| Tag | Content |
|---|
EnhancerAtlas ID | HS187-25752 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chrX:46988560-46989280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chrX:46988570-46988581 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chrX:46988570-46988580 | GCCCCGCCCC | + | 6.02 | | RREB1 | MA0073.1 | chrX:46989259-46989279 | CCCCCCCCCACCCCCCCGGA | + | 6.28 | | SP2 | MA0516.2 | chrX:46988720-46988737 | TCAATCCCCGCCCCCTT | + | 6.48 | | ZNF740 | MA0753.2 | chrX:46989257-46989270 | GCCCCCCCCCCAC | + | 6.29 | | ZNF740 | MA0753.2 | chrX:46989255-46989268 | CCGCCCCCCCCCC | + | 6.64 |
|
| | 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 |
| GH0XI047128 | chrX | 46988000 | 46989999 |
|
Enhancer Sequence | GCACTCAGTC GCCCCGCCCC CAACGCAAGT AGGCATGTTT ATTGGATGAT AAGAGGGTCA 60
GTCAAAGTAA GGACCAACCC TCTACTGCCA AAAGACACAT ACTACTCAAG GGCCCCTGAC 120
TCAGACGTTC TCACTGGTCG GAAATGCCAT CAATCAAGTT TCAATCCCCG CCCCCTTCTC 180
GCGGAAGAAC TATGGGTGCT AACCTCTCTC TCAGGCCTGC TGTCAATCGG CTCCGCATCC 240
TCTAGTTCTG CACATCCCCG GCCATCAGAG CACGAACTTC TGGTCGGTCC GCCTGCCGTT 300
CTTTCACCTA TAGAGCCCAC CCTCTAAAGG TGTCCAAGCT GCTCCAAAGA ACAATTGATT 360
AACCCAACGG CTGTCTTTGG CCCTCAGAAC TGTCACACCT GGCTCCGCCT CTTCCCGGAC 420
ATCATCTGTT GCACCAGAGA CTGGCGGGTC TGGAAAGAAG CTCTGAGCCC ATCCGCGTTT 480
CTCTGTTGGA CCCTGTCAGG TCTCTTGTTC CGTGTCCAAT GTCAGTCGGG TAGGGAGGCA 540
GTGGGGCAGT CTTGGTTCTC ATCCCACCCC GGAGTCTCTG CGCAGCCACA ATTCAGGAAA 600
ACAATCTGGA GGCGGGTTCA AAACACTAAG ATTGATTGAA CGCGCTGATG GTTTGGTTTT 660
CTCCTATAGC GCTTTGGTAG TGGCTTTTAT CCAGACCGCC CCCCCCCCAC CCCCCCGGAA 720
|
