Variant report

Variant	nsv433397
Chromosome Location	chr8:6940656-7053947
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	BACH1	chr8:6949393-6949420	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr8:7016048-7016290	GM12878	blood:	n/a	n/a
3	BATF	chr8:6976169-6976555	GM12878	blood:	n/a	n/a
4	BATF	chr8:6976187-6976452	GM12878	blood:	n/a	n/a
5	BATF	chr8:6998432-6998646	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:6963184-6963444	GM12878	blood:	n/a	n/a
7	BCL11A	chr8:6963128-6963505	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:6975956-6976114	GM12878	blood:	n/a	n/a
9	CBX3	chr8:7009532-7009840	K562	blood:	n/a	n/a
10	CEBPB	chr8:6948092-6948185	HepG2	liver:	n/a	chr8:6948133-6948142 chr8:6948131-6948144 chr8:6948132-6948143
11	CEBPB	chr8:6948106-6948176	K562	blood:	n/a	chr8:6948133-6948142 chr8:6948131-6948144 chr8:6948132-6948143
12	CEBPB	chr8:6990754-6990963	K562	blood:	n/a	n/a
13	CEBPB	chr8:7005971-7006346	K562	blood:	n/a	n/a
14	CEBPB	chr8:6948119-6948147	H1-hESC	embryonic stem cell:	n/a	chr8:6948133-6948142 chr8:6948131-6948144 chr8:6948132-6948143
15	CEBPB	chr8:6990758-6990880	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:7005819-7006426	K562	blood:	n/a	n/a
17	CEBPB	chr8:6990652-6990853	K562	blood:	n/a	n/a
18	CEBPB	chr8:7003781-7004139	K562	blood:	n/a	n/a
19	CEBPB	chr8:7003837-7004114	K562	blood:	n/a	n/a
20	CEBPD	chr8:7005807-7006267	K562	blood:	n/a	n/a
21	CTCF	chr8:6949287-6949594	GM13976	blood:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
22	CTCF	chr8:6954625-6954671	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr8:6949204-6949604	A549	lung:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
24	CTCF	chr8:6983652-6983796	H1-hESC	embryonic stem cell:	n/a	chr8:6983718-6983731
25	CTCF	chr8:6949360-6949510	GM12871	blood:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
26	CTCF	chr8:6948940-6949090	GM12866	blood:	n/a	n/a
27	CTCF	chr8:6949204-6949614	HCT-116	colon:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
28	CTCF	chr8:6983649-6983868	H1-hESC	embryonic stem cell:	n/a	chr8:6983718-6983731
29	CTCF	chr8:6950020-6950170	SAEC	small airway:	n/a	chr8:6950135-6950144 chr8:6950129-6950142
30	CTCF	chr8:6949260-6949410	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr8:6949260-6949410	NHLF	lung:	n/a	n/a
32	CTCF	chr8:6949275-6949577	GM12891	blood:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
33	CTCF	chr8:6949360-6949510	Caco-2	colon:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
34	CTCF	chr8:6949380-6949530	GM12868	blood:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
35	CTCF	chr8:6966280-6966430	K562	blood:	n/a	n/a
36	CTCF	chr8:6966280-6966430	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:7015452-7015527	GM13976	blood:	n/a	n/a
38	CTCF	chr8:6956243-6956295	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr8:6949239-6949605	H1-hESC	embryonic stem cell:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
40	CTCF	chr8:6949288-6949579	H1-hESC	embryonic stem cell:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
41	CTCF	chr8:6966300-6966450	HMEC	breast:	n/a	n/a
42	CTCF	chr8:6949304-6949593	Pancreas_OC	pancreas:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
43	CTCF	chr8:6949317-6949542	HepG2	liver:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
44	CTCF	chr8:6966259-6966381	HepG2	liver:	n/a	n/a
45	CTCF	chr8:6966115-6966499	A549	lung:	n/a	n/a
46	CTCF	chr8:6949303-6949593	LNCaP	prostate:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
47	CTCF	chr8:6949597-6949619	GM13976	blood:	n/a	n/a
48	CTCF	chr8:6949380-6949530	GM12865	blood:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462
49	CTCF	chr8:7020248-7020329	GM10266	blood:	n/a	n/a
50	CTCF	chr8:6949400-6949550	GM12873	blood:	n/a	chr8:6949447-6949468 chr8:6949445-6949463 chr8:6949448-6949461 chr8:6949448-6949461 chr8:6949446-6949462

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:7009699-7009749	LNCaP	prostate:	n/a
2	chr8:6953040-6953090	U87	brain:	n/a
3	chr8:7009699-7009749	SK-N-MC	brain:	n/a
4	chr8:7005562-7005612	HRE	kidney:	n/a
5	chr8:6949404-6949454	NHDF-neo	bronchial:	n/a
6	chr8:7004819-7004869	H1-hESC	embryonic stem cell:	embryo
7	chr8:6950038-6950088	HEK293	kidney:	embryo
8	chr8:6950160-6950210	Jurkat	blood:	n/a
9	chr8:6950038-6950088	GM12891	blood:	n/a
10	chr8:7005562-7005612	MCF-7	breast:	n/a
11	chr8:7004819-7004869	PANC-1	pancreas:	n/a
12	chr8:7005678-7005728	NHDF-neo	bronchial:	n/a
13	chr8:6949415-6949465	HEK293	kidney:	embryo
14	chr8:7009699-7009749	HPAEpiC	pulmonary alveolar:	n/a
15	chr8:6940702-6940752	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:6953040-6953090	SAEC	small airway:	n/a
17	chr8:6949404-6949454	ECC-1	luminal epithelium:	n/a
18	chr8:6949404-6949454	CMK	blood:	n/a
19	chr8:7005678-7005728	SK-N-SH_RA	brain:	n/a
20	chr8:6946366-6946416	SK-N-SH	brain:	n/a
21	chr8:7004819-7004869	HCT-116	colon:	n/a
22	chr8:6949415-6949465	U87	brain:	n/a
23	chr8:7005562-7005612	AG04449	skin:	fetal
24	chr8:6950160-6950210	HMEC	breast:	n/a
25	chr8:6949404-6949454	NH-A	brain:	n/a
26	chr8:6940624-6940674	Hela-S3	cervix:	n/a
27	chr8:6946366-6946416	LNCaP	prostate:	n/a
28	chr8:6950038-6950088	NHBE	bronchial:	n/a
29	chr8:7005011-7005061	AG04450	lung:	fetal
30	chr8:6953040-6953090	PrEC	prostate:	n/a
31	chr8:6940624-6940674	K562	blood:	n/a
32	chr8:7004738-7004788	BE2_C	brain:	n/a
33	chr8:7004944-7004994	HNPCEpiC	eye:	n/a
34	chr8:7004944-7004994	GM06990	blood:	n/a
35	chr8:6946366-6946416	HAEpiC	amniotic membrane:	n/a
36	chr8:7005562-7005612	HNPCEpiC	eye:	n/a
37	chr8:7004944-7004994	ProgFib	skin:	n/a
38	chr8:7004819-7004869	HL-60	blood:	n/a
39	chr8:7005678-7005728	GM12892	blood:	n/a
40	chr8:6946366-6946416	NB4	blood:	n/a
41	chr8:7009699-7009749	HEEpiC	esophagus:	n/a
42	chr8:6949404-6949454	NHBE	bronchial:	n/a
43	chr8:6949321-6949371	HCM	heart:	n/a
44	chr8:6949415-6949465	AG09309	skin:	n/a
45	chr8:6953040-6953090	PFSK-1	brain:	n/a
46	chr8:6949321-6949371	HCT-116	colon:	n/a
47	chr8:6949404-6949454	AoSMC	blood vessel:	n/a
48	chr8:6949415-6949465	HRCEpiC	kidney:	n/a
49	chr8:7005678-7005728	A549	lung:	n/a
50	chr8:6950038-6950088	HCF	heart:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB105B-4	chr8:7043806-7044422	NONHSAT124814
2	lnc-DEFB105B-4	chr8:7010239-7010328	NONHSAT124814
3	lnc-DEFA5-2	chr8:7001154-7001363	NONHSAT124813

Variant related genes	Relation type
ENSG00000254683	TF binding region
ENSG00000216206	TF binding region
ENSG00000234120	TF binding region
ENSG00000231930	TF binding region
ENSG00000221567	TF binding region
ENSG00000230106	TF binding region
RPS3AP30	TF binding region
RPS3AP33	TF binding region
ENSG00000254683	CpG island
ENSG00000216206	CpG island
ENSG00000234120	CpG island
ENSG00000231930	CpG island
ENSG00000221567	CpG island
ENSG00000230106	CpG island
RPS3AP30	CpG island
RPS3AP33	CpG island

Extended variants
information (count: 4059 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:4059 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4841834	chr8:6940656-6940657	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144806658	chr8:6940670-6940671	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs544203768	chr8:6940677-6940678	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs560753546	chr8:6940698-6940699	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs560774101	chr8:6940721-6940722	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs529861646	chr8:6940726-6940727	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs187080788	chr8:6940734-6940735	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs560702813	chr8:6940740-6940741	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs111503111	chr8:6940772-6940773	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs552568233	chr8:6940776-6940777	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs569551805	chr8:6940779-6940780	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs189910793	chr8:6940800-6940801	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs531552234	chr8:6944801-6944802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185814984	chr8:6944810-6944811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113235665	chr8:6944819-6944820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527242081	chr8:6944824-6944825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554830417	chr8:6944825-6944826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547116683	chr8:6944827-6944828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570507517	chr8:6944845-6944846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539195235	chr8:6944871-6944872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555858676	chr8:6944877-6944878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191003762	chr8:6944878-6944879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10099095	chr8:6944887-6944888	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs574559605	chr8:6944902-6944903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555600486	chr8:6944911-6944912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572691488	chr8:6944923-6944924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541413306	chr8:6944928-6944929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557893474	chr8:6944977-6944978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4841836	chr8:6944986-6944987	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs543901175	chr8:6944992-6944993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559249563	chr8:6944996-6944997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563791553	chr8:6944997-6944998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367876839	chr8:6945217-6945218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371910586	chr8:6945220-6945221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182355291	chr8:6945221-6945222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535040799	chr8:6945224-6945225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138124273	chr8:6945277-6945278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2978716	chr8:6945279-6945280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188451840	chr8:6945281-6945282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192675017	chr8:6945297-6945298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542040313	chr8:6945311-6945312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2979400	chr8:6945325-6945326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541258366	chr8:6945329-6945330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561770811	chr8:6945343-6945344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572223301	chr8:6945352-6945353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144122225	chr8:6945355-6945356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184663796	chr8:6945370-6945371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148703882	chr8:6945375-6945376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142162534	chr8:6945389-6945390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147393371	chr8:6945390-6945391	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
early-passage human iPS cells	21368824	CNVD
Chordoma	21215367	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	20369283	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6940600-6940800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:6940600-6940800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:6940600-6940800	Enhancers	Spleen	Spleen
4	chr8:6944800-6945000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:6945200-6945400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:6945200-6947000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr8:6945400-6945600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr8:6945400-6946400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr8:6945600-6945800	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:6945600-6946600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr8:6946000-6947200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr8:6946200-6946400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:6946400-6946800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr8:6946400-6948000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr8:6946400-6948000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:6946600-6947200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr8:6946800-6947000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr8:6946800-6947000	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr8:6947000-6947200	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr8:6947000-6947400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr8:6947000-6947800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr8:6947200-6947400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr8:6947200-6947400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
24	chr8:6947200-6947400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
25	chr8:6947200-6947400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr8:6947200-6947600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr8:6947200-6947600	Enhancers	H9 Cell Line	embryonic stem cell
28	chr8:6947200-6947600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr8:6947400-6947600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
30	chr8:6947400-6947600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
31	chr8:6947400-6947600	Enhancers	Dnd41	blood
32	chr8:6947400-6947800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr8:6947600-6948400	Weak transcription	Dnd41	blood
34	chr8:6947600-6949200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:6947600-6949600	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr8:6947800-6948000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
37	chr8:6947800-6948400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
38	chr8:6948000-6948200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
39	chr8:6948000-6949400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr8:6948200-6948400	Enhancers	Spleen	Spleen
41	chr8:6948400-6949200	Weak transcription	Spleen	Spleen
42	chr8:6948400-6949200	Enhancers	Dnd41	blood
43	chr8:6949000-6949200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
44	chr8:6949000-6949200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
45	chr8:6949000-6949200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
46	chr8:6949000-6949400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:6949000-6949400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
48	chr8:6949000-6949400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr8:6949000-6949600	Enhancers	Primary B cells from peripheral blood	blood
50	chr8:6949200-6949400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links