Variant report

Variant	nsv601489
Chromosome Location	chr6:31060162-31082361
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:385)
CpG islands
(count:1039)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31060873-31061356	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:31060884-31061162	K562	blood:	n/a	n/a
3	BACH1	chr6:31066438-31066679	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:31066429-31066707	K562	blood:	n/a	n/a
5	CEBPB	chr6:31074520-31074636	IMR90	lung:	n/a	chr6:31074567-31074578
6	CEBPB	chr6:31063018-31063195	H1-hESC	embryonic stem cell:	n/a	chr6:31063079-31063090 chr6:31063077-31063090 chr6:31063077-31063088
7	CEBPB	chr6:31062922-31063207	IMR90	lung:	n/a	chr6:31063079-31063090 chr6:31063077-31063090 chr6:31063077-31063088
8	CEBPB	chr6:31074557-31074582	K562	blood:	n/a	chr6:31074567-31074578
9	CEBPB	chr6:31063020-31063165	K562	blood:	n/a	chr6:31063079-31063090 chr6:31063077-31063090 chr6:31063077-31063088
10	CEBPB	chr6:31062952-31063173	HepG2	liver:	n/a	chr6:31063079-31063090 chr6:31063077-31063090 chr6:31063077-31063088
11	CEBPB	chr6:31063003-31063138	HepG2	liver:	n/a	chr6:31063079-31063090 chr6:31063077-31063090 chr6:31063077-31063088
12	CEBPB	chr6:31074451-31074709	HepG2	liver:	n/a	chr6:31074567-31074578
13	CHD2	chr6:31082207-31083041	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr6:31070182-31070458	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr6:31070200-31070350	HVMF	connective:	n/a	n/a
16	CTCF	chr6:31077128-31077161	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr6:31070263-31070396	GM13976	blood:	n/a	n/a
18	CTCF	chr6:31070215-31070453	GM12891	blood:	n/a	n/a
19	CTCF	chr6:31070260-31070410	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr6:31070259-31070262	GM13976	blood:	n/a	n/a
21	CTCF	chr6:31070300-31070450	BE2_C	brain:	n/a	n/a
22	CTCF	chr6:31070260-31070410	GM12866	blood:	n/a	n/a
23	CTCF	chr6:31070224-31070426	HepG2	liver:	n/a	n/a
24	CTCF	chr6:31070248-31070443	ProgFib	skin:	n/a	n/a
25	CTCF	chr6:31070240-31070390	GM06990	blood:	n/a	n/a
26	CTCF	chr6:31070240-31070390	AG04449	skin:	n/a	n/a
27	CTCF	chr6:31070180-31070330	RPTEC	kidney:	n/a	n/a
28	CTCF	chr6:31070260-31070410	GM12870	blood:	n/a	n/a
29	CTCF	chr6:31070220-31070456	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:31070260-31070410	GM12868	blood:	n/a	n/a
31	CTCF	chr6:31070240-31070390	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr6:31070197-31070443	GM12878	blood:	n/a	n/a
33	CTCF	chr6:31070046-31070532	K562	blood:	n/a	n/a
34	CTCF	chr6:31070248-31070426	GM19239	blood:	n/a	n/a
35	CTCF	chr6:31081620-31081770	HAc	cerebellar:	n/a	chr6:31081705-31081714
36	CTCF	chr6:31078787-31078948	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr6:31070260-31070410	AG04449	skin:	n/a	n/a
38	CTCF	chr6:31070220-31070370	BE2_C	brain:	n/a	n/a
39	CTCF	chr6:31081680-31081830	AG10803	skin:	n/a	chr6:31081705-31081714
40	CTCF	chr6:31078780-31078930	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr6:31070220-31070370	A549	lung:	n/a	n/a
42	CTCF	chr6:31070219-31070451	Fibrobl	skin:	n/a	n/a
43	CTCF	chr6:31070020-31070170	HCM	heart:	n/a	n/a
44	CTCF	chr6:31070142-31070487	K562	blood:	n/a	n/a
45	CTCF	chr6:31081640-31081790	AG09309	skin:	n/a	chr6:31081705-31081714
46	CTCF	chr6:31070300-31070450	GM12874	blood:	n/a	n/a
47	CTCF	chr6:31070260-31070410	HEK293	kidney:	n/a	n/a
48	CTCF	chr6:31070180-31070330	GM12864	blood:	n/a	n/a
49	CTCF	chr6:31070260-31070410	HCFaa	heart:	n/a	n/a
50	CTCF	chr6:31070195-31070478	Gliobla	brain:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31081617-31081667	CMK	blood:	n/a
2	chr6:31081617-31081667	GM12892	blood:	n/a
3	chr6:31081617-31081667	CMK	blood:	n/a
4	chr6:31081617-31081667	GM12892	blood:	n/a
5	chr6:31079698-31079748	PFSK-1	brain:	n/a
6	chr6:31079698-31079748	SK-N-SH	brain:	n/a
7	chr6:31080048-31080098	T-47D	breast:	n/a
8	chr6:31081617-31081667	NHBE	bronchial:	n/a
9	chr6:31079110-31079160	HRPEpiC	eye:	n/a
10	chr6:31082200-31082250	AG04450	lung:	fetal
11	chr6:31079110-31079160	BE2_C	brain:	n/a
12	chr6:31081323-31081373	NHBE	bronchial:	n/a
13	chr6:31079555-31079605	U87	brain:	n/a
14	chr6:31080048-31080098	SK-N-MC	brain:	n/a
15	chr6:31081617-31081667	NHDF-neo	bronchial:	n/a
16	chr6:31082187-31082237	ECC-1	luminal epithelium:	n/a
17	chr6:31079617-31079667	SK-N-SH_RA	brain:	n/a
18	chr6:31080529-31080579	HRCEpiC	kidney:	n/a
19	chr6:31081518-31081568	HAEpiC	amniotic membrane:	n/a
20	chr6:31079152-31079202	HL-60	blood:	n/a
21	chr6:31082200-31082250	Hepatocyte	liver:	n/a
22	chr6:31080529-31080579	ProgFib	skin:	n/a
23	chr6:31079110-31079160	HRE	kidney:	n/a
24	chr6:31082187-31082237	HMEC	breast:	n/a
25	chr6:31081905-31081955	Hepatocyte	liver:	n/a
26	chr6:31079698-31079748	AG09309	skin:	n/a
27	chr6:31072036-31072086	NHDF-neo	bronchial:	n/a
28	chr6:31079306-31079356	HRPEpiC	eye:	n/a
29	chr6:31082196-31082246	HCF	heart:	n/a
30	chr6:31081905-31081955	SKMC	muscle:	n/a
31	chr6:31079152-31079202	HMEC	breast:	n/a
32	chr6:31082200-31082250	Hela-S3	cervix:	n/a
33	chr6:31079617-31079667	HUVEC	blood vessel:	n/a
34	chr6:31079152-31079202	H1-hESC	embryonic stem cell:	embryo
35	chr6:31079617-31079667	SK-N-MC	brain:	n/a
36	chr6:31079306-31079356	SAEC	small airway:	n/a
37	chr6:31082200-31082250	ProgFib	skin:	n/a
38	chr6:31082200-31082250	RPTEC	kidney:	n/a
39	chr6:31079306-31079356	HepG2	liver:	n/a
40	chr6:31079110-31079160	NHDF-neo	bronchial:	n/a
41	chr6:31081905-31081955	GM06990	blood:	n/a
42	chr6:31079152-31079202	PFSK-1	brain:	n/a
43	chr6:31079698-31079748	CMK	blood:	n/a
44	chr6:31081323-31081373	MCF-7	breast:	n/a
45	chr6:31080048-31080098	LNCaP	prostate:	n/a
46	chr6:31079698-31079748	SAEC	small airway:	n/a
47	chr6:31081518-31081568	AG09319	gingival:	n/a
48	chr6:31081905-31081955	NHBE	bronchial:	n/a
49	chr6:31081518-31081568	SK-N-SH_RA	brain:	n/a
50	chr6:31081617-31081667	HCPEpiC	choroid plexus:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31073874..31075659-chr6:31079144..31080670,2	K562	blood:
2	chr6:31080693..31083957-chr6:31087484..31089976,3	K562	blood:
3	chr6:30780845..30782405-chr6:31060991..31063180,2	K562	blood:
4	chr6:31050562..31052756-chr6:31081245..31083912,2	MCF-7	breast:
5	chr6:30710595..30712129-chr6:31063748..31065436,2	MCF-7	breast:
6	chr6:31055515..31057079-chr6:31058653..31060271,2	K562	blood:
7	chr6:30850897..30852602-chr6:31080609..31083224,2	MCF-7	breast:
8	chr6:30688777..30690812-chr6:31058826..31061400,2	K562	blood:
9	chr6:31053892..31056272-chr6:31061858..31063779,2	K562	blood:
10	chr6:30701308..30703413-chr6:31060856..31063680,2	MCF-7	breast:
11	chr6:31060052..31062667-chr6:31078284..31080842,2	MCF-7	breast:
12	chr6:30882036..30883658-chr6:31081525..31084682,3	MCF-7	breast:
13	chr6:31075272..31076774-chr6:31094558..31097353,2	K562	blood:
14	chr6:31079457..31085209-chr6:31085850..31092700,13	MCF-7	breast:

No data

Variant related genes	Relation type
C6orf15	TF binding region
PSORS1C1	TF binding region
C6orf15	CpG island
PSORS1C1	CpG island
ENSG00000137411	chromatin interactions
ENSG00000204542	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000222895	chromatin interactions
ENSG00000196230	chromatin interactions
ENSG00000204580	chromatin interactions
ENSG00000204539	chromatin interactions

Extended variants
information (count: 1015 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1015 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2517452	chr6:31060162-31060163	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548123771	chr6:31060168-31060169	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs2535296	chr6:31060219-31060220	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs530489576	chr6:31060233-31060234	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs538812817	chr6:31060296-31060297	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188996401	chr6:31060309-31060310	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs113558311	chr6:31060320-31060321	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs3130962	chr6:31060343-31060344	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs12214039	chr6:31060362-31060363	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs377684795	chr6:31060387-31060388	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568339423	chr6:31060424-31060425	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs535386426	chr6:31060435-31060436	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs3130963	chr6:31060442-31060443	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs3130964	chr6:31060461-31060462	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs573667674	chr6:31060544-31060545	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs539911083	chr6:31060552-31060553	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs544594437	chr6:31060556-31060557	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs563181570	chr6:31060575-31060576	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs386698846	chr6:31060598-31060599	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs3130966	chr6:31060600-31060601	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs562148993	chr6:31060604-31060605	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs181696557	chr6:31060606-31060607	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs544594614	chr6:31060639-31060640	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs11755249	chr6:31060720-31060721	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs532487941	chr6:31060722-31060723	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562917298	chr6:31060728-31060729	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs530403847	chr6:31060734-31060735	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs373601392	chr6:31060749-31060750	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs551788638	chr6:31060758-31060759	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs563827680	chr6:31060772-31060773	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs368044822	chr6:31060797-31060798	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs535791295	chr6:31060852-31060853	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs528220745	chr6:31060901-31060902	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs560331279	chr6:31060937-31060938	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs186360650	chr6:31060946-31060947	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs114927745	chr6:31060953-31060954	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568168605	chr6:31060966-31060967	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs67565791	chr6:31061013-31061014	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs200469556	chr6:31061035-31061036	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs201188446	chr6:31061074-31061075	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs202101472	chr6:31061077-31061078	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs567292477	chr6:31061078-31061079	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs9281199	chr6:31061083-31061084	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs142410884	chr6:31061084-31061085	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs550913391	chr6:31061180-31061181	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs565175990	chr6:31061308-31061309	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs367666634	chr6:31061309-31061310	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs181044718	chr6:31061345-31061346	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs141593187	chr6:31061377-31061378	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs558231776	chr6:31061434-31061435	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	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
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	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
Breast cancer	21785460	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
Myelofibrosis	22110671	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
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31040600-31062400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr6:31051000-31062200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:31052000-31061000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr6:31055200-31060600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr6:31055200-31060600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:31055200-31062000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr6:31055200-31062200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr6:31055400-31060800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr6:31055400-31061000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr6:31055400-31061000	Weak transcription	Brain Hippocampus Middle	brain
11	chr6:31055400-31062400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr6:31055600-31060600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr6:31055800-31060600	Weak transcription	HUVEC	blood vessel
14	chr6:31055800-31061000	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr6:31055800-31061000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr6:31055800-31061800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr6:31058400-31061400	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr6:31058800-31060200	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr6:31058800-31062000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:31058800-31066400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:31059000-31060400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr6:31059200-31062000	Weak transcription	Stomach Mucosa	stomach
23	chr6:31059400-31060200	Enhancers	Duodenum Mucosa	Duodenum
24	chr6:31059400-31060400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr6:31059600-31060800	Weak transcription	K562	blood
26	chr6:31059800-31060400	Enhancers	A549	lung
27	chr6:31059800-31061000	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr6:31059800-31062200	Weak transcription	Gastric	stomach
29	chr6:31059800-31063000	Enhancers	HepG2	liver
30	chr6:31060000-31061600	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr6:31060000-31062000	Weak transcription	Colonic Mucosa	Colon
32	chr6:31060200-31062000	Weak transcription	Duodenum Mucosa	Duodenum
33	chr6:31060200-31062600	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr6:31060400-31060800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr6:31060400-31060800	Weak transcription	A549	lung
36	chr6:31060400-31061800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr6:31060600-31061000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:31060600-31061400	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr6:31060600-31062000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr6:31060600-31062200	Enhancers	HUVEC	blood vessel
41	chr6:31060600-31065200	Enhancers	Primary hematopoietic stem cells	blood
42	chr6:31060800-31061200	Enhancers	K562	blood
43	chr6:31060800-31061400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr6:31060800-31061400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr6:31060800-31062000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr6:31060800-31062800	Enhancers	A549	lung
47	chr6:31060800-31063200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr6:31060800-31066800	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr6:31061000-31061200	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr6:31061000-31061200	Enhancers	Brain Cingulate Gyrus	brain

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