Variant report

Variant	nsv901603
Chromosome Location	chr14:35371697-35435651
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:276)
CpG islands
(count:244)
Chromatin interactive
region (count:32)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:35382984-35383077	K562	blood:	n/a	n/a
2	CEBPB	chr14:35374364-35374623	HepG2	liver:	n/a	chr14:35374470-35374481
3	CEBPB	chr14:35420493-35420854	IMR90	lung:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
4	CEBPB	chr14:35417192-35417509	HepG2	liver:	n/a	chr14:35417352-35417365 chr14:35417353-35417364
5	CEBPB	chr14:35420557-35420750	Hela-S3	cervix:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
6	CEBPB	chr14:35382962-35383161	K562	blood:	n/a	n/a
7	CEBPB	chr14:35380437-35380803	IMR90	lung:	n/a	chr14:35380616-35380627
8	CEBPB	chr14:35380440-35380801	A549	lung:	n/a	chr14:35380616-35380627
9	CEBPB	chr14:35374417-35374597	A549	lung:	n/a	chr14:35374470-35374481
10	CEBPB	chr14:35380451-35380785	K562	blood:	n/a	chr14:35380616-35380627
11	CEBPB	chr14:35420541-35420728	HepG2	liver:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
12	CEBPB	chr14:35374339-35374549	IMR90	lung:	n/a	chr14:35374470-35374481
13	CEBPB	chr14:35378389-35378437	HepG2	liver:	n/a	chr14:35378420-35378431
14	CEBPB	chr14:35404663-35404976	HepG2	liver:	n/a	chr14:35404786-35404797
15	CEBPB	chr14:35380452-35380801	Hela-S3	cervix:	n/a	chr14:35380616-35380627
16	CEBPB	chr14:35420615-35420711	K562	blood:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
17	CEBPB	chr14:35420358-35420886	MCF-7	breast:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682 chr14:35420422-35420430
18	CEBPB	chr14:35380452-35380802	HepG2	liver:	n/a	chr14:35380616-35380627
19	CEBPB	chr14:35380540-35380740	H1-hESC	embryonic stem cell:	n/a	chr14:35380616-35380627
20	CEBPB	chr14:35424166-35424264	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:35420425-35420947	MCF-7	breast:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
22	CTCF	chr14:35381472-35381609	GM19239	blood:	n/a	n/a
23	CTCF	chr14:35381460-35381610	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr14:35381503-35381548	ProgFib	skin:	n/a	n/a
25	CTCF	chr14:35381470-35381627	MCF-7	breast:	n/a	n/a
26	CTCF	chr14:35381454-35381602	GM19238	blood:	n/a	n/a
27	CTCF	chr14:35411240-35411390	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr14:35381420-35381570	GM12874	blood:	n/a	n/a
29	CTCF	chr14:35381453-35381635	A549	lung:	n/a	n/a
30	CTCF	chr14:35381480-35381630	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr14:35411360-35411510	MCF-7	breast:	n/a	n/a
32	CTCF	chr14:35381440-35381590	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr14:35433530-35433573	GM20000	blood:	n/a	n/a
34	CTCF	chr14:35381480-35381630	GM12872	blood:	n/a	n/a
35	CTCF	chr14:35381500-35381650	GM12869	blood:	n/a	n/a
36	CTCF	chr14:35381360-35381510	HVMF	connective:	n/a	n/a
37	CTCF	chr14:35386406-35386516	GM10248	blood:	n/a	n/a
38	CTCF	chr14:35381420-35381570	HepG2	liver:	n/a	n/a
39	CTCF	chr14:35381420-35381570	HEK293	kidney:	n/a	n/a
40	CTCF	chr14:35381460-35381610	GM12864	blood:	n/a	n/a
41	CTCF	chr14:35381496-35381589	GM13976	blood:	n/a	n/a
42	CTCF	chr14:35381354-35381724	A549	lung:	n/a	n/a
43	CTCF	chr14:35381324-35381641	HepG2	liver:	n/a	n/a
44	CTCF	chr14:35381429-35381632	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:35381460-35381610	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr14:35381447-35381649	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:35381420-35381570	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr14:35381440-35381737	K562	blood:	n/a	n/a
49	CTCF	chr14:35381439-35381635	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:35381500-35381650	Hela-S3	cervix:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35409083-35409133	HPAEpiC	pulmonary alveolar:	n/a
2	chr14:35408689-35408739	HCT-116	colon:	n/a
3	chr14:35409641-35409691	NHBE	bronchial:	n/a
4	chr14:35408569-35408619	AG09309	skin:	n/a
5	chr14:35409083-35409133	MCF-7	breast:	n/a
6	chr14:35408689-35408739	AG09309	skin:	n/a
7	chr14:35409083-35409133	BE2_C	brain:	n/a
8	chr14:35408689-35408739	SK-N-MC	brain:	n/a
9	chr14:35408689-35408739	HCPEpiC	choroid plexus:	n/a
10	chr14:35408689-35408739	HEEpiC	esophagus:	n/a
11	chr14:35408689-35408739	HL-60	blood:	n/a
12	chr14:35409083-35409133	IMR90	lung:	fetal
13	chr14:35408689-35408739	GM12891	blood:	n/a
14	chr14:35408689-35408739	SAEC	small airway:	n/a
15	chr14:35408569-35408619	MCF-7	breast:	n/a
16	chr14:35408689-35408739	A549	lung:	n/a
17	chr14:35408569-35408619	U87	brain:	n/a
18	chr14:35409083-35409133	H1-hESC	embryonic stem cell:	embryo
19	chr14:35409641-35409691	SK-N-MC	brain:	n/a
20	chr14:35409083-35409133	Hepatocyte	liver:	n/a
21	chr14:35409083-35409133	ovcar-3	ovarian:	n/a
22	chr14:35409641-35409691	Jurkat	blood:	n/a
23	chr14:35408689-35408739	PrEC	prostate:	n/a
24	chr14:35408569-35408619	RPTEC	kidney:	n/a
25	chr14:35408569-35408619	BE2_C	brain:	n/a
26	chr14:35409083-35409133	Caco-2	colon:	n/a
27	chr14:35409641-35409691	Hepatocyte	liver:	n/a
28	chr14:35409641-35409691	AG04450	lung:	fetal
29	chr14:35409641-35409691	Hela-S3	cervix:	n/a
30	chr14:35409083-35409133	LNCaP	prostate:	n/a
31	chr14:35409641-35409691	T-47D	breast:	n/a
32	chr14:35409641-35409691	HEK293	kidney:	embryo
33	chr14:35408689-35408739	GM12892	blood:	n/a
34	chr14:35409641-35409691	BE2_C	brain:	n/a
35	chr14:35409641-35409691	PANC-1	pancreas:	n/a
36	chr14:35408689-35408739	SK-N-SH	brain:	n/a
37	chr14:35409641-35409691	NHDF-neo	bronchial:	n/a
38	chr14:35409083-35409133	HCT-116	colon:	n/a
39	chr14:35408569-35408619	MCF10A-Er-Src	breast:	n/a
40	chr14:35408689-35408739	HCM	heart:	n/a
41	chr14:35409641-35409691	MCF-7	breast:	n/a
42	chr14:35408569-35408619	Hela-S3	cervix:	n/a
43	chr14:35409083-35409133	HRE	kidney:	n/a
44	chr14:35409083-35409133	GM12891	blood:	n/a
45	chr14:35409641-35409691	GM12891	blood:	n/a
46	chr14:35409641-35409691	HEEpiC	esophagus:	n/a
47	chr14:35409083-35409133	AG09319	gingival:	n/a
48	chr14:35409641-35409691	HMEC	breast:	n/a
49	chr14:35409641-35409691	K562	blood:	n/a
50	chr14:35408689-35408739	H1-hESC	embryonic stem cell:	embryo

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:35393659..35395682-chr14:35403132..35405921,2	K562	blood:
2	chr14:35430162..35434482-chr14:35434976..35439153,5	K562	blood:
3	chr14:35376534..35379086-chr14:35381229..35383060,2	K562	blood:
4	chr14:35393659..35395682-chr14:35403132..35405921,2	K562	blood:
5	chr14:35376534..35379086-chr14:35381229..35383060,2	K562	blood:
6	chr14:35397975..35400662-chr14:35403521..35405781,3	K562	blood:
7	chr14:35347443..35349212-chr14:35398653..35401635,2	MCF-7	breast:
8	chr14:35397975..35400662-chr14:35403521..35405781,3	K562	blood:
9	chr14:35376044..35378197-chr14:35387149..35389854,2	MCF-7	breast:
10	chr14:35376044..35378197-chr14:35387149..35389854,2	MCF-7	breast:
11	chr14:35405852..35407525-chr14:35456925..35458489,2	K562	blood:
12	chr14:35347496..35349428-chr14:35395723..35397299,2	K562	blood:
13	chr14:35340774..35347210-chr14:35373911..35377911,7	K562	blood:
14	chr14:35343366..35345021-chr14:35390010..35392504,2	MCF-7	breast:
15	chr14:35342338..35344567-chr14:35370175..35372509,2	MCF-7	breast:
16	chr14:35344296..35346112-chr14:35380613..35383612,2	MCF-7	breast:
17	chr14:35342361..35345685-chr14:35383772..35387208,3	MCF-7	breast:
18	chr14:35342877..35345707-chr14:35420662..35422275,2	MCF-7	breast:
19	chr14:35344479..35347170-chr14:35376800..35378472,2	MCF-7	breast:
20	chr14:35342311..35345634-chr14:35398849..35401832,3	MCF-7	breast:
21	chr14:35342775..35345035-chr14:35387354..35389341,2	K562	blood:
22	chr14:35343121..35345679-chr14:35426875..35428541,2	K562	blood:
23	chr14:35430162..35434482-chr14:35434976..35439153,5	K562	blood:
24	chr14:35343070..35344827-chr14:35397804..35399646,2	MCF-7	breast:
25	chr14:35342308..35344409-chr14:35373836..35375775,2	K562	blood:
26	chr14:35370120..35372275-chr14:35372286..35374430,3	K562	blood:
27	chr14:35426260..35429015-chr14:35450690..35452638,2	K562	blood:
28	chr14:35381216..35383800-chr14:35450117..35451932,2	MCF-7	breast:
29	chr14:35342112..35344260-chr14:35376381..35377958,2	MCF-7	breast:
30	chr14:35424726..35426528-chr14:35427204..35429694,2	K562	blood:
31	chr14:35370120..35372275-chr14:35372286..35374430,3	K562	blood:
32	chr14:35424726..35426528-chr14:35427204..35429694,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRP54-3	chr14:35433120-35433246	NONHSAT036352
2	lnc-SRP54-5	chr14:35409128-35409702	NR_002937

No data

Variant related genes	Relation type
IGBP1P1	TF binding region
ENSG00000199980	TF binding region
ENSG00000258493	TF binding region
IGBP1P1	CpG island
ENSG00000199980	CpG island
ENSG00000258493	CpG island
ENSG00000100883	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000258738	chromatin interactions

Extended variants
information (count: 2335 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2335 , 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	rs6571690	chr14:35371697-35371698	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553669099	chr14:35371767-35371768	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs544405650	chr14:35371808-35371809	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs8005844	chr14:35371855-35371856	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs17508632	chr14:35371890-35371891	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs556240528	chr14:35371931-35371932	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs199569120	chr14:35372006-35372007	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs575988569	chr14:35372014-35372015	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557817542	chr14:35372026-35372027	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs372282546	chr14:35372028-35372029	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs545018639	chr14:35372144-35372145	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs572754018	chr14:35372145-35372146	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs138377391	chr14:35372172-35372173	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs527957879	chr14:35372210-35372211	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs143927565	chr14:35372235-35372236	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs192905790	chr14:35372263-35372264	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs549703478	chr14:35372275-35372276	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs530367753	chr14:35372276-35372277	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs549054246	chr14:35372284-35372285	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs183630783	chr14:35372336-35372337	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs144298630	chr14:35372338-35372339	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551371470	chr14:35372364-35372365	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs573425190	chr14:35372394-35372395	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs371982368	chr14:35372397-35372398	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs148708647	chr14:35372450-35372451	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187983752	chr14:35372465-35372466	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs141421440	chr14:35372467-35372468	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs112026560	chr14:35372508-35372509	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs74988910	chr14:35373865-35373866	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs370446167	chr14:35373866-35373867	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs61231449	chr14:35373886-35373887	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs534832529	chr14:35373934-35373935	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs77913567	chr14:35373941-35373942	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs112951154	chr14:35373948-35373949	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs79218441	chr14:35373955-35373956	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs17102833	chr14:35373957-35373958	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs577472907	chr14:35373976-35373977	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs546393657	chr14:35373990-35373991	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs558342840	chr14:35374016-35374017	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs180788559	chr14:35374032-35374033	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs540804904	chr14:35374033-35374034	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs34610240	chr14:35374058-35374059	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs149020691	chr14:35374202-35374203	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs529689865	chr14:35374294-35374295	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs543268895	chr14:35374338-35374339	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs142085893	chr14:35374344-35374345	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs563253951	chr14:35374369-35374370	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs61988055	chr14:35374484-35374485	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs151218884	chr14:35374528-35374529	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs565767550	chr14:35374529-35374530	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21858162	CNVD

Chromatin state (count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35374400-35389400	Weak transcription	Ovary	ovary
2	chr14:35380600-35381200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:35380600-35381400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr14:35380600-35381400	Enhancers	A549	lung
5	chr14:35380600-35381600	Enhancers	Osteobl	bone
6	chr14:35380600-35388400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr14:35380800-35381400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr14:35380800-35381400	Enhancers	HUVEC	blood vessel
9	chr14:35381000-35381400	Enhancers	Fetal Heart	heart
10	chr14:35381000-35381400	Enhancers	HSMMtube	muscle
11	chr14:35381000-35381400	Enhancers	NH-A	brain
12	chr14:35381000-35381600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr14:35381000-35398600	Weak transcription	Primary T cells from cord blood	blood
14	chr14:35381200-35381400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr14:35381200-35381600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr14:35381200-35381600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr14:35381200-35381600	Enhancers	NHLF	lung
18	chr14:35381200-35382800	Enhancers	K562	blood
19	chr14:35381400-35382000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr14:35381400-35382000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr14:35381400-35382000	Enhancers	Primary B cells from cord blood	blood
22	chr14:35381400-35382400	Weak transcription	A549	lung
23	chr14:35381400-35412200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr14:35381600-35382200	Weak transcription	Osteobl	bone
25	chr14:35381600-35382800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr14:35381600-35389800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr14:35381800-35382400	Enhancers	Primary B cells from peripheral blood	blood
28	chr14:35381800-35382400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:35381800-35382600	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr14:35382000-35387200	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr14:35382000-35387400	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr14:35382200-35382400	Enhancers	Osteobl	bone
33	chr14:35382400-35382600	Enhancers	GM12878-XiMat	blood
34	chr14:35382400-35382800	Enhancers	A549	lung
35	chr14:35382600-35387400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr14:35384600-35398200	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr14:35384800-35398600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr14:35387200-35388200	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr14:35387400-35387800	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr14:35387400-35387800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr14:35387400-35388200	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr14:35387400-35397000	Weak transcription	Fetal Intestine Small	intestine
43	chr14:35388200-35390000	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr14:35388200-35390000	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr14:35389400-35390000	Strong transcription	Ovary	ovary
46	chr14:35389400-35390200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr14:35389600-35390200	Enhancers	A549	lung
48	chr14:35389600-35390200	Enhancers	NH-A	brain
49	chr14:35389600-35411400	Weak transcription	Aorta	Aorta
50	chr14:35389800-35390200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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