Variant report

Variant	esv3341480
Chromosome Location	chr6:33418074-33422572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:540)
CpG islands
(count:3358)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:33421823-33422480	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:33422289-33422435	K562	blood:	n/a	n/a
3	ATF1	chr6:33422157-33422498	K562	blood:	n/a	n/a
4	ATF2	chr6:33421763-33422732	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:33421866-33422700	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:33421965-33422549	GM12878	blood:	n/a	n/a
7	BACH1	chr6:33421756-33421872	K562	blood:	n/a	n/a
8	BCLAF1	chr6:33421920-33422570	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:33421761-33422553	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:33421945-33422582	K562	blood:	n/a	chr6:33422174-33422190
11	BHLHE40	chr6:33422018-33422527	GM12878	blood:	n/a	chr6:33422174-33422190
12	BRCA1	chr6:33422150-33422519	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr6:33422020-33422212	HepG2	liver:	n/a	n/a
14	CBX3	chr6:33421427-33422762	K562	blood:	n/a	chr6:33421765-33421776
15	CCNT2	chr6:33421934-33422589	K562	blood:	n/a	n/a
16	CEBPB	chr6:33422297-33422583	K562	blood:	n/a	n/a
17	CEBPB	chr6:33422182-33422501	HepG2	liver:	n/a	chr6:33422254-33422262 chr6:33422290-33422298
18	CEBPD	chr6:33422146-33422752	K562	blood:	n/a	n/a
19	CEBPD	chr6:33421883-33422533	HepG2	liver:	n/a	n/a
20	CHD1	chr6:33422540-33422740	GM12878	blood:	n/a	n/a
21	CHD1	chr6:33422534-33422774	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr6:33421837-33422555	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr6:33421945-33422589	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr6:33421896-33422602	K562	blood:	n/a	n/a
25	CHD2	chr6:33421928-33422584	HepG2	liver:	n/a	n/a
26	CHD2	chr6:33421843-33422500	GM12878	blood:	n/a	n/a
27	CREB1	chr6:33421934-33422668	HepG2	liver:	n/a	n/a
28	CREB1	chr6:33422069-33422570	ECC-1	luminal epithelium:	n/a	n/a
29	CREB1	chr6:33421801-33422704	GM12878	blood:	n/a	n/a
30	CREB1	chr6:33421836-33422641	K562	blood:	n/a	n/a
31	CREB1	chr6:33422135-33422396	A549	lung:	n/a	n/a
32	CREB1	chr6:33421434-33422769	HepG2	liver:	n/a	n/a
33	CREB1	chr6:33421876-33422654	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr6:33421937-33422579	A549	lung:	n/a	n/a
35	CTCF	chr6:33422364-33422430	GM12891	blood:	n/a	n/a
36	CTCF	chr6:33422263-33422511	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr6:33422364-33422420	GM19238	blood:	n/a	n/a
38	CTCF	chr6:33422328-33422453	NHEK	skin:	n/a	n/a
39	CTCF	chr6:33422342-33422474	GM19239	blood:	n/a	n/a
40	CTCF	chr6:33422340-33422490	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr6:33422300-33422450	GM12872	blood:	n/a	n/a
42	CTCF	chr6:33422440-33422590	GM12878	blood:	n/a	n/a
43	CTCF	chr6:33422374-33422438	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:33422340-33422490	AG09319	gingival:	n/a	n/a
45	CTCF	chr6:33422140-33422290	GM12871	blood:	n/a	n/a
46	CTCF	chr6:33422380-33422530	AG04449	skin:	n/a	n/a
47	CTCF	chr6:33422251-33422507	GM12878	blood:	n/a	n/a
48	CTCF	chr6:33422388-33422415	GM12892	blood:	n/a	n/a
49	CTCF	chr6:33422320-33422470	GM12865	blood:	n/a	n/a
50	CTCF	chr6:33422500-33422650	HEK293	kidney:	n/a	n/a

(count:3358 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33422266-33422316	NHBE	bronchial:	n/a
2	chr6:33422426-33422476	MCF-7	breast:	n/a
3	chr6:33422185-33422235	HMEC	breast:	n/a
4	chr6:33422266-33422316	NHBE	bronchial:	n/a
5	chr6:33422426-33422476	MCF-7	breast:	n/a
6	chr6:33422185-33422235	HMEC	breast:	n/a
7	chr6:33419656-33419706	U87	brain:	n/a
8	chr6:33421468-33421518	SK-N-SH_RA	brain:	n/a
9	chr6:33422521-33422571	SKMC	muscle:	n/a
10	chr6:33421819-33421869	ovcar-3	ovarian:	n/a
11	chr6:33420805-33420855	HCPEpiC	choroid plexus:	n/a
12	chr6:33419510-33419560	PFSK-1	brain:	n/a
13	chr6:33420208-33420258	HRCEpiC	kidney:	n/a
14	chr6:33418869-33418919	K562	blood:	n/a
15	chr6:33422080-33422130	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:33422244-33422294	HRCEpiC	kidney:	n/a
17	chr6:33422526-33422576	GM19239	blood:	n/a
18	chr6:33421902-33421952	LNCaP	prostate:	n/a
19	chr6:33422526-33422576	CMK	blood:	n/a
20	chr6:33419633-33419683	NT2-D1	testis:	n/a
21	chr6:33418656-33418706	BJ	skin:	n/a
22	chr6:33419633-33419683	HRCEpiC	kidney:	n/a
23	chr6:33419790-33419840	SKMC	muscle:	n/a
24	chr6:33421963-33422013	Caco-2	colon:	n/a
25	chr6:33422516-33422566	ovcar-3	ovarian:	n/a
26	chr6:33419140-33419190	NH-A	brain:	n/a
27	chr6:33422521-33422571	NT2-D1	testis:	n/a
28	chr6:33418814-33418864	ECC-1	luminal epithelium:	n/a
29	chr6:33419510-33419560	HEK293	kidney:	embryo
30	chr6:33420227-33420277	BJ	skin:	n/a
31	chr6:33418869-33418919	CMK	blood:	n/a
32	chr6:33422080-33422130	SK-N-MC	brain:	n/a
33	chr6:33419496-33419546	CMK	blood:	n/a
34	chr6:33419653-33419703	HEEpiC	esophagus:	n/a
35	chr6:33419353-33419403	SK-N-SH_RA	brain:	n/a
36	chr6:33422459-33422509	NB4	blood:	n/a
37	chr6:33421476-33421526	H1-hESC	embryonic stem cell:	embryo
38	chr6:33420121-33420171	SK-N-SH_RA	brain:	n/a
39	chr6:33422516-33422566	SKMC	muscle:	n/a
40	chr6:33419512-33419562	HMEC	breast:	n/a
41	chr6:33422406-33422456	HCT-116	colon:	n/a
42	chr6:33421509-33421559	GM12878	blood:	n/a
43	chr6:33421704-33421754	GM19239	blood:	n/a
44	chr6:33419571-33419621	RPTEC	kidney:	n/a
45	chr6:33422102-33422152	SK-N-MC	brain:	n/a
46	chr6:33419653-33419703	ProgFib	skin:	n/a
47	chr6:33422300-33422350	Caco-2	colon:	n/a
48	chr6:33418656-33418706	GM12892	blood:	n/a
49	chr6:33421902-33421952	HRPEpiC	eye:	n/a
50	chr6:33419571-33419621	GM12892	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33422362..33424306-chr6:33561012..33562772,2	K562	blood:
2	chr6:33358950..33361251-chr6:33421997..33423819,3	K562	blood:
3	chr6:33377039..33379614-chr6:33421781..33424452,2	K562	blood:
4	chr6:33392449..33400629-chr6:33419013..33424035,12	MCF-7	breast:
5	chr6:33264374..33267492-chr6:33422246..33424652,3	K562	blood:
6	chr6:33245204..33246812-chr6:33420469..33423462,2	MCF-7	breast:
7	chr6:33398677..33403495-chr6:33419995..33423723,6	K562	blood:
8	chr6:33381847..33384907-chr6:33420236..33423106,3	MCF-7	breast:
9	chr6:33402335..33405767-chr6:33416394..33418965,3	MCF-7	breast:
10	chr6:33406190..33414491-chr6:33419287..33424467,10	MCF-7	breast:
11	chr6:33385453..33389637-chr6:33419628..33424957,5	MCF-7	breast:
12	chr6:33238561..33240428-chr6:33421904..33423704,2	K562	blood:
13	chr6:33357170..33359461-chr6:33419565..33421602,2	K562	blood:
14	chr19:5689875..5690838-chr6:33420626..33421397,2	Hela-S3	cervix:
15	chr6:33358627..33361285-chr6:33416169..33418601,2	MCF-7	breast:
16	chr6:33384548..33387250-chr6:33422114..33424496,2	K562	blood:
17	chr6:33395899..33401993-chr6:33420102..33423796,11	MCF-7	breast:
18	chr6:33392146..33394863-chr6:33415963..33418099,3	MCF-7	breast:
19	chr6:33416427..33418165-chr6:33432976..33435399,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SYNGAP1	hsa-miR-30c-5p	chr6:33421424-33421446

Variant related genes	Relation type
ZBTB9	TF binding region
ZBTB9	CpG island
ENSG00000235863	chromatin interactions
ENSG00000112514	chromatin interactions
ENSG00000197283	chromatin interactions
ENSG00000130255	chromatin interactions
ENSG00000197251	chromatin interactions
ENSG00000237441	chromatin interactions
ENSG00000112511	chromatin interactions
ENSG00000223501	chromatin interactions
ENSG00000231500	chromatin interactions
ENSG00000225644	chromatin interactions
ENSG00000237649	chromatin interactions

Extended variants
information (count: 131 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:131 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545961757	chr6:33418080-33418081	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs560064620	chr6:33418114-33418115	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs527535972	chr6:33418133-33418134	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs548918825	chr6:33418142-33418143	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs567424149	chr6:33418153-33418154	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs181810754	chr6:33418199-33418200	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs144754234	chr6:33418296-33418297	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs186499352	chr6:33418297-33418298	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs188095016	chr6:33418304-33418305	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs181048622	chr6:33418361-33418362	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs547370155	chr6:33418376-33418377	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs566250976	chr6:33418415-33418416	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs11753355	chr6:33418473-33418474	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs554888047	chr6:33418474-33418475	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs576605548	chr6:33418517-33418518	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs541954502	chr6:33418550-33418551	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs186344398	chr6:33418656-33418657	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs563337415	chr6:33418657-33418658	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs12111285	chr6:33418680-33418681	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs576924119	chr6:33418720-33418721	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs138402935	chr6:33418747-33418748	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs191544615	chr6:33418806-33418807	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs559286069	chr6:33418825-33418826	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs575332030	chr6:33418916-33418917	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs545840059	chr6:33418937-33418938	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572270755	chr6:33418947-33418948	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs141816467	chr6:33418964-33418965	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs150625247	chr6:33418971-33418972	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs368290349	chr6:33418974-33418975	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs371745179	chr6:33418979-33418980	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs531574446	chr6:33419144-33419145	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs549997755	chr6:33419202-33419203	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539821624	chr6:33419231-33419232	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs183375797	chr6:33419239-33419240	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs532732121	chr6:33419242-33419243	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs74379499	chr6:33419283-33419284	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs532202910	chr6:33419302-33419303	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs373999010	chr6:33419311-33419312	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs547433168	chr6:33419415-33419416	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs368168718	chr6:33419512-33419513	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs368894185	chr6:33419552-33419553	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs199694815	chr6:33419553-33419554	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs372190836	chr6:33419593-33419594	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs201509029	chr6:33419653-33419654	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs367907637	chr6:33419718-33419719	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs371821639	chr6:33419739-33419740	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs570246788	chr6:33419747-33419748	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs537296679	chr6:33419771-33419772	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs558681767	chr6:33419776-33419777	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs576935882	chr6:33419779-33419780	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Renal cell carcinoma	18765545	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
abnormal development	18461090	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
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20964600	CNVD
Autism	20531469	CNVD

Chromatin state (count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33399400-33421200	Weak transcription	HMEC	breast
2	chr6:33399400-33421600	Weak transcription	Stomach Mucosa	stomach
3	chr6:33399600-33421400	Weak transcription	HUVEC	blood vessel
4	chr6:33399800-33421400	Weak transcription	A549	lung
5	chr6:33400000-33420600	Strong transcription	Brain Germinal Matrix	brain
6	chr6:33401200-33420800	Strong transcription	Fetal Brain Female	brain
7	chr6:33401400-33418800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr6:33401400-33421400	Weak transcription	Right Atrium	heart
9	chr6:33402000-33418200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr6:33402000-33420600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:33402200-33418200	Strong transcription	Fetal Muscle Leg	muscle
12	chr6:33402200-33418600	Strong transcription	Dnd41	blood
13	chr6:33402200-33420000	Strong transcription	Fetal Thymus	thymus
14	chr6:33402200-33420800	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr6:33402400-33420800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:33402600-33420000	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr6:33402600-33420400	Strong transcription	Fetal Stomach	stomach
18	chr6:33402600-33421400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr6:33402800-33418400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr6:33402800-33418600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr6:33402800-33418600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
22	chr6:33402800-33419000	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr6:33402800-33420000	Strong transcription	H9 Cell Line	embryonic stem cell
24	chr6:33402800-33420000	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr6:33402800-33420000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr6:33402800-33420200	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr6:33402800-33420200	Strong transcription	Fetal Muscle Trunk	muscle
28	chr6:33403000-33418200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:33403000-33420600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr6:33403200-33420200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:33403600-33420400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:33404000-33421200	Weak transcription	HSMM	muscle
33	chr6:33405400-33420400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr6:33406200-33421200	Weak transcription	Liver	Liver
35	chr6:33406400-33420800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:33406400-33421200	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr6:33406400-33421400	Weak transcription	Colonic Mucosa	Colon
38	chr6:33406600-33421400	Weak transcription	HSMMtube	muscle
39	chr6:33406800-33421000	Weak transcription	NH-A	brain
40	chr6:33407200-33420400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr6:33408400-33421400	Weak transcription	Fetal Kidney	kidney
42	chr6:33408600-33418800	Strong transcription	Brain Anterior Caudate	brain
43	chr6:33408800-33419200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr6:33409400-33419800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr6:33410000-33420400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr6:33411200-33421400	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr6:33411200-33421400	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr6:33412400-33420800	Weak transcription	Primary B cells from peripheral blood	blood
49	chr6:33413000-33419800	Weak transcription	Fetal Heart	heart
50	chr6:33413000-33421400	Weak transcription	Left Ventricle	heart

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