| Tag | Content |
|---|
EnhancerAtlas ID | HS047-20607 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:236126860-236128130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NOTO | MA0710.1 | chr2:236127953-236127963 | GCTAATTAGC | + | 6.02 | | NOTO | MA0710.1 | chr2:236127953-236127963 | GCTAATTAGC | - | 6.02 | | NRF1 | MA0506.1 | chr2:236126908-236126919 | CGCGCATGCGC | - | 6.02 | | NRF1 | MA0506.1 | chr2:236126909-236126920 | GCGCATGCGCA | + | 6.32 | | POU4F2 | MA0683.1 | chr2:236127554-236127570 | CTCATTTAAAATTCAT | - | 6.29 | | SPI1 | MA0080.4 | chr2:236127283-236127297 | AAAAAAGGGAAGTA | + | 6.01 | | SPIC | MA0687.1 | chr2:236127283-236127297 | AAAAAAGGGAAGTA | + | 6.35 |
|
| | 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 |
| GH02I235218 | chr2 | 236127288 | 236128492 |
|
Enhancer Sequence | TGTGTGTGTG TGTGCGCGCG CGTGCGTGTG TGTGCGTGCG CGCGTGCGCG CGCATGCGCA 60
CGTATCTTCT TTACTTTTCT GTCATGGGCC CCAAAGCTGG GAAAACTATC AACATAAAAT 120
AAAAATGTTC TTGAAAAAGA AACATTTAAT AACATTCATT TTAAAATGCA TTATTTAAAC 180
ACATGTTTTC CTCTATATGC ATGAACTCTA TTACAACAAG TGATATCTGT TTGGAGAATG 240
AAATAAAACT CCCATTACTA CTGAGGATTG GGAGGCAGTA TGGATTCTTC CAGGGGGAGG 300
CCTGATTGGG TAACAGATGC CAGCAGCATT GTGGATGCCA ATGGCGTTCC AGTCCTCTAC 360
CGCCAGCAGT TAGCTACATA ATCTTGAGCA AGTTTCCAAA CTCTGAACCG AGGTTTCCTC 420
ATCAAAAAAG GGAAGTAATA GCACCAGCTT CATAGGGTTG TTTGTGGAAT GAAGATAATG 480
AGTGAAAAGG ACTTGGCACG GGAGAAAGTC AACACATGTT GGGTTTTAAT CTCATCGCTA 540
GAAGTTTCAT CAGCGAGGCG GAGCTGACGT GATCAGGATG GGTTGCATGG AAACTTGGGT 600
CCTGAGACTC ACTCTTCCAG GAACAGCGAG GAAGTCTCTT CCCCTGTCTG TGCTCCAGCT 660
CCCTCACTTA CAGTCTCAGG AGATCCGACT AGACCTCATT TAAAATTCAT CCAATCCCCC 720
AGTCCTGTGC TTCAAATTCA GCCTCCACTA AATACTCCTT GCCATTGTCT CATTTACTTT 780
TCGGAAGGGC CCAATAAAGT GGAGATCGGC CAATCTGTTT GTCCCAGGCA AGGACACCAG 840
GGTTCACAGA GGGTCTCAGA GCCAGGCTGG GGAGGAGCTG AGTGTTGGCC CCACTGACTC 900
ACACCTTTCT GATTCTCCTG AGTTCAGAGT ATGTGCAAGG AGATTCAATC AGAGGCACGT 960
TGCATACCTC ATTAAGCTGA GGCCACGACC CAGAGTCCAG ATTGGTCCCT GAGCTCAGAG 1020
TCCATTGACT GGCTTCTCCC ACGGGGTCCC CTTTGCCCTG TGTTCATCCA CGTGTCCTCT 1080
CAGTCATCTG GCAGCTAATT AGCCTGGAAA TGACAGCCTG GACACTGATG TAAGGTTATG 1140
ATTCCCAAGC TTCCCTTGGA GCTGTGAATG GTGACTCTGT GAACACATTT ACCAGGATTC 1200
GTATGGAGGA ATTCTGATTC ATTTCAGATT TTTTTAAAAG TCAAAACACA TGCCCCTTCA 1260
ACCCCCAACA 1270
|
