Variant report

Variant	nsv522741
Chromosome Location	chr4:98873667-99057457
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	ARID3A	chr4:99014048-99014354	HepG2	liver:	n/a	n/a
2	BCL3	chr4:98905816-98906082	GM12878	blood:	n/a	n/a
3	BCL3	chr4:98906959-98907234	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:98908240-98908390	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr4:98989787-98989990	HepG2	liver:	n/a	chr4:98989872-98989883
6	CEBPB	chr4:98967948-98968326	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr4:99026254-99026525	HepG2	liver:	n/a	chr4:99026390-99026401
8	CEBPB	chr4:99056571-99056577	K562	blood:	n/a	n/a
9	CEBPB	chr4:99026262-99026519	IMR90	lung:	n/a	chr4:99026390-99026401
10	CEBPB	chr4:98999062-98999081	K562	blood:	n/a	n/a
11	CEBPB	chr4:99005951-99006103	A549	lung:	n/a	chr4:99006022-99006033
12	CEBPB	chr4:99056464-99056708	HepG2	liver:	n/a	chr4:99056544-99056561 chr4:99056547-99056558
13	CEBPB	chr4:99026275-99026452	H1-hESC	embryonic stem cell:	n/a	chr4:99026390-99026401
14	CEBPB	chr4:98998918-98999191	HepG2	liver:	n/a	chr4:98999042-98999051 chr4:98999042-98999051 chr4:98999042-98999051 chr4:98999041-98999052 chr4:98999040-98999051 chr4:98999042-98999051 chr4:98999040-98999053
15	CEBPB	chr4:99005909-99006159	IMR90	lung:	n/a	chr4:99006022-99006033
16	CEBPB	chr4:98910863-98911031	A549	lung:	n/a	n/a
17	CEBPB	chr4:98898912-98899245	HepG2	liver:	n/a	chr4:98899094-98899105
18	CEBPB	chr4:99005881-99006191	HepG2	liver:	n/a	chr4:99006022-99006033
19	CEBPB	chr4:98975792-98975954	HepG2	liver:	n/a	chr4:98975918-98975929
20	CEBPB	chr4:99030855-99030922	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:98973085-98973241	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:99056440-99056698	IMR90	lung:	n/a	chr4:99056544-99056561 chr4:99056547-99056558
23	CEBPB	chr4:98950612-98950807	HepG2	liver:	n/a	chr4:98950662-98950673
24	CHD2	chr4:99001733-99001756	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr4:98977400-98977550	GM12865	blood:	n/a	n/a
26	CTCF	chr4:99034266-99034435	Pancreas_OC	pancreas:	n/a	n/a
27	CTCF	chr4:99034240-99034390	RPTEC	kidney:	n/a	n/a
28	CTCF	chr4:98905800-98905950	BE2_C	brain:	n/a	n/a
29	CTCF	chr4:98905839-98905954	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr4:99014120-99014270	HMEC	breast:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
31	CTCF	chr4:99014080-99014230	GM06990	blood:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
32	CTCF	chr4:99034293-99034437	GM19239	blood:	n/a	n/a
33	CTCF	chr4:98908280-98908430	GM12869	blood:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
34	CTCF	chr4:98905860-98906010	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr4:99014102-99014304	A549	lung:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
36	CTCF	chr4:98908340-98908490	GM12873	blood:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
37	CTCF	chr4:98905780-98905930	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr4:98905722-98906060	GM12878	blood:	n/a	n/a
39	CTCF	chr4:98908320-98908470	HL-60	blood:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
40	CTCF	chr4:98908300-98908450	HCT-116	colon:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
41	CTCF	chr4:98977380-98977530	GM12864	blood:	n/a	n/a
42	CTCF	chr4:98928140-98928290	HMEC	breast:	n/a	n/a
43	CTCF	chr4:98905780-98905930	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr4:98905700-98905850	AG09309	skin:	n/a	n/a
45	CTCF	chr4:98949111-98949212	K562	blood:	n/a	n/a
46	CTCF	chr4:98908220-98908370	GM12864	blood:	n/a	n/a
47	CTCF	chr4:98949080-98949230	SAEC	small airway:	n/a	n/a
48	CTCF	chr4:99014080-99014230	NHEK	skin:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
49	CTCF	chr4:99014780-99014930	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr4:98905875-98906003	Fibrobl	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99008595-99008645	CMK	blood:	n/a
2	chr4:99031533-99031583	SK-N-SH_RA	brain:	n/a
3	chr4:99031533-99031583	HMEC	breast:	n/a
4	chr4:99008595-99008645	HAEpiC	amniotic membrane:	n/a
5	chr4:99031533-99031583	Caco-2	colon:	n/a
6	chr4:99008595-99008645	MCF10A-Er-Src	breast:	n/a
7	chr4:99031533-99031583	SK-N-SH	brain:	n/a
8	chr4:99008595-99008645	HUVEC	blood vessel:	n/a
9	chr4:99008595-99008645	SKMC	muscle:	n/a
10	chr4:99031533-99031583	H1-hESC	embryonic stem cell:	embryo
11	chr4:99031533-99031583	AoSMC	blood vessel:	n/a
12	chr4:99008595-99008645	HNPCEpiC	eye:	n/a
13	chr4:99008595-99008645	NH-A	brain:	n/a
14	chr4:99008595-99008645	HRE	kidney:	n/a
15	chr4:99008595-99008645	NT2-D1	testis:	n/a
16	chr4:99008595-99008645	AG09319	gingival:	n/a
17	chr4:99031533-99031583	HAEpiC	amniotic membrane:	n/a
18	chr4:99031533-99031583	HCT-116	colon:	n/a
19	chr4:99031533-99031583	PFSK-1	brain:	n/a
20	chr4:99031533-99031583	HIPEpiC	eye:	n/a
21	chr4:99008595-99008645	PrEC	prostate:	n/a
22	chr4:99031533-99031583	IMR90	lung:	fetal
23	chr4:99008595-99008645	HRPEpiC	eye:	n/a
24	chr4:99008595-99008645	Caco-2	colon:	n/a
25	chr4:99008595-99008645	HCPEpiC	choroid plexus:	n/a
26	chr4:99031533-99031583	Hela-S3	cervix:	n/a
27	chr4:99008595-99008645	H1-hESC	embryonic stem cell:	embryo
28	chr4:99008595-99008645	GM19239	blood:	n/a
29	chr4:99008595-99008645	IMR90	lung:	fetal
30	chr4:99008595-99008645	HRCEpiC	kidney:	n/a
31	chr4:99031533-99031583	PrEC	prostate:	n/a
32	chr4:99031533-99031583	GM19239	blood:	n/a
33	chr4:99008595-99008645	HIPEpiC	eye:	n/a
34	chr4:99008595-99008645	NHDF-neo	bronchial:	n/a
35	chr4:99031533-99031583	GM12891	blood:	n/a
36	chr4:99008595-99008645	MCF-7	breast:	n/a
37	chr4:99008595-99008645	GM06990	blood:	n/a
38	chr4:99008595-99008645	SK-N-SH_RA	brain:	n/a
39	chr4:99031533-99031583	ProgFib	skin:	n/a
40	chr4:99008595-99008645	PANC-1	pancreas:	n/a
41	chr4:99008595-99008645	AG09309	skin:	n/a
42	chr4:99008595-99008645	Hela-S3	cervix:	n/a
43	chr4:99031533-99031583	MCF10A-Er-Src	breast:	n/a
44	chr4:99031533-99031583	K562	blood:	n/a
45	chr4:99031533-99031583	GM12892	blood:	n/a
46	chr4:99008595-99008645	HCT-116	colon:	n/a
47	chr4:99031533-99031583	NT2-D1	testis:	n/a
48	chr4:99031533-99031583	ovcar-3	ovarian:	n/a
49	chr4:99031533-99031583	HUVEC	blood vessel:	n/a
50	chr4:99031533-99031583	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:99001766..99003673-chr4:99063340..99066059,2	MCF-7	breast:
2	chr4:98967509..98968412-chr4:99013843..99014513,4	MCF-7	breast:
3	chr4:99034025..99034574-chr4:99308766..99309435,2	MCF-7	breast:
4	chr4:99002780..99005606-chr4:99010089..99012416,2	MCF-7	breast:
5	chr4:97404242..97405044-chr4:98905771..98906367,3	MCF-7	breast:
6	chr4:99033892..99034970-chr4:99063844..99064725,8	MCF-7	breast:
7	chr4:98765331..98767165-chr4:99012892..99015543,2	K562	blood:
8	chr4:98641928..98642827-chr4:98905748..98906362,2	MCF-7	breast:
9	chr4:98896668..98898608-chr4:98901811..98903490,2	K562	blood:
10	chr4:98995356..98997429-chr4:98998775..99000432,2	MCF-7	breast:
11	chr4:98995356..98997429-chr4:98998775..99000432,2	MCF-7	breast:
12	chr4:99037506..99039090-chr4:99060858..99063344,2	MCF-7	breast:
13	chr4:98896668..98898608-chr4:98901811..98903490,2	K562	blood:
14	chr4:99002780..99005606-chr4:99010089..99012416,2	MCF-7	breast:
15	chr4:99012356..99014792-chr4:99062792..99064417,2	MCF-7	breast:
16	chr4:98967509..98968412-chr4:99013843..99014513,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAP1GDS1-6	chr4:98969706-98970194	NONHSAT097481

Variant related genes	Relation type
STPG2	TF binding region
RPL5P12	TF binding region
DUTP8	TF binding region
STPG2	CpG island
RPL5P12	CpG island
DUTP8	CpG island
ENSG00000163116	chromatin interactions

Extended variants
information (count: 1914 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1914 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2162369	chr4:98873667-98873668	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182010137	chr4:98873678-98873679	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs374401380	chr4:98873689-98873690	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs569916313	chr4:98873691-98873692	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs187271197	chr4:98873703-98873704	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs377494082	chr4:98873733-98873734	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs572820718	chr4:98873801-98873802	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs144802053	chr4:98873830-98873831	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs568131336	chr4:98873861-98873862	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs535132103	chr4:98873885-98873886	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs115222185	chr4:98873904-98873905	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs572030595	chr4:98873920-98873921	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs138645555	chr4:98873963-98873964	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs57396208	chr4:98873989-98873990	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs576346656	chr4:98874023-98874024	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs543589878	chr4:98874111-98874112	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs562071250	chr4:98874131-98874132	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs148912562	chr4:98874152-98874153	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs531119036	chr4:98874161-98874162	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs192023228	chr4:98874182-98874183	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs559328366	chr4:98874184-98874185	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs182654858	chr4:98874221-98874222	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs370649496	chr4:98874284-98874285	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs1426661	chr4:98874303-98874304	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570002806	chr4:98874324-98874325	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs531044949	chr4:98874325-98874326	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs367590699	chr4:98874327-98874328	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs371858731	chr4:98874340-98874341	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs71610686	chr4:98874341-98874342	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs535553254	chr4:98874342-98874343	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs375055394	chr4:98874381-98874382	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs186670237	chr4:98874418-98874419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62320997	chr4:98874441-98874442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539432918	chr4:98874450-98874451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558119517	chr4:98874482-98874483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576267258	chr4:98874499-98874500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543327122	chr4:98874515-98874516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555556469	chr4:98874624-98874625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573711684	chr4:98874640-98874641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544224444	chr4:98874662-98874663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541515371	chr4:98874697-98874698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559416490	chr4:98874698-98874699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190062924	chr4:98874767-98874768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570696928	chr4:98874771-98874772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530289070	chr4:98874806-98874807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544984192	chr4:98874820-98874821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143593592	chr4:98874830-98874831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531256633	chr4:98874874-98874875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549377865	chr4:98874878-98874879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540755196	chr4:98874909-98874910	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	16891809	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98864400-98874800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:98873600-98874400	Flanking Active TSS	Dnd41	blood
3	chr4:98874400-98875600	Enhancers	Dnd41	blood
4	chr4:98874800-98875000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:98877800-98878200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:98882800-98884600	Weak transcription	Pancreas	Pancrea
7	chr4:98883000-98884000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
8	chr4:98884000-98886000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr4:98884600-98884800	ZNF genes & repeats	Pancreas	Pancrea
10	chr4:98885200-98885600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr4:98886000-98886600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
12	chr4:98886400-98886800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:98890200-98890600	ZNF genes & repeats	Brain Anterior Caudate	brain
14	chr4:98894800-98895200	ZNF genes & repeats	Pancreas	Pancrea
15	chr4:98895000-98895200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:98895200-98895600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:98907600-98907800	Enhancers	Fetal Kidney	kidney
18	chr4:98908000-98908400	Enhancers	Brain Angular Gyrus	brain
19	chr4:98908000-98908400	Enhancers	Dnd41	blood
20	chr4:98909000-98909400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr4:98915800-98916800	Enhancers	HMEC	breast
22	chr4:98916000-98916600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:98916000-98916800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:98916800-98918400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:98922400-98923000	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr4:98927400-98927600	Weak transcription	Gastric	stomach
27	chr4:98927800-98928000	ZNF genes & repeats	Gastric	stomach
28	chr4:98932200-98932400	ZNF genes & repeats	Pancreas	Pancrea
29	chr4:98932400-98938000	Weak transcription	Pancreas	Pancrea
30	chr4:98938000-98938200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr4:98938000-98938600	ZNF genes & repeats	Pancreas	Pancrea
32	chr4:98938000-98938800	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr4:98946800-98947000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:98947000-98948800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:98948400-98949600	Enhancers	Fetal Brain Male	brain
36	chr4:98948800-98949600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr4:98967400-98968600	Enhancers	HSMMtube	muscle
38	chr4:98968000-98968400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr4:98968000-98968600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr4:98968000-98968600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr4:98968200-98968400	ZNF genes & repeats	Pancreas	Pancrea
42	chr4:98968200-98968600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr4:98968400-98972000	Weak transcription	Pancreas	Pancrea
44	chr4:98982400-98982800	Enhancers	Dnd41	blood
45	chr4:98998600-99000000	Enhancers	Dnd41	blood
46	chr4:99014600-99015800	Enhancers	HMEC	breast
47	chr4:99014600-99016000	Enhancers	Fetal Intestine Large	intestine
48	chr4:99014600-99016000	Enhancers	Fetal Intestine Small	intestine
49	chr4:99014800-99015800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr4:99014800-99015800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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