Variant report

Variant	nsv1022912
Chromosome Location	chr6:46093409-46116449
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:242)
CpG islands
(count:857)
Chromatin interactive
region (count:8)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:242 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:46097505-46098200	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr6:46097227-46098039	GM12878	blood:	n/a	chr6:46097771-46097784 chr6:46097770-46097783
3	BCLAF1	chr6:46097487-46098159	GM12878	blood:	n/a	chr6:46097771-46097784 chr6:46097770-46097783 chr6:46098064-46098073 chr6:46098062-46098075
4	BHLHE40	chr6:46106049-46106509	GM12878	blood:	n/a	n/a
5	CCNT2	chr6:46104596-46104857	K562	blood:	n/a	n/a
6	CEBPB	chr6:46111277-46111381	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr6:46093430-46093697	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr6:46097346-46098106	GM12878	blood:	n/a	chr6:46097936-46097946
9	CHD2	chr6:46097436-46097875	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr6:46097456-46097808	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTBP2	chr6:46097260-46098229	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr6:46097620-46097770	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr6:46097720-46097870	GM12875	blood:	n/a	n/a
14	CTCF	chr6:46097680-46097830	GM12866	blood:	n/a	n/a
15	CTCF	chr6:46097696-46097728	A549	lung:	n/a	n/a
16	CTCF	chr6:46097700-46097850	GM12869	blood:	n/a	n/a
17	CTCF	chr6:46097615-46097836	GM12892	blood:	n/a	n/a
18	CTCF	chr6:46097600-46097750	GM12872	blood:	n/a	n/a
19	CTCF	chr6:46097620-46097770	GM12878	blood:	n/a	n/a
20	CTCF	chr6:46097700-46097850	GM12873	blood:	n/a	n/a
21	CTCF	chr6:46097664-46097789	MCF-7	breast:	n/a	n/a
22	CTCF	chr6:46097676-46097750	MCF-7	breast:	n/a	n/a
23	CTCF	chr6:46097660-46097810	GM12870	blood:	n/a	n/a
24	CTCF	chr6:46097600-46097750	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr6:46097580-46097730	GM12864	blood:	n/a	n/a
26	CTCF	chr6:46097693-46097767	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr6:46097600-46097750	GM12868	blood:	n/a	n/a
28	CTCF	chr6:46097740-46097890	GM12872	blood:	n/a	n/a
29	CTCF	chr6:46097700-46097850	HRE	kidney:	n/a	n/a
30	CTCF	chr6:46097580-46097730	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr6:46097690-46097694	A549	lung:	n/a	n/a
32	CTCF	chr6:46097635-46097816	GM12891	blood:	n/a	n/a
33	CTCF	chr6:46097700-46097850	GM12866	blood:	n/a	n/a
34	CTCF	chr6:46097620-46097770	BJ	skin:	n/a	n/a
35	CTCF	chr6:46097960-46098110	GM12864	blood:	n/a	n/a
36	CTCF	chr6:46097662-46097736	Fibrobl	skin:	n/a	n/a
37	CTCF	chr6:46097700-46097850	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr6:46097540-46097690	GM12873	blood:	n/a	n/a
39	CTCF	chr6:46097640-46097790	AG09319	gingival:	n/a	n/a
40	CTCF	chr6:46097673-46097972	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr6:46097713-46097748	LNCaP	prostate:	n/a	n/a
42	CTCF	chr6:46097680-46097830	GM12875	blood:	n/a	n/a
43	CTCF	chr6:46097620-46097770	GM12865	blood:	n/a	n/a
44	CTCF	chr6:46097660-46097810	Caco-2	colon:	n/a	n/a
45	CTCF	chr6:46097643-46097783	GM19238	blood:	n/a	n/a
46	CTCF	chr6:46097661-46097775	GM13977	blood:	n/a	n/a
47	CTCF	chr6:46097620-46097770	HCM	heart:	n/a	n/a
48	CTCF	chr6:46097642-46097808	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:46097700-46097850	GM12864	blood:	n/a	n/a
50	CTCF	chr6:46097760-46097910	GM12878	blood:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:46112967-46113017	HRCEpiC	kidney:	n/a
2	chr6:46097392-46097442	HAEpiC	amniotic membrane:	n/a
3	chr6:46097392-46097442	Hela-S3	cervix:	n/a
4	chr6:46112967-46113017	HRCEpiC	kidney:	n/a
5	chr6:46097392-46097442	HAEpiC	amniotic membrane:	n/a
6	chr6:46097392-46097442	Hela-S3	cervix:	n/a
7	chr6:46097784-46097834	PANC-1	pancreas:	n/a
8	chr6:46097468-46097518	PANC-1	pancreas:	n/a
9	chr6:46097468-46097518	CMK	blood:	n/a
10	chr6:46094735-46094785	T-47D	breast:	n/a
11	chr6:46110412-46110462	IMR90	lung:	fetal
12	chr6:46098122-46098172	CMK	blood:	n/a
13	chr6:46097784-46097834	SK-N-SH_RA	brain:	n/a
14	chr6:46097521-46097571	HCPEpiC	choroid plexus:	n/a
15	chr6:46112967-46113017	HCM	heart:	n/a
16	chr6:46097468-46097518	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:46097650-46097700	HNPCEpiC	eye:	n/a
18	chr6:46098122-46098172	AG09319	gingival:	n/a
19	chr6:46097521-46097571	HEEpiC	esophagus:	n/a
20	chr6:46101741-46101791	IMR90	lung:	fetal
21	chr6:46097468-46097518	H1-hESC	embryonic stem cell:	embryo
22	chr6:46097784-46097834	GM12891	blood:	n/a
23	chr6:46097695-46097745	ProgFib	skin:	n/a
24	chr6:46097392-46097442	SK-N-SH_RA	brain:	n/a
25	chr6:46110412-46110462	Jurkat	blood:	n/a
26	chr6:46112967-46113017	Jurkat	blood:	n/a
27	chr6:46097784-46097834	Jurkat	blood:	n/a
28	chr6:46097671-46097721	SK-N-SH	brain:	n/a
29	chr6:46097671-46097721	AG04450	lung:	fetal
30	chr6:46112967-46113017	ovcar-3	ovarian:	n/a
31	chr6:46110412-46110462	H1-hESC	embryonic stem cell:	embryo
32	chr6:46112967-46113017	HCPEpiC	choroid plexus:	n/a
33	chr6:46110412-46110462	RPTEC	kidney:	n/a
34	chr6:46097650-46097700	HepG2	liver:	n/a
35	chr6:46097392-46097442	CMK	blood:	n/a
36	chr6:46112967-46113017	IMR90	lung:	fetal
37	chr6:46101741-46101791	NT2-D1	testis:	n/a
38	chr6:46097521-46097571	GM12891	blood:	n/a
39	chr6:46097650-46097700	SK-N-SH	brain:	n/a
40	chr6:46097784-46097834	NHDF-neo	bronchial:	n/a
41	chr6:46097671-46097721	ovcar-3	ovarian:	n/a
42	chr6:46097650-46097700	HL-60	blood:	n/a
43	chr6:46101741-46101791	NH-A	brain:	n/a
44	chr6:46097441-46097491	HL-60	blood:	n/a
45	chr6:46098122-46098172	HCF	heart:	n/a
46	chr6:46094735-46094785	HL-60	blood:	n/a
47	chr6:46110412-46110462	BE2_C	brain:	n/a
48	chr6:46094735-46094785	CMK	blood:	n/a
49	chr6:46097671-46097721	HRE	kidney:	n/a
50	chr6:46112967-46113017	AG04450	lung:	fetal

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:46110640..46112825-chr6:46112958..46115144,2	K562	blood:
2	chr6:46110640..46112825-chr6:46112958..46115144,2	K562	blood:
3	chr6:46112224..46114185-chr6:46116270..46118117,2	K562	blood:
4	chr6:46107057..46110054-chr6:46111949..46114711,2	K562	blood:
5	chr6:46112224..46114185-chr6:46116270..46118117,2	K562	blood:
6	chr6:46097274..46099373-chr6:46101188..46103755,2	K562	blood:
7	chr6:46106023..46108072-chr6:46120783..46123181,2	MCF-7	breast:
8	chr6:46107057..46110054-chr6:46111949..46114711,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLIC5-1	chr6:46097241-46097328	ENSG00000231769.1
2	lnc-CLIC5-1	chr6:46097327-46097443	ENSG00000231769.2
3	lnc-CLIC5-1	chr6:46097327-46097443	ENSG00000231769.1
4	lnc-CLIC5-1	chr6:46097241-46097328	ENSG00000231769.2
5	lnc-CLIC5-1	chr6:46097241-46097571	NONHSAT113004

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ENPP4	hsa-miR-16-5p	chr6:46113911-46113930
2	ENPP4	hsa-miR-16-5p	chr6:46113745-46113767
3	ENPP4	hsa-miR-103a-3p	chr6:46113744-46113766

Variant related genes	Relation type
ENSG00000231769	TF binding region
ENPP4	TF binding region
ENSG00000231769	CpG island
ENPP4	CpG island
ENSG00000001561	chromatin interactions
ENSG00000231769	chromatin interactions

Extended variants
information (count: 839 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:839 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184833375	chr6:46093411-46093412	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs12665453	chr6:46093481-46093482	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs12530009	chr6:46093527-46093528	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs189159492	chr6:46093552-46093553	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200330875	chr6:46093562-46093563	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs192330266	chr6:46093570-46093571	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs577255335	chr6:46093581-46093582	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs562577361	chr6:46093587-46093588	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs34093379	chr6:46093627-46093628	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs11759657	chr6:46093667-46093668	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs546072577	chr6:46093671-46093672	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs551712183	chr6:46093713-46093714	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs567045424	chr6:46093727-46093728	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs534544975	chr6:46093817-46093818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184343668	chr6:46093818-46093819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570685258	chr6:46093829-46093830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538066111	chr6:46093838-46093839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149718878	chr6:46093853-46093854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556199355	chr6:46093874-46093875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574922108	chr6:46093880-46093881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113160446	chr6:46094102-46094103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554172128	chr6:46094160-46094161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573030557	chr6:46094181-46094182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181530662	chr6:46094205-46094206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201919766	chr6:46094230-46094231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565191746	chr6:46094281-46094282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577069419	chr6:46094331-46094332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574544673	chr6:46094348-46094349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544424124	chr6:46094454-46094455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562569176	chr6:46094457-46094458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373803880	chr6:46094472-46094473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369926961	chr6:46094513-46094514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2223778	chr6:46094538-46094539	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs2223777	chr6:46094541-46094542	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs527310829	chr6:46094542-46094543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552420944	chr6:46094546-46094547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149176479	chr6:46094564-46094565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376729704	chr6:46094620-46094621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547536157	chr6:46094629-46094630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531784434	chr6:46094653-46094654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550000601	chr6:46094663-46094664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568446844	chr6:46094681-46094682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535971706	chr6:46094689-46094690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145060894	chr6:46094695-46094696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185693556	chr6:46094719-46094720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189237314	chr6:46094735-46094736	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs558840703	chr6:46094759-46094760	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs567285061	chr6:46094794-46094795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577259223	chr6:46094835-46094836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181469865	chr6:46094841-46094842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
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
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
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	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
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:46080200-46095600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr6:46080600-46095400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:46081600-46096400	Weak transcription	Thymus	Thymus
4	chr6:46083000-46096200	Weak transcription	Primary T cells from cord blood	blood
5	chr6:46087400-46095400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:46087400-46095600	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr6:46087400-46097000	Weak transcription	Aorta	Aorta
8	chr6:46088000-46094800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr6:46088400-46095600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr6:46088400-46095600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr6:46092200-46093600	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr6:46093400-46093600	Enhancers	Psoas Muscle	Psoas
13	chr6:46093400-46094000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr6:46093400-46096400	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr6:46093600-46094000	Enhancers	Primary T cells fromperipheralblood	blood
16	chr6:46093600-46095400	Weak transcription	Psoas Muscle	Psoas
17	chr6:46093800-46094000	Enhancers	Right Ventricle	heart
18	chr6:46093800-46094200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr6:46094000-46095400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr6:46094000-46095800	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr6:46094200-46096800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr6:46094400-46094600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:46094400-46094600	Enhancers	Stomach Mucosa	stomach
24	chr6:46094400-46094800	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr6:46094400-46096800	Enhancers	Primary B cells from cord blood	blood
26	chr6:46094600-46094800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:46094600-46094800	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr6:46094600-46095200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr6:46094600-46095600	Weak transcription	Stomach Mucosa	stomach
30	chr6:46094800-46095200	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr6:46094800-46095600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr6:46094800-46096800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr6:46095000-46097000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:46095200-46096400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr6:46095200-46097000	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr6:46095400-46095600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr6:46095400-46095600	Enhancers	GM12878-XiMat	blood
38	chr6:46095400-46095800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:46095400-46096000	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr6:46095400-46096000	Enhancers	Dnd41	blood
41	chr6:46095400-46096200	Enhancers	Primary hematopoietic stem cells	blood
42	chr6:46095400-46096200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr6:46095400-46096200	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr6:46095400-46096400	Enhancers	Psoas Muscle	Psoas
45	chr6:46095400-46096600	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr6:46095400-46096600	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr6:46095400-46096800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr6:46095400-46097000	Enhancers	Primary B cells from peripheral blood	blood
49	chr6:46095400-46097000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr6:46095400-46097000	Enhancers	Brain Substantia Nigra	brain

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