Variant report

Variant	nsv878671
Chromosome Location	chr4:9766888-9912101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1118)
CpG islands
(count:1163)
Chromatin interactive
region (count:28)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1118 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:9850013-9850273	K562	blood:	n/a	n/a
2	ATF2	chr4:9814641-9815054	GM12878	blood:	n/a	n/a
3	ATF2	chr4:9809744-9810072	GM12878	blood:	n/a	n/a
4	ATF3	chr4:9849946-9850297	K562	blood:	n/a	n/a
5	BACH1	chr4:9885168-9885286	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:9806067-9806321	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:9784048-9784153	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr4:9813621-9813815	GM12878	blood:	n/a	n/a
9	BATF	chr4:9814682-9815071	GM12878	blood:	n/a	n/a
10	BATF	chr4:9779146-9779367	GM12878	blood:	n/a	n/a
11	BATF	chr4:9809777-9810086	GM12878	blood:	n/a	n/a
12	BATF	chr4:9814742-9814999	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:9809752-9810069	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:9779122-9779297	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:9809742-9810117	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:9851100-9851523	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:9814557-9814998	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:9814677-9815008	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:9851148-9851550	GM12878	blood:	n/a	n/a
20	BCL3	chr4:9826836-9827129	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:9814583-9815072	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:9802635-9802910	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:9882590-9882646	K562	blood:	n/a	n/a
24	BHLHE40	chr4:9851061-9851588	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:9872224-9872359	K562	blood:	n/a	n/a
26	BHLHE40	chr4:9809778-9810107	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:9867363-9867483	K562	blood:	n/a	n/a
28	BHLHE40	chr4:9809308-9809346	GM12878	blood:	n/a	n/a
29	BRCA1	chr4:9871086-9871272	GM12878	blood:	n/a	n/a
30	BRCA1	chr4:9829608-9829617	H1-hESC	embryonic stem cell:	n/a	n/a
31	CCNT2	chr4:9895028-9895704	K562	blood:	n/a	n/a
32	CEBPB	chr4:9849824-9850326	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
33	CEBPB	chr4:9900375-9900657	K562	blood:	n/a	n/a
34	CEBPB	chr4:9876127-9876348	HepG2	liver:	n/a	chr4:9876241-9876252
35	CEBPB	chr4:9849869-9850308	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
36	CEBPB	chr4:9876209-9876280	K562	blood:	n/a	chr4:9876241-9876252
37	CEBPB	chr4:9900230-9900797	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr4:9876089-9876404	IMR90	lung:	n/a	chr4:9876241-9876252
39	CEBPB	chr4:9849900-9850296	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
40	CEBPB	chr4:9849942-9850300	IMR90	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
41	CEBPB	chr4:9849949-9850302	HepG2	liver:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
42	CEBPB	chr4:9849980-9850299	H1-hESC	embryonic stem cell:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
43	CEBPB	chr4:9849998-9850279	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
44	CEBPB	chr4:9895337-9895676	K562	blood:	n/a	n/a
45	CEBPB	chr4:9867161-9867312	HepG2	liver:	n/a	chr4:9867238-9867249
46	CEBPB	chr4:9900393-9900739	MCF-7	breast:	n/a	n/a
47	CEBPB	chr4:9849994-9850220	MCF-7	breast:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
48	CEBPB	chr4:9849913-9850318	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
49	CEBPB	chr4:9895305-9895547	K562	blood:	n/a	n/a
50	CEBPB	chr4:9849953-9850289	Hela-S3	cervix:	n/a	chr4:9850045-9850056 chr4:9850120-9850131

(count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9782891-9782941	MCF-7	breast:	n/a
2	chr4:9783246-9783296	HMEC	breast:	n/a
3	chr4:9783059-9783109	GM12878	blood:	n/a
4	chr4:9783206-9783256	ovcar-3	ovarian:	n/a
5	chr4:9782891-9782941	MCF-7	breast:	n/a
6	chr4:9783246-9783296	HMEC	breast:	n/a
7	chr4:9783059-9783109	GM12878	blood:	n/a
8	chr4:9783206-9783256	ovcar-3	ovarian:	n/a
9	chr4:9783206-9783256	PFSK-1	brain:	n/a
10	chr4:9884128-9884178	AG04450	lung:	fetal
11	chr4:9783206-9783256	GM19239	blood:	n/a
12	chr4:9783206-9783256	Jurkat	blood:	n/a
13	chr4:9782891-9782941	AG04450	lung:	fetal
14	chr4:9780269-9780319	HCF	heart:	n/a
15	chr4:9782931-9782981	PANC-1	pancreas:	n/a
16	chr4:9892887-9892937	GM06990	blood:	n/a
17	chr4:9892887-9892937	AG04449	skin:	fetal
18	chr4:9782891-9782941	SK-N-MC	brain:	n/a
19	chr4:9783965-9784015	AG04449	skin:	fetal
20	chr4:9892887-9892937	NHBE	bronchial:	n/a
21	chr4:9783198-9783248	NH-A	brain:	n/a
22	chr4:9783198-9783248	SK-N-SH	brain:	n/a
23	chr4:9782243-9782293	HIPEpiC	eye:	n/a
24	chr4:9784508-9784558	MCF-7	breast:	n/a
25	chr4:9780269-9780319	NH-A	brain:	n/a
26	chr4:9783192-9783242	SAEC	small airway:	n/a
27	chr4:9783965-9784015	HIPEpiC	eye:	n/a
28	chr4:9782891-9782941	HAEpiC	amniotic membrane:	n/a
29	chr4:9783965-9784015	BE2_C	brain:	n/a
30	chr4:9783246-9783296	NHDF-neo	bronchial:	n/a
31	chr4:9783623-9783673	HMEC	breast:	n/a
32	chr4:9782243-9782293	HRE	kidney:	n/a
33	chr4:9782931-9782981	HEK293	kidney:	embryo
34	chr4:9783192-9783242	HIPEpiC	eye:	n/a
35	chr4:9783623-9783673	AG09319	gingival:	n/a
36	chr4:9783246-9783296	T-47D	breast:	n/a
37	chr4:9783623-9783673	BE2_C	brain:	n/a
38	chr4:9784508-9784558	ECC-1	luminal epithelium:	n/a
39	chr4:9892887-9892937	T-47D	breast:	n/a
40	chr4:9783192-9783242	HEEpiC	esophagus:	n/a
41	chr4:9783953-9784003	PFSK-1	brain:	n/a
42	chr4:9783363-9783413	HIPEpiC	eye:	n/a
43	chr4:9783206-9783256	ProgFib	skin:	n/a
44	chr4:9783196-9783246	GM12891	blood:	n/a
45	chr4:9783198-9783248	AG09319	gingival:	n/a
46	chr4:9782243-9782293	GM06990	blood:	n/a
47	chr4:9783206-9783256	LNCaP	prostate:	n/a
48	chr4:9783196-9783246	SKMC	muscle:	n/a
49	chr4:9782891-9782941	HRE	kidney:	n/a
50	chr4:9782931-9782981	SKMC	muscle:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
2	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
3	chr2:91818363..91818948-chr4:9766445..9767270,6	MCF-7	breast:
4	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
5	chr2:91818108..91819097-chr4:9766527..9767180,2	K562	blood:
6	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
7	chr2:91818675..91820415-chr4:9765033..9768552,3	K562	blood:
8	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
9	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
10	chr2:91816088..91820118-chr4:9765029..9767622,10	MCF-7	breast:
11	chr4:9765483..9767943-chr4:10007316..10009788,2	MCF-7	breast:
12	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
13	chr4:9705037..9705657-chr4:9778184..9778690,2	K562	blood:
14	chr4:9766550..9767471-chr4:10020110..10020837,2	MCF-7	breast:
15	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
16	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
17	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
18	chr2:91817635..91819182-chr4:9766044..9767255,9	MCF-7	breast:
19	chr4:9770192..9773137-chr4:10024212..10026749,2	K562	blood:
20	chr1:149220703..149225113-chr4:9764948..9767069,4	MCF-7	breast:
21	chr4:9898528..9900449-chr4:10019179..10021130,2	MCF-7	breast:
22	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
23	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
24	chr2:91815162..91820044-chr4:9763391..9768700,25	MCF-7	breast:
25	chr4:9766486..9767204-chr4:10064960..10065893,2	MCF-7	breast:
26	chr4:9827283..9829135-chr4:9829200..9831465,2	K562	blood:
27	chr2:91816400..91817015-chr4:9766701..9767270,2	MCF-7	breast:
28	chr4:9766485..9767197-chr4:10016698..10017481,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-12	chr4:9870401-9871383	NONHSAT095146
2	lnc-DRD5-13	chr4:9814207-9814604	NONHSAT095145
3	lnc-DRD5-13	chr4:9807330-9807762	NONHSAT095145
4	lnc-WDR1-12	chr4:9873428-9874487	NONHSAT095146
5	lnc-DRD5-13	chr4:9810799-9811038	NONHSAT095145

No data

Variant related genes	Relation type
RNA5SP154	TF binding region
DRD5	TF binding region
SLC2A9	TF binding region
RNA5SP154	CpG island
DRD5	CpG island
SLC2A9	CpG island
ENSG00000206737	chromatin interactions
ENSG00000109667	chromatin interactions
ENSG00000250413	chromatin interactions

Extended variants
information (count: 6488 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:6488 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1878943	chr4:9766888-9766889	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs80119365	chr4:9766891-9766892	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs184818508	chr4:9766908-9766909	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs535789727	chr4:9766910-9766911	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs550776452	chr4:9766915-9766916	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs569110638	chr4:9766916-9766917	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs371839287	chr4:9766943-9766944	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs189232459	chr4:9766950-9766951	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs559116238	chr4:9766997-9766998	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs551671268	chr4:9767007-9767008	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs560384009	chr4:9767008-9767009	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs534718257	chr4:9767019-9767020	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs553374149	chr4:9767101-9767102	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575028580	chr4:9767102-9767103	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527906801	chr4:9767122-9767123	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs542144719	chr4:9767145-9767146	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs563523830	chr4:9767151-9767152	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs111301609	chr4:9767154-9767155	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs11731100	chr4:9767180-9767181	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs182174175	chr4:9767187-9767188	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185120070	chr4:9767188-9767189	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs112042890	chr4:9767230-9767231	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs150030926	chr4:9767231-9767232	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs111752813	chr4:9767240-9767241	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs112121633	chr4:9767263-9767264	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs111456310	chr4:9767267-9767268	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs561752972	chr4:9767276-9767277	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs112979264	chr4:9767294-9767295	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs11726288	chr4:9767309-9767310	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs550909281	chr4:9767338-9767339	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs569048828	chr4:9767350-9767351	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs140989013	chr4:9767353-9767354	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs552602420	chr4:9767365-9767366	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs10939504	chr4:9767370-9767371	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs375816945	chr4:9767378-9767379	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189871898	chr4:9767382-9767383	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs181187574	chr4:9767396-9767397	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs574808090	chr4:9767397-9767398	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs535713849	chr4:9767401-9767402	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs557252835	chr4:9767402-9767403	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs111502994	chr4:9767409-9767410	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs73805834	chr4:9767417-9767418	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs545996159	chr4:9767426-9767427	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs564740912	chr4:9767438-9767439	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs147864662	chr4:9767442-9767443	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs540358851	chr4:9767459-9767460	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs561491609	chr4:9767474-9767475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528918698	chr4:9767484-9767485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141539501	chr4:9767488-9767489	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562782733	chr4:9767489-9767490	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Wilms tumour	21544195	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
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
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
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
early-passage human iPS cells	21368824	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Obesity	21131291	CNVD
Schizophrenia	23813976	CNVD
Hepatocellular carcinoma	22267523	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9763600-9767600	Weak transcription	Right Atrium	heart
2	chr4:9766600-9767200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:9766800-9771800	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr4:9766800-9782000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:9767000-9767200	Bivalent Enhancer	Stomach Mucosa	stomach
6	chr4:9769400-9773600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr4:9769600-9773400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr4:9771000-9771200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:9771400-9772400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:9771800-9772000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr4:9772000-9772400	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr4:9772000-9773600	Enhancers	HMEC	breast
13	chr4:9772400-9773600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:9772400-9773600	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr4:9772600-9773400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:9775000-9775600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:9775200-9775600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr4:9775200-9776800	Enhancers	Brain Cingulate Gyrus	brain
19	chr4:9781200-9781600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr4:9781400-9781600	Enhancers	HMEC	breast
21	chr4:9781400-9781800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:9781400-9781800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:9781400-9781800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:9781400-9781800	Bivalent Enhancer	NHEK	skin
25	chr4:9781600-9781800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr4:9781600-9781800	Bivalent Enhancer	Small Intestine	intestine
27	chr4:9781800-9782200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr4:9782000-9782200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:9782400-9783000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:9782400-9783400	Bivalent Enhancer	Fetal Muscle Leg	muscle
31	chr4:9782600-9783800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
32	chr4:9782600-9784000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
33	chr4:9782800-9783000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:9782800-9783400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:9782800-9783400	Active TSS	Colonic Mucosa	Colon
36	chr4:9782800-9783400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr4:9782800-9783600	Active TSS	H9 Cell Line	embryonic stem cell
38	chr4:9782800-9783600	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:9782800-9783800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
40	chr4:9782800-9783800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
41	chr4:9782800-9783800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
42	chr4:9782800-9784000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
43	chr4:9782800-9784000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
44	chr4:9782800-9784000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
45	chr4:9783000-9783200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr4:9783000-9783400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr4:9783000-9783400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
48	chr4:9783000-9783600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr4:9783000-9783600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:9783000-9783600	Bivalent/Poised TSS	Fetal Brain Female	brain

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