Variant report

Variant	esv3451290
Chromosome Location	chr7:6911323-6993815
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1139)
CpG islands
(count:1099)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1139 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:6962881-6963081	K562	blood:	n/a	n/a
2	BATF	chr7:6993800-6993986	GM12878	blood:	n/a	n/a
3	BATF	chr7:6967778-6968070	GM12878	blood:	n/a	n/a
4	BATF	chr7:6911459-6911623	GM12878	blood:	n/a	n/a
5	BATF	chr7:6967768-6968127	GM12878	blood:	n/a	n/a
6	BATF	chr7:6992805-6993006	GM12878	blood:	n/a	n/a
7	BATF	chr7:6967256-6967613	GM12878	blood:	n/a	n/a
8	BATF	chr7:6959520-6959921	GM12878	blood:	n/a	chr7:6959720-6959731
9	BATF	chr7:6959640-6959863	GM12878	blood:	n/a	chr7:6959720-6959731
10	BATF	chr7:6965792-6966222	GM12878	blood:	n/a	n/a
11	BATF	chr7:6965828-6966219	GM12878	blood:	n/a	n/a
12	BATF	chr7:6970367-6970679	GM12878	blood:	n/a	n/a
13	BATF	chr7:6930048-6930266	GM12878	blood:	n/a	chr7:6930144-6930155
14	BATF	chr7:6911365-6911638	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:6967281-6967607	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:6966697-6966858	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:6970443-6970693	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:6965764-6966259	GM12878	blood:	n/a	chr7:6966028-6966037
19	BCL11A	chr7:6968204-6968549	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:6967360-6967540	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:6965815-6966145	GM12878	blood:	n/a	chr7:6966028-6966037
22	BCL3	chr7:6916434-6916785	GM12878	blood:	n/a	n/a
23	BCL3	chr7:6928637-6929472	GM12878	blood:	n/a	n/a
24	BCL3	chr7:6928564-6929398	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:6967280-6967585	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:6943039-6943099	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:6962913-6963006	K562	blood:	n/a	n/a
28	BHLHE40	chr7:6929175-6929309	K562	blood:	n/a	n/a
29	BHLHE40	chr7:6968034-6968094	GM12878	blood:	n/a	n/a
30	CBX3	chr7:6965814-6966339	K562	blood:	n/a	n/a
31	CBX3	chr7:6962809-6962993	K562	blood:	n/a	n/a
32	CBX3	chr7:6962801-6963079	K562	blood:	n/a	n/a
33	CBX3	chr7:6977915-6978267	K562	blood:	n/a	n/a
34	CBX3	chr7:6940710-6940918	K562	blood:	n/a	n/a
35	CEBPB	chr7:6936030-6936175	A549	lung:	n/a	n/a
36	CEBPB	chr7:6912527-6912646	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:6975688-6975969	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:6968040-6968133	K562	blood:	n/a	n/a
39	CEBPB	chr7:6962825-6963113	K562	blood:	n/a	n/a
40	CEBPB	chr7:6973635-6973950	A549	lung:	n/a	chr7:6973791-6973802
41	CEBPB	chr7:6973609-6973984	K562	blood:	n/a	chr7:6973791-6973802
42	CEBPB	chr7:6935911-6936099	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:6962895-6963023	K562	blood:	n/a	n/a
44	CEBPB	chr7:6973611-6973982	HepG2	liver:	n/a	chr7:6973791-6973802
45	CEBPB	chr7:6973659-6973952	H1-hESC	embryonic stem cell:	n/a	chr7:6973791-6973802
46	CEBPB	chr7:6973599-6973979	K562	blood:	n/a	chr7:6973791-6973802
47	CEBPB	chr7:6936027-6936120	K562	blood:	n/a	n/a
48	CEBPB	chr7:6967985-6968236	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:6914862-6914979	K562	blood:	n/a	n/a
50	CEBPD	chr7:6962813-6963184	K562	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6979239-6979289	HEK293	kidney:	embryo
2	chr7:6979239-6979289	HEK293	kidney:	embryo
3	chr7:6974956-6975006	SK-N-MC	brain:	n/a
4	chr7:6990107-6990157	GM19239	blood:	n/a
5	chr7:6915508-6915558	HCT-116	colon:	n/a
6	chr7:6993429-6993479	PFSK-1	brain:	n/a
7	chr7:6921561-6921611	AG04449	skin:	fetal
8	chr7:6914498-6914548	AG09309	skin:	n/a
9	chr7:6977556-6977606	Caco-2	colon:	n/a
10	chr7:6979239-6979289	HAEpiC	amniotic membrane:	n/a
11	chr7:6916089-6916139	CMK	blood:	n/a
12	chr7:6979239-6979289	HRE	kidney:	n/a
13	chr7:6974956-6975006	ECC-1	luminal epithelium:	n/a
14	chr7:6974270-6974320	GM12891	blood:	n/a
15	chr7:6977556-6977606	HCF	heart:	n/a
16	chr7:6974956-6975006	ovcar-3	ovarian:	n/a
17	chr7:6974892-6974942	GM19239	blood:	n/a
18	chr7:6993429-6993479	MCF10A-Er-Src	breast:	n/a
19	chr7:6974758-6974808	Caco-2	colon:	n/a
20	chr7:6974270-6974320	NHDF-neo	bronchial:	n/a
21	chr7:6914498-6914548	Hela-S3	cervix:	n/a
22	chr7:6993393-6993443	PrEC	prostate:	n/a
23	chr7:6974956-6975006	A549	lung:	n/a
24	chr7:6916089-6916139	ECC-1	luminal epithelium:	n/a
25	chr7:6921561-6921611	Caco-2	colon:	n/a
26	chr7:6915373-6915423	HRE	kidney:	n/a
27	chr7:6915894-6915944	HUVEC	blood vessel:	n/a
28	chr7:6915373-6915423	NHBE	bronchial:	n/a
29	chr7:6915373-6915423	GM06990	blood:	n/a
30	chr7:6974892-6974942	HL-60	blood:	n/a
31	chr7:6974956-6975006	HEEpiC	esophagus:	n/a
32	chr7:6921561-6921611	SAEC	small airway:	n/a
33	chr7:6915508-6915558	BE2_C	brain:	n/a
34	chr7:6915894-6915944	HRE	kidney:	n/a
35	chr7:6977556-6977606	PrEC	prostate:	n/a
36	chr7:6979488-6979538	SKMC	muscle:	n/a
37	chr7:6990107-6990157	CMK	blood:	n/a
38	chr7:6990107-6990157	GM12878	blood:	n/a
39	chr7:6993429-6993479	Hela-S3	cervix:	n/a
40	chr7:6915508-6915558	NH-A	brain:	n/a
41	chr7:6914289-6914339	HepG2	liver:	n/a
42	chr7:6977556-6977606	HCM	heart:	n/a
43	chr7:6993429-6993479	HNPCEpiC	eye:	n/a
44	chr7:6979488-6979538	HUVEC	blood vessel:	n/a
45	chr7:6974270-6974320	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:6915373-6915423	GM19239	blood:	n/a
47	chr7:6914289-6914339	NB4	blood:	n/a
48	chr7:6977556-6977606	GM19239	blood:	n/a
49	chr7:6990107-6990157	MCF-7	breast:	n/a
50	chr7:6974892-6974942	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:6362339..6362861-chr7:6969838..6970665,2	K562	blood:
2	chr7:6144018..6145898-chr7:6967333..6970236,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCZ1B-5	chr7:6963709-6964144	NONHSAT119086

No data

Variant related genes	Relation type
ALG1L5P	TF binding region
ENSG00000241539	TF binding region
ENSG00000243531	TF binding region
FAM86LP	TF binding region
OR7E136P	TF binding region
ENSG00000263457	TF binding region
OR7E59P	TF binding region
ALG1L5P	CpG island
ENSG00000241539	CpG island
ENSG00000243531	CpG island
FAM86LP	CpG island
OR7E136P	CpG island
ENSG00000263457	CpG island
OR7E59P	CpG island
ENSG00000106346	chromatin interactions

Extended variants
information (count: 4707 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4707 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182542530	chr7:6911324-6911325	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs550665578	chr7:6911339-6911340	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs185878070	chr7:6911342-6911343	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs10275812	chr7:6911345-6911346	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs549344177	chr7:6911352-6911353	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs561163539	chr7:6911365-6911366	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs573173038	chr7:6911381-6911382	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs145255430	chr7:6911393-6911394	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs112525329	chr7:6911410-6911411	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs540402306	chr7:6911417-6911418	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs567538662	chr7:6911443-6911444	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs141283172	chr7:6911448-6911449	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs111906123	chr7:6911449-6911450	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs182631573	chr7:6911503-6911504	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs185731914	chr7:6911504-6911505	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs542913500	chr7:6911516-6911517	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs111396544	chr7:6911538-6911539	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs146713320	chr7:6911550-6911551	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs573200651	chr7:6911558-6911559	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs140335114	chr7:6911566-6911567	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs79826312	chr7:6911567-6911568	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs148053946	chr7:6911569-6911570	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs141646676	chr7:6911602-6911603	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs551081251	chr7:6911609-6911610	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs562735906	chr7:6911629-6911630	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs190446687	chr7:6911638-6911639	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs201032533	chr7:6911648-6911649	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs548611541	chr7:6911672-6911673	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs567521101	chr7:6911675-6911676	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs138500113	chr7:6911681-6911682	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs546444590	chr7:6911696-6911697	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs183524398	chr7:6911699-6911700	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs538335469	chr7:6911725-6911726	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs142727879	chr7:6911727-6911728	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs550758171	chr7:6911732-6911733	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs76463423	chr7:6911745-6911746	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs535807593	chr7:6911760-6911761	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs554163450	chr7:6911765-6911766	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs573163587	chr7:6911775-6911776	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs540953877	chr7:6911791-6911792	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs112439084	chr7:6911803-6911804	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs369299401	chr7:6911807-6911808	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs147302237	chr7:6911817-6911818	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs577412312	chr7:6911818-6911819	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs77873671	chr7:6911826-6911827	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs139287796	chr7:6911856-6911857	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs188912272	chr7:6911864-6911865	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs75438699	chr7:6911867-6911868	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs6949808	chr7:6911874-6911875	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs560494579	chr7:6911881-6911882	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	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
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6910800-6911600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:6910800-6914000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:6911200-6912400	Weak transcription	Stomach Mucosa	stomach
4	chr7:6911400-6913600	Enhancers	Fetal Intestine Small	intestine
5	chr7:6911800-6913000	Enhancers	HepG2	liver
6	chr7:6912400-6912800	Enhancers	Fetal Intestine Large	intestine
7	chr7:6912400-6912800	Enhancers	Stomach Mucosa	stomach
8	chr7:6913000-6913600	Weak transcription	HepG2	liver
9	chr7:6913400-6913800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr7:6913400-6914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:6913600-6913800	Enhancers	HepG2	liver
12	chr7:6913600-6914800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:6914000-6914400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:6914400-6915000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:6921000-6923000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:6921400-6922600	Enhancers	NH-A	brain
17	chr7:6921400-6922800	Enhancers	HSMM	muscle
18	chr7:6921400-6923000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:6921600-6922200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr7:6921600-6923000	Enhancers	HSMMtube	muscle
21	chr7:6922000-6922200	Enhancers	Osteobl	bone
22	chr7:6922200-6922600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:6922200-6922600	Flanking Active TSS	Osteobl	bone
24	chr7:6922600-6922800	Enhancers	Osteobl	bone
25	chr7:6922600-6927600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:6923000-6927800	Weak transcription	HSMMtube	muscle
27	chr7:6925200-6925400	Active TSS	Primary T cells from cord blood	blood
28	chr7:6926400-6928800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr7:6926400-6928800	Weak transcription	Right Atrium	heart
30	chr7:6927000-6930200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr7:6927200-6928200	Enhancers	Brain Hippocampus Middle	brain
32	chr7:6927400-6928200	Enhancers	Left Ventricle	heart
33	chr7:6927400-6928600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr7:6927400-6929000	Enhancers	Fetal Heart	heart
35	chr7:6927600-6928600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:6927800-6928200	Enhancers	Brain Cingulate Gyrus	brain
37	chr7:6927800-6928400	Enhancers	HSMMtube	muscle
38	chr7:6927800-6929200	Enhancers	NHDF-Ad	bronchial
39	chr7:6928000-6928200	Enhancers	Fetal Muscle Trunk	muscle
40	chr7:6928200-6929400	Weak transcription	Brain Hippocampus Middle	brain
41	chr7:6928800-6929200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:6928800-6929200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr7:6928800-6929200	Enhancers	Esophagus	oesophagus
44	chr7:6928800-6929200	ZNF genes & repeats	Fetal Brain Male	brain
45	chr7:6928800-6929200	Enhancers	Gastric	stomach
46	chr7:6928800-6929200	Enhancers	Right Atrium	heart
47	chr7:6928800-6929400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:6928800-6929400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr7:6928800-6929400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:6928800-6929400	ZNF genes & repeats	Fetal Kidney	kidney

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