Variant report

Variant	esv2759476
Chromosome Location	chr6:143916621-144079976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1651)
CpG islands
(count:2138)
Chromatin interactive
region (count:112)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1651 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:144013747-144014189	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:144008022-144008119	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:144010530-144010772	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:143999613-144001057	K562	blood:	n/a	n/a
5	ARID3A	chr6:143999086-143999263	K562	blood:	n/a	n/a
6	ARID3A	chr6:144022774-144022836	K562	blood:	n/a	n/a
7	ARID3A	chr6:143996538-143996643	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:144048068-144048556	K562	blood:	n/a	n/a
9	ARID3A	chr6:144017583-144017744	K562	blood:	n/a	n/a
10	ARID3A	chr6:144012273-144012766	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:144026822-144027051	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:144020067-144020138	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:143976730-143977030	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:144065690-144067812	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:144000195-144000496	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:143999084-143999976	HepG2	liver:	n/a	n/a
17	ATF1	chr6:143919513-143919893	K562	blood:	n/a	n/a
18	ATF1	chr6:144078467-144078874	K562	blood:	n/a	n/a
19	ATF1	chr6:143961157-143961293	K562	blood:	n/a	n/a
20	ATF1	chr6:144012634-144012655	K562	blood:	n/a	n/a
21	ATF1	chr6:143940224-143940393	K562	blood:	n/a	n/a
22	ATF1	chr6:144048151-144048412	K562	blood:	n/a	n/a
23	ATF1	chr6:144068421-144069008	K562	blood:	n/a	n/a
24	ATF2	chr6:144067075-144068247	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr6:144067217-144068081	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr6:143996723-143996912	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:144072409-144072444	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr6:144067444-144068191	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:143999128-143999331	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:144064537-144064699	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:144029583-144029584	H1-hESC	embryonic stem cell:	n/a	n/a
32	BATF	chr6:143968326-143968565	GM12878	blood:	n/a	n/a
33	BATF	chr6:143968337-143968614	GM12878	blood:	n/a	n/a
34	BCL11A	chr6:144067630-144067972	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL3	chr6:144066414-144067359	A549	lung:	n/a	n/a
36	BCL3	chr6:144078994-144079337	GM12878	blood:	n/a	n/a
37	BCL3	chr6:144066457-144067271	A549	lung:	n/a	n/a
38	BHLHE40	chr6:144016025-144016151	K562	blood:	n/a	n/a
39	BHLHE40	chr6:143999032-143999882	K562	blood:	n/a	n/a
40	BHLHE40	chr6:144068428-144069066	K562	blood:	n/a	n/a
41	BHLHE40	chr6:144065690-144067663	HepG2	liver:	n/a	n/a
42	BHLHE40	chr6:143999059-143999707	HepG2	liver:	n/a	n/a
43	BHLHE40	chr6:144021865-144022157	K562	blood:	n/a	n/a
44	BHLHE40	chr6:143938045-143938156	K562	blood:	n/a	n/a
45	BHLHE40	chr6:144028946-144029155	K562	blood:	n/a	n/a
46	BHLHE40	chr6:143994776-143995092	A549	lung:	n/a	chr6:143994920-143994941
47	BHLHE40	chr6:143976720-143977003	HepG2	liver:	n/a	n/a
48	BHLHE40	chr6:143994820-143995075	HepG2	liver:	n/a	chr6:143994920-143994941
49	BHLHE40	chr6:143994790-143995073	K562	blood:	n/a	chr6:143994920-143994941
50	BRCA1	chr6:143996583-143996851	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:143968714-143968764	HUVEC	blood vessel:	n/a
2	chr6:144018564-144018614	HepG2	liver:	n/a
3	chr6:144009131-144009181	HIPEpiC	eye:	n/a
4	chr6:143968714-143968764	HUVEC	blood vessel:	n/a
5	chr6:144018564-144018614	HepG2	liver:	n/a
6	chr6:144009131-144009181	HIPEpiC	eye:	n/a
7	chr6:144013969-144014019	HCF	heart:	n/a
8	chr6:143929406-143929456	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:144018564-144018614	SKMC	muscle:	n/a
10	chr6:143998958-143999008	SAEC	small airway:	n/a
11	chr6:143998961-143999011	ECC-1	luminal epithelium:	n/a
12	chr6:143998952-143999002	SK-N-SH	brain:	n/a
13	chr6:143999105-143999155	U87	brain:	n/a
14	chr6:144018564-144018614	SK-N-MC	brain:	n/a
15	chr6:144013969-144014019	U87	brain:	n/a
16	chr6:143958167-143958217	K562	blood:	n/a
17	chr6:143999504-143999554	BJ	skin:	n/a
18	chr6:144074617-144074667	ECC-1	luminal epithelium:	n/a
19	chr6:143998967-143999017	HCF	heart:	n/a
20	chr6:143999236-143999286	CMK	blood:	n/a
21	chr6:143928514-143928564	AoSMC	blood vessel:	n/a
22	chr6:144021172-144021222	HCF	heart:	n/a
23	chr6:143999715-143999765	SKMC	muscle:	n/a
24	chr6:143932803-143932853	MCF10A-Er-Src	breast:	n/a
25	chr6:143932803-143932853	H1-hESC	embryonic stem cell:	embryo
26	chr6:143999504-143999554	AG04449	skin:	fetal
27	chr6:143998869-143998919	Caco-2	colon:	n/a
28	chr6:143999715-143999765	GM12891	blood:	n/a
29	chr6:143996509-143996559	HCM	heart:	n/a
30	chr6:143997701-143997751	ovcar-3	ovarian:	n/a
31	chr6:143999715-143999765	U87	brain:	n/a
32	chr6:144009131-144009181	PANC-1	pancreas:	n/a
33	chr6:144033157-144033207	NHDF-neo	bronchial:	n/a
34	chr6:143996509-143996559	RPTEC	kidney:	n/a
35	chr6:143998869-143998919	SK-N-SH_RA	brain:	n/a
36	chr6:144009131-144009181	BE2_C	brain:	n/a
37	chr6:144056673-144056723	LNCaP	prostate:	n/a
38	chr6:143999236-143999286	HRPEpiC	eye:	n/a
39	chr6:143942465-143942515	NT2-D1	testis:	n/a
40	chr6:143999236-143999286	U87	brain:	n/a
41	chr6:143929406-143929456	K562	blood:	n/a
42	chr6:144066847-144066897	Caco-2	colon:	n/a
43	chr6:143942465-143942515	HNPCEpiC	eye:	n/a
44	chr6:144013969-144014019	ProgFib	skin:	n/a
45	chr6:143942465-143942515	HEK293	kidney:	embryo
46	chr6:143998869-143998919	GM12891	blood:	n/a
47	chr6:144018564-144018614	ECC-1	luminal epithelium:	n/a
48	chr6:143929511-143929561	LNCaP	prostate:	n/a
49	chr6:144074617-144074667	HCM	heart:	n/a
50	chr6:143942465-143942515	MCF10A-Er-Src	breast:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:144002192..144005187-chr6:144008261..144010591,3	MCF-7	breast:
2	chr6:144026361..144028111-chr6:144034125..144036106,2	MCF-7	breast:
3	chr6:144019071..144021984-chr6:144030527..144032678,2	MCF-7	breast:
4	chr6:144074038..144075721-chr6:144077621..144079711,2	K562	blood:
5	chr6:144005095..144007441-chr6:144008353..144010500,3	K562	blood:
6	chr6:143936810..143939021-chr6:143939704..143941251,2	K562	blood:
7	chr6:143916961..143919434-chr6:143921245..143924950,3	K562	blood:
8	chr6:144063490..144065500-chr6:144068197..144069773,2	K562	blood:
9	chr6:143831227..143833944-chr6:144017748..144020555,2	MCF-7	breast:
10	chr6:143998977..144000615-chr6:144001616..144004213,2	MCF-7	breast:
11	chr6:143977398..143979098-chr6:143982621..143985331,2	MCF-7	breast:
12	chr6:144015602..144018341-chr6:144021601..144023244,2	K562	blood:
13	chr6:143993920..143996702-chr6:144021547..144023983,2	MCF-7	breast:
14	chr6:143940682..143942289-chr6:143942415..143944107,2	MCF-7	breast:
15	chr6:143916961..143919434-chr6:143921245..143924950,3	K562	blood:
16	chr6:144037482..144039752-chr6:144079011..144080855,2	K562	blood:
17	chr6:144063490..144065500-chr6:144068197..144069773,2	K562	blood:
18	chr6:144018054..144020954-chr6:144022528..144024554,3	MCF-7	breast:
19	chr6:143979031..143980675-chr6:143980783..143983550,2	MCF-7	breast:
20	chr6:144011387..144013559-chr6:144018568..144021455,2	MCF-7	breast:
21	chr6:143923576..143926302-chr6:143926359..143929305,3	K562	blood:
22	chr6:144011351..144015622-chr6:144016784..144019989,3	K562	blood:
23	chr6:143966000..143968139-chr6:143973368..143975325,2	MCF-7	breast:
24	chr6:144060296..144062270-chr6:144062738..144065749,3	MCF-7	breast:
25	chr6:144075659..144077408-chr6:144078604..144081076,2	K562	blood:
26	chr6:144076953..144079572-chr6:144081415..144086815,4	K562	blood:
27	chr14:67903168..67904681-chr6:144023662..144026476,2	MCF-7	breast:
28	chr6:144075659..144077408-chr6:144078604..144081076,2	K562	blood:
29	chr6:144071732..144074823-chr6:144075904..144078859,3	MCF-7	breast:
30	chr6:143966000..143968139-chr6:143973368..143975325,2	MCF-7	breast:
31	chr6:143933160..143936004-chr6:143939923..143941547,2	K562	blood:
32	chr17:56707615..56709515-chr6:144027101..144029427,2	MCF-7	breast:
33	chr6:143933160..143936004-chr6:143939923..143941547,2	K562	blood:
34	chr6:143993282..143995063-chr6:144073784..144075986,2	MCF-7	breast:
35	chr6:144025959..144030073-chr6:144031546..144034604,3	K562	blood:
36	chr6:144005095..144007441-chr6:144008353..144010500,3	K562	blood:
37	chr6:143997975..143999811-chr6:144003059..144004885,2	K562	blood:
38	chr6:144000686..144002814-chr6:144004185..144006059,2	K562	blood:
39	chr6:144020099..144020600-chr6:144334156..144334754,2	K562	blood:
40	chr6:143958411..143960649-chr6:143968320..143970149,2	K562	blood:
41	chr6:143919523..143922006-chr6:143930988..143932681,2	K562	blood:
42	chr6:144002192..144005187-chr6:144008261..144010591,3	MCF-7	breast:
43	chr6:143999802..144002439-chr6:144003209..144005357,2	MCF-7	breast:
44	chr6:144018054..144020954-chr6:144022528..144024554,3	MCF-7	breast:
45	chr6:143997575..144000803-chr6:144010017..144014247,5	MCF-7	breast:
46	chr6:144069372..144071037-chr6:144077042..144078678,2	MCF-7	breast:
47	chr6:144022138..144024563-chr6:144033976..144035577,2	K562	blood:
48	chr6:144009959..144011502-chr6:144013449..144016270,2	K562	blood:
49	chr6:144015602..144018341-chr6:144021601..144023244,2	K562	blood:
50	chr6:143998944..144000506-chr6:144415343..144418005,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FUCA2-1	chr6:143921092-143921694	NONHSAT115358
2	lnc-FUCA2-2	chr6:143931690-143932169	ucscGeneNc_uc003qjp_1

No data

Variant related genes	Relation type
PHACTR2	TF binding region
PHACTR2	CpG island
ENSG00000212195	chromatin interactions
ENSG00000118495	chromatin interactions
ENSG00000112419	chromatin interactions
ENSG00000001036	chromatin interactions
ENSG00000169976	chromatin interactions
ENSG00000120694	chromatin interactions
ENSG00000135521	chromatin interactions

Extended variants
information (count: 5988 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:5988 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149720407	chr6:143916630-143916631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530949161	chr6:143916640-143916641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184437940	chr6:143916708-143916709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114427445	chr6:143916747-143916748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533704516	chr6:143916757-143916758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374321126	chr6:143916762-143916763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553391928	chr6:143916817-143916818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145551164	chr6:143916885-143916886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535761977	chr6:143916909-143916910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75711264	chr6:143916944-143916945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575884753	chr6:143916956-143916957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9386039	chr6:143916992-143916993	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs560299361	chr6:143917013-143917014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557851080	chr6:143917054-143917055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187718836	chr6:143917115-143917116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529347848	chr6:143917116-143917117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs193232170	chr6:143917177-143917178	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs185446267	chr6:143917194-143917195	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189536416	chr6:143917213-143917214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562374243	chr6:143917239-143917240	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs532935144	chr6:143917302-143917303	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552271720	chr6:143917385-143917386	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148907257	chr6:143917397-143917398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs181480275	chr6:143917402-143917403	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs143622641	chr6:143917416-143917417	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs573544397	chr6:143917442-143917443	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568346659	chr6:143917523-143917524	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536175222	chr6:143917634-143917635	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs369348760	chr6:143917638-143917639	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569487958	chr6:143917639-143917640	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs539999666	chr6:143917662-143917663	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs148055503	chr6:143917694-143917695	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536836127	chr6:143917698-143917699	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs11155308	chr6:143917700-143917701	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs533642700	chr6:143917711-143917712	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs555379088	chr6:143917713-143917714	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545627917	chr6:143917724-143917725	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs544519362	chr6:143917756-143917757	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562411049	chr6:143917789-143917790	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs13219404	chr6:143917982-143917983	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184554717	chr6:143918010-143918011	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs117736864	chr6:143918011-143918012	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142009717	chr6:143918024-143918025	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs590526	chr6:143918092-143918093	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs565433503	chr6:143918124-143918125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs145759570	chr6:143918151-143918152	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368543187	chr6:143918162-143918163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs11155309	chr6:143918183-143918184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529236436	chr6:143918282-143918283	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs551304114	chr6:143918301-143918302	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Autism	22495311	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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3661 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143895600-143918200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr6:143899400-143918000	Weak transcription	Spleen	Spleen
3	chr6:143899800-143919200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr6:143900800-143918200	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr6:143901200-143918000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:143903400-143918200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr6:143903600-143918600	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr6:143910400-143918200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr6:143910600-143918000	Weak transcription	Right Atrium	heart
10	chr6:143911200-143929200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr6:143912200-143916800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:143912800-143918200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr6:143913000-143918800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr6:143913200-143919000	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr6:143913200-143928400	Weak transcription	Aorta	Aorta
16	chr6:143914400-143917400	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr6:143914800-143919400	Weak transcription	Stomach Mucosa	stomach
18	chr6:143915600-143916800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr6:143915600-143917000	Enhancers	Hela-S3	cervix
20	chr6:143915600-143917200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr6:143915600-143918400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr6:143915600-143919000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:143915800-143917200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr6:143915800-143917400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:143915800-143918200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr6:143916000-143917000	Enhancers	NH-A	brain
27	chr6:143916000-143917400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:143916000-143917600	Weak transcription	Fetal Muscle Leg	muscle
29	chr6:143916000-143917800	Weak transcription	Left Ventricle	heart
30	chr6:143916000-143919400	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr6:143916200-143917000	Enhancers	Fetal Intestine Small	intestine
32	chr6:143916200-143917000	Enhancers	Osteobl	bone
33	chr6:143916200-143917200	Weak transcription	Ovary	ovary
34	chr6:143916200-143917600	Weak transcription	Lung	lung
35	chr6:143916200-143918000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr6:143916200-143918800	Enhancers	NHDF-Ad	bronchial
37	chr6:143916400-143916800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr6:143916600-143917000	Weak transcription	Fetal Intestine Large	intestine
39	chr6:143916600-143917000	Weak transcription	Placenta	Placenta
40	chr6:143916600-143917200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr6:143916600-143917400	Enhancers	HSMMtube	muscle
42	chr6:143916600-143917600	Weak transcription	NHLF	lung
43	chr6:143916600-143918200	Weak transcription	Stomach Smooth Muscle	stomach
44	chr6:143916800-143917200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr6:143916800-143918200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:143917000-143917200	Enhancers	Fetal Intestine Large	intestine
47	chr6:143917000-143918200	Weak transcription	Hela-S3	cervix
48	chr6:143917000-143920200	Enhancers	Placenta	Placenta
49	chr6:143917000-143973600	Weak transcription	Fetal Intestine Small	intestine
50	chr6:143917200-143918200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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