Variant report

Variant	rs6701819
Chromosome Location	chr1:151541162-151541163
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:151482728..151486205-chr1:151540004..151544693,5	MCF-7	breast:
2	chr1:151538923..151541258-chr1:151872642..151874684,2	K562	blood:
3	chr1:151526616..151529320-chr1:151540801..151542682,2	MCF-7	breast:
4	chr1:151428600..151431654-chr1:151540611..151542217,3	MCF-7	breast:
5	chr1:151511950..151514146-chr1:151540485..151542423,2	MCF-7	breast:
6	chr1:151540484..151542860-chr1:151546818..151548619,2	MCF-7	breast:
7	chr1:151415037..151418672-chr1:151540855..151543962,3	MCF-7	breast:
8	chr1:151534117..151538483-chr1:151538584..151542578,5	MCF-7	breast:
9	chr1:151535253..151539972-chr1:151541025..151545495,6	MCF-7	breast:
10	chr1:151520214..151522047-chr1:151540698..151542766,2	MCF-7	breast:
11	chr1:151539929..151545457-chr1:151553538..151558687,9	MCF-7	breast:
12	chr1:151522558..151525413-chr1:151540386..151543231,3	MCF-7	breast:
13	chr1:151510961..151514204-chr1:151540033..151544637,10	MCF-7	breast:
14	chr1:151514171..151515908-chr1:151540816..151544051,3	MCF-7	breast:
15	chr1:151539778..151542331-chr1:151689893..151691713,2	MCF-7	breast:
16	chr1:151539684..151544323-chr1:151552691..151557234,8	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000232536	Chromatin interaction
ENSG00000143367	Chromatin interaction
ENSG00000143375	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10888422	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1196359	0.82[EUR][1000 genomes]
rs1196361	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1196362	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12749	0.90[MEX][hapmap]
rs1539492	1.00[CHB][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1781415	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2337363	0.87[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4394658	1.00[CHB][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4970920	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6660238	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6683478	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6702889	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916272	chr1:150961809-151557253	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
2	nsv997511	chr1:151491765-151595902	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151514400-151556800	Weak transcription	Fetal Brain Male	brain
2	chr1:151520600-151542000	Weak transcription	Right Ventricle	heart
3	chr1:151520600-151545200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:151521800-151541800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:151521800-151559000	Weak transcription	Small Intestine	intestine
6	chr1:151531800-151542200	Strong transcription	HSMM	muscle
7	chr1:151532000-151542200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:151532200-151546400	Weak transcription	Spleen	Spleen
9	chr1:151532600-151551200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr1:151533000-151557200	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr1:151533600-151541600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr1:151533800-151541400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr1:151533800-151561600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr1:151534200-151542000	Strong transcription	Fetal Intestine Large	intestine
15	chr1:151534200-151542200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:151534200-151542400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr1:151534200-151549400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr1:151534200-151550200	Strong transcription	Stomach Smooth Muscle	stomach
19	chr1:151535000-151547000	Strong transcription	HSMMtube	muscle
20	chr1:151535200-151541800	Weak transcription	NHDF-Ad	bronchial
21	chr1:151535600-151547000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr1:151535800-151561800	Weak transcription	Brain Substantia Nigra	brain
23	chr1:151536000-151544600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:151536000-151546800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:151536000-151547000	Strong transcription	Placenta	Placenta
26	chr1:151536400-151546000	Strong transcription	Placenta Amnion	Placenta Amnion
27	chr1:151537000-151542000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:151537000-151556800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr1:151537400-151541400	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr1:151537400-151556000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr1:151537400-151558400	Weak transcription	Fetal Kidney	kidney
32	chr1:151537600-151542200	Weak transcription	Brain Cingulate Gyrus	brain
33	chr1:151537600-151546800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr1:151537800-151541600	Weak transcription	Colonic Mucosa	Colon
35	chr1:151537800-151541800	Weak transcription	NHLF	lung
36	chr1:151538000-151546400	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr1:151538000-151557400	Weak transcription	Brain Hippocampus Middle	brain
38	chr1:151538200-151541200	Weak transcription	Aorta	Aorta
39	chr1:151538200-151541400	Weak transcription	Ovary	ovary
40	chr1:151538200-151541600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:151538200-151543800	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr1:151538200-151545200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr1:151538400-151541800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr1:151538600-151546800	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr1:151538800-151541600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr1:151538800-151544800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr1:151538800-151548800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
48	chr1:151539000-151541200	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr1:151539000-151541200	Weak transcription	Gastric	stomach
50	chr1:151539000-151541200	Weak transcription	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links