Variant report

Variant	rs10273005
Chromosome Location	chr7:140274858-140274859
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10227869	1.00[AMR][1000 genomes]
rs10242266	0.89[AFR][1000 genomes]
rs10245737	0.89[AFR][1000 genomes]
rs10255623	1.00[AMR][1000 genomes]
rs11983453	1.00[AMR][1000 genomes]
rs55816014	1.00[AMR][1000 genomes]
rs56711326	1.00[AMR][1000 genomes]
rs59489402	1.00[AMR][1000 genomes]
rs6951766	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6972562	1.00[AMR][1000 genomes]
rs6979290	1.00[AMR][1000 genomes]
rs7780213	1.00[AMR][1000 genomes]
rs7795017	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1802929	chr7:140212566-140285491	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv831157	chr7:140241339-140426876	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1021133	chr7:140270797-140338653	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140247000-140276400	Weak transcription	Duodenum Mucosa	Duodenum
2	chr7:140247000-140297400	Weak transcription	Spleen	Spleen
3	chr7:140261800-140284000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:140263400-140278400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:140263800-140276000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr7:140263800-140277800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr7:140263800-140286800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr7:140263800-140303600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr7:140263800-140303600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr7:140263800-140305200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr7:140263800-140305600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:140264600-140290400	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr7:140265200-140304400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr7:140266200-140275400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:140266400-140285200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr7:140267600-140281000	Strong transcription	Fetal Muscle Leg	muscle
17	chr7:140267800-140275000	Strong transcription	Fetal Stomach	stomach
18	chr7:140267800-140275200	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr7:140267800-140281000	Weak transcription	Brain Angular Gyrus	brain
20	chr7:140267800-140281200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr7:140267800-140283000	Weak transcription	Liver	Liver
22	chr7:140267800-140285000	Weak transcription	Colon Smooth Muscle	Colon
23	chr7:140267800-140285000	Weak transcription	NH-A	brain
24	chr7:140267800-140290600	Weak transcription	Rectal Smooth Muscle	rectum
25	chr7:140267800-140291200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr7:140267800-140300800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr7:140267800-140326000	Weak transcription	Gastric	stomach
28	chr7:140268400-140281000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:140268400-140281000	Strong transcription	Fetal Muscle Trunk	muscle
30	chr7:140268600-140278200	Weak transcription	Fetal Heart	heart
31	chr7:140269400-140282000	Weak transcription	Lung	lung
32	chr7:140269400-140306600	Weak transcription	Right Atrium	heart
33	chr7:140272200-140287000	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr7:140273600-140281400	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr7:140273600-140284200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr7:140273600-140285000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr7:140273800-140277400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:140273800-140280800	Weak transcription	Brain Hippocampus Middle	brain
39	chr7:140273800-140281000	Weak transcription	Brain Cingulate Gyrus	brain
40	chr7:140273800-140281200	Weak transcription	Left Ventricle	heart
41	chr7:140273800-140281400	Weak transcription	Brain Anterior Caudate	brain
42	chr7:140273800-140282200	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr7:140273800-140285800	Weak transcription	Fetal Brain Male	brain
44	chr7:140274000-140281000	Weak transcription	Brain Substantia Nigra	brain
45	chr7:140274000-140281200	Weak transcription	Fetal Brain Female	brain
46	chr7:140274000-140281400	Weak transcription	NHDF-Ad	bronchial
47	chr7:140274000-140284200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:140274000-140284800	Weak transcription	Fetal Kidney	kidney
49	chr7:140274000-140285200	Weak transcription	Fetal Intestine Large	intestine
50	chr7:140274000-140301400	Weak transcription	Right Ventricle	heart

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