Variant report

Variant	nsv1014701
Chromosome Location	chr3:23257658-23416094
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:710)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:710 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:23270274-23270325	K562	blood:	n/a	n/a
2	ATF2	chr3:23367108-23367548	GM12878	blood:	n/a	n/a
3	ATF2	chr3:23259313-23259723	GM12878	blood:	n/a	n/a
4	ATF2	chr3:23259335-23259791	GM12878	blood:	n/a	n/a
5	ATF2	chr3:23367105-23367549	GM12878	blood:	n/a	n/a
6	ATF2	chr3:23382835-23383365	GM12878	blood:	n/a	n/a
7	BACH1	chr3:23299743-23299785	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr3:23367272-23367502	GM12878	blood:	n/a	n/a
9	BATF	chr3:23298327-23298695	GM12878	blood:	n/a	n/a
10	BATF	chr3:23367094-23367570	GM12878	blood:	n/a	n/a
11	BATF	chr3:23313878-23314156	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:23260741-23261087	GM12878	blood:	n/a	chr3:23260800-23260807
13	BCL11A	chr3:23367192-23367517	GM12878	blood:	n/a	n/a
14	BCL3	chr3:23367262-23367545	GM12878	blood:	n/a	n/a
15	BCLAF1	chr3:23367134-23367570	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:23270311-23270369	A549	lung:	n/a	n/a
17	BRCA1	chr3:23261437-23261514	GM12878	blood:	n/a	n/a
18	CCNT2	chr3:23330795-23330876	K562	blood:	n/a	n/a
19	CEBPB	chr3:23314983-23315065	A549	lung:	n/a	n/a
20	CEBPB	chr3:23280707-23280985	HepG2	liver:	n/a	chr3:23280843-23280854 chr3:23280807-23280818
21	CEBPB	chr3:23319866-23320309	IMR90	lung:	n/a	n/a
22	CEBPB	chr3:23320082-23320198	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:23397720-23397889	Hela-S3	cervix:	n/a	chr3:23397809-23397820
24	CEBPB	chr3:23397764-23397950	HepG2	liver:	n/a	chr3:23397809-23397820
25	CEBPB	chr3:23404653-23405172	IMR90	lung:	n/a	chr3:23404763-23404774
26	CEBPB	chr3:23313998-23314235	IMR90	lung:	n/a	chr3:23314083-23314094 chr3:23314083-23314096 chr3:23314083-23314094
27	CEBPB	chr3:23404659-23405168	HepG2	liver:	n/a	chr3:23404763-23404774
28	CEBPB	chr3:23356948-23357212	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:23404642-23405196	A549	lung:	n/a	chr3:23404763-23404774
30	CEBPB	chr3:23404746-23404806	Hela-S3	cervix:	n/a	chr3:23404763-23404774
31	CEBPB	chr3:23320068-23320261	K562	blood:	n/a	n/a
32	CEBPB	chr3:23320037-23320201	A549	lung:	n/a	n/a
33	CEBPB	chr3:23280694-23280996	Hela-S3	cervix:	n/a	chr3:23280843-23280854 chr3:23280807-23280818
34	CHD1	chr3:23366250-23366294	GM12878	blood:	n/a	n/a
35	CTCF	chr3:23412120-23412270	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr3:23413900-23414050	GM12872	blood:	n/a	n/a
37	CTCF	chr3:23412120-23412270	HMF	breast:	n/a	n/a
38	CTCF	chr3:23413980-23414130	HCM	heart:	n/a	n/a
39	CTCF	chr3:23413880-23414030	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr3:23413820-23413970	HMEC	breast:	n/a	n/a
41	CTCF	chr3:23413860-23414010	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr3:23281460-23281610	RPTEC	kidney:	n/a	n/a
43	CTCF	chr3:23412111-23412325	MCF-7	breast:	n/a	n/a
44	CTCF	chr3:23281440-23281590	AG09319	gingival:	n/a	n/a
45	CTCF	chr3:23413880-23414030	HMF	breast:	n/a	n/a
46	CTCF	chr3:23412216-23412270	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr3:23413840-23413990	AG04449	skin:	n/a	n/a
48	CTCF	chr3:23413880-23414030	HAc	cerebellar:	n/a	n/a
49	CTCF	chr3:23281380-23281530	HMF	breast:	n/a	n/a
50	CTCF	chr3:23413900-23414050	HMF	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:23313729-23313779	GM12878	blood:	n/a
2	chr3:23415040-23415090	SAEC	small airway:	n/a
3	chr3:23415040-23415090	T-47D	breast:	n/a
4	chr3:23331228-23331278	RPTEC	kidney:	n/a
5	chr3:23331228-23331278	HL-60	blood:	n/a
6	chr3:23313729-23313779	HRPEpiC	eye:	n/a
7	chr3:23415040-23415090	PANC-1	pancreas:	n/a
8	chr3:23313729-23313779	PrEC	prostate:	n/a
9	chr3:23305946-23305996	HNPCEpiC	eye:	n/a
10	chr3:23305946-23305996	SK-N-SH	brain:	n/a
11	chr3:23331228-23331278	GM06990	blood:	n/a
12	chr3:23305946-23305996	HEEpiC	esophagus:	n/a
13	chr3:23331228-23331278	HCPEpiC	choroid plexus:	n/a
14	chr3:23313729-23313779	HepG2	liver:	n/a
15	chr3:23331228-23331278	SAEC	small airway:	n/a
16	chr3:23305946-23305996	AG04449	skin:	fetal
17	chr3:23313729-23313779	K562	blood:	n/a
18	chr3:23305946-23305996	GM12891	blood:	n/a
19	chr3:23313729-23313779	LNCaP	prostate:	n/a
20	chr3:23305946-23305996	HRCEpiC	kidney:	n/a
21	chr3:23305946-23305996	HepG2	liver:	n/a
22	chr3:23305946-23305996	HUVEC	blood vessel:	n/a
23	chr3:23415040-23415090	HRPEpiC	eye:	n/a
24	chr3:23313729-23313779	GM06990	blood:	n/a
25	chr3:23305946-23305996	H1-hESC	embryonic stem cell:	embryo
26	chr3:23415040-23415090	ovcar-3	ovarian:	n/a
27	chr3:23331228-23331278	BJ	skin:	n/a
28	chr3:23415040-23415090	MCF-7	breast:	n/a
29	chr3:23331228-23331278	GM12891	blood:	n/a
30	chr3:23313729-23313779	AG09319	gingival:	n/a
31	chr3:23415040-23415090	GM12892	blood:	n/a
32	chr3:23305946-23305996	IMR90	lung:	fetal
33	chr3:23415040-23415090	MCF10A-Er-Src	breast:	n/a
34	chr3:23305946-23305996	SK-N-SH_RA	brain:	n/a
35	chr3:23331228-23331278	NB4	blood:	n/a
36	chr3:23305946-23305996	AG10803	skin:	n/a
37	chr3:23415040-23415090	HCT-116	colon:	n/a
38	chr3:23305946-23305996	HEK293	kidney:	embryo
39	chr3:23305946-23305996	PrEC	prostate:	n/a
40	chr3:23331228-23331278	MCF-7	breast:	n/a
41	chr3:23305946-23305996	HRE	kidney:	n/a
42	chr3:23305946-23305996	ProgFib	skin:	n/a
43	chr3:23305946-23305996	U87	brain:	n/a
44	chr3:23331228-23331278	K562	blood:	n/a
45	chr3:23305946-23305996	RPTEC	kidney:	n/a
46	chr3:23331228-23331278	CMK	blood:	n/a
47	chr3:23305946-23305996	Hepatocyte	liver:	n/a
48	chr3:23313729-23313779	SKMC	muscle:	n/a
49	chr3:23313729-23313779	GM19239	blood:	n/a
50	chr3:23331228-23331278	ECC-1	luminal epithelium:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:23375136..23376980-chr3:23383143..23385276,2	MCF-7	breast:
2	chr3:23245705..23247404-chr3:23258369..23260756,2	K562	blood:
3	chr3:23284952..23287695-chr3:23289326..23291059,2	K562	blood:
4	chr3:23247004..23248744-chr3:23272999..23274643,2	K562	blood:
5	chr3:23266677..23268446-chr3:23270132..23272875,2	K562	blood:
6	chr3:23333702..23336217-chr3:23346722..23349222,2	MCF-7	breast:
7	chr3:23245352..23245950-chr3:23374735..23375546,2	MCF-7	breast:
8	chr3:23370714..23373096-chr3:23375354..23377337,2	K562	blood:
9	chr3:23413992..23416641-chr3:23420982..23423774,2	MCF-7	breast:
10	chr3:23361011..23363823-chr3:23364424..23367156,3	MCF-7	breast:
11	chr3:23243052..23244840-chr3:23256645..23259135,2	K562	blood:
12	chr3:23255785..23258216-chr3:23259980..23262399,2	MCF-7	breast:
13	chr3:23398268..23400293-chr3:23402710..23405112,2	MCF-7	breast:
14	chr3:23370714..23373096-chr3:23375354..23377337,2	K562	blood:
15	chr3:23360954..23362532-chr3:23363082..23365861,2	MCF-7	breast:
16	chr3:23247857..23249626-chr3:23258764..23261200,2	MCF-7	breast:
17	chr3:23361011..23363823-chr3:23364424..23367156,3	MCF-7	breast:
18	chr3:23252644..23254931-chr3:23257139..23259977,2	MCF-7	breast:
19	chr3:23266677..23268446-chr3:23270132..23272875,2	K562	blood:
20	chr3:23240535..23243490-chr3:23256250..23257758,2	MCF-7	breast:
21	chr3:23375136..23376980-chr3:23383143..23385276,2	MCF-7	breast:
22	chr3:23255785..23258216-chr3:23259980..23262399,2	MCF-7	breast:
23	chr3:23284952..23287695-chr3:23289326..23291059,2	K562	blood:
24	chr3:23243585..23246598-chr3:23255369..23258477,4	MCF-7	breast:
25	chr3:23360954..23362532-chr3:23363082..23365861,2	MCF-7	breast:
26	chr3:23398268..23400293-chr3:23402710..23405112,2	MCF-7	breast:
27	chr3:23267196..23270682-chr3:23275861..23279079,3	MCF-7	breast:
28	chr3:23333702..23336217-chr3:23346722..23349222,2	MCF-7	breast:
29	chr3:23267196..23270682-chr3:23275861..23279079,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000206728	TF binding region
ENSG00000206728	CpG island
ENSG00000182247	chromatin interactions
ENSG00000233153	chromatin interactions

Extended variants
information (count: 6744 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:6744 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540474827	chr3:23257675-23257676	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs529531599	chr3:23257678-23257679	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs561937729	chr3:23257694-23257695	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs141121265	chr3:23257714-23257715	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs563737063	chr3:23257763-23257764	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs528989979	chr3:23257819-23257820	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs1013460	chr3:23257860-23257861	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs562217401	chr3:23257882-23257883	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs532950370	chr3:23257910-23257911	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs551041114	chr3:23257913-23257914	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs560444644	chr3:23257949-23257950	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs541114173	chr3:23257961-23257962	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs527581798	chr3:23257964-23257965	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs549231730	chr3:23257974-23257975	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs192984822	chr3:23258025-23258026	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs141795264	chr3:23258077-23258078	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs551109226	chr3:23258078-23258079	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs569215962	chr3:23258079-23258080	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs150597909	chr3:23258098-23258099	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs570033530	chr3:23258133-23258134	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185282274	chr3:23258197-23258198	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs139610505	chr3:23258212-23258213	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs188767421	chr3:23258237-23258238	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs143637754	chr3:23258269-23258270	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs113298222	chr3:23258270-23258271	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs544366768	chr3:23258276-23258277	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs73821295	chr3:23258313-23258314	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs577660797	chr3:23258339-23258340	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs192542248	chr3:23258347-23258348	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs527236374	chr3:23258349-23258350	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs559876782	chr3:23258385-23258386	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs527609263	chr3:23258394-23258395	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549317820	chr3:23258441-23258442	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561130263	chr3:23258476-23258477	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs538615364	chr3:23258525-23258526	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs367584627	chr3:23258564-23258565	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs1495135	chr3:23258571-23258572	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs549957560	chr3:23258586-23258587	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs184567073	chr3:23258593-23258594	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs11926494	chr3:23258614-23258615	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs551787066	chr3:23258631-23258632	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs566732475	chr3:23258644-23258645	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533906044	chr3:23258668-23258669	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373933102	chr3:23258684-23258685	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs555657778	chr3:23258707-23258708	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs573947697	chr3:23258771-23258772	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs202201847	chr3:23258809-23258810	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs375268809	chr3:23258829-23258830	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs373193048	chr3:23258848-23258849	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs377470506	chr3:23258850-23258851	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1556 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23245800-23262800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr3:23246000-23260800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr3:23246200-23258800	Weak transcription	HSMM	muscle
4	chr3:23246200-23259000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:23246200-23259000	Weak transcription	Colon Smooth Muscle	Colon
6	chr3:23246200-23259200	Weak transcription	NH-A	brain
7	chr3:23246200-23260600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr3:23246200-23264200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr3:23246400-23259400	Weak transcription	Osteobl	bone
10	chr3:23246400-23261200	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr3:23246400-23273400	Weak transcription	Aorta	Aorta
12	chr3:23246600-23258800	Weak transcription	Fetal Lung	lung
13	chr3:23246600-23259000	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr3:23246600-23259000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr3:23246600-23259200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr3:23246600-23259200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr3:23246600-23260000	Weak transcription	NHEK	skin
18	chr3:23246600-23260800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr3:23246600-23262400	Weak transcription	Primary hematopoietic stem cells	blood
20	chr3:23246800-23259000	Weak transcription	NHLF	lung
21	chr3:23246800-23259800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:23247400-23258400	Weak transcription	Brain Cingulate Gyrus	brain
23	chr3:23248200-23258400	Weak transcription	Brain Anterior Caudate	brain
24	chr3:23248200-23259000	Weak transcription	A549	lung
25	chr3:23248200-23260600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr3:23248800-23265800	Weak transcription	Primary T cells from cord blood	blood
27	chr3:23249000-23273400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr3:23249400-23260600	Weak transcription	HSMMtube	muscle
29	chr3:23251400-23258200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr3:23251600-23259200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr3:23251600-23260400	Weak transcription	HMEC	breast
32	chr3:23251600-23262800	Weak transcription	Adipose Nuclei	Adipose
33	chr3:23251800-23260600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr3:23251800-23260600	Weak transcription	Esophagus	oesophagus
35	chr3:23251800-23260800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr3:23252400-23258800	Weak transcription	GM12878-XiMat	blood
37	chr3:23252600-23258800	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr3:23252800-23260600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr3:23253400-23260800	Weak transcription	Primary B cells from peripheral blood	blood
40	chr3:23253600-23258400	Weak transcription	Primary B cells from cord blood	blood
41	chr3:23255600-23260600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:23257000-23259600	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr3:23257000-23263200	Enhancers	Brain Hippocampus Middle	brain
44	chr3:23257200-23259600	Enhancers	Brain Angular Gyrus	brain
45	chr3:23257400-23259600	Enhancers	Brain Substantia Nigra	brain
46	chr3:23257600-23260600	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr3:23258000-23259600	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr3:23258200-23258400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr3:23258200-23258400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr3:23258200-23259000	Enhancers	Psoas Muscle	Psoas

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