Variant report

Variant	esv3424432
Chromosome Location	chr6:146041308-146057603
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:859)
CpG islands
(count:428)
Chromatin interactive
region (count:42)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:859 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:146054941-146055183	K562	blood:	n/a	n/a
2	ARID3A	chr6:146056640-146056950	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:146055459-146056158	K562	blood:	n/a	n/a
4	ARID3A	chr6:146057198-146057248	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:146044817-146044902	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:146055703-146056408	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:146053984-146054603	K562	blood:	n/a	n/a
8	ATF2	chr6:146055751-146056303	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr6:146056839-146057271	GM12878	blood:	n/a	n/a
10	ATF2	chr6:146055583-146056126	GM12878	blood:	n/a	n/a
11	ATF2	chr6:146055700-146056255	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr6:146056722-146057541	GM12878	blood:	n/a	n/a
13	BACH1	chr6:146055950-146056520	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:146056742-146057090	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCLAF1	chr6:146056511-146057323	GM12878	blood:	n/a	chr6:146056929-146056938 chr6:146056638-146056651 chr6:146056681-146056694 chr6:146056643-146056652 chr6:146056635-146056648 chr6:146056640-146056649
16	BCLAF1	chr6:146055709-146056329	GM12878	blood:	n/a	chr6:146055898-146055911 chr6:146056085-146056098
17	BCLAF1	chr6:146055584-146057472	GM12878	blood:	n/a	chr6:146056929-146056938 chr6:146056638-146056651 chr6:146056681-146056694 chr6:146055898-146055911 chr6:146056643-146056652 chr6:146056085-146056098 chr6:146056635-146056648 chr6:146056640-146056649
18	BCLAF1	chr6:146055626-146057292	K562	blood:	n/a	chr6:146056929-146056938 chr6:146056638-146056651 chr6:146056681-146056694 chr6:146055898-146055911 chr6:146056643-146056652 chr6:146056085-146056098 chr6:146056635-146056648 chr6:146056640-146056649
19	BHLHE40	chr6:146055762-146057226	HepG2	liver:	n/a	chr6:146056676-146056692
20	BHLHE40	chr6:146055796-146057399	K562	blood:	n/a	chr6:146056676-146056692
21	BHLHE40	chr6:146056682-146057034	A549	lung:	n/a	n/a
22	BHLHE40	chr6:146055480-146057455	GM12878	blood:	n/a	chr6:146056676-146056692
23	BRCA1	chr6:146056878-146057138	GM12878	blood:	n/a	n/a
24	BRCA1	chr6:146055875-146056062	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr6:146055847-146056407	HepG2	liver:	n/a	n/a
26	BRCA1	chr6:146055627-146056142	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr6:146055627-146056522	K562	blood:	n/a	n/a
28	CBX3	chr6:146056547-146057279	K562	blood:	n/a	n/a
29	CBX3	chr6:146050097-146050441	K562	blood:	n/a	n/a
30	CBX3	chr6:146050015-146050508	K562	blood:	n/a	n/a
31	CBX3	chr6:146048942-146049338	K562	blood:	n/a	n/a
32	CCNT2	chr6:146055680-146057243	K562	blood:	n/a	n/a
33	CEBPB	chr6:146053887-146054047	H1-hESC	embryonic stem cell:	n/a	chr6:146053910-146053919 chr6:146053910-146053921 chr6:146053908-146053919
34	CEBPB	chr6:146056664-146057343	K562	blood:	n/a	n/a
35	CEBPB	chr6:146054359-146054707	K562	blood:	n/a	n/a
36	CEBPB	chr6:146056880-146057388	K562	blood:	n/a	n/a
37	CEBPB	chr6:146047673-146047873	A549	lung:	n/a	n/a
38	CEBPB	chr6:146054958-146055072	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr6:146057008-146057150	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr6:146053737-146054092	K562	blood:	n/a	chr6:146053910-146053919 chr6:146053910-146053921 chr6:146053908-146053919
41	CEBPB	chr6:146055884-146057293	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr6:146054908-146055221	K562	blood:	n/a	n/a
43	CEBPB	chr6:146053774-146054051	HepG2	liver:	n/a	chr6:146053910-146053919 chr6:146053910-146053921 chr6:146053908-146053919
44	CEBPB	chr6:146055891-146056118	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr6:146053803-146054053	A549	lung:	n/a	chr6:146053910-146053919 chr6:146053910-146053921 chr6:146053908-146053919
46	CEBPB	chr6:146053777-146054062	Hela-S3	cervix:	n/a	chr6:146053910-146053919 chr6:146053910-146053921 chr6:146053908-146053919
47	CEBPB	chr6:146051152-146051336	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:146056919-146057280	A549	lung:	n/a	n/a
49	CEBPD	chr6:146055689-146056733	HepG2	liver:	n/a	n/a
50	CEBPD	chr6:146056385-146056653	HepG2	liver:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:146056083-146056133	A549	lung:	n/a
2	chr6:146056083-146056133	A549	lung:	n/a
3	chr6:146056083-146056133	SK-N-SH_RA	brain:	n/a
4	chr6:146056793-146056843	AG10803	skin:	n/a
5	chr6:146056793-146056843	NT2-D1	testis:	n/a
6	chr6:146056793-146056843	Jurkat	blood:	n/a
7	chr6:146056419-146056469	BE2_C	brain:	n/a
8	chr6:146056083-146056133	NHBE	bronchial:	n/a
9	chr6:146057055-146057105	HEK293	kidney:	embryo
10	chr6:146056793-146056843	SAEC	small airway:	n/a
11	chr6:146056083-146056133	AG10803	skin:	n/a
12	chr6:146056419-146056469	GM12878	blood:	n/a
13	chr6:146051934-146051984	AG04449	skin:	fetal
14	chr6:146057073-146057123	SK-N-SH_RA	brain:	n/a
15	chr6:146051934-146051984	GM06990	blood:	n/a
16	chr6:146056083-146056133	NHDF-neo	bronchial:	n/a
17	chr6:146056419-146056469	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:146056083-146056133	Hela-S3	cervix:	n/a
19	chr6:146056770-146056820	BJ	skin:	n/a
20	chr6:146056770-146056820	AG04449	skin:	fetal
21	chr6:146056083-146056133	CMK	blood:	n/a
22	chr6:146056793-146056843	Hepatocyte	liver:	n/a
23	chr6:146057073-146057123	AG10803	skin:	n/a
24	chr6:146056083-146056133	AG09319	gingival:	n/a
25	chr6:146051934-146051984	PFSK-1	brain:	n/a
26	chr6:146056770-146056820	AG04450	lung:	fetal
27	chr6:146056793-146056843	ovcar-3	ovarian:	n/a
28	chr6:146056419-146056469	GM19239	blood:	n/a
29	chr6:146056419-146056469	HRCEpiC	kidney:	n/a
30	chr6:146057073-146057123	SK-N-MC	brain:	n/a
31	chr6:146056770-146056820	HUVEC	blood vessel:	n/a
32	chr6:146057073-146057123	GM12878	blood:	n/a
33	chr6:146057055-146057105	K562	blood:	n/a
34	chr6:146056083-146056133	ProgFib	skin:	n/a
35	chr6:146056419-146056469	HL-60	blood:	n/a
36	chr6:146057055-146057105	PANC-1	pancreas:	n/a
37	chr6:146057055-146057105	MCF-7	breast:	n/a
38	chr6:146056083-146056133	NB4	blood:	n/a
39	chr6:146057073-146057123	HEEpiC	esophagus:	n/a
40	chr6:146056083-146056133	HCT-116	colon:	n/a
41	chr6:146056770-146056820	HNPCEpiC	eye:	n/a
42	chr6:146056793-146056843	RPTEC	kidney:	n/a
43	chr6:146057055-146057105	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:146056770-146056820	HCM	heart:	n/a
45	chr6:146057055-146057105	PrEC	prostate:	n/a
46	chr6:146056770-146056820	SK-N-SH_RA	brain:	n/a
47	chr6:146056083-146056133	K562	blood:	n/a
48	chr6:146056419-146056469	AG09309	skin:	n/a
49	chr6:146056083-146056133	MCF10A-Er-Src	breast:	n/a
50	chr6:146056770-146056820	PrEC	prostate:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:146044114..146046476-chr6:146084502..146087117,2	K562	blood:
2	chr12:44199788..44200535-chr6:146055682..146056650,2	Hela-S3	cervix:
3	chr6:146054188..146056153-chr6:146627133..146629580,2	K562	blood:
4	chr6:146047111..146049534-chr6:146133059..146136238,3	K562	blood:
5	chr2:38977833..38978509-chr6:146055931..146056536,2	Hela-S3	cervix:
6	chr10:75012200..75012758-chr6:146055684..146056249,2	Hela-S3	cervix:
7	chr6:146047690..146050384-chr6:146050492..146052811,2	K562	blood:
8	chr6:146040935..146043789-chr6:146048451..146050573,2	K562	blood:
9	chr6:146021020..146022840-chr6:146050602..146052412,2	K562	blood:
10	chr19:16770512..16771052-chr6:146055843..146056790,2	Hela-S3	cervix:
11	chr6:146056240..146056988-chr7:100424823..100425448,2	HCT-116	colon:
12	chr6:146023773..146025394-chr6:146054656..146056157,2	K562	blood:
13	chr13:98794348..98794868-chr6:146056065..146056713,2	HCT-116	colon:
14	chr6:146040316..146042577-chr6:146048417..146050382,3	K562	blood:
15	chr6:146047690..146050384-chr6:146050492..146052811,2	K562	blood:
16	chr6:146040316..146042577-chr6:146048417..146050382,3	K562	blood:
17	chr6:146054743..146057884-chr6:146276241..146279001,3	K562	blood:
18	chr6:43595203..43596723-chr6:146055866..146057723,2	MCF-7	breast:
19	chr6:146055972..146056545-chr6:146135397..146135982,2	MCF-7	breast:
20	chr6:146054764..146058281-chr6:146133205..146137397,13	MCF-7	breast:
21	chr6:146051601..146058492-chr6:146282422..146286666,8	K562	blood:
22	chr6:146056051..146056947-chr9:33025138..33025814,2	Hela-S3	cervix:
23	chr6:146042289..146044000-chr6:146051001..146052592,2	MCF-7	breast:
24	chr6:146043919..146045619-chr6:146047459..146050321,2	K562	blood:
25	chr6:146055814..146058166-chr6:146135376..146138309,3	MCF-7	breast:
26	chr6:146043919..146045619-chr6:146047459..146050321,2	K562	blood:
27	chr6:146052203..146054409-chr6:146284749..146287037,2	K562	blood:
28	chr1:110950353..110950869-chr6:146056622..146057613,2	Hela-S3	cervix:
29	chr6:146040708..146045667-chr6:146052083..146058701,12	K562	blood:
30	chr6:146054881..146058754-chr6:146284576..146286666,3	K562	blood:
31	chr6:146047378..146061811-chr6:146118130..146137627,77	K562	blood:
32	chr6:146040825..146042704-chr6:146055386..146057604,2	MCF-7	breast:
33	chr6:146040935..146043789-chr6:146048451..146050573,2	K562	blood:
34	chr19:55770065..55771348-chr6:146056333..146057332,3	Hela-S3	cervix:
35	chr1:228327693..228328321-chr6:146055580..146056537,2	Hela-S3	cervix:
36	chr11:62608720..62609583-chr6:146056117..146056835,2	NB4	blood:
37	chr6:146052168..146062191-chr6:146124046..146141258,59	K562	blood:
38	chr6:146042690..146044450-chr6:146054852..146056800,2	MCF-7	breast:
39	chr6:146042289..146044000-chr6:146051001..146052592,2	MCF-7	breast:
40	chr6:146043150..146050221-chr6:146053202..146058792,11	MCF-7	breast:
41	chr6:146055478..146057329-chr6:146213622..146216410,2	K562	blood:
42	chr6:146041485..146043057-chr6:146133059..146134567,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM1-11	chr6:146056706-146058354	ENSG00000270638.1
2	lnc-GRM1-1	chr6:146056005-146056056	NONHSAT115397

No data

Variant related genes	Relation type
ENSG00000270638	TF binding region
EPM2A	TF binding region
ENSG00000270638	CpG island
EPM2A	CpG island
ENSG00000143774	chromatin interactions
ENSG00000214046	chromatin interactions
ENSG00000152767	chromatin interactions
ENSG00000086061	chromatin interactions
ENSG00000224699	chromatin interactions
ENSG00000137074	chromatin interactions
ENSG00000227540	chromatin interactions
ENSG00000172432	chromatin interactions
ENSG00000196411	chromatin interactions
ENSG00000134248	chromatin interactions
ENSG00000270828	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000270638	chromatin interactions
ENSG00000151239	chromatin interactions
ENSG00000268790	chromatin interactions
ENSG00000235652	chromatin interactions
ENSG00000182180	chromatin interactions
ENSG00000105063	chromatin interactions
ENSG00000112425	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000118496	chromatin interactions
ENSG00000146414	chromatin interactions

Extended variants
information (count: 598 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:598 , 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	rs556902075	chr6:146041321-146041322	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs543693155	chr6:146041325-146041326	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs183582333	chr6:146041333-146041334	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs188168794	chr6:146041347-146041348	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs139781266	chr6:146041350-146041351	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs117248440	chr6:146041377-146041378	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs539975751	chr6:146041394-146041395	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs113110393	chr6:146041402-146041403	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs573756514	chr6:146041499-146041500	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs4896841	chr6:146041522-146041523	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs151098189	chr6:146041628-146041629	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs531532842	chr6:146041661-146041662	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs191648871	chr6:146041687-146041688	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs565155500	chr6:146041722-146041723	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs559708404	chr6:146041731-146041732	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs560356356	chr6:146041777-146041778	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs528532071	chr6:146041924-146041925	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs527748531	chr6:146041956-146041957	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs528459812	chr6:146041973-146041974	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs567803728	chr6:146042041-146042042	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs574058222	chr6:146042054-146042055	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs139763276	chr6:146042073-146042074	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs374090557	chr6:146042095-146042096	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs182241210	chr6:146042105-146042106	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs149803229	chr6:146042124-146042125	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs557758891	chr6:146042151-146042152	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs577580952	chr6:146042180-146042181	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs541658019	chr6:146042191-146042192	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs561536978	chr6:146042209-146042210	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs551311792	chr6:146042218-146042219	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs147869748	chr6:146042264-146042265	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs141545692	chr6:146042294-146042295	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs368383255	chr6:146042306-146042307	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs542397645	chr6:146042367-146042368	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs186479264	chr6:146042368-146042369	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs575902356	chr6:146042395-146042396	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs79070285	chr6:146042417-146042418	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs370127124	chr6:146042459-146042460	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs544914692	chr6:146042511-146042512	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs565240532	chr6:146042532-146042533	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs527691661	chr6:146042540-146042541	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs1337840	chr6:146042558-146042559	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs530751216	chr6:146042559-146042560	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs74461216	chr6:146042560-146042561	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs367765580	chr6:146042603-146042604	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs192603905	chr6:146042657-146042658	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs146998905	chr6:146042722-146042723	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs371595415	chr6:146042725-146042726	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs570286176	chr6:146042787-146042788	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs539306617	chr6:146042824-146042825	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:542 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:146006800-146050000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr6:146007400-146043800	Weak transcription	Liver	Liver
3	chr6:146026800-146055800	Weak transcription	Left Ventricle	heart
4	chr6:146027600-146043400	Weak transcription	Psoas Muscle	Psoas
5	chr6:146028600-146049200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:146030000-146043000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:146030200-146054000	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr6:146035800-146055200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr6:146036200-146044200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr6:146036200-146049800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:146036200-146054800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr6:146036600-146044600	Weak transcription	Brain Hippocampus Middle	brain
13	chr6:146036800-146050000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:146036800-146050000	Weak transcription	Thymus	Thymus
15	chr6:146037000-146052000	Weak transcription	Ovary	ovary
16	chr6:146037600-146043600	Weak transcription	Primary T cells from cord blood	blood
17	chr6:146037800-146044800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:146038400-146052600	Weak transcription	Fetal Heart	heart
19	chr6:146041200-146042000	Strong transcription	Primary B cells from cord blood	blood
20	chr6:146041400-146043800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:146041800-146050000	Weak transcription	Fetal Stomach	stomach
22	chr6:146042000-146044800	Weak transcription	Primary B cells from cord blood	blood
23	chr6:146043600-146044000	ZNF genes & repeats	Primary T cells from cord blood	blood
24	chr6:146043800-146044000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:146043800-146044200	ZNF genes & repeats	Liver	Liver
26	chr6:146044200-146044800	Weak transcription	Liver	Liver
27	chr6:146044800-146045000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr6:146044800-146045200	Enhancers	HepG2	liver
29	chr6:146044800-146045400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:146045000-146055200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr6:146045400-146045800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:146045600-146054800	Weak transcription	Primary T cells from cord blood	blood
33	chr6:146045800-146046200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr6:146046200-146050000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:146046800-146047000	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr6:146047000-146049800	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr6:146047800-146055000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr6:146049200-146051200	Strong transcription	Stomach Smooth Muscle	stomach
39	chr6:146049200-146051400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
40	chr6:146049200-146051800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr6:146049400-146049800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr6:146049800-146050200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:146049800-146050200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
44	chr6:146049800-146050800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:146050000-146050200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr6:146050000-146050400	ZNF genes & repeats	Brain Cingulate Gyrus	brain
47	chr6:146050000-146050400	ZNF genes & repeats	Colon Smooth Muscle	Colon
48	chr6:146050000-146050600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:146050000-146050600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr6:146050000-146050600	ZNF genes & repeats	Fetal Stomach	stomach

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