Variant report

Variant	esv3330928
Chromosome Location	chr6:35759074-35768272
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	BHLHE40	chr6:35760699-35760763	K562	blood:	n/a	n/a
3	CEBPB	chr6:35762562-35762885	K562	blood:	n/a	n/a
4	CTCF	chr6:35766010-35766063	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr6:35760640-35760790	GM12868	blood:	n/a	n/a
6	CTCF	chr6:35760300-35760450	AG04449	skin:	n/a	n/a
7	CTCF	chr6:35767700-35767850	GM06990	blood:	n/a	n/a
8	CTCF	chr6:35765740-35765890	GM12864	blood:	n/a	n/a
9	E2F4	chr6:35759420-35759424	MCF10A-Er-Src	breast:	n/a	n/a
10	E2F6	chr6:35766372-35766946	H1-hESC	embryonic stem cell:	n/a	n/a
11	E2F6	chr6:35761091-35761480	H1-hESC	embryonic stem cell:	n/a	chr6:35761248-35761260
12	E2F6	chr6:35761154-35761630	H1-hESC	embryonic stem cell:	n/a	chr6:35761248-35761260
13	E2F6	chr6:35766297-35766870	H1-hESC	embryonic stem cell:	n/a	n/a
14	E2F6	chr6:35761233-35761368	K562	blood:	n/a	chr6:35761248-35761260
15	EGR1	chr6:35763349-35763621	K562	blood:	n/a	chr6:35763477-35763491 chr6:35763478-35763491 chr6:35763479-35763490 chr6:35763479-35763490 chr6:35763479-35763488
16	EGR1	chr6:35765030-35765252	K562	blood:	n/a	n/a
17	ELF1	chr6:35764865-35765253	GM12878	blood:	n/a	n/a
18	FOXA1	chr6:35764086-35764407	T-47D	breast:	n/a	n/a
19	FOXA1	chr6:35764145-35764400	T-47D	breast:	n/a	n/a
20	GTF2F1	chr6:35765022-35765053	H1-hESC	embryonic stem cell:	n/a	n/a
21	GTF2F1	chr6:35763645-35763723	K562	blood:	n/a	n/a
22	GTF2F1	chr6:35766681-35766722	H1-hESC	embryonic stem cell:	n/a	n/a
23	JUN	chr6:35765331-35765335	H1-hESC	embryonic stem cell:	n/a	n/a
24	MAFF	chr6:35762574-35762875	K562	blood:	n/a	chr6:35762725-35762739 chr6:35762719-35762737
25	MAFF	chr6:35767908-35767981	HepG2	liver:	n/a	chr6:35767933-35767951
26	MAFF	chr6:35762658-35762770	HepG2	liver:	n/a	chr6:35762725-35762739 chr6:35762719-35762737
27	MAFK	chr6:35767812-35768012	HepG2	liver:	n/a	n/a
28	MAFK	chr6:35762633-35762864	Hela-S3	cervix:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
29	MAFK	chr6:35762557-35762899	K562	blood:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
30	MAFK	chr6:35762562-35762855	HepG2	liver:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
31	MAFK	chr6:35762579-35762870	HepG2	liver:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
32	MAX	chr6:35766413-35766899	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738
33	MAX	chr6:35765943-35766141	K562	blood:	n/a	chr6:35766039-35766048 chr6:35766038-35766048 chr6:35766038-35766049 chr6:35766039-35766048 chr6:35766040-35766047
34	MAX	chr6:35766425-35766854	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738
35	MAX	chr6:35766457-35766910	ECC-1	luminal epithelium:	n/a	chr6:35766728-35766738
36	MAX	chr6:35761196-35761505	K562	blood:	n/a	n/a
37	MAX	chr6:35761223-35761454	H1-hESC	embryonic stem cell:	n/a	n/a
38	MAX	chr6:35766531-35766863	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738
39	MAX	chr6:35761205-35761542	H1-hESC	embryonic stem cell:	n/a	n/a
40	MAX	chr6:35765902-35766195	K562	blood:	n/a	chr6:35766039-35766048 chr6:35766038-35766048 chr6:35766038-35766049 chr6:35766039-35766048 chr6:35766040-35766047
41	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
42	MAX	chr6:35761136-35761546	H1-hESC	embryonic stem cell:	n/a	n/a
43	MYC	chr6:35766566-35766816	MCF10A-Er-Src	breast:	n/a	chr6:35766728-35766738
44	MYC	chr6:35766546-35766859	MCF10A-Er-Src	breast:	n/a	chr6:35766728-35766738
45	MYC	chr6:35762319-35762823	K562	blood:	n/a	chr6:35762704-35762713
46	MYC	chr6:35766615-35766772	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738
47	NFYB	chr6:35767650-35767865	K562	blood:	n/a	n/a
48	NR2F2	chr6:35765015-35765305	K562	blood:	n/a	n/a
49	POLR2A	chr6:35764276-35764323	GM12878	blood:	n/a	n/a
50	RCOR1	chr6:35763033-35763323	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35765589-35765639	ovcar-3	ovarian:	n/a
2	chr6:35765589-35765639	ovcar-3	ovarian:	n/a
3	chr6:35762844-35762894	HEEpiC	esophagus:	n/a
4	chr6:35766051-35766101	GM12892	blood:	n/a
5	chr6:35766021-35766071	Caco-2	colon:	n/a
6	chr6:35765093-35765143	SK-N-SH	brain:	n/a
7	chr6:35765176-35765226	NB4	blood:	n/a
8	chr6:35765093-35765143	SK-N-MC	brain:	n/a
9	chr6:35765589-35765639	HEK293	kidney:	embryo
10	chr6:35765146-35765196	AG04449	skin:	fetal
11	chr6:35766051-35766101	ProgFib	skin:	n/a
12	chr6:35764958-35765008	AG04449	skin:	fetal
13	chr6:35765589-35765639	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:35765215-35765265	AG09319	gingival:	n/a
15	chr6:35765176-35765226	HCF	heart:	n/a
16	chr6:35765146-35765196	A549	lung:	n/a
17	chr6:35766051-35766101	BJ	skin:	n/a
18	chr6:35765176-35765226	PFSK-1	brain:	n/a
19	chr6:35765215-35765265	HIPEpiC	eye:	n/a
20	chr6:35765093-35765143	CMK	blood:	n/a
21	chr6:35762844-35762894	PrEC	prostate:	n/a
22	chr6:35766051-35766101	K562	blood:	n/a
23	chr6:35765215-35765265	GM19239	blood:	n/a
24	chr6:35764958-35765008	NT2-D1	testis:	n/a
25	chr6:35765093-35765143	ovcar-3	ovarian:	n/a
26	chr6:35765215-35765265	NHBE	bronchial:	n/a
27	chr6:35765146-35765196	HCF	heart:	n/a
28	chr6:35766051-35766101	HNPCEpiC	eye:	n/a
29	chr6:35766021-35766071	AG10803	skin:	n/a
30	chr6:35762844-35762894	ovcar-3	ovarian:	n/a
31	chr6:35765093-35765143	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:35765146-35765196	ovcar-3	ovarian:	n/a
33	chr6:35765146-35765196	ProgFib	skin:	n/a
34	chr6:35766051-35766101	ovcar-3	ovarian:	n/a
35	chr6:35764958-35765008	HUVEC	blood vessel:	n/a
36	chr6:35766051-35766101	AG10803	skin:	n/a
37	chr6:35765215-35765265	SKMC	muscle:	n/a
38	chr6:35765215-35765265	SAEC	small airway:	n/a
39	chr6:35766021-35766071	PrEC	prostate:	n/a
40	chr6:35765146-35765196	AG10803	skin:	n/a
41	chr6:35764958-35765008	PANC-1	pancreas:	n/a
42	chr6:35762844-35762894	GM12892	blood:	n/a
43	chr6:35766051-35766101	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:35762844-35762894	SKMC	muscle:	n/a
45	chr6:35765589-35765639	Hela-S3	cervix:	n/a
46	chr6:35766051-35766101	ECC-1	luminal epithelium:	n/a
47	chr6:35765093-35765143	NHDF-neo	bronchial:	n/a
48	chr6:35766021-35766071	HRPEpiC	eye:	n/a
49	chr6:35765093-35765143	HEEpiC	esophagus:	n/a
50	chr6:35765093-35765143	NB4	blood:	n/a

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

Variant related genes	Relation type
CLPS	TF binding region
LHFPL5	TF binding region
CLPS	CpG island
LHFPL5	CpG island
ENSG00000246982	chromatin interactions
ENSG00000196748	chromatin interactions
ENSG00000197753	chromatin interactions
ENSG00000096070	chromatin interactions
ENSG00000204140	chromatin interactions
ENSG00000137392	chromatin interactions

Extended variants
information (count: 505 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114293288	chr6:35759082-35759083	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs373682258	chr6:35759109-35759110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557434552	chr6:35759110-35759111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374740444	chr6:35759116-35759117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150443533	chr6:35759120-35759121	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs546308228	chr6:35759125-35759126	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs538942503	chr6:35759134-35759135	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs138556660	chr6:35759137-35759138	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs148848808	chr6:35759151-35759152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs146940819	chr6:35759163-35759164	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs540004382	chr6:35759183-35759184	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190449098	chr6:35759187-35759188	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs529187625	chr6:35759191-35759192	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs374490678	chr6:35759197-35759198	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201260041	chr6:35759246-35759247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs6907913	chr6:35759251-35759252	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs532750458	chr6:35759252-35759253	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs59313399	chr6:35759272-35759273	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs188865680	chr6:35759278-35759279	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs535224989	chr6:35759306-35759307	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553250683	chr6:35759316-35759317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568660846	chr6:35759317-35759318	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs536203684	chr6:35759319-35759320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs557668832	chr6:35759329-35759330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575744872	chr6:35759333-35759334	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs143392372	chr6:35759340-35759341	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs9470097	chr6:35759354-35759355	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs72328042	chr6:35759386-35759387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558233367	chr6:35759387-35759388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576322105	chr6:35759397-35759398	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs573213426	chr6:35759398-35759399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs540709724	chr6:35759404-35759405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371954481	chr6:35759428-35759429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs375581602	chr6:35759444-35759445	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146189846	chr6:35759455-35759456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs192149138	chr6:35759470-35759471	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs6908914	chr6:35759518-35759519	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs182617019	chr6:35759519-35759520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370488995	chr6:35759533-35759534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374660919	chr6:35759539-35759540	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs6931331	chr6:35759553-35759554	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs6908647	chr6:35759563-35759564	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs114626523	chr6:35759566-35759567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs369887050	chr6:35759584-35759585	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs6908638	chr6:35759587-35759588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187692652	chr6:35759642-35759643	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536043731	chr6:35759643-35759644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs563560613	chr6:35759651-35759652	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551314053	chr6:35759659-35759660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs576988689	chr6:35759688-35759689	Weak transcription	Chromatin interactive region	1 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:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35755400-35765600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:35757000-35760400	Weak transcription	Pancreas	Pancrea
3	chr6:35758800-35760400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:35760400-35760600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:35760400-35760600	Enhancers	Pancreas	Pancrea
6	chr6:35760400-35761600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr6:35760600-35760800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr6:35760600-35760800	Flanking Active TSS	Pancreas	Pancrea
9	chr6:35760600-35760800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
10	chr6:35760600-35762600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:35760800-35761200	Enhancers	Pancreas	Pancrea
12	chr6:35761200-35761400	Active TSS	Pancreas	Pancrea
13	chr6:35761200-35761600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr6:35761400-35761600	Flanking Active TSS	Pancreas	Pancrea
15	chr6:35761600-35762400	Active TSS	Pancreas	Pancrea
16	chr6:35762200-35762400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:35762200-35765200	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr6:35762400-35764000	Transcr. at gene 5' and 3'	Pancreas	Pancrea
19	chr6:35762600-35763000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr6:35762800-35763000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr6:35762800-35763600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:35763000-35772800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:35763400-35763600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr6:35763600-35773000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:35764000-35765600	Active TSS	Pancreas	Pancrea
26	chr6:35765600-35766000	Flanking Active TSS	Pancreas	Pancrea
27	chr6:35765600-35766200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:35765600-35766600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:35765800-35766000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:35765800-35766000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr6:35765800-35766200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr6:35765800-35766800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
33	chr6:35765800-35767400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr6:35766000-35766200	Bivalent Enhancer	HepG2	liver
35	chr6:35766000-35766800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:35766000-35766800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr6:35766000-35766800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr6:35766000-35768200	Enhancers	Pancreas	Pancrea
39	chr6:35766200-35769200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr6:35766400-35767000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr6:35766400-35767000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr6:35766600-35766800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr6:35766600-35767000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:35766600-35767000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr6:35766600-35767200	Enhancers	H9 Cell Line	embryonic stem cell
46	chr6:35766600-35772800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:35766800-35767400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr6:35766800-35769200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr6:35766800-35772800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr6:35766800-35772800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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