Variant report

Variant	nsv528632
Chromosome Location	chr6:119380885-119397860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:79)
CpG islands
(count:367)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:79 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:119388308-119388636	K562	blood:	n/a	n/a
2	ARID3A	chr6:119387925-119388005	K562	blood:	n/a	n/a
3	ATF1	chr6:119388315-119388618	K562	blood:	n/a	n/a
4	BACH1	chr6:119396652-119396663	K562	blood:	n/a	n/a
5	BHLHE40	chr6:119388304-119388720	K562	blood:	n/a	n/a
6	CCNT2	chr6:119388430-119388532	K562	blood:	n/a	n/a
7	CCNT2	chr6:119387842-119387939	K562	blood:	n/a	n/a
8	CEBPB	chr6:119392777-119393105	HepG2	liver:	n/a	chr6:119392926-119392939
9	CEBPB	chr6:119382408-119382730	K562	blood:	n/a	chr6:119382576-119382587
10	CEBPB	chr6:119382386-119382720	K562	blood:	n/a	chr6:119382576-119382587
11	CEBPB	chr6:119387843-119388105	K562	blood:	n/a	n/a
12	CEBPB	chr6:119392760-119393082	HepG2	liver:	n/a	chr6:119392926-119392939
13	CEBPB	chr6:119382420-119382741	HepG2	liver:	n/a	chr6:119382576-119382587
14	CEBPB	chr6:119387869-119388061	K562	blood:	n/a	n/a
15	CEBPB	chr6:119387803-119388161	K562	blood:	n/a	n/a
16	CEBPB	chr6:119392836-119393008	HepG2	liver:	n/a	chr6:119392926-119392939
17	CEBPB	chr6:119382507-119382707	H1-hESC	embryonic stem cell:	n/a	chr6:119382576-119382587
18	CEBPB	chr6:119382501-119382724	IMR90	lung:	n/a	chr6:119382576-119382587
19	CEBPB	chr6:119382478-119382648	K562	blood:	n/a	chr6:119382576-119382587
20	CEBPB	chr6:119382451-119382662	HepG2	liver:	n/a	chr6:119382576-119382587
21	CUX1	chr6:119387846-119387944	K562	blood:	n/a	chr6:119387918-119387932
22	CUX1	chr6:119381443-119381511	K562	blood:	n/a	n/a
23	CUX1	chr6:119388312-119388857	K562	blood:	n/a	n/a
24	E2F4	chr6:119386374-119386419	MCF10A-Er-Src	breast:	n/a	n/a
25	EBF1	chr6:119394666-119394866	GM12878	blood:	n/a	chr6:119394758-119394769
26	EBF1	chr6:119394632-119394906	GM12878	blood:	n/a	chr6:119394758-119394769
27	ELK1	chr6:119381437-119381496	GM12878	blood:	n/a	n/a
28	EP300	chr6:119392679-119393080	HepG2	liver:	n/a	n/a
29	EP300	chr6:119381742-119381927	K562	blood:	n/a	n/a
30	EP300	chr6:119387829-119388645	K562	blood:	n/a	chr6:119388242-119388256
31	GATA3	chr6:119385555-119385833	T-47D	breast:	n/a	n/a
32	HNF4A	chr6:119392801-119393087	HepG2	liver:	n/a	chr6:119393001-119393016 chr6:119393001-119393016
33	HNF4A	chr6:119392821-119393091	HepG2	liver:	n/a	chr6:119393001-119393016 chr6:119393001-119393016
34	HNF4G	chr6:119392757-119393091	HepG2	liver:	n/a	chr6:119393001-119393016 chr6:119393001-119393016
35	IRF1	chr6:119387392-119387412	K562	blood:	n/a	n/a
36	JUND	chr6:119388288-119388678	K562	blood:	n/a	n/a
37	JUND	chr6:119382595-119382600	HepG2	liver:	n/a	n/a
38	JUND	chr6:119381784-119381947	K562	blood:	n/a	n/a
39	JUND	chr6:119387750-119388024	K562	blood:	n/a	chr6:119387762-119387770 chr6:119387761-119387771
40	KAP1	chr6:119397303-119397773	U2OS	brain:	n/a	n/a
41	KAP1	chr6:119381638-119382084	U2OS	brain:	n/a	n/a
42	MAFF	chr6:119388374-119388498	K562	blood:	n/a	n/a
43	MAFF	chr6:119394144-119394387	HepG2	liver:	n/a	n/a
44	MAFF	chr6:119394130-119394367	K562	blood:	n/a	n/a
45	MAFK	chr6:119394158-119394422	HepG2	liver:	n/a	n/a
46	MAFK	chr6:119394165-119394397	HepG2	liver:	n/a	n/a
47	MAX	chr6:119381744-119382128	K562	blood:	n/a	n/a
48	MAZ	chr6:119381769-119381941	K562	blood:	n/a	n/a
49	MYC	chr6:119396069-119396137	MCF10A-Er-Src	breast:	n/a	n/a
50	MYC	chr6:119381457-119381480	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:119390418-119390468	HCT-116	colon:	n/a
2	chr6:119390418-119390468	HCT-116	colon:	n/a
3	chr6:119390286-119390336	SK-N-SH	brain:	n/a
4	chr6:119390418-119390468	HCM	heart:	n/a
5	chr6:119395189-119395239	PrEC	prostate:	n/a
6	chr6:119390286-119390336	A549	lung:	n/a
7	chr6:119397402-119397452	GM12891	blood:	n/a
8	chr6:119395189-119395239	NT2-D1	testis:	n/a
9	chr6:119395189-119395239	HIPEpiC	eye:	n/a
10	chr6:119397402-119397452	MCF10A-Er-Src	breast:	n/a
11	chr6:119390286-119390336	HCT-116	colon:	n/a
12	chr6:119390286-119390336	ECC-1	luminal epithelium:	n/a
13	chr6:119390646-119390696	NHDF-neo	bronchial:	n/a
14	chr6:119390712-119390762	HAEpiC	amniotic membrane:	n/a
15	chr6:119390418-119390468	HEEpiC	esophagus:	n/a
16	chr6:119390646-119390696	ovcar-3	ovarian:	n/a
17	chr6:119390646-119390696	HL-60	blood:	n/a
18	chr6:119390646-119390696	HCM	heart:	n/a
19	chr6:119390418-119390468	AG04449	skin:	fetal
20	chr6:119390418-119390468	MCF10A-Er-Src	breast:	n/a
21	chr6:119390712-119390762	MCF-7	breast:	n/a
22	chr6:119390712-119390762	GM12891	blood:	n/a
23	chr6:119390418-119390468	AG09309	skin:	n/a
24	chr6:119390712-119390762	A549	lung:	n/a
25	chr6:119395189-119395239	ECC-1	luminal epithelium:	n/a
26	chr6:119390712-119390762	HRE	kidney:	n/a
27	chr6:119390712-119390762	GM19239	blood:	n/a
28	chr6:119390418-119390468	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:119390646-119390696	HCT-116	colon:	n/a
30	chr6:119390418-119390468	AG04450	lung:	fetal
31	chr6:119395189-119395239	A549	lung:	n/a
32	chr6:119390712-119390762	NB4	blood:	n/a
33	chr6:119390418-119390468	AoSMC	blood vessel:	n/a
34	chr6:119390712-119390762	HIPEpiC	eye:	n/a
35	chr6:119390712-119390762	SAEC	small airway:	n/a
36	chr6:119390286-119390336	AoSMC	blood vessel:	n/a
37	chr6:119390646-119390696	HCF	heart:	n/a
38	chr6:119390418-119390468	HEK293	kidney:	embryo
39	chr6:119390286-119390336	AG04450	lung:	fetal
40	chr6:119390286-119390336	GM06990	blood:	n/a
41	chr6:119397402-119397452	IMR90	lung:	fetal
42	chr6:119390646-119390696	AG04449	skin:	fetal
43	chr6:119390646-119390696	HRPEpiC	eye:	n/a
44	chr6:119390712-119390762	HCT-116	colon:	n/a
45	chr6:119390712-119390762	HCF	heart:	n/a
46	chr6:119390712-119390762	Caco-2	colon:	n/a
47	chr6:119390286-119390336	H1-hESC	embryonic stem cell:	embryo
48	chr6:119390646-119390696	HNPCEpiC	eye:	n/a
49	chr6:119390646-119390696	HRCEpiC	kidney:	n/a
50	chr6:119390712-119390762	HPAEpiC	pulmonary alveolar:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:119383826..119386462-chr6:119386776..119389889,4	K562	blood:
2	chr6:119357800..119360745-chr6:119397203..119399369,2	K562	blood:
3	chr6:119384109..119386949-chr6:119396336..119398560,2	K562	blood:
4	chr6:119384109..119386949-chr6:119396336..119398560,2	K562	blood:
5	chr6:119253156..119256806-chr6:119394976..119399977,7	K562	blood:
6	chr6:119381731..119385519-chr6:119386330..119388707,4	K562	blood:
7	chr6:119282607..119285041-chr6:119393256..119395593,2	K562	blood:
8	chr6:119254512..119256806-chr6:119396471..119398017,2	K562	blood:
9	chr6:119366419..119369327-chr6:119386975..119389213,2	K562	blood:
10	chr6:119381731..119385519-chr6:119386330..119388707,4	K562	blood:
11	chr6:119215094..119217164-chr6:119391963..119394614,2	K562	blood:
12	chr6:119383826..119386462-chr6:119386776..119389889,4	K562	blood:
13	chr6:119384404..119387073-chr6:119389709..119391211,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548b-3p	chr6:119390227-119390248	MIMAT0003254
hsa-miR-548b-5p	chr6:119390263-119390284	MIMAT0004798

No data

Variant related genes	Relation type
MIR548B	TF binding region
MIR548B	CpG island
ENSG00000111875	chromatin interactions
ENSG00000207982	chromatin interactions
ENSG00000253194	chromatin interactions
ENSG00000111877	chromatin interactions
TET3	Mature miRNA region
COX7A2	Mature miRNA region
PRC1	Mature miRNA region
ZBTB18	Mature miRNA region
FRS2	Mature miRNA region
TMEM167A	Mature miRNA region
AREL1	Mature miRNA region
AKAP11	Mature miRNA region
INADL	Mature miRNA region
ZBTB21	Mature miRNA region
SNRNP200	Mature miRNA region
RER1	Mature miRNA region
ZBTB39	Mature miRNA region
NBEA	Mature miRNA region
SPRTN	Mature miRNA region
CD46	Mature miRNA region
FAT2	Mature miRNA region
TLE4	Mature miRNA region
SLC25A44	Mature miRNA region
CLCN3	Mature miRNA region
TST	Mature miRNA region
KCTD20	Mature miRNA region
SATB1	Mature miRNA region

Extended variants
information (count: 587 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17080799	chr6:119380885-119380886	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191425454	chr6:119380899-119380900	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564928332	chr6:119381000-119381001	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572069878	chr6:119381002-119381003	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541128663	chr6:119381066-119381067	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181121941	chr6:119381084-119381085	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs17080802	chr6:119381086-119381087	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs11966857	chr6:119381102-119381103	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563852649	chr6:119381154-119381155	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559083927	chr6:119381192-119381193	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142653356	chr6:119381250-119381251	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551434809	chr6:119381253-119381254	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571270497	chr6:119381254-119381255	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533742638	chr6:119381263-119381264	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs371856535	chr6:119381299-119381300	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567342153	chr6:119381306-119381307	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577643964	chr6:119381314-119381315	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112289875	chr6:119381338-119381339	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556320967	chr6:119381372-119381373	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576299614	chr6:119381382-119381383	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559809888	chr6:119381431-119381432	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76214260	chr6:119381462-119381463	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185662272	chr6:119381483-119381484	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs639266	chr6:119381502-119381503	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs540991683	chr6:119381515-119381516	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146012819	chr6:119381548-119381549	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542320734	chr6:119381653-119381654	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574854477	chr6:119381705-119381706	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531548440	chr6:119381733-119381734	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543702700	chr6:119381770-119381771	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111780449	chr6:119381797-119381798	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532710748	chr6:119381813-119381814	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182955261	chr6:119381870-119381871	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373110308	chr6:119381879-119381880	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139919549	chr6:119381915-119381916	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527320820	chr6:119381955-119381956	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs35621042	chr6:119381965-119381966	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188029617	chr6:119382004-119382005	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199826783	chr6:119382021-119382022	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141235985	chr6:119382047-119382048	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1570493	chr6:119382101-119382102	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs549739642	chr6:119382118-119382119	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549571666	chr6:119382188-119382189	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571095082	chr6:119382234-119382235	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17513308	chr6:119382351-119382352	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs558442632	chr6:119382384-119382385	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369181613	chr6:119382390-119382391	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77137077	chr6:119382442-119382443	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565623128	chr6:119382461-119382462	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72953076	chr6:119382464-119382465	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119375000-119382000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr6:119375200-119381200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:119375800-119381400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr6:119378000-119381400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:119378200-119381400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr6:119378200-119381400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr6:119378200-119388400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr6:119380800-119383000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:119380800-119384400	Weak transcription	Fetal Lung	lung
10	chr6:119381200-119382600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr6:119381200-119383000	Enhancers	K562	blood
12	chr6:119381400-119381600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr6:119381400-119382000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:119381400-119382000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:119381400-119382200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr6:119381400-119382400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:119381400-119382400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr6:119381400-119382400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr6:119381600-119382200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr6:119381800-119382000	Enhancers	Fetal Intestine Large	intestine
21	chr6:119381800-119382600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr6:119382000-119382400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr6:119382000-119384800	Weak transcription	Fetal Intestine Large	intestine
24	chr6:119382000-119387200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr6:119382200-119382400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr6:119383000-119385800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:119383000-119387000	Weak transcription	K562	blood
28	chr6:119384400-119385000	Enhancers	Fetal Lung	lung
29	chr6:119384800-119385600	Enhancers	Fetal Intestine Large	intestine
30	chr6:119385000-119385800	Enhancers	Fetal Intestine Small	intestine
31	chr6:119385000-119386600	Weak transcription	Fetal Lung	lung
32	chr6:119385000-119397200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr6:119385600-119386800	Weak transcription	Fetal Intestine Large	intestine
34	chr6:119385800-119387200	Weak transcription	Fetal Intestine Small	intestine
35	chr6:119385800-119388800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:119386600-119388000	Enhancers	Fetal Lung	lung
37	chr6:119386800-119387000	Enhancers	Fetal Intestine Large	intestine
38	chr6:119387000-119387400	Weak transcription	Fetal Intestine Large	intestine
39	chr6:119387000-119388200	Enhancers	K562	blood
40	chr6:119387200-119387800	Enhancers	Fetal Intestine Small	intestine
41	chr6:119387200-119389200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr6:119387400-119387800	Enhancers	Duodenum Mucosa	Duodenum
43	chr6:119387400-119388600	Enhancers	Fetal Intestine Large	intestine
44	chr6:119387600-119388000	Enhancers	Fetal Heart	heart
45	chr6:119387800-119388200	Weak transcription	Duodenum Mucosa	Duodenum
46	chr6:119387800-119391800	Weak transcription	Fetal Intestine Small	intestine
47	chr6:119388200-119388800	Enhancers	Duodenum Mucosa	Duodenum
48	chr6:119388200-119389000	Flanking Active TSS	K562	blood
49	chr6:119388400-119388600	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr6:119388600-119392200	Weak transcription	Fetal Intestine Large	intestine

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