Variant report

Variant	nsv1022577
Chromosome Location	chr6:56263674-56289698
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:259)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:56263473-56265397	HepG2	liver:	n/a	n/a
2	ATF1	chr6:56264363-56264569	K562	blood:	n/a	n/a
3	ATF2	chr6:56270988-56271507	GM12878	blood:	n/a	n/a
4	BATF	chr6:56271074-56271396	GM12878	blood:	n/a	n/a
5	BATF	chr6:56271086-56271407	GM12878	blood:	n/a	n/a
6	BCL3	chr6:56264282-56264850	A549	lung:	n/a	n/a
7	BCL3	chr6:56264124-56264740	A549	lung:	n/a	n/a
8	BHLHE40	chr6:56264159-56265149	HepG2	liver:	n/a	n/a
9	BRCA1	chr6:56264285-56264368	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:56267187-56267387	HepG2	liver:	n/a	chr6:56267277-56267288
11	CEBPB	chr6:56264434-56264730	A549	lung:	n/a	n/a
12	CEBPB	chr6:56267163-56267334	Hela-S3	cervix:	n/a	chr6:56267277-56267288
13	CEBPB	chr6:56264156-56264381	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:56264167-56264816	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:56269034-56269965	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr6:56264359-56264766	HepG2	liver:	n/a	n/a
17	CEBPD	chr6:56264464-56264823	HepG2	liver:	n/a	n/a
18	CEBPD	chr6:56264469-56264780	HepG2	liver:	n/a	n/a
19	CHD2	chr6:56264294-56264993	HepG2	liver:	n/a	n/a
20	CREB1	chr6:56264440-56264775	HepG2	liver:	n/a	n/a
21	CTCF	chr6:56282760-56282910	HEK293	kidney:	n/a	n/a
22	CTCF	chr6:56282760-56282910	A549	lung:	n/a	n/a
23	CTCF	chr6:56282540-56282690	BE2_C	brain:	n/a	n/a
24	CTCF	chr6:56282800-56282950	GM12864	blood:	n/a	n/a
25	CTCF	chr6:56263940-56264090	GM12865	blood:	n/a	n/a
26	CTCF	chr6:56264500-56264650	RPTEC	kidney:	n/a	n/a
27	CTCF	chr6:56282760-56282910	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr6:56282732-56282967	MCF-7	breast:	n/a	n/a
29	CTCF	chr6:56282780-56282930	RPTEC	kidney:	n/a	n/a
30	CTCF	chr6:56282760-56282910	Caco-2	colon:	n/a	n/a
31	CTCF	chr6:56282761-56282944	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr6:56282780-56282930	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr6:56282700-56282850	BE2_C	brain:	n/a	n/a
34	CTCF	chr6:56282774-56282941	GM12878	blood:	n/a	n/a
35	CTCF	chr6:56283000-56283150	GM06990	blood:	n/a	n/a
36	CTCF	chr6:56282732-56282950	GM12878	blood:	n/a	n/a
37	CTCF	chr6:56282700-56282850	GM12871	blood:	n/a	n/a
38	CTCF	chr6:56282745-56282946	HepG2	liver:	n/a	n/a
39	CTCF	chr6:56282740-56282890	GM12878	blood:	n/a	n/a
40	CTCF	chr6:56282800-56282950	GM12873	blood:	n/a	n/a
41	CTCF	chr6:56282700-56282850	GM12865	blood:	n/a	n/a
42	CTCF	chr6:56282836-56282896	K562	blood:	n/a	n/a
43	CTCF	chr6:56282700-56282850	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:56282840-56282990	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr6:56282680-56282830	GM12872	blood:	n/a	n/a
46	CTCF	chr6:56264620-56264770	RPTEC	kidney:	n/a	n/a
47	CTCF	chr6:56282740-56282890	HRE	kidney:	n/a	n/a
48	CTCF	chr6:56264580-56264730	HRE	kidney:	n/a	n/a
49	CTCF	chr6:56282772-56282938	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:56283000-56283150	GM12864	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:56269391-56269441	HRCEpiC	kidney:	n/a
2	chr6:56269391-56269441	LNCaP	prostate:	n/a
3	chr6:56269391-56269441	HRPEpiC	eye:	n/a
4	chr6:56269391-56269441	AG04449	skin:	fetal
5	chr6:56269391-56269441	HMEC	breast:	n/a
6	chr6:56269391-56269441	PFSK-1	brain:	n/a
7	chr6:56269391-56269441	GM06990	blood:	n/a
8	chr6:56269391-56269441	PANC-1	pancreas:	n/a
9	chr6:56269391-56269441	Jurkat	blood:	n/a
10	chr6:56269391-56269441	HNPCEpiC	eye:	n/a
11	chr6:56269391-56269441	NH-A	brain:	n/a
12	chr6:56269391-56269441	HCF	heart:	n/a
13	chr6:56269391-56269441	BE2_C	brain:	n/a
14	chr6:56269391-56269441	ovcar-3	ovarian:	n/a
15	chr6:56269391-56269441	ECC-1	luminal epithelium:	n/a
16	chr6:56269391-56269441	AG10803	skin:	n/a
17	chr6:56269391-56269441	GM12878	blood:	n/a
18	chr6:56269391-56269441	HepG2	liver:	n/a
19	chr6:56269391-56269441	HCM	heart:	n/a
20	chr6:56269391-56269441	ProgFib	skin:	n/a
21	chr6:56269391-56269441	NT2-D1	testis:	n/a
22	chr6:56269391-56269441	GM12891	blood:	n/a
23	chr6:56269391-56269441	HAEpiC	amniotic membrane:	n/a
24	chr6:56269391-56269441	NB4	blood:	n/a
25	chr6:56269391-56269441	MCF-7	breast:	n/a
26	chr6:56269391-56269441	SK-N-SH_RA	brain:	n/a
27	chr6:56269391-56269441	HCPEpiC	choroid plexus:	n/a
28	chr6:56269391-56269441	SK-N-SH	brain:	n/a
29	chr6:56269391-56269441	H1-hESC	embryonic stem cell:	embryo
30	chr6:56269391-56269441	Hela-S3	cervix:	n/a
31	chr6:56269391-56269441	HL-60	blood:	n/a
32	chr6:56269391-56269441	HIPEpiC	eye:	n/a
33	chr6:56269391-56269441	MCF10A-Er-Src	breast:	n/a
34	chr6:56269391-56269441	HRE	kidney:	n/a
35	chr6:56269391-56269441	SAEC	small airway:	n/a
36	chr6:56269391-56269441	Hepatocyte	liver:	n/a
37	chr6:56269391-56269441	U87	brain:	n/a
38	chr6:56269391-56269441	GM12892	blood:	n/a
39	chr6:56269391-56269441	CMK	blood:	n/a
40	chr6:56269391-56269441	AG09309	skin:	n/a
41	chr6:56269391-56269441	Caco-2	colon:	n/a
42	chr6:56269391-56269441	HEEpiC	esophagus:	n/a
43	chr6:56269391-56269441	GM19239	blood:	n/a
44	chr6:56269391-56269441	HUVEC	blood vessel:	n/a
45	chr6:56269391-56269441	NHDF-neo	bronchial:	n/a
46	chr6:56269391-56269441	HEK293	kidney:	embryo
47	chr6:56269391-56269441	K562	blood:	n/a
48	chr6:56269391-56269441	AG04450	lung:	fetal
49	chr6:56269391-56269441	T-47D	breast:	n/a
50	chr6:56269391-56269441	HCT-116	colon:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:56272573..56275309-chr6:56286381..56288171,2	K562	blood:
2	chr6:56282151..56283969-chr6:56288478..56291005,2	MCF-7	breast:
3	chr6:56252272..56255163-chr6:56263455..56266276,3	MCF-7	breast:
4	chr6:56263868..56266502-chr6:56269861..56271738,2	MCF-7	breast:
5	chr6:56272573..56275309-chr6:56286381..56288171,2	K562	blood:
6	chr6:56281288..56284077-chr6:56298863..56300687,2	MCF-7	breast:
7	chr6:56267636..56269580-chr6:56284501..56287415,2	K562	blood:
8	chr6:56234561..56235796-chr6:56282457..56283322,3	MCF-7	breast:
9	chr6:56233543..56236471-chr6:56278322..56281271,2	MCF-7	breast:
10	chr6:56234569..56235702-chr6:56282589..56283337,3	MCF-7	breast:
11	chr6:56282151..56283969-chr6:56288478..56291005,2	MCF-7	breast:
12	chr6:56268256..56270109-chr6:56270332..56272934,2	MCF-7	breast:
13	chr6:56268256..56270109-chr6:56270332..56272934,2	MCF-7	breast:
14	chr6:56263704..56266113-chr6:56287391..56289066,2	MCF-7	breast:
15	chr6:56263868..56266502-chr6:56269861..56271738,2	MCF-7	breast:
16	chr6:56263704..56266113-chr6:56287391..56289066,2	MCF-7	breast:
17	chr6:56288567..56292393-chr6:56296577..56299834,5	MCF-7	breast:
18	chr6:56258236..56262021-chr6:56262029..56264794,4	MCF-7	breast:
19	chr6:56235077..56236646-chr6:56284091..56285833,2	MCF-7	breast:
20	chr6:56267636..56269580-chr6:56284501..56287415,2	K562	blood:

No data

Variant related genes	Relation type
COL21A1	TF binding region
COL21A1	CpG island
ENSG00000220666	chromatin interactions
ENSG00000266793	chromatin interactions
ENSG00000124749	chromatin interactions

Extended variants
information (count: 784 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:784 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571859936	chr6:56263706-56263707	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs147646391	chr6:56263713-56263714	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554540953	chr6:56263731-56263732	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs540477481	chr6:56263793-56263794	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs566456539	chr6:56263852-56263853	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs201120766	chr6:56263883-56263884	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs113965839	chr6:56263885-56263886	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs646884	chr6:56263915-56263916	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs12214233	chr6:56263918-56263919	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs573664676	chr6:56263929-56263930	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544347312	chr6:56263987-56263988	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556082237	chr6:56263991-56263992	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182737456	chr6:56264011-56264012	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs544886550	chr6:56264073-56264074	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113354091	chr6:56264085-56264086	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113263129	chr6:56264105-56264106	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs66585274	chr6:56264106-56264107	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs527415061	chr6:56264107-56264108	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs3031083	chr6:56264127-56264128	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs57470018	chr6:56264129-56264130	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs572077927	chr6:56264208-56264209	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542625146	chr6:56264222-56264223	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs568959263	chr6:56264267-56264268	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561389904	chr6:56264275-56264276	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140572203	chr6:56264308-56264309	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550294092	chr6:56264327-56264328	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192719501	chr6:56264342-56264343	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs184709674	chr6:56264363-56264364	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144445791	chr6:56264377-56264378	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571189055	chr6:56264415-56264416	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548082775	chr6:56264430-56264431	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs2179519	chr6:56264435-56264436	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs533730058	chr6:56264448-56264449	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548704852	chr6:56264455-56264456	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs567300757	chr6:56264508-56264509	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs552737012	chr6:56264532-56264533	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs376984853	chr6:56264535-56264536	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537534623	chr6:56264536-56264537	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556257490	chr6:56264600-56264601	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575438734	chr6:56264613-56264614	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs553626890	chr6:56264620-56264621	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs116797495	chr6:56264623-56264624	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566864434	chr6:56264651-56264652	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs643246	chr6:56264727-56264728	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs149177947	chr6:56264730-56264731	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs71549709	chr6:56264804-56264805	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs542563535	chr6:56264839-56264840	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs561118558	chr6:56264856-56264857	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs576419884	chr6:56264877-56264878	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs375246371	chr6:56264890-56264891	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	22522925	CNVD
Central neurocytomas	17123091	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56253000-56282600	Weak transcription	Aorta	Aorta
2	chr6:56259200-56264800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:56261800-56265600	Enhancers	Fetal Intestine Large	intestine
4	chr6:56263400-56264000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:56263400-56264200	Enhancers	Duodenum Mucosa	Duodenum
6	chr6:56263400-56265000	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr6:56263400-56265200	Enhancers	Hela-S3	cervix
8	chr6:56263400-56265600	Enhancers	Fetal Intestine Small	intestine
9	chr6:56263600-56264000	Flanking Active TSS	A549	lung
10	chr6:56263600-56264200	Flanking Active TSS	Liver	Liver
11	chr6:56263600-56264400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr6:56263600-56264400	Enhancers	Small Intestine	intestine
13	chr6:56263600-56264400	Flanking Active TSS	HepG2	liver
14	chr6:56263600-56264600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr6:56263600-56265200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr6:56263800-56264200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr6:56263800-56264200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr6:56263800-56264200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr6:56263800-56264400	Enhancers	Fetal Kidney	kidney
20	chr6:56263800-56265200	Enhancers	Stomach Mucosa	stomach
21	chr6:56263800-56265400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr6:56264000-56264200	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr6:56264000-56265000	Active TSS	A549	lung
24	chr6:56264200-56264400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:56264200-56264400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr6:56264200-56264800	Enhancers	Liver	Liver
27	chr6:56264200-56264800	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr6:56264200-56265200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr6:56264200-56265400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr6:56264200-56265400	Enhancers	Pancreas	Pancrea
31	chr6:56264200-56265800	Active TSS	Duodenum Mucosa	Duodenum
32	chr6:56264400-56264800	Active TSS	HepG2	liver
33	chr6:56264400-56265200	Weak transcription	Fetal Kidney	kidney
34	chr6:56264400-56268600	Weak transcription	Small Intestine	intestine
35	chr6:56264600-56265200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr6:56264600-56265600	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr6:56264800-56265200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr6:56264800-56265200	Flanking Active TSS	Liver	Liver
39	chr6:56264800-56265200	Enhancers	Lung	lung
40	chr6:56264800-56265200	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr6:56264800-56265400	Enhancers	Gastric	stomach
42	chr6:56264800-56265800	Flanking Active TSS	HepG2	liver
43	chr6:56265000-56265200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr6:56265000-56265200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr6:56265000-56265400	Flanking Active TSS	A549	lung
46	chr6:56265200-56265400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr6:56265200-56265400	Active TSS	Liver	Liver
48	chr6:56265200-56265400	Enhancers	Fetal Kidney	kidney
49	chr6:56265200-56265600	Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr6:56265200-56268600	Weak transcription	Hela-S3	cervix

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