Variant report

Variant	nsv969376
Chromosome Location	chr6:30601427-30608408
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	CEBPB	chr6:30602799-30603123	K562	blood:	n/a	chr6:30602966-30602977 chr6:30602965-30602978 chr6:30602965-30602976 chr6:30602967-30602976
2	CEBPB	chr6:30602823-30603133	IMR90	lung:	n/a	chr6:30602966-30602977 chr6:30602965-30602978 chr6:30602965-30602976 chr6:30602967-30602976
3	CEBPB	chr6:30602853-30603078	A549	lung:	n/a	chr6:30602966-30602977 chr6:30602965-30602978 chr6:30602965-30602976 chr6:30602967-30602976
4	CEBPB	chr6:30602834-30603127	HepG2	liver:	n/a	chr6:30602966-30602977 chr6:30602965-30602978 chr6:30602965-30602976 chr6:30602967-30602976
5	CEBPB	chr6:30602935-30602983	Hela-S3	cervix:	n/a	chr6:30602966-30602977 chr6:30602965-30602978 chr6:30602965-30602976 chr6:30602967-30602976
6	CTCF	chr6:30608324-30608576	MCF-7	breast:	n/a	n/a
7	CTCF	chr6:30608160-30608430	HL-60	blood:	n/a	n/a
8	CTCF	chr6:30608214-30608615	MCF-7	breast:	n/a	n/a
9	CTCF	chr6:30608360-30608510	SAEC	small airway:	n/a	n/a
10	CTCF	chr6:30608320-30608470	HMEC	breast:	n/a	n/a
11	CTCF	chr6:30608407-30608530	GM12878	blood:	n/a	n/a
12	CTCF	chr6:30608380-30608530	NB4	blood:	n/a	n/a
13	CTCF	chr6:30608364-30608542	Gliobla	brain:	n/a	n/a
14	CTCF	chr6:30608240-30608390	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr6:30608340-30608490	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr6:30608336-30608526	MCF-7	breast:	n/a	n/a
17	CTCF	chr6:30608379-30608523	A549	lung:	n/a	n/a
18	CTCF	chr6:30608300-30608450	GM12872	blood:	n/a	n/a
19	CTCF	chr6:30608399-30608509	GM12878	blood:	n/a	n/a
20	CTCF	chr6:30608334-30608503	MCF-7	breast:	n/a	n/a
21	CTCF	chr6:30608380-30608530	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr6:30608380-30608530	GM12873	blood:	n/a	n/a
23	CTCF	chr6:30608380-30608530	HEK293	kidney:	n/a	n/a
24	CTCF	chr6:30608340-30608490	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr6:30608380-30608530	GM12878	blood:	n/a	n/a
26	CTCF	chr6:30608344-30608549	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr6:30608406-30608487	HepG2	liver:	n/a	n/a
28	CTCF	chr6:30608300-30608450	GM12865	blood:	n/a	n/a
29	CTCF	chr6:30608338-30608563	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:30608347-30608523	MCF-7	breast:	n/a	n/a
31	EGR1	chr6:30603663-30604000	K562	blood:	n/a	n/a
32	EGR1	chr6:30603667-30603893	K562	blood:	n/a	n/a
33	JUND	chr6:30603763-30603902	HepG2	liver:	n/a	n/a
34	MAX	chr6:30608215-30608587	MCF-7	breast:	n/a	n/a
35	POLR2A	chr6:30604663-30604687	MCF-7	breast:	n/a	n/a
36	POLR2A	chr6:30607593-30607835	HepG2	liver:	n/a	n/a
37	POLR2A	chr6:30605574-30605817	HepG2	liver:	n/a	n/a
38	POLR2A	chr6:30601305-30601519	HepG2	liver:	n/a	n/a
39	POLR2A	chr6:30606923-30606925	HepG2	liver:	n/a	n/a
40	POLR2A	chr6:30608306-30608391	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr6:30601257-30601845	HepG2	liver:	n/a	n/a
42	POLR2A	chr6:30607562-30607590	HepG2	liver:	n/a	n/a
43	POLR2A	chr6:30606121-30606230	HepG2	liver:	n/a	n/a
44	POLR2A	chr6:30606838-30606920	HepG2	liver:	n/a	n/a
45	RAD21	chr6:30608229-30608704	MCF-7	breast:	n/a	n/a
46	RAD21	chr6:30608297-30608575	Hela-S3	cervix:	n/a	n/a
47	RAD21	chr6:30608399-30608463	A549	lung:	n/a	n/a
48	SMC3	chr6:30608368-30608518	Hela-S3	cervix:	n/a	n/a
49	STAT3	chr6:30603541-30603741	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:30600893..30602967-chr6:30606710..30608465,2	MCF-7	breast:
2	chr6:30601918..30605372-chr6:30687012..30690435,4	K562	blood:
3	chr6:30603404..30605348-chr6:30605560..30609450,3	MCF-7	breast:
4	chr6:30581846..30586345-chr6:30599769..30603372,4	MCF-7	breast:
5	chr6:30598934..30603301-chr6:30608761..30613584,7	MCF-7	breast:
6	chr6:30591157..30598732-chr6:30607879..30619621,21	K562	blood:
7	chr6:30455831..30458376-chr6:30599698..30601458,2	MCF-7	breast:
8	chr6:30592203..30595028-chr6:30602897..30604567,2	MCF-7	breast:
9	chr6:30584082..30586982-chr6:30608127..30610003,2	MCF-7	breast:
10	chr6:30603404..30605348-chr6:30605560..30609450,3	MCF-7	breast:
11	chr6:30608315..30616989-chr6:30683761..30694958,31	K562	blood:
12	chr6:30604583..30606646-chr6:30606974..30609651,2	MCF-7	breast:
13	chr6:30584090..30585907-chr6:30604843..30607556,2	MCF-7	breast:
14	chr6:30607674..30610215-chr6:30640154..30642448,2	K562	blood:

Variant related genes	Relation type
ATAT1	TF binding region
ENSG00000204560	chromatin interactions
ENSG00000137343	chromatin interactions
ENSG00000272540	chromatin interactions
ENSG00000196230	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000204592	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000228415	chromatin interactions
ENSG00000137337	chromatin interactions

Extended variants
information (count: 254 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530736701	chr6:30601437-30601438	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs550656467	chr6:30601439-30601440	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs374792624	chr6:30601479-30601480	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs567273605	chr6:30601515-30601516	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs368677302	chr6:30601530-30601531	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs556040090	chr6:30601561-30601562	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs140732210	chr6:30601588-30601589	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs566277898	chr6:30601589-30601590	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs189584782	chr6:30601607-30601608	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs557972828	chr6:30601621-30601622	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs577805427	chr6:30601627-30601628	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs9501026	chr6:30601644-30601645	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs144363175	chr6:30601652-30601653	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs573996887	chr6:30601653-30601654	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs542693552	chr6:30601686-30601687	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs559679958	chr6:30601692-30601693	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs528423067	chr6:30601694-30601695	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs148768246	chr6:30601730-30601731	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs112682543	chr6:30601779-30601780	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs374971826	chr6:30601797-30601798	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs570741039	chr6:30601818-30601819	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs386698781	chr6:30601821-30601822	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs115444444	chr6:30601822-30601823	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs550715626	chr6:30601869-30601870	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs542235912	chr6:30601928-30601929	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs529780315	chr6:30601982-30601983	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs371396394	chr6:30602021-30602022	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs368761717	chr6:30602052-30602053	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs566189505	chr6:30602068-30602069	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs2894041	chr6:30602091-30602092	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs557986906	chr6:30602101-30602102	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs571508114	chr6:30602105-30602106	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs537216748	chr6:30602110-30602111	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs557119776	chr6:30602158-30602159	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs574082202	chr6:30602172-30602173	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs28445993	chr6:30602349-30602350	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs117021444	chr6:30602376-30602377	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs576414285	chr6:30602382-30602383	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs553133912	chr6:30602403-30602404	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs3094105	chr6:30602414-30602415	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs545327235	chr6:30602418-30602419	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs560116784	chr6:30602441-30602442	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs565147202	chr6:30602452-30602453	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs575524511	chr6:30602476-30602477	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs544452632	chr6:30602523-30602524	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs558864197	chr6:30602553-30602554	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs529795449	chr6:30602562-30602563	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs550843613	chr6:30602593-30602594	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs577118223	chr6:30602596-30602597	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs546663590	chr6:30602651-30602652	Weak transcription Strong transcription	Chromatin interactive region	5 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
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
Lung cancer	21569311	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

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30593600-30613800	Weak transcription	Hela-S3	cervix
2	chr6:30595200-30607000	Weak transcription	Right Atrium	heart
3	chr6:30595200-30609000	Weak transcription	Colonic Mucosa	Colon
4	chr6:30595400-30607800	Weak transcription	Right Ventricle	heart
5	chr6:30595400-30608200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:30595400-30608400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr6:30595400-30614000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr6:30595400-30614800	Weak transcription	Small Intestine	intestine
9	chr6:30595600-30605200	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr6:30595600-30608000	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr6:30595600-30608200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr6:30595600-30608600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr6:30595600-30611000	Weak transcription	Primary B cells from cord blood	blood
14	chr6:30595600-30613000	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:30595600-30613800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:30595600-30614200	Strong transcription	Fetal Muscle Trunk	muscle
17	chr6:30595600-30614200	Strong transcription	Fetal Stomach	stomach
18	chr6:30595600-30614200	Weak transcription	Psoas Muscle	Psoas
19	chr6:30595600-30614400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr6:30595800-30601800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr6:30595800-30602000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:30595800-30602000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:30595800-30602000	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr6:30595800-30602200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr6:30595800-30602400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr6:30595800-30602400	Strong transcription	Fetal Intestine Large	intestine
27	chr6:30595800-30602400	Strong transcription	Fetal Thymus	thymus
28	chr6:30595800-30603200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr6:30595800-30604200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr6:30595800-30608200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr6:30595800-30608800	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr6:30595800-30613000	Strong transcription	Fetal Lung	lung
33	chr6:30595800-30613600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:30595800-30613600	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr6:30595800-30614000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr6:30595800-30614200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr6:30596000-30601800	Strong transcription	Ovary	ovary
38	chr6:30596000-30602000	Strong transcription	Brain Anterior Caudate	brain
39	chr6:30596000-30602000	Strong transcription	Brain Cingulate Gyrus	brain
40	chr6:30596000-30602000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr6:30596000-30602400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr6:30596000-30602400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr6:30596000-30602800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:30596000-30604200	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr6:30596000-30605200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:30596000-30605400	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr6:30596000-30605800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:30596000-30613800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr6:30596000-30613800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr6:30596000-30614000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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