Variant report

Variant	esv1794906
Chromosome Location	chr6:34067792-34082563
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:80)
CpG islands
(count:183)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:80 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr6:34073719-34073871	K562	blood:	n/a	n/a
2	CCNT2	chr6:34075046-34075070	K562	blood:	n/a	n/a
3	CEBPB	chr6:34073410-34073648	HepG2	liver:	n/a	n/a
4	CEBPB	chr6:34081936-34082024	HepG2	liver:	n/a	n/a
5	CTCF	chr6:34069680-34069830	MCF-7	breast:	n/a	n/a
6	CTCF	chr6:34080024-34080114	Medullo	brain:	n/a	n/a
7	CTCF	chr6:34069720-34069870	WERI-Rb-1	eye:	n/a	n/a
8	CTCF	chr6:34075060-34075216	HepG2	liver:	n/a	n/a
9	CTCF	chr6:34069660-34069810	Caco-2	colon:	n/a	n/a
10	CTCF	chr6:34075102-34075214	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr6:34075088-34075234	MCF-7	breast:	n/a	n/a
12	CTCF	chr6:34075129-34075175	Gliobla	brain:	n/a	n/a
13	CTCF	chr6:34075094-34075230	MCF-7	breast:	n/a	n/a
14	CTCF	chr6:34078447-34078492	Pancreas_OC	pancreas:	n/a	n/a
15	CTCF	chr6:34075104-34075220	MCF-7	breast:	n/a	n/a
16	CTCF	chr6:34075097-34075233	K562	blood:	n/a	n/a
17	CTCF	chr6:34074979-34075276	K562	blood:	n/a	chr6:34075009-34075022
18	CTCF	chr6:34075080-34075230	HEK293	kidney:	n/a	n/a
19	CTCF	chr6:34075060-34075210	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr6:34075100-34075250	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr6:34074880-34075030	GM12873	blood:	n/a	chr6:34075009-34075022
22	CTCF	chr6:34069718-34069787	MCF-7	breast:	n/a	n/a
23	CTCF	chr6:34074997-34075285	K562	blood:	n/a	chr6:34075009-34075022
24	CTCF	chr6:34069680-34069830	HEK293	kidney:	n/a	n/a
25	CTCF	chr6:34075096-34075226	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:34075092-34075223	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:34069684-34069849	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr6:34074996-34075320	K562	blood:	n/a	chr6:34075009-34075022
29	CTCF	chr6:34069680-34069830	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr6:34075060-34075210	NB4	blood:	n/a	n/a
31	CTCF	chr6:34073740-34073890	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr6:34075160-34075310	HCT-116	colon:	n/a	n/a
33	CTCF	chr6:34075082-34075250	K562	blood:	n/a	n/a
34	CTCF	chr6:34075100-34075250	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr6:34075040-34075190	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr6:34078196-34078253	GM20000	blood:	n/a	n/a
37	CTCF	chr6:34079999-34080142	K562	blood:	n/a	n/a
38	CTCF	chr6:34069680-34069830	HepG2	liver:	n/a	n/a
39	CTCF	chr6:34075060-34075210	HepG2	liver:	n/a	n/a
40	CTCF	chr6:34080000-34080150	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr6:34080000-34080150	BE2_C	brain:	n/a	n/a
42	CTCF	chr6:34075040-34075190	NHEK	skin:	n/a	n/a
43	EGR1	chr6:34073641-34073922	K562	blood:	n/a	n/a
44	EGR1	chr6:34073647-34073895	K562	blood:	n/a	n/a
45	EGR1	chr6:34071088-34071431	K562	blood:	n/a	chr6:34071264-34071273 chr6:34071261-34071274 chr6:34071261-34071274 chr6:34071262-34071273 chr6:34071264-34071274 chr6:34071261-34071274 chr6:34071257-34071279 chr6:34071260-34071270
46	EGR1	chr6:34071055-34071452	K562	blood:	n/a	chr6:34071264-34071273 chr6:34071261-34071274 chr6:34071261-34071274 chr6:34071262-34071273 chr6:34071264-34071274 chr6:34071261-34071274 chr6:34071257-34071279 chr6:34071260-34071270
47	ELF1	chr6:34073635-34073836	K562	blood:	n/a	n/a
48	ELF1	chr6:34070642-34070946	GM12878	blood:	n/a	n/a
49	GATA2	chr6:34070890-34071359	SH-SY5Y	brain:	n/a	chr6:34071240-34071247 chr6:34071238-34071247 chr6:34071240-34071247 chr6:34070936-34070952 chr6:34071240-34071247 chr6:34071238-34071248 chr6:34070938-34070950 chr6:34071238-34071247
50	HNF4A	chr6:34073455-34073651	HepG2	liver:	n/a	chr6:34073533-34073548

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34074955-34075005	AG04450	lung:	fetal
2	chr6:34074955-34075005	SK-N-SH	brain:	n/a
3	chr6:34073788-34073838	BJ	skin:	n/a
4	chr6:34073788-34073838	Hela-S3	cervix:	n/a
5	chr6:34074282-34074332	AG10803	skin:	n/a
6	chr6:34073788-34073838	SK-N-MC	brain:	n/a
7	chr6:34074282-34074332	NH-A	brain:	n/a
8	chr6:34074955-34075005	K562	blood:	n/a
9	chr6:34074282-34074332	HEEpiC	esophagus:	n/a
10	chr6:34073788-34073838	A549	lung:	n/a
11	chr6:34073788-34073838	NHDF-neo	bronchial:	n/a
12	chr6:34074282-34074332	HNPCEpiC	eye:	n/a
13	chr6:34074282-34074332	ovcar-3	ovarian:	n/a
14	chr6:34074955-34075005	SKMC	muscle:	n/a
15	chr6:34074282-34074332	Hela-S3	cervix:	n/a
16	chr6:34074955-34075005	MCF10A-Er-Src	breast:	n/a
17	chr6:34074955-34075005	HCPEpiC	choroid plexus:	n/a
18	chr6:34073788-34073838	AG04450	lung:	fetal
19	chr6:34073788-34073838	HCPEpiC	choroid plexus:	n/a
20	chr6:34074282-34074332	GM12891	blood:	n/a
21	chr6:34074955-34075005	HRE	kidney:	n/a
22	chr6:34074955-34075005	CMK	blood:	n/a
23	chr6:34073788-34073838	U87	brain:	n/a
24	chr6:34074282-34074332	AoSMC	blood vessel:	n/a
25	chr6:34074282-34074332	Caco-2	colon:	n/a
26	chr6:34074955-34075005	Hepatocyte	liver:	n/a
27	chr6:34074955-34075005	IMR90	lung:	fetal
28	chr6:34074955-34075005	HEEpiC	esophagus:	n/a
29	chr6:34074955-34075005	GM12891	blood:	n/a
30	chr6:34074282-34074332	NB4	blood:	n/a
31	chr6:34074282-34074332	HCPEpiC	choroid plexus:	n/a
32	chr6:34074955-34075005	ovcar-3	ovarian:	n/a
33	chr6:34073788-34073838	SK-N-SH_RA	brain:	n/a
34	chr6:34073788-34073838	LNCaP	prostate:	n/a
35	chr6:34073788-34073838	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:34073788-34073838	HIPEpiC	eye:	n/a
37	chr6:34074955-34075005	HEK293	kidney:	embryo
38	chr6:34074955-34075005	GM06990	blood:	n/a
39	chr6:34074282-34074332	SAEC	small airway:	n/a
40	chr6:34074282-34074332	HUVEC	blood vessel:	n/a
41	chr6:34074282-34074332	A549	lung:	n/a
42	chr6:34073788-34073838	NT2-D1	testis:	n/a
43	chr6:34074955-34075005	SK-N-SH_RA	brain:	n/a
44	chr6:34073788-34073838	PrEC	prostate:	n/a
45	chr6:34074282-34074332	GM19239	blood:	n/a
46	chr6:34074282-34074332	HCT-116	colon:	n/a
47	chr6:34074282-34074332	Jurkat	blood:	n/a
48	chr6:34074282-34074332	GM12878	blood:	n/a
49	chr6:34074282-34074332	HAEpiC	amniotic membrane:	n/a
50	chr6:34073788-34073838	AG09319	gingival:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:34066615..34070590-chr6:34071095..34073197,4	K562	blood:
2	chr6:34082169..34084838-chr6:34084845..34087062,3	K562	blood:
3	chr6:34069851..34072638-chr6:34076441..34079307,2	MCF-7	breast:
4	chr6:34067961..34070856-chr6:34074799..34076460,2	K562	blood:
5	chr6:34072071..34075419-chr6:34078119..34081173,3	K562	blood:
6	chr6:34065737..34070590-chr6:34071331..34077866,9	K562	blood:
7	chr6:34066615..34070590-chr6:34071095..34073197,4	K562	blood:
8	chr6:34080081..34083212-chr6:34095884..34099849,3	MCF-7	breast:
9	chr6:34070999..34073655-chr6:34074573..34077003,3	K562	blood:
10	chr6:34065737..34067488-chr6:34074520..34076745,2	K562	blood:
11	chr6:34069851..34072638-chr6:34076441..34079307,2	MCF-7	breast:
12	chr6:34072071..34075419-chr6:34078119..34081173,3	K562	blood:
13	chr6:34081522..34084838-chr6:34084875..34087062,3	K562	blood:
14	chr6:34080760..34083112-chr6:34091391..34094093,2	K562	blood:
15	chr6:34074512..34076677-chr6:34090043..34092410,2	MCF-7	breast:
16	chr6:34065737..34070590-chr6:34071331..34077866,9	K562	blood:
17	chr6:34074373..34075890-chr6:34082068..34084619,2	MCF-7	breast:
18	chr6:34071722..34076075-chr6:34081654..34085311,5	K562	blood:
19	chr6:34074373..34075890-chr6:34082068..34084619,2	MCF-7	breast:
20	chr6:34070510..34073396-chr6:34076306..34077910,2	MCF-7	breast:

No data

Variant related genes	Relation type
GRM4	TF binding region
GRM4	CpG island
ENSG00000124493	chromatin interactions

Extended variants
information (count: 600 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:600 , 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	rs9380406	chr6:34067792-34067793	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139736485	chr6:34067836-34067837	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184171573	chr6:34067878-34067879	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546743480	chr6:34067924-34067925	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs568691512	chr6:34067950-34067951	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs536005116	chr6:34067982-34067983	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs553083162	chr6:34068004-34068005	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs75356096	chr6:34068043-34068044	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs144522153	chr6:34068044-34068045	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs539739539	chr6:34068047-34068048	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs188969028	chr6:34068052-34068053	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs557764281	chr6:34068069-34068070	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572737126	chr6:34068089-34068090	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540340697	chr6:34068104-34068105	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs561418794	chr6:34068134-34068135	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573504344	chr6:34068166-34068167	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541456651	chr6:34068226-34068227	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs543964393	chr6:34068289-34068290	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs115203635	chr6:34068307-34068308	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs533084065	chr6:34068367-34068368	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551369863	chr6:34068381-34068382	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs146597885	chr6:34068390-34068391	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528447480	chr6:34068402-34068403	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs733457	chr6:34068408-34068409	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs568523656	chr6:34068415-34068416	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs181764768	chr6:34068423-34068424	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs141362866	chr6:34068431-34068432	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs569453876	chr6:34068494-34068495	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs149903199	chr6:34068593-34068594	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs187502939	chr6:34068671-34068672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566487465	chr6:34068672-34068673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs745501	chr6:34068719-34068720	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs373909276	chr6:34068736-34068737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2395555	chr6:34068767-34068768	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs190731317	chr6:34068774-34068775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs555973251	chr6:34068799-34068800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181063308	chr6:34068807-34068808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs114420565	chr6:34068813-34068814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186342504	chr6:34068814-34068815	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528493129	chr6:34068815-34068816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369725484	chr6:34068844-34068845	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144974066	chr6:34068846-34068847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs149060697	chr6:34068905-34068906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs16894846	chr6:34068923-34068924	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs201194437	chr6:34068944-34068945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs190066775	chr6:34068978-34068979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs143006773	chr6:34069047-34069048	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs3887555	chr6:34069062-34069063	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs533338934	chr6:34069066-34069067	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs182714901	chr6:34069135-34069136	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Urothelial carcinoma	21177765	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
Breast cancer	22522925	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34025000-34101800	Weak transcription	Right Atrium	heart
2	chr6:34051400-34089000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:34063600-34068600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:34066600-34069200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:34066800-34067800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr6:34067000-34067800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr6:34067000-34097000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:34067200-34080600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:34067200-34089000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr6:34067400-34089000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:34067600-34068000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:34067800-34068000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr6:34068000-34068200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:34068000-34068200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:34068200-34078200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:34068600-34071800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:34070600-34070800	Enhancers	Brain Anterior Caudate	brain
18	chr6:34070600-34071600	Enhancers	Fetal Intestine Small	intestine
19	chr6:34070800-34071200	Enhancers	Fetal Intestine Large	intestine
20	chr6:34070800-34071400	Weak transcription	Brain Anterior Caudate	brain
21	chr6:34071200-34071600	Bivalent Enhancer	Fetal Intestine Large	intestine
22	chr6:34071400-34071600	Enhancers	Brain Anterior Caudate	brain
23	chr6:34071400-34071600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
24	chr6:34071400-34071600	Bivalent Enhancer	HepG2	liver
25	chr6:34071400-34071600	Bivalent Enhancer	K562	blood
26	chr6:34071600-34073600	Weak transcription	Fetal Intestine Small	intestine
27	chr6:34071600-34081800	Weak transcription	Brain Anterior Caudate	brain
28	chr6:34071800-34072000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:34072000-34072200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr6:34072200-34073200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:34073200-34073400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:34073200-34073800	Enhancers	Duodenum Mucosa	Duodenum
33	chr6:34073400-34073600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr6:34073600-34073800	Enhancers	Fetal Intestine Small	intestine
35	chr6:34073600-34074400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr6:34074400-34075200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:34075000-34075400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr6:34075000-34075800	Enhancers	Spleen	Spleen
39	chr6:34075200-34075600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr6:34075600-34076400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:34075800-34076000	Flanking Active TSS	Spleen	Spleen
42	chr6:34076000-34076200	Active TSS	Spleen	Spleen
43	chr6:34076400-34076800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:34076800-34077400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr6:34077200-34077400	Bivalent Enhancer	Right Ventricle	heart
46	chr6:34077400-34080200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:34078200-34078800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:34078400-34078600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr6:34078400-34079200	Bivalent Enhancer	Fetal Brain Male	brain
50	chr6:34078400-34080800	Enhancers	Fetal Brain Female	brain

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