Variant report

Variant	nsv877895
Chromosome Location	chr3:164046501-164126802
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr3:164065590-164065659	K562	blood:	n/a	n/a
2	CEBPB	chr3:164097994-164098357	MCF-7	breast:	n/a	n/a
3	CEBPB	chr3:164121426-164121694	K562	blood:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
4	CEBPB	chr3:164085628-164085750	K562	blood:	n/a	n/a
5	CEBPB	chr3:164077996-164078260	A549	lung:	n/a	chr3:164078134-164078145
6	CEBPB	chr3:164066095-164066166	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:164107081-164107356	A549	lung:	n/a	chr3:164107227-164107236 chr3:164107225-164107238 chr3:164107227-164107236 chr3:164107227-164107236 chr3:164107226-164107237 chr3:164107225-164107238 chr3:164107225-164107236 chr3:164107227-164107236
8	CEBPB	chr3:164093320-164093640	HepG2	liver:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
9	CEBPB	chr3:164093357-164093663	A549	lung:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
10	CEBPB	chr3:164107093-164107343	IMR90	lung:	n/a	chr3:164107227-164107236 chr3:164107225-164107238 chr3:164107227-164107236 chr3:164107227-164107236 chr3:164107226-164107237 chr3:164107225-164107238 chr3:164107225-164107236 chr3:164107227-164107236
11	CEBPB	chr3:164121454-164121666	H1-hESC	embryonic stem cell:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
12	CEBPB	chr3:164107072-164107346	HepG2	liver:	n/a	chr3:164107227-164107236 chr3:164107225-164107238 chr3:164107227-164107236 chr3:164107227-164107236 chr3:164107226-164107237 chr3:164107225-164107238 chr3:164107225-164107236 chr3:164107227-164107236
13	CEBPB	chr3:164077987-164078333	Hela-S3	cervix:	n/a	chr3:164078134-164078145
14	CEBPB	chr3:164078064-164078196	HepG2	liver:	n/a	chr3:164078134-164078145
15	CEBPB	chr3:164093370-164093659	Hela-S3	cervix:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
16	CEBPB	chr3:164121359-164121699	IMR90	lung:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
17	CEBPB	chr3:164077961-164078328	HepG2	liver:	n/a	chr3:164078134-164078145
18	CEBPB	chr3:164078081-164078324	MCF-7	breast:	n/a	chr3:164078134-164078145
19	CEBPB	chr3:164078036-164078173	H1-hESC	embryonic stem cell:	n/a	chr3:164078134-164078145
20	CEBPB	chr3:164085608-164085831	IMR90	lung:	n/a	chr3:164085753-164085766
21	CEBPB	chr3:164121369-164121693	A549	lung:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
22	CEBPB	chr3:164093408-164093523	K562	blood:	n/a	chr3:164093476-164093487
23	CEBPB	chr3:164121373-164121695	HepG2	liver:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
24	CTCF	chr3:164107980-164108130	HCFaa	heart:	n/a	n/a
25	CTCF	chr3:164050660-164050810	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr3:164118967-164119038	Pancreas_OC	pancreas:	n/a	n/a
27	CTCF	chr3:164107920-164108070	HAc	cerebellar:	n/a	n/a
28	CTCF	chr3:164111080-164111230	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr3:164108020-164108170	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr3:164093897-164094066	MCF-7	breast:	n/a	n/a
31	CTCF	chr3:164108000-164108150	GM12871	blood:	n/a	n/a
32	CTCF	chr3:164066300-164066450	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:164093920-164094070	AG09319	gingival:	n/a	n/a
34	CTCF	chr3:164111000-164111150	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:164107840-164108130	GM12866	blood:	n/a	n/a
36	CTCF	chr3:164107820-164107970	RPTEC	kidney:	n/a	n/a
37	CTCF	chr3:164050660-164050810	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr3:164108000-164108150	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr3:164094008-164094019	GM13977	blood:	n/a	n/a
40	CTCF	chr3:164108060-164108210	HRE	kidney:	n/a	n/a
41	CTCF	chr3:164111042-164111266	Medullo	brain:	n/a	n/a
42	CTCF	chr3:164108027-164108136	GM12878	blood:	n/a	n/a
43	CTCF	chr3:164111074-164111221	MCF-7	breast:	n/a	n/a
44	CTCF	chr3:164093987-164093999	GM13977	blood:	n/a	n/a
45	CTCF	chr3:164093880-164094030	RPTEC	kidney:	n/a	n/a
46	CTCF	chr3:164093932-164094044	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:164050700-164050850	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr3:164111240-164111390	RPTEC	kidney:	n/a	n/a
49	CTCF	chr3:164107340-164107490	NHEK	skin:	n/a	n/a
50	CTCF	chr3:164107980-164108130	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:164119959-164120009	ProgFib	skin:	n/a
2	chr3:164059011-164059061	SK-N-SH_RA	brain:	n/a
3	chr3:164059124-164059174	SAEC	small airway:	n/a
4	chr3:164119020-164119070	Caco-2	colon:	n/a
5	chr3:164059124-164059174	A549	lung:	n/a
6	chr3:164059124-164059174	HNPCEpiC	eye:	n/a
7	chr3:164119959-164120009	HepG2	liver:	n/a
8	chr3:164059255-164059305	NT2-D1	testis:	n/a
9	chr3:164119737-164119787	ECC-1	luminal epithelium:	n/a
10	chr3:164119737-164119787	HIPEpiC	eye:	n/a
11	chr3:164119020-164119070	HCT-116	colon:	n/a
12	chr3:164056753-164056803	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:164119737-164119787	HL-60	blood:	n/a
14	chr3:164119020-164119070	MCF10A-Er-Src	breast:	n/a
15	chr3:164059011-164059061	HPAEpiC	pulmonary alveolar:	n/a
16	chr3:164059255-164059305	ECC-1	luminal epithelium:	n/a
17	chr3:164119020-164119070	BJ	skin:	n/a
18	chr3:164059011-164059061	NHDF-neo	bronchial:	n/a
19	chr3:164056753-164056803	Hepatocyte	liver:	n/a
20	chr3:164119020-164119070	A549	lung:	n/a
21	chr3:164059011-164059061	A549	lung:	n/a
22	chr3:164119959-164120009	BJ	skin:	n/a
23	chr3:164056463-164056513	GM19239	blood:	n/a
24	chr3:164050953-164051003	HEK293	kidney:	embryo
25	chr3:164059255-164059305	NHDF-neo	bronchial:	n/a
26	chr3:164056463-164056513	K562	blood:	n/a
27	chr3:164059255-164059305	AG10803	skin:	n/a
28	chr3:164056463-164056513	HCF	heart:	n/a
29	chr3:164056463-164056513	GM12878	blood:	n/a
30	chr3:164059124-164059174	GM12892	blood:	n/a
31	chr3:164119959-164120009	HCT-116	colon:	n/a
32	chr3:164059255-164059305	Jurkat	blood:	n/a
33	chr3:164056463-164056513	H1-hESC	embryonic stem cell:	embryo
34	chr3:164050953-164051003	HNPCEpiC	eye:	n/a
35	chr3:164119959-164120009	Jurkat	blood:	n/a
36	chr3:164059011-164059061	HCF	heart:	n/a
37	chr3:164056753-164056803	HUVEC	blood vessel:	n/a
38	chr3:164119737-164119787	GM12878	blood:	n/a
39	chr3:164056463-164056513	Hepatocyte	liver:	n/a
40	chr3:164059255-164059305	BJ	skin:	n/a
41	chr3:164056463-164056513	HL-60	blood:	n/a
42	chr3:164059124-164059174	SK-N-SH	brain:	n/a
43	chr3:164059255-164059305	NHBE	bronchial:	n/a
44	chr3:164119737-164119787	MCF-7	breast:	n/a
45	chr3:164119020-164119070	IMR90	lung:	fetal
46	chr3:164119737-164119787	PANC-1	pancreas:	n/a
47	chr3:164056753-164056803	NHBE	bronchial:	n/a
48	chr3:164056753-164056803	HRCEpiC	kidney:	n/a
49	chr3:164050953-164051003	IMR90	lung:	fetal
50	chr3:164119737-164119787	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
2	chr3:164050649..164051226-chr3:164523700..164524566,2	MCF-7	breast:
3	chr3:164093244..164094225-chr3:164903325..164904113,2	MCF-7	breast:
4	chr3:164097731..164098551-chr3:164154660..164155422,4	MCF-7	breast:
5	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
6	chr3:164097647..164098715-chr3:164154502..164155534,19	MCF-7	breast:
7	chr3:164097711..164098324-chr3:164241488..164242187,2	MCF-7	breast:
8	chr3:164097711..164099012-chr3:164352332..164353250,14	MCF-7	breast:
9	chr3:164097709..164098424-chr3:164241494..164242452,3	MCF-7	breast:
10	chr3:164097647..164098678-chr3:164154502..164155534,10	MCF-7	breast:
11	chr3:164097708..164098703-chr3:164352353..164353241,9	MCF-7	breast:
12	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
13	chr3:164097659..164099012-chr3:164352282..164353331,34	MCF-7	breast:
14	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
15	chr3:164097711..164098324-chr3:164241488..164242482,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTOL1-4	chr3:164078868-164078917	XLOC_002899
2	lnc-OTOL1-4	chr3:164088402-164088464	XLOC_002899

Variant related genes	Relation type
MIR720	TF binding region
MIR720	CpG island

Extended variants
information (count: 2189 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2189 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7623391	chr3:164046501-164046502	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559986308	chr3:164046524-164046525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139642363	chr3:164046530-164046531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144390323	chr3:164046577-164046578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548627089	chr3:164046582-164046583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576809686	chr3:164046595-164046596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536660450	chr3:164046611-164046612	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550507264	chr3:164046638-164046639	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570565164	chr3:164046652-164046653	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573822449	chr3:164046715-164046716	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534774960	chr3:164046719-164046720	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539587970	chr3:164046725-164046726	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189696796	chr3:164046773-164046774	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146137586	chr3:164046778-164046779	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182669603	chr3:164046779-164046780	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577421323	chr3:164046786-164046787	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555390635	chr3:164046825-164046826	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139886451	chr3:164046831-164046832	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543458309	chr3:164046887-164046888	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557374483	chr3:164046965-164046966	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144326862	chr3:164046990-164046991	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149841075	chr3:164047014-164047015	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545930142	chr3:164047052-164047053	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376943728	chr3:164047066-164047067	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186942907	chr3:164047086-164047087	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559398118	chr3:164047099-164047100	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370586284	chr3:164047105-164047106	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192203052	chr3:164047109-164047110	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145874024	chr3:164047148-164047149	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542372003	chr3:164047196-164047197	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562249888	chr3:164047240-164047241	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73876589	chr3:164047246-164047247	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563452186	chr3:164047250-164047251	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4473557	chr3:164047251-164047252	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs2366086	chr3:164047279-164047280	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs532939897	chr3:164047293-164047294	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114375702	chr3:164047306-164047307	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566540302	chr3:164047313-164047314	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535300153	chr3:164047360-164047361	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77285745	chr3:164047362-164047363	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551133802	chr3:164047393-164047394	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568958400	chr3:164047395-164047396	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528236814	chr3:164047402-164047403	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546715725	chr3:164047404-164047405	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538183902	chr3:164047415-164047416	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2366087	chr3:164047467-164047468	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs576855821	chr3:164047471-164047472	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148817078	chr3:164047502-164047503	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs71298313	chr3:164047531-164047532	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs573246285	chr3:164047537-164047538	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Bladder cancer	21909424	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Alcoholism	21790672	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	19651600	CNVD
Autism	19287141	CNVD
Incontinentia Pigmenti	22033527	CNVD
Rett syndrome	21593744	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:164039200-164050000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:164039400-164048800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr3:164044800-164049000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:164044800-164049400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:164044800-164049400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr3:164045000-164048800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr3:164045000-164048800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr3:164045000-164050200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr3:164045200-164049000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr3:164045200-164049600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr3:164046400-164046600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr3:164046400-164046800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:164046600-164046800	Enhancers	H9 Cell Line	embryonic stem cell
14	chr3:164046800-164047400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr3:164046800-164048000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:164047400-164047600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr3:164047400-164047600	Enhancers	H9 Cell Line	embryonic stem cell
18	chr3:164047600-164049600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr3:164047600-164050400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr3:164048000-164049000	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:164048800-164050600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:164048800-164050800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr3:164048800-164051600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr3:164049000-164049800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:164049000-164051000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr3:164049000-164051600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr3:164049400-164049600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr3:164049400-164049800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr3:164049400-164051600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:164049600-164050200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr3:164049600-164050400	Enhancers	Dnd41	blood
32	chr3:164049600-164051600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr3:164049600-164051600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr3:164049600-164051600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr3:164049800-164050000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr3:164049800-164051400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:164050000-164051400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr3:164050000-164051600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr3:164050200-164050800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr3:164050200-164051000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr3:164050200-164051200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr3:164050200-164051600	Enhancers	Fetal Stomach	stomach
43	chr3:164050200-164052200	Enhancers	Fetal Intestine Small	intestine
44	chr3:164050400-164050600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr3:164050400-164050800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr3:164050400-164051400	Enhancers	H9 Cell Line	embryonic stem cell
47	chr3:164050400-164051400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr3:164050400-164051600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr3:164050400-164051600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr3:164050400-164051600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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