Variant report

Variant	rs6937379
Chromosome Location	chr6:15525997-15525998
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:15513759..15516208-chr6:15524311..15526503,2	K562	blood:
2	chr6:15522144..15525319-chr6:15525407..15528669,4	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11756738	0.88[CEU][hapmap]
rs13192791	0.80[EUR][1000 genomes]
rs13195001	0.83[CEU][hapmap]
rs13212086	0.81[EUR][1000 genomes]
rs1988856	0.84[EUR][1000 genomes]
rs2056942	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2619531	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6903266	0.87[CEU][hapmap];0.92[YRI][hapmap];0.82[AMR][1000 genomes]
rs6906100	0.90[EUR][1000 genomes]
rs6918834	0.92[EUR][1000 genomes]
rs71533648	0.81[EUR][1000 genomes]
rs760665	0.87[EUR][1000 genomes]
rs760666	1.00[ASW][hapmap];0.94[CEU][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];0.95[MKK][hapmap];0.85[TSI][hapmap];0.92[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7738263	0.81[EUR][1000 genomes]
rs7745876	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7745907	0.93[AMR][1000 genomes]
rs7758659	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7760564	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7765924	0.82[EUR][1000 genomes]
rs875462	0.94[CEU][hapmap];0.93[GIH][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9296983	1.00[ASW][hapmap];0.94[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.95[MKK][hapmap];0.85[TSI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9296986	0.94[CEU][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9383063	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9396593	0.82[ASW][hapmap];0.93[GIH][hapmap];0.91[MKK][hapmap];0.97[TSI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9464796	0.94[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][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	nsv538140	chr6:15217899-15547127	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS 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	29 gene(s)	inside rSNPs	diseases
2	nsv522265	chr6:15494177-15546213	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv428473	chr6:15522653-15595739	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6937379	MYLIP	cis	cerebellum	SCAN

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15492200-15527000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr6:15492400-15527200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr6:15492800-15527000	Strong transcription	Primary T helper cells PMA-I stimulated	--
4	chr6:15494800-15527000	Strong transcription	Primary B cells from peripheral blood	blood
5	chr6:15495000-15527200	Strong transcription	Dnd41	blood
6	chr6:15495000-15529200	Strong transcription	Primary T cells from cord blood	blood
7	chr6:15496000-15526600	Strong transcription	Primary T helper cells fromperipheralblood	blood
8	chr6:15496000-15528400	Strong transcription	Primary B cells from cord blood	blood
9	chr6:15497400-15526600	Strong transcription	Fetal Intestine Large	intestine
10	chr6:15506000-15527000	Strong transcription	Fetal Intestine Small	intestine
11	chr6:15506600-15527400	Strong transcription	Duodenum Mucosa	Duodenum
12	chr6:15507000-15533200	Weak transcription	HSMM	muscle
13	chr6:15507400-15529400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr6:15509200-15527200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr6:15510000-15526800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:15510800-15527000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:15511600-15528200	Weak transcription	Right Atrium	heart
18	chr6:15512600-15531000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr6:15512600-15536400	Weak transcription	Psoas Muscle	Psoas
20	chr6:15515200-15527000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:15515800-15533600	Strong transcription	Thymus	Thymus
22	chr6:15517400-15527000	Strong transcription	Rectal Mucosa Donor 31	rectum
23	chr6:15518400-15531400	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr6:15519400-15534200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr6:15521800-15526600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:15522200-15527000	Strong transcription	Aorta	Aorta
27	chr6:15522600-15526800	Strong transcription	Fetal Muscle Trunk	muscle
28	chr6:15522800-15526800	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr6:15523000-15527200	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr6:15523000-15533800	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr6:15523200-15527000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
32	chr6:15523400-15526600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:15523400-15526800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr6:15523400-15527000	Strong transcription	Fetal Muscle Leg	muscle
35	chr6:15523400-15528000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:15523400-15534000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr6:15523400-15534400	Weak transcription	HUVEC	blood vessel
38	chr6:15523600-15535800	Weak transcription	Small Intestine	intestine
39	chr6:15523600-15540000	Weak transcription	NHEK	skin
40	chr6:15523800-15533400	Weak transcription	HMEC	breast
41	chr6:15523800-15534200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr6:15524000-15527000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:15524200-15527200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
44	chr6:15524200-15535800	Weak transcription	Stomach Mucosa	stomach
45	chr6:15524400-15526200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr6:15524400-15533800	Weak transcription	NHDF-Ad	bronchial
47	chr6:15524400-15535400	Weak transcription	A549	lung
48	chr6:15524400-15549400	Weak transcription	Hela-S3	cervix
49	chr6:15524600-15526800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr6:15524600-15526800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links