Variant report

Variant	rs3735355
Chromosome Location	chr7:139657328-139657329
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs917147	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020234	chr7:139377822-139661964	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1032711	chr7:139411404-139684043	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1018712	chr7:139429703-139658014	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv831156	chr7:139532318-139694326	Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1019001	chr7:139558216-139841268	Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv1029099	chr7:139558216-139869148	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:139646800-139658600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr7:139647000-139660600	Weak transcription	K562	blood
3	chr7:139649800-139658400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:139651400-139662400	Weak transcription	Pancreas	Pancrea
5	chr7:139651400-139670000	Weak transcription	Gastric	stomach
6	chr7:139652000-139668400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr7:139652200-139691600	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr7:139652800-139668000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:139653000-139678200	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr7:139653200-139658000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:139653200-139672200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:139653200-139678000	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr7:139653400-139659800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr7:139653400-139676000	Weak transcription	Adipose Nuclei	Adipose
15	chr7:139653600-139661600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr7:139653800-139657800	Weak transcription	Primary T cells from cord blood	blood
17	chr7:139654600-139677600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr7:139655000-139657800	Weak transcription	Fetal Kidney	kidney
19	chr7:139655000-139660400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr7:139655000-139667800	Weak transcription	Colonic Mucosa	Colon
21	chr7:139655000-139677800	Weak transcription	Primary B cells from cord blood	blood
22	chr7:139655200-139658200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr7:139655200-139660200	Strong transcription	Spleen	Spleen
24	chr7:139656000-139659000	Strong transcription	Fetal Thymus	thymus
25	chr7:139656200-139658000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr7:139656400-139657400	Strong transcription	Lung	lung
27	chr7:139656400-139660400	Strong transcription	Primary hematopoietic stem cells	blood
28	chr7:139656600-139657600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr7:139656800-139657600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr7:139656800-139658000	Strong transcription	Thymus	Thymus
31	chr7:139656800-139660200	Enhancers	Fetal Stomach	stomach
32	chr7:139657000-139657600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr7:139657000-139658400	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr7:139657200-139657800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr7:139657200-139658000	Flanking Active TSS	Brain Germinal Matrix	brain
36	chr7:139657200-139658400	Enhancers	HUES48 Cell Line	embryonic stem cell

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