Variant report

Variant	nsv979339
Chromosome Location	chr2:114430138-114495192
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:853)
CpG islands
(count:183)
Chromatin interactive
region (count:37)
LncRNA
region (count:14)
Mature miRNA
region (count: 2)
miRNA target
sites (count:3)

(count:853 , 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	chr2:114457692-114458213	K562	blood:	n/a	n/a
2	ARID3A	chr2:114457824-114457937	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:114464702-114465021	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:114469664-114469667	HepG2	liver:	n/a	n/a
5	ATF1	chr2:114437071-114437425	K562	blood:	n/a	n/a
6	ATF2	chr2:114450181-114450739	GM12878	blood:	n/a	n/a
7	ATF2	chr2:114457703-114458119	GM12878	blood:	n/a	n/a
8	ATF2	chr2:114451050-114451495	GM12878	blood:	n/a	n/a
9	ATF2	chr2:114450125-114450742	GM12878	blood:	n/a	n/a
10	ATF2	chr2:114456570-114457191	GM12878	blood:	n/a	n/a
11	ATF2	chr2:114457610-114458053	GM12878	blood:	n/a	n/a
12	ATF2	chr2:114450992-114451895	GM12878	blood:	n/a	n/a
13	BATF	chr2:114450302-114450614	GM12878	blood:	n/a	n/a
14	BATF	chr2:114451104-114451470	GM12878	blood:	n/a	n/a
15	BATF	chr2:114450245-114450607	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:114450307-114450523	GM12878	blood:	n/a	chr2:114450467-114450476
17	BCL11A	chr2:114451170-114451502	GM12878	blood:	n/a	n/a
18	BCL11A	chr2:114450249-114450705	GM12878	blood:	n/a	chr2:114450467-114450476
19	BCL11A	chr2:114451174-114451583	GM12878	blood:	n/a	n/a
20	BCL3	chr2:114451106-114451503	GM12878	blood:	n/a	n/a
21	BCLAF1	chr2:114451062-114451648	GM12878	blood:	n/a	n/a
22	BCLAF1	chr2:114450204-114450653	GM12878	blood:	n/a	chr2:114450467-114450476
23	BCLAF1	chr2:114457710-114458179	GM12878	blood:	n/a	n/a
24	BCLAF1	chr2:114451057-114451505	GM12878	blood:	n/a	n/a
25	BCLAF1	chr2:114450139-114450709	GM12878	blood:	n/a	chr2:114450467-114450476
26	BHLHE40	chr2:114451064-114451611	GM12878	blood:	n/a	n/a
27	BHLHE40	chr2:114457890-114458374	K562	blood:	n/a	n/a
28	CBX3	chr2:114457750-114458241	K562	blood:	n/a	n/a
29	CEBPB	chr2:114491045-114491452	MCF-7	breast:	n/a	chr2:114491265-114491276
30	CEBPB	chr2:114445176-114445376	K562	blood:	n/a	n/a
31	CEBPB	chr2:114473898-114474244	K562	blood:	n/a	chr2:114474047-114474058
32	CEBPB	chr2:114491246-114491384	A549	lung:	n/a	chr2:114491265-114491276
33	CEBPB	chr2:114464751-114465030	K562	blood:	n/a	chr2:114464905-114464916
34	CEBPB	chr2:114491117-114491491	MCF-7	breast:	n/a	chr2:114491265-114491276
35	CEBPB	chr2:114464760-114465040	H1-hESC	embryonic stem cell:	n/a	chr2:114464905-114464916
36	CEBPB	chr2:114476569-114476786	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:114491124-114491437	K562	blood:	n/a	chr2:114491265-114491276
38	CEBPB	chr2:114459301-114459451	K562	blood:	n/a	chr2:114459371-114459382
39	CEBPB	chr2:114451065-114451686	GM12878	blood:	n/a	n/a
40	CEBPB	chr2:114459265-114459473	HepG2	liver:	n/a	chr2:114459371-114459382
41	CEBPB	chr2:114464737-114465089	K562	blood:	n/a	chr2:114464905-114464916
42	CEBPB	chr2:114479224-114479386	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:114464677-114465090	Hela-S3	cervix:	n/a	chr2:114464905-114464916
44	CEBPB	chr2:114451144-114451505	GM12878	blood:	n/a	n/a
45	CEBPB	chr2:114473875-114474173	K562	blood:	n/a	chr2:114474047-114474058
46	CEBPB	chr2:114473954-114474140	A549	lung:	n/a	chr2:114474047-114474058
47	CEBPB	chr2:114464687-114465094	IMR90	lung:	n/a	chr2:114464905-114464916
48	CEBPB	chr2:114473857-114474244	IMR90	lung:	n/a	chr2:114474047-114474058
49	CEBPB	chr2:114473942-114474194	HepG2	liver:	n/a	chr2:114474047-114474058
50	CEBPB	chr2:114469389-114469899	ECC-1	luminal epithelium:	n/a	chr2:114469520-114469537

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114463932-114463982	U87	brain:	n/a
2	chr2:114463932-114463982	HEK293	kidney:	embryo
3	chr2:114474155-114474205	BJ	skin:	n/a
4	chr2:114430284-114430334	HCM	heart:	n/a
5	chr2:114463932-114463982	HRE	kidney:	n/a
6	chr2:114430284-114430334	AG09309	skin:	n/a
7	chr2:114474155-114474205	NHDF-neo	bronchial:	n/a
8	chr2:114463932-114463982	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:114474155-114474205	AoSMC	blood vessel:	n/a
10	chr2:114474155-114474205	HRCEpiC	kidney:	n/a
11	chr2:114430284-114430334	NH-A	brain:	n/a
12	chr2:114474155-114474205	IMR90	lung:	fetal
13	chr2:114430284-114430334	ECC-1	luminal epithelium:	n/a
14	chr2:114463932-114463982	LNCaP	prostate:	n/a
15	chr2:114430284-114430334	CMK	blood:	n/a
16	chr2:114430284-114430334	AG04449	skin:	fetal
17	chr2:114430284-114430334	HRPEpiC	eye:	n/a
18	chr2:114463932-114463982	HEEpiC	esophagus:	n/a
19	chr2:114430284-114430334	MCF10A-Er-Src	breast:	n/a
20	chr2:114463932-114463982	Caco-2	colon:	n/a
21	chr2:114430284-114430334	IMR90	lung:	fetal
22	chr2:114463932-114463982	ovcar-3	ovarian:	n/a
23	chr2:114463932-114463982	GM06990	blood:	n/a
24	chr2:114463932-114463982	NT2-D1	testis:	n/a
25	chr2:114430284-114430334	GM19239	blood:	n/a
26	chr2:114430284-114430334	ovcar-3	ovarian:	n/a
27	chr2:114463932-114463982	CMK	blood:	n/a
28	chr2:114463932-114463982	AG09309	skin:	n/a
29	chr2:114430284-114430334	NT2-D1	testis:	n/a
30	chr2:114474155-114474205	SAEC	small airway:	n/a
31	chr2:114474155-114474205	T-47D	breast:	n/a
32	chr2:114474155-114474205	LNCaP	prostate:	n/a
33	chr2:114474155-114474205	SKMC	muscle:	n/a
34	chr2:114430284-114430334	SK-N-SH_RA	brain:	n/a
35	chr2:114474155-114474205	GM19239	blood:	n/a
36	chr2:114463932-114463982	Hela-S3	cervix:	n/a
37	chr2:114474155-114474205	NHBE	bronchial:	n/a
38	chr2:114463932-114463982	NB4	blood:	n/a
39	chr2:114474155-114474205	GM12891	blood:	n/a
40	chr2:114463932-114463982	HCM	heart:	n/a
41	chr2:114474155-114474205	ECC-1	luminal epithelium:	n/a
42	chr2:114463932-114463982	MCF10A-Er-Src	breast:	n/a
43	chr2:114430284-114430334	SK-N-MC	brain:	n/a
44	chr2:114430284-114430334	HRCEpiC	kidney:	n/a
45	chr2:114474155-114474205	HIPEpiC	eye:	n/a
46	chr2:114430284-114430334	BJ	skin:	n/a
47	chr2:114430284-114430334	HCPEpiC	choroid plexus:	n/a
48	chr2:114430284-114430334	HCF	heart:	n/a
49	chr2:114474155-114474205	AG09319	gingival:	n/a
50	chr2:114463932-114463982	GM12891	blood:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:114458048..114459604-chr2:114646095..114648927,2	MCF-7	breast:
2	chr2:114467029..114469645-chr2:114471402..114474213,2	K562	blood:
3	chr2:114492884..114495202-chr2:114498895..114501885,3	K562	blood:
4	chr2:114485598..114489125-chr2:114489448..114492903,4	MCF-7	breast:
5	chr2:114477814..114479515-chr2:114484887..114487513,2	K562	blood:
6	chr2:114476035..114479420-chr2:114481411..114484659,3	K562	blood:
7	chr2:114489926..114491643-chr2:114503029..114505332,2	K562	blood:
8	chr2:114467029..114469645-chr2:114471402..114474213,2	K562	blood:
9	chr2:114480781..114482978-chr2:114512798..114514341,2	K562	blood:
10	chr2:114490228..114492803-chr2:114497199..114499336,2	K562	blood:
11	chr2:114284812..114285348-chr2:114457736..114458446,2	MCF-7	breast:
12	chr2:114476035..114479420-chr2:114481411..114484659,3	K562	blood:
13	chr2:114450920..114453589-chr2:114487817..114489810,2	K562	blood:
14	chr2:114482332..114485532-chr2:114485677..114488517,3	K562	blood:
15	chr2:114476831..114479473-chr2:114488755..114491285,2	K562	blood:
16	chr2:114488891..114491412-chr2:114512139..114514622,2	K562	blood:
17	chr2:114446767..114449661-chr2:114451262..114453281,2	K562	blood:
18	chr2:114480320..114482087-chr2:114485684..114488123,2	K562	blood:
19	chr2:114480320..114482087-chr2:114485684..114488123,2	K562	blood:
20	chr2:114437381..114438920-chr2:114440621..114443610,2	K562	blood:
21	chr2:114361263..114362251-chr2:114457536..114458288,3	MCF-7	breast:
22	chr2:114477814..114479515-chr2:114484887..114487513,2	K562	blood:
23	chr2:114446767..114449661-chr2:114451262..114453281,2	K562	blood:
24	chr2:114361344..114362249-chr2:114457515..114458330,2	MCF-7	breast:
25	chr2:114489220..114494215-chr2:114513189..114517576,5	K562	blood:
26	chr2:114495189..114499777-chr2:114499993..114505139,6	K562	blood:
27	chr2:114491572..114494215-chr2:114513189..114515373,3	K562	blood:
28	chr2:114490228..114492106-chr2:114494949..114498699,3	K562	blood:
29	chr2:114482332..114485532-chr2:114485677..114488517,3	K562	blood:
30	chr2:114490228..114492106-chr2:114494949..114498699,3	K562	blood:
31	chr2:114470204..114472162-chr2:114473968..114476714,2	K562	blood:
32	chr2:114473851..114476041-chr2:114476528..114479274,2	K562	blood:
33	chr2:114450920..114453589-chr2:114487817..114489810,2	K562	blood:
34	chr2:114437420..114439660-chr2:114441343..114445054,3	K562	blood:
35	chr2:114482159..114484951-chr2:114491076..114492999,2	MCF-7	breast:
36	chr2:114359257..114359811-chr2:114457510..114458087,2	MCF-7	breast:
37	chr2:114470204..114472162-chr2:114473968..114476714,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RABL2A-3	chr2:114432688-114433000	expReg_chr2_8797_+
2	lnc-RABL2A-5	chr2:114450947-114454451	l_1932_chr2:114450946-114476823_testes
3	lnc-RABL2A-5	chr2:114457238-114457575	l_1932_chr2:114450946-114476823_testes
4	lnc-RABL2A-1	chr2:114430157-114430315	XLOC_001633
5	lnc-RABL2A-5	chr2:114481066-114481354	l_1932_chr2:114450946-114476823_testes
6	lnc-RABL2A-5	chr2:114481066-114481349	NONHSAT073828
7	lnc-RABL2A-5	chr2:114453956-114454175	NONHSAT073829
8	lnc-RABL2A-5	chr2:114475938-114476823	l_1932_chr2:114450946-114476823_testes
9	lnc-RABL2A-5	chr2:114456711-114456810	l_1932_chr2:114450946-114476823_testes
10	lnc-RABL2A-5	chr2:114456711-114457305	NONHSAT073829
11	lnc-RABL2A-1	chr2:114430446-114430768	XLOC_001633
12	lnc-RABL2A-5	chr2:114453616-114454175	NONHSAT073828
13	lnc-AC016745.1-2	chr2:114466280-114467816	XLOC_002282
14	lnc-AC016745.1-2	chr2:114464370-114465202	XLOC_002282

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4782-5p	chr2:114478915-114478936	MIMAT0019944
hsa-miR-4782-3p	chr2:114478875-114478896	MIMAT0019945

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	SLC35F5	hsa-miR-142-3p	chr2:114474760-114474753
2	SLC35F5	hsa-miR-142-3p	chr2:114472197-114472219
3	SLC35F5	hsa-miR-142-3p	chr2:114472585-114472607

Variant related genes	Relation type
ENSG00000227359	TF binding region
RNU6-744P	TF binding region
ENSG00000175509	TF binding region
MIR4782	TF binding region
SLC35F5	TF binding region
ENSG00000227359	CpG island
RNU6-744P	CpG island
ENSG00000175509	CpG island
MIR4782	CpG island
SLC35F5	CpG island
ENSG00000265429	chromatin interactions
ENSG00000270019	chromatin interactions
ENSG00000115091	chromatin interactions
ENSG00000115084	chromatin interactions
ENSG00000202427	chromatin interactions
TDG	miRNA target sites
OSBP	miRNA target sites
SNX4	miRNA target sites

Extended variants
information (count: 2322 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12711778	chr2:114430166-114430167	Bivalent Enhancer Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567864817	chr2:114430194-114430195	Bivalent Enhancer Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs559030462	chr2:114430212-114430213	Bivalent Enhancer Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs536405797	chr2:114430224-114430225	Bivalent Enhancer Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs556899998	chr2:114430226-114430227	Bivalent Enhancer Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs112895378	chr2:114430285-114430286	Bivalent Enhancer Enhancers Weak transcription	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs570410386	chr2:114430322-114430323	Bivalent Enhancer Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs139499700	chr2:114430331-114430332	Bivalent Enhancer Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs558620028	chr2:114430350-114430351	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182095095	chr2:114430351-114430352	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541139781	chr2:114430397-114430398	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs59544264	chr2:114430402-114430403	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199980191	chr2:114430403-114430404	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144746054	chr2:114430406-114430407	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528149338	chr2:114430461-114430462	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs554330904	chr2:114430496-114430497	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs574583493	chr2:114430514-114430515	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs149251947	chr2:114430553-114430554	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs144432523	chr2:114430560-114430561	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs532309656	chr2:114430590-114430591	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs545674124	chr2:114430606-114430607	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs565305571	chr2:114430763-114430764	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs527651566	chr2:114430904-114430905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551066187	chr2:114430920-114430921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547880217	chr2:114430974-114430975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567606711	chr2:114430975-114430976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114793763	chr2:114430988-114430989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550436442	chr2:114431043-114431044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570247620	chr2:114431085-114431086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539368933	chr2:114431087-114431088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139779951	chr2:114431102-114431103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11899799	chr2:114431220-114431221	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs534278795	chr2:114431235-114431236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75265906	chr2:114431262-114431263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113134726	chr2:114431304-114431305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574492398	chr2:114431324-114431325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144513904	chr2:114431361-114431362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556768111	chr2:114431364-114431365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576602665	chr2:114431378-114431379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185077031	chr2:114431379-114431380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559345148	chr2:114431382-114431383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189514412	chr2:114431408-114431409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112252491	chr2:114431428-114431429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs72944622	chr2:114431432-114431433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368235707	chr2:114431449-114431450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530250092	chr2:114431485-114431486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550275487	chr2:114431503-114431504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563894432	chr2:114431505-114431506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532715097	chr2:114431527-114431528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111945265	chr2:114431530-114431531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Neuroticism	17667963	CNVD

Chromatin state (count:1198 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114424800-114433400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr2:114429400-114430600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
3	chr2:114429400-114430600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr2:114429400-114430600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:114429400-114430800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr2:114429400-114434800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr2:114429600-114430200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:114429600-114430400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr2:114429600-114430600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
10	chr2:114429600-114430600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr2:114429600-114430600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr2:114429600-114431000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr2:114429800-114430200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr2:114429800-114430600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:114429800-114433000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:114430000-114430400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
17	chr2:114430000-114431200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:114430200-114430600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr2:114432000-114432200	Enhancers	K562	blood
20	chr2:114432200-114433200	Weak transcription	K562	blood
21	chr2:114432800-114433000	Enhancers	Left Ventricle	heart
22	chr2:114432800-114433000	Enhancers	Right Atrium	heart
23	chr2:114432800-114434600	Enhancers	Spleen	Spleen
24	chr2:114433000-114433600	Weak transcription	Left Ventricle	heart
25	chr2:114433000-114434000	Weak transcription	Right Atrium	heart
26	chr2:114433200-114433600	Bivalent Enhancer	HepG2	liver
27	chr2:114433200-114434000	Enhancers	K562	blood
28	chr2:114433200-114434600	Enhancers	Adipose Nuclei	Adipose
29	chr2:114433400-114434200	Enhancers	Fetal Muscle Leg	muscle
30	chr2:114433600-114433800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:114433600-114433800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:114433600-114433800	Flanking Bivalent TSS/Enh	HepG2	liver
33	chr2:114433600-114434600	Enhancers	Left Ventricle	heart
34	chr2:114433800-114434000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
35	chr2:114433800-114434000	Bivalent Enhancer	HepG2	liver
36	chr2:114434000-114435200	Weak transcription	K562	blood
37	chr2:114434000-114435600	Enhancers	Fetal Heart	heart
38	chr2:114434000-114435800	Enhancers	Right Atrium	heart
39	chr2:114434200-114435800	Enhancers	Right Ventricle	heart
40	chr2:114434800-114435000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:114435200-114435800	Enhancers	K562	blood
42	chr2:114435200-114436400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:114435800-114437000	Weak transcription	K562	blood
44	chr2:114436400-114437800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:114436800-114437200	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr2:114437000-114437600	Enhancers	K562	blood
47	chr2:114437000-114438000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr2:114437000-114438000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr2:114437600-114438400	Enhancers	Fetal Lung	lung
50	chr2:114437600-114443000	Weak transcription	K562	blood

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