Variant report

Variant	esv1805371
Chromosome Location	chr6:35761684-35766871
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	BHLHE40	chr6:35765017-35765289	K562	blood:	n/a	n/a
2	CEBPB	chr6:35762562-35762885	K562	blood:	n/a	n/a
3	CTCF	chr6:35765740-35765890	GM12864	blood:	n/a	n/a
4	CTCF	chr6:35766010-35766063	H1-hESC	embryonic stem cell:	n/a	n/a
5	E2F6	chr6:35766297-35766870	H1-hESC	embryonic stem cell:	n/a	n/a
6	E2F6	chr6:35766372-35766946	H1-hESC	embryonic stem cell:	n/a	n/a
7	EGR1	chr6:35765030-35765252	K562	blood:	n/a	n/a
8	EGR1	chr6:35763349-35763621	K562	blood:	n/a	chr6:35763477-35763491 chr6:35763478-35763491 chr6:35763479-35763490 chr6:35763479-35763490 chr6:35763479-35763488
9	ELF1	chr6:35764865-35765253	GM12878	blood:	n/a	n/a
10	FOXA1	chr6:35764086-35764407	T-47D	breast:	n/a	n/a
11	FOXA1	chr6:35764145-35764400	T-47D	breast:	n/a	n/a
12	GTF2F1	chr6:35765022-35765053	H1-hESC	embryonic stem cell:	n/a	n/a
13	GTF2F1	chr6:35763645-35763723	K562	blood:	n/a	n/a
14	GTF2F1	chr6:35766681-35766722	H1-hESC	embryonic stem cell:	n/a	n/a
15	JUN	chr6:35765331-35765335	H1-hESC	embryonic stem cell:	n/a	n/a
16	MAFF	chr6:35762658-35762770	HepG2	liver:	n/a	chr6:35762725-35762739 chr6:35762719-35762737
17	MAFF	chr6:35762574-35762875	K562	blood:	n/a	chr6:35762725-35762739 chr6:35762719-35762737
18	MAFK	chr6:35762562-35762855	HepG2	liver:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
19	MAFK	chr6:35762579-35762870	HepG2	liver:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
20	MAFK	chr6:35762557-35762899	K562	blood:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
21	MAFK	chr6:35762633-35762864	Hela-S3	cervix:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
22	MAX	chr6:35765943-35766141	K562	blood:	n/a	chr6:35766039-35766048 chr6:35766038-35766048 chr6:35766038-35766049 chr6:35766039-35766048 chr6:35766040-35766047
23	MAX	chr6:35766531-35766863	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738
24	MAX	chr6:35765792-35766276	H1-hESC	embryonic stem cell:	n/a	chr6:35766039-35766048 chr6:35766038-35766048 chr6:35766038-35766049 chr6:35766039-35766048 chr6:35766040-35766047
25	MAX	chr6:35766413-35766899	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738
26	MAX	chr6:35766457-35766910	ECC-1	luminal epithelium:	n/a	chr6:35766728-35766738
27	MAX	chr6:35766425-35766854	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738
28	MAX	chr6:35765902-35766195	K562	blood:	n/a	chr6:35766039-35766048 chr6:35766038-35766048 chr6:35766038-35766049 chr6:35766039-35766048 chr6:35766040-35766047
29	MYC	chr6:35766566-35766816	MCF10A-Er-Src	breast:	n/a	chr6:35766728-35766738
30	MYC	chr6:35766615-35766772	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738
31	MYC	chr6:35766546-35766859	MCF10A-Er-Src	breast:	n/a	chr6:35766728-35766738
32	MYC	chr6:35762319-35762823	K562	blood:	n/a	chr6:35762704-35762713
33	NR2F2	chr6:35765015-35765305	K562	blood:	n/a	n/a
34	POLR2A	chr6:35764276-35764323	GM12878	blood:	n/a	n/a
35	RCOR1	chr6:35762534-35762855	K562	blood:	n/a	n/a
36	RCOR1	chr6:35765222-35765251	K562	blood:	n/a	n/a
37	RCOR1	chr6:35763033-35763323	K562	blood:	n/a	n/a
38	RCOR1	chr6:35763125-35763350	K562	blood:	n/a	n/a
39	RCOR1	chr6:35764985-35765081	K562	blood:	n/a	n/a
40	TAL1	chr6:35765136-35765354	K562	blood:	n/a	n/a
41	ZNF143	chr6:35763131-35763340	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35765589-35765639	K562	blood:	n/a
2	chr6:35762844-35762894	HNPCEpiC	eye:	n/a
3	chr6:35765093-35765143	RPTEC	kidney:	n/a
4	chr6:35766051-35766101	ovcar-3	ovarian:	n/a
5	chr6:35762844-35762894	ECC-1	luminal epithelium:	n/a
6	chr6:35762844-35762894	SKMC	muscle:	n/a
7	chr6:35765589-35765639	GM12892	blood:	n/a
8	chr6:35766021-35766071	H1-hESC	embryonic stem cell:	embryo
9	chr6:35765146-35765196	MCF-7	breast:	n/a
10	chr6:35766021-35766071	CMK	blood:	n/a
11	chr6:35765176-35765226	SKMC	muscle:	n/a
12	chr6:35765215-35765265	GM12892	blood:	n/a
13	chr6:35766021-35766071	HIPEpiC	eye:	n/a
14	chr6:35766051-35766101	SK-N-SH_RA	brain:	n/a
15	chr6:35765093-35765143	U87	brain:	n/a
16	chr6:35765093-35765143	SK-N-SH	brain:	n/a
17	chr6:35766051-35766101	PFSK-1	brain:	n/a
18	chr6:35766021-35766071	GM12892	blood:	n/a
19	chr6:35762844-35762894	HCT-116	colon:	n/a
20	chr6:35765589-35765639	Hela-S3	cervix:	n/a
21	chr6:35765093-35765143	GM19239	blood:	n/a
22	chr6:35766021-35766071	Caco-2	colon:	n/a
23	chr6:35765176-35765226	PFSK-1	brain:	n/a
24	chr6:35765215-35765265	K562	blood:	n/a
25	chr6:35765093-35765143	BE2_C	brain:	n/a
26	chr6:35765589-35765639	BJ	skin:	n/a
27	chr6:35762844-35762894	GM06990	blood:	n/a
28	chr6:35766051-35766101	HCPEpiC	choroid plexus:	n/a
29	chr6:35766051-35766101	Jurkat	blood:	n/a
30	chr6:35766021-35766071	Hela-S3	cervix:	n/a
31	chr6:35765215-35765265	GM06990	blood:	n/a
32	chr6:35762844-35762894	HL-60	blood:	n/a
33	chr6:35762844-35762894	Caco-2	colon:	n/a
34	chr6:35765093-35765143	NHDF-neo	bronchial:	n/a
35	chr6:35765589-35765639	SK-N-SH	brain:	n/a
36	chr6:35764958-35765008	SK-N-SH_RA	brain:	n/a
37	chr6:35765176-35765226	GM12891	blood:	n/a
38	chr6:35765146-35765196	A549	lung:	n/a
39	chr6:35765589-35765639	HepG2	liver:	n/a
40	chr6:35765215-35765265	T-47D	breast:	n/a
41	chr6:35766021-35766071	Hepatocyte	liver:	n/a
42	chr6:35766051-35766101	NT2-D1	testis:	n/a
43	chr6:35766021-35766071	BE2_C	brain:	n/a
44	chr6:35765146-35765196	LNCaP	prostate:	n/a
45	chr6:35766051-35766101	ProgFib	skin:	n/a
46	chr6:35765146-35765196	NHBE	bronchial:	n/a
47	chr6:35764958-35765008	HEK293	kidney:	embryo
48	chr6:35765589-35765639	RPTEC	kidney:	n/a
49	chr6:35766021-35766071	ovcar-3	ovarian:	n/a
50	chr6:35766021-35766071	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:35762091..35764853-chr6:35765476..35768100,2	MCF-7	breast:
2	chr6:35753638..35758618-chr6:35762629..35767095,7	K562	blood:
3	chr6:35762307..35765078-chr6:35772426..35774241,2	MCF-7	breast:
4	chr6:35760846..35763760-chr6:36163836..36166432,2	K562	blood:
5	chr6:35760015..35761880-chr6:35763280..35765561,2	K562	blood:
6	chr6:35747942..35750162-chr6:35760132..35762411,2	MCF-7	breast:
7	chr6:35762283..35764266-chr6:35764644..35767426,2	MCF-7	breast:
8	chr6:35742984..35745597-chr6:35763979..35765844,2	MCF-7	breast:
9	chr6:35753847..35759789-chr6:35762486..35768711,9	K562	blood:
10	chr6:35762091..35764853-chr6:35765476..35768100,2	MCF-7	breast:

Variant related genes	Relation type
CLPS	TF binding region
CLPS	CpG island
ENSG00000204140	chromatin interactions
ENSG00000196748	chromatin interactions
ENSG00000197753	chromatin interactions
ENSG00000096070	chromatin interactions
ENSG00000137392	chromatin interactions
ENSG00000246982	chromatin interactions

Extended variants
information (count: 308 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2817013	chr6:35761684-35761685	Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576830212	chr6:35761697-35761698	Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs2766592	chr6:35761755-35761756	Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs6921084	chr6:35761781-35761782	Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs147579109	chr6:35761792-35761793	Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs572284085	chr6:35761812-35761813	Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs542948427	chr6:35761816-35761817	Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs181316505	chr6:35761842-35761843	Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs368865881	chr6:35761875-35761876	Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs531621216	chr6:35761884-35761885	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs141965884	chr6:35761910-35761911	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs563422550	chr6:35761921-35761922	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs145716446	chr6:35761950-35761951	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs540043974	chr6:35761953-35761954	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs185390101	chr6:35761966-35761967	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs147369633	chr6:35761986-35761987	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs112061930	chr6:35761989-35761990	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs138672437	chr6:35762008-35762009	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs565914405	chr6:35762016-35762017	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs536414671	chr6:35762041-35762042	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs368161612	chr6:35762051-35762052	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs149321266	chr6:35762072-35762073	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs569919176	chr6:35762077-35762078	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs557150127	chr6:35762087-35762088	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs375544694	chr6:35762095-35762096	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs67661036	chr6:35762097-35762098	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs75442675	chr6:35762098-35762099	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558563291	chr6:35762103-35762104	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs9470100	chr6:35762108-35762109	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs201528951	chr6:35762122-35762123	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs189999645	chr6:35762137-35762138	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs534745600	chr6:35762225-35762226	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs181590685	chr6:35762242-35762243	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs572323546	chr6:35762282-35762283	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs10633959	chr6:35762333-35762334	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs10643068	chr6:35762334-35762335	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs542786877	chr6:35762349-35762350	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs35428303	chr6:35762372-35762373	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs375298401	chr6:35762375-35762376	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs543753631	chr6:35762376-35762377	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs2817014	chr6:35762380-35762381	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs532384493	chr6:35762406-35762407	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs547882628	chr6:35762411-35762412	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs35732000	chr6:35762419-35762420	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs2817015	chr6:35762432-35762433	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs371655610	chr6:35762438-35762439	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs376687578	chr6:35762461-35762462	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs374112941	chr6:35762463-35762464	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs61345527	chr6:35762468-35762469	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs9462119	chr6:35762472-35762473	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Lung cancer	19153074	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35755400-35765600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:35760600-35762600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:35761600-35762400	Active TSS	Pancreas	Pancrea
4	chr6:35762200-35762400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:35762200-35765200	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr6:35762400-35764000	Transcr. at gene 5' and 3'	Pancreas	Pancrea
7	chr6:35762600-35763000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:35762800-35763000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:35762800-35763600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:35763000-35772800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:35763400-35763600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:35763600-35773000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:35764000-35765600	Active TSS	Pancreas	Pancrea
14	chr6:35765600-35766000	Flanking Active TSS	Pancreas	Pancrea
15	chr6:35765600-35766200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:35765600-35766600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:35765800-35766000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr6:35765800-35766000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr6:35765800-35766200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:35765800-35766800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
21	chr6:35765800-35767400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr6:35766000-35766200	Bivalent Enhancer	HepG2	liver
23	chr6:35766000-35766800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr6:35766000-35766800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr6:35766000-35766800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr6:35766000-35768200	Enhancers	Pancreas	Pancrea
27	chr6:35766200-35769200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:35766400-35767000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr6:35766400-35767000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr6:35766600-35766800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr6:35766600-35767000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr6:35766600-35767000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr6:35766600-35767200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr6:35766600-35772800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:35766800-35767400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr6:35766800-35769200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr6:35766800-35772800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr6:35766800-35772800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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