Variant report

Variant	nsv1025553
Chromosome Location	chr6:210077-266046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1870)
CpG islands
(count:732)
Chromatin interactive
region (count:24)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1870 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:221474-221994	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:220004-220874	HepG2	liver:	n/a	n/a
3	ATF1	chr6:232965-233203	K562	blood:	n/a	n/a
4	ATF1	chr6:246458-246690	K562	blood:	n/a	n/a
5	ATF2	chr6:209691-210220	GM12878	blood:	n/a	n/a
6	ATF2	chr6:231354-232300	GM12878	blood:	n/a	n/a
7	ATF2	chr6:250576-251222	GM12878	blood:	n/a	n/a
8	ATF2	chr6:235849-236489	GM12878	blood:	n/a	n/a
9	ATF2	chr6:220648-222383	GM12878	blood:	n/a	n/a
10	ATF2	chr6:235845-236520	GM12878	blood:	n/a	n/a
11	ATF2	chr6:217063-217455	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr6:230263-230821	GM12878	blood:	n/a	n/a
13	ATF2	chr6:209433-210258	GM12878	blood:	n/a	n/a
14	ATF2	chr6:259642-260384	GM12878	blood:	n/a	n/a
15	ATF2	chr6:216952-217397	GM12878	blood:	n/a	n/a
16	ATF2	chr6:226477-229964	GM12878	blood:	n/a	n/a
17	ATF2	chr6:250519-251229	GM12878	blood:	n/a	n/a
18	ATF2	chr6:226748-228552	GM12878	blood:	n/a	n/a
19	ATF2	chr6:230249-231059	GM12878	blood:	n/a	n/a
20	ATF2	chr6:221081-222611	GM12878	blood:	n/a	n/a
21	ATF2	chr6:224802-226028	GM12878	blood:	n/a	n/a
22	ATF2	chr6:259708-260417	GM12878	blood:	n/a	n/a
23	ATF2	chr6:251841-252484	GM12878	blood:	n/a	n/a
24	ATF2	chr6:231396-232311	GM12878	blood:	n/a	n/a
25	ATF2	chr6:217880-219360	GM12878	blood:	n/a	n/a
26	ATF2	chr6:252707-253298	GM12878	blood:	n/a	n/a
27	ATF2	chr6:224893-225951	GM12878	blood:	n/a	n/a
28	ATF2	chr6:216810-217515	GM12878	blood:	n/a	n/a
29	ATF2	chr6:217828-219955	GM12878	blood:	n/a	n/a
30	ATF2	chr6:228803-229965	GM12878	blood:	n/a	n/a
31	ATF3	chr6:219928-220235	K562	blood:	n/a	n/a
32	BACH1	chr6:219988-220177	K562	blood:	n/a	chr6:220124-220138
33	BACH1	chr6:220702-221015	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:219912-220319	H1-hESC	embryonic stem cell:	n/a	chr6:220124-220138
35	BATF	chr6:235892-236368	GM12878	blood:	n/a	n/a
36	BATF	chr6:231671-232067	GM12878	blood:	n/a	n/a
37	BATF	chr6:253185-253459	GM12878	blood:	n/a	chr6:253319-253330
38	BATF	chr6:230393-230768	GM12878	blood:	n/a	n/a
39	BATF	chr6:228992-229816	GM12878	blood:	n/a	n/a
40	BATF	chr6:209735-210135	GM12878	blood:	n/a	n/a
41	BATF	chr6:228909-229827	GM12878	blood:	n/a	n/a
42	BATF	chr6:224948-225808	GM12878	blood:	n/a	n/a
43	BATF	chr6:235921-236302	GM12878	blood:	n/a	n/a
44	BATF	chr6:217000-217388	GM12878	blood:	n/a	n/a
45	BATF	chr6:230389-230679	GM12878	blood:	n/a	n/a
46	BATF	chr6:250687-251007	GM12878	blood:	n/a	n/a
47	BATF	chr6:221656-222204	GM12878	blood:	n/a	chr6:221879-221890
48	BATF	chr6:218090-218656	GM12878	blood:	n/a	n/a
49	BATF	chr6:255760-256053	GM12878	blood:	n/a	n/a
50	BATF	chr6:251891-252302	GM12878	blood:	n/a	chr6:252121-252132

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:236559-236609	HCM	heart:	n/a
2	chr6:236559-236609	NT2-D1	testis:	n/a
3	chr6:230959-231009	GM06990	blood:	n/a
4	chr6:236559-236609	GM12878	blood:	n/a
5	chr6:225666-225716	RPTEC	kidney:	n/a
6	chr6:224339-224389	IMR90	lung:	fetal
7	chr6:236559-236609	HRPEpiC	eye:	n/a
8	chr6:224713-224763	T-47D	breast:	n/a
9	chr6:230932-230982	HEEpiC	esophagus:	n/a
10	chr6:236559-236609	AoSMC	blood vessel:	n/a
11	chr6:230908-230958	MCF10A-Er-Src	breast:	n/a
12	chr6:225666-225716	Caco-2	colon:	n/a
13	chr6:226092-226142	ovcar-3	ovarian:	n/a
14	chr6:236559-236609	ovcar-3	ovarian:	n/a
15	chr6:225824-225874	AG10803	skin:	n/a
16	chr6:225824-225874	HCT-116	colon:	n/a
17	chr6:224713-224763	MCF-7	breast:	n/a
18	chr6:230908-230958	HCM	heart:	n/a
19	chr6:236559-236609	HCPEpiC	choroid plexus:	n/a
20	chr6:225824-225874	Jurkat	blood:	n/a
21	chr6:225666-225716	HEEpiC	esophagus:	n/a
22	chr6:220928-220978	HCT-116	colon:	n/a
23	chr6:224713-224763	ovcar-3	ovarian:	n/a
24	chr6:224713-224763	HCF	heart:	n/a
25	chr6:224339-224389	AoSMC	blood vessel:	n/a
26	chr6:230959-231009	HEEpiC	esophagus:	n/a
27	chr6:224339-224389	GM19239	blood:	n/a
28	chr6:225666-225716	HCF	heart:	n/a
29	chr6:220928-220978	K562	blood:	n/a
30	chr6:236559-236609	HepG2	liver:	n/a
31	chr6:230908-230958	HUVEC	blood vessel:	n/a
32	chr6:235035-235085	HRE	kidney:	n/a
33	chr6:230932-230982	LNCaP	prostate:	n/a
34	chr6:230932-230982	Hela-S3	cervix:	n/a
35	chr6:224713-224763	SAEC	small airway:	n/a
36	chr6:220928-220978	SK-N-MC	brain:	n/a
37	chr6:236559-236609	HIPEpiC	eye:	n/a
38	chr6:230959-231009	NT2-D1	testis:	n/a
39	chr6:224339-224389	HNPCEpiC	eye:	n/a
40	chr6:224339-224389	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:225824-225874	HAEpiC	amniotic membrane:	n/a
42	chr6:226092-226142	GM12892	blood:	n/a
43	chr6:220928-220978	AG09309	skin:	n/a
44	chr6:230932-230982	HL-60	blood:	n/a
45	chr6:235035-235085	HCF	heart:	n/a
46	chr6:220928-220978	Jurkat	blood:	n/a
47	chr6:224733-224783	BE2_C	brain:	n/a
48	chr6:225666-225716	NH-A	brain:	n/a
49	chr6:230959-231009	HL-60	blood:	n/a
50	chr6:230932-230982	GM12892	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:215085..218653-chr6:219608..222374,3	K562	blood:
2	chr6:204380..207081-chr6:218001..219962,2	K562	blood:
3	chr6:217782..221161-chr6:291544..295345,3	MCF-7	breast:
4	chr6:226916..227829-chr6:408545..409059,2	K562	blood:
5	chr6:215085..218653-chr6:219608..222374,3	K562	blood:
6	chr6:221469..223469-chr6:224100..226474,2	K562	blood:
7	chr6:221194..223469-chr6:223525..225600,3	K562	blood:
8	chr6:257151..259180-chr6:290748..292745,2	MCF-7	breast:
9	chr6:221194..223469-chr6:223525..225600,3	K562	blood:
10	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
11	chr6:256291..258797-chr6:266153..268904,2	K562	blood:
12	chr6:228323..230023-chr6:368553..371061,2	K562	blood:
13	chr6:215135..217089-chr6:292102..293904,2	MCF-7	breast:
14	chr6:226271..228027-chr6:231480..233250,2	K562	blood:
15	chr6:264177..266345-chr6:291888..293660,2	MCF-7	breast:
16	chr6:256291..259560-chr6:266153..268904,3	K562	blood:
17	chr6:226271..228027-chr6:231480..233250,2	K562	blood:
18	chr6:201924..204091-chr6:207759..211489,3	K562	blood:
19	chr6:218667..220722-chr6:290754..293697,2	MCF-7	breast:
20	chr6:257661..259747-chr6:263345..265684,2	K562	blood:
21	chr6:216802..217456-chr6:1436640..1437220,2	K562	blood:
22	chr6:230872..233357-chr6:348225..349996,2	K562	blood:
23	chr6:217204..217743-chr6:408573..409085,2	K562	blood:
24	chr6:221469..223469-chr6:224100..226474,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOC2-17	chr6:222864-223155	l_3086_chr6:222863-230359_lymphNode
2	lnc-AL035696.1-3	chr6:225686-226068	XLOC_005118
3	lnc-EXOC2-17	chr6:230321-230359	l_3086_chr6:222863-230359_lymphNode
4	lnc-AL035696.1-3	chr6:226079-226400	XLOC_005118
5	lnc-AL035696.1-3	chr6:224950-225088	XLOC_005118

No data

Variant related genes	Relation type
ENSG00000263667	TF binding region
ENSG00000263667	CpG island
ENSG00000112679	chromatin interactions
ENSG00000205653	chromatin interactions
ENSG00000263667	chromatin interactions

Extended variants
information (count: 2644 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2644 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534253590	chr6:210113-210114	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs553155608	chr6:210114-210115	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs542922464	chr6:210193-210194	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs560113825	chr6:210210-210211	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs148657353	chr6:210213-210214	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs189110309	chr6:210256-210257	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs564170876	chr6:210315-210316	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs202060396	chr6:210322-210323	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs367633597	chr6:210323-210324	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs533012946	chr6:210360-210361	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs80067053	chr6:210389-210390	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs569517494	chr6:210401-210402	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs535455539	chr6:210403-210404	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs375487114	chr6:210421-210422	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs548984325	chr6:210450-210451	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs143395249	chr6:210463-210464	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs534506336	chr6:210466-210467	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs565077976	chr6:210542-210543	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs193041499	chr6:210577-210578	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs146744581	chr6:210579-210580	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs183769683	chr6:210588-210589	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs74691055	chr6:210623-210624	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573928006	chr6:210630-210631	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543038877	chr6:210653-210654	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575145461	chr6:210656-210657	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75465367	chr6:210660-210661	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368831802	chr6:210664-210665	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140411000	chr6:210689-210690	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144175708	chr6:210697-210698	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs532230669	chr6:210706-210707	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531153591	chr6:210790-210791	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs9502968	chr6:210815-210816	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs71548189	chr6:210832-210833	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs146421210	chr6:210835-210836	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs71548190	chr6:210836-210837	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs372136323	chr6:210893-210894	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs375506872	chr6:210903-210904	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111408476	chr6:210911-210912	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs9392309	chr6:210917-210918	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs551277142	chr6:210945-210946	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs571080300	chr6:211010-211011	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187456220	chr6:211047-211048	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs140739405	chr6:211147-211148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs60181389	chr6:211182-211183	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs200884935	chr6:211183-211184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs191926927	chr6:211213-211214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs17133783	chr6:211215-211216	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs538501425	chr6:211290-211291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs75292070	chr6:211315-211316	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545685163	chr6:211346-211347	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Prader-willi syndrome	20588305	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495311	CNVD
small cell lung cancer	20016488	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:934 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:196800-211800	Weak transcription	Right Atrium	heart
2	chr6:208800-210400	Flanking Active TSS	GM12878-XiMat	blood
3	chr6:209000-210200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr6:209200-210400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
5	chr6:209400-210200	Active TSS	Primary T helper naive cells from peripheral blood	blood
6	chr6:209400-210200	Active TSS	Colonic Mucosa	Colon
7	chr6:209400-210200	Active TSS	Duodenum Mucosa	Duodenum
8	chr6:209600-210200	Flanking Active TSS	Primary B cells from peripheral blood	blood
9	chr6:209600-210200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
10	chr6:209600-210200	Active TSS	Primary T helper cells fromperipheralblood	blood
11	chr6:209600-210200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
12	chr6:209600-210200	Active TSS	Primary T killer memory cells from peripheral blood	blood
13	chr6:209600-210200	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr6:209600-211000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:209800-210200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
16	chr6:209800-210800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:210000-210200	Active TSS	Primary T helper cells PMA-I stimulated	--
18	chr6:210000-210400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
19	chr6:210000-210400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
20	chr6:210000-210400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr6:210000-210600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr6:210200-210400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr6:210200-210400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
24	chr6:210200-210400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
25	chr6:210200-210400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr6:210200-210400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr6:210200-210400	Enhancers	Esophagus	oesophagus
28	chr6:210200-210600	Enhancers	Primary B cells from peripheral blood	blood
29	chr6:210200-210600	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr6:210200-210600	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr6:210400-210600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr6:210400-210600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr6:210400-210800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr6:210400-211000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr6:210400-211800	Weak transcription	Esophagus	oesophagus
36	chr6:210400-213600	Enhancers	GM12878-XiMat	blood
37	chr6:210400-215200	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr6:210600-215400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr6:210600-215400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr6:210800-211000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:210800-211000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr6:210800-215400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:211000-211800	Enhancers	Fetal Thymus	thymus
44	chr6:211200-211400	Enhancers	Brain Substantia Nigra	brain
45	chr6:211400-211600	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr6:211400-212000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
47	chr6:211400-212200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
48	chr6:211600-211800	Enhancers	Brain Substantia Nigra	brain
49	chr6:211600-212000	Bivalent Enhancer	Brain Hippocampus Middle	brain
50	chr6:211600-212000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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