Variant report

Variant	nsv595334
Chromosome Location	chr4:121623057-121765527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:998)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:998 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:121670498-121670947	GM12878	blood:	n/a	n/a
2	BACH1	chr4:121642846-121642911	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:121640212-121640444	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:121686870-121687098	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:121670672-121671060	GM12878	blood:	n/a	n/a
6	BRCA1	chr4:121651232-121651259	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr4:121644141-121644145	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:121690199-121690775	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr4:121754428-121754544	K562	blood:	n/a	n/a
10	CEBPB	chr4:121676743-121677031	HepG2	liver:	n/a	chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676918-121676929
11	CEBPB	chr4:121690345-121690783	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:121631112-121631528	IMR90	lung:	n/a	chr4:121631295-121631306
13	CEBPB	chr4:121645169-121646234	Hela-S3	cervix:	n/a	chr4:121645385-121645402 chr4:121645889-121645902 chr4:121645891-121645902 chr4:121645891-121645900
14	CEBPB	chr4:121643338-121643603	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:121631141-121631341	HepG2	liver:	n/a	chr4:121631295-121631306
16	CEBPB	chr4:121762328-121762678	IMR90	lung:	n/a	chr4:121762495-121762508
17	CEBPB	chr4:121635451-121636206	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr4:121750290-121751025	Hela-S3	cervix:	n/a	chr4:121750852-121750863
19	CEBPB	chr4:121645254-121645513	IMR90	lung:	n/a	chr4:121645385-121645402
20	CEBPB	chr4:121704092-121704827	IMR90	lung:	n/a	chr4:121704325-121704338 chr4:121704325-121704338 chr4:121704196-121704209
21	CEBPB	chr4:121640171-121640485	MCF-7	breast:	n/a	chr4:121640181-121640192
22	CEBPB	chr4:121762437-121762637	A549	lung:	n/a	chr4:121762495-121762508
23	CEBPB	chr4:121631130-121631448	Hela-S3	cervix:	n/a	chr4:121631295-121631306
24	CEBPB	chr4:121750678-121751008	IMR90	lung:	n/a	chr4:121750852-121750863
25	CHD2	chr4:121655980-121656247	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	chr4:121693120-121693270	AG09319	gingival:	n/a	n/a
30	CTCF	chr4:121765100-121765250	RPTEC	kidney:	n/a	n/a
31	CTCF	chr4:121765120-121765270	HMEC	breast:	n/a	chr4:121765246-121765254
32	CTCF	chr4:121640240-121640390	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr4:121765080-121765230	GM12871	blood:	n/a	n/a
34	CTCF	chr4:121765160-121765310	AG09319	gingival:	n/a	chr4:121765246-121765254
35	CTCF	chr4:121640260-121640410	GM12864	blood:	n/a	n/a
36	CTCF	chr4:121765120-121765270	HEEpiC	esophagus:	n/a	chr4:121765246-121765254
37	CTCF	chr4:121640200-121640350	HL-60	blood:	n/a	n/a
38	CTCF	chr4:121640220-121640370	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr4:121730676-121731029	GM12878	blood:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
40	CTCF	chr4:121765080-121765324	H1-hESC	embryonic stem cell:	n/a	chr4:121765246-121765254
41	CTCF	chr4:121765180-121765330	Hela-S3	cervix:	n/a	chr4:121765246-121765254
42	CTCF	chr4:121640178-121640411	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr4:121693200-121693350	GM12865	blood:	n/a	n/a
44	CTCF	chr4:121640240-121640390	AG04449	skin:	n/a	n/a
45	CTCF	chr4:121730780-121730930	HVMF	connective:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
46	CTCF	chr4:121640240-121640390	GM12878	blood:	n/a	n/a
47	CTCF	chr4:121765072-121765295	HepG2	liver:	n/a	chr4:121765246-121765254
48	CTCF	chr4:121693180-121693330	Caco-2	colon:	n/a	n/a
49	CTCF	chr4:121693180-121693330	GM06990	blood:	n/a	n/a
50	CTCF	chr4:121730780-121730930	GM12875	blood:	n/a	chr4:121730831-121730849 chr4:121730826-121730847

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:121763322-121763372	HCF	heart:	n/a
2	chr4:121763322-121763372	AG10803	skin:	n/a
3	chr4:121763322-121763372	ECC-1	luminal epithelium:	n/a
4	chr4:121763322-121763372	Caco-2	colon:	n/a
5	chr4:121763322-121763372	HEEpiC	esophagus:	n/a
6	chr4:121763322-121763372	K562	blood:	n/a
7	chr4:121763322-121763372	RPTEC	kidney:	n/a
8	chr4:121763322-121763372	HRCEpiC	kidney:	n/a
9	chr4:121763322-121763372	SAEC	small airway:	n/a
10	chr4:121763322-121763372	NH-A	brain:	n/a
11	chr4:121763322-121763372	AG04450	lung:	fetal
12	chr4:121763322-121763372	U87	brain:	n/a
13	chr4:121763322-121763372	T-47D	breast:	n/a
14	chr4:121763322-121763372	HRPEpiC	eye:	n/a
15	chr4:121763322-121763372	PFSK-1	brain:	n/a
16	chr4:121763322-121763372	AoSMC	blood vessel:	n/a
17	chr4:121763322-121763372	HUVEC	blood vessel:	n/a
18	chr4:121763322-121763372	MCF-7	breast:	n/a
19	chr4:121763322-121763372	HepG2	liver:	n/a
20	chr4:121763322-121763372	SK-N-MC	brain:	n/a
21	chr4:121763322-121763372	BJ	skin:	n/a
22	chr4:121763322-121763372	GM12891	blood:	n/a
23	chr4:121763322-121763372	H1-hESC	embryonic stem cell:	embryo
24	chr4:121763322-121763372	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:121763322-121763372	LNCaP	prostate:	n/a
26	chr4:121763322-121763372	HL-60	blood:	n/a
27	chr4:121763322-121763372	HRE	kidney:	n/a
28	chr4:121763322-121763372	HIPEpiC	eye:	n/a
29	chr4:121763322-121763372	Hepatocyte	liver:	n/a
30	chr4:121763322-121763372	HCPEpiC	choroid plexus:	n/a
31	chr4:121763322-121763372	IMR90	lung:	fetal
32	chr4:121763322-121763372	HCT-116	colon:	n/a
33	chr4:121763322-121763372	GM06990	blood:	n/a
34	chr4:121763322-121763372	SKMC	muscle:	n/a
35	chr4:121763322-121763372	Jurkat	blood:	n/a
36	chr4:121763322-121763372	GM19239	blood:	n/a
37	chr4:121763322-121763372	MCF10A-Er-Src	breast:	n/a
38	chr4:121763322-121763372	BE2_C	brain:	n/a
39	chr4:121763322-121763372	Hela-S3	cervix:	n/a
40	chr4:121763322-121763372	A549	lung:	n/a
41	chr4:121763322-121763372	PANC-1	pancreas:	n/a
42	chr4:121763322-121763372	CMK	blood:	n/a
43	chr4:121763322-121763372	AG09309	skin:	n/a
44	chr4:121763322-121763372	PrEC	prostate:	n/a
45	chr4:121763322-121763372	ovcar-3	ovarian:	n/a
46	chr4:121763322-121763372	NB4	blood:	n/a
47	chr4:121763322-121763372	HCM	heart:	n/a
48	chr4:121763322-121763372	HMEC	breast:	n/a
49	chr4:121763322-121763372	NHDF-neo	bronchial:	n/a
50	chr4:121763322-121763372	HEK293	kidney:	embryo

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:121646983..121649694-chr4:121650404..121652066,2	K562	blood:
2	chr4:121633676..121636146-chr4:121637384..121639291,2	K562	blood:
3	chr4:121396849..121398573-chr4:121700140..121702182,2	K562	blood:
4	chr4:121622815..121625386-chr4:121625794..121628188,2	K562	blood:
5	chr4:121763712..121766459-chr4:121767957..121770236,3	MCF-7	breast:
6	chr4:121745652..121748462-chr4:121750150..121752192,2	MCF-7	breast:
7	chr4:121651698..121654667-chr4:121660319..121662690,2	MCF-7	breast:
8	chr4:121650109..121652030-chr4:121655352..121657399,2	K562	blood:
9	chr4:121633676..121636146-chr4:121637384..121639291,2	K562	blood:
10	chr4:121646983..121649694-chr4:121650404..121652066,2	K562	blood:
11	chr4:121639899..121640642-chr4:121840005..121841112,3	MCF-7	breast:
12	chr4:121077068..121077961-chr4:121639964..121640817,3	MCF-7	breast:
13	chr4:121764972..121765670-chr4:121898848..121899366,2	MCF-7	breast:
14	chr4:121622815..121625386-chr4:121625794..121628188,2	K562	blood:
15	chr4:121745652..121748462-chr4:121750150..121752192,2	MCF-7	breast:
16	chr4:121651698..121654667-chr4:121660319..121662690,2	MCF-7	breast:
17	chr4:121650109..121652030-chr4:121655352..121657399,2	K562	blood:

(count:1 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 5606 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:5606 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1874442	chr4:121623057-121623058	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549824563	chr4:121623079-121623080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569686194	chr4:121623119-121623120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538364001	chr4:121623121-121623122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558658007	chr4:121623130-121623131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572142269	chr4:121623135-121623136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528387948	chr4:121623137-121623138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534844662	chr4:121623165-121623166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554425181	chr4:121623170-121623171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574416592	chr4:121623175-121623176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6534204	chr4:121623193-121623194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs13119260	chr4:121623209-121623210	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs13143781	chr4:121623224-121623225	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs56029376	chr4:121623236-121623237	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs565407352	chr4:121623244-121623245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13119281	chr4:121623246-121623247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs74905157	chr4:121623263-121623264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139262860	chr4:121623296-121623297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs13119501	chr4:121623301-121623302	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs530420892	chr4:121623314-121623315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549755740	chr4:121623345-121623346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569540093	chr4:121623350-121623351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538672343	chr4:121623354-121623355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76823020	chr4:121623364-121623365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113761994	chr4:121623365-121623366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7437685	chr4:121623366-121623367	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs534474082	chr4:121623382-121623383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34807908	chr4:121623409-121623410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77956370	chr4:121623420-121623421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191440146	chr4:121623428-121623429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536940732	chr4:121623433-121623434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557272297	chr4:121623443-121623444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576337869	chr4:121623460-121623461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145070579	chr4:121623474-121623475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs199673977	chr4:121623490-121623491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558747847	chr4:121623514-121623515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1496276	chr4:121623516-121623517	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs541591784	chr4:121623531-121623532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561475610	chr4:121623537-121623538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148620880	chr4:121623562-121623563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544123179	chr4:121623575-121623576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142070391	chr4:121623578-121623579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183611641	chr4:121623612-121623613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552163829	chr4:121623613-121623614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555775547	chr4:121623620-121623621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575750116	chr4:121623633-121623634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76160836	chr4:121623663-121623664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547924289	chr4:121623665-121623666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538233532	chr4:121623668-121623669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567913668	chr4:121623679-121623680	Weak transcription	n/a	n/a	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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121610200-121624600	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr4:121615200-121624200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr4:121616800-121631000	Weak transcription	NHEK	skin
4	chr4:121617400-121629200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:121617600-121630200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:121618600-121630600	Weak transcription	Fetal Lung	lung
7	chr4:121620800-121637600	Weak transcription	Psoas Muscle	Psoas
8	chr4:121620800-121654400	Weak transcription	Left Ventricle	heart
9	chr4:121620800-121671400	Weak transcription	Pancreas	Pancrea
10	chr4:121621000-121630600	Weak transcription	Fetal Heart	heart
11	chr4:121624600-121625600	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr4:121625000-121625400	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr4:121625000-121625800	Enhancers	Colon Smooth Muscle	Colon
14	chr4:121625000-121626800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:121625200-121626000	Enhancers	Brain Substantia Nigra	brain
16	chr4:121625200-121626000	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr4:121625600-121657600	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr4:121625800-121626000	ZNF genes & repeats	Aorta	Aorta
19	chr4:121625800-121630800	Weak transcription	Colon Smooth Muscle	Colon
20	chr4:121626000-121630600	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr4:121626000-121658200	Weak transcription	Aorta	Aorta
22	chr4:121626200-121629000	Weak transcription	Ovary	ovary
23	chr4:121626800-121631400	Weak transcription	Right Ventricle	heart
24	chr4:121629000-121630000	Strong transcription	Ovary	ovary
25	chr4:121629600-121643400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr4:121630000-121671400	Weak transcription	Ovary	ovary
27	chr4:121630200-121631600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:121630200-121631800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr4:121630400-121631600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr4:121630400-121631600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:121630400-121631600	Enhancers	NHDF-Ad	bronchial
32	chr4:121630600-121631200	Enhancers	Fetal Lung	lung
33	chr4:121630600-121631600	Enhancers	Fetal Heart	heart
34	chr4:121630600-121631600	Enhancers	Osteobl	bone
35	chr4:121630600-121631800	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr4:121630800-121631400	Enhancers	Colon Smooth Muscle	Colon
37	chr4:121630800-121631600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr4:121630800-121631600	Enhancers	HSMMtube	muscle
39	chr4:121631000-121631400	Enhancers	Fetal Kidney	kidney
40	chr4:121631000-121631600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr4:121631000-121631600	Enhancers	HSMM	muscle
42	chr4:121631000-121631600	Enhancers	NHEK	skin
43	chr4:121631000-121631600	Enhancers	NHLF	lung
44	chr4:121631200-121631600	Enhancers	Fetal Brain Male	brain
45	chr4:121631200-121631600	Flanking Active TSS	Fetal Lung	lung
46	chr4:121631200-121631600	Enhancers	Rectal Smooth Muscle	rectum
47	chr4:121631600-121631800	Enhancers	Fetal Lung	lung
48	chr4:121631600-121641200	Weak transcription	Fetal Heart	heart
49	chr4:121631800-121642200	Weak transcription	Fetal Lung	lung
50	chr4:121633600-121634000	Enhancers	HUES48 Cell Line	embryonic stem cell

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