Variant report

Variant	nsv964620
Chromosome Location	chr22:31452981-31465140
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:222)
CpG islands
(count:62)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:222 , 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	chr22:31460329-31460536	K562	blood:	n/a	n/a
2	ARID3A	chr22:31459729-31459847	HepG2	liver:	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	chr22:31457100-31457435	A549	lung:	n/a	n/a
7	CEBPB	chr22:31457110-31457420	IMR90	lung:	n/a	n/a
8	CEBPB	chr22:31456248-31456448	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	chr22:31457086-31457506	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr22:31458881-31459117	A549	lung:	n/a	n/a
13	CEBPB	chr22:31460052-31460081	HepG2	liver:	n/a	n/a
14	CEBPB	chr22:31457096-31457436	K562	blood:	n/a	n/a
15	CEBPB	chr22:31457126-31457397	K562	blood:	n/a	n/a
16	CEBPB	chr22:31457122-31457366	HepG2	liver:	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	chr22:31461710-31461770	LNCaP	prostate:	n/a	n/a
21	CTCF	chr22:31456265-31456307	GM20000	blood:	n/a	n/a
22	CUX1	chr22:31459143-31459144	K562	blood:	n/a	n/a
23	E2F6	chr22:31459777-31460500	K562	blood:	n/a	n/a
24	E2F6	chr22:31460010-31460214	K562	blood:	n/a	n/a
25	EBF1	chr22:31464857-31465053	GM12878	blood:	n/a	chr22:31464938-31464949
26	EBF1	chr22:31464812-31465045	GM12878	blood:	n/a	chr22:31464938-31464949
27	ELF1	chr22:31457180-31457406	K562	blood:	n/a	chr22:31457295-31457308
28	ELF1	chr22:31459994-31460341	K562	blood:	n/a	chr22:31460147-31460158 chr22:31460146-31460159
29	EP300	chr22:31457202-31457424	Hela-S3	cervix:	n/a	n/a
30	EP300	chr22:31459812-31460451	GM12878	blood:	n/a	n/a
31	EP300	chr22:31457279-31457312	K562	blood:	n/a	n/a
32	ETS1	chr22:31459990-31460348	K562	blood:	n/a	n/a
33	FOS	chr22:31457099-31457527	MCF10A-Er-Src	breast:	n/a	chr22:31457306-31457317 chr22:31457334-31457346 chr22:31457336-31457344
34	FOS	chr22:31457111-31457520	MCF10A-Er-Src	breast:	n/a	chr22:31457306-31457317 chr22:31457334-31457346 chr22:31457336-31457344
35	FOS	chr22:31462970-31463147	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr22:31458800-31459203	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr22:31455812-31455929	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr22:31455808-31455978	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr22:31458577-31459311	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr22:31457120-31457526	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	chr22:31457125-31457523	MCF10A-Er-Src	breast:	n/a	chr22:31457306-31457317 chr22:31457334-31457346 chr22:31457336-31457344
43	FOS	chr22:31459809-31460299	K562	blood:	n/a	n/a
44	FOS	chr22:31458609-31459232	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr22:31458645-31459214	MCF10A-Er-Src	breast:	n/a	n/a
46	FOSL2	chr22:31457166-31457437	HepG2	liver:	n/a	chr22:31457306-31457317 chr22:31457334-31457346 chr22:31457336-31457344
47	FOSL2	chr22:31455699-31456050	HepG2	liver:	n/a	n/a
48	FOXA1	chr22:31459754-31460249	HepG2	liver:	n/a	n/a
49	FOXA1	chr22:31459788-31460350	HepG2	liver:	n/a	n/a
50	FOXA1	chr22:31459661-31460299	HepG2	liver:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:31460131-31460181	AG09309	skin:	n/a
2	chr22:31460131-31460181	AG09309	skin:	n/a
3	chr22:31460131-31460181	Hepatocyte	liver:	n/a
4	chr22:31460131-31460181	AoSMC	blood vessel:	n/a
5	chr22:31460131-31460181	NHBE	bronchial:	n/a
6	chr22:31460131-31460181	GM12891	blood:	n/a
7	chr22:31460131-31460181	U87	brain:	n/a
8	chr22:31460131-31460181	NT2-D1	testis:	n/a
9	chr22:31460131-31460181	T-47D	breast:	n/a
10	chr22:31460131-31460181	ECC-1	luminal epithelium:	n/a
11	chr22:31460131-31460181	LNCaP	prostate:	n/a
12	chr22:31460131-31460181	NB4	blood:	n/a
13	chr22:31460131-31460181	HCPEpiC	choroid plexus:	n/a
14	chr22:31460131-31460181	HMEC	breast:	n/a
15	chr22:31460131-31460181	K562	blood:	n/a
16	chr22:31460131-31460181	HNPCEpiC	eye:	n/a
17	chr22:31460131-31460181	Hela-S3	cervix:	n/a
18	chr22:31460131-31460181	PFSK-1	brain:	n/a
19	chr22:31460131-31460181	HEEpiC	esophagus:	n/a
20	chr22:31460131-31460181	SAEC	small airway:	n/a
21	chr22:31460131-31460181	ovcar-3	ovarian:	n/a
22	chr22:31460131-31460181	HEK293	kidney:	embryo
23	chr22:31460131-31460181	A549	lung:	n/a
24	chr22:31460131-31460181	SK-N-SH_RA	brain:	n/a
25	chr22:31460131-31460181	PANC-1	pancreas:	n/a
26	chr22:31460131-31460181	CMK	blood:	n/a
27	chr22:31460131-31460181	HRE	kidney:	n/a
28	chr22:31460131-31460181	Jurkat	blood:	n/a
29	chr22:31460131-31460181	HUVEC	blood vessel:	n/a
30	chr22:31460131-31460181	SKMC	muscle:	n/a
31	chr22:31460131-31460181	NH-A	brain:	n/a
32	chr22:31460131-31460181	AG10803	skin:	n/a
33	chr22:31460131-31460181	IMR90	lung:	fetal
34	chr22:31460131-31460181	Caco-2	colon:	n/a
35	chr22:31460131-31460181	MCF-7	breast:	n/a
36	chr22:31460131-31460181	HepG2	liver:	n/a
37	chr22:31460131-31460181	GM06990	blood:	n/a
38	chr22:31460131-31460181	MCF10A-Er-Src	breast:	n/a
39	chr22:31460131-31460181	HIPEpiC	eye:	n/a
40	chr22:31460131-31460181	PrEC	prostate:	n/a
41	chr22:31460131-31460181	GM19239	blood:	n/a
42	chr22:31460131-31460181	RPTEC	kidney:	n/a
43	chr22:31460131-31460181	AG09319	gingival:	n/a
44	chr22:31460131-31460181	BE2_C	brain:	n/a
45	chr22:31460131-31460181	HCT-116	colon:	n/a
46	chr22:31460131-31460181	HAEpiC	amniotic membrane:	n/a
47	chr22:31460131-31460181	HCM	heart:	n/a
48	chr22:31460131-31460181	AG04449	skin:	fetal
49	chr22:31460131-31460181	HRPEpiC	eye:	n/a
50	chr22:31460131-31460181	NHDF-neo	bronchial:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:31460561..31462331-chr22:31465438..31468064,2	K562	blood:
2	chr22:31450684..31454190-chr22:31458624..31461519,3	K562	blood:
3	chr22:31464585..31466786-chr22:31479626..31481207,2	MCF-7	breast:
4	chr22:31363691..31369255-chr22:31456002..31460514,7	MCF-7	breast:
5	chr22:31458274..31462644-chr22:31476246..31482425,10	K562	blood:
6	chr22:31450083..31452668-chr22:31463620..31466392,3	MCF-7	breast:
7	chr22:31450718..31452880-chr22:31457371..31459942,3	MCF-7	breast:
8	chr22:31451720..31453462-chr22:31457824..31459739,2	MCF-7	breast:
9	chr22:31360377..31363179-chr22:31451258..31453241,3	K562	blood:
10	chr22:31363469..31366268-chr22:31450278..31456884,6	MCF-7	breast:
11	chr22:31445856..31448467-chr22:31451849..31454142,3	K562	blood:
12	chr22:31448944..31454267-chr22:31475725..31482456,15	MCF-7	breast:
13	chr22:31455769..31462183-chr22:31475245..31482356,13	K562	blood:
14	chr22:31450722..31454659-chr22:31476861..31481048,4	K562	blood:
15	chr22:31452690..31454726-chr22:31460173..31463712,3	MCF-7	breast:
16	chr22:31364481..31367281-chr22:31457492..31460562,3	MCF-7	breast:
17	chr22:31455775..31461842-chr22:31476267..31480955,13	MCF-7	breast:
18	chr22:31451720..31453462-chr22:31457824..31459739,2	MCF-7	breast:
19	chr22:31449294..31454779-chr22:31475265..31480255,11	MCF-7	breast:
20	chr22:31363776..31366652-chr22:31458331..31460655,2	K562	blood:
21	chr22:31457775..31462699-chr22:31474304..31478789,5	MCF-7	breast:
22	chr22:31459554..31462165-chr22:31463445..31465017,2	K562	blood:
23	chr22:31432776..31435079-chr22:31450665..31453170,2	MCF-7	breast:
24	chr22:31362787..31366384-chr22:31450123..31453347,3	MCF-7	breast:
25	chr22:31452690..31454726-chr22:31460173..31463712,3	MCF-7	breast:
26	chr22:31449984..31454484-chr22:31456787..31462654,7	K562	blood:

(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
ENSG00000183963	chromatin interactions
ENSG00000133422	chromatin interactions
ENSG00000273387	chromatin interactions
ENSG00000253352	chromatin interactions

Extended variants
information (count: 446 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144386272	chr22:31453017-31453018	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs532229300	chr22:31453018-31453019	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs528281649	chr22:31453023-31453024	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs559097771	chr22:31453031-31453032	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs528058463	chr22:31453042-31453043	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs187233781	chr22:31453064-31453065	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs552012048	chr22:31453066-31453067	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs373281980	chr22:31453068-31453069	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs568175853	chr22:31453112-31453113	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs577243342	chr22:31453117-31453118	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs16989281	chr22:31453205-31453206	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs191371198	chr22:31453219-31453220	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs570311601	chr22:31453263-31453264	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs4820933	chr22:31453264-31453265	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs7291565	chr22:31453321-31453322	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs147832979	chr22:31453336-31453337	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs550182843	chr22:31453434-31453435	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs141428311	chr22:31453436-31453437	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs555451786	chr22:31453438-31453439	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs575723952	chr22:31453460-31453461	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs544707843	chr22:31453540-31453541	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs558434957	chr22:31453552-31453553	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs578188719	chr22:31453577-31453578	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs182964370	chr22:31453580-31453581	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs569965785	chr22:31453608-31453609	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs539873212	chr22:31453751-31453752	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs188770599	chr22:31453758-31453759	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs541843604	chr22:31453788-31453789	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs150419619	chr22:31453853-31453854	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs193295346	chr22:31453944-31453945	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs185602023	chr22:31453946-31453947	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs5997858	chr22:31453961-31453962	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs5997859	chr22:31454023-31454024	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs536118262	chr22:31454024-31454025	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs188765480	chr22:31454096-31454097	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs5749211	chr22:31454118-31454119	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs142199929	chr22:31454129-31454130	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs549397005	chr22:31454157-31454158	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs569152748	chr22:31454164-31454165	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs199544370	chr22:31454206-31454207	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs538354619	chr22:31454241-31454242	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs192147098	chr22:31454386-31454387	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs578231041	chr22:31454387-31454388	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs534425255	chr22:31454394-31454395	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs554058617	chr22:31454395-31454396	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs183911156	chr22:31454404-31454405	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs4624487	chr22:31454441-31454442	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs574316802	chr22:31454500-31454501	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs542949448	chr22:31454514-31454515	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs375226404	chr22:31454579-31454580	Weak transcription Enhancers	TF binding region 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:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31440000-31453200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr22:31441600-31455000	Enhancers	Fetal Stomach	stomach
3	chr22:31443600-31455400	Weak transcription	K562	blood
4	chr22:31449200-31453400	Enhancers	Fetal Muscle Leg	muscle
5	chr22:31449800-31453200	Enhancers	Fetal Lung	lung
6	chr22:31450000-31453000	Enhancers	Fetal Muscle Trunk	muscle
7	chr22:31450200-31454400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr22:31450800-31453000	Enhancers	Placenta	Placenta
9	chr22:31450800-31453200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr22:31450800-31453200	Enhancers	Fetal Intestine Small	intestine
11	chr22:31450800-31453600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr22:31450800-31454600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr22:31451000-31453200	Enhancers	Fetal Intestine Large	intestine
14	chr22:31451000-31453400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr22:31451000-31453400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr22:31451400-31455400	Weak transcription	Right Ventricle	heart
17	chr22:31451600-31453400	Enhancers	Rectal Smooth Muscle	rectum
18	chr22:31451600-31453600	Enhancers	Colon Smooth Muscle	Colon
19	chr22:31451600-31453600	Enhancers	A549	lung
20	chr22:31452000-31453200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr22:31452000-31458000	Weak transcription	Adipose Nuclei	Adipose
22	chr22:31452200-31453200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr22:31452200-31453200	Weak transcription	Lung	lung
24	chr22:31452200-31453400	Enhancers	Stomach Smooth Muscle	stomach
25	chr22:31452200-31453400	Enhancers	HepG2	liver
26	chr22:31452200-31455600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr22:31452200-31455600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr22:31452200-31455600	Weak transcription	Ovary	ovary
29	chr22:31452200-31455800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr22:31452200-31455800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr22:31452200-31456000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr22:31452200-31456000	Weak transcription	NHEK	skin
33	chr22:31452800-31453000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr22:31452800-31453200	Enhancers	Fetal Heart	heart
35	chr22:31452800-31453800	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr22:31452800-31455600	Weak transcription	HMEC	breast
37	chr22:31452800-31456800	Weak transcription	Hela-S3	cervix
38	chr22:31452800-31458200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr22:31453000-31453400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr22:31453000-31455600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr22:31453000-31455600	Weak transcription	Fetal Muscle Trunk	muscle
42	chr22:31453000-31455600	Weak transcription	Placenta	Placenta
43	chr22:31453200-31453400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr22:31453200-31453600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr22:31453200-31455400	Weak transcription	Fetal Lung	lung
46	chr22:31453200-31455600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr22:31453200-31455600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr22:31453200-31455600	Weak transcription	Fetal Intestine Large	intestine
49	chr22:31453200-31455600	Weak transcription	Fetal Intestine Small	intestine
50	chr22:31453400-31454200	Weak transcription	Stomach Smooth Muscle	stomach

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