Variant report

Variant	esv2763548
Chromosome Location	chr6:33496201-33524779
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:297)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:33505986-33506047	K562	blood:	n/a	n/a
2	ATF2	chr6:33524650-33525045	GM12878	blood:	n/a	n/a
3	ATF2	chr6:33524534-33525041	GM12878	blood:	n/a	n/a
4	BATF	chr6:33524632-33525042	GM12878	blood:	n/a	chr6:33524830-33524841
5	BATF	chr6:33507961-33508146	GM12878	blood:	n/a	chr6:33508060-33508071
6	BATF	chr6:33524682-33524969	GM12878	blood:	n/a	chr6:33524830-33524841
7	BCL11A	chr6:33524690-33524969	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:33524554-33525001	GM12878	blood:	n/a	n/a
9	BCL3	chr6:33507290-33507657	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:33524661-33525119	GM12878	blood:	n/a	n/a
11	BCLAF1	chr6:33524623-33525016	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:33524697-33525135	GM12878	blood:	n/a	n/a
13	CEBPB	chr6:33502527-33502711	K562	blood:	n/a	chr6:33502571-33502582
14	CEBPB	chr6:33519414-33519654	HepG2	liver:	n/a	chr6:33519497-33519508
15	CEBPB	chr6:33499797-33500036	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr6:33502466-33502692	A549	lung:	n/a	chr6:33502571-33502582
17	CEBPB	chr6:33519451-33519543	H1-hESC	embryonic stem cell:	n/a	chr6:33519497-33519508
18	CEBPB	chr6:33520785-33520890	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:33520666-33521078	MCF-7	breast:	n/a	n/a
20	CEBPB	chr6:33524568-33525165	GM12878	blood:	n/a	n/a
21	CEBPB	chr6:33514598-33514637	K562	blood:	n/a	n/a
22	CEBPB	chr6:33502456-33502701	HepG2	liver:	n/a	chr6:33502571-33502582
23	CEBPB	chr6:33520754-33520895	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr6:33507674-33507854	K562	blood:	n/a	n/a
25	CEBPB	chr6:33499777-33500000	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:33518917-33518921	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr6:33498944-33498955	K562	blood:	n/a	n/a
28	CEBPB	chr6:33517831-33518035	K562	blood:	n/a	n/a
29	CHD2	chr6:33524661-33525001	GM12878	blood:	n/a	n/a
30	CREB1	chr6:33524691-33525121	GM12878	blood:	n/a	n/a
31	CREB1	chr6:33524515-33525068	GM12878	blood:	n/a	n/a
32	CTCF	chr6:33503052-33503099	GM12878	blood:	n/a	n/a
33	CTCF	chr6:33502920-33503070	HCM	heart:	n/a	n/a
34	CTCF	chr6:33502995-33503198	K562	blood:	n/a	n/a
35	CTCF	chr6:33503043-33503104	GM19240	blood:	n/a	n/a
36	CTCF	chr6:33503079-33503099	IMR90	lung:	n/a	n/a
37	CTCF	chr6:33502992-33503100	LNCaP	prostate:	n/a	n/a
38	CTCF	chr6:33502960-33503110	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:33507740-33507890	GM12874	blood:	n/a	n/a
40	CTCF	chr6:33503023-33503151	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:33503020-33503170	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr6:33503020-33503154	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:33503019-33503108	HepG2	liver:	n/a	n/a
44	CTCF	chr6:33503030-33503096	GM19238	blood:	n/a	n/a
45	CTCF	chr6:33503009-33503133	K562	blood:	n/a	n/a
46	CTCF	chr6:33502900-33503200	K562	blood:	n/a	n/a
47	CTCF	chr6:33502988-33503175	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:33502960-33503110	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr6:33496500-33496650	HEK293	kidney:	n/a	n/a
50	CTCF	chr6:33503002-33503152	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33501379-33501429	ovcar-3	ovarian:	n/a
2	chr6:33501379-33501429	GM06990	blood:	n/a
3	chr6:33500486-33500536	AG09319	gingival:	n/a
4	chr6:33500486-33500536	NT2-D1	testis:	n/a
5	chr6:33500486-33500536	ECC-1	luminal epithelium:	n/a
6	chr6:33501379-33501429	HEK293	kidney:	embryo
7	chr6:33500486-33500536	GM12878	blood:	n/a
8	chr6:33500486-33500536	AG10803	skin:	n/a
9	chr6:33501379-33501429	AG04450	lung:	fetal
10	chr6:33501379-33501429	NH-A	brain:	n/a
11	chr6:33500486-33500536	GM12892	blood:	n/a
12	chr6:33501379-33501429	SK-N-SH	brain:	n/a
13	chr6:33500486-33500536	LNCaP	prostate:	n/a
14	chr6:33500486-33500536	IMR90	lung:	fetal
15	chr6:33501379-33501429	HRCEpiC	kidney:	n/a
16	chr6:33501379-33501429	GM12892	blood:	n/a
17	chr6:33500486-33500536	SAEC	small airway:	n/a
18	chr6:33500486-33500536	MCF-7	breast:	n/a
19	chr6:33500486-33500536	HEEpiC	esophagus:	n/a
20	chr6:33500486-33500536	BE2_C	brain:	n/a
21	chr6:33500486-33500536	Jurkat	blood:	n/a
22	chr6:33500486-33500536	PrEC	prostate:	n/a
23	chr6:33501379-33501429	ProgFib	skin:	n/a
24	chr6:33500486-33500536	AoSMC	blood vessel:	n/a
25	chr6:33501379-33501429	GM12878	blood:	n/a
26	chr6:33501379-33501429	PFSK-1	brain:	n/a
27	chr6:33500486-33500536	Hela-S3	cervix:	n/a
28	chr6:33500486-33500536	NB4	blood:	n/a
29	chr6:33500486-33500536	MCF10A-Er-Src	breast:	n/a
30	chr6:33501379-33501429	HAEpiC	amniotic membrane:	n/a
31	chr6:33500486-33500536	SKMC	muscle:	n/a
32	chr6:33501379-33501429	LNCaP	prostate:	n/a
33	chr6:33500486-33500536	HEK293	kidney:	embryo
34	chr6:33500486-33500536	HepG2	liver:	n/a
35	chr6:33500486-33500536	RPTEC	kidney:	n/a
36	chr6:33500486-33500536	CMK	blood:	n/a
37	chr6:33501379-33501429	HRPEpiC	eye:	n/a
38	chr6:33501379-33501429	NT2-D1	testis:	n/a
39	chr6:33501379-33501429	H1-hESC	embryonic stem cell:	embryo
40	chr6:33501379-33501429	MCF-7	breast:	n/a
41	chr6:33501379-33501429	ECC-1	luminal epithelium:	n/a
42	chr6:33500486-33500536	HMEC	breast:	n/a
43	chr6:33501379-33501429	HMEC	breast:	n/a
44	chr6:33500486-33500536	HIPEpiC	eye:	n/a
45	chr6:33501379-33501429	HCF	heart:	n/a
46	chr6:33500486-33500536	HCF	heart:	n/a
47	chr6:33500486-33500536	HAEpiC	amniotic membrane:	n/a
48	chr6:33501379-33501429	T-47D	breast:	n/a
49	chr6:33500486-33500536	ovcar-3	ovarian:	n/a
50	chr6:33501379-33501429	HNPCEpiC	eye:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33385003..33387538-chr6:33494085..33496852,2	K562	blood:
2	chr6:33265668..33268001-chr6:33494684..33497652,2	MCF-7	breast:
3	chr6:33517814..33520773-chr6:33534546..33536789,2	K562	blood:
4	chr6:33521966..33523890-chr6:33538624..33540317,3	MCF-7	breast:
5	chr6:33510727..33512644-chr6:33523375..33526015,2	MCF-7	breast:
6	chr6:33511493..33513337-chr6:33513833..33516085,2	K562	blood:
7	chr6:33511493..33513337-chr6:33513833..33516085,2	K562	blood:
8	chr6:33507165..33509178-chr6:33510190..33512427,2	MCF-7	breast:
9	chr6:33419305..33423714-chr6:33512758..33516549,4	MCF-7	breast:
10	chr6:33510727..33512644-chr6:33523375..33526015,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GGNBP1-5	chr6:33524549-33524840	expReg_chr6_3652_+
2	lnc-GGNBP1-6	chr6:33517527-33517951	NONHSAT109003
3	lnc-GGNBP1-7	chr6:33508471-33508774	NONHSAT109002

No data

Variant related genes	Relation type
RN7SL26P	TF binding region
RN7SL26P	CpG island
ENSG00000213588	chromatin interactions
ENSG00000242014	chromatin interactions
ENSG00000112514	chromatin interactions
ENSG00000237441	chromatin interactions

Extended variants
information (count: 1362 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1362 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9469465	chr6:33496201-33496202	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141224693	chr6:33496217-33496218	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552108236	chr6:33496229-33496230	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs375475703	chr6:33496233-33496234	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs564843615	chr6:33496241-33496242	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188776462	chr6:33496263-33496264	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs368834958	chr6:33496296-33496297	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs138427007	chr6:33496301-33496302	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs569496875	chr6:33496348-33496349	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs386699944	chr6:33496349-33496350	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs547235170	chr6:33496350-33496351	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs374258597	chr6:33496353-33496354	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs71565386	chr6:33496370-33496371	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs535995825	chr6:33496477-33496478	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs112782605	chr6:33496513-33496514	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
16	rs9469466	chr6:33496523-33496524	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs577326319	chr6:33496530-33496531	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs558579520	chr6:33496533-33496534	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs375816336	chr6:33496593-33496594	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs73743727	chr6:33496609-33496610	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs78935424	chr6:33496611-33496612	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs435945	chr6:33496632-33496633	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs75598103	chr6:33496633-33496634	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs1794686	chr6:33496663-33496664	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs386699945	chr6:33496687-33496688	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs139040090	chr6:33496688-33496689	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs562412470	chr6:33496691-33496692	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs529761563	chr6:33496693-33496694	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs73743728	chr6:33496701-33496702	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs449242	chr6:33496714-33496715	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs73743729	chr6:33496736-33496737	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs559348989	chr6:33496737-33496738	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs370865094	chr6:33496740-33496741	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533482750	chr6:33496763-33496764	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs75778583	chr6:33496766-33496767	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs563112485	chr6:33496781-33496782	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548031142	chr6:33496802-33496803	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs73743730	chr6:33496804-33496805	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs113352061	chr6:33496805-33496806	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs202198406	chr6:33496860-33496861	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552232228	chr6:33496917-33496918	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs62405923	chr6:33497037-33497038	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147868680	chr6:33497067-33497068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs534566109	chr6:33497075-33497076	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs112177246	chr6:33497118-33497119	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143781767	chr6:33497169-33497170	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs113014868	chr6:33497177-33497178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs376891414	chr6:33497179-33497180	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181676831	chr6:33497185-33497186	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs77520385	chr6:33497219-33497220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
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
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	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
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
Acute lymphoblastic leukemia	22237106	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33494600-33497400	Weak transcription	HepG2	liver
2	chr6:33496200-33496800	Enhancers	Fetal Stomach	stomach
3	chr6:33496400-33496800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:33496400-33496800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:33496400-33496800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:33497400-33498200	Enhancers	HepG2	liver
7	chr6:33498200-33501000	Weak transcription	HepG2	liver
8	chr6:33500000-33501000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr6:33500000-33501000	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr6:33500400-33501000	Enhancers	Primary T cells fromperipheralblood	blood
11	chr6:33500400-33501000	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr6:33500400-33501000	Enhancers	Dnd41	blood
13	chr6:33500600-33501000	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr6:33500600-33501000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr6:33500600-33502000	Enhancers	Fetal Thymus	thymus
16	chr6:33500800-33501000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr6:33500800-33501200	Enhancers	Thymus	Thymus
18	chr6:33501000-33501200	Active TSS	Primary T cells from cord blood	blood
19	chr6:33501000-33501200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
20	chr6:33501000-33501200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
21	chr6:33501000-33501200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr6:33501000-33501200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
23	chr6:33501000-33501400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
24	chr6:33501000-33501400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr6:33501000-33501400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
26	chr6:33501000-33501600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:33501000-33501600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
28	chr6:33501000-33501600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr6:33501000-33501600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
30	chr6:33501000-33501800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
31	chr6:33501000-33501800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr6:33501000-33501800	Flanking Active TSS	Dnd41	blood
33	chr6:33501000-33501800	Enhancers	HepG2	liver
34	chr6:33501200-33501400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
35	chr6:33501200-33501400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
36	chr6:33501200-33501600	Flanking Active TSS	Primary T cells from cord blood	blood
37	chr6:33501200-33501600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
38	chr6:33501200-33501600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
39	chr6:33501200-33501600	Active TSS	Primary T killer memory cells from peripheral blood	blood
40	chr6:33501200-33501800	Flanking Active TSS	Thymus	Thymus
41	chr6:33501400-33501600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
42	chr6:33501400-33501600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
43	chr6:33501400-33501600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
44	chr6:33501400-33501600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr6:33501400-33501600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
46	chr6:33501400-33501600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
47	chr6:33501600-33501800	Active TSS	Primary T cells from cord blood	blood
48	chr6:33501600-33501800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr6:33501600-33501800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr6:33501600-33501800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood

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