| Tag | Content |
|---|
EnhancerAtlas ID | HS136-20849 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chrX:46988220-46989380 |
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: 2 | Chromosome | Start | End |
| chrX | 46988600 | 46988657 | | chrX | 46988400 | 46988600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI047128 | chrX | 46988000 | 46989999 |
|
Enhancer Sequence | GGCGGATCAA TTGAGGTCAG GAGATCGAGA CCAGCCTGGC CAACATGGTG AAACCCCGTC 60
TCTACTAAAA ATACAAAAAT TAGCCGGGCG TGATGGTGGG CGCCTGTAAT CCCAGCTACT 120
CAGGAGGCTG AGGCACGAGA ATCGCTGGAA CCCGGGAGGC GGAGGTTGCA GTGAGCGGAG 180
ATCGTGCCAC TGCACTCCAG CCTGGGCGAC AGAGCTAGAT TCCGTCTCAA AAAAATAAAA 240
AATATAAAAT AAAAAACAGA TAAGCGGGTA GGGAGCTACC GGTGGAACTG AGTTTCCTCT 300
TTAAGGGAAA CGAGGACAAG GACAAGATCC CGTCTTTTCT GCACTCAGTC GCCCCGCCCC 360
CAACGCAAGT AGGCATGTTT ATTGGATGAT AAGAGGGTCA GTCAAAGTAA GGACCAACCC 420
TCTACTGCCA AAAGACACAT ACTACTCAAG GGCCCCTGAC TCAGACGTTC TCACTGGTCG 480
GAAATGCCAT CAATCAAGTT TCAATCCCCG CCCCCTTCTC GCGGAAGAAC TATGGGTGCT 540
AACCTCTCTC TCAGGCCTGC TGTCAATCGG CTCCGCATCC TCTAGTTCTG CACATCCCCG 600
GCCATCAGAG CACGAACTTC TGGTCGGTCC GCCTGCCGTT CTTTCACCTA TAGAGCCCAC 660
CCTCTAAAGG TGTCCAAGCT GCTCCAAAGA ACAATTGATT AACCCAACGG CTGTCTTTGG 720
CCCTCAGAAC TGTCACACCT GGCTCCGCCT CTTCCCGGAC ATCATCTGTT GCACCAGAGA 780
CTGGCGGGTC TGGAAAGAAG CTCTGAGCCC ATCCGCGTTT CTCTGTTGGA CCCTGTCAGG 840
TCTCTTGTTC CGTGTCCAAT GTCAGTCGGG TAGGGAGGCA GTGGGGCAGT CTTGGTTCTC 900
ATCCCACCCC GGAGTCTCTG CGCAGCCACA ATTCAGGAAA ACAATCTGGA GGCGGGTTCA 960
AAACACTAAG ATTGATTGAA CGCGCTGATG GTTTGGTTTT CTCCTATAGC GCTTTGGTAG 1020
TGGCTTTTAT CCAGACCGCC CCCCCCCCAC CCCCCCGGAA TGAACCCTGG TATAGAAATG 1080
TTACCCGTAT GTGTGCATAT GATTGTTTTT AATATATTTC AATTTGATGA ATCAGCCTTT 1140
TTCAAGGTCA GATTCCAGAC 1160
|
