Variant report

Variant	nsv884733
Chromosome Location	chr6:32318036-32349946
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:148)
CpG islands
(count:1221)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:148 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:32341778-32342105	HepG2	liver:	n/a	n/a
2	BRCA1	chr6:32337516-32337917	Hela-S3	cervix:	n/a	n/a
3	CBX3	chr6:32341732-32342198	HCT-116	colon:	n/a	n/a
4	CBX3	chr6:32337349-32337928	HCT-116	colon:	n/a	n/a
5	CEBPB	chr6:32338339-32338640	A549	lung:	n/a	chr6:32338479-32338490
6	CEBPB	chr6:32334419-32334604	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr6:32337490-32337785	IMR90	lung:	n/a	n/a
8	CEBPB	chr6:32334428-32334621	K562	blood:	n/a	n/a
9	CEBPB	chr6:32337397-32337887	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:32321136-32321610	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:32338237-32338741	Hela-S3	cervix:	n/a	chr6:32338479-32338490
12	CEBPB	chr6:32338366-32338566	HepG2	liver:	n/a	chr6:32338479-32338490
13	CEBPB	chr6:32338273-32338693	A549	lung:	n/a	chr6:32338479-32338490
14	CEBPB	chr6:32341733-32341934	A549	lung:	n/a	n/a
15	CHD1	chr6:32337451-32338056	IMR90	lung:	n/a	n/a
16	CHD2	chr6:32337443-32337845	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr6:32333160-32333310	HFF-Myc	foreskin:	n/a	n/a
18	CTCF	chr6:32341860-32342010	GM12864	blood:	n/a	n/a
19	E2F4	chr6:32337560-32337756	MCF10A-Er-Src	breast:	n/a	n/a
20	EBF1	chr6:32344047-32344247	GM12878	blood:	n/a	chr6:32344133-32344144
21	ELK1	chr6:32337477-32337817	Hela-S3	cervix:	n/a	n/a
22	EP300	chr6:32338263-32338802	Hela-S3	cervix:	n/a	chr6:32338504-32338511
23	EP300	chr6:32341731-32342181	A549	lung:	n/a	n/a
24	EP300	chr6:32321139-32321500	Hela-S3	cervix:	n/a	n/a
25	EP300	chr6:32337414-32337932	Hela-S3	cervix:	n/a	n/a
26	EP300	chr6:32345420-32345547	K562	blood:	n/a	n/a
27	FAM48A	chr6:32344986-32345116	GM12878	blood:	n/a	n/a
28	FOS	chr6:32337477-32337880	Hela-S3	cervix:	n/a	chr6:32337653-32337664
29	FOS	chr6:32321122-32321561	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr6:32337460-32337846	MCF10A-Er-Src	breast:	n/a	chr6:32337653-32337664
31	FOS	chr6:32321132-32321502	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr6:32321184-32321501	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr6:32337393-32337942	MCF10A-Er-Src	breast:	n/a	chr6:32337653-32337664
34	FOS	chr6:32338259-32338662	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr6:32337452-32337994	MCF10A-Er-Src	breast:	n/a	chr6:32337653-32337664
36	FOS	chr6:32338246-32338672	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr6:32337437-32338092	HUVEC	blood vessel:	n/a	chr6:32337653-32337664
38	FOS	chr6:32337382-32337953	MCF10A-Er-Src	breast:	n/a	chr6:32337653-32337664
39	FOS	chr6:32338376-32338636	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr6:32321115-32321505	MCF10A-Er-Src	breast:	n/a	n/a
41	FOSL1	chr6:32337406-32337937	HCT-116	colon:	n/a	n/a
42	FOSL1	chr6:32341707-32342134	HCT-116	colon:	n/a	n/a
43	FOSL1	chr6:32341675-32342200	HCT-116	colon:	n/a	n/a
44	FOSL1	chr6:32337350-32338010	HCT-116	colon:	n/a	n/a
45	FOSL2	chr6:32337515-32337847	A549	lung:	n/a	n/a
46	FOSL2	chr6:32337424-32337907	SK-N-SH	brain:	n/a	n/a
47	FOSL2	chr6:32341780-32342110	A549	lung:	n/a	n/a
48	FOSL2	chr6:32337443-32337925	A549	lung:	n/a	n/a
49	FOSL2	chr6:32341699-32342222	A549	lung:	n/a	n/a
50	FOXA1	chr6:32341766-32342200	HepG2	liver:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32336160-32336210	CMK	blood:	n/a
2	chr6:32336160-32336210	CMK	blood:	n/a
3	chr6:32340208-32340258	HNPCEpiC	eye:	n/a
4	chr6:32326581-32326631	HEK293	kidney:	embryo
5	chr6:32337970-32338020	T-47D	breast:	n/a
6	chr6:32337970-32338020	HL-60	blood:	n/a
7	chr6:32330197-32330247	HepG2	liver:	n/a
8	chr6:32337906-32337956	NHDF-neo	bronchial:	n/a
9	chr6:32340354-32340404	IMR90	lung:	fetal
10	chr6:32337906-32337956	GM12892	blood:	n/a
11	chr6:32324878-32324928	NHDF-neo	bronchial:	n/a
12	chr6:32320708-32320758	SK-N-SH_RA	brain:	n/a
13	chr6:32339208-32339258	HCM	heart:	n/a
14	chr6:32326581-32326631	NB4	blood:	n/a
15	chr6:32335123-32335173	U87	brain:	n/a
16	chr6:32339208-32339258	NH-A	brain:	n/a
17	chr6:32340354-32340404	RPTEC	kidney:	n/a
18	chr6:32335123-32335173	GM12878	blood:	n/a
19	chr6:32340354-32340404	SAEC	small airway:	n/a
20	chr6:32320708-32320758	GM12891	blood:	n/a
21	chr6:32337930-32337980	HRPEpiC	eye:	n/a
22	chr6:32339208-32339258	AG04450	lung:	fetal
23	chr6:32339554-32339604	Jurkat	blood:	n/a
24	chr6:32330197-32330247	AG10803	skin:	n/a
25	chr6:32337906-32337956	IMR90	lung:	fetal
26	chr6:32339554-32339604	LNCaP	prostate:	n/a
27	chr6:32320715-32320765	HepG2	liver:	n/a
28	chr6:32329440-32329490	CMK	blood:	n/a
29	chr6:32320715-32320765	K562	blood:	n/a
30	chr6:32326581-32326631	Hepatocyte	liver:	n/a
31	chr6:32339208-32339258	HMEC	breast:	n/a
32	chr6:32335060-32335110	HCT-116	colon:	n/a
33	chr6:32326581-32326631	PFSK-1	brain:	n/a
34	chr6:32340354-32340404	HRPEpiC	eye:	n/a
35	chr6:32333231-32333281	NB4	blood:	n/a
36	chr6:32335123-32335173	SK-N-SH	brain:	n/a
37	chr6:32339208-32339258	HCF	heart:	n/a
38	chr6:32335060-32335110	CMK	blood:	n/a
39	chr6:32320715-32320765	Hela-S3	cervix:	n/a
40	chr6:32324878-32324928	SK-N-MC	brain:	n/a
41	chr6:32337970-32338020	Jurkat	blood:	n/a
42	chr6:32333231-32333281	GM12891	blood:	n/a
43	chr6:32339511-32339561	AG04449	skin:	fetal
44	chr6:32340955-32341005	A549	lung:	n/a
45	chr6:32340955-32341005	PANC-1	pancreas:	n/a
46	chr6:32330188-32330238	HAEpiC	amniotic membrane:	n/a
47	chr6:32324878-32324928	GM12891	blood:	n/a
48	chr6:32339511-32339561	Jurkat	blood:	n/a
49	chr6:32337970-32338020	H1-hESC	embryonic stem cell:	embryo
50	chr6:32330188-32330238	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:32340623..32343267-chr6:32371760..32373920,2	K562	blood:
2	chr6:32312156..32313758-chr6:32316689..32318846,2	MCF-7	breast:
3	chr6:32338535..32340842-chr6:32342130..32344081,2	K562	blood:
4	chr6:32341767..32343740-chr6:32372075..32373920,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-603P	TF binding region
C6orf10	TF binding region
RNU6-603P	CpG island
C6orf10	CpG island
ENSG00000204296	chromatin interactions

Extended variants
information (count: 1071 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:1071 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs761187	chr6:32318036-32318037	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181155795	chr6:32318052-32318053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139265273	chr6:32318120-32318121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144166679	chr6:32318123-32318124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528929160	chr6:32318170-32318171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564335232	chr6:32318269-32318270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78834018	chr6:32318284-32318285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562310652	chr6:32318325-32318326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376149166	chr6:32318337-32318338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs151003771	chr6:32318357-32318358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs377242131	chr6:32318365-32318366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114365500	chr6:32318384-32318385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566339401	chr6:32318387-32318388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140961206	chr6:32318406-32318407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549114115	chr6:32318430-32318431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559069428	chr6:32318539-32318540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3117119	chr6:32318610-32318611	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs12662503	chr6:32318644-32318645	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs2143463	chr6:32318729-32318730	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs112285143	chr6:32318747-32318748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186467048	chr6:32318770-32318771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188757604	chr6:32318771-32318772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539320560	chr6:32318831-32318832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113858268	chr6:32318847-32318848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572717853	chr6:32318935-32318936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149769381	chr6:32319011-32319012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561794644	chr6:32319017-32319018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs60863947	chr6:32319019-32319020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs80206624	chr6:32319084-32319085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73396965	chr6:32319122-32319123	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs186024225	chr6:32319141-32319142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs17208405	chr6:32319173-32319174	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs375568215	chr6:32319174-32319175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62405785	chr6:32319189-32319190	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs560014871	chr6:32319214-32319215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533752437	chr6:32319239-32319240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190881631	chr6:32319247-32319248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546241899	chr6:32319295-32319296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3117118	chr6:32319387-32319388	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs147712241	chr6:32319412-32319413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371150666	chr6:32319496-32319497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575778818	chr6:32319502-32319503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9268301	chr6:32319637-32319638	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
44	rs561138267	chr6:32319640-32319641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184007518	chr6:32319674-32319675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs59880608	chr6:32319798-32319799	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs554550910	chr6:32319840-32319841	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs572754489	chr6:32319908-32319909	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs536881854	chr6:32320112-32320113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3132963	chr6:32320153-32320154	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:125)

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
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	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
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
Ovarian cancer	21781307	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
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
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
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:32317800-32320800	Weak transcription	Hela-S3	cervix
2	chr6:32320800-32321800	Enhancers	Hela-S3	cervix
3	chr6:32320800-32322000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:32321800-32323000	Weak transcription	Hela-S3	cervix
5	chr6:32322000-32323200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:32322800-32323600	Enhancers	HUVEC	blood vessel
7	chr6:32323000-32323400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:32323000-32324200	Enhancers	Hela-S3	cervix
9	chr6:32323200-32324000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:32324200-32324600	Weak transcription	Hela-S3	cervix
11	chr6:32324600-32325600	Enhancers	Hela-S3	cervix
12	chr6:32325600-32332600	Weak transcription	Hela-S3	cervix
13	chr6:32332600-32332800	Enhancers	Hela-S3	cervix
14	chr6:32332800-32335800	Weak transcription	Hela-S3	cervix
15	chr6:32335800-32337800	Enhancers	Hela-S3	cervix
16	chr6:32336000-32339200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:32337200-32339000	Enhancers	HUVEC	blood vessel
18	chr6:32337400-32337800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr6:32337400-32338000	Enhancers	Osteobl	bone
20	chr6:32337400-32338200	Enhancers	A549	lung
21	chr6:32337400-32338200	Enhancers	NH-A	brain
22	chr6:32337400-32338800	Enhancers	NHDF-Ad	bronchial
23	chr6:32337400-32339000	Enhancers	HMEC	breast
24	chr6:32337400-32339400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:32337400-32339600	Enhancers	NHEK	skin
26	chr6:32337600-32337800	Enhancers	Small Intestine	intestine
27	chr6:32337600-32338400	Enhancers	Muscle Satellite Cultured Cells	--
28	chr6:32337800-32338200	Flanking Active TSS	Hela-S3	cervix
29	chr6:32337800-32338800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:32337800-32342000	Weak transcription	Small Intestine	intestine
31	chr6:32338200-32338600	Weak transcription	A549	lung
32	chr6:32338200-32338600	Weak transcription	NH-A	brain
33	chr6:32338200-32339800	Enhancers	Hela-S3	cervix
34	chr6:32338400-32338800	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr6:32338600-32339400	Enhancers	A549	lung
36	chr6:32338600-32339600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr6:32338600-32339600	Enhancers	NH-A	brain
38	chr6:32338800-32339200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr6:32339000-32339200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr6:32339000-32339400	Flanking Active TSS	HUVEC	blood vessel
41	chr6:32339400-32340000	Enhancers	HUVEC	blood vessel
42	chr6:32339400-32341000	Weak transcription	A549	lung
43	chr6:32341000-32342600	Enhancers	A549	lung
44	chr6:32341400-32343200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr6:32341400-32345000	Enhancers	Duodenum Mucosa	Duodenum
46	chr6:32341600-32342400	Enhancers	HepG2	liver
47	chr6:32341800-32342000	Enhancers	HUVEC	blood vessel
48	chr6:32341800-32343400	Weak transcription	Fetal Stomach	stomach
49	chr6:32342000-32342200	Enhancers	Small Intestine	intestine
50	chr6:32342000-32342400	Enhancers	Fetal Intestine Small	intestine

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