| Tag | Content |
|---|
EnhancerAtlas ID | HS176-21609 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:136544340-136545410 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:136545160-136545178 | GGAAAGGAGGAAGGAAAC | + | 6.44 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 136544467 | 136544688 | | chr2 | 136544400 | 136545000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I135786 | chr2 | 136544041 | 136545410 |
|
Enhancer Sequence | AGCCAGGATG GTCTCGATCT CCTGACCTCG TGATCTGCCC ACCTCAGCCT CCCAAAGTGC 60
TGGGATTACA GGTGTGCGCC ACCGTGCCCG GCCAACAAAT GTCTTTAATA TCAATTTTAG 120
AACCACCCCC ACCCCCATCT GACAAACTTT TCCAGTCGAT TGATGGAGAA AAATGCTTGT 180
GCACCACAAG CTCCTGACTG CCAGGTTGGG ACTCATGGCG TTGGAATGTT TTGATAGGGA 240
AAGGAATGCT TACAAGAAGC AAATTTCAAG TGTGATCATC CTTTTAAGAC CAGCCCAAAA 300
TTACTCTGTT GTTACAAAAC ATTTTCCCAG CTATCTAGAT GTAATATATG GGCCAATCAA 360
GTGTTTAGGT GTTTCACACT GAGATTGTCT CTCAGCACAT TTGAGGGGAT TATAAAGAAC 420
ATATCTCTGC TCCCACCACT GCCCTGGAAA TGCTATGTGA ATGGGTGAAC ACACGAAAGG 480
AGCATTTGTG CTTTTCATTG CTCTCTCCAA GTTGTGCTTG CCAGAGACAA TGAGACATGG 540
TCCTTGGCCT TAAGAAGCTG ATGATAGAGA AATACGCAAT TCCAGTATAG AAACTGGATG 600
GTCAAGTTGT AATAGGGGAT ATTTACAAGC AAAGCAGACG AAGGAGAATC TGCCTGGGGA 660
TTTCAGGGAA GCCATTCAGA GGAGGAAGTA CATTATTTCA GCTGAGACTT AAAGGCATTT 720
TCAGAAGAAA GGGCATCCTA GGTGGAAGGA GTAGCATTTG GGAAGACACA AAGGAATATG 780
GATAGTTGTC CTATGTGCCG TTTAGAACTA CCACAAATTG GGAAAGGAGG AAGGAAACAG 840
ACTAAATGAA CCAAGGTCAG ATGGGAGAGC TGGGGATGGC ATAAAAAGTG GCAGTGGGGG 900
TGTTCGAGGG GTGGGAAAAG GCCACTTTCT GCATGTTGTG GTATTTGCCC CAAGGAATAT 960
AATGTCAACA GAAAGACTTG GTCTGGTGAG AAAGCTTAAT CGGAGCTCCA GATGGCTTGT 1020
GTGACTTCAT AACTTCTCTT GAACCTACTT TCTCAAGGAG GGGCAACCAT 1070
|
