Variant report

Variant	nsv1000392
Chromosome Location	chr4:78273146-78301467
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	CEBPB	chr4:78296891-78297161	A549	lung:	n/a	chr4:78297047-78297058 chr4:78297049-78297058
2	CEBPB	chr4:78296898-78297215	HepG2	liver:	n/a	chr4:78297047-78297058 chr4:78297049-78297058
3	CEBPB	chr4:78296971-78297162	IMR90	lung:	n/a	chr4:78297047-78297058 chr4:78297049-78297058
4	CTCF	chr4:78288025-78288292	A549	lung:	n/a	chr4:78288200-78288218 chr4:78288203-78288216 chr4:78288202-78288223
5	CTCF	chr4:78279519-78279800	GM13977	blood:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
6	CTCF	chr4:78274946-78275271	NHEK	skin:	n/a	chr4:78275103-78275121 chr4:78275105-78275126 chr4:78275106-78275119
7	CTCF	chr4:78279920-78280070	SAEC	small airway:	n/a	n/a
8	CTCF	chr4:78288086-78288337	GM20000	blood:	n/a	chr4:78288200-78288218 chr4:78288203-78288216 chr4:78288202-78288223
9	CTCF	chr4:78279600-78279750	WERI-Rb-1	eye:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
10	CTCF	chr4:78279591-78279808	NHEK	skin:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
11	CTCF	chr4:78279360-78279866	HCT-116	colon:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
12	CTCF	chr4:78279620-78279770	HCPEpiC	choroid plexus:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
13	CTCF	chr4:78287960-78288110	HA-sp	spinal cord:	n/a	n/a
14	CTCF	chr4:78287960-78288110	NHEK	skin:	n/a	n/a
15	CTCF	chr4:78287940-78288090	GM12878	blood:	n/a	n/a
16	CTCF	chr4:78279385-78279822	MCF-7	breast:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
17	CTCF	chr4:78279936-78280009	GM20000	blood:	n/a	n/a
18	CTCF	chr4:78274840-78274990	HCFaa	heart:	n/a	n/a
19	CTCF	chr4:78274927-78275297	MCF-7	breast:	n/a	chr4:78275103-78275121 chr4:78275105-78275126 chr4:78275106-78275119
20	CTCF	chr4:78279637-78279804	GM12891	blood:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
21	CTCF	chr4:78279620-78279770	BJ	skin:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
22	CTCF	chr4:78274983-78275239	Lung_OC	lung:	n/a	chr4:78275103-78275121 chr4:78275105-78275126 chr4:78275106-78275119
23	CTCF	chr4:78274840-78274990	HL-60	blood:	n/a	n/a
24	CTCF	chr4:78279600-78279750	HPAF	blood vessel:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
25	CTCF	chr4:78279520-78279670	HVMF	connective:	n/a	n/a
26	CTCF	chr4:78287960-78288110	HMEC	breast:	n/a	n/a
27	CTCF	chr4:78287920-78288070	GM12869	blood:	n/a	n/a
28	CTCF	chr4:78279545-78279823	A549	lung:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
29	CTCF	chr4:78298000-78298150	GM12875	blood:	n/a	n/a
30	CTCF	chr4:78274966-78275245	Medullo	brain:	n/a	chr4:78275103-78275121 chr4:78275105-78275126 chr4:78275106-78275119
31	CTCF	chr4:78298070-78298167	Fibrobl	skin:	n/a	n/a
32	CTCF	chr4:78287920-78288070	HVMF	connective:	n/a	n/a
33	CTCF	chr4:78275200-78275350	GM12872	blood:	n/a	n/a
34	CTCF	chr4:78287960-78288110	GM12878	blood:	n/a	n/a
35	CTCF	chr4:78280180-78280330	AG04450	lung:	n/a	n/a
36	CTCF	chr4:78279200-78279350	WI-38	lung:	n/a	n/a
37	CTCF	chr4:78275260-78275410	GM12872	blood:	n/a	n/a
38	CTCF	chr4:78275280-78275430	HVMF	connective:	n/a	n/a
39	CTCF	chr4:78274860-78275010	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr4:78274840-78274990	NHLF	lung:	n/a	n/a
41	CTCF	chr4:78287960-78288110	GM12870	blood:	n/a	n/a
42	CTCF	chr4:78288340-78288490	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr4:78279620-78279770	GM12868	blood:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
44	CTCF	chr4:78287940-78288090	GM12874	blood:	n/a	n/a
45	CTCF	chr4:78274860-78275010	HFF	foreskin:	n/a	n/a
46	CTCF	chr4:78274963-78275282	A549	lung:	n/a	chr4:78275103-78275121 chr4:78275105-78275126 chr4:78275106-78275119
47	CTCF	chr4:78288055-78288363	H1-hESC	embryonic stem cell:	n/a	chr4:78288200-78288218 chr4:78288203-78288216 chr4:78288202-78288223
48	CTCF	chr4:78279860-78280010	HVMF	connective:	n/a	n/a
49	CTCF	chr4:78279662-78279767	MCF-7	breast:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
50	CTCF	chr4:78288340-78288490	HA-sp	spinal cord:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78298282-78298332	ECC-1	luminal epithelium:	n/a
2	chr4:78298282-78298332	Jurkat	blood:	n/a
3	chr4:78298282-78298332	ovcar-3	ovarian:	n/a
4	chr4:78298282-78298332	CMK	blood:	n/a
5	chr4:78298282-78298332	AG04449	skin:	fetal
6	chr4:78298282-78298332	BE2_C	brain:	n/a
7	chr4:78298282-78298332	AG04450	lung:	fetal
8	chr4:78298282-78298332	AG09319	gingival:	n/a
9	chr4:78298282-78298332	MCF-7	breast:	n/a
10	chr4:78298282-78298332	HMEC	breast:	n/a
11	chr4:78298282-78298332	AG10803	skin:	n/a
12	chr4:78298282-78298332	HIPEpiC	eye:	n/a
13	chr4:78298282-78298332	HCF	heart:	n/a
14	chr4:78298282-78298332	BJ	skin:	n/a
15	chr4:78298282-78298332	HCM	heart:	n/a
16	chr4:78298282-78298332	HL-60	blood:	n/a
17	chr4:78298282-78298332	GM12892	blood:	n/a
18	chr4:78298282-78298332	RPTEC	kidney:	n/a
19	chr4:78298282-78298332	AG09309	skin:	n/a
20	chr4:78298282-78298332	NB4	blood:	n/a
21	chr4:78298282-78298332	HepG2	liver:	n/a
22	chr4:78298282-78298332	HEK293	kidney:	embryo
23	chr4:78298282-78298332	ProgFib	skin:	n/a
24	chr4:78298282-78298332	HNPCEpiC	eye:	n/a
25	chr4:78298282-78298332	HRCEpiC	kidney:	n/a
26	chr4:78298282-78298332	GM19239	blood:	n/a
27	chr4:78298282-78298332	SAEC	small airway:	n/a
28	chr4:78298282-78298332	NHBE	bronchial:	n/a
29	chr4:78298282-78298332	SKMC	muscle:	n/a
30	chr4:78298282-78298332	IMR90	lung:	fetal
31	chr4:78298282-78298332	T-47D	breast:	n/a
32	chr4:78298282-78298332	GM06990	blood:	n/a
33	chr4:78298282-78298332	H1-hESC	embryonic stem cell:	embryo
34	chr4:78298282-78298332	GM12878	blood:	n/a
35	chr4:78298282-78298332	Caco-2	colon:	n/a
36	chr4:78298282-78298332	LNCaP	prostate:	n/a
37	chr4:78298282-78298332	HRE	kidney:	n/a
38	chr4:78298282-78298332	HCPEpiC	choroid plexus:	n/a
39	chr4:78298282-78298332	HUVEC	blood vessel:	n/a
40	chr4:78298282-78298332	PFSK-1	brain:	n/a
41	chr4:78298282-78298332	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:78298282-78298332	SK-N-MC	brain:	n/a
43	chr4:78298282-78298332	MCF10A-Er-Src	breast:	n/a
44	chr4:78298282-78298332	PrEC	prostate:	n/a
45	chr4:78298282-78298332	A549	lung:	n/a
46	chr4:78298282-78298332	K562	blood:	n/a
47	chr4:78298282-78298332	SK-N-SH_RA	brain:	n/a
48	chr4:78298282-78298332	PANC-1	pancreas:	n/a
49	chr4:78298282-78298332	SK-N-SH	brain:	n/a
50	chr4:78298282-78298332	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:78278110..78280443-chr4:78281438..78283101,2	MCF-7	breast:
2	chr4:78287359..78291622-chr4:78351702..78357008,5	MCF-7	breast:
3	chr4:78289830..78292754-chr4:78299148..78300754,2	K562	blood:
4	chr4:78161365..78162334-chr4:78279195..78280134,7	K562	blood:
5	chr1:118958475..118959178-chr4:78279470..78280113,2	MCF-7	breast:
6	chr4:78161324..78162321-chr4:78279149..78280134,4	MCF-7	breast:
7	chr4:78236163..78238480-chr4:78287943..78289669,2	K562	blood:
8	chr4:78229797..78230625-chr4:78279333..78280102,3	MCF-7	breast:
9	chr4:78287667..78288571-chr4:78353781..78354626,3	MCF-7	breast:
10	chr4:78230184..78230702-chr4:78278364..78278865,2	MCF-7	breast:
11	chr4:78298658..78300930-chr4:78308885..78310955,2	MCF-7	breast:
12	chr4:78161721..78162270-chr4:78279119..78279681,2	MCF-7	breast:
13	chr4:78287913..78288436-chr4:78619834..78620825,2	MCF-7	breast:
14	chr4:78289830..78292754-chr4:78299148..78300754,2	K562	blood:
15	chr4:78292160..78295150-chr4:78297091..78299092,2	MCF-7	breast:
16	chr4:78278110..78280443-chr4:78281438..78283101,2	MCF-7	breast:
17	chr4:78292160..78295150-chr4:78297091..78299092,2	MCF-7	breast:
18	chr4:78296565..78297450-chr4:78353933..78354751,2	MCF-7	breast:
19	chr4:78270382..78272050-chr4:78274178..78276131,2	K562	blood:

Variant related genes	Relation type
ENSG00000248831	TF binding region
ENSG00000248831	CpG island

Extended variants
information (count: 1075 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1075 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17002578	chr4:78273146-78273147	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556761874	chr4:78273152-78273153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565154510	chr4:78273161-78273162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533018582	chr4:78273197-78273198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189743494	chr4:78273272-78273273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569620672	chr4:78273296-78273297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567076250	chr4:78273306-78273307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6849731	chr4:78273333-78273334	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs72648559	chr4:78273353-78273354	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs565932315	chr4:78273371-78273372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113270865	chr4:78273426-78273427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374044554	chr4:78273427-78273428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6819777	chr4:78273451-78273452	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs541101275	chr4:78273480-78273481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537529107	chr4:78273481-78273482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141668837	chr4:78273501-78273502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147026887	chr4:78273561-78273562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558149685	chr4:78273585-78273586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181026049	chr4:78273631-78273632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs578158063	chr4:78273651-78273652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573167497	chr4:78273660-78273661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543889792	chr4:78273777-78273778	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs112018908	chr4:78273790-78273791	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs565116096	chr4:78273853-78273854	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs142843864	chr4:78273854-78273855	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs375024134	chr4:78273864-78273865	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs563880225	chr4:78273871-78273872	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs549840627	chr4:78273881-78273882	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs367695591	chr4:78273891-78273892	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs563288911	chr4:78273916-78273917	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs186644792	chr4:78273919-78273920	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs111533011	chr4:78273955-78273956	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs138028367	chr4:78273990-78273991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374609818	chr4:78274042-78274043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78174291	chr4:78274097-78274098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111663293	chr4:78274102-78274103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370218511	chr4:78274103-78274104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551726649	chr4:78274112-78274113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368932392	chr4:78274139-78274140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113299201	chr4:78274156-78274157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143939575	chr4:78274197-78274198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139848313	chr4:78274211-78274212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114074341	chr4:78274230-78274231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527761504	chr4:78274292-78274293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377158890	chr4:78274296-78274297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191331673	chr4:78274301-78274302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs74883070	chr4:78274315-78274316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs72648560	chr4:78274318-78274319	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs143280977	chr4:78274357-78274358	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs117946141	chr4:78274363-78274364	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
lymphocytic leukemia	21291569	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
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78271800-78276800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:78272000-78276800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:78272000-78277000	Weak transcription	HMEC	breast
4	chr4:78272600-78273800	Enhancers	Fetal Heart	heart
5	chr4:78273000-78274600	Enhancers	Stomach Mucosa	stomach
6	chr4:78273800-78277000	Weak transcription	Fetal Heart	heart
7	chr4:78275400-78277400	Enhancers	Fetal Thymus	thymus
8	chr4:78275600-78276200	Enhancers	Thymus	Thymus
9	chr4:78275600-78276400	Enhancers	Primary B cells from peripheral blood	blood
10	chr4:78275600-78276600	Enhancers	Fetal Muscle Leg	muscle
11	chr4:78276000-78276600	Enhancers	Fetal Kidney	kidney
12	chr4:78276000-78277000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:78276400-78281400	Weak transcription	Primary B cells from peripheral blood	blood
14	chr4:78276600-78277000	Weak transcription	Fetal Muscle Leg	muscle
15	chr4:78276600-78281200	Weak transcription	Fetal Kidney	kidney
16	chr4:78276800-78277600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:78276800-78277800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:78276800-78277800	Enhancers	NHEK	skin
19	chr4:78277000-78277800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:78277000-78277800	Enhancers	Fetal Muscle Leg	muscle
21	chr4:78277000-78277800	Enhancers	HMEC	breast
22	chr4:78277000-78278000	Enhancers	Fetal Heart	heart
23	chr4:78277400-78287800	Weak transcription	Fetal Thymus	thymus
24	chr4:78281400-78281600	Enhancers	Fetal Kidney	kidney
25	chr4:78281400-78282000	Enhancers	Primary B cells from peripheral blood	blood
26	chr4:78281600-78282000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:78281600-78282000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:78282600-78283000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:78282800-78283400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr4:78282800-78283400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr4:78283000-78283200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
32	chr4:78283000-78283600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:78283200-78283400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr4:78283200-78283600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:78285400-78285600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr4:78287200-78289200	Enhancers	Fetal Muscle Leg	muscle
37	chr4:78287800-78289600	Enhancers	Fetal Thymus	thymus
38	chr4:78288400-78289400	Enhancers	Primary B cells from peripheral blood	blood
39	chr4:78291800-78292800	ZNF genes & repeats	Aorta	Aorta
40	chr4:78293400-78293600	Enhancers	Fetal Intestine Small	intestine
41	chr4:78294200-78294800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:78294800-78295600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:78297000-78297400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr4:78297000-78297400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:78297000-78297400	Enhancers	Primary T cells from cord blood	blood
46	chr4:78297000-78297800	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:78297000-78297800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr4:78297000-78298000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr4:78297000-78298400	Enhancers	H1 Cell Line	embryonic stem cell
50	chr4:78297200-78297600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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