Variant report

Variant	nsv538708
Chromosome Location	chr7:4928087-4962190
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:104)
CpG islands
(count:366)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:104 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:4946335-4946650	K562	blood:	n/a	n/a
2	ATF2	chr7:4946333-4946705	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:4946260-4946603	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr7:4946355-4946692	K562	blood:	n/a	n/a
5	CBX3	chr7:4933736-4934034	K562	blood:	n/a	n/a
6	CEBPB	chr7:4929346-4929739	K562	blood:	n/a	chr7:4929483-4929494
7	CEBPB	chr7:4955641-4955811	K562	blood:	n/a	n/a
8	CEBPB	chr7:4929371-4929693	MCF-7	breast:	n/a	chr7:4929483-4929494
9	CEBPB	chr7:4929347-4929642	A549	lung:	n/a	chr7:4929483-4929494
10	CEBPB	chr7:4929377-4929668	IMR90	lung:	n/a	chr7:4929483-4929494
11	CEBPB	chr7:4952325-4952525	HepG2	liver:	n/a	chr7:4952392-4952403
12	CEBPB	chr7:4929319-4929640	HepG2	liver:	n/a	chr7:4929483-4929494
13	CEBPB	chr7:4932943-4933143	K562	blood:	n/a	n/a
14	CEBPB	chr7:4929309-4929916	Hela-S3	cervix:	n/a	chr7:4929483-4929494
15	CEBPD	chr7:4931012-4931750	K562	blood:	n/a	n/a
16	CEBPD	chr7:4930863-4931822	K562	blood:	n/a	n/a
17	CREB1	chr7:4946376-4946678	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr7:4928107-4928230	K562	blood:	n/a	chr7:4928159-4928177
19	CTCF	chr7:4955813-4956031	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr7:4928100-4928250	MCF-7	breast:	n/a	chr7:4928159-4928177
21	CTCF	chr7:4955800-4955950	GM12873	blood:	n/a	n/a
22	CTCF	chr7:4928120-4928200	HepG2	liver:	n/a	chr7:4928159-4928177
23	CTCF	chr7:4952998-4953123	Lung_OC	lung:	n/a	n/a
24	CTCF	chr7:4928097-4928218	HepG2	liver:	n/a	chr7:4928159-4928177
25	CTCF	chr7:4929799-4929827	GM13976	blood:	n/a	n/a
26	CTCF	chr7:4928140-4928196	MCF-7	breast:	n/a	chr7:4928159-4928177
27	CTCF	chr7:4928148-4928226	MCF-7	breast:	n/a	chr7:4928159-4928177
28	CTCF	chr7:4928156-4928189	MCF-7	breast:	n/a	chr7:4928159-4928177
29	CTCF	chr7:4955880-4956014	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr7:4955860-4956010	A549	lung:	n/a	n/a
31	CTCF	chr7:4928121-4928231	K562	blood:	n/a	chr7:4928159-4928177
32	CTCF	chr7:4928040-4928190	MCF-7	breast:	n/a	chr7:4928159-4928177
33	CTCF	chr7:4955840-4955990	HepG2	liver:	n/a	n/a
34	CTCF	chr7:4951075-4951194	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr7:4928088-4928250	MCF-7	breast:	n/a	chr7:4928159-4928177
36	EGR1	chr7:4959474-4959690	K562	blood:	n/a	n/a
37	ELF1	chr7:4959645-4959874	K562	blood:	n/a	n/a
38	FOXA1	chr7:4927688-4928177	T-47D	breast:	n/a	n/a
39	FOXA1	chr7:4927750-4928147	T-47D	breast:	n/a	n/a
40	FOXA2	chr7:4927825-4928133	A549	lung:	n/a	n/a
41	GABPA	chr7:4959688-4960038	K562	blood:	n/a	n/a
42	GATA2	chr7:4930954-4931631	K562	blood:	n/a	n/a
43	GATA2	chr7:4930993-4931702	K562	blood:	n/a	n/a
44	GATA3	chr7:4927733-4928128	MCF-7	breast:	n/a	n/a
45	GATA3	chr7:4927693-4928244	T-47D	breast:	n/a	n/a
46	GATA3	chr7:4927573-4928317	MCF-7	breast:	n/a	n/a
47	GATA3	chr7:4931110-4931748	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr7:4927696-4928253	T-47D	breast:	n/a	n/a
49	HDAC2	chr7:4927715-4928163	MCF-7	breast:	n/a	n/a
50	JUN	chr7:4946376-4946657	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4939325-4939375	HIPEpiC	eye:	n/a
2	chr7:4945896-4945946	U87	brain:	n/a
3	chr7:4945896-4945946	HMEC	breast:	n/a
4	chr7:4939325-4939375	GM12891	blood:	n/a
5	chr7:4948052-4948102	PANC-1	pancreas:	n/a
6	chr7:4939403-4939453	HCM	heart:	n/a
7	chr7:4948064-4948114	MCF10A-Er-Src	breast:	n/a
8	chr7:4948064-4948114	SK-N-SH_RA	brain:	n/a
9	chr7:4948064-4948114	ECC-1	luminal epithelium:	n/a
10	chr7:4945896-4945946	Hepatocyte	liver:	n/a
11	chr7:4945896-4945946	AG04450	lung:	fetal
12	chr7:4948064-4948114	K562	blood:	n/a
13	chr7:4939325-4939375	A549	lung:	n/a
14	chr7:4948052-4948102	HRE	kidney:	n/a
15	chr7:4948052-4948102	HCT-116	colon:	n/a
16	chr7:4945896-4945946	HEK293	kidney:	embryo
17	chr7:4948052-4948102	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:4948052-4948102	CMK	blood:	n/a
19	chr7:4948613-4948663	NHDF-neo	bronchial:	n/a
20	chr7:4948613-4948663	HRCEpiC	kidney:	n/a
21	chr7:4939325-4939375	AoSMC	blood vessel:	n/a
22	chr7:4948052-4948102	AoSMC	blood vessel:	n/a
23	chr7:4948613-4948663	HRE	kidney:	n/a
24	chr7:4948613-4948663	H1-hESC	embryonic stem cell:	embryo
25	chr7:4939403-4939453	IMR90	lung:	fetal
26	chr7:4945896-4945946	GM12891	blood:	n/a
27	chr7:4945896-4945946	HIPEpiC	eye:	n/a
28	chr7:4939403-4939453	AG04449	skin:	fetal
29	chr7:4948052-4948102	GM19239	blood:	n/a
30	chr7:4948613-4948663	Hepatocyte	liver:	n/a
31	chr7:4945896-4945946	AG04449	skin:	fetal
32	chr7:4939403-4939453	SAEC	small airway:	n/a
33	chr7:4948052-4948102	HAEpiC	amniotic membrane:	n/a
34	chr7:4948064-4948114	HL-60	blood:	n/a
35	chr7:4948052-4948102	GM12892	blood:	n/a
36	chr7:4939325-4939375	NH-A	brain:	n/a
37	chr7:4939403-4939453	HRE	kidney:	n/a
38	chr7:4945896-4945946	NH-A	brain:	n/a
39	chr7:4948613-4948663	HCT-116	colon:	n/a
40	chr7:4939325-4939375	AG09309	skin:	n/a
41	chr7:4948064-4948114	AG04450	lung:	fetal
42	chr7:4939325-4939375	HCF	heart:	n/a
43	chr7:4948613-4948663	U87	brain:	n/a
44	chr7:4948064-4948114	NHBE	bronchial:	n/a
45	chr7:4948052-4948102	HRPEpiC	eye:	n/a
46	chr7:4948064-4948114	T-47D	breast:	n/a
47	chr7:4948613-4948663	HUVEC	blood vessel:	n/a
48	chr7:4948052-4948102	MCF-7	breast:	n/a
49	chr7:4948613-4948663	K562	blood:	n/a
50	chr7:4948064-4948114	HEEpiC	esophagus:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4943284..4944790-chr7:4959243..4960927,2	MCF-7	breast:
2	chr7:4937830..4939738-chr7:4942280..4944560,2	MCF-7	breast:
3	chr7:4920467..4922780-chr7:4952296..4954216,2	MCF-7	breast:
4	chr7:4943284..4944790-chr7:4959243..4960927,2	MCF-7	breast:
5	chr7:4937830..4939738-chr7:4942280..4944560,2	MCF-7	breast:
6	chr7:4813542..4816432-chr7:4945729..4948675,2	MCF-7	breast:
7	chr7:4927849..4928583-chr7:5124843..5125774,2	MCF-7	breast:
8	chr7:4909223..4912201-chr7:4926426..4928312,2	MCF-7	breast:
9	chr20:57918982..57919503-chr7:4943405..4943905,2	MCF-7	breast:
10	chr7:4920631..4924250-chr7:4926781..4929390,5	K562	blood:
11	chr7:4960887..4962459-chr7:4962868..4964450,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMD2-2	chr7:4936899-4938466	NONHSAT118885

No data

Variant related genes	Relation type
RADIL	TF binding region
RADIL	CpG island
ENSG00000242802	chromatin interactions
ENSG00000157927	chromatin interactions

Extended variants
information (count: 1639 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1639 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567849051	chr7:4928094-4928095	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs183764391	chr7:4928098-4928099	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563691413	chr7:4928101-4928102	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs79716623	chr7:4928122-4928123	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs117055159	chr7:4928127-4928128	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs114195760	chr7:4928165-4928166	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs55773258	chr7:4928176-4928177	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs371316570	chr7:4928183-4928184	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557426640	chr7:4928217-4928218	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs139863485	chr7:4928256-4928257	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs543233511	chr7:4928287-4928288	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373977752	chr7:4928294-4928295	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs35805997	chr7:4928354-4928355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs187441902	chr7:4928366-4928367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559696835	chr7:4928373-4928374	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533356959	chr7:4928394-4928395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545466434	chr7:4928423-4928424	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs77934351	chr7:4928452-4928453	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531068579	chr7:4928474-4928475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs549226697	chr7:4928479-4928480	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567799851	chr7:4928487-4928488	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs193273971	chr7:4928534-4928535	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs535230441	chr7:4928568-4928569	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546878427	chr7:4928583-4928584	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs571653304	chr7:4928610-4928611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs572050985	chr7:4928615-4928616	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546153654	chr7:4928631-4928632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550994506	chr7:4928653-4928654	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs569562751	chr7:4928665-4928666	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs537123882	chr7:4928666-4928667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374984391	chr7:4928674-4928675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111393602	chr7:4928676-4928677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs143297216	chr7:4928705-4928706	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554491327	chr7:4928739-4928740	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs573741949	chr7:4928749-4928750	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534857796	chr7:4928755-4928756	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs185417095	chr7:4928771-4928772	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs146602327	chr7:4928778-4928779	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs114975962	chr7:4928798-4928799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs563666945	chr7:4928800-4928801	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs452102	chr7:4928833-4928834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs115882014	chr7:4928841-4928842	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561265272	chr7:4928854-4928855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs62451386	chr7:4928863-4928864	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs74667370	chr7:4928895-4928896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs12666642	chr7:4928896-4928897	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs149843529	chr7:4928901-4928902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs190565446	chr7:4928916-4928917	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs79976584	chr7:4928939-4928940	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs372652638	chr7:4929021-4929022	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4923400-4928200	Weak transcription	Right Atrium	heart
2	chr7:4923400-4933800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:4928000-4928200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr7:4928000-4928400	Enhancers	Lung	lung
5	chr7:4928200-4928400	Enhancers	Brain Germinal Matrix	brain
6	chr7:4928200-4928400	Enhancers	Right Atrium	heart
7	chr7:4929200-4929400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:4933800-4934600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr7:4933800-4934600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr7:4939400-4939600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:4939800-4941200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:4940200-4940400	Enhancers	Brain Anterior Caudate	brain
13	chr7:4940400-4946800	Weak transcription	Brain Anterior Caudate	brain
14	chr7:4941200-4941400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:4941400-4942200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr7:4942200-4943400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:4943000-4943200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr7:4943000-4943600	Enhancers	Lung	lung
19	chr7:4944600-4957600	Weak transcription	Brain Cingulate Gyrus	brain
20	chr7:4946600-4964000	Weak transcription	Brain Hippocampus Middle	brain
21	chr7:4946800-4947600	Strong transcription	Brain Anterior Caudate	brain
22	chr7:4947600-4957600	Weak transcription	Brain Anterior Caudate	brain
23	chr7:4949400-4949800	Enhancers	Fetal Muscle Trunk	muscle
24	chr7:4949600-4950000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr7:4949600-4950000	Enhancers	Fetal Muscle Leg	muscle
26	chr7:4952000-4952800	Enhancers	HepG2	liver
27	chr7:4957600-4957800	ZNF genes & repeats	Brain Cingulate Gyrus	brain
28	chr7:4957600-4958000	ZNF genes & repeats	Brain Anterior Caudate	brain
29	chr7:4957800-4971400	Weak transcription	Brain Cingulate Gyrus	brain
30	chr7:4958000-4971400	Weak transcription	Brain Anterior Caudate	brain
31	chr7:4959000-4959800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:4959800-4960000	ZNF genes & repeats	Spleen	Spleen
33	chr7:4960000-4960200	Bivalent Enhancer	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links