| Tag | Content |
|---|
EnhancerAtlas ID | HS187-17499 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:107629330-107630360 |
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 | CTCCGGAGTC CACCGCCCCC CTTTCACTAC CTGTTATGGG TTTAAATTGT GTCCTCCCCC 60
AGAAGATAGG CTGAACTCTT AACTTCTAGA ACTTCTCAAT ATGACCTTAT TTGGAAACAG 120
GGTCTTTGCA GACATAATCA AGTCTAGATG AGGTCACACA GGAGTAGAGT GAGCCCTGAT 180
CCAGTATGAC TGGTGTTCTT ATAAGAAGAG AAGAGGCAAG TAGAGGGAAG GCAATGTGAA 240
GACACACAGG GAGAGTGCCA TGTGATGTCA CAGGCAGCAT GGAGTGCTGC ACACAAATGA 300
CAGAAGGAAG GGTTTTCCCC TACAGGTTTC AGATGAGCAC GGCCCTGCCA ACACCTGGAT 360
TTCAGTCTTT CAGCCTCCAG AGCTGTGAGG CAATACATTT CTGCTGTTTT AAGCCATCTA 420
GGTTGTGGTA CTTTGTTGTG GTGGCCCTAG CAAAATAATA TACTCTCTCT AAGTCCCACC 480
CCCGCCCCCT TCCTCCCAGG TTGTAGGATG CAGGCAGCTG CCTCTCCCAC ACCTACTAAT 540
GCCAGCCTTG TTGGGGTGAG CACTACAGAT TGTCTTCTTG GCTTCCTCAT GCCTCAGTCC 600
CCGGTCTGGC CTCCTGAGGG TCATGGAGTC CACGGGCTTC TGTTCCTTCT TGATCTTTCA 660
GAGAAAGATG AACAGGATGT GGACTTATTA GGGCACTTTC AGGATGAAAC CAAAGGCCCA 720
CTGGCTGTGA GGGGAACTGG AAGAGAAACC AAGTGAAGCT CCCACTTCAA TCCTAAATTG 780
TCTGTTTCTC TGGAGCTAGA GAAAATGAAC TTTTTGAGTA AAAGCAGGAC CCAGCCATGC 840
TGTTGCATGT CTAGGAATTC CCTGTGGTTC TGAGCTTTCA TTGCATTTGT TCCAGGGGTG 900
TCTGCAATTT GTCACAGAGG TCCCTGACTT TCTAGGCAGA GGGAGAAAAG GAAAGCGAGT 960
GGGGTGGTGA CTGTGGAAGT GCTCTCTAAA CATCTCCAGG GCCATGCAAA CTGTCAACAT 1020
TAAGGGAGGT 1030
|
