Variant report

Variant	nsv886774
Chromosome Location	chr6:150931131-150983318
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:404)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150949256-150950060	HepG2	liver:	n/a	n/a
2	ATF2	chr6:150943923-150944597	GM12878	blood:	n/a	n/a
3	ATF2	chr6:150943968-150944604	GM12878	blood:	n/a	n/a
4	ATF2	chr6:150953746-150954406	GM12878	blood:	n/a	n/a
5	ATF2	chr6:150953738-150954355	GM12878	blood:	n/a	n/a
6	ATF2	chr6:150959858-150960397	GM12878	blood:	n/a	n/a
7	ATF2	chr6:150957790-150958485	GM12878	blood:	n/a	n/a
8	ATF2	chr6:150957789-150958421	GM12878	blood:	n/a	n/a
9	BATF	chr6:150957948-150958356	GM12878	blood:	n/a	n/a
10	BATF	chr6:150944087-150944448	GM12878	blood:	n/a	n/a
11	BATF	chr6:150933150-150933360	GM12878	blood:	n/a	n/a
12	BATF	chr6:150960980-150961295	GM12878	blood:	n/a	n/a
13	BATF	chr6:150944066-150944453	GM12878	blood:	n/a	n/a
14	BATF	chr6:150961003-150961211	GM12878	blood:	n/a	n/a
15	BATF	chr6:150957954-150958244	GM12878	blood:	n/a	n/a
16	BATF	chr6:150962069-150962311	GM12878	blood:	n/a	n/a
17	BCL11A	chr6:150957974-150958311	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:150943957-150944490	GM12878	blood:	n/a	chr6:150944264-150944273
19	BCL11A	chr6:150957878-150958315	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:150944049-150944445	GM12878	blood:	n/a	chr6:150944264-150944273
21	BCL3	chr6:150944002-150944433	GM12878	blood:	n/a	chr6:150944264-150944273
22	BCL3	chr6:150957958-150958343	GM12878	blood:	n/a	n/a
23	BCLAF1	chr6:150943922-150944627	GM12878	blood:	n/a	chr6:150944264-150944273
24	BCLAF1	chr6:150957906-150958414	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:150962390-150962913	GM12878	blood:	n/a	chr6:150962884-150962893
26	BHLHE40	chr6:150956631-150956671	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:150961641-150961772	A549	lung:	n/a	n/a
28	BHLHE40	chr6:150952740-150952944	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:150953805-150954373	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:150957956-150958420	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:150943998-150944813	GM12878	blood:	n/a	n/a
32	BRCA1	chr6:150943651-150943678	GM12878	blood:	n/a	n/a
33	CEBPB	chr6:150942791-150943053	A549	lung:	n/a	chr6:150942883-150942894 chr6:150942884-150942895
34	CEBPB	chr6:150958748-150958822	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:150949214-150949437	A549	lung:	n/a	n/a
36	CEBPB	chr6:150949145-150949541	HepG2	liver:	n/a	n/a
37	CEBPB	chr6:150952474-150952588	HepG2	liver:	n/a	chr6:150952522-150952539 chr6:150952524-150952535 chr6:150952523-150952536
38	CEBPB	chr6:150942748-150943065	K562	blood:	n/a	chr6:150942883-150942894 chr6:150942884-150942895
39	CEBPB	chr6:150942760-150943059	IMR90	lung:	n/a	chr6:150942883-150942894 chr6:150942884-150942895
40	CEBPB	chr6:150942720-150943070	HepG2	liver:	n/a	chr6:150942883-150942894 chr6:150942884-150942895
41	CEBPB	chr6:150952498-150952565	A549	lung:	n/a	chr6:150952522-150952539 chr6:150952524-150952535 chr6:150952523-150952536
42	CEBPB	chr6:150949223-150949357	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:150947101-150947303	HepG2	liver:	n/a	chr6:150947260-150947273 chr6:150947138-150947149
44	CEBPB	chr6:150957847-150958497	GM12878	blood:	n/a	n/a
45	CEBPB	chr6:150952504-150952605	K562	blood:	n/a	chr6:150952522-150952539 chr6:150952524-150952535 chr6:150952523-150952536
46	CHD1	chr6:150956610-150956903	GM12878	blood:	n/a	n/a
47	CHD1	chr6:150954878-150955069	GM12878	blood:	n/a	n/a
48	CHD1	chr6:150957964-150958668	GM12878	blood:	n/a	n/a
49	CHD2	chr6:150943942-150944657	GM12878	blood:	n/a	n/a
50	CHD2	chr6:150945589-150945605	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150953085-150953135	HNPCEpiC	eye:	n/a
2	chr6:150953085-150953135	GM12891	blood:	n/a
3	chr6:150953085-150953135	HUVEC	blood vessel:	n/a
4	chr6:150953085-150953135	Hepatocyte	liver:	n/a
5	chr6:150953085-150953135	HRPEpiC	eye:	n/a
6	chr6:150953085-150953135	SK-N-SH_RA	brain:	n/a
7	chr6:150953085-150953135	SKMC	muscle:	n/a
8	chr6:150953085-150953135	HIPEpiC	eye:	n/a
9	chr6:150953085-150953135	A549	lung:	n/a
10	chr6:150953085-150953135	NT2-D1	testis:	n/a
11	chr6:150953085-150953135	AG09319	gingival:	n/a
12	chr6:150953085-150953135	K562	blood:	n/a
13	chr6:150953085-150953135	HRE	kidney:	n/a
14	chr6:150953085-150953135	AG04450	lung:	fetal
15	chr6:150953085-150953135	LNCaP	prostate:	n/a
16	chr6:150953085-150953135	ProgFib	skin:	n/a
17	chr6:150953085-150953135	HRCEpiC	kidney:	n/a
18	chr6:150953085-150953135	RPTEC	kidney:	n/a
19	chr6:150953085-150953135	PFSK-1	brain:	n/a
20	chr6:150953085-150953135	PANC-1	pancreas:	n/a
21	chr6:150953085-150953135	NH-A	brain:	n/a
22	chr6:150953085-150953135	HL-60	blood:	n/a
23	chr6:150953085-150953135	NHDF-neo	bronchial:	n/a
24	chr6:150953085-150953135	Caco-2	colon:	n/a
25	chr6:150953085-150953135	HAEpiC	amniotic membrane:	n/a
26	chr6:150953085-150953135	Jurkat	blood:	n/a
27	chr6:150953085-150953135	GM06990	blood:	n/a
28	chr6:150953085-150953135	AoSMC	blood vessel:	n/a
29	chr6:150953085-150953135	NHBE	bronchial:	n/a
30	chr6:150953085-150953135	AG10803	skin:	n/a
31	chr6:150953085-150953135	MCF-7	breast:	n/a
32	chr6:150953085-150953135	T-47D	breast:	n/a
33	chr6:150953085-150953135	SK-N-SH	brain:	n/a
34	chr6:150953085-150953135	HPAEpiC	pulmonary alveolar:	n/a
35	chr6:150953085-150953135	HCPEpiC	choroid plexus:	n/a
36	chr6:150953085-150953135	Hela-S3	cervix:	n/a
37	chr6:150953085-150953135	HCF	heart:	n/a
38	chr6:150953085-150953135	HEEpiC	esophagus:	n/a
39	chr6:150953085-150953135	ovcar-3	ovarian:	n/a
40	chr6:150953085-150953135	U87	brain:	n/a
41	chr6:150953085-150953135	GM12892	blood:	n/a
42	chr6:150953085-150953135	AG04449	skin:	fetal
43	chr6:150953085-150953135	CMK	blood:	n/a
44	chr6:150953085-150953135	NB4	blood:	n/a
45	chr6:150953085-150953135	HCT-116	colon:	n/a
46	chr6:150953085-150953135	BJ	skin:	n/a
47	chr6:150953085-150953135	SK-N-MC	brain:	n/a
48	chr6:150953085-150953135	AG09309	skin:	n/a
49	chr6:150953085-150953135	HepG2	liver:	n/a
50	chr6:150953085-150953135	IMR90	lung:	fetal

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:150982869..150985340-chr6:150985871..150988445,2	MCF-7	breast:
2	chr6:150952990..150955187-chr6:150959095..150960724,2	MCF-7	breast:
3	chr6:150933927..150936291-chr6:150938696..150941603,2	K562	blood:
4	chr6:150975378..150977551-chr6:150979774..150981508,2	K562	blood:
5	chr6:150944124..150946424-chr6:150947908..150950533,2	MCF-7	breast:
6	chr6:150956857..150958367-chr6:150960142..150962219,2	K562	blood:
7	chr6:150954086..150955641-chr6:150957684..150959729,2	MCF-7	breast:
8	chr6:150951151..150953690-chr6:150954298..150957054,3	K562	blood:
9	chr6:150931083..150932995-chr6:150934617..150936390,2	K562	blood:
10	chr6:150951151..150953690-chr6:150954298..150957054,3	K562	blood:
11	chr6:150969221..150971594-chr6:150972938..150975653,2	K562	blood:
12	chr6:150920338..150922218-chr6:150932618..150934873,2	K562	blood:
13	chr6:150956857..150958367-chr6:150960142..150962219,2	K562	blood:
14	chr6:150960489..150962367-chr6:150966319..150968724,2	MCF-7	breast:
15	chr6:150932085..150934107-chr6:150971901..150974703,2	K562	blood:
16	chr6:150975378..150977551-chr6:150979774..150981508,2	K562	blood:
17	chr6:150952990..150955187-chr6:150959095..150960724,2	MCF-7	breast:
18	chr6:150960489..150962367-chr6:150966319..150968724,2	MCF-7	breast:
19	chr6:150966591..150968646-chr6:150981306..150983343,2	MCF-7	breast:
20	chr6:150951658..150953857-chr6:150954928..150957054,2	K562	blood:
21	chr6:150947452..150949419-chr6:150952657..150955576,2	MCF-7	breast:
22	chr6:150951658..150953857-chr6:150954928..150957054,2	K562	blood:
23	chr6:150947452..150949419-chr6:150952657..150955576,2	MCF-7	breast:
24	chr6:150933927..150936291-chr6:150938696..150941603,2	K562	blood:
25	chr6:150954086..150955641-chr6:150957684..150959729,2	MCF-7	breast:
26	chr6:150966591..150968646-chr6:150981306..150983343,2	MCF-7	breast:
27	chr6:150931083..150932995-chr6:150934617..150936390,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULBP3-2	chr6:150972957-150973161	ENSG00000226599
2	lnc-ULBP3-2	chr6:150971908-150972316	ENSG00000226599
3	lnc-IYD-2	chr6:150945813-150946095	ENSG00000224029.1
4	lnc-IYD-2	chr6:150946867-150947222	ENSG00000224029.1

No data

Variant related genes	Relation type
ENSG00000226599	TF binding region
ENSG00000224029	TF binding region
ENSG00000226599	CpG island
ENSG00000224029	CpG island
ENSG00000226599	chromatin interactions
ENSG00000224029	chromatin interactions
ENSG00000232891	chromatin interactions
ENSG00000120278	chromatin interactions

Extended variants
information (count: 1938 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1938 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1492577	chr6:150931131-150931132	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561315936	chr6:150931137-150931138	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs192319849	chr6:150931138-150931139	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs574196883	chr6:150931153-150931154	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs543070956	chr6:150931167-150931168	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs370632189	chr6:150931200-150931201	ZNF genes & repeats Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs570760795	chr6:150931246-150931247	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562958131	chr6:150931253-150931254	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531950860	chr6:150931301-150931302	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373908316	chr6:150931318-150931319	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145346173	chr6:150931320-150931321	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145221589	chr6:150931328-150931329	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528338984	chr6:150931339-150931340	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113845682	chr6:150931355-150931356	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78873122	chr6:150931436-150931437	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543711105	chr6:150931454-150931455	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184525703	chr6:150931455-150931456	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373147568	chr6:150931465-150931466	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75843927	chr6:150931496-150931497	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564018433	chr6:150931520-150931521	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371599411	chr6:150931530-150931531	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117868374	chr6:150931579-150931580	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6901976	chr6:150931666-150931667	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs368830037	chr6:150931764-150931765	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs151290840	chr6:150931767-150931768	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9478766	chr6:150931777-150931778	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs115366061	chr6:150931786-150931787	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs377583985	chr6:150931817-150931818	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574654427	chr6:150931852-150931853	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189577239	chr6:150931880-150931881	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140560848	chr6:150931919-150931920	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528184762	chr6:150931944-150931945	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548310593	chr6:150932108-150932109	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576473286	chr6:150932112-150932113	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs545300133	chr6:150932137-150932138	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs373723570	chr6:150932142-150932143	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559258234	chr6:150932151-150932152	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs192471707	chr6:150932167-150932168	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs76616591	chr6:150932200-150932201	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs561886031	chr6:150932223-150932224	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs75205528	chr6:150932277-150932278	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs184566605	chr6:150932314-150932315	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs9478767	chr6:150932346-150932347	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs373697360	chr6:150932388-150932389	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs145848679	chr6:150932443-150932444	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566023491	chr6:150932480-150932481	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535019726	chr6:150932497-150932498	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs556939322	chr6:150932527-150932528	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs62432656	chr6:150932536-150932537	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs188983235	chr6:150932538-150932539	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1126 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150922400-150941400	Weak transcription	Colonic Mucosa	Colon
2	chr6:150923000-150938600	Weak transcription	Duodenum Mucosa	Duodenum
3	chr6:150925600-150931600	Genic enhancers	Fetal Thymus	thymus
4	chr6:150928000-150937400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:150928200-150938600	Weak transcription	Fetal Intestine Small	intestine
6	chr6:150928200-150944800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr6:150928400-150938600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:150928400-150938600	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr6:150928400-150939600	Weak transcription	Brain Angular Gyrus	brain
10	chr6:150928400-150940600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr6:150928400-150952800	Weak transcription	Right Ventricle	heart
12	chr6:150928600-150933800	Weak transcription	Lung	lung
13	chr6:150928600-150933800	Weak transcription	HUVEC	blood vessel
14	chr6:150928600-150938200	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr6:150928600-150938600	Weak transcription	Brain Substantia Nigra	brain
16	chr6:150928600-150948800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr6:150928800-150933800	Weak transcription	Liver	Liver
18	chr6:150929000-150932200	Weak transcription	Ovary	ovary
19	chr6:150929000-150938600	Weak transcription	Brain Cingulate Gyrus	brain
20	chr6:150929000-150938800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:150929400-150941400	Weak transcription	Fetal Stomach	stomach
22	chr6:150930000-150931800	Weak transcription	Primary B cells from cord blood	blood
23	chr6:150930000-150934400	Genic enhancers	Primary B cells from peripheral blood	blood
24	chr6:150930400-150931200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:150930600-150931200	ZNF genes & repeats	Aorta	Aorta
26	chr6:150930600-150931200	Enhancers	Spleen	Spleen
27	chr6:150930800-150931200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:150930800-150931200	Bivalent Enhancer	Esophagus	oesophagus
29	chr6:150930800-150931200	Genic enhancers	Thymus	Thymus
30	chr6:150930800-150931600	Enhancers	Right Atrium	heart
31	chr6:150931000-150933600	Weak transcription	Left Ventricle	heart
32	chr6:150931000-150934000	Weak transcription	Gastric	stomach
33	chr6:150931000-150938600	Weak transcription	Fetal Kidney	kidney
34	chr6:150931000-150947400	Weak transcription	Placenta	Placenta
35	chr6:150931200-150931800	Weak transcription	Aorta	Aorta
36	chr6:150931200-150932400	Enhancers	Thymus	Thymus
37	chr6:150931200-150933800	Weak transcription	Spleen	Spleen
38	chr6:150931200-150938000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:150931600-150932600	Strong transcription	Fetal Thymus	thymus
40	chr6:150931600-150934600	Weak transcription	Right Atrium	heart
41	chr6:150931800-150932600	Genic enhancers	Primary B cells from cord blood	blood
42	chr6:150932200-150932400	Enhancers	Ovary	ovary
43	chr6:150932400-150933200	Weak transcription	Thymus	Thymus
44	chr6:150932600-150933400	Enhancers	Primary B cells from cord blood	blood
45	chr6:150932600-150937600	Genic enhancers	Fetal Thymus	thymus
46	chr6:150933200-150937000	Genic enhancers	Thymus	Thymus
47	chr6:150933400-150933800	Weak transcription	Primary B cells from cord blood	blood
48	chr6:150933600-150934200	Enhancers	Left Ventricle	heart
49	chr6:150933800-150934200	Enhancers	HUVEC	blood vessel
50	chr6:150933800-150934800	Strong transcription	Primary B cells from cord blood	blood

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