| Tag | Content |
|---|
EnhancerAtlas ID | HS060-24824 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:107629360-107630360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr3:107629804-107629821 | CCCACCCCCGCCCCCTT | + | 6.48 | | SRF | MA0083.3 | chr3:107629431-107629447 | TGACCTTATTTGGAAA | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 107629437 | 107629889 | | chr3 | 107629410 | 107629800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I107910 | chr3 | 107629841 | 107630154 |
|
Enhancer Sequence | CTGTTATGGG TTTAAATTGT GTCCTCCCCC AGAAGATAGG CTGAACTCTT AACTTCTAGA 60
ACTTCTCAAT ATGACCTTAT TTGGAAACAG GGTCTTTGCA GACATAATCA AGTCTAGATG 120
AGGTCACACA GGAGTAGAGT GAGCCCTGAT CCAGTATGAC TGGTGTTCTT ATAAGAAGAG 180
AAGAGGCAAG TAGAGGGAAG GCAATGTGAA GACACACAGG GAGAGTGCCA TGTGATGTCA 240
CAGGCAGCAT GGAGTGCTGC ACACAAATGA CAGAAGGAAG GGTTTTCCCC TACAGGTTTC 300
AGATGAGCAC GGCCCTGCCA ACACCTGGAT TTCAGTCTTT CAGCCTCCAG AGCTGTGAGG 360
CAATACATTT CTGCTGTTTT AAGCCATCTA GGTTGTGGTA CTTTGTTGTG GTGGCCCTAG 420
CAAAATAATA TACTCTCTCT AAGTCCCACC CCCGCCCCCT TCCTCCCAGG TTGTAGGATG 480
CAGGCAGCTG CCTCTCCCAC ACCTACTAAT GCCAGCCTTG TTGGGGTGAG CACTACAGAT 540
TGTCTTCTTG GCTTCCTCAT GCCTCAGTCC CCGGTCTGGC CTCCTGAGGG TCATGGAGTC 600
CACGGGCTTC TGTTCCTTCT TGATCTTTCA GAGAAAGATG AACAGGATGT GGACTTATTA 660
GGGCACTTTC AGGATGAAAC CAAAGGCCCA CTGGCTGTGA GGGGAACTGG AAGAGAAACC 720
AAGTGAAGCT CCCACTTCAA TCCTAAATTG TCTGTTTCTC TGGAGCTAGA GAAAATGAAC 780
TTTTTGAGTA AAAGCAGGAC CCAGCCATGC TGTTGCATGT CTAGGAATTC CCTGTGGTTC 840
TGAGCTTTCA TTGCATTTGT TCCAGGGGTG TCTGCAATTT GTCACAGAGG TCCCTGACTT 900
TCTAGGCAGA GGGAGAAAAG GAAAGCGAGT GGGGTGGTGA CTGTGGAAGT GCTCTCTAAA 960
CATCTCCAGG GCCATGCAAA CTGTCAACAT TAAGGGAGGT 1000
|
