Variant report
Variant | rs11849999 |
---|---|
Chromosome Location | chr14:37731443-37731444 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:5 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr14:37724973..37727829-chr14:37731230..37733021,2 | MCF-7 | breast: | |
2 | chr14:37730985..37733871-chr14:37737549..37739404,2 | MCF-7 | breast: | |
3 | chr14:37708906..37733371-chr14:38048131..38068843,170 | MCF-7 | breast: | |
4 | chr14:37729939..37731852-chr14:37742042..37744319,2 | K562 | blood: | |
5 | chr14:37723534..37725938-chr14:37730959..37732560,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000139865 | Chromatin interaction |
ENSG00000129514 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1005539 | 1.00[EUR][1000 genomes] |
rs1005540 | 1.00[EUR][1000 genomes] |
rs10129341 | 1.00[EUR][1000 genomes] |
rs10132652 | 1.00[EUR][1000 genomes] |
rs10132727 | 1.00[EUR][1000 genomes] |
rs10134672 | 1.00[EUR][1000 genomes] |
rs10135014 | 1.00[EUR][1000 genomes] |
rs10136240 | 1.00[EUR][1000 genomes] |
rs10137554 | 1.00[EUR][1000 genomes] |
rs10141822 | 1.00[EUR][1000 genomes] |
rs10144237 | 1.00[EUR][1000 genomes] |
rs10144304 | 1.00[EUR][1000 genomes] |
rs10145246 | 1.00[EUR][1000 genomes] |
rs10146919 | 1.00[EUR][1000 genomes] |
rs1014880 | 1.00[EUR][1000 genomes] |
rs10150559 | 1.00[EUR][1000 genomes] |
rs10782386 | 1.00[EUR][1000 genomes] |
rs11845464 | 0.87[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs11846576 | 0.87[EUR][1000 genomes] |
rs11848827 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11851719 | 0.81[AFR][1000 genomes] |
rs12434053 | 1.00[EUR][1000 genomes] |
rs12437318 | 1.00[EUR][1000 genomes] |
rs12586942 | 1.00[EUR][1000 genomes] |
rs12717263 | 1.00[EUR][1000 genomes] |
rs1474887 | 1.00[EUR][1000 genomes] |
rs1474888 | 1.00[EUR][1000 genomes] |
rs1546973 | 1.00[EUR][1000 genomes] |
rs1950518 | 1.00[EUR][1000 genomes] |
rs1950525 | 1.00[EUR][1000 genomes] |
rs1950528 | 1.00[EUR][1000 genomes] |
rs1950535 | 1.00[EUR][1000 genomes] |
rs1955932 | 1.00[EUR][1000 genomes] |
rs1955933 | 1.00[EUR][1000 genomes] |
rs1955935 | 1.00[EUR][1000 genomes] |
rs1955937 | 1.00[EUR][1000 genomes] |
rs1955953 | 1.00[EUR][1000 genomes] |
rs1955954 | 1.00[EUR][1000 genomes] |
rs1955956 | 1.00[EUR][1000 genomes] |
rs1956517 | 1.00[EUR][1000 genomes] |
rs1998019 | 1.00[EUR][1000 genomes] |
rs2144582 | 1.00[EUR][1000 genomes] |
rs2180252 | 1.00[EUR][1000 genomes] |
rs2180253 | 1.00[EUR][1000 genomes] |
rs2207861 | 1.00[EUR][1000 genomes] |
rs2207863 | 1.00[EUR][1000 genomes] |
rs2224155 | 1.00[EUR][1000 genomes] |
rs2224157 | 1.00[EUR][1000 genomes] |
rs2415390 | 0.87[EUR][1000 genomes] |
rs2415392 | 1.00[EUR][1000 genomes] |
rs2415394 | 1.00[EUR][1000 genomes] |
rs2415395 | 1.00[EUR][1000 genomes] |
rs2899856 | 1.00[EUR][1000 genomes] |
rs2899858 | 1.00[EUR][1000 genomes] |
rs34172996 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs41307090 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4522332 | 1.00[EUR][1000 genomes] |
rs4898593 | 1.00[EUR][1000 genomes] |
rs4900779 | 1.00[EUR][1000 genomes] |
rs4900823 | 1.00[EUR][1000 genomes] |
rs4900834 | 1.00[EUR][1000 genomes] |
rs57167835 | 0.87[EUR][1000 genomes] |
rs57900485 | 0.87[EUR][1000 genomes] |
rs58520096 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59258105 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59542560 | 0.87[EUR][1000 genomes] |
rs59544181 | 0.87[EUR][1000 genomes] |
rs60287404 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6571804 | 1.00[EUR][1000 genomes] |
rs6571805 | 1.00[EUR][1000 genomes] |
rs6571809 | 1.00[EUR][1000 genomes] |
rs7142072 | 1.00[EUR][1000 genomes] |
rs7142933 | 1.00[EUR][1000 genomes] |
rs7143412 | 1.00[EUR][1000 genomes] |
rs7146631 | 1.00[EUR][1000 genomes] |
rs7150214 | 1.00[EUR][1000 genomes] |
rs7150986 | 0.87[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs7154479 | 1.00[EUR][1000 genomes] |
rs7154977 | 1.00[EUR][1000 genomes] |
rs7157931 | 1.00[EUR][1000 genomes] |
rs7158473 | 1.00[EUR][1000 genomes] |
rs7160824 | 1.00[EUR][1000 genomes] |
rs7161464 | 1.00[EUR][1000 genomes] |
rs719135 | 1.00[EUR][1000 genomes] |
rs8013329 | 1.00[EUR][1000 genomes] |
rs8014311 | 1.00[EUR][1000 genomes] |
rs8015886 | 1.00[EUR][1000 genomes] |
rs8016309 | 1.00[EUR][1000 genomes] |
rs8019167 | 1.00[EUR][1000 genomes] |
rs8019673 | 1.00[EUR][1000 genomes] |
rs8020631 | 1.00[EUR][1000 genomes] |
rs8022961 | 1.00[EUR][1000 genomes] |
rs987859 | 1.00[EUR][1000 genomes] |
rs9989228 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530038 | chr14:37590543-38336191 | Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 58 gene(s) | inside rSNPs | diseases |
2 | nsv915783 | chr14:37607836-38002966 | Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
3 | nsv1036854 | chr14:37609535-38013533 | Active TSS ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
4 | nsv542045 | chr14:37609535-38013533 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
5 | nsv901635 | chr14:37623177-37782273 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
6 | esv3528451 | chr14:37631483-37771365 | Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
7 | esv3527359 | chr14:37631504-37771435 | Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
8 | esv3370191 | chr14:37631508-37771354 | Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
9 | esv3527360 | chr14:37631521-37771311 | Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
10 | esv3528462 | chr14:37631535-37771345 | Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
11 | esv3528473 | chr14:37631543-37771255 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
12 | esv3527361 | chr14:37631554-37771408 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
13 | esv3528484 | chr14:37631599-37771228 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
14 | esv3527363 | chr14:37631608-37771230 | Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
15 | nsv901636 | chr14:37702799-37736054 | Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS | TF binding regionChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
16 | nsv901637 | chr14:37702799-37743583 | Active TSS Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
17 | nsv901638 | chr14:37702799-37814824 | Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:37694800-37756400 | Weak transcription | Aorta | Aorta |
2 | chr14:37716000-37732800 | Weak transcription | Fetal Lung | lung |
3 | chr14:37716000-37770600 | Weak transcription | A549 | lung |
4 | chr14:37717800-37738600 | Weak transcription | Fetal Intestine Small | intestine |
5 | chr14:37718000-37737600 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
6 | chr14:37724000-37737400 | Weak transcription | HUVEC | blood vessel |
7 | chr14:37724600-37731800 | Weak transcription | HepG2 | liver |
8 | chr14:37726800-37740000 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
9 | chr14:37727000-37740400 | Weak transcription | HSMMtube | muscle |
10 | chr14:37727400-37731600 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
11 | chr14:37730000-37735400 | Weak transcription | Stomach Mucosa | stomach |
12 | chr14:37730800-37732400 | Enhancers | Pancreatic Islets | Pancreatic Islet |
13 | chr14:37731000-37732000 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
14 | chr14:37731200-37732200 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
15 | chr14:37731200-37732400 | Weak transcription | Liver | Liver |
16 | chr14:37731200-37734000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |