Variant report

Variant	nsv883412
Chromosome Location	chr6:4349808-4376376
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:843)
CpG islands
(count:245)
Chromatin interactive
region (count:27)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:4358943-4359212	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:4358995-4359244	K562	blood:	n/a	n/a
3	ARID3A	chr6:4371555-4372189	K562	blood:	n/a	n/a
4	ATF1	chr6:4371386-4372137	K562	blood:	n/a	n/a
5	ATF1	chr6:4358933-4359347	K562	blood:	n/a	n/a
6	ATF3	chr6:4358772-4359356	A549	lung:	n/a	chr6:4359087-4359101
7	ATF3	chr6:4352090-4352762	A549	lung:	n/a	n/a
8	ATF3	chr6:4358697-4359404	A549	lung:	n/a	chr6:4359087-4359101
9	BACH1	chr6:4359681-4359836	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:4358618-4359481	H1-hESC	embryonic stem cell:	n/a	chr6:4358987-4359001
11	BACH1	chr6:4358909-4359109	K562	blood:	n/a	chr6:4358987-4359001
12	BCL3	chr6:4358806-4359364	A549	lung:	n/a	n/a
13	BCL3	chr6:4358658-4359374	A549	lung:	n/a	n/a
14	BHLHE40	chr6:4358824-4359540	K562	blood:	n/a	n/a
15	BHLHE40	chr6:4349843-4349883	K562	blood:	n/a	n/a
16	BHLHE40	chr6:4371434-4372512	K562	blood:	n/a	n/a
17	BHLHE40	chr6:4358856-4359271	HepG2	liver:	n/a	n/a
18	BRCA1	chr6:4350805-4351110	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr6:4358829-4359310	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr6:4358607-4359510	HCT-116	colon:	n/a	n/a
21	CBX3	chr6:4371514-4372140	K562	blood:	n/a	n/a
22	CBX3	chr6:4358901-4359260	K562	blood:	n/a	n/a
23	CCNT2	chr6:4358812-4359272	K562	blood:	n/a	n/a
24	CCNT2	chr6:4352256-4352363	K562	blood:	n/a	n/a
25	CCNT2	chr6:4371578-4372104	K562	blood:	n/a	n/a
26	CEBPB	chr6:4358793-4359217	A549	lung:	n/a	n/a
27	CEBPB	chr6:4359586-4359903	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr6:4358818-4359118	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:4358732-4359944	IMR90	lung:	n/a	n/a
30	CEBPB	chr6:4358813-4359207	A549	lung:	n/a	n/a
31	CEBPB	chr6:4351965-4352633	A549	lung:	n/a	n/a
32	CEBPB	chr6:4358722-4359319	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr6:4363963-4364244	IMR90	lung:	n/a	n/a
34	CEBPB	chr6:4355406-4355923	A549	lung:	n/a	chr6:4355849-4355861 chr6:4355497-4355505
35	CEBPB	chr6:4358807-4359083	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr6:4358713-4359337	MCF-7	breast:	n/a	n/a
37	CEBPB	chr6:4355383-4355888	Hela-S3	cervix:	n/a	chr6:4355849-4355861 chr6:4355497-4355505
38	CEBPB	chr6:4358670-4359832	A549	lung:	n/a	n/a
39	CEBPB	chr6:4358923-4359044	K562	blood:	n/a	n/a
40	CEBPB	chr6:4355266-4355860	A549	lung:	n/a	chr6:4355497-4355505
41	CEBPB	chr6:4350829-4351135	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr6:4351986-4352685	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr6:4359605-4359798	HepG2	liver:	n/a	n/a
44	CEBPB	chr6:4355084-4355941	IMR90	lung:	n/a	chr6:4355849-4355861 chr6:4355497-4355505
45	CEBPB	chr6:4351854-4352643	IMR90	lung:	n/a	n/a
46	CEBPB	chr6:4355260-4355956	A549	lung:	n/a	chr6:4355849-4355861 chr6:4355497-4355505
47	CEBPD	chr6:4371633-4372105	K562	blood:	n/a	n/a
48	CHD2	chr6:4358723-4359391	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr6:4350774-4351386	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr6:4355144-4355937	Hela-S3	cervix:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4350359-4350409	SK-N-MC	brain:	n/a
2	chr6:4350359-4350409	SK-N-MC	brain:	n/a
3	chr6:4358810-4358860	AG04449	skin:	fetal
4	chr6:4370460-4370510	HCF	heart:	n/a
5	chr6:4352453-4352503	ProgFib	skin:	n/a
6	chr6:4370460-4370510	HAEpiC	amniotic membrane:	n/a
7	chr6:4358810-4358860	HMEC	breast:	n/a
8	chr6:4352453-4352503	GM12878	blood:	n/a
9	chr6:4352453-4352503	HRCEpiC	kidney:	n/a
10	chr6:4352453-4352503	A549	lung:	n/a
11	chr6:4370460-4370510	HCPEpiC	choroid plexus:	n/a
12	chr6:4350359-4350409	HMEC	breast:	n/a
13	chr6:4352453-4352503	AoSMC	blood vessel:	n/a
14	chr6:4352453-4352503	SK-N-SH	brain:	n/a
15	chr6:4352453-4352503	LNCaP	prostate:	n/a
16	chr6:4358810-4358860	BE2_C	brain:	n/a
17	chr6:4370460-4370510	BJ	skin:	n/a
18	chr6:4358810-4358860	Caco-2	colon:	n/a
19	chr6:4370460-4370510	HepG2	liver:	n/a
20	chr6:4358810-4358860	Hepatocyte	liver:	n/a
21	chr6:4350359-4350409	HAEpiC	amniotic membrane:	n/a
22	chr6:4370460-4370510	A549	lung:	n/a
23	chr6:4358810-4358860	HCF	heart:	n/a
24	chr6:4352453-4352503	GM12891	blood:	n/a
25	chr6:4358810-4358860	SK-N-SH_RA	brain:	n/a
26	chr6:4350359-4350409	HCF	heart:	n/a
27	chr6:4370460-4370510	SK-N-SH_RA	brain:	n/a
28	chr6:4358810-4358860	HEEpiC	esophagus:	n/a
29	chr6:4370460-4370510	SKMC	muscle:	n/a
30	chr6:4370460-4370510	Hela-S3	cervix:	n/a
31	chr6:4352453-4352503	PrEC	prostate:	n/a
32	chr6:4350359-4350409	HCM	heart:	n/a
33	chr6:4358810-4358860	HAEpiC	amniotic membrane:	n/a
34	chr6:4370460-4370510	K562	blood:	n/a
35	chr6:4358810-4358860	NB4	blood:	n/a
36	chr6:4358810-4358860	H1-hESC	embryonic stem cell:	embryo
37	chr6:4370460-4370510	HRE	kidney:	n/a
38	chr6:4370460-4370510	HEEpiC	esophagus:	n/a
39	chr6:4370460-4370510	AG09319	gingival:	n/a
40	chr6:4358810-4358860	IMR90	lung:	fetal
41	chr6:4352453-4352503	Hela-S3	cervix:	n/a
42	chr6:4350359-4350409	AG04450	lung:	fetal
43	chr6:4370460-4370510	HRCEpiC	kidney:	n/a
44	chr6:4350359-4350409	PANC-1	pancreas:	n/a
45	chr6:4352453-4352503	CMK	blood:	n/a
46	chr6:4370460-4370510	GM06990	blood:	n/a
47	chr6:4358810-4358860	Jurkat	blood:	n/a
48	chr6:4352453-4352503	HL-60	blood:	n/a
49	chr6:4352453-4352503	Hepatocyte	liver:	n/a
50	chr6:4370460-4370510	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:4357867..4361282-chr6:4367398..4370344,4	MCF-7	breast:
2	chr6:4349515..4351510-chr6:4353133..4355673,2	MCF-7	breast:
3	chr6:4358711..4363126-chr6:4363507..4365655,4	MCF-7	breast:
4	chr13:96329105..96329998-chr6:4358903..4359458,2	Hela-S3	cervix:
5	chr6:4365316..4368041-chr6:5177218..5180072,2	K562	blood:
6	chr6:4319275..4321491-chr6:4359897..4362207,2	MCF-7	breast:
7	chr6:4359577..4361173-chr6:4490171..4493110,2	MCF-7	breast:
8	chr6:4368958..4371929-chr6:4378307..4380468,2	K562	blood:
9	chr6:4340460..4343142-chr6:4357521..4360296,2	MCF-7	breast:
10	chr6:4342872..4345232-chr6:4351018..4352663,2	MCF-7	breast:
11	chr6:4358711..4363126-chr6:4363507..4365655,4	MCF-7	breast:
12	chr6:4368833..4371140-chr6:4377835..4379659,2	MCF-7	breast:
13	chr6:4351209..4353665-chr6:4356006..4358889,4	MCF-7	breast:
14	chr6:4321843..4323529-chr6:4350636..4352389,2	MCF-7	breast:
15	chr6:4353848..4355960-chr6:4776598..4779085,2	K562	blood:
16	chr6:4357867..4361282-chr6:4367398..4370344,4	MCF-7	breast:
17	chr6:4352359..4354263-chr6:4776426..4779094,2	MCF-7	breast:
18	chr6:4340786..4343119-chr6:4351135..4354014,2	K562	blood:
19	chr6:4365852..4368376-chr6:4465065..4467160,2	MCF-7	breast:
20	chr6:4371859..4373766-chr6:4377826..4380202,2	MCF-7	breast:
21	chr6:4351209..4353665-chr6:4356006..4358889,4	MCF-7	breast:
22	chr6:4349515..4351510-chr6:4353133..4355673,2	MCF-7	breast:
23	chr6:4359417..4361025-chr6:4363589..4366332,2	MCF-7	breast:
24	chr6:4358738..4361729-chr6:4368799..4370354,2	K562	blood:
25	chr6:4359417..4361025-chr6:4363589..4366332,2	MCF-7	breast:
26	chr6:4358738..4361729-chr6:4368799..4370354,2	K562	blood:
27	chr11:65192592..65193389-chr6:4359179..4360144,2	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf201-22	chr6:4370140-4370561	NONHSAT107410
2	lnc-C6orf201-22	chr6:4369433-4369742	NONHSAT107410
3	lnc-C6orf201-20	chr6:4371497-4371760	NONHSAT107406
4	lnc-C6orf201-20	chr6:4367057-4367156	NONHSAT107406

No data

Variant related genes	Relation type
ENSG00000231811	TF binding region
ENSG00000231811	CpG island
ENSG00000260239	chromatin interactions
ENSG00000247400	chromatin interactions
ENSG00000102580	chromatin interactions
ENSG00000153046	chromatin interactions

Extended variants
information (count: 1111 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1111 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9504059	chr6:4349808-4349809	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186253224	chr6:4349812-4349813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1265207	chr6:4349814-4349815	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs375688969	chr6:4349821-4349822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190731494	chr6:4349844-4349845	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs7740780	chr6:4349893-4349894	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs539398584	chr6:4349913-4349914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116406729	chr6:4349931-4349932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182788223	chr6:4349933-4349934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139890267	chr6:4349941-4349942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535506877	chr6:4349966-4349967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143272682	chr6:4349997-4349998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572020650	chr6:4350048-4350049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187244199	chr6:4350057-4350058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557511259	chr6:4350099-4350100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146200754	chr6:4350101-4350102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546209893	chr6:4350128-4350129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562729440	chr6:4350133-4350134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576363957	chr6:4350167-4350168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148563320	chr6:4350179-4350180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532218081	chr6:4350180-4350181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142907268	chr6:4350237-4350238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191652984	chr6:4350266-4350267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535201610	chr6:4350283-4350284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527639385	chr6:4350305-4350306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs151123508	chr6:4350315-4350316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555536228	chr6:4350375-4350376	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs533237892	chr6:4350397-4350398	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs78676338	chr6:4350416-4350417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569837399	chr6:4350491-4350492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535647162	chr6:4350526-4350527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541302210	chr6:4350554-4350555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183060490	chr6:4350684-4350685	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs6933759	chr6:4350698-4350699	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs141088632	chr6:4350758-4350759	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs144660831	chr6:4350791-4350792	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs578015196	chr6:4350797-4350798	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs557717371	chr6:4350846-4350847	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs529962126	chr6:4350904-4350905	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs571190765	chr6:4350908-4350909	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs540092960	chr6:4350912-4350913	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs372535415	chr6:4350947-4350948	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs188179424	chr6:4350955-4350956	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs147876746	chr6:4350963-4350964	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs542028792	chr6:4350967-4350968	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs562878097	chr6:4350979-4350980	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs9392588	chr6:4350992-4350993	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs541200025	chr6:4351036-4351037	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs564469625	chr6:4351054-4351055	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs9392589	chr6:4351062-4351063	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:97)

Disease	PMID	Source
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
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Schizophrenia	20967226	CNVD
Basal cell lymphoma	21115979	CNVD

Chromatin state (count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4345000-4351600	Weak transcription	HSMMtube	muscle
2	chr6:4345200-4351400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:4345800-4353600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:4346200-4350600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr6:4346200-4350800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:4346200-4350800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr6:4347000-4350800	Weak transcription	Brain Substantia Nigra	brain
8	chr6:4347200-4351800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:4347400-4358600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:4347600-4351800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr6:4347600-4351800	Enhancers	NHLF	lung
12	chr6:4348000-4350200	Enhancers	Stomach Smooth Muscle	stomach
13	chr6:4348000-4351200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:4348000-4351800	Weak transcription	HSMM	muscle
15	chr6:4348200-4351400	Weak transcription	Right Ventricle	heart
16	chr6:4348200-4352000	Enhancers	Rectal Smooth Muscle	rectum
17	chr6:4348400-4350200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr6:4348400-4350400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:4348400-4350400	Weak transcription	Left Ventricle	heart
20	chr6:4348400-4350600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:4348400-4351600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:4348800-4350600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:4349000-4351000	Weak transcription	NH-A	brain
24	chr6:4349000-4351600	Weak transcription	Fetal Heart	heart
25	chr6:4349000-4351800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr6:4349200-4350600	Weak transcription	Fetal Stomach	stomach
27	chr6:4349400-4350800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr6:4349600-4351600	Enhancers	NHDF-Ad	bronchial
29	chr6:4349800-4351000	Weak transcription	Colon Smooth Muscle	Colon
30	chr6:4349800-4351400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr6:4349800-4351800	Enhancers	Right Atrium	heart
32	chr6:4350000-4350600	Enhancers	Spleen	Spleen
33	chr6:4350000-4351800	Enhancers	Hela-S3	cervix
34	chr6:4350000-4351800	Enhancers	HMEC	breast
35	chr6:4350200-4350400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr6:4350200-4350600	Weak transcription	Stomach Smooth Muscle	stomach
37	chr6:4350200-4351200	Enhancers	Lung	lung
38	chr6:4350200-4351400	Enhancers	Fetal Muscle Trunk	muscle
39	chr6:4350200-4352000	Enhancers	Fetal Muscle Leg	muscle
40	chr6:4350200-4352800	Enhancers	HUVEC	blood vessel
41	chr6:4350200-4353200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr6:4350400-4351600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr6:4350400-4351800	Enhancers	Adipose Nuclei	Adipose
44	chr6:4350400-4352000	Enhancers	Left Ventricle	heart
45	chr6:4350400-4352800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:4350400-4353600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr6:4350600-4351000	Enhancers	Stomach Smooth Muscle	stomach
48	chr6:4350600-4351400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:4350600-4351800	Enhancers	Brain Cingulate Gyrus	brain
50	chr6:4350600-4351800	Enhancers	Brain Hippocampus Middle	brain

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