Variant report

Variant	nsv962852
Chromosome Location	chr22:31455516-31465140
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:219)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:219 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:31459729-31459847	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:31460329-31460536	K562	blood:	n/a	n/a
3	ATF3	chr22:31459943-31460164	K562	blood:	n/a	n/a
4	ATF3	chr22:31457219-31457506	K562	blood:	n/a	n/a
5	BHLHE40	chr22:31460091-31460296	K562	blood:	n/a	n/a
6	CEBPB	chr22:31460052-31460081	HepG2	liver:	n/a	n/a
7	CEBPB	chr22:31456248-31456448	K562	blood:	n/a	n/a
8	CEBPB	chr22:31457126-31457397	K562	blood:	n/a	n/a
9	CEBPB	chr22:31460023-31460279	K562	blood:	n/a	n/a
10	CEBPB	chr22:31457105-31457459	K562	blood:	n/a	n/a
11	CEBPB	chr22:31457100-31457435	A549	lung:	n/a	n/a
12	CEBPB	chr22:31457110-31457420	IMR90	lung:	n/a	n/a
13	CEBPB	chr22:31457096-31457436	K562	blood:	n/a	n/a
14	CEBPB	chr22:31457122-31457366	HepG2	liver:	n/a	n/a
15	CEBPB	chr22:31457086-31457506	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr22:31458881-31459117	A549	lung:	n/a	n/a
17	CHD2	chr22:31459772-31460410	K562	blood:	n/a	n/a
18	CHD2	chr22:31462184-31462198	K562	blood:	n/a	n/a
19	CHD2	chr22:31460015-31460145	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr22:31456265-31456307	GM20000	blood:	n/a	n/a
21	CTCF	chr22:31461710-31461770	LNCaP	prostate:	n/a	n/a
22	CUX1	chr22:31459143-31459144	K562	blood:	n/a	n/a
23	E2F6	chr22:31460010-31460214	K562	blood:	n/a	n/a
24	E2F6	chr22:31459777-31460500	K562	blood:	n/a	n/a
25	EBF1	chr22:31464812-31465045	GM12878	blood:	n/a	chr22:31464938-31464949
26	EBF1	chr22:31464857-31465053	GM12878	blood:	n/a	chr22:31464938-31464949
27	ELF1	chr22:31459994-31460341	K562	blood:	n/a	chr22:31460147-31460158 chr22:31460146-31460159
28	ELF1	chr22:31457180-31457406	K562	blood:	n/a	chr22:31457295-31457308
29	EP300	chr22:31457279-31457312	K562	blood:	n/a	n/a
30	EP300	chr22:31457202-31457424	Hela-S3	cervix:	n/a	n/a
31	EP300	chr22:31459812-31460451	GM12878	blood:	n/a	n/a
32	ETS1	chr22:31459990-31460348	K562	blood:	n/a	n/a
33	FOS	chr22:31459809-31460299	K562	blood:	n/a	n/a
34	FOS	chr22:31458800-31459203	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr22:31458577-31459311	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr22:31457125-31457523	MCF10A-Er-Src	breast:	n/a	chr22:31457306-31457317 chr22:31457334-31457346 chr22:31457336-31457344
37	FOS	chr22:31458609-31459232	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr22:31462970-31463147	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr22:31455808-31455978	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr22:31457099-31457527	MCF10A-Er-Src	breast:	n/a	chr22:31457306-31457317 chr22:31457334-31457346 chr22:31457336-31457344
41	FOS	chr22:31455807-31455969	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr22:31457120-31457526	MCF10A-Er-Src	breast:	n/a	chr22:31457306-31457317 chr22:31457334-31457346 chr22:31457336-31457344
43	FOS	chr22:31457111-31457520	MCF10A-Er-Src	breast:	n/a	chr22:31457306-31457317 chr22:31457334-31457346 chr22:31457336-31457344
44	FOS	chr22:31458645-31459214	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr22:31455812-31455929	MCF10A-Er-Src	breast:	n/a	n/a
46	FOSL2	chr22:31455699-31456050	HepG2	liver:	n/a	n/a
47	FOSL2	chr22:31457166-31457437	HepG2	liver:	n/a	chr22:31457306-31457317 chr22:31457334-31457346 chr22:31457336-31457344
48	FOXA1	chr22:31459661-31460299	HepG2	liver:	n/a	n/a
49	FOXA1	chr22:31459788-31460350	HepG2	liver:	n/a	n/a
50	FOXA1	chr22:31459754-31460249	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:31460131-31460181	HMEC	breast:	n/a
2	chr22:31460131-31460181	BJ	skin:	n/a
3	chr22:31460131-31460181	HCPEpiC	choroid plexus:	n/a
4	chr22:31460131-31460181	Jurkat	blood:	n/a
5	chr22:31460131-31460181	HRE	kidney:	n/a
6	chr22:31460131-31460181	AG04450	lung:	fetal
7	chr22:31460131-31460181	NB4	blood:	n/a
8	chr22:31460131-31460181	HCT-116	colon:	n/a
9	chr22:31460131-31460181	ovcar-3	ovarian:	n/a
10	chr22:31460131-31460181	GM06990	blood:	n/a
11	chr22:31460131-31460181	NHDF-neo	bronchial:	n/a
12	chr22:31460131-31460181	HIPEpiC	eye:	n/a
13	chr22:31460131-31460181	U87	brain:	n/a
14	chr22:31460131-31460181	HAEpiC	amniotic membrane:	n/a
15	chr22:31460131-31460181	MCF-7	breast:	n/a
16	chr22:31460131-31460181	ECC-1	luminal epithelium:	n/a
17	chr22:31460131-31460181	K562	blood:	n/a
18	chr22:31460131-31460181	HNPCEpiC	eye:	n/a
19	chr22:31460131-31460181	MCF10A-Er-Src	breast:	n/a
20	chr22:31460131-31460181	HRCEpiC	kidney:	n/a
21	chr22:31460131-31460181	GM12892	blood:	n/a
22	chr22:31460131-31460181	AoSMC	blood vessel:	n/a
23	chr22:31460131-31460181	CMK	blood:	n/a
24	chr22:31460131-31460181	Hela-S3	cervix:	n/a
25	chr22:31460131-31460181	IMR90	lung:	fetal
26	chr22:31460131-31460181	AG10803	skin:	n/a
27	chr22:31460131-31460181	HCM	heart:	n/a
28	chr22:31460131-31460181	HepG2	liver:	n/a
29	chr22:31460131-31460181	BE2_C	brain:	n/a
30	chr22:31460131-31460181	H1-hESC	embryonic stem cell:	embryo
31	chr22:31460131-31460181	PFSK-1	brain:	n/a
32	chr22:31460131-31460181	SAEC	small airway:	n/a
33	chr22:31460131-31460181	SKMC	muscle:	n/a
34	chr22:31460131-31460181	GM12891	blood:	n/a
35	chr22:31460131-31460181	HRPEpiC	eye:	n/a
36	chr22:31460131-31460181	AG09319	gingival:	n/a
37	chr22:31460131-31460181	RPTEC	kidney:	n/a
38	chr22:31460131-31460181	AG09309	skin:	n/a
39	chr22:31460131-31460181	GM12878	blood:	n/a
40	chr22:31460131-31460181	AG04449	skin:	fetal
41	chr22:31460131-31460181	SK-N-MC	brain:	n/a
42	chr22:31460131-31460181	NH-A	brain:	n/a
43	chr22:31460131-31460181	SK-N-SH	brain:	n/a
44	chr22:31460131-31460181	NHBE	bronchial:	n/a
45	chr22:31460131-31460181	NT2-D1	testis:	n/a
46	chr22:31460131-31460181	HEK293	kidney:	embryo
47	chr22:31460131-31460181	LNCaP	prostate:	n/a
48	chr22:31460131-31460181	Caco-2	colon:	n/a
49	chr22:31460131-31460181	T-47D	breast:	n/a
50	chr22:31460131-31460181	ProgFib	skin:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:31458274..31462644-chr22:31476246..31482425,10	K562	blood:
2	chr22:31364481..31367281-chr22:31457492..31460562,3	MCF-7	breast:
3	chr22:31455769..31462183-chr22:31475245..31482356,13	K562	blood:
4	chr22:31459554..31462165-chr22:31463445..31465017,2	K562	blood:
5	chr22:31363691..31369255-chr22:31456002..31460514,7	MCF-7	breast:
6	chr22:31455775..31461842-chr22:31476267..31480955,13	MCF-7	breast:
7	chr22:31450083..31452668-chr22:31463620..31466392,3	MCF-7	breast:
8	chr22:31363469..31366268-chr22:31450278..31456884,6	MCF-7	breast:
9	chr22:31457775..31462699-chr22:31474304..31478789,5	MCF-7	breast:
10	chr22:31363776..31366652-chr22:31458331..31460655,2	K562	blood:
11	chr22:31460561..31462331-chr22:31465438..31468064,2	K562	blood:
12	chr22:31452690..31454726-chr22:31460173..31463712,3	MCF-7	breast:
13	chr22:31451720..31453462-chr22:31457824..31459739,2	MCF-7	breast:
14	chr22:31464585..31466786-chr22:31479626..31481207,2	MCF-7	breast:
15	chr22:31450718..31452880-chr22:31457371..31459942,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMTN-2	chr22:31455975-31456269	NONHSAT084842

No data

Variant related genes	Relation type
RN7SL633P	TF binding region
SMTN	TF binding region
RN7SL633P	CpG island
SMTN	CpG island
ENSG00000253352	chromatin interactions
ENSG00000183963	chromatin interactions
ENSG00000133422	chromatin interactions
ENSG00000273387	chromatin interactions

Extended variants
information (count: 362 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182207753	chr22:31455549-31455550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs187300564	chr22:31455634-31455635	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551840989	chr22:31455640-31455641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571665898	chr22:31455670-31455671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs527790233	chr22:31455673-31455674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs57300566	chr22:31455693-31455694	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs190503600	chr22:31455706-31455707	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs183154799	chr22:31455718-31455719	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs145273768	chr22:31455719-31455720	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs570048819	chr22:31455756-31455757	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs185623812	chr22:31455774-31455775	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs538933947	chr22:31455799-31455800	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs5994367	chr22:31455816-31455817	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs577169279	chr22:31455825-31455826	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs190434915	chr22:31455846-31455847	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs573561747	chr22:31455916-31455917	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs35865412	chr22:31455993-31455994	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs4820934	chr22:31456006-31456007	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs148921203	chr22:31456058-31456059	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
20	rs182543367	chr22:31456089-31456090	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
21	rs367836512	chr22:31456128-31456129	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
22	rs187727682	chr22:31456137-31456138	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs531684322	chr22:31456141-31456142	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
24	rs190803802	chr22:31456152-31456153	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs371358173	chr22:31456189-31456190	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs545277749	chr22:31456226-31456227	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
27	rs374850852	chr22:31456228-31456229	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs141298089	chr22:31456292-31456293	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs552890279	chr22:31456294-31456295	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs547890627	chr22:31456320-31456321	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs567681336	chr22:31456323-31456324	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs9621173	chr22:31456352-31456353	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs113451210	chr22:31456383-31456384	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs549999194	chr22:31456387-31456388	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs569910035	chr22:31456388-31456389	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs146835017	chr22:31456409-31456410	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs183907528	chr22:31456449-31456450	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs571244550	chr22:31456496-31456497	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs111655049	chr22:31456511-31456512	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs533583056	chr22:31456559-31456560	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs553715206	chr22:31456560-31456561	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs199773121	chr22:31456565-31456566	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs12159096	chr22:31456587-31456588	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs536350073	chr22:31456596-31456597	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs556397503	chr22:31456614-31456615	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs576265673	chr22:31456616-31456617	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs545339609	chr22:31456623-31456624	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs565147222	chr22:31456657-31456658	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs187880104	chr22:31456664-31456665	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs541101254	chr22:31456683-31456684	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20858604	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31452000-31458000	Weak transcription	Adipose Nuclei	Adipose
2	chr22:31452200-31455600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr22:31452200-31455600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr22:31452200-31455600	Weak transcription	Ovary	ovary
5	chr22:31452200-31455800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr22:31452200-31455800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr22:31452200-31456000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr22:31452200-31456000	Weak transcription	NHEK	skin
9	chr22:31452800-31455600	Weak transcription	HMEC	breast
10	chr22:31452800-31456800	Weak transcription	Hela-S3	cervix
11	chr22:31452800-31458200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr22:31453000-31455600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr22:31453000-31455600	Weak transcription	Fetal Muscle Trunk	muscle
14	chr22:31453000-31455600	Weak transcription	Placenta	Placenta
15	chr22:31453200-31455600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr22:31453200-31455600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr22:31453200-31455600	Weak transcription	Fetal Intestine Large	intestine
18	chr22:31453200-31455600	Weak transcription	Fetal Intestine Small	intestine
19	chr22:31453400-31455600	Weak transcription	Fetal Muscle Leg	muscle
20	chr22:31453400-31455600	Weak transcription	Rectal Smooth Muscle	rectum
21	chr22:31453400-31455600	Weak transcription	HepG2	liver
22	chr22:31453400-31455800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr22:31453600-31455600	Weak transcription	A549	lung
24	chr22:31454400-31455600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr22:31454400-31455800	Weak transcription	Stomach Smooth Muscle	stomach
26	chr22:31454600-31455600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr22:31454600-31455600	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr22:31455400-31455600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr22:31455400-31456200	Enhancers	Fetal Lung	lung
30	chr22:31455400-31456200	Enhancers	Fetal Stomach	stomach
31	chr22:31455400-31458400	Enhancers	K562	blood
32	chr22:31455600-31455800	Enhancers	Right Ventricle	heart
33	chr22:31455600-31456000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr22:31455600-31456000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr22:31455600-31456000	Enhancers	Fetal Muscle Trunk	muscle
36	chr22:31455600-31456000	Enhancers	Fetal Muscle Leg	muscle
37	chr22:31455600-31456000	Enhancers	Lung	lung
38	chr22:31455600-31456000	Enhancers	Ovary	ovary
39	chr22:31455600-31456000	Enhancers	HMEC	breast
40	chr22:31455600-31456200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr22:31455600-31456200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr22:31455600-31456200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr22:31455600-31456200	Enhancers	A549	lung
44	chr22:31455600-31456400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr22:31455600-31456400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr22:31455600-31456400	Enhancers	Fetal Intestine Large	intestine
47	chr22:31455600-31456400	Enhancers	Fetal Intestine Small	intestine
48	chr22:31455600-31456400	Enhancers	Placenta	Placenta
49	chr22:31455600-31456400	Enhancers	Placenta Amnion	Placenta Amnion
50	chr22:31455600-31456600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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