Variant report

Variant	rs6573755
Chromosome Location	chr14:67654476-67654477
allele	G/T
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	NFIC	chr14:67653705-67655047	SK-N-SH	brain:	n/a	n/a
2	FOSL2	chr14:67653792-67654502	A549	lung:	n/a	chr14:67654090-67654101 chr14:67654119-67654130
3	FOSL2	chr14:67653829-67655008	MCF-7	breast:	n/a	chr14:67654776-67654784 chr14:67654090-67654101 chr14:67654119-67654130
4	JUND	chr14:67653977-67654807	MCF-7	breast:	n/a	chr14:67654776-67654784 chr14:67654118-67654129 chr14:67654089-67654100
5	POLR2A	chr14:67654409-67654979	PANC-1	pancreas:	n/a	n/a
6	EP300	chr14:67653773-67654871	SK-N-SH	brain:	n/a	chr14:67653884-67653891
7	NFIC	chr14:67654475-67655007	SK-N-SH	brain:	n/a	n/a
8	TEAD4	chr14:67654474-67655009	ECC-1	luminal epithelium:	n/a	n/a
9	RCOR1	chr14:67653528-67655064	IMR90	lung:	n/a	n/a
10	FOS	chr14:67653651-67655330	MCF10A-Er-Src	breast:	n/a	chr14:67654776-67654784 chr14:67654089-67654100 chr14:67654118-67654129
11	CBX3	chr14:67653814-67654476	HCT-116	colon:	n/a	n/a
12	JUND	chr14:67653510-67655097	HCT-116	colon:	n/a	chr14:67654776-67654784 chr14:67654118-67654129 chr14:67654089-67654100
13	GATA3	chr14:67653821-67655023	MCF-7	breast:	n/a	n/a
14	FOS	chr14:67653536-67655363	MCF10A-Er-Src	breast:	n/a	chr14:67654776-67654784 chr14:67654089-67654100 chr14:67654118-67654129
15	FOSL1	chr14:67653739-67655016	HCT-116	colon:	n/a	chr14:67654776-67654784
16	SP1	chr14:67653752-67655047	HCT-116	colon:	n/a	n/a
17	JUND	chr14:67653377-67654920	SK-N-SH	brain:	n/a	chr14:67654776-67654784 chr14:67654118-67654129 chr14:67654089-67654100
18	NR2F2	chr14:67654396-67654972	MCF-7	breast:	n/a	n/a
19	FOS	chr14:67653639-67654841	MCF10A-Er-Src	breast:	n/a	chr14:67654776-67654784 chr14:67654089-67654100 chr14:67654118-67654129
20	NFIC	chr14:67654472-67654944	ECC-1	luminal epithelium:	n/a	n/a
21	FOSL1	chr14:67653652-67655070	HCT-116	colon:	n/a	chr14:67654776-67654784
22	EP300	chr14:67653839-67654951	ECC-1	luminal epithelium:	n/a	chr14:67653884-67653891
23	TCF7L2	chr14:67653990-67654834	PANC-1	pancreas:	n/a	n/a
24	TCF12	chr14:67653731-67654981	SK-N-SH	brain:	n/a	n/a
25	GATA3	chr14:67654266-67655416	MCF-7	breast:	n/a	n/a
26	FOSL2	chr14:67653809-67654961	SK-N-SH	brain:	n/a	chr14:67654776-67654784 chr14:67654090-67654101 chr14:67654119-67654130
27	SP1	chr14:67653698-67655015	HCT-116	colon:	n/a	n/a
28	STAT3	chr14:67653524-67654765	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr14:67653698-67654930	MCF10A-Er-Src	breast:	n/a	chr14:67654776-67654784 chr14:67654089-67654100 chr14:67654118-67654129
30	NFIC	chr14:67653763-67655076	ECC-1	luminal epithelium:	n/a	n/a
31	JUND	chr14:67653708-67654935	HCT-116	colon:	n/a	chr14:67654776-67654784 chr14:67654118-67654129 chr14:67654089-67654100
32	GATA3	chr14:67653808-67655050	SK-N-SH	brain:	n/a	n/a
33	GATA3	chr14:67653727-67655043	SK-N-SH	brain:	n/a	n/a
34	JUND	chr14:67653861-67654487	MCF-7	breast:	n/a	chr14:67654118-67654129 chr14:67654089-67654100
35	CBX3	chr14:67653506-67655062	HCT-116	colon:	n/a	n/a

Variant related genes	Relation type
FAM71D	TF binding region

Extended variants
information (count: 167 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:160)

rs_ID	r²[population]
rs10129779	0.90[JPT][hapmap]
rs10130796	0.80[ASN][1000 genomes]
rs10131175	0.91[JPT][hapmap]
rs10131212	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs10131242	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10131984	0.89[ASN][1000 genomes]
rs10132088	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10134592	0.97[ASN][1000 genomes]
rs10135100	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10135903	0.91[JPT][hapmap]
rs10136073	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10137557	0.90[JPT][hapmap]
rs10137618	0.82[AMR][1000 genomes]
rs10138631	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10138755	0.89[JPT][hapmap]
rs10138824	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs10138850	0.83[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap];0.92[LWK][hapmap];0.82[MKK][hapmap];0.83[YRI][hapmap];0.93[ASN][1000 genomes]
rs10138865	0.83[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.90[JPT][hapmap];0.89[LWK][hapmap];0.82[YRI][hapmap];0.93[ASN][1000 genomes]
rs10139792	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10140817	0.91[JPT][hapmap]
rs10141815	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10141879	0.85[CHD][hapmap];0.81[JPT][hapmap]
rs10141952	0.83[ASN][1000 genomes]
rs10144090	0.86[CHD][hapmap];0.90[JPT][hapmap]
rs10144371	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10144401	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs10144417	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs10145508	0.86[ASN][1000 genomes]
rs10145511	0.84[ASN][1000 genomes]
rs10145586	0.90[JPT][hapmap]
rs10146304	0.85[AMR][1000 genomes]
rs10146663	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs10146722	0.89[JPT][hapmap]
rs10147852	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs10150902	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs10151464	0.91[JPT][hapmap]
rs10220477	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10431718	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs1045060	0.83[CHD][hapmap];0.90[JPT][hapmap]
rs10459453	0.91[JPT][hapmap]
rs10483793	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1073607	0.91[JPT][hapmap]
rs1078194	0.82[JPT][hapmap]
rs10873200	0.91[JPT][hapmap]
rs11158655	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs11158658	0.86[JPT][hapmap]
rs12323494	0.90[JPT][hapmap]
rs12323911	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs12586402	0.80[ASN][1000 genomes]
rs12586552	0.89[JPT][hapmap]
rs12588478	0.90[JPT][hapmap]
rs12589091	0.89[JPT][hapmap]
rs12589218	0.91[JPT][hapmap]
rs12589671	0.91[JPT][hapmap]
rs12590689	0.80[ASN][1000 genomes]
rs12590956	0.82[JPT][hapmap]
rs1318914	0.91[JPT][hapmap]
rs13379142	0.90[JPT][hapmap]
rs13379368	0.91[JPT][hapmap]
rs1535491	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs1536271	0.91[JPT][hapmap]
rs1536272	0.91[JPT][hapmap]
rs17104103	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs17104106	0.91[JPT][hapmap]
rs17104109	0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs17104114	0.81[CHD][hapmap];0.82[JPT][hapmap]
rs17248252	0.84[ASN][1000 genomes]
rs17248357	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17248421	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17248526	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs17248616	0.90[JPT][hapmap]
rs1885589	0.90[JPT][hapmap]
rs1918483	0.83[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap];0.92[LWK][hapmap];0.82[MKK][hapmap];0.84[YRI][hapmap];0.93[ASN][1000 genomes]
rs1918484	0.80[ASN][1000 genomes]
rs1950284	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1952337	0.83[CHB][hapmap]
rs2031563	0.83[CHD][hapmap];0.86[JPT][hapmap]
rs2039055	0.81[ASN][1000 genomes]
rs2057396	0.91[JPT][hapmap]
rs2146229	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs2146230	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs2236333	0.91[JPT][hapmap]
rs2274335	0.91[JPT][hapmap]
rs2274338	0.91[JPT][hapmap]
rs2281676	0.88[ASN][1000 genomes]
rs2295903	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2296560	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs28368552	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28662990	0.97[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28678515	0.88[AMR][1000 genomes]
rs28685619	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3752993	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3759755	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs3818467	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs3866760	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4058254	0.86[JPT][hapmap]
rs58221168	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59774616	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6573744	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6573745	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6573746	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6573749	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6573750	0.92[AMR][1000 genomes]
rs6573751	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6573752	1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs6573753	0.82[AMR][1000 genomes]
rs6573754	0.91[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs6573760	0.83[CHD][hapmap];0.82[JPT][hapmap]
rs7141519	0.95[CHB][hapmap];0.93[CHD][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap]
rs7144434	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7144580	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7145005	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7146638	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7147207	0.87[ASN][1000 genomes]
rs7147534	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7148044	0.96[ASN][1000 genomes]
rs7148425	0.96[ASN][1000 genomes]
rs7149535	0.91[JPT][hapmap]
rs7150089	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7150739	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7150934	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7151086	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7151898	0.88[ASN][1000 genomes]
rs7152217	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7152231	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7152903	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs7154905	0.85[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7155042	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7156119	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7156441	0.83[CHD][hapmap];0.90[JPT][hapmap]
rs7157394	0.84[ASN][1000 genomes]
rs7157418	0.84[ASN][1000 genomes]
rs7158228	0.84[ASN][1000 genomes]
rs7161664	0.95[CHB][hapmap];0.93[CHD][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap]
rs7161698	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7493580	0.81[ASN][1000 genomes]
rs768770	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8004148	0.83[CHD][hapmap];0.81[JPT][hapmap]
rs8004488	0.81[CHD][hapmap];0.82[JPT][hapmap]
rs8005981	0.87[ASN][1000 genomes]
rs8006281	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8006391	0.90[JPT][hapmap]
rs8006519	0.83[CHD][hapmap]
rs8007033	0.85[CHD][hapmap];0.91[JPT][hapmap]
rs8008236	0.91[JPT][hapmap]
rs8008619	0.85[CHD][hapmap];0.91[JPT][hapmap]
rs8008724	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs8008739	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8009318	0.91[JPT][hapmap]
rs8010261	1.00[CHB][hapmap];0.95[CHD][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs8012944	0.88[EUR][1000 genomes]
rs8013724	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8014966	0.91[JPT][hapmap]
rs8015862	0.91[JPT][hapmap]
rs8016037	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs8019510	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs8021896	0.86[CHD][hapmap];0.91[JPT][hapmap]
rs9323494	0.92[ASN][1000 genomes]
rs9743842	1.00[CEU][hapmap]
rs9743911	0.91[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902058	chr14:67310195-67760538	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv902059	chr14:67352226-67760538	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	esv2751285	chr14:67364747-67886781	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv902060	chr14:67417083-67760538	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv1045518	chr14:67529049-67959582	Strong transcription Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv832821	chr14:67590418-67828169	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv1040257	chr14:67634585-67762806	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs6573755	EIF2S1	cis	lymphoblastoid	seeQTL
rs6573755	EIF2S1	Cis_1M	lymphoblastoid	RTeQTL
rs6573755	EIF2S1	cis	multi-tissue	Pritchard

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67618400-67658200	Weak transcription	Brain Angular Gyrus	brain
2	chr14:67639600-67658600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr14:67645800-67656400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr14:67645800-67658200	Weak transcription	Brain Anterior Caudate	brain
5	chr14:67646000-67655800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr14:67646200-67656200	Weak transcription	Psoas Muscle	Psoas
7	chr14:67647800-67658400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr14:67648200-67656000	Weak transcription	Aorta	Aorta
9	chr14:67648200-67656000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr14:67648200-67656000	Weak transcription	Spleen	Spleen
11	chr14:67648200-67656200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr14:67648200-67658200	Weak transcription	Brain Hippocampus Middle	brain
13	chr14:67648200-67658200	Weak transcription	Brain Substantia Nigra	brain
14	chr14:67648200-67660400	Weak transcription	Ovary	ovary
15	chr14:67648400-67656000	Weak transcription	Fetal Stomach	stomach
16	chr14:67648400-67658000	Weak transcription	Brain Cingulate Gyrus	brain
17	chr14:67648400-67658000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr14:67648400-67658400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr14:67648400-67658800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:67648600-67656000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr14:67648800-67656000	Weak transcription	Liver	Liver
22	chr14:67650200-67656000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr14:67652400-67656200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr14:67652600-67656200	Enhancers	HMEC	breast
25	chr14:67652800-67654600	Enhancers	Colon Smooth Muscle	Colon
26	chr14:67652800-67654800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr14:67652800-67655400	Enhancers	NHEK	skin
28	chr14:67653000-67654600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr14:67653000-67654600	Enhancers	Stomach Mucosa	stomach
30	chr14:67653000-67655400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr14:67653000-67655600	Enhancers	HSMM	muscle
32	chr14:67653200-67654600	Enhancers	Rectal Smooth Muscle	rectum
33	chr14:67653200-67654800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr14:67653200-67654800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr14:67653200-67655000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr14:67653200-67655000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr14:67653200-67655000	Enhancers	NHDF-Ad	bronchial
38	chr14:67653200-67655000	Enhancers	NHLF	lung
39	chr14:67653200-67655400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr14:67653200-67655400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr14:67653200-67655400	Enhancers	HSMMtube	muscle
42	chr14:67653200-67656200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr14:67653200-67656400	Enhancers	Osteobl	bone
44	chr14:67653400-67654600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr14:67653400-67654600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr14:67653400-67655000	Enhancers	HUVEC	blood vessel
47	chr14:67653400-67655400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr14:67653400-67656200	Enhancers	NH-A	brain
49	chr14:67653600-67654800	Enhancers	K562	blood
50	chr14:67653600-67655000	Enhancers	Fetal Thymus	thymus

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