Variant report

Variant	nsv517891
Chromosome Location	chr6:45899823-45915088
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	CEBPB	chr6:45909675-45909746	K562	blood:	n/a	chr6:45909704-45909715
2	CEBPB	chr6:45914739-45914939	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr6:45909550-45909824	HepG2	liver:	n/a	chr6:45909704-45909715
4	CEBPB	chr6:45909550-45909865	IMR90	lung:	n/a	chr6:45909704-45909715
5	CEBPB	chr6:45909594-45909769	Hela-S3	cervix:	n/a	chr6:45909704-45909715
6	CTCF	chr6:45914049-45914518	MCF-7	breast:	n/a	chr6:45914308-45914326 chr6:45914436-45914444 chr6:45914303-45914324
7	CTCF	chr6:45914200-45914350	BJ	skin:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
8	CTCF	chr6:45914220-45914370	SK-N-SH_RA	brain:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
9	CTCF	chr6:45914240-45914390	GM06990	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
10	CTCF	chr6:45914200-45914350	GM12878	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
11	CTCF	chr6:45914270-45914333	HUVEC	blood vessel:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
12	CTCF	chr6:45914160-45914310	MCF-7	breast:	n/a	n/a
13	CTCF	chr6:45914220-45914370	WERI-Rb-1	eye:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
14	CTCF	chr6:45914240-45914390	WERI-Rb-1	eye:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
15	CTCF	chr6:45914240-45914390	GM12874	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
16	CTCF	chr6:45914213-45914420	GM12878	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
17	CTCF	chr6:45914300-45914450	HAc	cerebellar:	n/a	chr6:45914308-45914326 chr6:45914436-45914444 chr6:45914303-45914324
18	CTCF	chr6:45914220-45914370	HCM	heart:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
19	CTCF	chr6:45914103-45914456	SK-N-SH_RA	brain:	n/a	chr6:45914308-45914326 chr6:45914436-45914444 chr6:45914303-45914324
20	CTCF	chr6:45914220-45914370	NB4	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
21	CTCF	chr6:45914120-45914493	K562	blood:	n/a	chr6:45914308-45914326 chr6:45914436-45914444 chr6:45914303-45914324
22	CTCF	chr6:45914160-45914310	GM12871	blood:	n/a	n/a
23	CTCF	chr6:45914140-45914290	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr6:45914160-45914310	WI-38	lung:	n/a	n/a
25	CTCF	chr6:45914160-45914310	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr6:45914180-45914330	GM12878	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
27	CTCF	chr6:45914248-45914385	GM13977	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
28	CTCF	chr6:45914240-45914390	GM12865	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
29	CTCF	chr6:45914235-45914436	H1-hESC	embryonic stem cell:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
30	CTCF	chr6:45914160-45914310	K562	blood:	n/a	n/a
31	CTCF	chr6:45914180-45914330	GM12866	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
32	CTCF	chr6:45914240-45914390	AG10803	skin:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
33	CTCF	chr6:45914234-45914418	GM19240	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
34	CTCF	chr6:45914240-45914390	AG04450	lung:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
35	CTCF	chr6:45914220-45914370	Hela-S3	cervix:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
36	CTCF	chr6:45914200-45914350	HBMEC	blood vessel:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
37	CTCF	chr6:45914240-45914390	K562	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
38	CTCF	chr6:45914165-45914390	HepG2	liver:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
39	CTCF	chr6:45914249-45914416	A549	lung:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
40	CTCF	chr6:45914240-45914390	HCT-116	colon:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
41	CTCF	chr6:45914249-45914420	GM19238	blood:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
42	CTCF	chr6:45914203-45914468	ProgFib	skin:	n/a	chr6:45914308-45914326 chr6:45914436-45914444 chr6:45914303-45914324
43	CTCF	chr6:45914220-45914370	HVMF	connective:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
44	CTCF	chr6:45914228-45914433	MCF-7	breast:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
45	CTCF	chr6:45914081-45914488	HepG2	liver:	n/a	chr6:45914308-45914326 chr6:45914436-45914444 chr6:45914303-45914324
46	CTCF	chr6:45914213-45914403	SK-N-SH_RA	brain:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
47	CTCF	chr6:45914720-45914870	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr6:45914320-45914470	GM12864	blood:	n/a	chr6:45914436-45914444
49	CTCF	chr6:45914200-45914350	HMF	breast:	n/a	chr6:45914308-45914326 chr6:45914303-45914324
50	CTCF	chr6:45913400-45913550	GM06990	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:45905524-45905574	ovcar-3	ovarian:	n/a
2	chr6:45905407-45905457	LNCaP	prostate:	n/a
3	chr6:45906675-45906725	HCT-116	colon:	n/a
4	chr6:45914282-45914332	NT2-D1	testis:	n/a
5	chr6:45905407-45905457	HRPEpiC	eye:	n/a
6	chr6:45905524-45905574	CMK	blood:	n/a
7	chr6:45905407-45905457	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:45905524-45905574	T-47D	breast:	n/a
9	chr6:45905524-45905574	HRCEpiC	kidney:	n/a
10	chr6:45906675-45906725	HUVEC	blood vessel:	n/a
11	chr6:45906675-45906725	HAEpiC	amniotic membrane:	n/a
12	chr6:45914282-45914332	U87	brain:	n/a
13	chr6:45901289-45901339	HRE	kidney:	n/a
14	chr6:45914282-45914332	HMEC	breast:	n/a
15	chr6:45905524-45905574	U87	brain:	n/a
16	chr6:45906675-45906725	SKMC	muscle:	n/a
17	chr6:45905524-45905574	AG09319	gingival:	n/a
18	chr6:45906675-45906725	NB4	blood:	n/a
19	chr6:45914282-45914332	PrEC	prostate:	n/a
20	chr6:45906408-45906458	PFSK-1	brain:	n/a
21	chr6:45905407-45905457	HepG2	liver:	n/a
22	chr6:45905524-45905574	HRPEpiC	eye:	n/a
23	chr6:45906675-45906725	SK-N-MC	brain:	n/a
24	chr6:45901289-45901339	HNPCEpiC	eye:	n/a
25	chr6:45914282-45914332	SK-N-SH_RA	brain:	n/a
26	chr6:45905524-45905574	K562	blood:	n/a
27	chr6:45914282-45914332	CMK	blood:	n/a
28	chr6:45914282-45914332	ovcar-3	ovarian:	n/a
29	chr6:45914282-45914332	LNCaP	prostate:	n/a
30	chr6:45906675-45906725	AG04450	lung:	fetal
31	chr6:45906408-45906458	SK-N-SH_RA	brain:	n/a
32	chr6:45906675-45906725	BJ	skin:	n/a
33	chr6:45906408-45906458	HRPEpiC	eye:	n/a
34	chr6:45905524-45905574	HMEC	breast:	n/a
35	chr6:45906675-45906725	NH-A	brain:	n/a
36	chr6:45914282-45914332	SKMC	muscle:	n/a
37	chr6:45914282-45914332	HCPEpiC	choroid plexus:	n/a
38	chr6:45906675-45906725	HRPEpiC	eye:	n/a
39	chr6:45906408-45906458	Caco-2	colon:	n/a
40	chr6:45901289-45901339	IMR90	lung:	fetal
41	chr6:45905524-45905574	GM19239	blood:	n/a
42	chr6:45901289-45901339	AG09319	gingival:	n/a
43	chr6:45905524-45905574	GM12878	blood:	n/a
44	chr6:45901289-45901339	HL-60	blood:	n/a
45	chr6:45914282-45914332	GM12878	blood:	n/a
46	chr6:45906408-45906458	NH-A	brain:	n/a
47	chr6:45901289-45901339	GM06990	blood:	n/a
48	chr6:45906675-45906725	HIPEpiC	eye:	n/a
49	chr6:45906675-45906725	RPTEC	kidney:	n/a
50	chr6:45914282-45914332	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr6:45896173..45899025-chr6:45900583..45902149,3	K562	blood:
2	chr6:45896169..45897673-chr6:45900583..45902413,2	K562	blood:
3	chr6:45903397..45906040-chr6:45911474..45913451,2	MCF-7	breast:
4	chr6:45908480..45910653-chr6:45930951..45933315,2	MCF-7	breast:
5	chr6:45898210..45898759-chr6:45913836..45914644,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ENPP5-2	chr6:45905142-45905201	NONHSAT113000
2	lnc-ENPP5-2	chr6:45901961-45902068	NONHSAT113000
3	lnc-ENPP5-2	chr6:45900431-45900535	NONHSAT113000

Variant related genes	Relation type
CLIC5	TF binding region
CLIC5	CpG island
ENSG00000112782	chromatin interactions

Extended variants
information (count: 683 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12055836	chr6:45899823-45899824	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562193755	chr6:45899978-45899979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200630660	chr6:45899983-45899984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117740142	chr6:45899984-45899985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142586300	chr6:45899996-45899997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183632868	chr6:45900021-45900022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188967327	chr6:45900034-45900035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552146782	chr6:45900035-45900036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs193236676	chr6:45900059-45900060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537795940	chr6:45900072-45900073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150957245	chr6:45900086-45900087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139828459	chr6:45900124-45900125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563659049	chr6:45900137-45900138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111988811	chr6:45900140-45900141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553468875	chr6:45900154-45900155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182629028	chr6:45900226-45900227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371723819	chr6:45900227-45900228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113854862	chr6:45900258-45900259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539058560	chr6:45900265-45900266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76027655	chr6:45900277-45900278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576672816	chr6:45900278-45900279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543802288	chr6:45900287-45900288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532453773	chr6:45900301-45900302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562293350	chr6:45900313-45900314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574313199	chr6:45900334-45900335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541510270	chr6:45900373-45900374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559895456	chr6:45900383-45900384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116195372	chr6:45900400-45900401	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35046780	chr6:45900410-45900411	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551748099	chr6:45900425-45900426	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563572195	chr6:45900495-45900496	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs531615409	chr6:45900515-45900516	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs72871469	chr6:45900530-45900531	Enhancers Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs186559286	chr6:45900531-45900532	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs535280829	chr6:45900547-45900548	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs3777567	chr6:45900566-45900567	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs565443104	chr6:45900656-45900657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191692778	chr6:45900702-45900703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs56766806	chr6:45900703-45900704	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs61564220	chr6:45900732-45900733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183824504	chr6:45900748-45900749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373744541	chr6:45900769-45900770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529892470	chr6:45900790-45900791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188498377	chr6:45900820-45900821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556116905	chr6:45900913-45900914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574250743	chr6:45900925-45900926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373696828	chr6:45901005-45901006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112337313	chr6:45901007-45901008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs578136864	chr6:45901031-45901032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375822310	chr6:45901081-45901082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:202 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45881200-45908000	Weak transcription	Duodenum Mucosa	Duodenum
2	chr6:45886800-45910600	Weak transcription	Psoas Muscle	Psoas
3	chr6:45890600-45901600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:45895400-45910800	Weak transcription	Placenta	Placenta
5	chr6:45896200-45901400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:45897800-45901400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:45898200-45901600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr6:45898200-45904400	Weak transcription	Spleen	Spleen
9	chr6:45898600-45901200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:45898600-45901400	Weak transcription	Osteobl	bone
11	chr6:45898600-45914600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr6:45898600-45916800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr6:45898800-45900400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr6:45898800-45903400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr6:45898800-45904200	Weak transcription	Colonic Mucosa	Colon
16	chr6:45898800-45911000	Weak transcription	Adipose Nuclei	Adipose
17	chr6:45898800-45919200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr6:45899000-45900600	Weak transcription	Fetal Intestine Large	intestine
19	chr6:45899000-45910600	Weak transcription	Fetal Heart	heart
20	chr6:45899200-45900200	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr6:45899200-45900200	Weak transcription	Right Ventricle	heart
22	chr6:45899200-45900200	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr6:45899200-45901400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:45899200-45901400	Weak transcription	Fetal Kidney	kidney
25	chr6:45899200-45910000	Strong transcription	Fetal Intestine Small	intestine
26	chr6:45899400-45905400	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr6:45899600-45902000	Strong transcription	Left Ventricle	heart
28	chr6:45899800-45908000	Weak transcription	Lung	lung
29	chr6:45900200-45900800	Strong transcription	Right Ventricle	heart
30	chr6:45900200-45901800	Strong transcription	Skeletal Muscle Male	skeletal muscle
31	chr6:45900200-45904800	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr6:45900400-45900600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr6:45900400-45901400	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr6:45900600-45901200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:45900600-45902000	Strong transcription	Fetal Intestine Large	intestine
36	chr6:45900800-45901200	Weak transcription	Right Ventricle	heart
37	chr6:45901200-45901800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
38	chr6:45901200-45901800	Strong transcription	Right Ventricle	heart
39	chr6:45901200-45902000	Enhancers	NH-A	brain
40	chr6:45901200-45902200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:45901200-45903200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr6:45901400-45901600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
43	chr6:45901400-45901600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
44	chr6:45901400-45902000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:45901400-45902000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
46	chr6:45901400-45902000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:45901400-45902000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:45901400-45902000	Enhancers	Osteobl	bone
49	chr6:45901400-45902200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr6:45901400-45902200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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