Variant report

Variant	rs10737319
Chromosome Location	chr1:171471672-171471673
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:171471248..171472959-chr1:171477758..171480196,2	MCF-7	breast:
2	chr1:171454829..171458429-chr1:171468344..171472224,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000117523	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs1980512	0.83[AMR][1000 genomes]
rs2207191	0.80[AMR][1000 genomes]
rs4916395	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6661903	0.91[AMR][1000 genomes]
rs7543159	0.94[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv14617	chr1:171016086-171726961	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv3512995	chr1:171329123-171994470	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers 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 miRNA target site	56 gene(s)	inside rSNPs	diseases
3	esv3512997	chr1:171329123-171994470	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	nsv465639	chr1:171459507-171545051	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv548190	chr1:171459507-171545051	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171456000-171481800	Weak transcription	Placenta	Placenta
2	chr1:171456200-171475000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:171456400-171473000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr1:171456400-171481800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr1:171456400-171483600	Weak transcription	Fetal Intestine Large	intestine
6	chr1:171456800-171474800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr1:171457800-171482000	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr1:171457800-171482200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr1:171459000-171482000	Weak transcription	HMEC	breast
10	chr1:171460400-171471800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr1:171460800-171481400	Weak transcription	HSMM	muscle
12	chr1:171462600-171478000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:171462600-171482400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:171463000-171483200	Weak transcription	Fetal Muscle Leg	muscle
15	chr1:171464000-171475200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr1:171464000-171483200	Weak transcription	Esophagus	oesophagus
17	chr1:171464200-171474600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:171464200-171476000	Weak transcription	NHDF-Ad	bronchial
19	chr1:171464200-171476800	Weak transcription	Brain Angular Gyrus	brain
20	chr1:171464200-171481600	Weak transcription	NHEK	skin
21	chr1:171464400-171475400	Weak transcription	NH-A	brain
22	chr1:171465000-171473400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:171465000-171475000	Weak transcription	Rectal Smooth Muscle	rectum
24	chr1:171465000-171476200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:171465200-171472400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:171465200-171475200	Weak transcription	Osteobl	bone
27	chr1:171465200-171475400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:171465200-171481800	Weak transcription	HUVEC	blood vessel
29	chr1:171465200-171482200	Weak transcription	Fetal Lung	lung
30	chr1:171465200-171483200	Weak transcription	NHLF	lung
31	chr1:171465200-171483600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr1:171466200-171475000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr1:171466200-171475600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr1:171466400-171475600	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr1:171466800-171476200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:171467000-171471800	Weak transcription	Lung	lung
37	chr1:171467600-171472000	Weak transcription	Aorta	Aorta
38	chr1:171467600-171472200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
39	chr1:171467800-171472200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:171468000-171471800	Strong transcription	Primary T cells from cord blood	blood
41	chr1:171468000-171482200	Weak transcription	Hela-S3	cervix
42	chr1:171468200-171475400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:171468200-171475600	Weak transcription	A549	lung
44	chr1:171468400-171471800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr1:171468400-171471800	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr1:171468400-171474200	Weak transcription	Psoas Muscle	Psoas
47	chr1:171468400-171483200	Weak transcription	Fetal Muscle Trunk	muscle
48	chr1:171468600-171471800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr1:171468800-171483600	Weak transcription	Gastric	stomach
50	chr1:171469000-171483600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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