Variant report

Variant	nsv1013704
Chromosome Location	chr4:121657648-121791601
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	ATF2	chr4:121765601-121766141	GM12878	blood:	n/a	n/a
2	ATF2	chr4:121765662-121766071	GM12878	blood:	n/a	n/a
3	ATF2	chr4:121670498-121670947	GM12878	blood:	n/a	n/a
4	BATF	chr4:121765654-121766090	GM12878	blood:	n/a	chr4:121765916-121765927
5	BATF	chr4:121765635-121766159	GM12878	blood:	n/a	chr4:121765916-121765927
6	BCL11A	chr4:121765689-121766051	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:121670672-121671060	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:121686870-121687098	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:121765706-121766156	GM12878	blood:	n/a	n/a
10	BRCA1	chr4:121690199-121690775	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr4:121754428-121754544	K562	blood:	n/a	n/a
12	CEBPB	chr4:121762328-121762678	IMR90	lung:	n/a	chr4:121762495-121762508
13	CEBPB	chr4:121676743-121677031	HepG2	liver:	n/a	chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676918-121676929
14	CEBPB	chr4:121750678-121751008	IMR90	lung:	n/a	chr4:121750852-121750863
15	CEBPB	chr4:121790971-121791073	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:121780159-121780359	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:121704092-121704827	IMR90	lung:	n/a	chr4:121704325-121704338 chr4:121704325-121704338 chr4:121704196-121704209
18	CEBPB	chr4:121762437-121762637	A549	lung:	n/a	chr4:121762495-121762508
19	CEBPB	chr4:121790388-121790628	HepG2	liver:	n/a	chr4:121790512-121790521 chr4:121790510-121790523 chr4:121790512-121790521 chr4:121790512-121790521 chr4:121790512-121790521 chr4:121790511-121790522
20	CEBPB	chr4:121750290-121751025	Hela-S3	cervix:	n/a	chr4:121750852-121750863
21	CEBPB	chr4:121690345-121690783	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr4:121780193-121780369	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:121790875-121791190	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:121779973-121780422	IMR90	lung:	n/a	n/a
25	CHD2	chr4:121765651-121765948	GM12878	blood:	n/a	n/a
26	CHD2	chr4:121765109-121765358	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr4:121690442-121690766	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr4:121670552-121671041	GM12878	blood:	n/a	n/a
29	CTCF	chr4:121765140-121765290	NHDF-neo	bronchial:	n/a	chr4:121765246-121765254
30	CTCF	chr4:121791580-121791730	GM12871	blood:	n/a	chr4:121791623-121791636 chr4:121791628-121791635
31	CTCF	chr4:121765072-121765295	HepG2	liver:	n/a	chr4:121765246-121765254
32	CTCF	chr4:121730800-121730950	AG09319	gingival:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
33	CTCF	chr4:121791572-121791713	MCF-7	breast:	n/a	chr4:121791623-121791636 chr4:121791628-121791635
34	CTCF	chr4:121765120-121765270	HBMEC	blood vessel:	n/a	chr4:121765246-121765254
35	CTCF	chr4:121670912-121671008	GM12878	blood:	n/a	n/a
36	CTCF	chr4:121791560-121791710	GM12874	blood:	n/a	chr4:121791623-121791636 chr4:121791628-121791635
37	CTCF	chr4:121765080-121765230	GM12874	blood:	n/a	n/a
38	CTCF	chr4:121765120-121765270	HVMF	connective:	n/a	chr4:121765246-121765254
39	CTCF	chr4:121714221-121714341	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr4:121730721-121730957	H1-hESC	embryonic stem cell:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
41	CTCF	chr4:121765100-121765250	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr4:121730688-121730999	K562	blood:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
43	CTCF	chr4:121730760-121730910	GM12872	blood:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
44	CTCF	chr4:121765120-121765270	K562	blood:	n/a	chr4:121765246-121765254
45	CTCF	chr4:121765100-121765250	AG04450	lung:	n/a	n/a
46	CTCF	chr4:121730700-121730850	HRPEpiC	eye:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
47	CTCF	chr4:121693220-121693370	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr4:121765093-121765290	LNCaP	prostate:	n/a	chr4:121765246-121765254
49	CTCF	chr4:121693200-121693350	GM12865	blood:	n/a	n/a
50	CTCF	chr4:121730780-121730930	AG04449	skin:	n/a	chr4:121730831-121730849 chr4:121730826-121730847

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:121770445-121770495	HUVEC	blood vessel:	n/a
2	chr4:121770445-121770495	ProgFib	skin:	n/a
3	chr4:121786690-121786740	HRCEpiC	kidney:	n/a
4	chr4:121770445-121770495	AG04449	skin:	fetal
5	chr4:121770445-121770495	NHBE	bronchial:	n/a
6	chr4:121786690-121786740	NB4	blood:	n/a
7	chr4:121763322-121763372	NT2-D1	testis:	n/a
8	chr4:121763322-121763372	H1-hESC	embryonic stem cell:	embryo
9	chr4:121770445-121770495	HIPEpiC	eye:	n/a
10	chr4:121770445-121770495	MCF10A-Er-Src	breast:	n/a
11	chr4:121786690-121786740	PFSK-1	brain:	n/a
12	chr4:121763322-121763372	GM19239	blood:	n/a
13	chr4:121763322-121763372	SK-N-SH_RA	brain:	n/a
14	chr4:121763322-121763372	Jurkat	blood:	n/a
15	chr4:121770445-121770495	HRCEpiC	kidney:	n/a
16	chr4:121786690-121786740	SAEC	small airway:	n/a
17	chr4:121763322-121763372	A549	lung:	n/a
18	chr4:121763322-121763372	AG04450	lung:	fetal
19	chr4:121786690-121786740	HAEpiC	amniotic membrane:	n/a
20	chr4:121786690-121786740	ECC-1	luminal epithelium:	n/a
21	chr4:121770445-121770495	SK-N-MC	brain:	n/a
22	chr4:121786690-121786740	HEK293	kidney:	embryo
23	chr4:121763322-121763372	AG09309	skin:	n/a
24	chr4:121786690-121786740	LNCaP	prostate:	n/a
25	chr4:121770445-121770495	HCT-116	colon:	n/a
26	chr4:121763322-121763372	SK-N-SH	brain:	n/a
27	chr4:121786690-121786740	CMK	blood:	n/a
28	chr4:121770445-121770495	GM19239	blood:	n/a
29	chr4:121786690-121786740	GM12891	blood:	n/a
30	chr4:121786690-121786740	GM12892	blood:	n/a
31	chr4:121786690-121786740	HIPEpiC	eye:	n/a
32	chr4:121763322-121763372	HMEC	breast:	n/a
33	chr4:121763322-121763372	HL-60	blood:	n/a
34	chr4:121786690-121786740	Hepatocyte	liver:	n/a
35	chr4:121770445-121770495	HRE	kidney:	n/a
36	chr4:121786690-121786740	AG09309	skin:	n/a
37	chr4:121786690-121786740	HMEC	breast:	n/a
38	chr4:121786690-121786740	GM19239	blood:	n/a
39	chr4:121786690-121786740	A549	lung:	n/a
40	chr4:121786690-121786740	H1-hESC	embryonic stem cell:	embryo
41	chr4:121786690-121786740	AG09319	gingival:	n/a
42	chr4:121763322-121763372	LNCaP	prostate:	n/a
43	chr4:121786690-121786740	SK-N-SH	brain:	n/a
44	chr4:121763322-121763372	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:121786690-121786740	IMR90	lung:	fetal
46	chr4:121763322-121763372	HUVEC	blood vessel:	n/a
47	chr4:121770445-121770495	SAEC	small airway:	n/a
48	chr4:121770445-121770495	GM12878	blood:	n/a
49	chr4:121786690-121786740	NH-A	brain:	n/a
50	chr4:121786690-121786740	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:121768312..121769256-chr5:10250360..10250922,2	NB4	blood:
2	chr4:121764972..121765670-chr4:121898848..121899366,2	MCF-7	breast:
3	chr4:121763712..121766459-chr4:121767957..121770236,3	MCF-7	breast:
4	chr4:121745652..121748462-chr4:121750150..121752192,2	MCF-7	breast:
5	chr4:121651698..121654667-chr4:121660319..121662690,2	MCF-7	breast:
6	chr4:121396849..121398573-chr4:121700140..121702182,2	K562	blood:
7	chr4:121763712..121766459-chr4:121767957..121770236,3	MCF-7	breast:
8	chr4:121769272..121771821-chr4:121774320..121777055,2	MCF-7	breast:
9	chr4:121769272..121771821-chr4:121774320..121777055,2	MCF-7	breast:
10	chr4:121745652..121748462-chr4:121750150..121752192,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDNF-4	chr4:121751724-121752408	NONHSAT098129

Variant related genes	Relation type
PRDM5	TF binding region
RNU6-550P	TF binding region
PRDM5	CpG island
RNU6-550P	CpG island
ENSG00000150753	chromatin interactions

Extended variants
information (count: 5149 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:5149 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116552806	chr4:121657688-121657689	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114704633	chr4:121657759-121657760	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs17051236	chr4:121657767-121657768	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs530446736	chr4:121657773-121657774	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550607782	chr4:121657795-121657796	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570550825	chr4:121657816-121657817	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543057034	chr4:121657828-121657829	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539585923	chr4:121657849-121657850	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183617893	chr4:121657853-121657854	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs151206617	chr4:121657854-121657855	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139144634	chr4:121657881-121657882	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555394820	chr4:121657914-121657915	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs17051237	chr4:121657939-121657940	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs114179070	chr4:121657946-121657947	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs17347219	chr4:121657950-121657951	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576922671	chr4:121658031-121658032	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538816159	chr4:121658061-121658062	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188715571	chr4:121658117-121658118	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553137760	chr4:121658193-121658194	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192933284	chr4:121658256-121658257	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34608745	chr4:121658271-121658272	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558762401	chr4:121658280-121658281	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184567501	chr4:121658291-121658292	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146512205	chr4:121658294-121658295	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141076836	chr4:121658313-121658314	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377177918	chr4:121658325-121658326	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544220792	chr4:121658364-121658365	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557344082	chr4:121658367-121658368	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190325241	chr4:121658369-121658370	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114895241	chr4:121658422-121658423	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144614959	chr4:121658430-121658431	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115640728	chr4:121658436-121658437	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370994643	chr4:121658481-121658482	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529079698	chr4:121658482-121658483	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145437917	chr4:121658510-121658511	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549221157	chr4:121658546-121658547	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569048621	chr4:121658547-121658548	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541371892	chr4:121658563-121658564	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538187998	chr4:121658642-121658643	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375120370	chr4:121658649-121658650	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs78092970	chr4:121658653-121658654	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35678961	chr4:121658716-121658717	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570549266	chr4:121658736-121658737	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112405512	chr4:121658750-121658751	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553074333	chr4:121658792-121658793	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17051238	chr4:121658798-121658799	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs574728738	chr4:121658885-121658886	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542046745	chr4:121658920-121658921	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555970758	chr4:121659009-121659010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185046302	chr4:121659130-121659131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Esophageal squamous carcinoma	18350619	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
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	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
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD

Chromatin state (count:1035 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121620800-121671400	Weak transcription	Pancreas	Pancrea
2	chr4:121626000-121658200	Weak transcription	Aorta	Aorta
3	chr4:121630000-121671400	Weak transcription	Ovary	ovary
4	chr4:121641200-121670400	Weak transcription	Fetal Muscle Leg	muscle
5	chr4:121641400-121669600	Weak transcription	Fetal Intestine Small	intestine
6	chr4:121642800-121670600	Weak transcription	Fetal Stomach	stomach
7	chr4:121644200-121658200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:121645800-121662000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr4:121647200-121671400	Weak transcription	Fetal Lung	lung
10	chr4:121647400-121670600	Weak transcription	Stomach Smooth Muscle	stomach
11	chr4:121648200-121671600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:121648200-121671600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr4:121648400-121660200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:121648400-121670600	Weak transcription	Adipose Nuclei	Adipose
15	chr4:121649600-121670800	Weak transcription	Fetal Intestine Large	intestine
16	chr4:121651200-121669200	Weak transcription	Fetal Muscle Trunk	muscle
17	chr4:121652000-121673600	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr4:121652400-121670800	Weak transcription	Right Ventricle	heart
19	chr4:121652600-121687000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:121653000-121658600	Weak transcription	Right Atrium	heart
21	chr4:121653000-121660400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr4:121653000-121662000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:121653000-121662600	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr4:121653000-121662800	Weak transcription	Lung	lung
25	chr4:121653200-121671600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:121653200-121672200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr4:121654600-121660200	Weak transcription	Esophagus	oesophagus
28	chr4:121655200-121659200	Enhancers	Fetal Heart	heart
29	chr4:121656000-121670600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr4:121656200-121661600	Weak transcription	Fetal Thymus	thymus
31	chr4:121657000-121657800	Weak transcription	Left Ventricle	heart
32	chr4:121657200-121658000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr4:121657600-121659000	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr4:121657800-121658200	Enhancers	Left Ventricle	heart
35	chr4:121658200-121658800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr4:121658200-121658800	Strong transcription	Aorta	Aorta
37	chr4:121658200-121658800	Genic enhancers	Left Ventricle	heart
38	chr4:121658600-121658800	Enhancers	Right Atrium	heart
39	chr4:121658800-121668600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr4:121658800-121670600	Weak transcription	Aorta	Aorta
41	chr4:121658800-121671400	Weak transcription	Left Ventricle	heart
42	chr4:121659000-121669600	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr4:121660400-121668800	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr4:121661600-121663400	Enhancers	Fetal Thymus	thymus
45	chr4:121661600-121670800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:121662000-121662400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr4:121662000-121662400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr4:121662000-121662400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr4:121662000-121662600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr4:121662000-121662600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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