Variant report

Variant	nsv819978
Chromosome Location	chr6:31713259-31721119
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	chr6:31714881-31715171	HepG2	liver:	n/a	n/a
2	BCL3	chr6:31720469-31721258	A549	lung:	n/a	n/a
3	BCL3	chr6:31717427-31717639	GM12878	blood:	n/a	n/a
4	BCL3	chr6:31720485-31720932	GM12878	blood:	n/a	n/a
5	BCL3	chr6:31720559-31720843	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:31718199-31718477	K562	blood:	n/a	n/a
7	BHLHE40	chr6:31715066-31715243	HepG2	liver:	n/a	n/a
8	CCNT2	chr6:31717533-31717619	K562	blood:	n/a	n/a
9	CCNT2	chr6:31718275-31718425	K562	blood:	n/a	n/a
10	CEBPB	chr6:31720550-31720996	IMR90	lung:	n/a	n/a
11	CHD2	chr6:31714906-31715144	HepG2	liver:	n/a	n/a
12	CTCF	chr6:31718044-31718077	Pancreas_OC	pancreas:	n/a	n/a
13	CUX1	chr6:31718241-31718516	K562	blood:	n/a	n/a
14	EGR1	chr6:31716267-31716487	K562	blood:	n/a	n/a
15	EP300	chr6:31714815-31715262	HepG2	liver:	n/a	n/a
16	EP300	chr6:31718122-31718454	K562	blood:	n/a	n/a
17	EP300	chr6:31718134-31718511	K562	blood:	n/a	n/a
18	EP300	chr6:31715132-31715215	HepG2	liver:	n/a	n/a
19	FOS	chr6:31720565-31720901	MCF10A-Er-Src	breast:	n/a	chr6:31720711-31720723 chr6:31720711-31720722 chr6:31720713-31720721 chr6:31720714-31720725
20	FOS	chr6:31720580-31720925	HUVEC	blood vessel:	n/a	chr6:31720711-31720723 chr6:31720711-31720722 chr6:31720713-31720721 chr6:31720714-31720725
21	FOS	chr6:31720215-31720919	MCF10A-Er-Src	breast:	n/a	chr6:31720711-31720723 chr6:31720711-31720722 chr6:31720713-31720721 chr6:31720714-31720725
22	FOS	chr6:31720216-31720362	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr6:31720205-31720919	MCF10A-Er-Src	breast:	n/a	chr6:31720711-31720723 chr6:31720711-31720722 chr6:31720713-31720721 chr6:31720714-31720725
24	FOS	chr6:31718217-31718398	MCF10A-Er-Src	breast:	n/a	chr6:31718360-31718372 chr6:31718362-31718370
25	FOS	chr6:31720526-31720929	MCF10A-Er-Src	breast:	n/a	chr6:31720711-31720723 chr6:31720711-31720722 chr6:31720713-31720721 chr6:31720714-31720725
26	FOS	chr6:31718337-31718375	MCF10A-Er-Src	breast:	n/a	chr6:31718360-31718372 chr6:31718362-31718370
27	FOSL1	chr6:31718147-31718606	K562	blood:	n/a	chr6:31718360-31718372 chr6:31718362-31718370
28	FOSL2	chr6:31720557-31720834	A549	lung:	n/a	chr6:31720711-31720723 chr6:31720713-31720721 chr6:31720714-31720725
29	FOSL2	chr6:31720415-31721014	SK-N-SH	brain:	n/a	chr6:31720711-31720723 chr6:31720713-31720721 chr6:31720714-31720725
30	FOSL2	chr6:31720489-31720977	A549	lung:	n/a	chr6:31720711-31720723 chr6:31720713-31720721 chr6:31720714-31720725
31	FOSL2	chr6:31714755-31715281	HepG2	liver:	n/a	n/a
32	FOXA1	chr6:31717427-31717720	T-47D	breast:	n/a	n/a
33	FOXA1	chr6:31714787-31715367	HepG2	liver:	n/a	n/a
34	FOXA1	chr6:31714785-31715259	HepG2	liver:	n/a	n/a
35	FOXA1	chr6:31714781-31715297	HepG2	liver:	n/a	n/a
36	FOXA1	chr6:31717409-31717755	HepG2	liver:	n/a	n/a
37	FOXA1	chr6:31717421-31717812	HepG2	liver:	n/a	n/a
38	FOXA1	chr6:31717420-31717759	HepG2	liver:	n/a	n/a
39	FOXA1	chr6:31714730-31715323	HepG2	liver:	n/a	n/a
40	FOXA1	chr6:31717416-31717766	T-47D	breast:	n/a	n/a
41	FOXA2	chr6:31717486-31717727	HepG2	liver:	n/a	n/a
42	FOXA2	chr6:31714823-31715232	HepG2	liver:	n/a	n/a
43	GATA3	chr6:31717366-31718064	MCF-7	breast:	n/a	n/a
44	GATA3	chr6:31717493-31717905	T-47D	breast:	n/a	n/a
45	GATA3	chr6:31717524-31717885	T-47D	breast:	n/a	n/a
46	GATA3	chr6:31717697-31718202	SH-SY5Y	brain:	n/a	n/a
47	HEY1	chr6:31715063-31715283	HepG2	liver:	n/a	n/a
48	IRF1	chr6:31718063-31718477	K562	blood:	n/a	n/a
49	JUN	chr6:31717449-31717767	HepG2	liver:	n/a	chr6:31717610-31717619 chr6:31717609-31717622
50	JUND	chr6:31714846-31715145	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31712086..31714995-chr6:31716083..31718162,2	MCF-7	breast:
2	chr6:31715039..31718016-chr6:31863817..31867579,3	K562	blood:
3	chr6:31712951..31714634-chr6:31717603..31719135,2	MCF-7	breast:
4	chr6:31704043..31706840-chr6:31719670..31721434,2	MCF-7	breast:
5	chr6:31717258..31719013-chr6:31760100..31762521,2	MCF-7	breast:
6	chr6:31707439..31709705-chr6:31719652..31722031,2	MCF-7	breast:
7	chr6:31711941..31713458-chr6:31842956..31845692,2	K562	blood:
8	chr6:31719193..31720715-chr6:31725277..31726950,2	MCF-7	breast:
9	chr6:31712951..31714634-chr6:31717603..31719135,2	MCF-7	breast:
10	chr6:31710678..31714958-chr6:31739473..31744061,4	MCF-7	breast:
11	chr6:31719655..31721426-chr6:31723732..31727179,3	MCF-7	breast:
12	chr6:31717928..31719785-chr6:31735295..31738183,2	MCF-7	breast:
13	chr6:31711834..31714451-chr6:31829809..31833042,3	K562	blood:

Variant related genes	Relation type
MSH5	TF binding region
ENSG00000255152	chromatin interactions
ENSG00000166278	chromatin interactions
ENSG00000204410	chromatin interactions
ENSG00000204371	chromatin interactions
ENSG00000204394	chromatin interactions
ENSG00000204396	chromatin interactions
ENSG00000204386	chromatin interactions
ENSG00000252743	chromatin interactions
ENSG00000213719	chromatin interactions
ENSG00000204385	chromatin interactions

Extended variants
information (count: 234 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:234 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191774159	chr6:31713261-31713262	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs138015643	chr6:31713304-31713305	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs554883031	chr6:31713364-31713365	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs576575223	chr6:31713391-31713392	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs28381363	chr6:31713393-31713394	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs562563834	chr6:31713394-31713395	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs577681291	chr6:31713399-31713400	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs3828922	chr6:31713454-31713455	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs560171018	chr6:31713462-31713463	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs527320939	chr6:31713499-31713500	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs9279404	chr6:31713543-31713544	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs3132444	chr6:31713565-31713566	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
13	rs531490287	chr6:31713575-31713576	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs182504014	chr6:31713584-31713585	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs371180482	chr6:31713676-31713677	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs538734594	chr6:31713690-31713691	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs141947965	chr6:31713727-31713728	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs565727403	chr6:31713728-31713729	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs536293472	chr6:31713734-31713735	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs186828768	chr6:31713748-31713749	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs576673803	chr6:31713765-31713766	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs4947330	chr6:31713785-31713786	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs558909221	chr6:31713794-31713795	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs191292906	chr6:31713822-31713823	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs12177823	chr6:31713823-31713824	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs368880246	chr6:31713833-31713834	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs572069705	chr6:31713834-31713835	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs41315808	chr6:31713835-31713836	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs561199146	chr6:31713857-31713858	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs61036903	chr6:31713892-31713893	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs543727225	chr6:31713904-31713905	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs572675654	chr6:31713942-31713943	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs3132443	chr6:31714031-31714032	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs547482690	chr6:31714039-31714040	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs565838166	chr6:31714109-31714110	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs561479424	chr6:31714160-31714161	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs149863825	chr6:31714170-31714171	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs570302830	chr6:31714173-31714174	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs529699959	chr6:31714174-31714175	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs185782768	chr6:31714186-31714187	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs201411694	chr6:31714210-31714211	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs12191233	chr6:31714220-31714221	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs140330258	chr6:31714302-31714303	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs565114603	chr6:31714330-31714331	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs190305567	chr6:31714382-31714383	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs532573998	chr6:31714406-31714407	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs183143899	chr6:31714444-31714445	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs572184129	chr6:31714505-31714506	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs542614482	chr6:31714506-31714507	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112247386	chr6:31714603-31714604	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

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
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
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
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	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
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
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31707400-31724600	Weak transcription	Fetal Heart	heart
2	chr6:31708200-31733800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:31708400-31714800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:31708400-31715000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:31708400-31715000	Weak transcription	Esophagus	oesophagus
6	chr6:31708400-31715000	Weak transcription	Ovary	ovary
7	chr6:31708400-31715000	Weak transcription	Pancreas	Pancrea
8	chr6:31708400-31717600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr6:31708400-31727000	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr6:31708400-31729600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:31708400-31731000	Weak transcription	HSMMtube	muscle
12	chr6:31708400-31731200	Weak transcription	Gastric	stomach
13	chr6:31708400-31731200	Weak transcription	Lung	lung
14	chr6:31708400-31731200	Weak transcription	Right Atrium	heart
15	chr6:31708600-31714800	Weak transcription	Colon Smooth Muscle	Colon
16	chr6:31708600-31715000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:31708600-31715000	Weak transcription	Stomach Smooth Muscle	stomach
18	chr6:31708600-31715200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr6:31708600-31717000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr6:31708600-31728200	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr6:31708600-31729400	Weak transcription	Fetal Lung	lung
22	chr6:31708600-31731200	Weak transcription	Brain Hippocampus Middle	brain
23	chr6:31708600-31732000	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr6:31708600-31734400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr6:31708800-31713400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:31708800-31714600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:31708800-31714800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr6:31708800-31715000	Weak transcription	Fetal Brain Female	brain
29	chr6:31708800-31716200	Strong transcription	Fetal Stomach	stomach
30	chr6:31708800-31717000	Weak transcription	Small Intestine	intestine
31	chr6:31708800-31723200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr6:31708800-31727400	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr6:31708800-31727600	Weak transcription	Spleen	Spleen
34	chr6:31708800-31731200	Weak transcription	Brain Anterior Caudate	brain
35	chr6:31708800-31737400	Weak transcription	Liver	Liver
36	chr6:31709000-31713400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:31709000-31715000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr6:31709000-31718200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:31709000-31719000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:31709000-31720400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr6:31709000-31720400	Weak transcription	NH-A	brain
42	chr6:31709000-31720400	Weak transcription	NHDF-Ad	bronchial
43	chr6:31709000-31721000	Weak transcription	Brain Substantia Nigra	brain
44	chr6:31709000-31722400	Weak transcription	Fetal Brain Male	brain
45	chr6:31709000-31726800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr6:31709000-31727000	Weak transcription	Primary T cells from cord blood	blood
47	chr6:31709000-31727600	Weak transcription	Colonic Mucosa	Colon
48	chr6:31709000-31738200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr6:31709200-31713400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr6:31709200-31715000	Weak transcription	HMEC	breast

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