Variant report
Variant | rs573970472 |
---|---|
Chromosome Location | chr1:166572717-166572718 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:37)
- CpG islands (count:61)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:37 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | GATA3 | chr1:166572340-166572891 | MCF-7 | breast: | n/a | chr1:166572492-166572508 chr1:166572554-166572567 |
2 | GATA3 | chr1:166572220-166573146 | MCF-7 | breast: | n/a | chr1:166572492-166572508 chr1:166572554-166572567 |
3 | HDAC2 | chr1:166572357-166572896 | MCF-7 | breast: | n/a | chr1:166572395-166572404 |
4 | FOS | chr1:166572573-166572930 | MCF10A-Er-Src | breast: | n/a | n/a |
5 | TCF7L2 | chr1:166572373-166572803 | MCF-7 | breast: | n/a | n/a |
6 | EP300 | chr1:166572432-166572956 | MCF-7 | breast: | n/a | n/a |
7 | FOS | chr1:166572542-166572950 | MCF10A-Er-Src | breast: | n/a | n/a |
8 | FOS | chr1:166572414-166572955 | MCF10A-Er-Src | breast: | n/a | n/a |
9 | STAT3 | chr1:166572517-166572925 | MCF10A-Er-Src | breast: | n/a | n/a |
10 | NR2F2 | chr1:166572252-166572952 | MCF-7 | breast: | n/a | n/a |
11 | EGR1 | chr1:166572440-166572910 | MCF-7 | breast: | n/a | n/a |
12 | MYC | chr1:166572489-166572882 | MCF10A-Er-Src | breast: | n/a | n/a |
13 | ELF1 | chr1:166572385-166572898 | MCF-7 | breast: | n/a | n/a |
14 | STAT3 | chr1:166572591-166572847 | MCF10A-Er-Src | breast: | n/a | n/a |
15 | STAT3 | chr1:166572586-166572856 | MCF10A-Er-Src | breast: | n/a | n/a |
16 | FOSL2 | chr1:166572419-166572885 | MCF-7 | breast: | n/a | n/a |
17 | JUND | chr1:166572494-166572897 | MCF-7 | breast: | n/a | n/a |
18 | MAX | chr1:166572461-166572928 | MCF-7 | breast: | n/a | n/a |
19 | NR2F2 | chr1:166572279-166572919 | MCF-7 | breast: | n/a | n/a |
20 | CEBPB | chr1:166572416-166572866 | MCF-7 | breast: | n/a | chr1:166572450-166572463 chr1:166572452-166572463 chr1:166572452-166572463 |
21 | GATA3 | chr1:166572218-166573079 | MCF-7 | breast: | n/a | chr1:166572492-166572508 chr1:166572554-166572567 |
22 | SIN3AK20 | chr1:166572238-166572892 | MCF-7 | breast: | n/a | n/a |
23 | SIN3AK20 | chr1:166572292-166573142 | MCF-7 | breast: | n/a | n/a |
24 | REST | chr1:166572397-166572856 | MCF-7 | breast: | n/a | n/a |
25 | FOS | chr1:166572442-166572950 | MCF10A-Er-Src | breast: | n/a | n/a |
26 | REST | chr1:166572568-166572889 | MCF-7 | breast: | n/a | n/a |
27 | HDAC2 | chr1:166572488-166572888 | MCF-7 | breast: | n/a | n/a |
28 | GATA3 | chr1:166572380-166572748 | MCF-7 | breast: | n/a | chr1:166572492-166572508 chr1:166572554-166572567 |
29 | MYC | chr1:166572547-166572745 | MCF10A-Er-Src | breast: | n/a | n/a |
30 | JUND | chr1:166572383-166572896 | MCF-7 | breast: | n/a | n/a |
31 | CEBPB | chr1:166572326-166572939 | MCF-7 | breast: | n/a | chr1:166572450-166572463 chr1:166572452-166572463 chr1:166572452-166572463 |
32 | STAT3 | chr1:166572549-166572865 | MCF10A-Er-Src | breast: | n/a | n/a |
33 | E2F4 | chr1:166572547-166572893 | MCF10A-Er-Src | breast: | n/a | n/a |
34 | STAT3 | chr1:166572596-166572745 | MCF10A-Er-Src | breast: | n/a | n/a |
35 | ZNF217 | chr1:166572380-166573223 | MCF-7 | breast: | n/a | n/a |
36 | FOSL2 | chr1:166572389-166572887 | MCF-7 | breast: | n/a | n/a |
37 | EGR1 | chr1:166572326-166572860 | MCF-7 | breast: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:166572716-166572766 | T-47D | breast: | n/a |
2 | chr1:166572716-166572766 | PFSK-1 | brain: | n/a |
3 | chr1:166572716-166572766 | Hepatocyte | liver: | n/a |
4 | chr1:166572716-166572766 | HepG2 | liver: | n/a |
5 | chr1:166572716-166572766 | HEEpiC | esophagus: | n/a |
6 | chr1:166572716-166572766 | NHDF-neo | bronchial: | n/a |
7 | chr1:166572716-166572766 | LNCaP | prostate: | n/a |
8 | chr1:166572716-166572766 | SK-N-MC | brain: | n/a |
9 | chr1:166572716-166572766 | HRCEpiC | kidney: | n/a |
10 | chr1:166572716-166572766 | Jurkat | blood: | n/a |
11 | chr1:166572716-166572766 | ECC-1 | luminal epithelium: | n/a |
12 | chr1:166572716-166572766 | HIPEpiC | eye: | n/a |
13 | chr1:166572716-166572766 | SKMC | muscle: | n/a |
14 | chr1:166572716-166572766 | Caco-2 | colon: | n/a |
15 | chr1:166572716-166572766 | SAEC | small airway: | n/a |
16 | chr1:166572716-166572766 | BJ | skin: | n/a |
17 | chr1:166572716-166572766 | SK-N-SH | brain: | n/a |
18 | chr1:166572716-166572766 | AG04449 | skin: | fetal |
19 | chr1:166572716-166572766 | AG10803 | skin: | n/a |
20 | chr1:166572716-166572766 | HL-60 | blood: | n/a |
21 | chr1:166572716-166572766 | NH-A | brain: | n/a |
22 | chr1:166572716-166572766 | BE2_C | brain: | n/a |
23 | chr1:166572716-166572766 | NB4 | blood: | n/a |
24 | chr1:166572716-166572766 | HAEpiC | amniotic membrane: | n/a |
25 | chr1:166572716-166572766 | HRPEpiC | eye: | n/a |
26 | chr1:166572716-166572766 | U87 | brain: | n/a |
27 | chr1:166572716-166572766 | CMK | blood: | n/a |
28 | chr1:166572716-166572766 | AoSMC | blood vessel: | n/a |
29 | chr1:166572716-166572766 | K562 | blood: | n/a |
30 | chr1:166572716-166572766 | HMEC | breast: | n/a |
31 | chr1:166572716-166572766 | HPAEpiC | pulmonary alveolar: | n/a |
32 | chr1:166572716-166572766 | GM12892 | blood: | n/a |
33 | chr1:166572716-166572766 | GM06990 | blood: | n/a |
34 | chr1:166572716-166572766 | AG09319 | gingival: | n/a |
35 | chr1:166572716-166572766 | MCF10A-Er-Src | breast: | n/a |
36 | chr1:166572716-166572766 | ProgFib | skin: | n/a |
37 | chr1:166572716-166572766 | RPTEC | kidney: | n/a |
38 | chr1:166572716-166572766 | H1-hESC | embryonic stem cell: | embryo |
39 | chr1:166572716-166572766 | PANC-1 | pancreas: | n/a |
40 | chr1:166572716-166572766 | AG09309 | skin: | n/a |
41 | chr1:166572716-166572766 | ovcar-3 | ovarian: | n/a |
42 | chr1:166572716-166572766 | GM19239 | blood: | n/a |
43 | chr1:166572716-166572766 | HEK293 | kidney: | embryo |
44 | chr1:166572716-166572766 | GM12878 | blood: | n/a |
45 | chr1:166572716-166572766 | NHBE | bronchial: | n/a |
46 | chr1:166572716-166572766 | HCF | heart: | n/a |
47 | chr1:166572716-166572766 | HCPEpiC | choroid plexus: | n/a |
48 | chr1:166572716-166572766 | MCF-7 | breast: | n/a |
49 | chr1:166572716-166572766 | HRE | kidney: | n/a |
50 | chr1:166572716-166572766 | AG04450 | lung: | fetal |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
FMO9P | TF binding region |
FMO9P | CpG island |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv916491 | chr1:166000783-166948513 | Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
2 | esv2757759 | chr1:166491879-166650985 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | esv2758975 | chr1:166491879-166650985 | ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv872511 | chr1:166505186-166590046 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | nsv872512 | chr1:166532565-166581706 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
6 | nsv872513 | chr1:166532565-166590046 | Weak transcription Enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
7 | nsv872514 | chr1:166532565-166595209 | Weak transcription Enhancers Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
8 | nsv872515 | chr1:166532565-166595692 | Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
9 | nsv872516 | chr1:166536198-166590046 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
10 | nsv872517 | chr1:166539001-166590046 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
11 | esv2756869 | chr1:166543542-166601778 | Enhancers Weak transcription Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
12 | nsv872519 | chr1:166545275-166616786 | Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
13 | nsv872518 | chr1:166545275-166623180 | Weak transcription Enhancers Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
14 | esv34401 | chr1:166546342-166617601 | Enhancers Flanking Active TSS Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
15 | nsv872520 | chr1:166546851-166590046 | Weak transcription Enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
16 | nsv872521 | chr1:166568908-166593683 | Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
17 | nsv872522 | chr1:166571770-166593683 | Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:166571400-166574400 | Weak transcription | K562 | blood |
2 | chr1:166572400-166572800 | Enhancers | HMEC | breast |