Variant report

Variant	nsv970676
Chromosome Location	chr6:30966672-30987268
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:30979120-30979201	HepG2	liver:	n/a	n/a
2	ATF2	chr6:30972016-30972489	GM12878	blood:	n/a	n/a
3	ATF2	chr6:30972005-30972491	GM12878	blood:	n/a	n/a
4	ATF2	chr6:30973365-30973754	GM12878	blood:	n/a	n/a
5	BATF	chr6:30972019-30972487	GM12878	blood:	n/a	n/a
6	BATF	chr6:30973281-30973770	GM12878	blood:	n/a	n/a
7	BCL3	chr6:30973432-30973825	GM12878	blood:	n/a	n/a
8	BCL3	chr6:30972024-30972512	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:30973591-30973592	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:30979042-30979231	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:30976628-30976872	IMR90	lung:	n/a	chr6:30976725-30976736
12	CEBPB	chr6:30976650-30976850	A549	lung:	n/a	chr6:30976725-30976736
13	CEBPB	chr6:30971959-30972577	GM12878	blood:	n/a	n/a
14	CEBPB	chr6:30966681-30966941	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr6:30982027-30982185	IMR90	lung:	n/a	n/a
16	CEBPB	chr6:30976622-30976873	HepG2	liver:	n/a	chr6:30976725-30976736
17	CHD1	chr6:30978038-30978834	IMR90	lung:	n/a	n/a
18	CREB1	chr6:30973235-30973814	GM12878	blood:	n/a	n/a
19	CREB1	chr6:30972028-30972614	GM12878	blood:	n/a	n/a
20	CREB1	chr6:30972035-30972586	GM12878	blood:	n/a	n/a
21	CTCF	chr6:30976100-30976250	HVMF	connective:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
22	CTCF	chr6:30976140-30976290	BE2_C	brain:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
23	CTCF	chr6:30976040-30976190	MCF-7	breast:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
24	CTCF	chr6:30976100-30976250	HBMEC	blood vessel:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
25	CTCF	chr6:30976160-30976310	HCT-116	colon:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
26	CTCF	chr6:30976020-30976170	HMF	breast:	n/a	n/a
27	CTCF	chr6:30976080-30976230	HRE	kidney:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
28	CTCF	chr6:30976040-30976190	HAc	cerebellar:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
29	CTCF	chr6:30976140-30976290	K562	blood:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
30	CTCF	chr6:30976010-30976305	H1-hESC	embryonic stem cell:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
31	CTCF	chr6:30976080-30976230	HCFaa	heart:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
32	CTCF	chr6:30976140-30976290	HA-sp	spinal cord:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
33	CTCF	chr6:30976060-30976210	AG10803	skin:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
34	CTCF	chr6:30976133-30976140	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr6:30976135-30976139	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:30976089-30976239	Gliobla	brain:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
37	CTCF	chr6:30976127-30976166	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:30969162-30969235	Medullo	brain:	n/a	n/a
39	CTCF	chr6:30976040-30976190	HMF	breast:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
40	CTCF	chr6:30976060-30976210	HEEpiC	esophagus:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
41	CTCF	chr6:30976111-30976176	A549	lung:	n/a	n/a
42	CTCF	chr6:30976100-30976250	HEK293	kidney:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
43	CTCF	chr6:30976118-30976228	SK-N-SH_RA	brain:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
44	CTCF	chr6:30985540-30985690	GM12868	blood:	n/a	n/a
45	CTCF	chr6:30976085-30976234	K562	blood:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
46	CTCF	chr6:30976040-30976190	HRPEpiC	eye:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
47	CTCF	chr6:30976100-30976250	AG04450	lung:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
48	CTCF	chr6:30976141-30976177	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr6:30976140-30976290	A549	lung:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
50	CTCF	chr6:30976100-30976250	AG04449	skin:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30981960-30982010	NHDF-neo	bronchial:	n/a
2	chr6:30981960-30982010	NHDF-neo	bronchial:	n/a
3	chr6:30981960-30982010	HCF	heart:	n/a
4	chr6:30981960-30982010	HCPEpiC	choroid plexus:	n/a
5	chr6:30984791-30984841	GM12892	blood:	n/a
6	chr6:30984791-30984841	HEK293	kidney:	embryo
7	chr6:30984668-30984718	NB4	blood:	n/a
8	chr6:30984668-30984718	PFSK-1	brain:	n/a
9	chr6:30981960-30982010	HepG2	liver:	n/a
10	chr6:30968402-30968452	ovcar-3	ovarian:	n/a
11	chr6:30984668-30984718	MCF10A-Er-Src	breast:	n/a
12	chr6:30968402-30968452	RPTEC	kidney:	n/a
13	chr6:30968402-30968452	MCF10A-Er-Src	breast:	n/a
14	chr6:30980847-30980897	GM12878	blood:	n/a
15	chr6:30984668-30984718	GM19239	blood:	n/a
16	chr6:30984668-30984718	AG04450	lung:	fetal
17	chr6:30968402-30968452	HCF	heart:	n/a
18	chr6:30968402-30968452	H1-hESC	embryonic stem cell:	embryo
19	chr6:30984668-30984718	SK-N-MC	brain:	n/a
20	chr6:30981960-30982010	AG09309	skin:	n/a
21	chr6:30980847-30980897	PFSK-1	brain:	n/a
22	chr6:30981960-30982010	BE2_C	brain:	n/a
23	chr6:30984668-30984718	AG04449	skin:	fetal
24	chr6:30981960-30982010	SK-N-MC	brain:	n/a
25	chr6:30968402-30968452	HCM	heart:	n/a
26	chr6:30980847-30980897	AG04450	lung:	fetal
27	chr6:30980847-30980897	MCF-7	breast:	n/a
28	chr6:30980847-30980897	CMK	blood:	n/a
29	chr6:30980847-30980897	AG10803	skin:	n/a
30	chr6:30968402-30968452	AG09319	gingival:	n/a
31	chr6:30984791-30984841	AG09319	gingival:	n/a
32	chr6:30981960-30982010	SK-N-SH	brain:	n/a
33	chr6:30968402-30968452	U87	brain:	n/a
34	chr6:30980847-30980897	Jurkat	blood:	n/a
35	chr6:30984668-30984718	HMEC	breast:	n/a
36	chr6:30984668-30984718	GM06990	blood:	n/a
37	chr6:30980847-30980897	HPAEpiC	pulmonary alveolar:	n/a
38	chr6:30984668-30984718	MCF-7	breast:	n/a
39	chr6:30968402-30968452	CMK	blood:	n/a
40	chr6:30968402-30968452	AG10803	skin:	n/a
41	chr6:30981960-30982010	HL-60	blood:	n/a
42	chr6:30980847-30980897	MCF10A-Er-Src	breast:	n/a
43	chr6:30984668-30984718	HUVEC	blood vessel:	n/a
44	chr6:30981960-30982010	HMEC	breast:	n/a
45	chr6:30984791-30984841	H1-hESC	embryonic stem cell:	embryo
46	chr6:30980847-30980897	SK-N-SH	brain:	n/a
47	chr6:30968402-30968452	BE2_C	brain:	n/a
48	chr6:30980847-30980897	AG04449	skin:	fetal
49	chr6:30980847-30980897	HIPEpiC	eye:	n/a
50	chr6:30984668-30984718	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:30969067..30971818-chr6:30977942..30979590,2	K562	blood:
2	chr6:26157901..26159583-chr6:30975186..30977903,2	K562	blood:
3	chr6:26026654..26028309-chr6:30981430..30984025,2	K562	blood:
4	chr6:30956761..30958639-chr6:30968903..30970825,2	MCF-7	breast:
5	chr6:30966029..30968135-chr6:30974071..30975905,2	MCF-7	breast:
6	chr6:30781714..30783791-chr6:30982862..30984438,2	K562	blood:
7	chr6:30954105..30955673-chr6:30975592..30977694,2	K562	blood:
8	chr6:30976019..30976653-chr6:31010220..31010809,2	MCF-7	breast:
9	chr6:30967966..30971967-chr6:30974378..30977539,3	K562	blood:
10	chr6:30967966..30971967-chr6:30974378..30977539,3	K562	blood:
11	chr6:30971805..30974320-chr6:30984460..30987060,2	K562	blood:
12	chr6:30945892..30947709-chr6:30965242..30967995,2	K562	blood:
13	chr6:30953051..30955055-chr6:30968288..30971008,2	K562	blood:
14	chr6:30971805..30974320-chr6:30984460..30987060,2	K562	blood:
15	chr6:30966029..30968135-chr6:30974071..30975905,2	MCF-7	breast:

Variant related genes	Relation type
MUC22	TF binding region
MUC22	CpG island
ENSG00000158373	chromatin interactions
ENSG00000261272	chromatin interactions
ENSG00000124529	chromatin interactions

Extended variants
information (count: 977 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560854743	chr6:30966690-30966691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531365278	chr6:30966745-30966746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376789443	chr6:30966760-30966761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114982948	chr6:30966789-30966790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114753740	chr6:30966801-30966802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532285318	chr6:30966804-30966805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375044155	chr6:30966915-30966916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113993508	chr6:30966917-30966918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73393942	chr6:30966921-30966922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536123876	chr6:30966924-30966925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554470405	chr6:30966925-30966926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569685491	chr6:30966935-30966936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537063159	chr6:30966938-30966939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115335082	chr6:30966969-30966970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559832230	chr6:30967028-30967029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181422263	chr6:30967034-30967035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553283386	chr6:30967058-30967059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534749866	chr6:30967199-30967200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2530690	chr6:30967202-30967203	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs2530689	chr6:30967256-30967257	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs2517406	chr6:30967279-30967280	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs118160129	chr6:30967305-30967306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146266349	chr6:30967324-30967325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111746594	chr6:30967345-30967346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547503521	chr6:30967387-30967388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565714863	chr6:30967438-30967439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529860828	chr6:30967448-30967449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111897727	chr6:30967471-30967472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144184679	chr6:30967488-30967489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2530688	chr6:30967499-30967500	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs547624329	chr6:30967516-30967517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368390268	chr6:30967524-30967525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186620549	chr6:30967577-30967578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs55928860	chr6:30967587-30967588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570866863	chr6:30967595-30967596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534793816	chr6:30967612-30967613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190136991	chr6:30967788-30967789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575060493	chr6:30967792-30967793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536062154	chr6:30967826-30967827	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112005720	chr6:30967946-30967947	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557638302	chr6:30967947-30967948	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576003760	chr6:30967975-30967976	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs117712575	chr6:30967991-30967992	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551522396	chr6:30968030-30968031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576799317	chr6:30968035-30968036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540741590	chr6:30968036-30968037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114625453	chr6:30968045-30968046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111071055	chr6:30968070-30968071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2844671	chr6:30968109-30968110	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs145263566	chr6:30968180-30968181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30950800-30972200	Weak transcription	Right Atrium	heart
2	chr6:30965200-30975800	Weak transcription	Gastric	stomach
3	chr6:30966200-30966800	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr6:30966200-30967200	Enhancers	Hela-S3	cervix
5	chr6:30966200-30967400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:30966400-30967000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:30966400-30967000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr6:30966600-30967000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:30966600-30967800	Weak transcription	Esophagus	oesophagus
10	chr6:30966800-30972400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr6:30967000-30972200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:30967000-30972400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:30967200-30967800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:30967600-30968000	Enhancers	K562	blood
15	chr6:30967800-30968000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:30967800-30968000	Enhancers	Esophagus	oesophagus
17	chr6:30968000-30969800	Weak transcription	K562	blood
18	chr6:30969200-30969400	Enhancers	Thymus	Thymus
19	chr6:30969200-30969600	Enhancers	Fetal Kidney	kidney
20	chr6:30969200-30970600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr6:30969800-30970800	Enhancers	K562	blood
22	chr6:30970400-30970600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr6:30970400-30970600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:30970600-30971600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr6:30970600-30978000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:30970800-30972200	Weak transcription	K562	blood
27	chr6:30971200-30974800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:30971600-30972800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr6:30972200-30972400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:30972200-30972600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr6:30972200-30972600	Enhancers	Left Ventricle	heart
32	chr6:30972200-30972600	Enhancers	Lung	lung
33	chr6:30972200-30972600	Enhancers	Right Atrium	heart
34	chr6:30972200-30972600	Enhancers	Right Ventricle	heart
35	chr6:30972200-30972600	Enhancers	NHEK	skin
36	chr6:30972200-30973000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:30972200-30973200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr6:30972200-30973200	Enhancers	Small Intestine	intestine
39	chr6:30972200-30973400	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr6:30972200-30974000	Enhancers	GM12878-XiMat	blood
41	chr6:30972400-30972600	Enhancers	Psoas Muscle	Psoas
42	chr6:30972400-30972600	Enhancers	K562	blood
43	chr6:30972400-30973400	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr6:30972400-30973400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:30972400-30973400	Enhancers	Adipose Nuclei	Adipose
46	chr6:30972400-30973400	Enhancers	HMEC	breast
47	chr6:30972400-30973600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:30972400-30973800	Enhancers	Fetal Heart	heart
49	chr6:30972400-30974400	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr6:30972600-30972800	Enhancers	Primary T helper cells PMA-I stimulated	--

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