Variant report

Variant	nsv970110
Chromosome Location	chr6:33331311-33342922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:191)
CpG islands
(count:488)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:191 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:33332242-33332580	K562	blood:	n/a	n/a
2	ATF1	chr6:33332223-33332565	K562	blood:	n/a	n/a
3	BHLHE40	chr6:33332293-33332634	K562	blood:	n/a	n/a
4	CBX3	chr6:33332057-33332616	K562	blood:	n/a	n/a
5	CEBPB	chr6:33342861-33343412	A549	lung:	n/a	n/a
6	CEBPB	chr6:33342913-33343384	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr6:33342883-33343540	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr6:33342915-33343374	MCF-7	breast:	n/a	n/a
9	CTCF	chr6:33333120-33333270	GM12865	blood:	n/a	n/a
10	CTCF	chr6:33333120-33333270	GM12864	blood:	n/a	n/a
11	CTCF	chr6:33333100-33333250	GM12872	blood:	n/a	n/a
12	CTCF	chr6:33333120-33333270	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr6:33333120-33333270	Caco-2	colon:	n/a	n/a
14	CTCF	chr6:33333131-33333236	GM12878	blood:	n/a	n/a
15	CTCF	chr6:33333204-33333232	MCF-7	breast:	n/a	n/a
16	CTCF	chr6:33333100-33333250	GM12865	blood:	n/a	n/a
17	CTCF	chr6:33333080-33333230	GM12871	blood:	n/a	n/a
18	CTCF	chr6:33333120-33333270	NHEK	skin:	n/a	n/a
19	CTCF	chr6:33333082-33333316	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr6:33333120-33333270	RPTEC	kidney:	n/a	n/a
21	CTCF	chr6:33333080-33333230	GM12868	blood:	n/a	n/a
22	CTCF	chr6:33333160-33333310	GM12867	blood:	n/a	n/a
23	CTCF	chr6:33333120-33333270	GM12866	blood:	n/a	n/a
24	CTCF	chr6:33333140-33333290	RPTEC	kidney:	n/a	n/a
25	CTCF	chr6:33333120-33333270	GM12873	blood:	n/a	n/a
26	CTCF	chr6:33333100-33333250	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr6:33333140-33333290	GM12864	blood:	n/a	n/a
28	CTCF	chr6:33332973-33333311	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr6:33333121-33333264	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:33333183-33333242	Fibrobl	skin:	n/a	n/a
31	CTCF	chr6:33333120-33333270	HMEC	breast:	n/a	n/a
32	CTCF	chr6:33333119-33333278	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:33333161-33333247	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:33333120-33333270	GM12875	blood:	n/a	n/a
35	CTCF	chr6:33333100-33333250	HepG2	liver:	n/a	n/a
36	CTCF	chr6:33333010-33333269	K562	blood:	n/a	n/a
37	CTCF	chr6:33333078-33333300	K562	blood:	n/a	n/a
38	CTCF	chr6:33333120-33333270	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr6:33332300-33332450	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr6:33333140-33333290	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr6:33333100-33333250	GM12874	blood:	n/a	n/a
42	CTCF	chr6:33333100-33333250	SAEC	small airway:	n/a	n/a
43	CTCF	chr6:33333040-33333190	GM12870	blood:	n/a	n/a
44	CTCF	chr6:33333080-33333230	GM12872	blood:	n/a	n/a
45	CTCF	chr6:33333192-33333249	GM10266	blood:	n/a	n/a
46	CTCF	chr6:33333190-33333220	A549	lung:	n/a	n/a
47	CTCF	chr6:33333120-33333270	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr6:33333100-33333250	GM12878	blood:	n/a	n/a
49	CTCF	chr6:33333120-33333270	HRE	kidney:	n/a	n/a
50	CTCF	chr6:33333120-33333270	HEK293	kidney:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33333563-33333613	Jurkat	blood:	n/a
2	chr6:33340235-33340285	HCPEpiC	choroid plexus:	n/a
3	chr6:33333945-33333995	AG04450	lung:	fetal
4	chr6:33334602-33334652	HEK293	kidney:	embryo
5	chr6:33335436-33335486	Jurkat	blood:	n/a
6	chr6:33333563-33333613	Hela-S3	cervix:	n/a
7	chr6:33340235-33340285	IMR90	lung:	fetal
8	chr6:33334703-33334753	HEEpiC	esophagus:	n/a
9	chr6:33334602-33334652	MCF-7	breast:	n/a
10	chr6:33334703-33334753	HAEpiC	amniotic membrane:	n/a
11	chr6:33335152-33335202	Hepatocyte	liver:	n/a
12	chr6:33331358-33331408	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:33335152-33335202	PrEC	prostate:	n/a
14	chr6:33340235-33340285	ProgFib	skin:	n/a
15	chr6:33334703-33334753	SK-N-MC	brain:	n/a
16	chr6:33334602-33334652	K562	blood:	n/a
17	chr6:33331358-33331408	SK-N-SH_RA	brain:	n/a
18	chr6:33333563-33333613	SKMC	muscle:	n/a
19	chr6:33333563-33333613	AG10803	skin:	n/a
20	chr6:33331358-33331408	NHBE	bronchial:	n/a
21	chr6:33333563-33333613	AoSMC	blood vessel:	n/a
22	chr6:33331358-33331408	MCF-7	breast:	n/a
23	chr6:33333563-33333613	CMK	blood:	n/a
24	chr6:33333563-33333613	HIPEpiC	eye:	n/a
25	chr6:33333563-33333613	BE2_C	brain:	n/a
26	chr6:33331358-33331408	GM12892	blood:	n/a
27	chr6:33334602-33334652	U87	brain:	n/a
28	chr6:33334602-33334652	PANC-1	pancreas:	n/a
29	chr6:33333945-33333995	CMK	blood:	n/a
30	chr6:33333563-33333613	T-47D	breast:	n/a
31	chr6:33335152-33335202	SAEC	small airway:	n/a
32	chr6:33333563-33333613	HCF	heart:	n/a
33	chr6:33334703-33334753	LNCaP	prostate:	n/a
34	chr6:33334602-33334652	NHDF-neo	bronchial:	n/a
35	chr6:33340235-33340285	GM12878	blood:	n/a
36	chr6:33340235-33340285	AG04450	lung:	fetal
37	chr6:33334703-33334753	HMEC	breast:	n/a
38	chr6:33335152-33335202	HCM	heart:	n/a
39	chr6:33334602-33334652	SK-N-SH_RA	brain:	n/a
40	chr6:33335436-33335486	Hela-S3	cervix:	n/a
41	chr6:33335436-33335486	NB4	blood:	n/a
42	chr6:33335152-33335202	PFSK-1	brain:	n/a
43	chr6:33335436-33335486	BJ	skin:	n/a
44	chr6:33335152-33335202	MCF10A-Er-Src	breast:	n/a
45	chr6:33335152-33335202	HEK293	kidney:	embryo
46	chr6:33333563-33333613	HRE	kidney:	n/a
47	chr6:33333563-33333613	HAEpiC	amniotic membrane:	n/a
48	chr6:33340235-33340285	HUVEC	blood vessel:	n/a
49	chr6:33333945-33333995	LNCaP	prostate:	n/a
50	chr6:33331358-33331408	ECC-1	luminal epithelium:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33238517..33240709-chr6:33340722..33342916,2	MCF-7	breast:
2	chr6:33329636..33331673-chr6:34204067..34205822,2	K562	blood:
3	chr6:33285523..33287607-chr6:33332179..33334621,2	K562	blood:
4	chr6:33290417..33292020-chr6:33336190..33337751,2	K562	blood:
5	chr6:33337039..33338621-chr6:33358348..33360371,2	K562	blood:
6	chr6:33329577..33332620-chr6:33339048..33342098,3	K562	blood:
7	chr6:33324046..33327931-chr6:33328359..33332196,5	K562	blood:
8	chr6:33342917..33344696-chr6:33346321..33348520,4	K562	blood:
9	chr6:33280766..33282554-chr6:33333161..33335162,2	K562	blood:
10	chr6:33328288..33333241-chr6:33333249..33338819,6	K562	blood:
11	chr6:33286727..33289149-chr6:33332199..33333898,2	MCF-7	breast:
12	chr6:33331065..33333625-chr6:33356346..33358635,2	K562	blood:
13	chr6:33329103..33331586-chr6:33359172..33360806,2	K562	blood:
14	chr6:33243900..33246250-chr6:33334641..33337125,2	K562	blood:
15	chr6:33341840..33344393-chr6:33370227..33373059,2	K562	blood:
16	chr6:33329577..33332620-chr6:33339048..33342098,3	K562	blood:
17	chr6:33267122..33269021-chr6:33335374..33337142,2	K562	blood:

No data

Variant related genes	Relation type
LYPLA2P1	TF binding region
LYPLA2P1	CpG island
ENSG00000228285	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000223501	chromatin interactions
ENSG00000225644	chromatin interactions
ENSG00000235863	chromatin interactions
ENSG00000231925	chromatin interactions
ENSG00000236104	chromatin interactions
ENSG00000231500	chromatin interactions
ENSG00000237649	chromatin interactions
ENSG00000204209	chromatin interactions

Extended variants
information (count: 379 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114168323	chr6:33331350-33331351	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs373946281	chr6:33331359-33331360	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs77342790	chr6:33331452-33331453	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs531638810	chr6:33331493-33331494	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs189078329	chr6:33331496-33331497	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs373732672	chr6:33331509-33331510	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs556215861	chr6:33331516-33331517	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs113342171	chr6:33331612-33331613	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs544992080	chr6:33331655-33331656	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs541765200	chr6:33331671-33331672	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs563204703	chr6:33331686-33331687	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs144214305	chr6:33331733-33331734	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs111252751	chr6:33331751-33331752	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs540071308	chr6:33331782-33331783	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs561954739	chr6:33331810-33331811	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs529059034	chr6:33331816-33331817	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs9469408	chr6:33331860-33331861	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs144852990	chr6:33331862-33331863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs568967167	chr6:33331895-33331896	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs532970306	chr6:33331907-33331908	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs564042454	chr6:33331914-33331915	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551346920	chr6:33331942-33331943	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs147838796	chr6:33331943-33331944	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs76571168	chr6:33331946-33331947	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs377338040	chr6:33331998-33331999	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs200583480	chr6:33332050-33332051	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs546713791	chr6:33332051-33332052	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs555768037	chr6:33332081-33332082	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs148904568	chr6:33332096-33332097	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs568102992	chr6:33332124-33332125	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs3130275	chr6:33332137-33332138	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs556279164	chr6:33332172-33332173	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577675542	chr6:33332209-33332210	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs114965683	chr6:33332235-33332236	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs200517981	chr6:33332242-33332243	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs201818985	chr6:33332245-33332246	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs386699934	chr6:33332246-33332247	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs33954365	chr6:33332247-33332248	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs572333994	chr6:33332301-33332302	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs62768261	chr6:33332334-33332335	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs537260445	chr6:33332343-33332344	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs142616548	chr6:33332352-33332353	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs187972744	chr6:33332382-33332383	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs371171661	chr6:33332419-33332420	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs113421911	chr6:33332468-33332469	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs559139086	chr6:33332490-33332491	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs570763987	chr6:33332500-33332501	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs562577100	chr6:33332547-33332548	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs191875149	chr6:33332569-33332570	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs150995002	chr6:33332588-33332589	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
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
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
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
Acute lymphoblastic leukemia	22237106	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33322000-33332200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr6:33324400-33332600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:33324600-33340200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:33327600-33332000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr6:33327800-33332000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr6:33328200-33332200	Weak transcription	A549	lung
7	chr6:33328600-33332000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr6:33330000-33332200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:33330600-33331400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:33330600-33332200	Enhancers	K562	blood
11	chr6:33331000-33331400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:33331000-33332200	Weak transcription	Hela-S3	cervix
13	chr6:33331400-33331800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:33331400-33331800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:33331400-33332600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:33331800-33332400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:33331800-33333200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:33331800-33333600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr6:33332000-33332200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr6:33332000-33332200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr6:33332000-33332400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr6:33332000-33332600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr6:33332000-33332800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:33332000-33332800	Enhancers	Primary hematopoietic stem cells	blood
25	chr6:33332000-33333200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr6:33332000-33333200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr6:33332000-33333200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr6:33332000-33333600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr6:33332200-33332400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr6:33332200-33332400	Enhancers	Fetal Kidney	kidney
31	chr6:33332200-33332400	Enhancers	NHLF	lung
32	chr6:33332200-33332400	Enhancers	Osteobl	bone
33	chr6:33332200-33332600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr6:33332200-33332600	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr6:33332200-33332600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr6:33332200-33332600	Flanking Active TSS	K562	blood
37	chr6:33332200-33332800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr6:33332200-33332800	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr6:33332200-33332800	Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr6:33332200-33332800	Enhancers	A549	lung
41	chr6:33332200-33333000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:33332200-33333000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:33332200-33333000	Enhancers	Hela-S3	cervix
44	chr6:33332200-33333200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr6:33332400-33332600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:33332400-33332800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:33332600-33333000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:33332600-33333400	Enhancers	K562	blood
49	chr6:33332600-33333600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr6:33332800-33333000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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