Variant report

Variant	rs4915378
Chromosome Location	chr1:197161212-197161213
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:197159273..197161304-chr1:197164955..197167252,3	K562	blood:
2	chr1:197160099..197163590-chr1:197167883..197170766,5	MCF-7	breast:
3	chr1:197148315..197153030-chr1:197158427..197161690,6	K562	blood:
4	chr1:197158202..197161289-chr1:197163593..197166561,4	MCF-7	breast:
5	chr1:197108980..197111975-chr1:197160260..197161833,2	K562	blood:

Variant related genes	Relation type
ENSG00000134376	Chromatin interaction
ENSG00000177888	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs1034162	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10429911	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10494748	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10494749	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10494750	1.00[CHB][hapmap]
rs10732295	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.80[MKK][hapmap];0.87[YRI][hapmap];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10732296	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10754219	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs10801593	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10801594	1.00[CHB][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11801772	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11808524	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11808883	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11811295	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12092294	1.00[GIH][hapmap]
rs12677	1.00[GIH][hapmap];0.83[YRI][hapmap]
rs1332663	0.83[ASW][hapmap];1.00[GIH][hapmap];0.83[YRI][hapmap]
rs1412631	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs1412632	0.83[ASW][hapmap];1.00[GIH][hapmap];0.87[LWK][hapmap];0.93[MKK][hapmap];0.83[YRI][hapmap]
rs1415217	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1556763	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1571964	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs16841212	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16841214	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16841219	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16841220	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16841237	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1759013	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1764629	0.83[EUR][1000 genomes]
rs1764800	1.00[CEU][hapmap]
rs1794003	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1888991	1.00[GIH][hapmap]
rs2026429	0.83[ASW][hapmap];1.00[GIH][hapmap];0.87[LWK][hapmap];0.93[MKK][hapmap];0.83[YRI][hapmap]
rs2151134	1.00[CEU][hapmap]
rs4244141	0.97[EUR][1000 genomes]
rs4342879	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs4350226	1.00[CEU][hapmap]
rs476390	1.00[CEU][hapmap]
rs4915337	0.83[YRI][hapmap]
rs4915379	1.00[CEU][hapmap];0.95[GIH][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs5029273	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs510135	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs518149	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs615647	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs616675	1.00[CEU][hapmap]
rs6428390	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6656448	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs6656858	0.83[ASW][hapmap];1.00[GIH][hapmap];0.87[LWK][hapmap];0.93[MKK][hapmap];0.83[YRI][hapmap]
rs6677082	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs6701681	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6702739	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6703400	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs7513826	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7520503	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7523013	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7534439	1.00[JPT][hapmap]
rs7535048	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7542397	0.82[YRI][hapmap]
rs7554802	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7554890	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7554995	1.00[EUR][1000 genomes]
rs877897	0.83[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv528460	chr1:196542567-197446702	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2758990	chr1:196590837-197169772	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv427897	chr1:196590837-197169772	Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	esv2757767	chr1:196977799-197169772	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv873070	chr1:197079671-197165014	Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv873071	chr1:197079671-197187605	Active TSS Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv873072	chr1:197079671-197221248	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
8	nsv548871	chr1:197106604-197168233	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
9	nsv873073	chr1:197107074-197221248	Flanking Active TSS Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
10	nsv947366	chr1:197157398-197163669	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197116600-197169800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:197125400-197168400	Weak transcription	Psoas Muscle	Psoas
3	chr1:197125600-197169600	Weak transcription	Esophagus	oesophagus
4	chr1:197126400-197169600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:197135200-197161800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:197136000-197161600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr1:197141400-197166200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr1:197143200-197165800	Weak transcription	Small Intestine	intestine
9	chr1:197149800-197165400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr1:197152400-197168600	Weak transcription	Stomach Mucosa	stomach
11	chr1:197152800-197161600	Strong transcription	HSMM	muscle
12	chr1:197153200-197165000	Weak transcription	Fetal Heart	heart
13	chr1:197154200-197161400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:197154800-197163400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:197155400-197163600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr1:197156400-197164400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr1:197156600-197164000	Weak transcription	Hela-S3	cervix
18	chr1:197157200-197164000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:197157200-197165600	Weak transcription	Aorta	Aorta
20	chr1:197157200-197166800	Weak transcription	NHEK	skin
21	chr1:197157400-197162200	Weak transcription	Fetal Brain Male	brain
22	chr1:197157400-197162800	Weak transcription	Ovary	ovary
23	chr1:197157400-197164000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr1:197157400-197164000	Weak transcription	Colon Smooth Muscle	Colon
25	chr1:197157400-197164000	Weak transcription	GM12878-XiMat	blood
26	chr1:197157400-197164200	Weak transcription	Brain Angular Gyrus	brain
27	chr1:197157400-197166800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:197157400-197166800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:197157400-197166800	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr1:197157400-197166800	Weak transcription	Rectal Smooth Muscle	rectum
31	chr1:197157400-197166800	Weak transcription	Right Ventricle	heart
32	chr1:197157400-197166800	Weak transcription	Thymus	Thymus
33	chr1:197157400-197166800	Weak transcription	HSMMtube	muscle
34	chr1:197157400-197166800	Weak transcription	NHLF	lung
35	chr1:197157400-197167000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr1:197157400-197168400	Weak transcription	Left Ventricle	heart
37	chr1:197157400-197169400	Weak transcription	Colonic Mucosa	Colon
38	chr1:197157400-197169600	Weak transcription	Pancreas	Pancrea
39	chr1:197157600-197162200	Weak transcription	K562	blood
40	chr1:197157600-197164000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr1:197157600-197165000	Weak transcription	Brain Hippocampus Middle	brain
42	chr1:197157600-197165000	Weak transcription	Brain Substantia Nigra	brain
43	chr1:197157600-197167000	Weak transcription	HMEC	breast
44	chr1:197157600-197167000	Weak transcription	HUVEC	blood vessel
45	chr1:197157600-197167600	Weak transcription	Primary hematopoietic stem cells	blood
46	chr1:197157800-197165600	Weak transcription	HepG2	liver
47	chr1:197158000-197164600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr1:197158200-197163400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr1:197158200-197165800	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr1:197158400-197164400	Weak transcription	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links