| Tag | Content |
|---|
EnhancerAtlas ID | HS095-23313 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr4:166158830-166159920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Tcf12 | MA0521.1 | chr4:166159533-166159544 | CAGCAGCTGTT | - | 6.32 | | ZNF263 | MA0528.1 | chr4:166159117-166159138 | ATCCCTTCTCTTTCCTCCTTC | - | 6.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr4 | 166159000 | 166159400 | | chr4 | 166159234 | 166159642 | | chr4 | 166159552 | 166159735 |
|
Enhancer Sequence | GCTATGTTAT GGTTTAATAA GAGATGCTGG GTTAAAGTGA AGGTGATGAA TAGTGGCACG 60
TTCTCATGCT TCTTTTACCT TTGAAACTTA GTGAATTCTA GAGCCAAATC TTTTTTGCCC 120
ATGGCCCTCA GCATTATTCT TGGACTGTCC TTTTAGTTTT TAATTGAATC CCTCCCCACC 180
CGCATTCAAT TGCTTGTGTC TCCATGTATC ATAGTTCACT TATGTTGTCA CACCTCGGTG 240
CTTAAACTTG CCTCCTACTC TCCCCAAGTC TCCTTGGCTT AGGGACCATC CCTTCTCTTT 300
CCTCCTTCCC TATTTCTTTT CCACAAGTGG GTATTAGGAA GAAAGTCTTT TACTGTTTTC 360
TTTGCAGGCA GTTTTGTAGA AGGATACCTG GTTTTAGTAA TAAAGCTGGT ATGGAAATGA 420
CTTCAGCGTG AAGTTGCTGC AGTTGACAAA CAGGAACTGA ATCTGAGCTA GAAGATCTCT 480
GTAACAAGCT TTGTTGTTGA CTAACTCTTT GTTATTATTG TGATCCCTGT TATGCCTTGC 540
ATTCTCTAAG CATCATAAGT AATTTGTTTT CTCGTTGTCT CTGGCATGAG GGTTGTGACC 600
TCTCACTGAG GGTGGAGCCT CTGTGTCTGG TGCAGGCTAT GCATGCCCCG GCAGGCATTT 660
GTGTGTTTGT TGAAGGAGTA ATGCTAACCA GGTGGGTCCT TTTCAGCAGC TGTTCATTGC 720
TATTAGCCAA AGGCAGTAAC ATCGTTACTC TTCTAGTCAT GACTGGAAAT CCATAAAGAC 780
AACAAGTGCC CAAAAGCAGG GACAGCCTCA GCTACTGATC CTATAGCCAC AAGAATAGTT 840
CATGCAGCTG GACATATGGC ACGTTCATTG TTGTGATATG ATTTTCAGGT GCAAGTGGGT 900
AACAAAAGTA CATTTTATGA TTTGCTCAGG TGAGCTTTTG GAAGAGGAAG GGGGGAGTAT 960
TTTCGGCCTG CAAAAAGTGG CTGATTATGC TGCCTGTTGA ATACAGTGAG TGGCAAGAAG 1020
ATGTATCAAT CTACATTGGC ATTGGAACTT CCACAGCAGT GTCTTGCTGT AACATCACTC 1080
TTATTCCTTT 1090
|
