Variant report

Variant	nsv10813
Chromosome Location	chr6:31050018-31052784
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	ATF1	chr6:31051604-31051989	K562	blood:	n/a	n/a
2	ATF2	chr6:31051726-31052178	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr6:31051506-31051857	K562	blood:	n/a	n/a
4	BACH1	chr6:31051590-31051926	K562	blood:	n/a	n/a
5	BHLHE40	chr6:31051627-31052109	K562	blood:	n/a	n/a
6	CBX3	chr6:31051691-31052118	K562	blood:	n/a	n/a
7	CEBPB	chr6:31051557-31051731	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr6:31051481-31052064	K562	blood:	n/a	n/a
9	CEBPB	chr6:31051475-31052098	K562	blood:	n/a	n/a
10	CEBPB	chr6:31051500-31051800	IMR90	lung:	n/a	n/a
11	CTCF	chr6:31051838-31052094	ProgFib	skin:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
12	CTCF	chr6:31051900-31052050	GM12870	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
13	CTCF	chr6:31051844-31052097	Gliobla	brain:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
14	CTCF	chr6:31051840-31051990	GM06990	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
15	CTCF	chr6:31051841-31052098	GM12891	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
16	CTCF	chr6:31051820-31051970	RPTEC	kidney:	n/a	chr6:31051956-31051969
17	CTCF	chr6:31051880-31052030	GM12872	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
18	CTCF	chr6:31051820-31051970	HCM	heart:	n/a	chr6:31051956-31051969
19	CTCF	chr6:31051580-31051730	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr6:31051900-31052050	NHEK	skin:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
21	CTCF	chr6:31051560-31051710	AG04449	skin:	n/a	n/a
22	CTCF	chr6:31051820-31051970	BE2_C	brain:	n/a	chr6:31051956-31051969
23	CTCF	chr6:31051860-31052010	GM12865	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
24	CTCF	chr6:31051856-31052076	NHEK	skin:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
25	CTCF	chr6:31051860-31052010	GM12878	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
26	CTCF	chr6:31051600-31051750	GM12872	blood:	n/a	n/a
27	CTCF	chr6:31051774-31052132	IMR90	lung:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
28	CTCF	chr6:31051800-31051950	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr6:31051840-31051990	AG09319	gingival:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
30	CTCF	chr6:31051837-31052096	GM19240	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
31	CTCF	chr6:31051880-31052030	GM12873	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
32	CTCF	chr6:31051880-31052071	Hela-S3	cervix:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
33	CTCF	chr6:31051908-31052050	LNCaP	prostate:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
34	CTCF	chr6:31051920-31052070	AG10803	skin:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
35	CTCF	chr6:31051836-31052110	Medullo	brain:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
36	CTCF	chr6:31051860-31052010	HPF	lung:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
37	CTCF	chr6:31051900-31052050	K562	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
38	CTCF	chr6:31051760-31051910	WI-38	lung:	n/a	n/a
39	CTCF	chr6:31051774-31052088	HepG2	liver:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
40	CTCF	chr6:31051880-31052030	BJ	skin:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
41	CTCF	chr6:31051800-31051950	HVMF	connective:	n/a	n/a
42	CTCF	chr6:31051880-31052030	NHEK	skin:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
43	CTCF	chr6:31051820-31051970	HVMF	connective:	n/a	chr6:31051956-31051969
44	CTCF	chr6:31051920-31052070	GM12871	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
45	CTCF	chr6:31051820-31051970	NHDF-neo	bronchial:	n/a	chr6:31051956-31051969
46	CTCF	chr6:31051820-31051970	WI-38	lung:	n/a	chr6:31051956-31051969
47	CTCF	chr6:31051900-31052050	GM12869	blood:	n/a	chr6:31051956-31051969 chr6:31051954-31051972
48	CTCF	chr6:31051820-31051970	MCF-7	breast:	n/a	chr6:31051956-31051969
49	CTCF	chr6:31051600-31051750	GM12870	blood:	n/a	n/a
50	CTCF	chr6:31051864-31052042	Spleen_OC	spleen:	n/a	chr6:31051956-31051969 chr6:31051954-31051972

No.	Distal block	Cell Line	Cell type
1	chr6:30584043..30585831-chr6:31049669..31051731,2	K562	blood:
2	chr6:30582850..30585432-chr6:31048124..31050128,2	K562	blood:
3	chr6:30579948..30582370-chr6:31051290..31053645,2	K562	blood:
4	chr6:30839220..30842043-chr6:31051399..31053018,2	K562	blood:
5	chr6:30881341..30883550-chr6:31049543..31052360,3	K562	blood:
6	chr6:31050562..31052756-chr6:31081245..31083912,2	MCF-7	breast:
7	chr6:30881805..30883309-chr6:31050438..31053270,2	MCF-7	breast:
8	chr6:30795961..30796892-chr6:31051647..31052371,2	K562	blood:
9	chr6:30881341..30883528-chr6:31050692..31052360,2	K562	blood:
10	chr6:30789508..30790311-chr6:31051825..31052620,2	K562	blood:

Variant related genes	Relation type
RNU6-1133P	TF binding region
ENSG00000204540	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000137411	chromatin interactions

Extended variants
information (count: 81 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:81 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117614158	chr6:31050057-31050058	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs141086378	chr6:31050107-31050108	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs76358125	chr6:31050174-31050175	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs531430333	chr6:31050178-31050179	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs9263473	chr6:31050179-31050180	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs9263474	chr6:31050244-31050245	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs187122171	chr6:31050250-31050251	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs117631086	chr6:31050290-31050291	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs191660491	chr6:31050347-31050348	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs9263475	chr6:31050348-31050349	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs56171738	chr6:31050361-31050362	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs551750176	chr6:31050426-31050427	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs548297412	chr6:31050497-31050498	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs368485276	chr6:31050561-31050562	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs181362415	chr6:31050570-31050571	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs537233502	chr6:31050586-31050587	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs538707836	chr6:31050591-31050592	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs554129447	chr6:31050607-31050608	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs146962790	chr6:31050658-31050659	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs9380216	chr6:31050815-31050816	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs199727418	chr6:31050883-31050884	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs115661105	chr6:31050905-31050906	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs137958466	chr6:31050999-31051000	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs4713431	chr6:31051008-31051009	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs149512473	chr6:31051024-31051025	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs554386010	chr6:31051041-31051042	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs185495630	chr6:31051079-31051080	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs370282317	chr6:31051187-31051188	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs543247435	chr6:31051192-31051193	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs116931329	chr6:31051199-31051200	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs532231196	chr6:31051220-31051221	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs564873789	chr6:31051240-31051241	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs540928303	chr6:31051251-31051252	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs532225205	chr6:31051265-31051266	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs372667032	chr6:31051275-31051276	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs143151568	chr6:31051312-31051313	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs116767433	chr6:31051377-31051378	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs559303223	chr6:31051385-31051386	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs199950647	chr6:31051388-31051389	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs531080868	chr6:31051391-31051392	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs116639236	chr6:31051399-31051400	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs548095592	chr6:31051498-31051499	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs376758536	chr6:31051506-31051507	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs374565389	chr6:31051507-31051508	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs9380217	chr6:31051553-31051554	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs535290374	chr6:31051601-31051602	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs530646425	chr6:31051641-31051642	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs553727534	chr6:31051645-31051646	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs3095311	chr6:31051675-31051676	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs190060804	chr6:31051792-31051793	Weak transcription Enhancers	Chromatin interactive region	2 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
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
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
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31022200-31050800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:31040600-31055000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr6:31040600-31062400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr6:31041600-31053200	Weak transcription	NH-A	brain
5	chr6:31043200-31051200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr6:31046600-31053400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:31047600-31051400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr6:31047600-31051400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr6:31047600-31051400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:31047600-31051400	Weak transcription	Hela-S3	cervix
11	chr6:31047600-31051400	Weak transcription	HSMM	muscle
12	chr6:31047600-31053800	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr6:31047600-31054600	Weak transcription	A549	lung
14	chr6:31047600-31054800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:31047600-31054800	Weak transcription	Left Ventricle	heart
16	chr6:31047600-31054800	Weak transcription	Right Atrium	heart
17	chr6:31047800-31050800	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr6:31047800-31051000	Weak transcription	Adipose Nuclei	Adipose
19	chr6:31047800-31051200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr6:31047800-31051200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr6:31047800-31051200	Weak transcription	NHLF	lung
22	chr6:31047800-31051400	Weak transcription	HMEC	breast
23	chr6:31047800-31051600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr6:31047800-31051800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:31047800-31053800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr6:31047800-31054600	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr6:31047800-31055000	Weak transcription	Brain Hippocampus Middle	brain
28	chr6:31048000-31050800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:31048000-31051200	Weak transcription	Osteobl	bone
30	chr6:31048000-31051400	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr6:31048000-31051600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr6:31048000-31051600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:31048000-31053400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr6:31048000-31054200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:31048000-31054800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr6:31048000-31054800	Weak transcription	Dnd41	blood
37	chr6:31049200-31051000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr6:31049200-31052000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr6:31049400-31050400	Enhancers	NHEK	skin
40	chr6:31049400-31050600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr6:31049800-31050400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr6:31049800-31050400	Enhancers	HSMMtube	muscle
43	chr6:31050400-31051400	Weak transcription	HSMMtube	muscle
44	chr6:31050400-31051600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr6:31050400-31051600	Weak transcription	NHEK	skin
46	chr6:31050600-31051000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr6:31050800-31051000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr6:31050800-31052000	Enhancers	Fetal Muscle Trunk	muscle
49	chr6:31050800-31052000	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr6:31050800-31054400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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