Variant report

Variant	nsv869146
Chromosome Location	chr2:148787051-149060763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1271)
CpG islands
(count:305)
Chromatin interactive
region (count:78)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1271 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:148810230-148810584	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:148968850-148969044	HepG2	liver:	n/a	chr2:148969017-148969033
3	ARID3A	chr2:149002017-149002569	HepG2	liver:	n/a	chr2:149002050-149002066
4	ARID3A	chr2:148920439-148920729	K562	blood:	n/a	n/a
5	ARID3A	chr2:148959061-148959356	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:149009605-149009760	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:148888294-148888308	HepG2	liver:	n/a	n/a
8	ATF1	chr2:149017285-149017419	K562	blood:	n/a	n/a
9	ATF1	chr2:148967322-148967474	K562	blood:	n/a	n/a
10	ATF2	chr2:148799610-148800244	GM12878	blood:	n/a	n/a
11	ATF2	chr2:148805695-148807140	GM12878	blood:	n/a	n/a
12	ATF2	chr2:148805766-148807114	GM12878	blood:	n/a	n/a
13	ATF2	chr2:148799549-148800235	GM12878	blood:	n/a	n/a
14	BACH1	chr2:149017369-149017502	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr2:149030956-149031246	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr2:148936476-148936481	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:149017398-149017543	K562	blood:	n/a	n/a
18	BATF	chr2:148803918-148804156	GM12878	blood:	n/a	n/a
19	BATF	chr2:148803827-148804138	GM12878	blood:	n/a	n/a
20	BATF	chr2:148799772-148800076	GM12878	blood:	n/a	chr2:148799907-148799918
21	BATF	chr2:148789167-148789394	GM12878	blood:	n/a	n/a
22	BATF	chr2:148806449-148806848	GM12878	blood:	n/a	chr2:148806614-148806625
23	BATF	chr2:148799707-148800070	GM12878	blood:	n/a	chr2:148799907-148799918
24	BATF	chr2:148880380-148880646	GM12878	blood:	n/a	chr2:148880539-148880550
25	BATF	chr2:148806259-148806907	GM12878	blood:	n/a	chr2:148806614-148806625
26	BCL11A	chr2:148806525-148806767	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:148799776-148800128	GM12878	blood:	n/a	chr2:148800002-148800011
28	BCL11A	chr2:148799845-148800073	GM12878	blood:	n/a	chr2:148800002-148800011
29	BCL11A	chr2:148806110-148806885	GM12878	blood:	n/a	n/a
30	BCL3	chr2:148805871-148806863	GM12878	blood:	n/a	n/a
31	BCL3	chr2:148799732-148800218	GM12878	blood:	n/a	chr2:148800002-148800011
32	BCLAF1	chr2:148799725-148800084	GM12878	blood:	n/a	chr2:148800002-148800011
33	BCLAF1	chr2:148805628-148807044	GM12878	blood:	n/a	n/a
34	BCLAF1	chr2:148806074-148806967	GM12878	blood:	n/a	n/a
35	BCLAF1	chr2:148799581-148800151	GM12878	blood:	n/a	chr2:148800002-148800011
36	BHLHE40	chr2:148842666-148842699	A549	lung:	n/a	n/a
37	BHLHE40	chr2:149011302-149011613	K562	blood:	n/a	n/a
38	BHLHE40	chr2:149002150-149002345	HepG2	liver:	n/a	n/a
39	BHLHE40	chr2:148805899-148807141	GM12878	blood:	n/a	n/a
40	BHLHE40	chr2:149017230-149017473	K562	blood:	n/a	n/a
41	CBX3	chr2:148958977-148959378	K562	blood:	n/a	n/a
42	CBX3	chr2:149011246-149011697	HCT-116	colon:	n/a	n/a
43	CBX3	chr2:149011244-149011646	K562	blood:	n/a	n/a
44	CBX3	chr2:149017230-149017609	K562	blood:	n/a	n/a
45	CEBPB	chr2:148957140-148957407	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr2:148843505-148843790	A549	lung:	n/a	chr2:148843670-148843681
47	CEBPB	chr2:149045883-149046183	IMR90	lung:	n/a	n/a
48	CEBPB	chr2:148889991-148890325	Hela-S3	cervix:	n/a	chr2:148890137-148890150 chr2:148890137-148890150
49	CEBPB	chr2:149036854-149037024	HepG2	liver:	n/a	chr2:149036949-149036960
50	CEBPB	chr2:148890651-148890853	A549	lung:	n/a	chr2:148890713-148890724 chr2:148890713-148890726 chr2:148890713-148890726 chr2:148890713-148890726 chr2:148890714-148890725

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:149041060-149041110	K562	blood:	n/a
2	chr2:148839265-148839315	LNCaP	prostate:	n/a
3	chr2:149041060-149041110	RPTEC	kidney:	n/a
4	chr2:148839265-148839315	SKMC	muscle:	n/a
5	chr2:148815999-148816049	ECC-1	luminal epithelium:	n/a
6	chr2:149041060-149041110	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:148893152-148893202	IMR90	lung:	fetal
8	chr2:148976109-148976159	CMK	blood:	n/a
9	chr2:149041060-149041110	GM12878	blood:	n/a
10	chr2:148815999-148816049	HL-60	blood:	n/a
11	chr2:148893152-148893202	PFSK-1	brain:	n/a
12	chr2:148815999-148816049	HNPCEpiC	eye:	n/a
13	chr2:148815999-148816049	HAEpiC	amniotic membrane:	n/a
14	chr2:149041060-149041110	NHBE	bronchial:	n/a
15	chr2:148839265-148839315	AoSMC	blood vessel:	n/a
16	chr2:148839265-148839315	SK-N-MC	brain:	n/a
17	chr2:148839265-148839315	HRE	kidney:	n/a
18	chr2:148893152-148893202	PANC-1	pancreas:	n/a
19	chr2:148815999-148816049	BE2_C	brain:	n/a
20	chr2:149041060-149041110	BE2_C	brain:	n/a
21	chr2:148815999-148816049	SK-N-MC	brain:	n/a
22	chr2:148815999-148816049	ovcar-3	ovarian:	n/a
23	chr2:148893152-148893202	AG10803	skin:	n/a
24	chr2:149041060-149041110	T-47D	breast:	n/a
25	chr2:148815999-148816049	GM12892	blood:	n/a
26	chr2:148893152-148893202	Hepatocyte	liver:	n/a
27	chr2:148893152-148893202	Jurkat	blood:	n/a
28	chr2:148815999-148816049	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:148893152-148893202	U87	brain:	n/a
30	chr2:148839265-148839315	ovcar-3	ovarian:	n/a
31	chr2:148976109-148976159	NHBE	bronchial:	n/a
32	chr2:149041060-149041110	HL-60	blood:	n/a
33	chr2:148976109-148976159	SKMC	muscle:	n/a
34	chr2:148976109-148976159	HCT-116	colon:	n/a
35	chr2:148815999-148816049	NHDF-neo	bronchial:	n/a
36	chr2:148839265-148839315	AG09319	gingival:	n/a
37	chr2:148893152-148893202	HRPEpiC	eye:	n/a
38	chr2:148976109-148976159	GM06990	blood:	n/a
39	chr2:149041060-149041110	HIPEpiC	eye:	n/a
40	chr2:148893152-148893202	HNPCEpiC	eye:	n/a
41	chr2:148815999-148816049	HCPEpiC	choroid plexus:	n/a
42	chr2:148893152-148893202	HEEpiC	esophagus:	n/a
43	chr2:148815999-148816049	HEK293	kidney:	embryo
44	chr2:148976109-148976159	AG04450	lung:	fetal
45	chr2:148815999-148816049	NB4	blood:	n/a
46	chr2:148815999-148816049	PANC-1	pancreas:	n/a
47	chr2:148893152-148893202	HIPEpiC	eye:	n/a
48	chr2:148976109-148976159	HCM	heart:	n/a
49	chr2:148976109-148976159	SAEC	small airway:	n/a
50	chr2:148976109-148976159	NB4	blood:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:148869849..148872323-chr2:148885274..148887437,2	MCF-7	breast:
2	chr17:56708724..56710145-chr2:149008940..149009960,20	MCF-7	breast:
3	chr2:148839523..148841211-chr2:148842127..148844445,2	K562	blood:
4	chr2:148796353..148798191-chr2:148802415..148804582,2	K562	blood:
5	chr2:148862754..148865628-chr2:148893706..148895344,2	K562	blood:
6	chr2:148994771..148998300-chr2:149002088..149006299,3	K562	blood:
7	chr2:148747178..148748066-chr2:148853587..148854325,3	MCF-7	breast:
8	chr2:148831814..148833866-chr2:148838337..148840088,2	K562	blood:
9	chr2:148790035..148791910-chr2:148820838..148823392,2	K562	blood:
10	chr2:148995742..148998637-chr2:149000873..149004003,3	MCF-7	breast:
11	chr2:148888593..148891096-chr2:148894086..148896797,2	K562	blood:
12	chr2:148884069..148886701-chr2:148890123..148892046,2	MCF-7	breast:
13	chr2:148995742..148998637-chr2:149000873..149004003,3	MCF-7	breast:
14	chr2:148801242..148804386-chr2:148805992..148808157,4	K562	blood:
15	chr2:148795246..148798191-chr2:148802393..148803915,2	K562	blood:
16	chr2:148951330..148953430-chr2:148956133..148959129,2	K562	blood:
17	chr17:56707748..56709669-chr2:149007960..149010940,5	MCF-7	breast:
18	chr2:148784396..148788846-chr2:148789085..148797042,12	K562	blood:
19	chr2:148826768..148827504-chr6:20350150..20350710,2	MCF-7	breast:
20	chr2:148859675..148863197-chr2:148868107..148869963,3	MCF-7	breast:
21	chr2:148784529..148787318-chr2:148787850..148789462,2	MCF-7	breast:
22	chr2:148794522..148796703-chr2:148799769..148801375,2	K562	blood:
23	chr2:148996066..148998300-chr2:149002088..149004966,2	K562	blood:
24	chr2:148924504..148926944-chr2:148937289..148939887,2	MCF-7	breast:
25	chr2:148801242..148804386-chr2:148805992..148808157,4	K562	blood:
26	chr2:148931889..148933794-chr2:148936353..148939104,2	K562	blood:
27	chr2:148976677..148978352-chr2:149006227..149008013,2	MCF-7	breast:
28	chr2:148967081..148967666-chr2:149266757..149267493,2	MCF-7	breast:
29	chr2:148796353..148798191-chr2:148802415..148804582,2	K562	blood:
30	chr2:148818705..148820589-chr2:148824017..148825657,2	MCF-7	breast:
31	chr2:148746466..148747928-chr2:148959011..148960040,7	MCF-7	breast:
32	chr2:148951330..148953430-chr2:148956133..148959129,2	K562	blood:
33	chr2:148976677..148978352-chr2:149006227..149008013,2	MCF-7	breast:
34	chr17:56707881..56710421-chr2:149007960..149010940,2	K562	blood:
35	chr2:148892318..148894319-chr2:148896559..148898244,2	MCF-7	breast:
36	chr2:148852527..148854088-chr2:148860647..148862456,2	MCF-7	breast:
37	chr2:148801657..148804409-chr2:148807658..148809416,2	MCF-7	breast:
38	chr2:148852527..148854088-chr2:148860647..148862456,2	MCF-7	breast:
39	chr2:148793989..148796591-chr2:148815417..148817298,2	K562	blood:
40	chr2:148782652..148784833-chr2:148785431..148787188,2	MCF-7	breast:
41	chr17:56707733..56709409-chr2:149007940..149009460,7	MCF-7	breast:
42	chr2:148811506..148813577-chr2:148817603..148819976,2	K562	blood:
43	chr2:148778014..148780334-chr2:148791954..148794463,2	K562	blood:
44	chr2:148931889..148933794-chr2:148936353..148939104,2	K562	blood:
45	chr2:148784396..148788846-chr2:148789085..148797042,12	K562	blood:
46	chr2:148777400..148781221-chr2:148785788..148788815,4	MCF-7	breast:
47	chr2:148777816..148780257-chr2:148961269..148962957,2	MCF-7	breast:
48	chr2:148996066..148998300-chr2:149002088..149004966,2	K562	blood:
49	chr2:148964117..148966027-chr2:148967186..148969154,2	MCF-7	breast:
50	chr2:148784529..148787318-chr2:148787850..148789462,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBD5-1	chr2:148798775-148798934	NONHSAT074876
2	lnc-MBD5-1	chr2:148977516-148977602	NONHSAT074878
3	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074872
4	lnc-MBD5-1	chr2:148990814-148990964	NONHSAT074878
5	lnc-MBD5-1	chr2:148990814-148990964	NONHSAT074872
6	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074874
7	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074878
8	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074871
9	lnc-MBD5-1	chr2:148826141-148826162	NONHSAT074878
10	lnc-ORC4-3	chr2:149053225-149054248	NONHSAT074880
11	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074875
12	lnc-MBD5-1	chr2:148990814-148990896	NONHSAT074874
13	lnc-MBD5-1	chr2:148811960-148812018	NONHSAT074874

No data

Variant related genes	Relation type
MBD5	TF binding region
ENSG00000212181	TF binding region
ENSG00000224007	TF binding region
MBD5	CpG island
ENSG00000212181	CpG island
ENSG00000224007	CpG island
ENSG00000204406	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000115947	chromatin interactions

Extended variants
information (count: 9296 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:9296 , 50 per page) page: 1 2 3 4 5 6 7 ... 186

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377081424	chr2:148787091-148787092	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs114379305	chr2:148787095-148787096	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs367818274	chr2:148787119-148787120	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs571213371	chr2:148787172-148787173	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs13029038	chr2:148787308-148787309	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs551554023	chr2:148787322-148787323	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs569940703	chr2:148787327-148787328	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572152851	chr2:148787420-148787421	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs185052472	chr2:148787460-148787461	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs555604477	chr2:148787477-148787478	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs189561072	chr2:148787481-148787482	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs534665833	chr2:148787493-148787494	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs182217686	chr2:148787517-148787518	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs578029221	chr2:148787573-148787574	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs188944076	chr2:148787583-148787584	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs557173282	chr2:148787656-148787657	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs575545052	chr2:148787677-148787678	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs542864045	chr2:148787704-148787705	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs1234397	chr2:148787713-148787714	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs139689446	chr2:148787755-148787756	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs143722907	chr2:148787810-148787811	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs192017162	chr2:148787833-148787834	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs183576113	chr2:148787854-148787855	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs550293027	chr2:148787874-148787875	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs554625208	chr2:148787898-148787899	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs530982864	chr2:148787944-148787945	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs576483148	chr2:148787955-148787956	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs567824918	chr2:148787963-148787964	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs543523266	chr2:148788043-148788044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs146811105	chr2:148788097-148788098	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs188563516	chr2:148788113-148788114	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs115890190	chr2:148788114-148788115	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs139926960	chr2:148788191-148788192	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs556508449	chr2:148788225-148788226	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs13012455	chr2:148788236-148788237	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs191743103	chr2:148788244-148788245	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539619545	chr2:148788256-148788257	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs554789498	chr2:148788274-148788275	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs76106164	chr2:148788319-148788320	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs117975101	chr2:148788320-148788321	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs34805135	chr2:148788321-148788322	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs531944995	chr2:148788354-148788355	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs143344710	chr2:148788386-148788387	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs1234398	chr2:148788435-148788436	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs374439656	chr2:148788478-148788479	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs529751433	chr2:148788503-148788504	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs145626118	chr2:148788506-148788507	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs184003924	chr2:148788518-148788519	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs187179737	chr2:148788540-148788541	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs148913788	chr2:148788560-148788561	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	19904302	CNVD
Intellectual disability	19904302	CNVD
Microcephaly	19904302	CNVD
severe speech impairment	19904302	CNVD
Mental retardation	20152051	CNVD
2q23.1 microdeletion syndrome	18812405	CNVD
Mental retardation	19809484	CNVD
Autism	21981781	CNVD
Breast cancer	22522925	CNVD
Mental retardation	17847001	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20531469	CNVD

Chromatin state (count:2269 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148779600-148844600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:148779800-148788200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr2:148779800-148801600	Weak transcription	Aorta	Aorta
4	chr2:148779800-148803000	Weak transcription	Lung	lung
5	chr2:148779800-148811600	Weak transcription	Placenta	Placenta
6	chr2:148779800-148814800	Weak transcription	Small Intestine	intestine
7	chr2:148779800-148825600	Weak transcription	Left Ventricle	heart
8	chr2:148780200-148789800	Weak transcription	Brain Angular Gyrus	brain
9	chr2:148780200-148806600	Weak transcription	Brain Hippocampus Middle	brain
10	chr2:148780400-148788800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr2:148780400-148798800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr2:148780400-148806000	Weak transcription	HSMM	muscle
13	chr2:148780400-148809800	Weak transcription	Fetal Stomach	stomach
14	chr2:148780600-148792200	Weak transcription	NH-A	brain
15	chr2:148780800-148806400	Weak transcription	HSMMtube	muscle
16	chr2:148781200-148796400	Weak transcription	Primary hematopoietic stem cells	blood
17	chr2:148781200-148798600	Weak transcription	Adipose Nuclei	Adipose
18	chr2:148781200-148799600	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr2:148781200-148814200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:148781600-148798600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:148781600-148813400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr2:148781800-148794800	Weak transcription	NHDF-Ad	bronchial
23	chr2:148781800-148798400	Weak transcription	Fetal Thymus	thymus
24	chr2:148781800-148798600	Weak transcription	Primary B cells from cord blood	blood
25	chr2:148781800-148810000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr2:148781800-148814800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr2:148781800-148822800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:148781800-148829600	Weak transcription	Fetal Intestine Small	intestine
29	chr2:148781800-148833400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr2:148782000-148805600	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr2:148782200-148789200	Weak transcription	Fetal Lung	lung
32	chr2:148782200-148789400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:148782200-148790000	Weak transcription	Fetal Kidney	kidney
34	chr2:148782200-148791400	Weak transcription	Primary T cells from cord blood	blood
35	chr2:148782200-148791600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr2:148782200-148795200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr2:148782200-148798600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr2:148782200-148798600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr2:148782200-148798800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:148782200-148806000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:148782200-148806200	Weak transcription	K562	blood
42	chr2:148782200-148806400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:148782400-148799000	Weak transcription	Fetal Brain Male	brain
44	chr2:148782800-148788000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr2:148782800-148798600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:148782800-148804200	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr2:148783000-148798600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr2:148784200-148795600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr2:148784400-148811600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr2:148785400-148789400	Weak transcription	NHLF	lung

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