Variant report

Variant	nsv1012289
Chromosome Location	chr4:7361958-7395292
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:206)
CpG islands
(count:793)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:206 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr4:7389520-7389951	GM12878	blood:	n/a	n/a
2	BCL3	chr4:7389522-7390004	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:7394736-7394888	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:7371415-7371470	K562	blood:	n/a	n/a
5	BRCA1	chr4:7383701-7383753	HepG2	liver:	n/a	n/a
6	CEBPB	chr4:7381736-7381812	IMR90	lung:	n/a	n/a
7	CHD2	chr4:7391585-7391592	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr4:7373500-7373650	HBMEC	blood vessel:	n/a	n/a
9	CTCF	chr4:7394780-7394930	HPF	lung:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
10	CTCF	chr4:7383200-7383350	GM12872	blood:	n/a	n/a
11	CTCF	chr4:7394780-7394930	HMF	breast:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
12	CTCF	chr4:7383180-7383330	GM12865	blood:	n/a	n/a
13	CTCF	chr4:7394760-7394910	BJ	skin:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
14	CTCF	chr4:7373400-7373550	HBMEC	blood vessel:	n/a	chr4:7373457-7373470
15	CTCF	chr4:7388194-7388232	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr4:7394860-7395010	HFF	foreskin:	n/a	chr4:7394864-7394882
17	CTCF	chr4:7383180-7383330	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr4:7383220-7383370	GM12873	blood:	n/a	n/a
19	CTCF	chr4:7383260-7383410	NHEK	skin:	n/a	n/a
20	CTCF	chr4:7383180-7383330	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr4:7394900-7395050	NHDF-neo	bronchial:	n/a	n/a
22	CTCF	chr4:7387830-7388081	GM19239	blood:	n/a	n/a
23	CTCF	chr4:7394780-7394930	AG09319	gingival:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
24	CTCF	chr4:7394820-7394970	RPTEC	kidney:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
25	CTCF	chr4:7364729-7364993	GM19239	blood:	n/a	n/a
26	CTCF	chr4:7383258-7383304	MCF-7	breast:	n/a	n/a
27	CTCF	chr4:7383000-7383150	BJ	skin:	n/a	n/a
28	CTCF	chr4:7389318-7389414	GM19239	blood:	n/a	n/a
29	CTCF	chr4:7394760-7394910	HFF-Myc	foreskin:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
30	CTCF	chr4:7383218-7383337	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:7383100-7383370	NB4	blood:	n/a	n/a
32	CTCF	chr4:7383200-7383350	HMEC	breast:	n/a	n/a
33	CTCF	chr4:7394820-7394970	HBMEC	blood vessel:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
34	CTCF	chr4:7394660-7394810	HAc	cerebellar:	n/a	n/a
35	CTCF	chr4:7383188-7383409	K562	blood:	n/a	n/a
36	CTCF	chr4:7394860-7395010	HCM	heart:	n/a	chr4:7394864-7394882
37	CTCF	chr4:7388308-7388382	GM19239	blood:	n/a	n/a
38	CTCF	chr4:7394800-7394950	AG09309	skin:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
39	CTCF	chr4:7394800-7394950	HCFaa	heart:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
40	CTCF	chr4:7383240-7383390	HMEC	breast:	n/a	n/a
41	CTCF	chr4:7394740-7394890	AG04449	skin:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
42	CTCF	chr4:7383320-7383470	GM12873	blood:	n/a	n/a
43	CTCF	chr4:7383160-7383310	HepG2	liver:	n/a	n/a
44	CTCF	chr4:7394803-7394933	K562	blood:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
45	CTCF	chr4:7383240-7383390	HepG2	liver:	n/a	n/a
46	CTCF	chr4:7383240-7383390	GM12873	blood:	n/a	n/a
47	CTCF	chr4:7394772-7394967	LNCaP	prostate:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
48	CTCF	chr4:7383200-7383350	GM12869	blood:	n/a	n/a
49	CTCF	chr4:7394800-7394950	NHDF-neo	bronchial:	n/a	chr4:7394864-7394882 chr4:7394859-7394880
50	CTCF	chr4:7394800-7394950	HPAF	blood vessel:	n/a	chr4:7394864-7394882 chr4:7394859-7394880

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7394790-7394840	SKMC	muscle:	n/a
2	chr4:7374622-7374672	GM06990	blood:	n/a
3	chr4:7394902-7394952	NHBE	bronchial:	n/a
4	chr4:7373065-7373115	MCF10A-Er-Src	breast:	n/a
5	chr4:7373088-7373138	HRCEpiC	kidney:	n/a
6	chr4:7373343-7373393	Hela-S3	cervix:	n/a
7	chr4:7395027-7395077	HEEpiC	esophagus:	n/a
8	chr4:7373065-7373115	GM12878	blood:	n/a
9	chr4:7368808-7368858	PrEC	prostate:	n/a
10	chr4:7373451-7373501	Hela-S3	cervix:	n/a
11	chr4:7374582-7374632	CMK	blood:	n/a
12	chr4:7373065-7373115	HRCEpiC	kidney:	n/a
13	chr4:7368808-7368858	GM12891	blood:	n/a
14	chr4:7373088-7373138	Caco-2	colon:	n/a
15	chr4:7374582-7374632	PANC-1	pancreas:	n/a
16	chr4:7373088-7373138	GM12878	blood:	n/a
17	chr4:7394790-7394840	SK-N-SH	brain:	n/a
18	chr4:7373022-7373072	AG09319	gingival:	n/a
19	chr4:7374622-7374672	GM19239	blood:	n/a
20	chr4:7373343-7373393	HCF	heart:	n/a
21	chr4:7368808-7368858	SK-N-SH_RA	brain:	n/a
22	chr4:7373022-7373072	HCT-116	colon:	n/a
23	chr4:7373451-7373501	PrEC	prostate:	n/a
24	chr4:7373022-7373072	HL-60	blood:	n/a
25	chr4:7395027-7395077	HCPEpiC	choroid plexus:	n/a
26	chr4:7374669-7374719	HUVEC	blood vessel:	n/a
27	chr4:7374669-7374719	HCF	heart:	n/a
28	chr4:7374669-7374719	HNPCEpiC	eye:	n/a
29	chr4:7368808-7368858	AoSMC	blood vessel:	n/a
30	chr4:7395027-7395077	Hepatocyte	liver:	n/a
31	chr4:7394790-7394840	Hela-S3	cervix:	n/a
32	chr4:7373375-7373425	AG04449	skin:	fetal
33	chr4:7373343-7373393	HRE	kidney:	n/a
34	chr4:7394902-7394952	Caco-2	colon:	n/a
35	chr4:7374622-7374672	AG09309	skin:	n/a
36	chr4:7374622-7374672	NHDF-neo	bronchial:	n/a
37	chr4:7374582-7374632	NH-A	brain:	n/a
38	chr4:7373065-7373115	GM12891	blood:	n/a
39	chr4:7394902-7394952	AoSMC	blood vessel:	n/a
40	chr4:7373343-7373393	Jurkat	blood:	n/a
41	chr4:7373375-7373425	Caco-2	colon:	n/a
42	chr4:7373065-7373115	Caco-2	colon:	n/a
43	chr4:7373375-7373425	T-47D	breast:	n/a
44	chr4:7373022-7373072	PFSK-1	brain:	n/a
45	chr4:7373451-7373501	Hepatocyte	liver:	n/a
46	chr4:7373451-7373501	H1-hESC	embryonic stem cell:	embryo
47	chr4:7373088-7373138	SAEC	small airway:	n/a
48	chr4:7373065-7373115	NH-A	brain:	n/a
49	chr4:7373088-7373138	GM06990	blood:	n/a
50	chr4:7394902-7394952	PFSK-1	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7379670..7381494-chr4:7386089..7388164,2	MCF-7	breast:
2	chr4:7390826..7393048-chr4:7397978..7399599,2	K562	blood:
3	chr4:7383688..7386863-chr4:7391292..7393827,3	MCF-7	breast:
4	chr4:7343522..7345728-chr4:7361522..7364374,3	MCF-7	breast:
5	chr4:7385620..7387196-chr4:7395929..7398822,2	MCF-7	breast:
6	chr4:7368817..7370379-chr4:7371392..7373136,2	MCF-7	breast:
7	chr4:7368964..7371820-chr4:7419661..7422236,2	K562	blood:
8	chr4:7383688..7386863-chr4:7391292..7393827,3	MCF-7	breast:
9	chr4:7193444..7195418-chr4:7373102..7374832,2	MCF-7	breast:
10	chr1:9471245..9471745-chr4:7390618..7391126,2	K562	blood:
11	chr4:7368817..7370379-chr4:7371392..7373136,2	MCF-7	breast:
12	chr4:7379670..7381494-chr4:7386089..7388164,2	MCF-7	breast:
13	chr4:7375155..7379159-chr4:7380747..7383834,3	K562	blood:

No data

Variant related genes	Relation type
SORCS2	TF binding region
SORCS2	CpG island
ENSG00000184985	chromatin interactions

Extended variants
information (count: 2101 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2101 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576659619	chr4:7362006-7362007	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs537848140	chr4:7362018-7362019	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs556151596	chr4:7362019-7362020	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs577826961	chr4:7362031-7362032	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs545098177	chr4:7362036-7362037	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs186011667	chr4:7362038-7362039	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs3916114	chr4:7362054-7362055	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs141559424	chr4:7362055-7362056	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs561282600	chr4:7362084-7362085	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs531458602	chr4:7362089-7362090	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs375112953	chr4:7362090-7362091	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs150898108	chr4:7362124-7362125	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs189011823	chr4:7362130-7362131	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs532349420	chr4:7362154-7362155	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs181407324	chr4:7362164-7362165	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs566030719	chr4:7362168-7362169	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs112575177	chr4:7362188-7362189	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs548444088	chr4:7362193-7362194	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs570335266	chr4:7362194-7362195	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs6446593	chr4:7362229-7362230	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs138345277	chr4:7362242-7362243	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs112158963	chr4:7362275-7362276	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs544169978	chr4:7362368-7362369	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs556214925	chr4:7362391-7362392	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs571292931	chr4:7362435-7362436	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs538624683	chr4:7362469-7362470	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs565564346	chr4:7362473-7362474	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs553874621	chr4:7362474-7362475	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs548586514	chr4:7362484-7362485	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs375879056	chr4:7362485-7362486	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs3916115	chr4:7362523-7362524	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs372229098	chr4:7362524-7362525	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs542811517	chr4:7362531-7362532	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs554428606	chr4:7362532-7362533	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs576302286	chr4:7362535-7362536	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs187209107	chr4:7362549-7362550	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs564820910	chr4:7362550-7362551	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs192094571	chr4:7362575-7362576	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs7683584	chr4:7362598-7362599	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs559800721	chr4:7362603-7362604	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs17757615	chr4:7362647-7362648	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs548777176	chr4:7362678-7362679	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs570120883	chr4:7362702-7362703	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs55667900	chr4:7362724-7362725	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs116832958	chr4:7362737-7362738	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs571152500	chr4:7362755-7362756	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs143981064	chr4:7362797-7362798	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs529764733	chr4:7362832-7362833	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553443106	chr4:7362855-7362856	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186043892	chr4:7362875-7362876	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7346600-7367200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:7351400-7365000	Enhancers	Brain Cingulate Gyrus	brain
3	chr4:7351600-7365000	Enhancers	Brain Substantia Nigra	brain
4	chr4:7353600-7364800	Enhancers	Brain Anterior Caudate	brain
5	chr4:7358200-7365000	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr4:7358400-7362000	Enhancers	Fetal Brain Male	brain
7	chr4:7358800-7366800	Weak transcription	Right Ventricle	heart
8	chr4:7359000-7363000	Weak transcription	Right Atrium	heart
9	chr4:7359200-7362600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:7359200-7364600	Weak transcription	Gastric	stomach
11	chr4:7359600-7362000	Enhancers	Fetal Muscle Leg	muscle
12	chr4:7360000-7362200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr4:7360200-7367200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr4:7360400-7362000	Weak transcription	Fetal Brain Female	brain
15	chr4:7360400-7362600	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr4:7360400-7362800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr4:7360400-7362800	Weak transcription	Fetal Heart	heart
18	chr4:7360400-7364400	Weak transcription	Fetal Kidney	kidney
19	chr4:7360400-7367800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr4:7360600-7362600	Weak transcription	HSMMtube	muscle
21	chr4:7360600-7363000	Weak transcription	HSMM	muscle
22	chr4:7360600-7366800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:7360800-7362600	Weak transcription	Left Ventricle	heart
24	chr4:7360800-7364400	Enhancers	Fetal Lung	lung
25	chr4:7361000-7364000	Enhancers	Fetal Stomach	stomach
26	chr4:7361000-7364600	Enhancers	Stomach Smooth Muscle	stomach
27	chr4:7361000-7365000	Enhancers	Brain Angular Gyrus	brain
28	chr4:7361000-7365000	Enhancers	Brain Hippocampus Middle	brain
29	chr4:7361200-7362400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr4:7361400-7362000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr4:7361400-7364800	Enhancers	Ovary	ovary
32	chr4:7361400-7365000	Enhancers	Brain Germinal Matrix	brain
33	chr4:7362000-7362200	Enhancers	Fetal Brain Female	brain
34	chr4:7362000-7362400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr4:7362000-7362400	Weak transcription	Fetal Brain Male	brain
36	chr4:7362000-7363200	Enhancers	Lung	lung
37	chr4:7362000-7364600	Bivalent Enhancer	Fetal Muscle Leg	muscle
38	chr4:7362200-7362600	Weak transcription	Fetal Brain Female	brain
39	chr4:7362200-7363600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr4:7362400-7363600	Enhancers	Fetal Brain Male	brain
41	chr4:7362400-7364400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr4:7362400-7364400	Enhancers	Fetal Muscle Trunk	muscle
43	chr4:7362600-7362800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
44	chr4:7362600-7363200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:7362600-7363200	Enhancers	Fetal Brain Female	brain
46	chr4:7362600-7363400	Enhancers	Left Ventricle	heart
47	chr4:7362600-7363400	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr4:7362600-7364000	Enhancers	HSMMtube	muscle
49	chr4:7362800-7363000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:7362800-7363200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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