Variant report

Variant	nsv883535
Chromosome Location	chr6:29725321-29741338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:173)
CpG islands
(count:183)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:173 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:29725509-29725764	K562	blood:	n/a	n/a
2	BACH1	chr6:29739723-29739738	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:29725411-29725848	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:29727429-29727629	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:29731473-29731729	GM12878	blood:	n/a	chr6:29731606-29731617
6	BHLHE40	chr6:29728231-29728441	K562	blood:	n/a	n/a
7	BHLHE40	chr6:29725706-29726221	K562	blood:	n/a	n/a
8	CBX3	chr6:29728244-29728637	K562	blood:	n/a	n/a
9	CEBPB	chr6:29727210-29727395	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr6:29731423-29731764	IMR90	lung:	n/a	n/a
11	CEBPB	chr6:29731363-29731796	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr6:29731051-29731073	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr6:29731405-29731718	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr6:29727214-29727591	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr6:29725782-29725910	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr6:29739625-29739642	K562	blood:	n/a	n/a
17	CTCF	chr6:29733900-29734050	GM12864	blood:	n/a	n/a
18	CTCF	chr6:29729760-29729910	HepG2	liver:	n/a	n/a
19	CTCF	chr6:29731280-29731430	HAc	cerebellar:	n/a	n/a
20	CTCF	chr6:29739500-29739650	WERI-Rb-1	eye:	n/a	n/a
21	E2F4	chr6:29732259-29732331	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr6:29732717-29733005	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr6:29731466-29731684	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F6	chr6:29727007-29727990	H1-hESC	embryonic stem cell:	n/a	n/a
25	EGR1	chr6:29732244-29732699	MCF-7	breast:	n/a	n/a
26	EGR1	chr6:29725716-29726005	K562	blood:	n/a	chr6:29725894-29725907
27	EGR1	chr6:29725735-29725996	K562	blood:	n/a	chr6:29725894-29725907
28	ELF1	chr6:29727220-29727553	K562	blood:	n/a	chr6:29727358-29727371
29	EP300	chr6:29731435-29731788	Hela-S3	cervix:	n/a	n/a
30	EP300	chr6:29725873-29726164	K562	blood:	n/a	n/a
31	EP300	chr6:29727175-29727621	H1-hESC	embryonic stem cell:	n/a	chr6:29727360-29727369
32	EP300	chr6:29727140-29727527	H1-hESC	embryonic stem cell:	n/a	chr6:29727360-29727369
33	FOS	chr6:29731419-29731859	MCF10A-Er-Src	breast:	n/a	chr6:29731638-29731650 chr6:29731608-29731619
34	FOS	chr6:29732465-29733008	HUVEC	blood vessel:	n/a	chr6:29732834-29732845
35	FOS	chr6:29732577-29733086	MCF10A-Er-Src	breast:	n/a	chr6:29732834-29732845
36	FOS	chr6:29729895-29730095	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr6:29729902-29730090	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:29730648-29730727	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr6:29728586-29728637	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr6:29731355-29732022	MCF10A-Er-Src	breast:	n/a	chr6:29731638-29731650 chr6:29731608-29731619
41	FOS	chr6:29732525-29733086	MCF10A-Er-Src	breast:	n/a	chr6:29732834-29732845
42	FOS	chr6:29732629-29733025	MCF10A-Er-Src	breast:	n/a	chr6:29732834-29732845
43	FOS	chr6:29731418-29731842	MCF10A-Er-Src	breast:	n/a	chr6:29731638-29731650 chr6:29731608-29731619
44	FOS	chr6:29731366-29732011	MCF10A-Er-Src	breast:	n/a	chr6:29731638-29731650 chr6:29731608-29731619
45	FOS	chr6:29732630-29733042	MCF10A-Er-Src	breast:	n/a	chr6:29732834-29732845
46	FOS	chr6:29728565-29728723	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr6:29731200-29731900	HUVEC	blood vessel:	n/a	chr6:29731638-29731650 chr6:29731608-29731619
48	FOS	chr6:29729986-29730095	MCF10A-Er-Src	breast:	n/a	n/a
49	FOSL2	chr6:29741228-29741526	HepG2	liver:	n/a	n/a
50	FOXA1	chr6:29732720-29732969	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29726705-29726755	AG04450	lung:	fetal
2	chr6:29727844-29727894	ECC-1	luminal epithelium:	n/a
3	chr6:29726705-29726755	MCF-7	breast:	n/a
4	chr6:29727844-29727894	GM12891	blood:	n/a
5	chr6:29726626-29726676	HCM	heart:	n/a
6	chr6:29726705-29726755	HCT-116	colon:	n/a
7	chr6:29726626-29726676	HUVEC	blood vessel:	n/a
8	chr6:29726705-29726755	NHBE	bronchial:	n/a
9	chr6:29726705-29726755	T-47D	breast:	n/a
10	chr6:29726626-29726676	BE2_C	brain:	n/a
11	chr6:29726626-29726676	Jurkat	blood:	n/a
12	chr6:29726705-29726755	AG04449	skin:	fetal
13	chr6:29726626-29726676	GM12892	blood:	n/a
14	chr6:29726705-29726755	AG09309	skin:	n/a
15	chr6:29726705-29726755	HEEpiC	esophagus:	n/a
16	chr6:29726626-29726676	HRPEpiC	eye:	n/a
17	chr6:29727844-29727894	HCPEpiC	choroid plexus:	n/a
18	chr6:29727844-29727894	NB4	blood:	n/a
19	chr6:29726626-29726676	GM19239	blood:	n/a
20	chr6:29726626-29726676	SAEC	small airway:	n/a
21	chr6:29727844-29727894	HPAEpiC	pulmonary alveolar:	n/a
22	chr6:29727844-29727894	PrEC	prostate:	n/a
23	chr6:29726705-29726755	PANC-1	pancreas:	n/a
24	chr6:29726626-29726676	HepG2	liver:	n/a
25	chr6:29727844-29727894	AG04450	lung:	fetal
26	chr6:29726705-29726755	HEK293	kidney:	embryo
27	chr6:29726705-29726755	U87	brain:	n/a
28	chr6:29726626-29726676	RPTEC	kidney:	n/a
29	chr6:29726705-29726755	CMK	blood:	n/a
30	chr6:29726705-29726755	HMEC	breast:	n/a
31	chr6:29726705-29726755	Hepatocyte	liver:	n/a
32	chr6:29727844-29727894	HAEpiC	amniotic membrane:	n/a
33	chr6:29727844-29727894	Caco-2	colon:	n/a
34	chr6:29727844-29727894	NHDF-neo	bronchial:	n/a
35	chr6:29727844-29727894	GM12892	blood:	n/a
36	chr6:29726705-29726755	HepG2	liver:	n/a
37	chr6:29727844-29727894	NH-A	brain:	n/a
38	chr6:29727844-29727894	HRE	kidney:	n/a
39	chr6:29727844-29727894	MCF10A-Er-Src	breast:	n/a
40	chr6:29726626-29726676	ECC-1	luminal epithelium:	n/a
41	chr6:29726626-29726676	IMR90	lung:	fetal
42	chr6:29726705-29726755	GM06990	blood:	n/a
43	chr6:29727844-29727894	IMR90	lung:	fetal
44	chr6:29726705-29726755	Jurkat	blood:	n/a
45	chr6:29726626-29726676	AG10803	skin:	n/a
46	chr6:29726705-29726755	MCF10A-Er-Src	breast:	n/a
47	chr6:29726705-29726755	HIPEpiC	eye:	n/a
48	chr6:29726626-29726676	GM12878	blood:	n/a
49	chr6:29726705-29726755	H1-hESC	embryonic stem cell:	embryo
50	chr6:29726705-29726755	Hela-S3	cervix:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29717754..29720157-chr6:29738008..29740778,2	MCF-7	breast:
2	chr6:29719431..29722230-chr6:29728984..29731849,2	MCF-7	breast:
3	chr6:29725785..29727435-chr6:29736523..29738044,2	MCF-7	breast:
4	chr6:29725785..29727435-chr6:29736523..29738044,2	MCF-7	breast:
5	chr6:29718286..29720439-chr6:29724711..29726723,2	K562	blood:
6	chr6:29728325..29730576-chr6:29733816..29735445,2	K562	blood:
7	chr6:29728325..29730576-chr6:29733816..29735445,2	K562	blood:
8	chr6:29727884..29729689-chr6:29740628..29742305,2	K562	blood:
9	chr6:29725320..29727210-chr6:29727863..29730824,2	K562	blood:
10	chr6:29727884..29729689-chr6:29740628..29742305,2	K562	blood:
11	chr6:29740458..29744376-chr6:29780204..29783385,3	K562	blood:
12	chr6:29725320..29727210-chr6:29727863..29730824,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000270896	TF binding region
ENSG00000270896	CpG island
ENSG00000235821	chromatin interactions
ENSG00000272236	chromatin interactions
ENSG00000199290	chromatin interactions
ENSG00000237042	chromatin interactions

Extended variants
information (count: 677 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1737076	chr6:29725321-29725322	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200636476	chr6:29725399-29725400	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186231074	chr6:29725429-29725430	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs9258266	chr6:29725452-29725453	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs552778059	chr6:29725456-29725457	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs572921367	chr6:29725517-29725518	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs1626636	chr6:29725598-29725599	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs369177981	chr6:29725611-29725612	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142130653	chr6:29725696-29725697	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs564228245	chr6:29725718-29725719	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs1633065	chr6:29725721-29725722	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs1625695	chr6:29725724-29725725	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs535431383	chr6:29725841-29725842	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs532547686	chr6:29725843-29725844	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs149003431	chr6:29725872-29725873	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs3131858	chr6:29725898-29725899	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs113579162	chr6:29725906-29725907	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs1633064	chr6:29726015-29726016	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs1633063	chr6:29726046-29726047	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs542733329	chr6:29726062-29726063	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs77185414	chr6:29726149-29726150	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs571060468	chr6:29726163-29726164	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs6935107	chr6:29726169-29726170	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs114671844	chr6:29726185-29726186	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs1633062	chr6:29726196-29726197	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs535850232	chr6:29726211-29726212	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs146718156	chr6:29726239-29726240	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs188212123	chr6:29726357-29726358	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs373979344	chr6:29726371-29726372	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs566967084	chr6:29726407-29726408	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs140326023	chr6:29726413-29726414	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs1633061	chr6:29726423-29726424	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs578191794	chr6:29726472-29726473	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs544066772	chr6:29726474-29726475	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs1633060	chr6:29726475-29726476	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs574323261	chr6:29726480-29726481	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs112294621	chr6:29726525-29726526	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs1633059	chr6:29726550-29726551	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs554708761	chr6:29726573-29726574	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs59290930	chr6:29726578-29726579	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559657210	chr6:29726588-29726589	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs528477711	chr6:29726589-29726590	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs145468226	chr6:29726646-29726647	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs146503768	chr6:29726670-29726671	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs530602981	chr6:29726705-29726706	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs141163595	chr6:29726706-29726707	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs1737075	chr6:29726712-29726713	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs536588306	chr6:29726731-29726732	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs1633058	chr6:29726761-29726762	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs115344325	chr6:29726777-29726778	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29721600-29725400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:29721600-29729400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:29721800-29725400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:29721800-29725400	Weak transcription	Hela-S3	cervix
5	chr6:29721800-29725400	Weak transcription	HMEC	breast
6	chr6:29723000-29728600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr6:29723200-29728600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr6:29723200-29728600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr6:29723200-29728600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:29723600-29725400	Weak transcription	K562	blood
11	chr6:29723600-29726800	Weak transcription	Spleen	Spleen
12	chr6:29723600-29728000	Weak transcription	Primary B cells from peripheral blood	blood
13	chr6:29723800-29725400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr6:29723800-29725400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:29724200-29726800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr6:29724200-29728000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr6:29724200-29728400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr6:29724200-29728600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr6:29724200-29728600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr6:29724600-29725400	Enhancers	Liver	Liver
21	chr6:29724800-29725400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr6:29725000-29727600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr6:29725200-29725800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:29725200-29728200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:29725200-29728400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:29725400-29725800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr6:29725400-29725800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr6:29725400-29725800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr6:29725400-29726000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:29725400-29726000	Enhancers	HMEC	breast
31	chr6:29725400-29726600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:29725400-29727400	Enhancers	K562	blood
33	chr6:29725400-29728000	Enhancers	Hela-S3	cervix
34	chr6:29725600-29725800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr6:29725800-29726600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr6:29725800-29727400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:29725800-29727600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr6:29725800-29728400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:29725800-29728600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr6:29726000-29726400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr6:29726000-29729000	Weak transcription	HMEC	breast
42	chr6:29726200-29726400	Bivalent Enhancer	Fetal Kidney	kidney
43	chr6:29726400-29728400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr6:29726600-29727000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr6:29726600-29727000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:29726800-29727200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr6:29726800-29727800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:29726800-29728000	Bivalent Enhancer	HepG2	liver
49	chr6:29726800-29728400	Enhancers	Spleen	Spleen
50	chr6:29726800-29728600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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