Variant report

Variant	rs4989959
Chromosome Location	chr7:100032288-100032289
allele	C/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:13)
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	chr7:100032223-100033760	GM12891	blood:	n/a	n/a
2	POLR2A	chr7:100032140-100034606	GM12892	blood:	n/a	n/a
3	POLR2A	chr7:100032282-100034553	GM12878	blood:	n/a	n/a
4	POLR2A	chr7:100032169-100034606	GM12891	blood:	n/a	n/a
5	POLR2A	chr7:100032219-100034537	MCF10A-Er-Src	breast:	n/a	n/a
6	POLR2A	chr7:100032217-100034542	HL-60	blood:	n/a	n/a
7	POLR2A	chr7:100032284-100034495	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr7:100030180-100034516	HepG2	liver:	n/a	n/a
9	HCFC1	chr7:100032210-100034610	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr7:100032179-100032799	GM12878	blood:	n/a	n/a
11	POLR2A	chr7:100032227-100032826	GM12878	blood:	n/a	n/a
12	POLR2A	chr7:100032212-100034595	HL-60	blood:	n/a	n/a
13	MTA3	chr7:100030193-100034606	GM12878	blood:	n/a	n/a
14	POLR2A	chr7:100032245-100033680	GM12891	blood:	n/a	n/a
15	POLR2A	chr7:100032261-100032528	HCT-116	colon:	n/a	n/a
16	CBX3	chr7:100032265-100032821	K562	blood:	n/a	n/a
17	POLR2A	chr7:100029646-100033719	U87	brain:	n/a	n/a
18	POLR2A	chr7:100025552-100034611	GM12892	blood:	n/a	n/a
19	POLR2A	chr7:100025685-100034590	GM12892	blood:	n/a	n/a
20	POLR2A	chr7:100025716-100034505	K562	blood:	n/a	n/a
21	POLR2A	chr7:100032246-100034604	MCF-7	breast:	n/a	n/a
22	POLR2A	chr7:100032230-100034480	U87	brain:	n/a	n/a
23	POLR2A	chr7:100032240-100032527	ECC-1	luminal epithelium:	n/a	n/a
24	POLR2A	chr7:100025714-100034420	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr7:100032202-100034560	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr7:100025516-100034612	SK-N-MC	brain:	n/a	n/a
27	POLR2A	chr7:100032161-100033691	SK-N-MC	brain:	n/a	n/a
28	POLR2A	chr7:100025670-100034884	K562	blood:	n/a	n/a
29	POLR2A	chr7:100032163-100034571	K562	blood:	n/a	n/a
30	TEAD4	chr7:100032277-100033750	K562	blood:	n/a	n/a
31	POLR2A	chr7:100032170-100034619	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr7:100025555-100034612	GM12878	blood:	n/a	n/a
33	POLR2A	chr7:100028726-100034596	SK-N-SH	brain:	n/a	n/a
34	POLR2A	chr7:100031269-100034538	Raji	blood:	n/a	n/a
35	POLR2A	chr7:100032161-100034513	HCT-116	colon:	n/a	n/a
36	POLR2A	chr7:100029318-100034564	GM12891	blood:	n/a	n/a
37	POLR2A	chr7:100030346-100034589	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr7:100032175-100034511	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr7:100032224-100033771	HepG2	liver:	n/a	n/a
40	POLR2A	chr7:100032179-100034492	K562	blood:	n/a	n/a
41	MXI1	chr7:100032261-100034522	IMR90	lung:	n/a	n/a
42	POLR2A	chr7:100025731-100034623	PFSK-1	brain:	n/a	n/a
43	POLR2A	chr7:100029242-100034507	K562	blood:	n/a	n/a
44	HEY1	chr7:100031237-100034512	K562	blood:	n/a	chr7:100032696-100032705
45	POLR2A	chr7:100028473-100034599	PANC-1	pancreas:	n/a	n/a
46	BCL3	chr7:100032248-100033749	A549	lung:	n/a	n/a
47	POLR2A	chr7:100032279-100034480	U87	brain:	n/a	n/a
48	POLR2A	chr7:100032264-100033736	GM12892	blood:	n/a	n/a
49	POLR2A	chr7:100025471-100034582	PANC-1	pancreas:	n/a	n/a
50	PML	chr7:100032251-100033767	GM12878	blood:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100024700..100032514-chr7:100067180..100083143,31	K562	blood:
2	chr7:100001600..100003590-chr7:100030106..100032583,2	MCF-7	breast:
3	chr7:100029587..100032466-chr7:100040702..100044115,3	MCF-7	breast:
4	chr7:100031120..100032907-chr7:100059800..100061803,2	K562	blood:
5	chr7:99998688..100005691-chr7:100025198..100032529,13	K562	blood:
6	chr7:100025583..100035841-chr7:100071553..100080023,19	MCF-7	breast:
7	chr7:99677604..99679757-chr7:100032184..100034035,2	K562	blood:
8	chr7:100031790..100034595-chr7:100181557..100184454,2	MCF-7	breast:
9	chr7:100031924..100034212-chr7:100179842..100183716,3	MCF-7	breast:
10	chr7:100032100..100034084-chr7:100269925..100271746,2	MCF-7	breast:
11	chr20:62494852..62496761-chr7:100029731..100032578,2	MCF-7	breast:
12	chr7:100018468..100021635-chr7:100028917..100032766,4	K562	blood:
13	chr7:99691882..99693394-chr7:100030103..100032798,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000241357	TF binding region
ENSG00000240211	TF binding region
ENSG00000106336	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000166508	Chromatin interaction
ENSG00000185955	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000266372	Chromatin interaction
ENSG00000166924	Chromatin interaction
ENSG00000166925	Chromatin interaction
ENSG00000264758	Chromatin interaction
ENSG00000166526	Chromatin interaction
ENSG00000101150	Chromatin interaction
ENSG00000172354	Chromatin interaction

Extended variants
information (count: 85 )
Associated
traits (count: 46 )

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs1000215	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1073	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11559117	1.00[ASN][1000 genomes]
rs11761624	1.00[ASN][1000 genomes]
rs11761725	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11761784	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11763414	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11763511	1.00[ASN][1000 genomes]
rs11764818	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11766202	1.00[ASN][1000 genomes]
rs11766752	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769700	1.00[ASN][1000 genomes]
rs11769886	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11771241	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11771419	0.85[EUR][1000 genomes]
rs11772580	1.00[ASN][1000 genomes]
rs11773661	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1962269	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2003507	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2406253	1.00[ASN][1000 genomes]
rs2406255	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28490152	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28578163	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28629346	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28660238	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2897358	1.00[ASN][1000 genomes]
rs34989573	1.00[ASN][1000 genomes]
rs35111986	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3900792	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4074838	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4385401	1.00[ASN][1000 genomes]
rs4463351	1.00[ASN][1000 genomes]
rs4469386	1.00[ASN][1000 genomes]
rs4472444	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60257855	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60478351	1.00[ASN][1000 genomes]
rs60644673	1.00[ASN][1000 genomes]
rs60844404	1.00[ASN][1000 genomes]
rs66632384	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66648318	1.00[ASN][1000 genomes]
rs66958101	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67040465	0.86[ASN][1000 genomes]
rs67163493	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67196635	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67239991	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67315960	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67471932	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67483801	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67885733	1.00[ASN][1000 genomes]
rs68116612	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6948699	1.00[ASN][1000 genomes]
rs6953107	1.00[ASN][1000 genomes]
rs6953749	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6955362	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6957928	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6962151	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6970806	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6970828	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6972167	0.86[ASN][1000 genomes]
rs6974286	1.00[ASN][1000 genomes]
rs6975514	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975729	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6978739	1.00[ASN][1000 genomes]
rs6979335	1.00[ASN][1000 genomes]
rs73161759	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73161762	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73403312	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73405353	1.00[ASN][1000 genomes]
rs7783159	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7783550	0.85[EUR][1000 genomes]
rs7787620	1.00[ASN][1000 genomes]
rs7787825	1.00[ASN][1000 genomes]
rs7794485	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7800667	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7803454	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7809801	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7811142	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350965	chr7:99747460-100146105	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
2	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
3	nsv831071	chr7:99918025-100113413	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	287 gene(s)	inside rSNPs	diseases
4	nsv527107	chr7:100014711-100064719	Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	269 gene(s)	inside rSNPs	diseases
5	nsv888776	chr7:100014711-100198386	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	297 gene(s)	inside rSNPs	diseases
6	nsv888777	chr7:100014711-100221867	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
7	nsv888778	chr7:100014711-100236593	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
8	nsv888779	chr7:100014711-100313420	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	321 gene(s)	inside rSNPs	diseases

mRNA abundance (count:46)

SNP	Gene	Cis/trans	Tissue	Source
rs4989959	STAG3	Cis_1M	lymphoblastoid	RTeQTL
rs4989959	PVRIG2P	cis	Thyroid	GTEx
rs4989959	PILRA	cis	Heart Left Ventricle	GTEx
rs4989959	PILRA	cis	Stomach	GTEx
rs4989959	STAG3L5P	cis	Artery Tibial	GTEx
rs4989959	PILRB	cis	Adipose Subcutaneous	GTEx
rs4989959	PVRIG2P	cis	Adipose Subcutaneous	GTEx
rs4989959	PILRA	cis	Thyroid	GTEx
rs4989959	STAG3L5P	cis	Heart Left Ventricle	GTEx
rs4989959	PILRB	cis	Artery Tibial	GTEx
rs4989959	PVRIG2P	cis	Nerve Tibial	GTEx
rs4989959	PILRB	cis	Whole Blood	GTEx
rs4989959	PVRIG2P	cis	Artery Tibial	GTEx
rs4989959	PILRA	cis	Artery Aorta	GTEx
rs4989959	STAG3L5P	cis	Adipose Subcutaneous	GTEx
rs4989959	PILRB	cis	Esophagus Muscularis	GTEx
rs4989959	PILRA	cis	Esophagus Mucosa	GTEx
rs4989959	STAG3L5P	cis	Skin Sun Exposed Lower leg	GTEx
rs4989959	STAG3L5P	cis	Thyroid	GTEx
rs4989959	STAG3L5P	cis	Muscle Skeletal	GTEx
rs4989959	STAG3L5P	cis	Esophagus Muscularis	GTEx
rs4989959	PILRB	cis	Artery Aorta	GTEx
rs4989959	STAG3L5P	cis	Artery Aorta	GTEx
rs4989959	PILRB	cis	Skin Sun Exposed Lower leg	GTEx
rs4989959	PILRA	cis	Esophagus Muscularis	GTEx
rs4989959	PILRB	cis	lung	GTEx
rs4989959	PILRB	cis	multi-tissue	Pritchard
rs4989959	PILRB	cis	Nerve Tibial	GTEx
rs4989959	PVRIG2P	cis	lung	GTEx
rs4989959	PMS2P1	cis	Thyroid	GTEx
rs4989959	PILRB	Cis_1M	lymphoblastoid	RTeQTL
rs4989959	PILRA	cis	Skin Sun Exposed Lower leg	GTEx
rs4989959	PVRIG2P	cis	Esophagus Mucosa	GTEx
rs4989959	PILRB	cis	Thyroid	GTEx
rs4989959	STAG3L5P	cis	Nerve Tibial	GTEx
rs4989959	STAG3L5P	cis	lung	GTEx
rs4989959	PILRA	cis	Nerve Tibial	GTEx
rs4989959	PILRA	cis	Muscle Skeletal	GTEx
rs4989959	PILRA	cis	Adipose Subcutaneous	GTEx
rs4989959	STAG3L5P	cis	Esophagus Mucosa	GTEx
rs4989959	PILRB	cis	Muscle Skeletal	GTEx
rs4989959	PVRIG	Cis_1M	lymphoblastoid	RTeQTL
rs4989959	STAG3L5P	cis	Stomach	GTEx
rs4989959	PILRA	cis	Artery Tibial	GTEx
rs4989959	PILRB	cis	Heart Left Ventricle	GTEx
rs4989959	PILRB	cis	Esophagus Mucosa	GTEx

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100027400-100033600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:100028200-100033400	Transcr. at gene 5' and 3'	Dnd41	blood
3	chr7:100028600-100032400	Weak transcription	Small Intestine	intestine
4	chr7:100028600-100032600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:100028600-100032600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr7:100028600-100033600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr7:100028800-100032400	Genic enhancers	H1 Cell Line	embryonic stem cell
8	chr7:100028800-100032400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
9	chr7:100028800-100032400	Genic enhancers	A549	lung
10	chr7:100028800-100032600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:100028800-100032600	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:100028800-100032600	Genic enhancers	Primary T cells fromperipheralblood	blood
13	chr7:100028800-100032600	Genic enhancers	Fetal Muscle Trunk	muscle
14	chr7:100028800-100033000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:100028800-100033000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr7:100028800-100033000	Genic enhancers	Placenta	Placenta
17	chr7:100028800-100033000	Genic enhancers	Spleen	Spleen
18	chr7:100029000-100032600	Genic enhancers	Fetal Muscle Leg	muscle
19	chr7:100029000-100032600	Genic enhancers	Skeletal Muscle Female	skeletal muscle
20	chr7:100029000-100033000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
21	chr7:100029200-100032400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:100029200-100032600	Genic enhancers	Fetal Intestine Large	intestine
23	chr7:100029400-100032400	Genic enhancers	Primary T cells from cord blood	blood
24	chr7:100029400-100033000	Transcr. at gene 5' and 3'	Hela-S3	cervix
25	chr7:100029600-100032400	Genic enhancers	HepG2	liver
26	chr7:100029600-100032600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
27	chr7:100029800-100032400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr7:100029800-100032400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr7:100029800-100032400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr7:100029800-100032600	Genic enhancers	Liver	Liver
31	chr7:100029800-100032600	Strong transcription	Brain Substantia Nigra	brain
32	chr7:100030000-100032400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:100030000-100032400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:100030000-100032400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr7:100030000-100032400	Genic enhancers	Fetal Intestine Small	intestine
36	chr7:100030000-100032400	Genic enhancers	Stomach Smooth Muscle	stomach
37	chr7:100030000-100032600	Weak transcription	Fetal Brain Male	brain
38	chr7:100030000-100032600	Strong transcription	Lung	lung
39	chr7:100030200-100032400	Genic enhancers	Fetal Thymus	thymus
40	chr7:100030200-100032400	Strong transcription	HUVEC	blood vessel
41	chr7:100030200-100032400	Strong transcription	Osteobl	bone
42	chr7:100030200-100032600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:100030200-100032600	Weak transcription	Right Atrium	heart
44	chr7:100030200-100032600	Genic enhancers	Thymus	Thymus
45	chr7:100030400-100032400	Strong transcription	H9 Cell Line	embryonic stem cell
46	chr7:100030400-100032400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
47	chr7:100030400-100032400	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr7:100030400-100032400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr7:100030400-100032400	Genic enhancers	Adipose Nuclei	Adipose
50	chr7:100030400-100032400	Strong transcription	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links