Variant report

Variant	nsv471194
Chromosome Location	chr22:30103476-30128380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:541)
CpG islands
(count:1285)
Chromatin interactive
region (count:19)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:30112673-30113047	HepG2	liver:	n/a	n/a
2	ATF3	chr22:30123277-30123446	K562	blood:	n/a	n/a
3	BACH1	chr22:30117117-30117164	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr22:30112938-30112959	K562	blood:	n/a	n/a
5	BHLHE40	chr22:30123039-30123491	K562	blood:	n/a	chr22:30123301-30123317 chr22:30123298-30123314
6	BHLHE40	chr22:30128256-30128610	K562	blood:	n/a	n/a
7	BHLHE40	chr22:30122204-30122269	K562	blood:	n/a	n/a
8	CBX3	chr22:30128277-30128548	K562	blood:	n/a	n/a
9	CBX3	chr22:30122729-30123043	K562	blood:	n/a	n/a
10	CCNT2	chr22:30122115-30122354	K562	blood:	n/a	n/a
11	CEBPB	chr22:30120445-30120468	IMR90	lung:	n/a	chr22:30120448-30120459
12	CEBPB	chr22:30120297-30120612	HepG2	liver:	n/a	chr22:30120448-30120459
13	CEBPB	chr22:30112795-30113094	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr22:30106956-30107195	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr22:30120413-30120592	Hela-S3	cervix:	n/a	chr22:30120448-30120459
16	CEBPB	chr22:30112775-30113097	HepG2	liver:	n/a	n/a
17	CEBPB	chr22:30123189-30123587	MCF-7	breast:	n/a	n/a
18	CEBPB	chr22:30123242-30123551	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr22:30112804-30113093	IMR90	lung:	n/a	n/a
20	CEBPB	chr22:30123279-30123521	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr22:30112810-30112951	HepG2	liver:	n/a	n/a
22	CEBPB	chr22:30123253-30123563	K562	blood:	n/a	n/a
23	CEBPB	chr22:30120332-30120505	A549	lung:	n/a	chr22:30120448-30120459
24	CEBPB	chr22:30120302-30120606	MCF-7	breast:	n/a	chr22:30120448-30120459
25	CEBPB	chr22:30123245-30123541	IMR90	lung:	n/a	n/a
26	CEBPB	chr22:30123247-30123550	HepG2	liver:	n/a	n/a
27	CEBPB	chr22:30123286-30123530	A549	lung:	n/a	n/a
28	CEBPB	chr22:30112805-30112998	K562	blood:	n/a	n/a
29	CEBPD	chr22:30123286-30123454	HepG2	liver:	n/a	n/a
30	CHD2	chr22:30112908-30113057	HepG2	liver:	n/a	n/a
31	CHD2	chr22:30122854-30123003	K562	blood:	n/a	n/a
32	CHD2	chr22:30106924-30107562	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr22:30123260-30123410	AG04450	lung:	n/a	n/a
34	CTCF	chr22:30123279-30123448	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr22:30114693-30114717	MCF-7	breast:	n/a	n/a
36	CTCF	chr22:30119880-30120030	GM12873	blood:	n/a	n/a
37	CTCF	chr22:30123320-30123470	GM12864	blood:	n/a	n/a
38	CTCF	chr22:30123230-30123474	Fibrobl	skin:	n/a	n/a
39	CTCF	chr22:30119891-30120018	GM12878	blood:	n/a	n/a
40	CTCF	chr22:30122800-30122950	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr22:30108863-30108879	MCF-7	breast:	n/a	n/a
42	CTCF	chr22:30123300-30123450	WI-38	lung:	n/a	n/a
43	CTCF	chr22:30123256-30123477	A549	lung:	n/a	n/a
44	CTCF	chr22:30123280-30123430	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr22:30123280-30123430	BJ	skin:	n/a	n/a
46	CTCF	chr22:30108859-30108896	H1-hESC	embryonic stem cell:	n/a	chr22:30108862-30108875
47	CTCF	chr22:30119940-30120090	HCT-116	colon:	n/a	n/a
48	CTCF	chr22:30123280-30123430	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr22:30119892-30120041	GM12878	blood:	n/a	n/a
50	CTCF	chr22:30123300-30123450	AG09319	gingival:	n/a	n/a

(count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30125483-30125533	AoSMC	blood vessel:	n/a
2	chr22:30125483-30125533	NH-A	brain:	n/a
3	chr22:30107178-30107228	AG09309	skin:	n/a
4	chr22:30116953-30117003	AG09319	gingival:	n/a
5	chr22:30125483-30125533	AoSMC	blood vessel:	n/a
6	chr22:30125483-30125533	NH-A	brain:	n/a
7	chr22:30107178-30107228	AG09309	skin:	n/a
8	chr22:30116953-30117003	AG09319	gingival:	n/a
9	chr22:30125483-30125533	K562	blood:	n/a
10	chr22:30119712-30119762	SK-N-SH	brain:	n/a
11	chr22:30116037-30116087	SKMC	muscle:	n/a
12	chr22:30127118-30127168	BE2_C	brain:	n/a
13	chr22:30115154-30115204	SK-N-MC	brain:	n/a
14	chr22:30119712-30119762	HCPEpiC	choroid plexus:	n/a
15	chr22:30116328-30116378	Caco-2	colon:	n/a
16	chr22:30119712-30119762	ProgFib	skin:	n/a
17	chr22:30125642-30125692	BJ	skin:	n/a
18	chr22:30117734-30117784	AG04450	lung:	fetal
19	chr22:30107178-30107228	HRPEpiC	eye:	n/a
20	chr22:30115203-30115253	CMK	blood:	n/a
21	chr22:30115154-30115204	BJ	skin:	n/a
22	chr22:30117159-30117209	HMEC	breast:	n/a
23	chr22:30115203-30115253	HL-60	blood:	n/a
24	chr22:30125353-30125403	Jurkat	blood:	n/a
25	chr22:30112403-30112453	HEK293	kidney:	embryo
26	chr22:30116919-30116969	HRCEpiC	kidney:	n/a
27	chr22:30115203-30115253	GM12878	blood:	n/a
28	chr22:30127118-30127168	AG10803	skin:	n/a
29	chr22:30107178-30107228	AG10803	skin:	n/a
30	chr22:30115348-30115398	SK-N-SH	brain:	n/a
31	chr22:30122327-30122377	Caco-2	colon:	n/a
32	chr22:30107178-30107228	A549	lung:	n/a
33	chr22:30116439-30116489	Hepatocyte	liver:	n/a
34	chr22:30116328-30116378	PrEC	prostate:	n/a
35	chr22:30115154-30115204	PANC-1	pancreas:	n/a
36	chr22:30115203-30115253	GM12892	blood:	n/a
37	chr22:30125483-30125533	HCM	heart:	n/a
38	chr22:30116953-30117003	PFSK-1	brain:	n/a
39	chr22:30116919-30116969	NT2-D1	testis:	n/a
40	chr22:30117159-30117209	GM12878	blood:	n/a
41	chr22:30122327-30122377	PANC-1	pancreas:	n/a
42	chr22:30107178-30107228	HCT-116	colon:	n/a
43	chr22:30116328-30116378	HCM	heart:	n/a
44	chr22:30112403-30112453	SAEC	small airway:	n/a
45	chr22:30117734-30117784	NH-A	brain:	n/a
46	chr22:30115203-30115253	AG04449	skin:	fetal
47	chr22:30122327-30122377	HCF	heart:	n/a
48	chr22:30117159-30117209	PFSK-1	brain:	n/a
49	chr22:30125483-30125533	HCPEpiC	choroid plexus:	n/a
50	chr22:30115348-30115398	AG10803	skin:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:30103672..30106590-chr22:30107402..30109092,2	MCF-7	breast:
2	chr22:30119899..30121884-chr22:30123778..30126684,2	MCF-7	breast:
3	chr22:30122754..30125379-chr22:30128810..30131334,3	MCF-7	breast:
4	chr22:30124714..30127862-chr22:30128538..30131492,3	K562	blood:
5	chr22:30114234..30116768-chr22:30120016..30122557,3	MCF-7	breast:
6	chr22:30101634..30103485-chr22:30110793..30113259,2	K562	blood:
7	chr22:30101634..30103485-chr22:30110793..30113259,2	K562	blood:
8	chr22:30127476..30130014-chr22:30183535..30186061,2	MCF-7	breast:
9	chr22:30096968..30098760-chr22:30102459..30104662,3	MCF-7	breast:
10	chr22:30119899..30121884-chr22:30123778..30126684,2	MCF-7	breast:
11	chr22:30120187..30123071-chr22:30140004..30142315,2	K562	blood:
12	chr22:30126165..30128637-chr22:30161660..30163491,2	MCF-7	breast:
13	chr22:30103672..30106590-chr22:30107402..30109092,2	MCF-7	breast:
14	chr22:30117740..30119771-chr22:30165612..30167453,2	MCF-7	breast:
15	chr22:30126344..30127866-chr22:30201046..30202629,2	K562	blood:
16	chr22:30118032..30120779-chr22:30154984..30156711,2	K562	blood:
17	chr22:30123279..30125899-chr22:30126231..30128918,2	K562	blood:
18	chr22:30123279..30125899-chr22:30126231..30128918,2	K562	blood:
19	chr22:30096975..30100180-chr22:30101896..30105574,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZMAT5-1	chr22:30115537-30115756	NONHSAT084729
2	lnc-ZMAT5-1	chr22:30115558-30115703	XLOC_014338
3	lnc-ZMAT5-1	chr22:30107809-30107906	XLOC_014338
4	lnc-ZMAT5-1	chr22:30107802-30107984	XLOC_014338
5	lnc-ZMAT5-1	chr22:30115537-30115737	XLOC_014338
6	lnc-ZMAT5-1	chr22:30115537-30115848	XLOC_014338
7	lnc-ZMAT5-1	chr22:30114214-30114787	NONHSAT084729

No data

Variant related genes	Relation type
CABP7	TF binding region
ENSG00000232396	TF binding region
ENSG00000239446	TF binding region
CABP7	CpG island
ENSG00000232396	CpG island
ENSG00000239446	CpG island
ENSG00000232396	chromatin interactions
ENSG00000184076	chromatin interactions
ENSG00000100314	chromatin interactions
ENSG00000100319	chromatin interactions
ENSG00000239446	chromatin interactions
NHLRC3	miRNA target sites
NID1	miRNA target sites

Extended variants
information (count: 1000 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1000 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2530682	chr22:30103476-30103477	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182845487	chr22:30103519-30103520	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs574323141	chr22:30103547-30103548	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs544470191	chr22:30103600-30103601	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs563107939	chr22:30103685-30103686	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs35921780	chr22:30103701-30103702	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs577669444	chr22:30103704-30103705	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs548685974	chr22:30103706-30103707	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs73390954	chr22:30103747-30103748	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs531148032	chr22:30103797-30103798	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs2527342	chr22:30103819-30103820	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs186042453	chr22:30103832-30103833	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs571210249	chr22:30103837-30103838	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs561021072	chr22:30103858-30103859	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs531670431	chr22:30103924-30103925	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs147000515	chr22:30103980-30103981	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs34906197	chr22:30103997-30103998	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs571467160	chr22:30104005-30104006	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs138132370	chr22:30104019-30104020	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs375032491	chr22:30104037-30104038	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs547502308	chr22:30104052-30104053	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs369397719	chr22:30104077-30104078	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs565811626	chr22:30104148-30104149	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs535870155	chr22:30104159-30104160	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs554591434	chr22:30104264-30104265	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs558611861	chr22:30104274-30104275	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs564922985	chr22:30104284-30104285	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs131257	chr22:30104285-30104286	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs113710584	chr22:30104288-30104289	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs116844839	chr22:30104351-30104352	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs556310019	chr22:30104393-30104394	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs577830307	chr22:30104395-30104396	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs545230286	chr22:30104429-30104430	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs560191239	chr22:30104501-30104502	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs572251315	chr22:30104527-30104528	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs143096331	chr22:30104563-30104564	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs554656603	chr22:30104638-30104639	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148220165	chr22:30104640-30104641	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560656803	chr22:30104650-30104651	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141180285	chr22:30104706-30104707	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565215950	chr22:30104710-30104711	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546408815	chr22:30104739-30104740	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532325690	chr22:30104795-30104796	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191231460	chr22:30104815-30104816	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150721800	chr22:30104816-30104817	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536357687	chr22:30104827-30104828	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527709515	chr22:30104842-30104843	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376890157	chr22:30104856-30104857	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs35360305	chr22:30104857-30104858	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2530683	chr22:30104909-30104910	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:70)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	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
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	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
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30096000-30103600	Enhancers	Fetal Brain Male	brain
2	chr22:30096400-30103600	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr22:30096400-30107400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr22:30096600-30103800	Enhancers	Brain Cingulate Gyrus	brain
5	chr22:30097000-30106400	Weak transcription	Psoas Muscle	Psoas
6	chr22:30098800-30115600	Weak transcription	Right Atrium	heart
7	chr22:30099400-30103600	Enhancers	Brain Germinal Matrix	brain
8	chr22:30100800-30103600	Enhancers	Brain Substantia Nigra	brain
9	chr22:30101000-30103600	Enhancers	Brain Angular Gyrus	brain
10	chr22:30101400-30104800	Weak transcription	HSMMtube	muscle
11	chr22:30101600-30103800	Enhancers	Brain Hippocampus Middle	brain
12	chr22:30102400-30103600	Bivalent Enhancer	Fetal Muscle Leg	muscle
13	chr22:30102800-30103600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr22:30102800-30103600	Bivalent Enhancer	Fetal Stomach	stomach
15	chr22:30102800-30104200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr22:30102800-30105200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr22:30102800-30106000	Weak transcription	Spleen	Spleen
18	chr22:30103200-30106400	Weak transcription	Fetal Brain Female	brain
19	chr22:30103600-30106200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr22:30103600-30106400	Weak transcription	Fetal Brain Male	brain
21	chr22:30104600-30105200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr22:30104600-30108000	Enhancers	Fetal Muscle Leg	muscle
23	chr22:30104800-30105200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr22:30104800-30105200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr22:30104800-30105800	Enhancers	HSMMtube	muscle
26	chr22:30105000-30105200	Bivalent Enhancer	Right Ventricle	heart
27	chr22:30105800-30106200	Weak transcription	HSMMtube	muscle
28	chr22:30105800-30108400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr22:30106000-30106200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr22:30106000-30106200	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr22:30106000-30106600	Enhancers	Hela-S3	cervix
32	chr22:30106000-30107000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr22:30106000-30107400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr22:30106000-30107800	Enhancers	Spleen	Spleen
35	chr22:30106200-30106800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
36	chr22:30106200-30107600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr22:30106200-30107800	Enhancers	HSMMtube	muscle
38	chr22:30106400-30107200	Enhancers	Psoas Muscle	Psoas
39	chr22:30106400-30107400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
40	chr22:30106400-30107600	Enhancers	Fetal Brain Male	brain
41	chr22:30106400-30107800	Enhancers	Fetal Brain Female	brain
42	chr22:30106400-30107800	Enhancers	Pancreas	Pancrea
43	chr22:30106600-30106800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr22:30106600-30106800	Bivalent Enhancer	Fetal Intestine Large	intestine
45	chr22:30106600-30107000	Bivalent Enhancer	Brain Hippocampus Middle	brain
46	chr22:30106600-30107400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
47	chr22:30106600-30107400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
48	chr22:30106600-30107400	Flanking Active TSS	Hela-S3	cervix
49	chr22:30106800-30107000	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
50	chr22:30106800-30107000	Enhancers	Skeletal Muscle Female	skeletal muscle

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