Variant report

Variant	rs11156907
Chromosome Location	chr14:21733874-21733875
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr14:21728426-21734336	GM12891	blood:	n/a	n/a
2	POLR2A	chr14:21728614-21735024	GM12878	blood:	n/a	n/a
3	POLR2A	chr14:21733340-21734174	K562	blood:	n/a	n/a
4	TAF7	chr14:21733639-21734039	H1-hESC	embryonic stem cell:	n/a	n/a
5	RUNX3	chr14:21733849-21734300	GM12878	blood:	n/a	n/a
6	POLR2A	chr14:21733326-21734271	HepG2	liver:	n/a	n/a
7	POLR2A	chr14:21733603-21734036	HL-60	blood:	n/a	n/a
8	POLR2A	chr14:21728611-21734968	GM12878	blood:	n/a	n/a
9	NFATC1	chr14:21733604-21734106	GM12878	blood:	n/a	n/a
10	POLR2A	chr14:21733622-21733915	HepG2	liver:	n/a	n/a
11	POLR2A	chr14:21733493-21734634	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr14:21728514-21734782	HepG2	liver:	n/a	n/a
13	POLR2A	chr14:21731778-21734317	K562	blood:	n/a	n/a
14	CTCF	chr14:21733780-21733930	HepG2	liver:	n/a	n/a
15	POLR2A	chr14:21728424-21734236	HepG2	liver:	n/a	n/a
16	POU2F2	chr14:21733578-21733983	GM12891	blood:	n/a	n/a
17	POLR2A	chr14:21733579-21734286	GM12891	blood:	n/a	n/a
18	POLR2A	chr14:21731378-21738564	GM12878	blood:	n/a	n/a
19	CTCF	chr14:21733740-21733890	GM12872	blood:	n/a	n/a
20	POLR2A	chr14:21728578-21737722	K562	blood:	n/a	n/a
21	POLR2A	chr14:21733614-21733926	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr14:21733250-21734132	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr14:21733680-21734292	PFSK-1	brain:	n/a	n/a
24	POLR2A	chr14:21733605-21733913	GM12878	blood:	n/a	n/a
25	NFATC1	chr14:21731767-21734347	GM12878	blood:	n/a	n/a
26	POLR2A	chr14:21732643-21734493	GM12891	blood:	n/a	n/a
27	POLR2A	chr14:21732683-21734209	K562	blood:	n/a	n/a
28	POLR2A	chr14:21733496-21734675	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr14:21733400-21734273	GM12892	blood:	n/a	n/a
30	POLR2A	chr14:21733462-21734191	IMR90	lung:	n/a	n/a
31	POLR2A	chr14:21733555-21734681	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr14:21733320-21734555	GM12891	blood:	n/a	n/a
33	POLR2A	chr14:21733593-21733943	GM12878	blood:	n/a	n/a
34	HEY1	chr14:21733542-21734350	K562	blood:	n/a	n/a
35	POLR2A	chr14:21731404-21735357	GM12878	blood:	n/a	n/a
36	POLR2A	chr14:21731507-21734631	A549	lung:	n/a	n/a
37	POLR2A	chr14:21733536-21734020	K562	blood:	n/a	n/a
38	HEY1	chr14:21732591-21734438	HepG2	liver:	n/a	n/a
39	POLR2A	chr14:21731402-21734421	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr14:21731441-21734438	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr14:21733820-21733886	A549	lung:	n/a	n/a
42	POLR2A	chr14:21733375-21734659	HepG2	liver:	n/a	n/a
43	POLR2A	chr14:21733777-21734361	PANC-1	pancreas:	n/a	n/a
44	POLR2A	chr14:21732593-21735313	GM12892	blood:	n/a	n/a
45	POLR2A	chr14:21731555-21738535	GM18505	blood:	n/a	n/a
46	STAT5A	chr14:21733585-21734251	GM12878	blood:	n/a	n/a
47	POLR2A	chr14:21733514-21734078	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr14:21728279-21734371	HepG2	liver:	n/a	n/a
49	RUNX3	chr14:21733838-21734317	GM12878	blood:	n/a	n/a
50	POLR2A	chr14:21733371-21735264	SK-N-MC	brain:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21731892..21738562-chr14:21850801..21854193,10	MCF-7	breast:
2	chr14:21732878..21735093-chr14:21822568..21824225,2	K562	blood:
3	chr14:21687620..21689527-chr14:21733855..21735500,2	MCF-7	breast:
4	chr14:21731325..21733922-chr14:21791322..21794128,2	MCF-7	breast:
5	chr14:21732396..21736856-chr14:21795995..21798414,4	K562	blood:
6	chr14:21731127..21734828-chr14:21850549..21852828,3	K562	blood:
7	chr14:21731613..21734582-chr14:21826282..21828114,3	MCF-7	breast:

No data

Variant related genes	Relation type
HNRNPC	TF binding region
ENSG00000092200	Chromatin interaction
ENSG00000092201	Chromatin interaction
ENSG00000260830	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10131045	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10140863	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10148280	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12436255	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12590649	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12590783	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12590806	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17197037	0.94[ASN][1000 genomes]
rs34293304	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35141059	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4982434	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4982436	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4982438	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7141230	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7142590	0.90[AMR][1000 genomes]
rs7142957	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7147655	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7148026	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7153505	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72678663	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7495	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8009894	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8011312	0.81[AFR][1000 genomes]
rs8016099	0.84[ASN][1000 genomes]
rs8018410	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530009	chr14:21377022-22044608	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
2	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv916319	chr14:21507092-21896590	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1036762	chr14:21507093-22101805	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv541976	chr14:21507093-22101805	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv530770	chr14:21526410-21852363	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
7	nsv1043570	chr14:21575068-21899964	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv541977	chr14:21575068-21899964	Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1048032	chr14:21602341-21847247	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
10	nsv541978	chr14:21602341-21847247	Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS 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	29 gene(s)	inside rSNPs	diseases
11	nsv948957	chr14:21616875-21928338	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
12	nsv901477	chr14:21625262-21750308	Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
13	nsv901478	chr14:21626497-21750308	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
14	nsv1044822	chr14:21659344-21860081	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
15	nsv541979	chr14:21672540-21735893	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
16	nsv541980	chr14:21672540-21742729	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
17	nsv541982	chr14:21676221-21735893	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
18	nsv541983	chr14:21676221-21742729	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
19	esv1825348	chr14:21691941-21829404	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
20	nsv1051407	chr14:21692670-21907366	Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
21	nsv541984	chr14:21692670-21907366	Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
22	nsv530010	chr14:21692670-21923767	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
23	nsv541986	chr14:21692703-21735893	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
24	nsv541987	chr14:21692703-21742729	Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
25	nsv541988	chr14:21696056-21735893	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
26	nsv541989	chr14:21696056-21742729	Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking 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	16 gene(s)	inside rSNPs	diseases
27	esv3357025	chr14:21702262-21737534	Strong transcription Genic enhancers Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
28	nsv541990	chr14:21702771-21757737	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
29	nsv428617	chr14:21721165-21871164	Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
30	nsv983804	chr14:21730434-21759672	Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21702200-21735600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:21723800-21734200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr14:21724200-21735600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr14:21728600-21737400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
5	chr14:21729200-21735600	Genic enhancers	Primary B cells from peripheral blood	blood
6	chr14:21729200-21736800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
7	chr14:21729600-21734200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr14:21729600-21734800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr14:21729800-21735400	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
10	chr14:21730000-21734000	Genic enhancers	Brain Cingulate Gyrus	brain
11	chr14:21730000-21734000	Strong transcription	Placenta Amnion	Placenta Amnion
12	chr14:21730000-21734200	Genic enhancers	Brain Inferior Temporal Lobe	brain
13	chr14:21730000-21734200	Genic enhancers	Rectal Mucosa Donor 31	rectum
14	chr14:21730200-21737600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
15	chr14:21730400-21735000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr14:21730600-21734200	Genic enhancers	Left Ventricle	heart
17	chr14:21730600-21734200	Enhancers	Small Intestine	intestine
18	chr14:21730600-21734600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr14:21730600-21734600	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
20	chr14:21730600-21734600	Genic enhancers	Fetal Lung	lung
21	chr14:21730600-21734800	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
22	chr14:21730600-21735400	Genic enhancers	Primary monocytes fromperipheralblood	blood
23	chr14:21730600-21735400	Genic enhancers	Primary B cells from cord blood	blood
24	chr14:21730600-21736200	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr14:21730800-21736400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr14:21730800-21736800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr14:21731200-21734200	Transcr. at gene 5' and 3'	NH-A	brain
28	chr14:21731400-21734200	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr14:21731600-21735000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
30	chr14:21731600-21736800	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell
31	chr14:21731600-21737000	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
32	chr14:21731600-21737200	Transcr. at gene 5' and 3'	A549	lung
33	chr14:21731600-21737400	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
34	chr14:21731800-21734400	Genic enhancers	Skeletal Muscle Female	skeletal muscle
35	chr14:21731800-21734600	Enhancers	Stomach Mucosa	stomach
36	chr14:21731800-21735000	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr14:21731800-21735000	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
38	chr14:21731800-21735800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
39	chr14:21731800-21736800	Transcr. at gene 5' and 3'	HUVEC	blood vessel
40	chr14:21731800-21737200	Transcr. at gene 5' and 3'	Dnd41	blood
41	chr14:21731800-21737400	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
42	chr14:21732000-21734000	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
43	chr14:21732000-21734200	Transcr. at gene 5' and 3'	K562	blood
44	chr14:21732000-21734800	Genic enhancers	HSMM	muscle
45	chr14:21732000-21735800	Transcr. at gene 5' and 3'	HepG2	liver
46	chr14:21732000-21736800	Transcr. at gene 5' and 3'	iPS-18 Cell Line	embryonic stem cell
47	chr14:21732200-21734200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr14:21732200-21734200	Genic enhancers	Fetal Intestine Small	intestine
49	chr14:21732200-21734200	Genic enhancers	NHLF	lung
50	chr14:21732200-21734400	Genic enhancers	Adipose Nuclei	Adipose

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