Variant report

Variant	nsv887463
Chromosome Location	chr7:6928252-6990426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	chr7:6959640-6959863	GM12878	blood:	n/a	chr7:6959720-6959731
3	BATF	chr7:6970367-6970679	GM12878	blood:	n/a	n/a
4	BATF	chr7:6967768-6968127	GM12878	blood:	n/a	n/a
5	BATF	chr7:6967256-6967613	GM12878	blood:	n/a	n/a
6	BATF	chr7:6967778-6968070	GM12878	blood:	n/a	n/a
7	BATF	chr7:6965792-6966222	GM12878	blood:	n/a	n/a
8	BATF	chr7:6965828-6966219	GM12878	blood:	n/a	n/a
9	BATF	chr7:6930048-6930266	GM12878	blood:	n/a	chr7:6930144-6930155
10	BATF	chr7:6959520-6959921	GM12878	blood:	n/a	chr7:6959720-6959731
11	BCL11A	chr7:6967281-6967607	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:6965815-6966145	GM12878	blood:	n/a	chr7:6966028-6966037
13	BCL11A	chr7:6970443-6970693	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:6968204-6968549	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:6967360-6967540	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:6965764-6966259	GM12878	blood:	n/a	chr7:6966028-6966037
17	BCL11A	chr7:6966697-6966858	GM12878	blood:	n/a	n/a
18	BCL3	chr7:6928564-6929398	GM12878	blood:	n/a	n/a
19	BCL3	chr7:6928637-6929472	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:6967280-6967585	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:6943039-6943099	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:6962913-6963006	K562	blood:	n/a	n/a
23	BHLHE40	chr7:6929175-6929309	K562	blood:	n/a	n/a
24	BHLHE40	chr7:6968034-6968094	GM12878	blood:	n/a	n/a
25	CBX3	chr7:6962801-6963079	K562	blood:	n/a	n/a
26	CBX3	chr7:6940710-6940918	K562	blood:	n/a	n/a
27	CBX3	chr7:6977915-6978267	K562	blood:	n/a	n/a
28	CBX3	chr7:6965814-6966339	K562	blood:	n/a	n/a
29	CBX3	chr7:6962809-6962993	K562	blood:	n/a	n/a
30	CEBPB	chr7:6975688-6975969	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:6935911-6936099	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:6968040-6968133	K562	blood:	n/a	n/a
33	CEBPB	chr7:6973635-6973950	A549	lung:	n/a	chr7:6973791-6973802
34	CEBPB	chr7:6973611-6973982	HepG2	liver:	n/a	chr7:6973791-6973802
35	CEBPB	chr7:6973659-6973952	H1-hESC	embryonic stem cell:	n/a	chr7:6973791-6973802
36	CEBPB	chr7:6962895-6963023	K562	blood:	n/a	n/a
37	CEBPB	chr7:6973609-6973984	K562	blood:	n/a	chr7:6973791-6973802
38	CEBPB	chr7:6973599-6973979	K562	blood:	n/a	chr7:6973791-6973802
39	CEBPB	chr7:6936027-6936120	K562	blood:	n/a	n/a
40	CEBPB	chr7:6967985-6968236	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:6936030-6936175	A549	lung:	n/a	n/a
42	CEBPB	chr7:6962825-6963113	K562	blood:	n/a	n/a
43	CEBPD	chr7:6962813-6963184	K562	blood:	n/a	n/a
44	CTCF	chr7:6978040-6978190	GM12865	blood:	n/a	chr7:6978136-6978145 chr7:6978129-6978142 chr7:6978122-6978143 chr7:6978156-6978164 chr7:6978127-6978145
45	CTCF	chr7:6970580-6970730	HMF	breast:	n/a	chr7:6970596-6970606
46	CTCF	chr7:6970520-6970670	AG04449	skin:	n/a	chr7:6970596-6970606 chr7:6970557-6970570 chr7:6970555-6970573 chr7:6970556-6970572
47	CTCF	chr7:6978020-6978170	WERI-Rb-1	eye:	n/a	chr7:6978136-6978145 chr7:6978129-6978142 chr7:6978122-6978143 chr7:6978156-6978164 chr7:6978127-6978145
48	CTCF	chr7:6970060-6970210	GM12864	blood:	n/a	n/a
49	CTCF	chr7:6978040-6978190	AoAF	blood vessel:	n/a	chr7:6978136-6978145 chr7:6978129-6978142 chr7:6978122-6978143 chr7:6978156-6978164 chr7:6978127-6978145
50	CTCF	chr7:6970600-6970750	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6974758-6974808	HEK293	kidney:	embryo
2	chr7:6974956-6975006	HepG2	liver:	n/a
3	chr7:6974892-6974942	GM12892	blood:	n/a
4	chr7:6990107-6990157	PrEC	prostate:	n/a
5	chr7:6979488-6979538	PANC-1	pancreas:	n/a
6	chr7:6990107-6990157	AG04450	lung:	fetal
7	chr7:6974956-6975006	RPTEC	kidney:	n/a
8	chr7:6979239-6979289	AG04450	lung:	fetal
9	chr7:6990107-6990157	NHDF-neo	bronchial:	n/a
10	chr7:6979239-6979289	PrEC	prostate:	n/a
11	chr7:6990107-6990157	ProgFib	skin:	n/a
12	chr7:6977556-6977606	GM12891	blood:	n/a
13	chr7:6979488-6979538	HNPCEpiC	eye:	n/a
14	chr7:6974892-6974942	IMR90	lung:	fetal
15	chr7:6979239-6979289	RPTEC	kidney:	n/a
16	chr7:6979239-6979289	LNCaP	prostate:	n/a
17	chr7:6977556-6977606	SKMC	muscle:	n/a
18	chr7:6977556-6977606	MCF10A-Er-Src	breast:	n/a
19	chr7:6974270-6974320	Jurkat	blood:	n/a
20	chr7:6990107-6990157	HCF	heart:	n/a
21	chr7:6979239-6979289	AG10803	skin:	n/a
22	chr7:6979488-6979538	HEK293	kidney:	embryo
23	chr7:6979488-6979538	HRE	kidney:	n/a
24	chr7:6977556-6977606	T-47D	breast:	n/a
25	chr7:6977556-6977606	GM19239	blood:	n/a
26	chr7:6974758-6974808	MCF-7	breast:	n/a
27	chr7:6974758-6974808	SK-N-SH	brain:	n/a
28	chr7:6974892-6974942	K562	blood:	n/a
29	chr7:6977556-6977606	SAEC	small airway:	n/a
30	chr7:6979239-6979289	AG09319	gingival:	n/a
31	chr7:6979488-6979538	HRPEpiC	eye:	n/a
32	chr7:6974956-6975006	SKMC	muscle:	n/a
33	chr7:6977556-6977606	A549	lung:	n/a
34	chr7:6990107-6990157	HIPEpiC	eye:	n/a
35	chr7:6974956-6975006	Caco-2	colon:	n/a
36	chr7:6974892-6974942	HCT-116	colon:	n/a
37	chr7:6974892-6974942	HCPEpiC	choroid plexus:	n/a
38	chr7:6974758-6974808	AG04449	skin:	fetal
39	chr7:6979488-6979538	HIPEpiC	eye:	n/a
40	chr7:6974758-6974808	AoSMC	blood vessel:	n/a
41	chr7:6974892-6974942	SAEC	small airway:	n/a
42	chr7:6990107-6990157	Caco-2	colon:	n/a
43	chr7:6979488-6979538	NHDF-neo	bronchial:	n/a
44	chr7:6974956-6975006	GM12891	blood:	n/a
45	chr7:6979488-6979538	NHBE	bronchial:	n/a
46	chr7:6974956-6975006	H1-hESC	embryonic stem cell:	embryo
47	chr7:6974758-6974808	BJ	skin:	n/a
48	chr7:6977556-6977606	IMR90	lung:	fetal
49	chr7:6979239-6979289	AG04449	skin:	fetal
50	chr7:6974270-6974320	BJ	skin:	n/a

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:

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

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

Extended variants
information (count: 3431 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3431 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111554808	chr7:6928252-6928253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs34815690	chr7:6928258-6928259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185041108	chr7:6928272-6928273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189746393	chr7:6928276-6928277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182781009	chr7:6928288-6928289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558689523	chr7:6928289-6928290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188340830	chr7:6928346-6928347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575960147	chr7:6928388-6928389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140583817	chr7:6928394-6928395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556873193	chr7:6928399-6928400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192831268	chr7:6928418-6928419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565561745	chr7:6928425-6928426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs28709433	chr7:6928455-6928456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539212450	chr7:6928495-6928496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183589111	chr7:6928499-6928500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187603047	chr7:6928562-6928563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34682335	chr7:6928579-6928580	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs192516067	chr7:6928585-6928586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368268017	chr7:6928592-6928593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531573585	chr7:6928608-6928609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201524973	chr7:6928626-6928627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549792713	chr7:6928635-6928636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147760893	chr7:6928662-6928663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114264996	chr7:6928667-6928668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141115858	chr7:6928676-6928677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566500753	chr7:6928758-6928759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs13239505	chr7:6928766-6928767	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs552273078	chr7:6928770-6928771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13229186	chr7:6928783-6928784	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs537823537	chr7:6928792-6928793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555925267	chr7:6928828-6928829	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs541747239	chr7:6928835-6928836	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs367843899	chr7:6928874-6928875	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs199775304	chr7:6928878-6928879	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs386709861	chr7:6928886-6928887	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs377597077	chr7:6928891-6928892	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs140500629	chr7:6928896-6928897	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs71010931	chr7:6928897-6928898	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375763306	chr7:6928918-6928919	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs111066279	chr7:6928968-6928969	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs111162091	chr7:6928982-6928983	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs573568545	chr7:6928985-6928986	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs13226511	chr7:6929005-6929006	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs13239036	chr7:6929027-6929028	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs374242525	chr7:6929034-6929035	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs546012563	chr7:6929040-6929041	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs111066282	chr7:6929042-6929043	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs530146497	chr7:6929043-6929044	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs576166069	chr7:6929058-6929059	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs111211214	chr7:6929062-6929063	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	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:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6926400-6928800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:6926400-6928800	Weak transcription	Right Atrium	heart
3	chr7:6927000-6930200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr7:6927400-6928600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:6927400-6929000	Enhancers	Fetal Heart	heart
6	chr7:6927600-6928600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:6927800-6928400	Enhancers	HSMMtube	muscle
8	chr7:6927800-6929200	Enhancers	NHDF-Ad	bronchial
9	chr7:6928200-6929400	Weak transcription	Brain Hippocampus Middle	brain
10	chr7:6928800-6929200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:6928800-6929200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:6928800-6929200	Enhancers	Esophagus	oesophagus
13	chr7:6928800-6929200	ZNF genes & repeats	Fetal Brain Male	brain
14	chr7:6928800-6929200	Enhancers	Gastric	stomach
15	chr7:6928800-6929200	Enhancers	Right Atrium	heart
16	chr7:6928800-6929400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:6928800-6929400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:6928800-6929400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:6928800-6929400	ZNF genes & repeats	Fetal Kidney	kidney
20	chr7:6928800-6929400	Bivalent/Poised TSS	Fetal Lung	lung
21	chr7:6928800-6929400	Enhancers	Pancreas	Pancrea
22	chr7:6929000-6929200	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
23	chr7:6929000-6929400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
24	chr7:6929400-6929800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:6929600-6929800	Enhancers	Brain Hippocampus Middle	brain
26	chr7:6931400-6932200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:6935800-6937800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:6936600-6937600	Enhancers	Osteobl	bone
29	chr7:6936800-6937200	Enhancers	Dnd41	blood
30	chr7:6936800-6937600	Enhancers	Fetal Thymus	thymus
31	chr7:6936800-6937600	Enhancers	HSMM	muscle
32	chr7:6936800-6937800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:6937000-6937600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:6937200-6937400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr7:6937200-6937600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr7:6937400-6942400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr7:6937800-6946600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:6939600-6941000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:6940200-6940800	Enhancers	HepG2	liver
40	chr7:6940400-6940800	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr7:6940600-6941400	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr7:6940600-6942000	Enhancers	Stomach Mucosa	stomach
43	chr7:6940600-6943200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:6940800-6945600	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr7:6941000-6941200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:6941000-6941400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr7:6941000-6942600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr7:6941200-6941400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr7:6941200-6941600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr7:6941200-6941600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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