Variant report

Variant	esv1802115
Chromosome Location	chr6:34852176-34856501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:559)
CpG islands
(count:915)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34855719-34856923	K562	blood:	n/a	n/a
2	ATF1	chr6:34855487-34856397	K562	blood:	n/a	chr6:34855838-34855852
3	ATF2	chr6:34855549-34856136	H1-hESC	embryonic stem cell:	n/a	chr6:34855838-34855852
4	ATF2	chr6:34855528-34856206	GM12878	blood:	n/a	chr6:34855838-34855852
5	ATF2	chr6:34855474-34856393	H1-hESC	embryonic stem cell:	n/a	chr6:34855838-34855852
6	ATF2	chr6:34855555-34856110	GM12878	blood:	n/a	chr6:34855838-34855852
7	ATF3	chr6:34855626-34856017	H1-hESC	embryonic stem cell:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
8	ATF3	chr6:34855553-34856043	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
9	ATF3	chr6:34855748-34855947	GM12878	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
10	ATF3	chr6:34855569-34856012	HepG2	liver:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
11	ATF3	chr6:34855595-34856148	GM12878	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
12	ATF3	chr6:34855564-34856045	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
13	ATF3	chr6:34855611-34856089	A549	lung:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
14	ATF3	chr6:34855584-34856143	HepG2	liver:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
15	ATF3	chr6:34855575-34856023	H1-hESC	embryonic stem cell:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
16	ATF3	chr6:34855565-34856126	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
17	BCL3	chr6:34855610-34855991	GM12878	blood:	n/a	n/a
18	BCLAF1	chr6:34855583-34856152	GM12878	blood:	n/a	n/a
19	BCLAF1	chr6:34855498-34856151	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:34855612-34856038	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:34855593-34856100	K562	blood:	n/a	n/a
22	BRCA1	chr6:34855671-34856036	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr6:34855787-34856109	GM12878	blood:	n/a	n/a
24	BRCA1	chr6:34855662-34856196	HepG2	liver:	n/a	n/a
25	BRCA1	chr6:34855630-34856250	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr6:34855652-34856179	K562	blood:	n/a	n/a
27	CBX3	chr6:34855492-34857137	K562	blood:	n/a	n/a
28	CCNT2	chr6:34855577-34856270	K562	blood:	n/a	n/a
29	CEBPB	chr6:34855470-34856309	GM12878	blood:	n/a	n/a
30	CEBPB	chr6:34855691-34856203	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:34855573-34856151	K562	blood:	n/a	n/a
32	CEBPB	chr6:34853686-34853985	K562	blood:	n/a	n/a
33	CEBPB	chr6:34855604-34856267	K562	blood:	n/a	n/a
34	CEBPB	chr6:34853734-34853964	K562	blood:	n/a	n/a
35	CEBPD	chr6:34855485-34856206	K562	blood:	n/a	n/a
36	CEBPD	chr6:34855573-34856031	HepG2	liver:	n/a	n/a
37	CHD1	chr6:34855161-34855323	GM12878	blood:	n/a	n/a
38	CHD1	chr6:34855352-34856900	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr6:34855533-34856594	GM12878	blood:	n/a	n/a
40	CHD2	chr6:34855656-34857154	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr6:34855559-34856008	GM12878	blood:	n/a	n/a
42	CHD2	chr6:34855433-34856316	K562	blood:	n/a	n/a
43	CHD2	chr6:34855549-34856172	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr6:34855618-34856113	HepG2	liver:	n/a	n/a
45	CREB1	chr6:34856455-34857463	K562	blood:	n/a	n/a
46	CREB1	chr6:34855202-34856440	HepG2	liver:	n/a	chr6:34855839-34855852
47	CREB1	chr6:34855376-34856443	K562	blood:	n/a	chr6:34855839-34855852
48	CREB1	chr6:34855055-34856231	K562	blood:	n/a	chr6:34855839-34855852
49	CREB1	chr6:34855504-34856138	ECC-1	luminal epithelium:	n/a	chr6:34855839-34855852
50	CREB1	chr6:34855535-34856154	H1-hESC	embryonic stem cell:	n/a	chr6:34855839-34855852

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34855885-34855935	BE2_C	brain:	n/a
2	chr6:34855980-34856030	HMEC	breast:	n/a
3	chr6:34855834-34855884	BJ	skin:	n/a
4	chr6:34855980-34856030	CMK	blood:	n/a
5	chr6:34855885-34855935	HMEC	breast:	n/a
6	chr6:34855797-34855847	MCF-7	breast:	n/a
7	chr6:34855887-34855937	H1-hESC	embryonic stem cell:	embryo
8	chr6:34853620-34853670	GM12892	blood:	n/a
9	chr6:34856217-34856267	LNCaP	prostate:	n/a
10	chr6:34856158-34856208	Hela-S3	cervix:	n/a
11	chr6:34855834-34855884	SK-N-MC	brain:	n/a
12	chr6:34853620-34853670	HCM	heart:	n/a
13	chr6:34855980-34856030	HEK293	kidney:	embryo
14	chr6:34855470-34855520	BJ	skin:	n/a
15	chr6:34855797-34855847	HUVEC	blood vessel:	n/a
16	chr6:34856217-34856267	NH-A	brain:	n/a
17	chr6:34855980-34856030	LNCaP	prostate:	n/a
18	chr6:34852903-34852953	MCF-7	breast:	n/a
19	chr6:34856217-34856267	GM12891	blood:	n/a
20	chr6:34855635-34855685	HMEC	breast:	n/a
21	chr6:34855839-34855889	SKMC	muscle:	n/a
22	chr6:34855834-34855884	K562	blood:	n/a
23	chr6:34855839-34855889	SAEC	small airway:	n/a
24	chr6:34853620-34853670	HNPCEpiC	eye:	n/a
25	chr6:34852903-34852953	PrEC	prostate:	n/a
26	chr6:34855834-34855884	HCPEpiC	choroid plexus:	n/a
27	chr6:34855797-34855847	NB4	blood:	n/a
28	chr6:34855408-34855458	ProgFib	skin:	n/a
29	chr6:34855980-34856030	SAEC	small airway:	n/a
30	chr6:34855470-34855520	SAEC	small airway:	n/a
31	chr6:34855635-34855685	T-47D	breast:	n/a
32	chr6:34852903-34852953	HEK293	kidney:	embryo
33	chr6:34855797-34855847	BJ	skin:	n/a
34	chr6:34856217-34856267	SAEC	small airway:	n/a
35	chr6:34853620-34853670	MCF-7	breast:	n/a
36	chr6:34855885-34855935	PANC-1	pancreas:	n/a
37	chr6:34855834-34855884	HCT-116	colon:	n/a
38	chr6:34856217-34856267	MCF-7	breast:	n/a
39	chr6:34855885-34855935	HL-60	blood:	n/a
40	chr6:34855839-34855889	H1-hESC	embryonic stem cell:	embryo
41	chr6:34855885-34855935	HRPEpiC	eye:	n/a
42	chr6:34855980-34856030	HRE	kidney:	n/a
43	chr6:34855789-34855839	Caco-2	colon:	n/a
44	chr6:34853620-34853670	HepG2	liver:	n/a
45	chr6:34855789-34855839	BJ	skin:	n/a
46	chr6:34853620-34853670	Hepatocyte	liver:	n/a
47	chr6:34855839-34855889	SK-N-SH_RA	brain:	n/a
48	chr6:34855408-34855458	BE2_C	brain:	n/a
49	chr6:34853620-34853670	ovcar-3	ovarian:	n/a
50	chr6:34855980-34856030	GM12891	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:34834250..34837156-chr6:34851105..34853013,3	MCF-7	breast:
2	chr6:34843479..34847323-chr6:34849401..34853884,4	MCF-7	breast:
3	chr6:34392840..34394590-chr6:34855825..34858514,2	K562	blood:
4	chr6:34855693..34857942-chr6:35191744..35194149,2	MCF-7	breast:
5	chr4:2419677..2420373-chr6:34855480..34855994,2	Hela-S3	cervix:
6	chr15:41913003..41913826-chr6:34855469..34856066,2	Hela-S3	cervix:
7	chr6:34733163..34735637-chr6:34853537..34855573,2	K562	blood:
8	chr6:34853107..34854715-chr6:34857316..34859285,2	MCF-7	breast:
9	chr6:34758735..34762506-chr6:34853024..34858695,7	MCF-7	breast:
10	chr6:34759044..34761297-chr6:34854138..34856970,2	K562	blood:
11	chr6:34853391..34855742-chr6:34918404..34920858,2	K562	blood:
12	chr17:56708594..56709416-chr6:34855776..34856394,2	Hela-S3	cervix:
13	chr6:34837346..34838981-chr6:34850648..34853394,2	K562	blood:
14	chr6:34854986..34858344-chr6:35226281..35229493,3	K562	blood:
15	chr6:34855314..34856910-chr6:35435686..35437650,2	MCF-7	breast:
16	chr6:27798350..27799895-chr6:34855095..34857385,2	K562	blood:
17	chr12:120729250..120730043-chr6:34855337..34856229,2	Hela-S3	cervix:
18	chr6:34723520..34726444-chr6:34854512..34857469,3	MCF-7	breast:
19	chr3:156534879..156535549-chr6:34855191..34855795,2	Hela-S3	cervix:
20	chr17:73285374..73286157-chr6:34855342..34855976,2	Hela-S3	cervix:
21	chr6:34842945..34852488-chr6:34852501..34858927,16	MCF-7	breast:
22	chr6:34856224..34858095-chr6:35226235..35229197,2	MCF-7	breast:

No data

Variant related genes	Relation type
ANKS1A	TF binding region
TAF11	TF binding region
ANKS1A	CpG island
TAF11	CpG island
ENSG00000270800	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000065060	chromatin interactions
ENSG00000272374	chromatin interactions
ENSG00000174197	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000065029	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000124562	chromatin interactions
ENSG00000159733	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000125454	chromatin interactions
ENSG00000197914	chromatin interactions
ENSG00000064995	chromatin interactions
ENSG00000064999	chromatin interactions

Extended variants
information (count: 178 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:178 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4646929	chr6:34852176-34852177	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs4646928	chr6:34852177-34852178	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs537229891	chr6:34852185-34852186	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs550286770	chr6:34852194-34852195	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs568593719	chr6:34852211-34852212	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs4646927	chr6:34852217-34852218	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs151159731	chr6:34852234-34852235	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs182912297	chr6:34852236-34852237	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs4646926	chr6:34852253-34852254	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs539130314	chr6:34852260-34852261	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs185765122	chr6:34852276-34852277	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs573911111	chr6:34852379-34852380	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs544404771	chr6:34852504-34852505	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs4646925	chr6:34852546-34852547	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs76914477	chr6:34852583-34852584	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs546185678	chr6:34852610-34852611	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs141147850	chr6:34852623-34852624	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs541105479	chr6:34852661-34852662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528478862	chr6:34852666-34852667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537435775	chr6:34852679-34852680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540573134	chr6:34852753-34852754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139304442	chr6:34852771-34852772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113964841	chr6:34852773-34852774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs67450543	chr6:34852774-34852775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562020902	chr6:34852858-34852859	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4646923	chr6:34852879-34852880	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs545887909	chr6:34852882-34852883	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35445513	chr6:34852883-34852884	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs199972096	chr6:34852891-34852892	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs202086347	chr6:34852893-34852894	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532841969	chr6:34852904-34852905	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs182813891	chr6:34853046-34853047	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566384650	chr6:34853083-34853084	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200101803	chr6:34853091-34853092	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200852596	chr6:34853092-34853093	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs35025391	chr6:34853176-34853177	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs4646922	chr6:34853253-34853254	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs60096232	chr6:34853291-34853292	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542834268	chr6:34853325-34853326	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555734566	chr6:34853329-34853330	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs146918260	chr6:34853344-34853345	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368844063	chr6:34853375-34853376	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs538061388	chr6:34853381-34853382	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs4646921	chr6:34853398-34853399	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs187140597	chr6:34853414-34853415	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192264941	chr6:34853544-34853545	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548945232	chr6:34853580-34853581	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs4646920	chr6:34853635-34853636	Weak transcription Enhancers Genic enhancers Strong transcription	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558231068	chr6:34853642-34853643	Weak transcription Enhancers Genic enhancers Strong transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs573182652	chr6:34853656-34853657	Weak transcription Enhancers Genic enhancers Strong transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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
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
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34816800-34853600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:34818600-34853400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:34820200-34855000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr6:34821000-34854600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:34830000-34855000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:34834400-34853600	Strong transcription	Primary T helper cells fromperipheralblood	blood
7	chr6:34835800-34855200	Weak transcription	Small Intestine	intestine
8	chr6:34837000-34852400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr6:34840800-34854800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:34841400-34854600	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr6:34841400-34855200	Weak transcription	Fetal Heart	heart
12	chr6:34841600-34854600	Weak transcription	Fetal Kidney	kidney
13	chr6:34842600-34854800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:34844000-34854000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:34844000-34854800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:34844600-34853400	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr6:34844600-34854600	Weak transcription	Psoas Muscle	Psoas
18	chr6:34845000-34854600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr6:34845200-34853800	Weak transcription	Fetal Brain Male	brain
20	chr6:34845400-34854600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr6:34845600-34852200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:34846600-34854600	Weak transcription	HMEC	breast
23	chr6:34847600-34854600	Weak transcription	Right Ventricle	heart
24	chr6:34848000-34853600	Weak transcription	Fetal Brain Female	brain
25	chr6:34848000-34854400	Weak transcription	Stomach Smooth Muscle	stomach
26	chr6:34848000-34854600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr6:34848000-34854600	Weak transcription	Brain Germinal Matrix	brain
28	chr6:34848000-34854600	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr6:34848000-34854600	Weak transcription	Thymus	Thymus
30	chr6:34848000-34854600	Weak transcription	HSMMtube	muscle
31	chr6:34848000-34854600	Weak transcription	NHLF	lung
32	chr6:34848000-34854800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr6:34848000-34854800	Weak transcription	Gastric	stomach
34	chr6:34848200-34853400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:34848200-34853400	Weak transcription	Pancreas	Pancrea
36	chr6:34848200-34854000	Weak transcription	Fetal Muscle Leg	muscle
37	chr6:34848200-34854000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr6:34848200-34854000	Weak transcription	NHEK	skin
39	chr6:34848200-34854400	Weak transcription	Colonic Mucosa	Colon
40	chr6:34848200-34854600	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr6:34848200-34854600	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr6:34848200-34854600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr6:34848200-34854600	Weak transcription	Brain Angular Gyrus	brain
44	chr6:34848200-34854600	Weak transcription	Brain Hippocampus Middle	brain
45	chr6:34848200-34854600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr6:34848200-34854600	Weak transcription	Fetal Muscle Trunk	muscle
47	chr6:34848200-34854600	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr6:34848200-34854600	Weak transcription	Rectal Smooth Muscle	rectum
49	chr6:34848200-34854600	Weak transcription	Spleen	Spleen
50	chr6:34848200-34854600	Weak transcription	A549	lung

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