTCACAAC AGATGCTGTA 1200
TATTGGAAAA GGCCCCCAAC TGAGCACCAA AAGACTTAGG TGTGGGTCCT GGTTCCAAAT 1260
GAGCCAGGAG ATATGGGGTA TATCTTGGTT CTTCCTTTAT AAATTGGAAT ATATATCTAT 1320
TTCTTTTTAC TTCATAGAGT TCTCTGACTC TTAATTGAGC AAAGTTTACA AAGAGAAGTG 1380
AATTAGATCT AGAAATAGAA TTCAGGTTCC ACCGATAACT GGCTGTATAA TTTTATGCTA 1440
CCCACCTCGG GGAAAAGGAA AATGAAAAAC GGCTCTGAAA 1480
|
