Variant report

Variant	nsv1030889
Chromosome Location	chr6:38374812-38450432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:38418438-38418909	HepG2	liver:	n/a	n/a
2	ATF1	chr6:38411596-38411926	K562	blood:	n/a	n/a
3	ATF2	chr6:38445535-38446087	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:38445534-38446002	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:38395485-38396059	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:38385354-38385551	HepG2	liver:	n/a	n/a
7	BRCA1	chr6:38411408-38411424	GM12878	blood:	n/a	n/a
8	CEBPB	chr6:38385924-38386459	HepG2	liver:	n/a	chr6:38386031-38386040 chr6:38386031-38386042 chr6:38386029-38386040 chr6:38386029-38386042
9	CEBPB	chr6:38385354-38385599	HepG2	liver:	n/a	chr6:38385499-38385510
10	CEBPB	chr6:38385352-38385628	Hela-S3	cervix:	n/a	chr6:38385499-38385510
11	CEBPB	chr6:38385945-38386423	K562	blood:	n/a	chr6:38386031-38386040 chr6:38386031-38386042 chr6:38386029-38386040 chr6:38386029-38386042
12	CEBPB	chr6:38404599-38405042	MCF-7	breast:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
13	CEBPB	chr6:38385339-38385668	MCF-7	breast:	n/a	chr6:38385499-38385510
14	CEBPB	chr6:38385365-38385623	H1-hESC	embryonic stem cell:	n/a	chr6:38385499-38385510
15	CEBPB	chr6:38402959-38403241	HepG2	liver:	n/a	chr6:38403067-38403078
16	CEBPB	chr6:38404527-38405019	MCF-7	breast:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
17	CEBPB	chr6:38385282-38385651	HCT-116	colon:	n/a	chr6:38385499-38385510
18	CEBPB	chr6:38404552-38404999	IMR90	lung:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
19	CEBPB	chr6:38450125-38450728	MCF-7	breast:	n/a	n/a
20	CEBPB	chr6:38385427-38385694	ECC-1	luminal epithelium:	n/a	chr6:38385499-38385510 chr6:38385686-38385694
21	CEBPB	chr6:38385415-38385606	HepG2	liver:	n/a	chr6:38385499-38385510
22	CEBPB	chr6:38445586-38445959	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr6:38448119-38448354	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:38450326-38450570	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr6:38404618-38404982	A549	lung:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
26	CEBPB	chr6:38404748-38404953	H1-hESC	embryonic stem cell:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
27	CEBPB	chr6:38385374-38385622	IMR90	lung:	n/a	chr6:38385499-38385510
28	CEBPB	chr6:38448084-38448348	IMR90	lung:	n/a	n/a
29	CEBPB	chr6:38404452-38405116	HCT-116	colon:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
30	CEBPB	chr6:38404559-38405061	A549	lung:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
31	CEBPB	chr6:38385886-38386476	IMR90	lung:	n/a	chr6:38386031-38386040 chr6:38386031-38386042 chr6:38386029-38386040 chr6:38386029-38386042
32	CEBPB	chr6:38385284-38385708	HCT-116	colon:	n/a	chr6:38385499-38385510 chr6:38385686-38385694
33	CEBPB	chr6:38385296-38385779	MCF-7	breast:	n/a	chr6:38385499-38385510 chr6:38385686-38385694
34	CEBPB	chr6:38450272-38450650	MCF-7	breast:	n/a	n/a
35	CEBPB	chr6:38404623-38404982	HepG2	liver:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
36	CEBPB	chr6:38404606-38404974	Hela-S3	cervix:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
37	CHD2	chr6:38395664-38396087	GM12878	blood:	n/a	n/a
38	CREB1	chr6:38411557-38411937	GM12878	blood:	n/a	n/a
39	CTCF	chr6:38400920-38401070	GM12867	blood:	n/a	n/a
40	CTCF	chr6:38407481-38407514	Lung_OC	lung:	n/a	n/a
41	CTCF	chr6:38400460-38400610	HMEC	breast:	n/a	n/a
42	CTCF	chr6:38411720-38411870	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr6:38400471-38400579	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr6:38400380-38400530	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr6:38400420-38400570	BJ	skin:	n/a	n/a
46	CTCF	chr6:38400460-38400610	HEK293	kidney:	n/a	n/a
47	CTCF	chr6:38400472-38400511	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr6:38400481-38400572	Fibrobl	skin:	n/a	n/a
49	CTCF	chr6:38400440-38400590	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr6:38400420-38400570	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:38394278-38394328	Caco-2	colon:	n/a
2	chr6:38394278-38394328	HepG2	liver:	n/a
3	chr6:38394278-38394328	AG04449	skin:	fetal
4	chr6:38394278-38394328	HCM	heart:	n/a
5	chr6:38445981-38446031	MCF10A-Er-Src	breast:	n/a
6	chr6:38445981-38446031	GM12891	blood:	n/a
7	chr6:38445981-38446031	AG10803	skin:	n/a
8	chr6:38445981-38446031	HEK293	kidney:	embryo
9	chr6:38445981-38446031	A549	lung:	n/a
10	chr6:38394278-38394328	GM06990	blood:	n/a
11	chr6:38394278-38394328	ProgFib	skin:	n/a
12	chr6:38445981-38446031	GM12892	blood:	n/a
13	chr6:38394278-38394328	AoSMC	blood vessel:	n/a
14	chr6:38445981-38446031	AG09319	gingival:	n/a
15	chr6:38445981-38446031	BJ	skin:	n/a
16	chr6:38394278-38394328	U87	brain:	n/a
17	chr6:38394278-38394328	Hepatocyte	liver:	n/a
18	chr6:38394278-38394328	HCT-116	colon:	n/a
19	chr6:38394278-38394328	CMK	blood:	n/a
20	chr6:38394278-38394328	Hela-S3	cervix:	n/a
21	chr6:38445981-38446031	H1-hESC	embryonic stem cell:	embryo
22	chr6:38394278-38394328	NB4	blood:	n/a
23	chr6:38445981-38446031	HRE	kidney:	n/a
24	chr6:38445981-38446031	HCF	heart:	n/a
25	chr6:38394278-38394328	GM12891	blood:	n/a
26	chr6:38445981-38446031	NHDF-neo	bronchial:	n/a
27	chr6:38445981-38446031	CMK	blood:	n/a
28	chr6:38394278-38394328	ECC-1	luminal epithelium:	n/a
29	chr6:38394278-38394328	SAEC	small airway:	n/a
30	chr6:38445981-38446031	MCF-7	breast:	n/a
31	chr6:38445981-38446031	SK-N-SH_RA	brain:	n/a
32	chr6:38394278-38394328	AG04450	lung:	fetal
33	chr6:38394278-38394328	NT2-D1	testis:	n/a
34	chr6:38394278-38394328	Jurkat	blood:	n/a
35	chr6:38445981-38446031	AG09309	skin:	n/a
36	chr6:38445981-38446031	Hepatocyte	liver:	n/a
37	chr6:38445981-38446031	SK-N-MC	brain:	n/a
38	chr6:38394278-38394328	HNPCEpiC	eye:	n/a
39	chr6:38445981-38446031	ovcar-3	ovarian:	n/a
40	chr6:38394278-38394328	T-47D	breast:	n/a
41	chr6:38394278-38394328	ovcar-3	ovarian:	n/a
42	chr6:38394278-38394328	NHDF-neo	bronchial:	n/a
43	chr6:38445981-38446031	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:38445981-38446031	ECC-1	luminal epithelium:	n/a
45	chr6:38445981-38446031	PANC-1	pancreas:	n/a
46	chr6:38394278-38394328	GM12878	blood:	n/a
47	chr6:38394278-38394328	AG09319	gingival:	n/a
48	chr6:38394278-38394328	GM12892	blood:	n/a
49	chr6:38445981-38446031	NT2-D1	testis:	n/a
50	chr6:38445981-38446031	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr6:38443341..38445345-chr6:38445490..38448475,2	MCF-7	breast:
2	chr6:38421940..38424040-chr6:38426250..38428177,2	K562	blood:
3	chr6:38406164..38407857-chr6:38442817..38445173,2	K562	blood:
4	chr6:38449509..38451131-chr6:38453879..38455476,2	MCF-7	breast:
5	chr6:38382277..38384906-chr6:38386748..38389388,2	MCF-7	breast:
6	chr6:38415370..38417878-chr6:38418782..38420645,2	MCF-7	breast:
7	chr6:38375672..38377894-chr6:38379334..38382033,2	MCF-7	breast:
8	chr6:38421940..38424040-chr6:38426250..38428177,2	K562	blood:
9	chr6:38406164..38407857-chr6:38442817..38445173,2	K562	blood:
10	chr6:38229115..38229659-chr6:38404798..38405463,2	MCF-7	breast:
11	chr6:38410346..38413041-chr6:38421338..38423278,2	MCF-7	breast:
12	chr6:38435448..38438389-chr6:38439030..38441795,2	MCF-7	breast:
13	chr6:38382277..38384906-chr6:38386748..38389388,2	MCF-7	breast:
14	chr6:38415370..38417878-chr6:38418782..38420645,2	MCF-7	breast:
15	chr6:38443341..38445345-chr6:38445490..38448475,2	MCF-7	breast:
16	chr6:38411269..38413093-chr6:38413488..38416191,2	K562	blood:
17	chr6:38371909..38373449-chr6:38395704..38397463,2	K562	blood:
18	chr6:38410346..38413041-chr6:38421338..38423278,2	MCF-7	breast:
19	chr6:38441969..38444159-chr6:38445659..38447643,2	K562	blood:
20	chr6:38375672..38377894-chr6:38379334..38382033,2	MCF-7	breast:
21	chr6:38357729..38359260-chr6:38373840..38376265,2	MCF-7	breast:
22	chr6:38423292..38425801-chr6:38436010..38438215,2	K562	blood:
23	chr6:38409873..38411784-chr6:38412186..38413893,2	MCF-7	breast:
24	chr6:38423292..38425801-chr6:38436010..38438215,2	K562	blood:
25	chr6:38411269..38413093-chr6:38413488..38416191,2	K562	blood:
26	chr6:38441969..38444159-chr6:38445659..38447643,2	K562	blood:
27	chr6:38409873..38411784-chr6:38412186..38413893,2	MCF-7	breast:
28	chr6:38435448..38438389-chr6:38439030..38441795,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNAH8-3	chr6:38449468-38449562	ENSG00000226533.1
2	lnc-DNAH8-3	chr6:38449843-38450307	ENSG00000226533.1

Variant related genes	Relation type
BTBD9-AS1	TF binding region
BTBD9-AS1	CpG island

Extended variants
information (count: 2837 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2837 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6903767	chr6:38374812-38374813	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555932629	chr6:38374849-38374850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184584911	chr6:38374933-38374934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547795535	chr6:38374982-38374983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188555929	chr6:38374991-38374992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566949175	chr6:38375005-38375006	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528227762	chr6:38375008-38375009	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547958594	chr6:38375041-38375042	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568074108	chr6:38375069-38375070	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74758094	chr6:38375089-38375090	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35444141	chr6:38375107-38375108	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536667197	chr6:38375111-38375112	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556507321	chr6:38375147-38375148	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570425573	chr6:38375154-38375155	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539305077	chr6:38375176-38375177	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552797850	chr6:38375197-38375198	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368534102	chr6:38375218-38375219	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572944239	chr6:38375254-38375255	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542344993	chr6:38375255-38375256	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115592375	chr6:38375267-38375268	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570843782	chr6:38375270-38375271	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560727043	chr6:38375272-38375273	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558141180	chr6:38375286-38375287	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs4714158	chr6:38375334-38375335	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs552298886	chr6:38375353-38375354	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544626226	chr6:38375363-38375364	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540571029	chr6:38375377-38375378	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564425777	chr6:38375392-38375393	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35983276	chr6:38375398-38375399	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs578261476	chr6:38375423-38375424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562875175	chr6:38375447-38375448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570465255	chr6:38375516-38375517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553926303	chr6:38375665-38375666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375392609	chr6:38375715-38375716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs74531250	chr6:38375770-38375771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77951370	chr6:38375783-38375784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs78251185	chr6:38375787-38375788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150504493	chr6:38375831-38375832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116618178	chr6:38375858-38375859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561647071	chr6:38375899-38375900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371633581	chr6:38375942-38375943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550166286	chr6:38375952-38375953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570113237	chr6:38375963-38375964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs9380747	chr6:38375969-38375970	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs117925972	chr6:38375988-38375989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79546470	chr6:38375991-38375992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535313812	chr6:38376004-38376005	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555497120	chr6:38376051-38376052	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139443357	chr6:38376089-38376090	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116525682	chr6:38376124-38376125	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	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
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38354000-38376000	Weak transcription	Primary T cells from cord blood	blood
2	chr6:38370800-38375200	Enhancers	Fetal Brain Male	brain
3	chr6:38371200-38375600	Enhancers	Adipose Nuclei	Adipose
4	chr6:38371600-38376400	Enhancers	Liver	Liver
5	chr6:38372600-38375000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:38372800-38376200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr6:38373000-38376800	Weak transcription	Aorta	Aorta
8	chr6:38373200-38395600	Weak transcription	Fetal Intestine Small	intestine
9	chr6:38373800-38375200	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr6:38373800-38383400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr6:38374000-38375200	Weak transcription	Brain Hippocampus Middle	brain
12	chr6:38374000-38375200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr6:38374200-38383000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:38374400-38375400	Enhancers	Esophagus	oesophagus
15	chr6:38374600-38375400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:38374600-38375400	Enhancers	Primary B cells from peripheral blood	blood
17	chr6:38374600-38375400	Enhancers	Ovary	ovary
18	chr6:38374600-38375400	Enhancers	Psoas Muscle	Psoas
19	chr6:38374600-38376200	Enhancers	GM12878-XiMat	blood
20	chr6:38375000-38375400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:38375200-38375400	Enhancers	Brain Hippocampus Middle	brain
22	chr6:38375200-38375400	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr6:38375200-38375400	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr6:38375200-38376000	Weak transcription	Fetal Brain Male	brain
25	chr6:38375400-38376200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:38375400-38381000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr6:38375400-38381000	Weak transcription	Ovary	ovary
28	chr6:38375400-38387600	Weak transcription	Psoas Muscle	Psoas
29	chr6:38376000-38376800	Strong transcription	Primary T cells from cord blood	blood
30	chr6:38376000-38376800	Enhancers	Fetal Brain Male	brain
31	chr6:38376200-38376400	Flanking Active TSS	GM12878-XiMat	blood
32	chr6:38376200-38380800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:38376400-38376600	Enhancers	GM12878-XiMat	blood
34	chr6:38376600-38376800	Flanking Active TSS	GM12878-XiMat	blood
35	chr6:38376800-38377000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr6:38376800-38377000	Enhancers	Aorta	Aorta
37	chr6:38376800-38379200	Enhancers	GM12878-XiMat	blood
38	chr6:38376800-38380800	Weak transcription	Fetal Brain Male	brain
39	chr6:38376800-38411400	Weak transcription	Primary T cells from cord blood	blood
40	chr6:38379400-38379600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:38380800-38381000	Enhancers	Fetal Brain Male	brain
42	chr6:38380800-38381600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:38381000-38381200	Enhancers	Ovary	ovary
44	chr6:38381000-38381400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:38381400-38381800	Enhancers	Brain Angular Gyrus	brain
46	chr6:38381400-38382800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:38381600-38382800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:38382800-38383200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:38382800-38383800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:38383000-38383400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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