Variant report

Variant	esv16306
Chromosome Location	chr6:31948122-32014041
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:864)
CpG islands
(count:4154)
Chromatin interactive
region (count:11)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:32013622-32013705	K562	blood:	n/a	n/a
2	BHLHE40	chr6:31970701-31971047	HepG2	liver:	n/a	n/a
3	BHLHE40	chr6:32003438-32003784	HepG2	liver:	n/a	n/a
4	BHLHE40	chr6:32013765-32014659	K562	blood:	n/a	n/a
5	BHLHE40	chr6:32012916-32012940	K562	blood:	n/a	n/a
6	BHLHE40	chr6:31949559-31949880	HepG2	liver:	n/a	n/a
7	BHLHE40	chr6:31982297-31982618	HepG2	liver:	n/a	n/a
8	BHLHE40	chr6:32007706-32008062	HepG2	liver:	n/a	n/a
9	CBX3	chr6:31990712-31991199	K562	blood:	n/a	n/a
10	CBX3	chr6:31989920-31990157	K562	blood:	n/a	n/a
11	CBX3	chr6:31952664-31953239	K562	blood:	n/a	n/a
12	CBX3	chr6:31970603-31971015	K562	blood:	n/a	n/a
13	CBX3	chr6:32012704-32014465	K562	blood:	n/a	n/a
14	CBX3	chr6:32003387-32003757	K562	blood:	n/a	n/a
15	CBX3	chr6:32003260-32004138	K562	blood:	n/a	n/a
16	CBX3	chr6:31958022-31958441	K562	blood:	n/a	n/a
17	CBX3	chr6:31985480-31985931	K562	blood:	n/a	n/a
18	CBX3	chr6:31980155-31981063	K562	blood:	n/a	n/a
19	CBX3	chr6:31957963-31958493	K562	blood:	n/a	n/a
20	CBX3	chr6:31990799-31991208	K562	blood:	n/a	n/a
21	CBX3	chr6:31970387-31971162	K562	blood:	n/a	n/a
22	CBX3	chr6:31965417-31965721	K562	blood:	n/a	n/a
23	CBX3	chr6:31989858-31990273	K562	blood:	n/a	n/a
24	CBX3	chr6:31952793-31953135	K562	blood:	n/a	n/a
25	CBX3	chr6:31985535-31985921	K562	blood:	n/a	n/a
26	CBX3	chr6:31982302-31982628	K562	blood:	n/a	n/a
27	CEBPB	chr6:31970574-31971273	K562	blood:	n/a	n/a
28	CEBPB	chr6:31970725-31971176	K562	blood:	n/a	n/a
29	CEBPB	chr6:32003276-32004129	K562	blood:	n/a	n/a
30	CEBPB	chr6:32003420-32003920	K562	blood:	n/a	n/a
31	CEBPD	chr6:32013475-32013869	K562	blood:	n/a	n/a
32	CEBPD	chr6:31970600-31971236	K562	blood:	n/a	n/a
33	CEBPD	chr6:31972233-31972447	HepG2	liver:	n/a	n/a
34	CEBPD	chr6:31980664-31980987	K562	blood:	n/a	n/a
35	CEBPD	chr6:32003343-32003982	K562	blood:	n/a	n/a
36	CTCF	chr6:31990314-31990438	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:31960396-31960478	GM20000	blood:	n/a	n/a
38	CTCF	chr6:31989996-31990155	GM12892	blood:	n/a	n/a
39	CTCF	chr6:31989901-31990249	K562	blood:	n/a	n/a
40	CTCF	chr6:31989806-31990297	A549	lung:	n/a	n/a
41	CTCF	chr6:31979878-31980147	K562	blood:	n/a	chr6:31979916-31979925
42	CTCF	chr6:31989985-31990147	Lung_OC	lung:	n/a	n/a
43	CTCF	chr6:31996871-31996889	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:32008734-32008854	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr6:31976035-31976080	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:32012780-32012930	AG04449	skin:	n/a	n/a
47	CTCF	chr6:32012807-32012912	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr6:31990038-31990109	GM19238	blood:	n/a	n/a
49	CTCF	chr6:31985548-31985578	GM20000	blood:	n/a	n/a
50	CTCF	chr6:32007802-32007887	Hela-S3	cervix:	n/a	n/a

(count:4154 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32011633-32011683	HCF	heart:	n/a
2	chr6:31997059-31997109	NHBE	bronchial:	n/a
3	chr6:32005897-32005947	ovcar-3	ovarian:	n/a
4	chr6:31997059-31997109	HRPEpiC	eye:	n/a
5	chr6:31977506-31977556	BE2_C	brain:	n/a
6	chr6:32011687-32011737	HRCEpiC	kidney:	n/a
7	chr6:32011633-32011683	HCF	heart:	n/a
8	chr6:31997059-31997109	NHBE	bronchial:	n/a
9	chr6:32005897-32005947	ovcar-3	ovarian:	n/a
10	chr6:31997059-31997109	HRPEpiC	eye:	n/a
11	chr6:31977506-31977556	BE2_C	brain:	n/a
12	chr6:32011687-32011737	HRCEpiC	kidney:	n/a
13	chr6:31974906-31974956	ProgFib	skin:	n/a
14	chr6:31976548-31976598	NHDF-neo	bronchial:	n/a
15	chr6:31976548-31976598	BJ	skin:	n/a
16	chr6:31973180-31973230	NT2-D1	testis:	n/a
17	chr6:32011506-32011556	MCF-7	breast:	n/a
18	chr6:31976687-31976737	U87	brain:	n/a
19	chr6:31976548-31976598	CMK	blood:	n/a
20	chr6:31964315-31964365	Jurkat	blood:	n/a
21	chr6:31980046-31980096	HRCEpiC	kidney:	n/a
22	chr6:32007986-32008036	HL-60	blood:	n/a
23	chr6:31997564-31997614	SK-N-SH	brain:	n/a
24	chr6:31977599-31977649	HUVEC	blood vessel:	n/a
25	chr6:31963892-31963942	A549	lung:	n/a
26	chr6:32007986-32008036	RPTEC	kidney:	n/a
27	chr6:32011633-32011683	HPAEpiC	pulmonary alveolar:	n/a
28	chr6:31980043-31980093	PANC-1	pancreas:	n/a
29	chr6:31963912-31963962	AG09319	gingival:	n/a
30	chr6:32013845-32013895	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:31980052-31980102	NH-A	brain:	n/a
32	chr6:31963919-31963969	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:31980043-31980093	HUVEC	blood vessel:	n/a
34	chr6:31963526-31963576	AG09309	skin:	n/a
35	chr6:32013974-32014024	PrEC	prostate:	n/a
36	chr6:32013845-32013895	HL-60	blood:	n/a
37	chr6:31973180-31973230	NH-A	brain:	n/a
38	chr6:31980856-31980906	PANC-1	pancreas:	n/a
39	chr6:31980836-31980886	RPTEC	kidney:	n/a
40	chr6:31963892-31963942	AG09319	gingival:	n/a
41	chr6:32011583-32011633	SK-N-SH_RA	brain:	n/a
42	chr6:32013710-32013760	RPTEC	kidney:	n/a
43	chr6:31964315-31964365	ProgFib	skin:	n/a
44	chr6:32006074-32006124	Hela-S3	cervix:	n/a
45	chr6:31964193-31964243	NHDF-neo	bronchial:	n/a
46	chr6:32013845-32013895	PANC-1	pancreas:	n/a
47	chr6:31964754-31964804	ProgFib	skin:	n/a
48	chr6:31996931-31996981	ECC-1	luminal epithelium:	n/a
49	chr6:31964274-31964324	AG09319	gingival:	n/a
50	chr6:31976548-31976598	GM12891	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31631447..31633355-chr6:32013677..32016476,2	K562	blood:
2	chr6:31868623..31870778-chr6:31945874..31948322,2	K562	blood:
3	chr6:32013434..32015953-chr6:32095466..32097702,3	K562	blood:
4	chr6:31937794..31943427-chr6:31944150..31949640,18	K562	blood:
5	chr6:31868360..31870239-chr6:32012136..32014091,2	K562	blood:
6	chr6:31912743..31916758-chr6:31944927..31949257,3	K562	blood:
7	chr6:31938465..31944613-chr6:32012205..32018958,7	K562	blood:
8	chr6:31938465..31941001-chr6:32013795..32015947,2	K562	blood:
9	chr6:31868360..31871056-chr6:32011358..32014091,3	K562	blood:
10	chr6:31830912..31833686-chr6:32013315..32015593,2	K562	blood:
11	chr6:31938987..31942159-chr6:31944563..31949146,6	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOM3Z-2	chr6:31970797-31971298	ENSG00000233627.2
2	lnc-TNXB-6	chr6:32003534-32004035	ENSG00000229776.1
3	lnc-TNXB-6	chr6:32000490-32002082	ENSG00000229776.1
4	lnc-DOM3Z-2	chr6:31967753-31969345	ENSG00000233627.2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	STK19	hsa-miR-29c-3p	chr6:31949085-31949105
2	STK19	hsa-miR-29c-3p	chr6:31981823-31981843

Variant related genes	Relation type
TNXA	TF binding region
STK19P	TF binding region
CYP21A1P	TF binding region
C4B	TF binding region
C4B-AS1	TF binding region
CYP21A2	TF binding region
STK19	TF binding region
ENSG00000268923	TF binding region
TNXB	TF binding region
C4A-AS1	TF binding region
C4A	TF binding region
TNXA	CpG island
STK19P	CpG island
CYP21A1P	CpG island
C4B	CpG island
C4B-AS1	CpG island
CYP21A2	CpG island
STK19	CpG island
ENSG00000268923	CpG island
TNXB	CpG island
C4A-AS1	CpG island
C4A	CpG island
ENSG00000204344	chromatin interactions
ENSG00000204438	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000204435	chromatin interactions
ENSG00000213676	chromatin interactions
ENSG00000204385	chromatin interactions
ENSG00000166278	chromatin interactions
ENSG00000243649	chromatin interactions
ENSG00000204348	chromatin interactions

Extended variants
information (count: 1099 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533747654	chr6:31948131-31948132	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs182148351	chr6:31948155-31948156	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs569231522	chr6:31948201-31948202	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs376107079	chr6:31948202-31948203	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs558139309	chr6:31948217-31948218	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs369081587	chr6:31948226-31948227	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs573540461	chr6:31948255-31948256	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs373414495	chr6:31948256-31948257	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs534517982	chr6:31948260-31948261	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs151183324	chr6:31948272-31948273	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs140503088	chr6:31948275-31948276	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs267600972	chr6:31948278-31948279	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs200696149	chr6:31948311-31948312	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs28441225	chr6:31948400-31948401	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs200620398	chr6:31948422-31948423	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs70990293	chr6:31948425-31948426	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs201442394	chr6:31948433-31948434	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs371041447	chr6:31948452-31948453	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs142791776	chr6:31948473-31948474	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs41267122	chr6:31948474-31948475	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs201134143	chr6:31948502-31948503	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs561534965	chr6:31948507-31948508	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs529123063	chr6:31948524-31948525	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs550753928	chr6:31948533-31948534	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs569210209	chr6:31948542-31948543	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs533482344	chr6:31948557-31948558	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs551457703	chr6:31948635-31948636	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs566899533	chr6:31948640-31948641	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs534481779	chr6:31948659-31948660	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs556137098	chr6:31948715-31948716	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs56337326	chr6:31949352-31949353	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs112291543	chr6:31949636-31949637	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs148404715	chr6:31949688-31949689	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs56386803	chr6:31950266-31950267	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200199167	chr6:31950335-31950336	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs142556478	chr6:31950651-31950652	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs56001408	chr6:31951207-31951208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs56261921	chr6:31951367-31951368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567402938	chr6:31951502-31951503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs55954268	chr6:31951912-31951913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150969927	chr6:31952180-31952181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140897509	chr6:31952255-31952256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144856589	chr6:31952806-31952807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147934048	chr6:31952857-31952858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141809751	chr6:31952957-31952958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150064392	chr6:31952980-31952981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145187627	chr6:31953172-31953173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs56009677	chr6:31953467-31953468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs55809101	chr6:31954348-31954349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs202084040	chr6:31955186-31955187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
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
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	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
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	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
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31941000-31949600	Weak transcription	Right Ventricle	heart
2	chr6:31941000-31949800	Weak transcription	Gastric	stomach
3	chr6:31941200-31949200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr6:31941200-31949400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:31941200-31949400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:31941200-31950000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr6:31941400-31949000	Weak transcription	Colonic Mucosa	Colon
8	chr6:31941400-31949400	Weak transcription	Primary B cells from cord blood	blood
9	chr6:31941400-31949400	Weak transcription	NH-A	brain
10	chr6:31941400-31950000	Weak transcription	Fetal Kidney	kidney
11	chr6:31941600-31949200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:31941600-31949200	Weak transcription	Colon Smooth Muscle	Colon
13	chr6:31941600-31950000	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr6:31941800-31948600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr6:31941800-31950000	Weak transcription	Dnd41	blood
16	chr6:31944800-31948400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:31945400-31948400	Strong transcription	Fetal Muscle Leg	muscle
18	chr6:31945800-31948400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr6:31945800-31948400	Strong transcription	Fetal Brain Female	brain
20	chr6:31946000-31948200	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr6:31946000-31948200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr6:31946400-31948200	Strong transcription	Placenta	Placenta
23	chr6:31946400-31948400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr6:31946400-31948400	Strong transcription	Brain Germinal Matrix	brain
25	chr6:31946400-31948400	Strong transcription	Brain Hippocampus Middle	brain
26	chr6:31946400-31948400	Strong transcription	Duodenum Smooth Muscle	Duodenum
27	chr6:31946400-31948400	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr6:31946600-31948200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:31946600-31948200	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr6:31946600-31948400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:31946600-31948400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:31946600-31948400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:31946600-31948400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:31946600-31948400	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr6:31946600-31948400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:31946600-31948400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr6:31946600-31948400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr6:31946600-31948400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr6:31946600-31948400	Strong transcription	Fetal Intestine Large	intestine
40	chr6:31946600-31948400	Strong transcription	Left Ventricle	heart
41	chr6:31946600-31948400	Strong transcription	Lung	lung
42	chr6:31946600-31948400	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr6:31946600-31948600	Strong transcription	Fetal Intestine Small	intestine
44	chr6:31946600-31948600	Strong transcription	Fetal Muscle Trunk	muscle
45	chr6:31946600-31948600	Strong transcription	Fetal Stomach	stomach
46	chr6:31946800-31948200	Strong transcription	Primary B cells from peripheral blood	blood
47	chr6:31946800-31948400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:31946800-31948400	Strong transcription	Thymus	Thymus
49	chr6:31947000-31948200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:31947000-31948200	Strong transcription	Pancreas	Pancrea

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