Variant report

Variant	esv3352859
Chromosome Location	chr6:13713873-13716971
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	chr6:13715820-13716305	HepG2	liver:	n/a	n/a
2	ATF2	chr6:13715428-13716029	GM12878	blood:	n/a	n/a
3	ATF2	chr6:13715445-13716093	GM12878	blood:	n/a	n/a
4	BATF	chr6:13715475-13716015	GM12878	blood:	n/a	n/a
5	BATF	chr6:13715519-13715903	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:13715591-13715843	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:13715520-13715967	GM12878	blood:	n/a	n/a
8	CBX3	chr6:13715701-13716148	K562	blood:	n/a	n/a
9	CBX3	chr6:13716704-13717035	K562	blood:	n/a	n/a
10	CEBPB	chr6:13715724-13716278	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:13715714-13716319	HepG2	liver:	n/a	n/a
12	CEBPB	chr6:13715791-13716162	K562	blood:	n/a	n/a
13	CHD2	chr6:13715789-13715989	HepG2	liver:	n/a	n/a
14	CUX1	chr6:13714012-13714081	K562	blood:	n/a	n/a
15	E2F4	chr6:13715894-13716131	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr6:13715534-13716063	GM12878	blood:	n/a	n/a
17	EBF1	chr6:13715643-13716010	GM12878	blood:	n/a	n/a
18	ELF1	chr6:13715770-13716086	HepG2	liver:	n/a	n/a
19	ELF1	chr6:13715720-13716165	HepG2	liver:	n/a	n/a
20	EP300	chr6:13715788-13716089	HepG2	liver:	n/a	n/a
21	EP300	chr6:13715744-13716351	HepG2	liver:	n/a	n/a
22	EP300	chr6:13715630-13715881	GM12878	blood:	n/a	n/a
23	EP300	chr6:13715766-13716239	HepG2	liver:	n/a	n/a
24	EP300	chr6:13715672-13715790	GM12878	blood:	n/a	n/a
25	FOS	chr6:13715809-13716230	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr6:13715778-13716291	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr6:13715809-13716510	MCF10A-Er-Src	breast:	n/a	chr6:13716430-13716442
28	FOS	chr6:13715773-13716305	MCF10A-Er-Src	breast:	n/a	n/a
29	FOSL2	chr6:13715718-13716297	HepG2	liver:	n/a	chr6:13715987-13715998
30	FOSL2	chr6:13715689-13716241	HepG2	liver:	n/a	chr6:13715987-13715998
31	FOXA1	chr6:13715829-13716438	HepG2	liver:	n/a	n/a
32	FOXA2	chr6:13715850-13716388	HepG2	liver:	n/a	n/a
33	FOXM1	chr6:13715489-13715987	GM12878	blood:	n/a	n/a
34	GATA3	chr6:13713885-13714176	SH-SY5Y	brain:	n/a	chr6:13714130-13714151 chr6:13714134-13714144
35	IKZF1	chr6:13715425-13715999	GM12878	blood:	n/a	n/a
36	IRF1	chr6:13715952-13715963	K562	blood:	n/a	n/a
37	IRF4	chr6:13715539-13716009	GM12878	blood:	n/a	n/a
38	IRF4	chr6:13715475-13716028	GM12878	blood:	n/a	n/a
39	JUN	chr6:13715855-13716271	HepG2	liver:	n/a	n/a
40	JUND	chr6:13715794-13716200	HepG2	liver:	n/a	chr6:13715986-13715997
41	JUND	chr6:13715828-13716180	K562	blood:	n/a	chr6:13715986-13715997
42	JUND	chr6:13715813-13716245	HepG2	liver:	n/a	chr6:13715986-13715997
43	MAFF	chr6:13716492-13716783	K562	blood:	n/a	chr6:13716650-13716668
44	MAFF	chr6:13715754-13716199	HepG2	liver:	n/a	n/a
45	MAFF	chr6:13716469-13716819	HepG2	liver:	n/a	chr6:13716650-13716668
46	MAFK	chr6:13716469-13716832	HepG2	liver:	n/a	chr6:13716646-13716666 chr6:13716655-13716666 chr6:13716656-13716667 chr6:13716547-13716561 chr6:13716651-13716666 chr6:13716656-13716667 chr6:13716549-13716560 chr6:13716655-13716666 chr6:13716651-13716667 chr6:13716654-13716668
47	MAFK	chr6:13715721-13716174	HepG2	liver:	n/a	n/a
48	MAFK	chr6:13716478-13716826	HepG2	liver:	n/a	chr6:13716646-13716666 chr6:13716655-13716666 chr6:13716656-13716667 chr6:13716547-13716561 chr6:13716651-13716666 chr6:13716656-13716667 chr6:13716549-13716560 chr6:13716655-13716666 chr6:13716651-13716667 chr6:13716654-13716668
49	MAFK	chr6:13716494-13716823	IMR90	lung:	n/a	chr6:13716646-13716666 chr6:13716655-13716666 chr6:13716656-13716667 chr6:13716547-13716561 chr6:13716651-13716666 chr6:13716656-13716667 chr6:13716549-13716560 chr6:13716655-13716666 chr6:13716651-13716667 chr6:13716654-13716668
50	MAFK	chr6:13716492-13716816	K562	blood:	n/a	chr6:13716646-13716666 chr6:13716655-13716666 chr6:13716656-13716667 chr6:13716547-13716561 chr6:13716651-13716666 chr6:13716656-13716667 chr6:13716549-13716560 chr6:13716655-13716666 chr6:13716651-13716667 chr6:13716654-13716668

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:13715593-13715643	AG10803	skin:	n/a
2	chr6:13715593-13715643	PANC-1	pancreas:	n/a
3	chr6:13715593-13715643	A549	lung:	n/a
4	chr6:13715593-13715643	HCF	heart:	n/a
5	chr6:13715593-13715643	HRCEpiC	kidney:	n/a
6	chr6:13715593-13715643	MCF10A-Er-Src	breast:	n/a
7	chr6:13715593-13715643	AG04450	lung:	fetal
8	chr6:13715593-13715643	HEEpiC	esophagus:	n/a
9	chr6:13715593-13715643	HepG2	liver:	n/a
10	chr6:13715593-13715643	Caco-2	colon:	n/a
11	chr6:13715593-13715643	HEK293	kidney:	embryo
12	chr6:13715593-13715643	HNPCEpiC	eye:	n/a
13	chr6:13715593-13715643	H1-hESC	embryonic stem cell:	embryo
14	chr6:13715593-13715643	CMK	blood:	n/a
15	chr6:13715593-13715643	HAEpiC	amniotic membrane:	n/a
16	chr6:13715593-13715643	SK-N-MC	brain:	n/a
17	chr6:13715593-13715643	PrEC	prostate:	n/a
18	chr6:13715593-13715643	GM06990	blood:	n/a
19	chr6:13715593-13715643	K562	blood:	n/a
20	chr6:13715593-13715643	SKMC	muscle:	n/a
21	chr6:13715593-13715643	LNCaP	prostate:	n/a
22	chr6:13715593-13715643	GM12878	blood:	n/a
23	chr6:13715593-13715643	IMR90	lung:	fetal
24	chr6:13715593-13715643	Jurkat	blood:	n/a
25	chr6:13715593-13715643	HMEC	breast:	n/a
26	chr6:13715593-13715643	HRPEpiC	eye:	n/a
27	chr6:13715593-13715643	AG09319	gingival:	n/a
28	chr6:13715593-13715643	GM12891	blood:	n/a
29	chr6:13715593-13715643	SK-N-SH_RA	brain:	n/a
30	chr6:13715593-13715643	HRE	kidney:	n/a
31	chr6:13715593-13715643	NHDF-neo	bronchial:	n/a
32	chr6:13715593-13715643	GM19239	blood:	n/a
33	chr6:13715593-13715643	NHBE	bronchial:	n/a
34	chr6:13715593-13715643	ECC-1	luminal epithelium:	n/a
35	chr6:13715593-13715643	PFSK-1	brain:	n/a
36	chr6:13715593-13715643	HCPEpiC	choroid plexus:	n/a
37	chr6:13715593-13715643	HIPEpiC	eye:	n/a
38	chr6:13715593-13715643	NB4	blood:	n/a
39	chr6:13715593-13715643	BJ	skin:	n/a
40	chr6:13715593-13715643	BE2_C	brain:	n/a
41	chr6:13715593-13715643	AG09309	skin:	n/a
42	chr6:13715593-13715643	ovcar-3	ovarian:	n/a
43	chr6:13715593-13715643	Hepatocyte	liver:	n/a
44	chr6:13715593-13715643	U87	brain:	n/a
45	chr6:13715593-13715643	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:13715593-13715643	HCT-116	colon:	n/a
47	chr6:13715593-13715643	NT2-D1	testis:	n/a
48	chr6:13715593-13715643	NH-A	brain:	n/a
49	chr6:13715593-13715643	SAEC	small airway:	n/a
50	chr6:13715593-13715643	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:13709898..13716469-chr6:13809605..13815390,11	K562	blood:
2	chr6:13703743..13705757-chr6:13712344..13714353,2	MCF-7	breast:
3	chr6:13667308..13669773-chr6:13712805..13714594,2	K562	blood:
4	chr6:13658437..13687167-chr6:13707669..13717356,51	K562	blood:
5	chr6:13712294..13715235-chr6:13734842..13736345,2	K562	blood:
6	chr6:13614005..13616960-chr6:13716595..13718707,2	MCF-7	breast:
7	chr6:13712562..13715550-chr6:13731027..13734094,5	K562	blood:
8	chr6:13712256..13714398-chr6:13725384..13727195,2	MCF-7	breast:
9	chr6:13713710..13717343-chr6:13751875..13754798,3	MCF-7	breast:
10	chr6:13710420..13715821-chr6:13716871..13724473,13	MCF-7	breast:
11	chr6:13613655..13618769-chr6:13709987..13714197,10	MCF-7	breast:
12	chr6:13712160..13713873-chr6:13816640..13818344,2	K562	blood:
13	chr6:13659651..13661542-chr6:13715805..13717920,2	MCF-7	breast:
14	chr6:13613792..13617654-chr6:13711804..13714048,3	K562	blood:
15	chr6:13710738..13712943-chr6:13714753..13716732,2	MCF-7	breast:
16	chr6:13711887..13713957-chr6:13747635..13751147,3	K562	blood:
17	chr6:13615378..13616963-chr6:13714230..13716669,2	K562	blood:
18	chr6:13677099..13683232-chr6:13708060..13717356,16	K562	blood:
19	chr6:13711847..13714774-chr6:13741208..13742857,2	K562	blood:

Variant related genes	Relation type
RANBP9	TF binding region
RANBP9	CpG island
ENSG00000010017	chromatin interactions
ENSG00000261071	chromatin interactions
ENSG00000252966	chromatin interactions
ENSG00000225921	chromatin interactions
ENSG00000233075	chromatin interactions
ENSG00000050393	chromatin interactions

Extended variants
information (count: 130 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:130 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190031746	chr6:13713898-13713899	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs181108354	chr6:13713973-13713974	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs562080301	chr6:13713979-13713980	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs185997180	chr6:13714010-13714011	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs143085253	chr6:13714021-13714022	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs190358055	chr6:13714031-13714032	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs532488350	chr6:13714070-13714071	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs115263797	chr6:13714071-13714072	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs565773464	chr6:13714118-13714119	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs3757255	chr6:13714190-13714191	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs554392184	chr6:13714236-13714237	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs557638581	chr6:13714262-13714263	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs536658653	chr6:13714277-13714278	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs183352307	chr6:13714301-13714302	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs187193879	chr6:13714312-13714313	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs570695261	chr6:13714316-13714317	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs546209683	chr6:13714340-13714341	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs554633638	chr6:13714355-13714356	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs553515247	chr6:13714365-13714366	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs190807899	chr6:13714377-13714378	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs116714728	chr6:13714393-13714394	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs550246351	chr6:13714478-13714479	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs574197824	chr6:13714480-13714481	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs396869	chr6:13714482-13714483	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs544605765	chr6:13714484-13714485	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs373009539	chr6:13714491-13714492	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs183001269	chr6:13714651-13714652	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs532412288	chr6:13714674-13714675	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs552206017	chr6:13714717-13714718	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs559473346	chr6:13714768-13714769	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs148182023	chr6:13714788-13714789	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs555443767	chr6:13714853-13714854	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs187594263	chr6:13714861-13714862	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs191880125	chr6:13714879-13714880	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs536799217	chr6:13714889-13714890	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs182625769	chr6:13714948-13714949	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs187578153	chr6:13714979-13714980	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs141150391	chr6:13715102-13715103	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs553412343	chr6:13715109-13715110	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs573338597	chr6:13715116-13715117	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs539669726	chr6:13715161-13715162	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs78023392	chr6:13715165-13715166	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs556034697	chr6:13715167-13715168	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs146195110	chr6:13715168-13715169	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs558525131	chr6:13715186-13715187	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs192050333	chr6:13715260-13715261	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs24023	chr6:13715303-13715304	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs536843166	chr6:13715363-13715364	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs117932725	chr6:13715394-13715395	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs559399057	chr6:13715413-13715414	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
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
small cell lung cancer	20016488	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
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13712800-13715600	Weak transcription	Esophagus	oesophagus
2	chr6:13712800-13715600	Weak transcription	Gastric	stomach
3	chr6:13712800-13716800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:13712800-13717000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:13713000-13716600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:13713200-13714000	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr6:13713200-13714000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr6:13713200-13714000	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr6:13713200-13714200	Enhancers	Colon Smooth Muscle	Colon
10	chr6:13713200-13715000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr6:13713200-13715200	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr6:13713200-13715400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr6:13713200-13715400	Enhancers	Fetal Heart	heart
14	chr6:13713200-13716400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr6:13713400-13714000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr6:13713400-13714000	Enhancers	Dnd41	blood
17	chr6:13713400-13715600	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr6:13713400-13715800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:13713600-13715000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr6:13713600-13715000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr6:13713600-13715200	Weak transcription	GM12878-XiMat	blood
22	chr6:13713600-13715400	Weak transcription	HepG2	liver
23	chr6:13713600-13715600	Weak transcription	K562	blood
24	chr6:13713600-13715800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr6:13713600-13716000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr6:13713600-13717200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr6:13713800-13714000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr6:13713800-13715600	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr6:13713800-13716000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr6:13714000-13715800	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr6:13714000-13718000	Weak transcription	Dnd41	blood
32	chr6:13714000-13722800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr6:13714000-13723400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr6:13715000-13716400	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr6:13715000-13716600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr6:13715000-13717000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr6:13715200-13716200	Enhancers	GM12878-XiMat	blood
38	chr6:13715200-13716200	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr6:13715400-13716800	Enhancers	HepG2	liver
40	chr6:13715600-13716000	Enhancers	Primary T cells fromperipheralblood	blood
41	chr6:13715600-13716000	Enhancers	Esophagus	oesophagus
42	chr6:13715600-13716200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr6:13715600-13716200	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr6:13715600-13716200	Enhancers	K562	blood
45	chr6:13715800-13716000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr6:13715800-13716000	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr6:13715800-13716200	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr6:13716000-13716200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr6:13716000-13716200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr6:13716000-13717200	Weak transcription	Esophagus	oesophagus

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