Variant report

Variant	nsv884772
Chromosome Location	chr6:32442086-32525688
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:551)
CpG islands
(count:3051)
Chromatin interactive
region (count:20)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:32522777-32523015	HepG2	liver:	n/a	n/a
2	ATF1	chr6:32443384-32443601	K562	blood:	n/a	n/a
3	BATF	chr6:32497788-32498190	GM12878	blood:	n/a	n/a
4	BATF	chr6:32498191-32498485	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:32497757-32498420	GM12878	blood:	n/a	n/a
6	BCLAF1	chr6:32497233-32498192	GM12878	blood:	n/a	n/a
7	BCLAF1	chr6:32497559-32498097	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:32493926-32494025	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:32498065-32498253	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:32517788-32517836	K562	blood:	n/a	n/a
11	CEBPB	chr6:32504062-32504262	A549	lung:	n/a	n/a
12	CEBPB	chr6:32498063-32498112	K562	blood:	n/a	n/a
13	CEBPB	chr6:32443372-32443570	K562	blood:	n/a	n/a
14	CEBPB	chr6:32498060-32498200	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:32519464-32519577	K562	blood:	n/a	chr6:32519504-32519515
16	CEBPB	chr6:32519351-32519645	HepG2	liver:	n/a	chr6:32519504-32519515
17	CHD1	chr6:32497360-32498091	GM12878	blood:	n/a	n/a
18	CHD2	chr6:32497862-32498076	GM12878	blood:	n/a	n/a
19	CREB1	chr6:32497839-32498347	GM12878	blood:	n/a	n/a
20	CTCF	chr6:32445600-32445750	GM12872	blood:	n/a	n/a
21	CTCF	chr6:32445735-32445852	GM19239	blood:	n/a	n/a
22	CTCF	chr6:32489686-32489782	MCF-7	breast:	n/a	n/a
23	CTCF	chr6:32445680-32445830	Caco-2	colon:	n/a	n/a
24	CTCF	chr6:32521092-32521109	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr6:32525579-32525633	GM12878	blood:	n/a	n/a
26	CTCF	chr6:32443717-32443919	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:32443720-32443870	MCF-7	breast:	n/a	n/a
28	CTCF	chr6:32443734-32443938	HepG2	liver:	n/a	n/a
29	CTCF	chr6:32443760-32443910	HEK293	kidney:	n/a	n/a
30	CTCF	chr6:32443705-32443891	HepG2	liver:	n/a	n/a
31	CTCF	chr6:32445760-32445910	HCT-116	colon:	n/a	n/a
32	CTCF	chr6:32443621-32444080	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:32446454-32446561	Lung_OC	lung:	n/a	n/a
34	CTCF	chr6:32445690-32445873	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr6:32521260-32521322	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr6:32525560-32525624	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:32525555-32525603	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:32445681-32445909	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:32443756-32443875	K562	blood:	n/a	n/a
40	CTCF	chr6:32445590-32445937	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:32489506-32489582	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:32498355-32498377	GM10248	blood:	n/a	n/a
43	CTCF	chr6:32443578-32443939	HepG2	liver:	n/a	n/a
44	CTCF	chr6:32489693-32489802	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:32497760-32497910	GM12874	blood:	n/a	n/a
46	CTCF	chr6:32490644-32490657	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:32489705-32489765	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:32489501-32489503	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:32443700-32443938	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:32498279-32498368	Lung_OC	lung:	n/a	n/a

(count:3051 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32522872-32522922	Hela-S3	cervix:	n/a
2	chr6:32522872-32522922	Hela-S3	cervix:	n/a
3	chr6:32515069-32515119	HNPCEpiC	eye:	n/a
4	chr6:32522683-32522733	AG04450	lung:	fetal
5	chr6:32520620-32520670	HepG2	liver:	n/a
6	chr6:32522795-32522845	AG09319	gingival:	n/a
7	chr6:32515069-32515119	AG09309	skin:	n/a
8	chr6:32515069-32515119	GM12891	blood:	n/a
9	chr6:32515069-32515119	NB4	blood:	n/a
10	chr6:32522683-32522733	HCF	heart:	n/a
11	chr6:32489750-32489800	Jurkat	blood:	n/a
12	chr6:32451079-32451129	SK-N-MC	brain:	n/a
13	chr6:32489963-32490013	GM12878	blood:	n/a
14	chr6:32520615-32520665	IMR90	lung:	fetal
15	chr6:32522905-32522955	HCPEpiC	choroid plexus:	n/a
16	chr6:32493917-32493967	HCF	heart:	n/a
17	chr6:32490421-32490471	HNPCEpiC	eye:	n/a
18	chr6:32490421-32490471	BJ	skin:	n/a
19	chr6:32515773-32515823	HAEpiC	amniotic membrane:	n/a
20	chr6:32487314-32487364	A549	lung:	n/a
21	chr6:32489984-32490034	PrEC	prostate:	n/a
22	chr6:32486399-32486449	Hepatocyte	liver:	n/a
23	chr6:32498285-32498335	CMK	blood:	n/a
24	chr6:32489984-32490034	HCF	heart:	n/a
25	chr6:32515150-32515200	GM12891	blood:	n/a
26	chr6:32451079-32451129	PrEC	prostate:	n/a
27	chr6:32485396-32485446	A549	lung:	n/a
28	chr6:32489553-32489603	AG04450	lung:	fetal
29	chr6:32490350-32490400	AG10803	skin:	n/a
30	chr6:32449961-32450011	SK-N-MC	brain:	n/a
31	chr6:32449961-32450011	SAEC	small airway:	n/a
32	chr6:32520620-32520670	HAEpiC	amniotic membrane:	n/a
33	chr6:32489991-32490041	HNPCEpiC	eye:	n/a
34	chr6:32520615-32520665	SK-N-SH	brain:	n/a
35	chr6:32452388-32452438	NB4	blood:	n/a
36	chr6:32499368-32499418	ProgFib	skin:	n/a
37	chr6:32490421-32490471	HepG2	liver:	n/a
38	chr6:32490350-32490400	IMR90	lung:	fetal
39	chr6:32516004-32516054	GM06990	blood:	n/a
40	chr6:32489750-32489800	SK-N-SH_RA	brain:	n/a
41	chr6:32489555-32489605	CMK	blood:	n/a
42	chr6:32489801-32489851	SK-N-MC	brain:	n/a
43	chr6:32520620-32520670	HNPCEpiC	eye:	n/a
44	chr6:32451079-32451129	CMK	blood:	n/a
45	chr6:32490350-32490400	Caco-2	colon:	n/a
46	chr6:32490421-32490471	GM12891	blood:	n/a
47	chr6:32493917-32493967	RPTEC	kidney:	n/a
48	chr6:32522905-32522955	SK-N-SH_RA	brain:	n/a
49	chr6:32522683-32522733	GM12892	blood:	n/a
50	chr6:32499852-32499902	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:32383034..32383683-chr6:32443303..32444621,3	MCF-7	breast:
2	chr6:32496441..32498666-chr6:32501268..32503290,2	MCF-7	breast:
3	chr6:32521739..32522615-chr6:32530472..32531387,2	MCF-7	breast:
4	chr6:32483984..32486232-chr6:32528948..32530708,2	MCF-7	breast:
5	chr6:32492411..32495450-chr6:32552484..32555959,3	MCF-7	breast:
6	chr6:32446571..32447329-chr6:32534338..32534901,2	MCF-7	breast:
7	chr6:32428191..32430542-chr6:32458841..32460810,2	MCF-7	breast:
8	chr6:32086283..32087229-chr6:32443372..32443883,2	K562	blood:
9	chr6:32488425..32491082-chr6:32525421..32528152,2	MCF-7	breast:
10	chr6:32521673..32522686-chr6:32534361..32535388,13	MCF-7	breast:
11	chr6:32521673..32522686-chr6:32534361..32535349,9	MCF-7	breast:
12	chr6:32399459..32400332-chr6:32443390..32444188,2	MCF-7	breast:
13	chr6:32521739..32522687-chr6:32530472..32531394,3	MCF-7	breast:
14	chr6:32521669..32522700-chr6:32534356..32535262,5	MCF-7	breast:
15	chr6:32489338..32491320-chr6:32492335..32495194,2	MCF-7	breast:
16	chr6:32478863..32481240-chr6:32540968..32542884,2	K562	blood:
17	chr6:32497873..32498399-chr6:32557101..32557832,2	HCT-116	colon:
18	chr6:32400824..32401535-chr6:32443504..32444248,2	MCF-7	breast:
19	chr6:32519836..32522790-chr6:32547584..32550109,2	MCF-7	breast:
20	chr6:32489338..32491320-chr6:32492335..32495194,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-DQA1-7	chr6:32522517-32522570	NONHSAT108910
2	lnc-HLA-DRA-4	chr6:32474307-32474692	NONHSAT108908
3	lnc-HLA-DQA1-7	chr6:32487174-32487196	NONHSAT108910
4	lnc-HLA-DRA-5	chr6:32475256-32475512	NONHSAT108909
5	lnc-HLA-DQA1-7	chr6:32522471-32522593	NONHSAT108916

No data

Variant related genes	Relation type
RNU1-61P	TF binding region
HLA-DRB9	TF binding region
HLA-DRB5	TF binding region
RNU1-61P	CpG island
HLA-DRB9	CpG island
HLA-DRB5	CpG island
ENSG00000196126	chromatin interactions
ENSG00000198502	chromatin interactions
ENSG00000229391	chromatin interactions

Extended variants
information (count: 6274 )
Associated
traits (count: 132 )

Variant overlapped rSNPs/rCNVs (count:6274 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34442410	chr6:32442086-32442087	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs62404407	chr6:32442088-32442089	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs75711039	chr6:32442095-32442096	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs62404408	chr6:32442099-32442100	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs186765860	chr6:32442103-32442104	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs34452045	chr6:32442119-32442120	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs116236132	chr6:32442122-32442123	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs62404409	chr6:32442135-32442136	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs370504693	chr6:32442140-32442141	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs35661077	chr6:32442154-32442155	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs386699369	chr6:32442156-32442157	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs6901373	chr6:32442157-32442158	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
13	rs6901665	chr6:32442167-32442168	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs146622606	chr6:32442175-32442176	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs62404410	chr6:32442176-32442177	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs12197312	chr6:32442180-32442181	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs111887107	chr6:32442195-32442196	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs112642749	chr6:32442207-32442208	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs62404411	chr6:32442210-32442211	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs62404412	chr6:32442217-32442218	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs112312777	chr6:32442219-32442220	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs113459238	chr6:32442225-32442226	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs62404413	chr6:32442227-32442228	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs62404414	chr6:32442241-32442242	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs13192505	chr6:32442242-32442243	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs62404415	chr6:32442246-32442247	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs62404416	chr6:32442248-32442249	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs116450051	chr6:32442253-32442254	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs115745583	chr6:32442255-32442256	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs111728391	chr6:32442257-32442258	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs6901541	chr6:32442261-32442262	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
32	rs142876841	chr6:32442265-32442266	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs117911038	chr6:32442271-32442272	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs142156602	chr6:32442281-32442282	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs6924267	chr6:32442296-32442297	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs61550563	chr6:32442391-32442392	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs35168843	chr6:32442408-32442409	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs6901903	chr6:32442436-32442437	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs371474981	chr6:32442462-32442463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551910133	chr6:32442539-32442540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377750331	chr6:32442542-32442543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189964538	chr6:32442548-32442549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568655380	chr6:32442550-32442551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377081291	chr6:32442572-32442573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs61639069	chr6:32442573-32442574	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs182597895	chr6:32442592-32442593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201564460	chr6:32442602-32442603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113158408	chr6:32442616-32442617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111909262	chr6:32442627-32442628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150695887	chr6:32442633-32442634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:132)

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
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	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	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
Ovarian cancer	21781307	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
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
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
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	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
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
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	22522925	CNVD
Rheumatoid arthritis	22536334	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Oral cancer	21386901	CNVD

Chromatin state (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:32439600-32442200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr6:32440400-32442200	Flanking Active TSS	Primary B cells from peripheral blood	blood
3	chr6:32440800-32442200	Flanking Active TSS	GM12878-XiMat	blood
4	chr6:32441000-32442200	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr6:32441000-32442400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr6:32441200-32442200	Enhancers	Primary B cells from cord blood	blood
7	chr6:32441200-32442800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr6:32441800-32442200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr6:32441800-32442400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:32441800-32444600	Weak transcription	Duodenum Mucosa	Duodenum
11	chr6:32441800-32445400	Weak transcription	Brain Anterior Caudate	brain
12	chr6:32442200-32442400	Enhancers	GM12878-XiMat	blood
13	chr6:32442200-32442600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr6:32442200-32442800	Enhancers	Primary B cells from peripheral blood	blood
15	chr6:32442800-32443800	Weak transcription	Primary B cells from peripheral blood	blood
16	chr6:32443800-32444000	Enhancers	Primary B cells from peripheral blood	blood
17	chr6:32444600-32444800	Enhancers	Duodenum Mucosa	Duodenum
18	chr6:32444800-32445200	Active TSS	Duodenum Mucosa	Duodenum
19	chr6:32445400-32446000	ZNF genes & repeats	Brain Anterior Caudate	brain
20	chr6:32445600-32445800	Bivalent/Poised TSS	Psoas Muscle	Psoas
21	chr6:32445800-32446000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
22	chr6:32447000-32447200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:32447200-32452000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:32447800-32449800	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr6:32448200-32448400	Weak transcription	Primary B cells from peripheral blood	blood
26	chr6:32448400-32448600	Genic enhancers	Primary B cells from peripheral blood	blood
27	chr6:32448400-32448600	Enhancers	GM12878-XiMat	blood
28	chr6:32448600-32448800	Enhancers	Primary B cells from peripheral blood	blood
29	chr6:32448600-32449800	Weak transcription	GM12878-XiMat	blood
30	chr6:32448800-32449800	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr6:32448800-32450000	Weak transcription	Primary B cells from peripheral blood	blood
32	chr6:32449800-32450000	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr6:32449800-32450200	Enhancers	GM12878-XiMat	blood
34	chr6:32449800-32451000	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr6:32450000-32450200	Flanking Active TSS	Primary B cells from peripheral blood	blood
36	chr6:32450000-32450400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr6:32450000-32450600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:32450200-32450600	Active TSS	Primary B cells from peripheral blood	blood
39	chr6:32450600-32450800	Flanking Active TSS	Primary B cells from peripheral blood	blood
40	chr6:32450800-32451200	Enhancers	Primary B cells from peripheral blood	blood
41	chr6:32451200-32452200	Weak transcription	Primary B cells from peripheral blood	blood
42	chr6:32452000-32452200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr6:32452000-32452600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:32452000-32452600	Enhancers	Spleen	Spleen
45	chr6:32452200-32452600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:32452400-32452600	Enhancers	Primary B cells from peripheral blood	blood
47	chr6:32452400-32452600	Bivalent Enhancer	Esophagus	oesophagus
48	chr6:32452600-32452800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr6:32452600-32453000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr6:32453200-32453400	Enhancers	NHEK	skin

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