Variant report

Variant	esv3424537
Chromosome Location	chr11:47660545-47663980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:47663861-47664550	HepG2	liver:	n/a	n/a
2	ATF1	chr11:47663960-47664547	K562	blood:	n/a	n/a
3	ATF3	chr11:47663846-47664280	H1-hESC	embryonic stem cell:	n/a	chr11:47664073-47664093 chr11:47664167-47664176 chr11:47664225-47664234
4	ATF3	chr11:47663929-47664349	GM12878	blood:	n/a	chr11:47664073-47664093 chr11:47664167-47664176 chr11:47664225-47664234
5	ATF3	chr11:47663858-47664387	K562	blood:	n/a	chr11:47664073-47664093 chr11:47664167-47664176 chr11:47664225-47664234 chr11:47664369-47664382
6	ATF3	chr11:47663856-47664502	K562	blood:	n/a	chr11:47664073-47664093 chr11:47664167-47664176 chr11:47664225-47664234 chr11:47664369-47664382
7	ATF3	chr11:47663888-47664262	HepG2	liver:	n/a	chr11:47664073-47664093 chr11:47664167-47664176 chr11:47664225-47664234
8	ATF3	chr11:47663910-47664233	K562	blood:	n/a	chr11:47664073-47664093 chr11:47664167-47664176
9	ATF3	chr11:47663951-47664147	H1-hESC	embryonic stem cell:	n/a	chr11:47664073-47664093
10	ATF3	chr11:47663873-47664614	GM12878	blood:	n/a	chr11:47664073-47664093 chr11:47664167-47664176 chr11:47664225-47664234 chr11:47664369-47664382
11	BACH1	chr11:47663913-47664417	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr11:47663669-47664618	GM12878	blood:	n/a	chr11:47663804-47663813
13	BHLHE40	chr11:47662722-47662847	K562	blood:	n/a	n/a
14	BHLHE40	chr11:47663897-47664507	A549	lung:	n/a	chr11:47664144-47664160 chr11:47664084-47664093 chr11:47664082-47664095 chr11:47664078-47664099 chr11:47664084-47664093 chr11:47664085-47664094 chr11:47664083-47664092
15	BHLHE40	chr11:47663561-47664629	K562	blood:	n/a	chr11:47664144-47664160 chr11:47664084-47664093 chr11:47664082-47664095 chr11:47664078-47664099 chr11:47664084-47664093 chr11:47664085-47664094 chr11:47664083-47664092
16	BHLHE40	chr11:47663862-47664356	HepG2	liver:	n/a	chr11:47664144-47664160 chr11:47664084-47664093 chr11:47664082-47664095 chr11:47664078-47664099 chr11:47664084-47664093 chr11:47664085-47664094 chr11:47664083-47664092
17	BHLHE40	chr11:47663512-47664574	HepG2	liver:	n/a	chr11:47664144-47664160 chr11:47664084-47664093 chr11:47664082-47664095 chr11:47664078-47664099 chr11:47664084-47664093 chr11:47664085-47664094 chr11:47664083-47664092
18	BHLHE40	chr11:47663943-47664224	HepG2	liver:	n/a	chr11:47664144-47664160 chr11:47664084-47664093 chr11:47664082-47664095 chr11:47664078-47664099 chr11:47664084-47664093 chr11:47664085-47664094 chr11:47664083-47664092
19	BHLHE40	chr11:47663431-47664655	GM12878	blood:	n/a	chr11:47664144-47664160 chr11:47664084-47664093 chr11:47664082-47664095 chr11:47664078-47664099 chr11:47664084-47664093 chr11:47664085-47664094 chr11:47664083-47664092
20	BRCA1	chr11:47663971-47664513	GM12878	blood:	n/a	n/a
21	BRCA1	chr11:47663422-47664520	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr11:47663963-47664348	HepG2	liver:	n/a	n/a
23	BRCA1	chr11:47663805-47664482	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr11:47663711-47664614	K562	blood:	n/a	n/a
25	CCNT2	chr11:47663625-47664549	K562	blood:	n/a	chr11:47664167-47664176
26	CEBPB	chr11:47662215-47662478	IMR90	lung:	n/a	chr11:47662340-47662353 chr11:47662341-47662352
27	CEBPB	chr11:47663943-47664485	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr11:47663965-47664418	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:47662229-47662472	HepG2	liver:	n/a	chr11:47662340-47662353 chr11:47662341-47662352
30	CEBPB	chr11:47663876-47664315	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPD	chr11:47663872-47664402	HepG2	liver:	n/a	n/a
32	CEBPD	chr11:47663787-47664620	K562	blood:	n/a	n/a
33	CHD1	chr11:47663234-47664037	H1-hESC	embryonic stem cell:	n/a	chr11:47663726-47663736
34	CHD1	chr11:47663303-47664570	GM12878	blood:	n/a	chr11:47663726-47663736
35	CHD2	chr11:47663508-47664618	GM12878	blood:	n/a	chr11:47663726-47663736
36	CHD2	chr11:47662746-47662822	K562	blood:	n/a	n/a
37	CHD2	chr11:47663498-47664503	Hela-S3	cervix:	n/a	chr11:47663726-47663736
38	CHD2	chr11:47663799-47664406	HepG2	liver:	n/a	n/a
39	CHD2	chr11:47663924-47664505	K562	blood:	n/a	n/a
40	CHD2	chr11:47663665-47664445	H1-hESC	embryonic stem cell:	n/a	chr11:47663726-47663736
41	CREB1	chr11:47663808-47664605	K562	blood:	n/a	n/a
42	CREB1	chr11:47663667-47664436	A549	lung:	n/a	n/a
43	CREB1	chr11:47663687-47664651	K562	blood:	n/a	n/a
44	CREB1	chr11:47663980-47664434	A549	lung:	n/a	n/a
45	CREB1	chr11:47663493-47664599	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr11:47663618-47664619	GM12878	blood:	n/a	n/a
47	CREB1	chr11:47663790-47664535	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr11:47663496-47664638	HepG2	liver:	n/a	n/a
49	CTBP2	chr11:47663674-47664451	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr11:47663740-47663890	GM12873	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:47663666-47663716	PANC-1	pancreas:	n/a
2	chr11:47663538-47663588	SAEC	small airway:	n/a
3	chr11:47663538-47663588	U87	brain:	n/a
4	chr11:47663538-47663588	HUVEC	blood vessel:	n/a
5	chr11:47663538-47663588	AoSMC	blood vessel:	n/a
6	chr11:47663538-47663588	SK-N-SH_RA	brain:	n/a
7	chr11:47663538-47663588	PrEC	prostate:	n/a
8	chr11:47663666-47663716	HIPEpiC	eye:	n/a
9	chr11:47663538-47663588	CMK	blood:	n/a
10	chr11:47663538-47663588	Jurkat	blood:	n/a
11	chr11:47663666-47663716	GM12878	blood:	n/a
12	chr11:47663538-47663588	HCM	heart:	n/a
13	chr11:47663538-47663588	NB4	blood:	n/a
14	chr11:47663666-47663716	AoSMC	blood vessel:	n/a
15	chr11:47663538-47663588	GM06990	blood:	n/a
16	chr11:47663666-47663716	HUVEC	blood vessel:	n/a
17	chr11:47663666-47663716	PrEC	prostate:	n/a
18	chr11:47663538-47663588	AG10803	skin:	n/a
19	chr11:47663538-47663588	BE2_C	brain:	n/a
20	chr11:47663538-47663588	HIPEpiC	eye:	n/a
21	chr11:47663538-47663588	HNPCEpiC	eye:	n/a
22	chr11:47663666-47663716	K562	blood:	n/a
23	chr11:47663666-47663716	HepG2	liver:	n/a
24	chr11:47663538-47663588	HRPEpiC	eye:	n/a
25	chr11:47663538-47663588	HCT-116	colon:	n/a
26	chr11:47663538-47663588	ovcar-3	ovarian:	n/a
27	chr11:47663666-47663716	A549	lung:	n/a
28	chr11:47663538-47663588	GM19239	blood:	n/a
29	chr11:47663666-47663716	U87	brain:	n/a
30	chr11:47663666-47663716	NHDF-neo	bronchial:	n/a
31	chr11:47663666-47663716	HCPEpiC	choroid plexus:	n/a
32	chr11:47663666-47663716	GM12892	blood:	n/a
33	chr11:47663666-47663716	SK-N-SH_RA	brain:	n/a
34	chr11:47663538-47663588	NHBE	bronchial:	n/a
35	chr11:47663538-47663588	A549	lung:	n/a
36	chr11:47663666-47663716	AG04449	skin:	fetal
37	chr11:47663538-47663588	Hepatocyte	liver:	n/a
38	chr11:47663666-47663716	CMK	blood:	n/a
39	chr11:47663538-47663588	GM12891	blood:	n/a
40	chr11:47663538-47663588	K562	blood:	n/a
41	chr11:47663666-47663716	AG09309	skin:	n/a
42	chr11:47663666-47663716	BE2_C	brain:	n/a
43	chr11:47663666-47663716	ECC-1	luminal epithelium:	n/a
44	chr11:47663538-47663588	IMR90	lung:	fetal
45	chr11:47663666-47663716	NHBE	bronchial:	n/a
46	chr11:47663666-47663716	HL-60	blood:	n/a
47	chr11:47663538-47663588	NH-A	brain:	n/a
48	chr11:47663538-47663588	GM12878	blood:	n/a
49	chr11:47663538-47663588	LNCaP	prostate:	n/a
50	chr11:47663666-47663716	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:47660743..47662346-chr11:47776631..47779336,2	MCF-7	breast:
2	chr11:47662615..47665881-chr11:47786940..47791485,8	K562	blood:
3	chr1:35658580..35659199-chr11:47663778..47664281,2	Hela-S3	cervix:
4	chr11:47661534..47663358-chr11:47740296..47742508,2	K562	blood:
5	chr11:47660129..47661788-chr11:47662493..47664105,2	MCF-7	breast:
6	chr11:47648151..47655137-chr11:47656071..47661932,11	K562	blood:
7	chr11:47206285..47208872-chr11:47661768..47663771,2	K562	blood:
8	chr11:47663604..47664110-chr16:57836092..57836625,2	Hela-S3	cervix:
9	chr11:47572750..47576231-chr11:47662956..47665605,3	K562	blood:
10	chr11:47663126..47663917-chr11:47735845..47736412,2	MCF-7	breast:
11	chr11:47662579..47666117-chr11:47735408..47738256,8	MCF-7	breast:
12	chr11:47662615..47664358-chr11:47788211..47790386,2	K562	blood:
13	chr11:47660129..47661788-chr11:47662493..47664105,2	MCF-7	breast:
14	chr11:47663817..47664494-chr13:101326174..101327133,2	Hela-S3	cervix:
15	chr11:47660831..47663188-chr11:47962801..47965480,2	K562	blood:
16	chr11:47648507..47652310-chr11:47658295..47660637,4	K562	blood:
17	chr11:47663635..47664413-chr21:28217518..28218073,2	Hela-S3	cervix:
18	chr11:47663305..47664213-chr14:21737267..21737936,2	HCT-116	colon:
19	chr11:47663756..47666703-chr11:47730078..47732549,2	MCF-7	breast:
20	chr11:47663042..47663543-chr12:109536619..109537119,2	Hela-S3	cervix:
21	chr11:47599811..47601701-chr11:47661212..47663329,2	K562	blood:
22	chr11:47663509..47666496-chr11:47787150..47790595,4	MCF-7	breast:
23	chr11:47662583..47667763-chr11:47735291..47739208,6	MCF-7	breast:
24	chr11:47599184..47601918-chr11:47661794..47664226,4	MCF-7	breast:
25	chr11:47599811..47601393-chr11:47661829..47664063,2	K562	blood:
26	chr11:47586161..47588765-chr11:47660200..47662976,2	MCF-7	breast:
27	chr11:47663591..47664273-chr16:18812487..18813289,2	Hela-S3	cervix:
28	chr11:47661932..47663606-chr11:47755819..47758646,2	K562	blood:

Variant related genes	Relation type
MTCH2	TF binding region
MTCH2	CpG island
ENSG00000213619	chromatin interactions
ENSG00000109919	chromatin interactions
ENSG00000154734	chromatin interactions
ENSG00000125247	chromatin interactions
ENSG00000170540	chromatin interactions
ENSG00000123444	chromatin interactions
ENSG00000116560	chromatin interactions
ENSG00000231880	chromatin interactions
ENSG00000165912	chromatin interactions
ENSG00000260342	chromatin interactions
ENSG00000149187	chromatin interactions
ENSG00000140859	chromatin interactions
ENSG00000109920	chromatin interactions
ENSG00000110536	chromatin interactions
ENSG00000092199	chromatin interactions
ENSG00000165923	chromatin interactions

Extended variants
information (count: 129 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:129 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530381454	chr11:47660613-47660614	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs375501249	chr11:47660623-47660624	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs368853244	chr11:47660624-47660625	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs372508158	chr11:47660635-47660636	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs533713734	chr11:47660666-47660667	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs550494666	chr11:47660672-47660673	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs563703063	chr11:47660688-47660689	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs531167007	chr11:47660696-47660697	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs150128455	chr11:47660776-47660777	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs549325622	chr11:47660803-47660804	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs138953267	chr11:47660826-47660827	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs566063438	chr11:47660829-47660830	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs535070263	chr11:47660881-47660882	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs76225881	chr11:47660883-47660884	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs563500376	chr11:47660885-47660886	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs141403391	chr11:47660909-47660910	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs570309734	chr11:47660939-47660940	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs183262496	chr11:47661007-47661008	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs146940221	chr11:47661052-47661053	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs556023913	chr11:47661108-47661109	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs575896828	chr11:47661115-47661116	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs530275260	chr11:47661119-47661120	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs376572827	chr11:47661134-47661135	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs555293657	chr11:47661188-47661189	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs572052825	chr11:47661246-47661247	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs541115048	chr11:47661262-47661263	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs564719710	chr11:47661314-47661315	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs199641055	chr11:47661322-47661323	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs578203646	chr11:47661325-47661326	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs186450844	chr11:47661349-47661350	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs113754555	chr11:47661355-47661356	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs529584925	chr11:47661379-47661380	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs575502208	chr11:47661390-47661391	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs571680942	chr11:47661394-47661395	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs546853487	chr11:47661399-47661400	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs111255370	chr11:47661401-47661402	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs559659310	chr11:47661419-47661420	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs528624061	chr11:47661488-47661489	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs7129948	chr11:47661498-47661499	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs538977967	chr11:47661524-47661525	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs570346898	chr11:47661540-47661541	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs539263347	chr11:47661541-47661542	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs549534594	chr11:47661607-47661608	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs189688842	chr11:47661616-47661617	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs191594998	chr11:47661640-47661641	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs372280280	chr11:47661656-47661657	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs113589828	chr11:47661744-47661745	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs569276409	chr11:47661745-47661746	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs535697352	chr11:47661755-47661756	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs555106909	chr11:47661758-47661759	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47636600-47661400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr11:47637600-47660800	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr11:47637600-47661200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:47637600-47663200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr11:47637800-47661000	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr11:47637800-47661000	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr11:47638000-47661400	Strong transcription	Fetal Thymus	thymus
8	chr11:47638000-47661800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr11:47638200-47661200	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr11:47638200-47661200	Strong transcription	Stomach Smooth Muscle	stomach
11	chr11:47638200-47661600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:47638200-47661600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:47638400-47661200	Strong transcription	HUES6 Cell Line	embryonic stem cell
14	chr11:47638800-47661600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr11:47639000-47661200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:47639000-47661400	Strong transcription	Fetal Muscle Leg	muscle
17	chr11:47639000-47662600	Weak transcription	Stomach Mucosa	stomach
18	chr11:47639600-47661200	Strong transcription	Fetal Muscle Trunk	muscle
19	chr11:47640000-47661000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:47640200-47661200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr11:47640200-47661200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr11:47640200-47661200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr11:47640600-47661400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr11:47640800-47661400	Strong transcription	Fetal Intestine Small	intestine
25	chr11:47640800-47661400	Strong transcription	Fetal Stomach	stomach
26	chr11:47641800-47661200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:47641800-47661600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr11:47642000-47661400	Strong transcription	Placenta	Placenta
29	chr11:47642000-47661800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr11:47643400-47661200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr11:47644000-47661600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr11:47646800-47662600	Weak transcription	Aorta	Aorta
33	chr11:47648200-47662800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr11:47648200-47663200	Weak transcription	Gastric	stomach
35	chr11:47648400-47662800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr11:47649200-47662600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr11:47653400-47661600	Weak transcription	Pancreas	Pancrea
38	chr11:47653400-47662600	Weak transcription	Psoas Muscle	Psoas
39	chr11:47653600-47662200	Weak transcription	Fetal Brain Male	brain
40	chr11:47653600-47662200	Weak transcription	Fetal Heart	heart
41	chr11:47653800-47662400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr11:47654000-47660800	Strong transcription	Liver	Liver
43	chr11:47654000-47661200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr11:47654400-47661200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr11:47654400-47661400	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr11:47654600-47661200	Strong transcription	Thymus	Thymus
47	chr11:47654800-47660600	Strong transcription	Left Ventricle	heart
48	chr11:47655000-47661000	Strong transcription	Adipose Nuclei	Adipose
49	chr11:47655200-47661000	Strong transcription	Fetal Intestine Large	intestine
50	chr11:47655200-47661600	Strong transcription	HUES64 Cell Line	embryonic stem cell

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