Variant report

Variant	nsv527735
Chromosome Location	chr6:2028237-2097654
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:340)
CpG islands
(count:122)
Chromatin interactive
region (count:27)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:2054021-2054064	HepG2	liver:	n/a	n/a
2	ATF1	chr6:2063914-2064084	K562	blood:	n/a	n/a
3	ATF2	chr6:2081607-2082134	GM12878	blood:	n/a	n/a
4	ATF2	chr6:2079063-2079591	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:2079176-2079524	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:2048167-2048485	HepG2	liver:	n/a	n/a
7	BHLHE40	chr6:2087299-2087385	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:2095378-2095459	K562	blood:	n/a	n/a
9	BHLHE40	chr6:2081674-2082026	GM12878	blood:	n/a	n/a
10	BRCA1	chr6:2072748-2073063	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:2034545-2034902	K562	blood:	n/a	n/a
12	CEBPB	chr6:2048113-2048435	HepG2	liver:	n/a	chr6:2048259-2048270
13	CEBPB	chr6:2055021-2055222	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:2044762-2044922	HepG2	liver:	n/a	chr6:2044864-2044875
15	CEBPB	chr6:2033311-2033582	IMR90	lung:	n/a	chr6:2033416-2033429 chr6:2033416-2033427 chr6:2033418-2033429
16	CEBPB	chr6:2034538-2034900	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:2053964-2054391	HepG2	liver:	n/a	chr6:2054100-2054111 chr6:2054099-2054110 chr6:2054099-2054110
18	CEBPB	chr6:2034543-2034870	A549	lung:	n/a	n/a
19	CEBPB	chr6:2029321-2029825	MCF-7	breast:	n/a	n/a
20	CEBPB	chr6:2029420-2029800	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:2072688-2073130	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr6:2048200-2048402	A549	lung:	n/a	chr6:2048259-2048270
23	CEBPB	chr6:2048102-2048427	IMR90	lung:	n/a	chr6:2048259-2048270
24	CEBPB	chr6:2033343-2033501	K562	blood:	n/a	chr6:2033416-2033429 chr6:2033416-2033427 chr6:2033418-2033429
25	CEBPB	chr6:2029377-2029811	MCF-7	breast:	n/a	n/a
26	CEBPB	chr6:2054026-2054178	HepG2	liver:	n/a	chr6:2054100-2054111 chr6:2054099-2054110 chr6:2054099-2054110
27	CEBPB	chr6:2034532-2034911	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:2033285-2033574	HepG2	liver:	n/a	chr6:2033416-2033429 chr6:2033416-2033427 chr6:2033418-2033429
29	CHD2	chr6:2072789-2073050	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr6:2038080-2038230	HCM	heart:	n/a	n/a
31	CTCF	chr6:2037880-2038030	NHDF-neo	bronchial:	n/a	chr6:2037959-2037980
32	CTCF	chr6:2037880-2038030	HMF	breast:	n/a	chr6:2037959-2037980
33	CTCF	chr6:2037885-2038081	MCF-7	breast:	n/a	chr6:2037959-2037980
34	CTCF	chr6:2037834-2038115	IMR90	lung:	n/a	chr6:2037959-2037980
35	CTCF	chr6:2037832-2038116	MCF-7	breast:	n/a	chr6:2037959-2037980
36	CTCF	chr6:2037900-2038050	HEEpiC	esophagus:	n/a	chr6:2037959-2037980
37	CTCF	chr6:2049227-2049238	ProgFib	skin:	n/a	n/a
38	CTCF	chr6:2037857-2038045	SK-N-SH_RA	brain:	n/a	chr6:2037959-2037980
39	CTCF	chr6:2037860-2038010	AoAF	blood vessel:	n/a	chr6:2037959-2037980
40	CTCF	chr6:2037880-2038030	HPAF	blood vessel:	n/a	chr6:2037959-2037980
41	CTCF	chr6:2037860-2038010	AG09309	skin:	n/a	chr6:2037959-2037980
42	CTCF	chr6:2037632-2038235	SK-N-SH	brain:	n/a	chr6:2037959-2037980
43	CTCF	chr6:2037922-2038055	Medullo	brain:	n/a	chr6:2037959-2037980
44	CTCF	chr6:2037886-2038062	Gliobla	brain:	n/a	chr6:2037959-2037980
45	CTCF	chr6:2037940-2038090	HMEC	breast:	n/a	chr6:2037959-2037980
46	CTCF	chr6:2037891-2038060	NHEK	skin:	n/a	chr6:2037959-2037980
47	CTCF	chr6:2037960-2038110	NHEK	skin:	n/a	n/a
48	CTCF	chr6:2094900-2095050	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr6:2037960-2038110	AG09319	gingival:	n/a	n/a
50	CTCF	chr6:2037827-2038198	MCF-7	breast:	n/a	chr6:2037959-2037980

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:2063957-2064007	HL-60	blood:	n/a
2	chr6:2063957-2064007	HNPCEpiC	eye:	n/a
3	chr6:2063957-2064007	NT2-D1	testis:	n/a
4	chr6:2030637-2030687	HEK293	kidney:	embryo
5	chr6:2063957-2064007	HEEpiC	esophagus:	n/a
6	chr6:2030637-2030687	HCM	heart:	n/a
7	chr6:2063957-2064007	ProgFib	skin:	n/a
8	chr6:2063957-2064007	GM19239	blood:	n/a
9	chr6:2030637-2030687	AG09309	skin:	n/a
10	chr6:2030637-2030687	HRE	kidney:	n/a
11	chr6:2030637-2030687	Jurkat	blood:	n/a
12	chr6:2030637-2030687	GM19239	blood:	n/a
13	chr6:2030637-2030687	LNCaP	prostate:	n/a
14	chr6:2030637-2030687	PANC-1	pancreas:	n/a
15	chr6:2063957-2064007	K562	blood:	n/a
16	chr6:2063957-2064007	T-47D	breast:	n/a
17	chr6:2030637-2030687	ovcar-3	ovarian:	n/a
18	chr6:2030637-2030687	NHDF-neo	bronchial:	n/a
19	chr6:2063957-2064007	HAEpiC	amniotic membrane:	n/a
20	chr6:2030637-2030687	GM06990	blood:	n/a
21	chr6:2030637-2030687	AoSMC	blood vessel:	n/a
22	chr6:2030637-2030687	Hela-S3	cervix:	n/a
23	chr6:2063957-2064007	CMK	blood:	n/a
24	chr6:2030637-2030687	HCPEpiC	choroid plexus:	n/a
25	chr6:2030637-2030687	IMR90	lung:	fetal
26	chr6:2063957-2064007	ovcar-3	ovarian:	n/a
27	chr6:2063957-2064007	BE2_C	brain:	n/a
28	chr6:2063957-2064007	SAEC	small airway:	n/a
29	chr6:2030637-2030687	Hepatocyte	liver:	n/a
30	chr6:2063957-2064007	Hepatocyte	liver:	n/a
31	chr6:2063957-2064007	Caco-2	colon:	n/a
32	chr6:2030637-2030687	H1-hESC	embryonic stem cell:	embryo
33	chr6:2063957-2064007	PANC-1	pancreas:	n/a
34	chr6:2063957-2064007	PrEC	prostate:	n/a
35	chr6:2063957-2064007	HRPEpiC	eye:	n/a
36	chr6:2063957-2064007	GM12891	blood:	n/a
37	chr6:2030637-2030687	HPAEpiC	pulmonary alveolar:	n/a
38	chr6:2030637-2030687	HUVEC	blood vessel:	n/a
39	chr6:2030637-2030687	T-47D	breast:	n/a
40	chr6:2063957-2064007	SK-N-SH_RA	brain:	n/a
41	chr6:2063957-2064007	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:2030637-2030687	CMK	blood:	n/a
43	chr6:2063957-2064007	AG09319	gingival:	n/a
44	chr6:2063957-2064007	AG04449	skin:	fetal
45	chr6:2063957-2064007	IMR90	lung:	fetal
46	chr6:2030637-2030687	RPTEC	kidney:	n/a
47	chr6:2030637-2030687	HepG2	liver:	n/a
48	chr6:2030637-2030687	MCF10A-Er-Src	breast:	n/a
49	chr6:2063957-2064007	AoSMC	blood vessel:	n/a
50	chr6:2030637-2030687	AG04450	lung:	fetal

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:1641104..1642209-chr6:2040485..2041851,20	MCF-7	breast:
2	chr6:2081922..2083588-chr6:2088961..2091628,2	MCF-7	breast:
3	chr6:2070854..2072589-chr6:2073721..2075447,2	K562	blood:
4	chr6:2040678..2043654-chr6:2103622..2106281,2	MCF-7	breast:
5	chr6:1609442..1611153-chr6:2038341..2040817,2	MCF-7	breast:
6	chr6:1608425..1611671-chr6:2030333..2034108,4	MCF-7	breast:
7	chr6:2034659..2036744-chr6:2038441..2040012,2	K562	blood:
8	chr6:2034659..2036744-chr6:2038441..2040012,2	K562	blood:
9	chr6:2053179..2055343-chr6:2055921..2058664,2	K562	blood:
10	chr6:2070854..2072589-chr6:2073721..2075447,2	K562	blood:
11	chr6:1604389..1605339-chr6:2037539..2038714,6	MCF-7	breast:
12	chr6:1610286..1612830-chr6:2028603..2030738,2	MCF-7	breast:
13	chr6:2009784..2011598-chr6:2035176..2037362,2	MCF-7	breast:
14	chr6:2081922..2083588-chr6:2088961..2091628,2	MCF-7	breast:
15	chr6:1609057..1611446-chr6:2026298..2028309,2	MCF-7	breast:
16	chr6:2040794..2041414-chr6:2132566..2133423,2	MCF-7	breast:
17	chr6:1641472..1642157-chr6:2040778..2041465,3	MCF-7	breast:
18	chr6:1641339..1642209-chr6:2040485..2041381,10	MCF-7	breast:
19	chr6:2076391..2078469-chr6:2091267..2093676,2	MCF-7	breast:
20	chr6:2053179..2055343-chr6:2055921..2058664,2	K562	blood:
21	chr6:2076391..2078469-chr6:2091267..2093676,2	MCF-7	breast:
22	chr6:1616379..1619156-chr6:2096704..2099403,2	MCF-7	breast:
23	chr6:2030064..2032046-chr6:2035936..2037834,2	K562	blood:
24	chr6:1604328..1605242-chr6:2035866..2036724,2	MCF-7	breast:
25	chr6:2030064..2032046-chr6:2035936..2037834,2	K562	blood:
26	chr6:1607895..1612984-chr6:2025307..2029705,5	MCF-7	breast:
27	chr6:1597053..1598701-chr6:2028381..2030962,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf195-22	chr6:2037712-2038201	NONHSAT106589

No data

Variant related genes	Relation type
GMDS	TF binding region
GMDS	CpG island
ENSG00000054598	chromatin interactions

Extended variants
information (count: 2701 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2701 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9392354	chr6:2028237-2028238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181438023	chr6:2028250-2028251	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184700968	chr6:2028288-2028289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs555649532	chr6:2028292-2028293	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs200303871	chr6:2028306-2028307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567086569	chr6:2028324-2028325	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139290440	chr6:2028354-2028355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559122575	chr6:2028403-2028404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs56098578	chr6:2028436-2028437	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs537898037	chr6:2028481-2028482	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs150016396	chr6:2028519-2028520	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs13199123	chr6:2028531-2028532	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375172816	chr6:2028626-2028627	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs554344375	chr6:2028665-2028666	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs531424288	chr6:2028667-2028668	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs12164011	chr6:2028731-2028732	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs372888455	chr6:2028732-2028733	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542920258	chr6:2028751-2028752	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145557248	chr6:2028756-2028757	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572727525	chr6:2028806-2028807	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140363075	chr6:2028823-2028824	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561796837	chr6:2028842-2028843	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369809616	chr6:2028844-2028845	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189466552	chr6:2028875-2028876	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs543927415	chr6:2028957-2028958	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs527616078	chr6:2029028-2029029	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560951212	chr6:2029074-2029075	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs529623832	chr6:2029078-2029079	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547294301	chr6:2029116-2029117	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs116399376	chr6:2029155-2029156	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532789397	chr6:2029187-2029188	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182015632	chr6:2029198-2029199	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs57777283	chr6:2029213-2029214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs201787415	chr6:2029229-2029230	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs68128479	chr6:2029233-2029234	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs144147202	chr6:2029270-2029271	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568460076	chr6:2029283-2029284	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs146502111	chr6:2029315-2029316	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs552881936	chr6:2029368-2029369	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs572789744	chr6:2029415-2029416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs2504721	chr6:2029454-2029455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs540078594	chr6:2029463-2029464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544851797	chr6:2029469-2029470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs558336341	chr6:2029522-2029523	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs186031109	chr6:2029552-2029553	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs189038538	chr6:2029569-2029570	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs180993703	chr6:2029592-2029593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570213844	chr6:2029640-2029641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs75137370	chr6:2029737-2029738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs186166435	chr6:2029791-2029792	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
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
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164919	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Gastric cancer	22315472	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2006200-2034800	Weak transcription	HepG2	liver
2	chr6:2019800-2040000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:2021600-2028600	Weak transcription	GM12878-XiMat	blood
4	chr6:2022200-2030600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr6:2022200-2031600	Weak transcription	Esophagus	oesophagus
6	chr6:2022400-2035000	Weak transcription	Gastric	stomach
7	chr6:2022400-2042800	Weak transcription	Right Atrium	heart
8	chr6:2022400-2055600	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr6:2022400-2080600	Weak transcription	Duodenum Mucosa	Duodenum
10	chr6:2022600-2028800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:2022600-2028800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:2022600-2028800	Weak transcription	Stomach Mucosa	stomach
13	chr6:2023800-2028800	Weak transcription	Fetal Thymus	thymus
14	chr6:2024000-2028600	Weak transcription	Thymus	Thymus
15	chr6:2024000-2028800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr6:2024600-2028400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr6:2024600-2028600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr6:2024800-2028600	Weak transcription	Primary T cells from cord blood	blood
19	chr6:2024800-2028600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr6:2024800-2028600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr6:2024800-2028600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr6:2025000-2028600	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr6:2025000-2028600	Weak transcription	Dnd41	blood
24	chr6:2026600-2028600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr6:2026600-2030200	Weak transcription	Pancreas	Pancrea
26	chr6:2026600-2031600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr6:2026800-2031000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr6:2027000-2029000	Weak transcription	Small Intestine	intestine
29	chr6:2027000-2035000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:2027200-2029800	Weak transcription	Brain Germinal Matrix	brain
31	chr6:2027400-2030600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:2028000-2028600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:2028200-2028800	Enhancers	HUVEC	blood vessel
34	chr6:2028400-2028800	Weak transcription	Adipose Nuclei	Adipose
35	chr6:2028400-2029000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr6:2028400-2029200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr6:2028400-2030600	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr6:2028600-2028800	Enhancers	GM12878-XiMat	blood
39	chr6:2028600-2029000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr6:2028600-2029000	Enhancers	Colon Smooth Muscle	Colon
41	chr6:2028600-2029200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr6:2028600-2029200	Enhancers	Primary B cells from peripheral blood	blood
43	chr6:2028600-2029200	Enhancers	Primary T cells from cord blood	blood
44	chr6:2028600-2029200	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr6:2028600-2029200	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr6:2028600-2029200	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr6:2028600-2029200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr6:2028600-2029200	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr6:2028600-2029200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr6:2028600-2029200	Enhancers	Thymus	Thymus

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