Variant report

Variant	nsv1009045
Chromosome Location	chr3:69821621-69875782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:569)
CpG islands
(count:245)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:69860987-69861165	K562	blood:	n/a	n/a
2	ARID3A	chr3:69826468-69827001	K562	blood:	n/a	n/a
3	ARID3A	chr3:69834193-69834202	K562	blood:	n/a	n/a
4	ARID3A	chr3:69825508-69826152	K562	blood:	n/a	n/a
5	ARID3A	chr3:69840983-69841643	K562	blood:	n/a	n/a
6	ATF1	chr3:69841030-69841536	K562	blood:	n/a	n/a
7	ATF1	chr3:69830392-69830580	K562	blood:	n/a	n/a
8	ATF3	chr3:69841027-69841389	K562	blood:	n/a	n/a
9	BHLHE40	chr3:69838433-69838667	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:69826776-69827099	K562	blood:	n/a	n/a
11	BHLHE40	chr3:69841056-69841571	K562	blood:	n/a	n/a
12	BHLHE40	chr3:69834105-69834771	K562	blood:	n/a	n/a
13	BRCA1	chr3:69841313-69841639	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr3:69840987-69841586	K562	blood:	n/a	n/a
15	CCNT2	chr3:69826784-69827113	K562	blood:	n/a	n/a
16	CCNT2	chr3:69840895-69841552	K562	blood:	n/a	n/a
17	CCNT2	chr3:69824349-69824671	K562	blood:	n/a	n/a
18	CEBPB	chr3:69840273-69840502	K562	blood:	n/a	chr3:69840406-69840417 chr3:69840405-69840416 chr3:69840405-69840418
19	CEBPB	chr3:69860843-69861340	K562	blood:	n/a	chr3:69860984-69861001
20	CEBPB	chr3:69858278-69858594	K562	blood:	n/a	n/a
21	CEBPB	chr3:69869921-69869979	K562	blood:	n/a	n/a
22	CEBPB	chr3:69858401-69858897	IMR90	lung:	n/a	n/a
23	CEBPB	chr3:69823228-69823575	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:69858495-69858828	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:69840181-69840708	K562	blood:	n/a	chr3:69840633-69840644 chr3:69840406-69840417 chr3:69840405-69840416 chr3:69840405-69840418
26	CEBPB	chr3:69851164-69851462	K562	blood:	n/a	n/a
27	CEBPB	chr3:69823263-69823562	IMR90	lung:	n/a	n/a
28	CEBPB	chr3:69840211-69840808	IMR90	lung:	n/a	chr3:69840633-69840644 chr3:69840406-69840417 chr3:69840743-69840756 chr3:69840405-69840416 chr3:69840405-69840418
29	CEBPB	chr3:69826391-69826735	K562	blood:	n/a	chr3:69826561-69826574 chr3:69826561-69826572 chr3:69826561-69826574
30	CEBPB	chr3:69858261-69858876	K562	blood:	n/a	n/a
31	CEBPB	chr3:69840186-69840768	K562	blood:	n/a	chr3:69840633-69840644 chr3:69840406-69840417 chr3:69840743-69840756 chr3:69840405-69840416 chr3:69840405-69840418
32	CEBPB	chr3:69841010-69841581	K562	blood:	n/a	n/a
33	CEBPB	chr3:69872293-69872628	MCF-7	breast:	n/a	n/a
34	CEBPB	chr3:69839536-69839580	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr3:69840239-69840777	Hela-S3	cervix:	n/a	chr3:69840633-69840644 chr3:69840406-69840417 chr3:69840743-69840756 chr3:69840405-69840416 chr3:69840405-69840418
36	CEBPB	chr3:69840237-69840594	H1-hESC	embryonic stem cell:	n/a	chr3:69840406-69840417 chr3:69840405-69840416 chr3:69840405-69840418
37	CEBPB	chr3:69836647-69836949	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr3:69840158-69840658	A549	lung:	n/a	chr3:69840633-69840644 chr3:69840406-69840417 chr3:69840405-69840416 chr3:69840405-69840418
39	CEBPB	chr3:69834225-69834563	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr3:69839412-69839770	IMR90	lung:	n/a	n/a
41	CEBPB	chr3:69823352-69823762	K562	blood:	n/a	n/a
42	CEBPB	chr3:69840089-69840848	A549	lung:	n/a	chr3:69840633-69840644 chr3:69840406-69840417 chr3:69840743-69840756 chr3:69840405-69840416 chr3:69840405-69840418
43	CEBPB	chr3:69840214-69840749	A549	lung:	n/a	chr3:69840633-69840644 chr3:69840406-69840417 chr3:69840405-69840416 chr3:69840405-69840418
44	CEBPB	chr3:69825464-69825804	K562	blood:	n/a	n/a
45	CEBPB	chr3:69829063-69829367	K562	blood:	n/a	n/a
46	CEBPB	chr3:69847725-69847800	K562	blood:	n/a	n/a
47	CEBPB	chr3:69840997-69841554	K562	blood:	n/a	n/a
48	CEBPB	chr3:69839426-69839795	A549	lung:	n/a	n/a
49	CEBPB	chr3:69856850-69857214	MCF-7	breast:	n/a	n/a
50	CEBPB	chr3:69853196-69853443	IMR90	lung:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:69822512-69822562	AG04449	skin:	fetal
2	chr3:69822512-69822562	AG04449	skin:	fetal
3	chr3:69822512-69822562	NH-A	brain:	n/a
4	chr3:69822512-69822562	GM12891	blood:	n/a
5	chr3:69824707-69824757	AG04450	lung:	fetal
6	chr3:69822512-69822562	SK-N-SH	brain:	n/a
7	chr3:69822512-69822562	BE2_C	brain:	n/a
8	chr3:69822512-69822562	HCPEpiC	choroid plexus:	n/a
9	chr3:69822512-69822562	NHDF-neo	bronchial:	n/a
10	chr3:69859618-69859668	IMR90	lung:	fetal
11	chr3:69822512-69822562	HUVEC	blood vessel:	n/a
12	chr3:69834386-69834436	AG09309	skin:	n/a
13	chr3:69859618-69859668	SAEC	small airway:	n/a
14	chr3:69834386-69834436	HCT-116	colon:	n/a
15	chr3:69834386-69834436	HCF	heart:	n/a
16	chr3:69859618-69859668	SK-N-SH	brain:	n/a
17	chr3:69859618-69859668	SK-N-SH_RA	brain:	n/a
18	chr3:69824707-69824757	HEEpiC	esophagus:	n/a
19	chr3:69822512-69822562	H1-hESC	embryonic stem cell:	embryo
20	chr3:69824707-69824757	HAEpiC	amniotic membrane:	n/a
21	chr3:69859618-69859668	AG09309	skin:	n/a
22	chr3:69824707-69824757	ovcar-3	ovarian:	n/a
23	chr3:69834386-69834436	ProgFib	skin:	n/a
24	chr3:69834386-69834436	GM06990	blood:	n/a
25	chr3:69859618-69859668	U87	brain:	n/a
26	chr3:69859618-69859668	PANC-1	pancreas:	n/a
27	chr3:69859618-69859668	ovcar-3	ovarian:	n/a
28	chr3:69824707-69824757	PFSK-1	brain:	n/a
29	chr3:69859618-69859668	NB4	blood:	n/a
30	chr3:69822512-69822562	Caco-2	colon:	n/a
31	chr3:69859618-69859668	Jurkat	blood:	n/a
32	chr3:69824707-69824757	SK-N-MC	brain:	n/a
33	chr3:69824707-69824757	K562	blood:	n/a
34	chr3:69859618-69859668	GM12891	blood:	n/a
35	chr3:69834386-69834436	GM12878	blood:	n/a
36	chr3:69859618-69859668	Caco-2	colon:	n/a
37	chr3:69824707-69824757	NHBE	bronchial:	n/a
38	chr3:69822512-69822562	PANC-1	pancreas:	n/a
39	chr3:69834386-69834436	U87	brain:	n/a
40	chr3:69834386-69834436	AG04449	skin:	fetal
41	chr3:69822512-69822562	ovcar-3	ovarian:	n/a
42	chr3:69834386-69834436	HL-60	blood:	n/a
43	chr3:69834386-69834436	NT2-D1	testis:	n/a
44	chr3:69822512-69822562	GM12892	blood:	n/a
45	chr3:69822512-69822562	ECC-1	luminal epithelium:	n/a
46	chr3:69859618-69859668	HNPCEpiC	eye:	n/a
47	chr3:69822512-69822562	SK-N-SH_RA	brain:	n/a
48	chr3:69859618-69859668	NHDF-neo	bronchial:	n/a
49	chr3:69824707-69824757	AG09309	skin:	n/a
50	chr3:69834386-69834436	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:69845234..69848226-chr3:69856309..69859149,2	K562	blood:
2	chr3:69845234..69848226-chr3:69856309..69859149,2	K562	blood:
3	chr3:69839973..69842535-chr3:69843772..69847485,3	K562	blood:
4	chr3:69824164..69825783-chr3:69833410..69835761,2	MCF-7	breast:
5	chr3:69820056..69823613-chr3:69833464..69836716,3	K562	blood:
6	chr3:69846957..69848859-chr3:69852285..69853945,2	K562	blood:
7	chr3:69839973..69842535-chr3:69843772..69847485,3	K562	blood:
8	chr3:69820056..69823613-chr3:69833464..69836716,3	K562	blood:
9	chr3:69704610..69707455-chr3:69833061..69835848,2	K562	blood:
10	chr3:69826342..69828033-chr3:69835897..69837657,2	MCF-7	breast:
11	chr3:69747459..69749389-chr3:69820708..69823563,2	K562	blood:
12	chr3:69738782..69741265-chr3:69830156..69831749,2	K562	blood:
13	chr3:69846957..69848859-chr3:69852285..69853945,2	K562	blood:
14	chr3:69851811..69854439-chr3:69855052..69858049,3	K562	blood:
15	chr3:69839973..69842535-chr3:69844514..69847485,2	K562	blood:
16	chr3:69872958..69874845-chr3:69892360..69894536,2	K562	blood:
17	chr3:69740116..69741498-chr3:69840841..69842066,6	MCF-7	breast:
18	chr3:69771834..69774322-chr3:69822965..69825784,2	K562	blood:
19	chr3:69810847..69812666-chr3:69831696..69834546,2	MCF-7	breast:
20	chr3:69785154..69786856-chr3:69826242..69828364,2	K562	blood:
21	chr3:69824164..69825783-chr3:69833410..69835761,2	MCF-7	breast:
22	chr3:69732676..69733657-chr3:69841036..69841931,2	MCF-7	breast:
23	chr3:69851811..69854439-chr3:69855052..69858049,3	K562	blood:
24	chr3:69826342..69828033-chr3:69835897..69837657,2	MCF-7	breast:
25	chr3:69739960..69740874-chr3:69840742..69841549,4	MCF-7	breast:
26	chr3:69840174..69842626-chr3:70047188..70049024,2	K562	blood:
27	chr3:69739945..69740812-chr3:69840988..69842008,3	K562	blood:
28	chr3:69839973..69842535-chr3:69844514..69847485,2	K562	blood:

No data

Variant related genes	Relation type
RN7SL418P	TF binding region
RN7SL418P	CpG island
ENSG00000240405	chromatin interactions
ENSG00000187098	chromatin interactions

Extended variants
information (count: 2028 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2028 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546767808	chr3:69821768-69821769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560447206	chr3:69821830-69821831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532681574	chr3:69821833-69821834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552425172	chr3:69821887-69821888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146621124	chr3:69821898-69821899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180919622	chr3:69821899-69821900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185799089	chr3:69821900-69821901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141447024	chr3:69821966-69821967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374756086	chr3:69822006-69822007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534028738	chr3:69822019-69822020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554026353	chr3:69822021-69822022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536511420	chr3:69822078-69822079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539749918	chr3:69822087-69822088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556453106	chr3:69822097-69822098	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs576027007	chr3:69822098-69822099	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs541454747	chr3:69822117-69822118	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs377747038	chr3:69822137-69822138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370235238	chr3:69822159-69822160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144949841	chr3:69822193-69822194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189427516	chr3:69822216-69822217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138803316	chr3:69822260-69822261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369430217	chr3:69822333-69822334	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs550470871	chr3:69822373-69822374	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs532522315	chr3:69822411-69822412	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs182340938	chr3:69822440-69822441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148941672	chr3:69822456-69822457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545387479	chr3:69822513-69822514	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs531760973	chr3:69822593-69822594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187290215	chr3:69822599-69822600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143705565	chr3:69822621-69822622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs970393	chr3:69822630-69822631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148116714	chr3:69822678-69822679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547868395	chr3:69822698-69822699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190760711	chr3:69822748-69822749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182898973	chr3:69822753-69822754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556466174	chr3:69822771-69822772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576234071	chr3:69822786-69822787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112616518	chr3:69822825-69822826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34653854	chr3:69822861-69822862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373792159	chr3:69822878-69822879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185777753	chr3:69822944-69822945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367991555	chr3:69822986-69822987	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs571978629	chr3:69823002-69823003	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs540730017	chr3:69823013-69823014	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs563829569	chr3:69823052-69823053	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs577070593	chr3:69823061-69823062	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs113369908	chr3:69823064-69823065	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs112215467	chr3:69823081-69823082	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs531929912	chr3:69823138-69823139	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs542484013	chr3:69823139-69823140	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Malignant glioma	16001072	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Mental retardation	17847001	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:993 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69814000-69823800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:69814400-69823400	Weak transcription	Brain Angular Gyrus	brain
3	chr3:69814400-69823800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr3:69814400-69834000	Weak transcription	Right Ventricle	heart
5	chr3:69814600-69824400	Enhancers	Colon Smooth Muscle	Colon
6	chr3:69816000-69823200	Weak transcription	Right Atrium	heart
7	chr3:69816000-69823400	Weak transcription	Aorta	Aorta
8	chr3:69816200-69821800	Weak transcription	K562	blood
9	chr3:69816400-69822200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:69817600-69823200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr3:69818000-69823800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr3:69818200-69823000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr3:69819000-69821800	Weak transcription	Gastric	stomach
14	chr3:69819000-69821800	Weak transcription	Left Ventricle	heart
15	chr3:69819000-69821800	Weak transcription	Ovary	ovary
16	chr3:69819000-69822000	Enhancers	HSMM	muscle
17	chr3:69819000-69823000	Enhancers	Fetal Heart	heart
18	chr3:69819400-69822400	Enhancers	HSMMtube	muscle
19	chr3:69819400-69824600	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr3:69819400-69827200	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr3:69819600-69821800	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr3:69819600-69825800	Enhancers	Rectal Smooth Muscle	rectum
23	chr3:69819800-69822400	Enhancers	NHLF	lung
24	chr3:69820000-69824600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr3:69820400-69822600	Enhancers	Psoas Muscle	Psoas
26	chr3:69820600-69823200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:69820800-69821800	Weak transcription	Adipose Nuclei	Adipose
28	chr3:69820800-69821800	Weak transcription	Fetal Lung	lung
29	chr3:69820800-69821800	Weak transcription	Small Intestine	intestine
30	chr3:69820800-69823800	Enhancers	Fetal Muscle Leg	muscle
31	chr3:69820800-69825800	Weak transcription	Osteobl	bone
32	chr3:69820800-69826000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr3:69821000-69822400	Enhancers	Duodenum Mucosa	Duodenum
34	chr3:69821000-69822400	Enhancers	Stomach Smooth Muscle	stomach
35	chr3:69821000-69823000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr3:69821000-69823000	Weak transcription	HMEC	breast
37	chr3:69821000-69825800	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr3:69821200-69823000	Weak transcription	NHEK	skin
39	chr3:69821200-69823200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr3:69821200-69823200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr3:69821200-69825600	Weak transcription	HUVEC	blood vessel
42	chr3:69821200-69834000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr3:69821400-69821800	Weak transcription	NHDF-Ad	bronchial
44	chr3:69821400-69822800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:69821400-69823400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr3:69821600-69822200	Enhancers	Brain Hippocampus Middle	brain
47	chr3:69821600-69822200	Enhancers	Fetal Kidney	kidney
48	chr3:69821800-69822000	Enhancers	Fetal Lung	lung
49	chr3:69821800-69822000	Enhancers	Small Intestine	intestine
50	chr3:69821800-69822000	Enhancers	NHDF-Ad	bronchial

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