Variant report

Variant	rs7148637
Chromosome Location	chr14:64665060-64665061
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	REST	chr14:64662665-64665717	H1-neurons	neurons:	n/a	chr14:64663684-64663704 chr14:64663869-64663878 chr14:64663684-64663704 chr14:64663684-64663704 chr14:64663726-64663739

No.	Distal block	Cell Line	Cell type
1	chr14:64664909..64666611-chr14:64732886..64734717,2	MCF-7	breast:
2	chr14:64662559..64666637-chr14:64681435..64684914,4	MCF-7	breast:
3	chr14:64660992..64662814-chr14:64664224..64665884,2	MCF-7	breast:
4	chr14:64657113..64659774-chr14:64664998..64667785,2	MCF-7	breast:

Variant related genes	Relation type
SYNE2	TF binding region
ENSG00000054654	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10162323	0.83[CEU][hapmap];0.84[EUR][1000 genomes]
rs12435376	0.83[CEU][hapmap];0.84[GIH][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs17101765	0.80[MEX][hapmap]
rs17179404	0.86[CEU][hapmap]
rs1953234	0.80[EUR][1000 genomes]
rs2027094	0.86[EUR][1000 genomes]
rs2256191	0.84[GIH][hapmap];0.87[TSI][hapmap]
rs2772163	0.80[MEX][hapmap]
rs2776607	0.83[EUR][1000 genomes]
rs2781379	0.83[EUR][1000 genomes]
rs2781380	0.83[EUR][1000 genomes]
rs3020444	0.80[MEX][hapmap]
rs3020450	0.86[MEX][hapmap]
rs6573547	0.84[GIH][hapmap];0.91[TSI][hapmap];0.85[EUR][1000 genomes]
rs6573548	0.83[CEU][hapmap];0.84[GIH][hapmap];0.91[TSI][hapmap];0.84[EUR][1000 genomes]
rs7148072	0.83[CEU][hapmap];0.84[GIH][hapmap];0.91[TSI][hapmap];0.83[EUR][1000 genomes]
rs7154455	0.81[CEU][hapmap];0.87[MEX][hapmap]
rs8006145	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902019	chr14:64395569-64882380	Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv456326	chr14:64420413-64754361	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv564905	chr14:64420413-64754361	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv902021	chr14:64647646-64715794	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs7148637	ESR2	Cis_1M	lymphoblastoid	RTeQTL
rs7148637	KCNH5	cis	parietal	SCAN
rs7148637	MTHFD1	cis	cerebellum	SCAN
rs7148637	MTHFD1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64600600-64667400	Weak transcription	Stomach Mucosa	stomach
2	chr14:64650800-64671800	Strong transcription	Liver	Liver
3	chr14:64652800-64666200	Strong transcription	Dnd41	blood
4	chr14:64658200-64667000	Weak transcription	Esophagus	oesophagus
5	chr14:64660600-64665200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr14:64660800-64682600	Weak transcription	Hela-S3	cervix
7	chr14:64661600-64667000	Weak transcription	HepG2	liver
8	chr14:64661600-64675000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr14:64661600-64675000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:64661800-64675400	Weak transcription	NHEK	skin
11	chr14:64661800-64675600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr14:64662400-64675200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr14:64662600-64665400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr14:64662800-64665600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr14:64662800-64667400	Weak transcription	Lung	lung
16	chr14:64662800-64674800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr14:64663200-64665200	Active TSS	Brain Angular Gyrus	brain
18	chr14:64663200-64665400	Active TSS	Brain Anterior Caudate	brain
19	chr14:64663200-64667400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr14:64663800-64665400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr14:64663800-64668600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr14:64664000-64665200	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr14:64664000-64665800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr14:64664000-64665800	Weak transcription	Gastric	stomach
25	chr14:64664000-64667000	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr14:64664000-64667000	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr14:64664000-64667200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr14:64664000-64667400	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr14:64664000-64668000	Weak transcription	Spleen	Spleen
30	chr14:64664000-64699600	Weak transcription	Small Intestine	intestine
31	chr14:64664200-64665200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:64664200-64665200	Weak transcription	Pancreas	Pancrea
33	chr14:64664200-64665200	Weak transcription	Right Ventricle	heart
34	chr14:64664200-64665200	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr14:64664200-64665400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr14:64664200-64665400	Weak transcription	Psoas Muscle	Psoas
37	chr14:64664200-64665600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr14:64664200-64666200	Enhancers	Fetal Thymus	thymus
39	chr14:64664200-64666400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr14:64664200-64666600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr14:64664200-64666600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr14:64664200-64666600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr14:64664200-64666600	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr14:64664200-64666600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr14:64664200-64666600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr14:64664200-64666600	Weak transcription	Fetal Intestine Small	intestine
47	chr14:64664200-64666600	Weak transcription	Placenta	Placenta
48	chr14:64664200-64666800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr14:64664200-64666800	Weak transcription	Fetal Stomach	stomach
50	chr14:64664200-64666800	Weak transcription	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links