Variant report

Variant	nsv564196
Chromosome Location	chr14:35110512-35152084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:729)
CpG islands
(count:122)
Chromatin interactive
region (count:37)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35120180-35120293	K562	blood:	n/a	n/a
2	ARID3A	chr14:35122450-35122628	K562	blood:	n/a	n/a
3	ARID3A	chr14:35135438-35135510	K562	blood:	n/a	n/a
4	ATF1	chr14:35122319-35122681	K562	blood:	n/a	n/a
5	ATF2	chr14:35151763-35152397	GM12878	blood:	n/a	n/a
6	ATF3	chr14:35120100-35120458	K562	blood:	n/a	n/a
7	ATF3	chr14:35120025-35120546	A549	lung:	n/a	n/a
8	BCL3	chr14:35119887-35120614	A549	lung:	n/a	n/a
9	BHLHE40	chr14:35122438-35122531	K562	blood:	n/a	n/a
10	BHLHE40	chr14:35110689-35110801	K562	blood:	n/a	n/a
11	BHLHE40	chr14:35150485-35150595	K562	blood:	n/a	n/a
12	CBX3	chr14:35120163-35120474	K562	blood:	n/a	n/a
13	CBX3	chr14:35119980-35120560	HCT-116	colon:	n/a	n/a
14	CBX3	chr14:35119917-35120633	HCT-116	colon:	n/a	n/a
15	CCNT2	chr14:35125305-35125505	K562	blood:	n/a	n/a
16	CCNT2	chr14:35147270-35147358	K562	blood:	n/a	n/a
17	CEBPB	chr14:35117932-35118134	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:35119868-35120784	A549	lung:	n/a	n/a
19	CEBPB	chr14:35132919-35133126	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr14:35117904-35118191	K562	blood:	n/a	n/a
21	CEBPB	chr14:35119938-35120515	IMR90	lung:	n/a	n/a
22	CEBPB	chr14:35117900-35118387	MCF-7	breast:	n/a	n/a
23	CEBPB	chr14:35117912-35118148	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr14:35119923-35120648	HCT-116	colon:	n/a	n/a
25	CEBPB	chr14:35137416-35137498	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr14:35141597-35141623	A549	lung:	n/a	n/a
27	CEBPB	chr14:35119953-35120653	A549	lung:	n/a	n/a
28	CEBPB	chr14:35117951-35118138	A549	lung:	n/a	n/a
29	CEBPB	chr14:35119913-35120724	HCT-116	colon:	n/a	n/a
30	CEBPB	chr14:35147128-35147480	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:35119880-35120558	A549	lung:	n/a	n/a
32	CEBPB	chr14:35119933-35120650	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr14:35120153-35120445	K562	blood:	n/a	n/a
34	CEBPB	chr14:35135194-35135704	A549	lung:	n/a	n/a
35	CEBPB	chr14:35117908-35118150	IMR90	lung:	n/a	n/a
36	CEBPB	chr14:35120045-35120582	MCF-7	breast:	n/a	n/a
37	CEBPB	chr14:35122373-35122856	K562	blood:	n/a	n/a
38	CEBPB	chr14:35122283-35122841	K562	blood:	n/a	n/a
39	CEBPB	chr14:35117883-35118178	K562	blood:	n/a	n/a
40	CEBPB	chr14:35132959-35133093	K562	blood:	n/a	n/a
41	CEBPB	chr14:35147090-35147488	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr14:35132965-35132992	A549	lung:	n/a	n/a
43	CEBPB	chr14:35117871-35118372	MCF-7	breast:	n/a	n/a
44	CEBPB	chr14:35147136-35147443	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr14:35147054-35147685	HCT-116	colon:	n/a	n/a
46	CEBPD	chr14:35122219-35122589	K562	blood:	n/a	n/a
47	CEBPD	chr14:35122197-35122711	K562	blood:	n/a	n/a
48	CHD1	chr14:35141641-35142218	IMR90	lung:	n/a	n/a
49	CHD1	chr14:35151152-35151161	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr14:35146988-35147639	IMR90	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35119021-35119071	H1-hESC	embryonic stem cell:	embryo
2	chr14:35119021-35119071	AG09309	skin:	n/a
3	chr14:35135441-35135491	NT2-D1	testis:	n/a
4	chr14:35119021-35119071	HEEpiC	esophagus:	n/a
5	chr14:35119021-35119071	Hela-S3	cervix:	n/a
6	chr14:35135441-35135491	HCF	heart:	n/a
7	chr14:35135441-35135491	AoSMC	blood vessel:	n/a
8	chr14:35135441-35135491	AG09319	gingival:	n/a
9	chr14:35135441-35135491	SAEC	small airway:	n/a
10	chr14:35119021-35119071	NH-A	brain:	n/a
11	chr14:35135441-35135491	U87	brain:	n/a
12	chr14:35135441-35135491	NB4	blood:	n/a
13	chr14:35135441-35135491	ECC-1	luminal epithelium:	n/a
14	chr14:35119021-35119071	PANC-1	pancreas:	n/a
15	chr14:35119021-35119071	NT2-D1	testis:	n/a
16	chr14:35119021-35119071	GM12891	blood:	n/a
17	chr14:35119021-35119071	HEK293	kidney:	embryo
18	chr14:35119021-35119071	ProgFib	skin:	n/a
19	chr14:35135441-35135491	GM12892	blood:	n/a
20	chr14:35119021-35119071	ovcar-3	ovarian:	n/a
21	chr14:35119021-35119071	K562	blood:	n/a
22	chr14:35119021-35119071	GM06990	blood:	n/a
23	chr14:35119021-35119071	NHDF-neo	bronchial:	n/a
24	chr14:35135441-35135491	RPTEC	kidney:	n/a
25	chr14:35135441-35135491	HIPEpiC	eye:	n/a
26	chr14:35119021-35119071	HepG2	liver:	n/a
27	chr14:35135441-35135491	Hela-S3	cervix:	n/a
28	chr14:35135441-35135491	Caco-2	colon:	n/a
29	chr14:35135441-35135491	AG10803	skin:	n/a
30	chr14:35135441-35135491	GM12891	blood:	n/a
31	chr14:35119021-35119071	RPTEC	kidney:	n/a
32	chr14:35135441-35135491	HRE	kidney:	n/a
33	chr14:35119021-35119071	GM12878	blood:	n/a
34	chr14:35135441-35135491	A549	lung:	n/a
35	chr14:35135441-35135491	MCF-7	breast:	n/a
36	chr14:35135441-35135491	SK-N-MC	brain:	n/a
37	chr14:35135441-35135491	PFSK-1	brain:	n/a
38	chr14:35135441-35135491	BJ	skin:	n/a
39	chr14:35135441-35135491	CMK	blood:	n/a
40	chr14:35119021-35119071	NHBE	bronchial:	n/a
41	chr14:35135441-35135491	HRCEpiC	kidney:	n/a
42	chr14:35135441-35135491	HCT-116	colon:	n/a
43	chr14:35119021-35119071	CMK	blood:	n/a
44	chr14:35119021-35119071	MCF10A-Er-Src	breast:	n/a
45	chr14:35119021-35119071	HCPEpiC	choroid plexus:	n/a
46	chr14:35119021-35119071	HIPEpiC	eye:	n/a
47	chr14:35135441-35135491	H1-hESC	embryonic stem cell:	embryo
48	chr14:35119021-35119071	MCF-7	breast:	n/a
49	chr14:35135441-35135491	HL-60	blood:	n/a
50	chr14:35135441-35135491	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr14:35141536..35142451-chr14:35451492..35451997,2	MCF-7	breast:
2	chr14:35141525..35142623-chr14:35191837..35192837,6	MCF-7	breast:
3	chr14:35016452..35018611-chr14:35133910..35135545,2	K562	blood:
4	chr14:35129877..35132741-chr14:35133755..35136058,2	MCF-7	breast:
5	chr14:35120647..35123453-chr14:35134189..35136107,2	MCF-7	breast:
6	chr14:35114973..35117245-chr14:35342771..35344725,2	K562	blood:
7	chr14:35150818..35153695-chr14:36294438..36295963,2	MCF-7	breast:
8	chr14:35017489..35019232-chr14:35116363..35118749,2	MCF-7	breast:
9	chr14:35114358..35116141-chr14:35116901..35120753,3	MCF-7	breast:
10	chr14:35149872..35152773-chr14:35155685..35158486,2	MCF-7	breast:
11	chr14:35023387..35025537-chr14:35125652..35127152,2	MCF-7	breast:
12	chr14:35022004..35024254-chr14:35128832..35131570,2	MCF-7	breast:
13	chr14:35118550..35121820-chr14:35125434..35129120,4	MCF-7	breast:
14	chr14:35129877..35132741-chr14:35133755..35136058,2	MCF-7	breast:
15	chr14:35135275..35136944-chr14:35151040..35152580,2	MCF-7	breast:
16	chr14:35150230..35152765-chr14:35168085..35171120,3	MCF-7	breast:
17	chr14:35107496..35110407-chr14:35118041..35119624,2	MCF-7	breast:
18	chr14:35139485..35141346-chr14:35514418..35517178,2	MCF-7	breast:
19	chr14:35141750..35142455-chr14:35235000..35235957,3	MCF-7	breast:
20	chr14:35145594..35147705-chr14:35179557..35182556,3	MCF-7	breast:
21	chr14:35130824..35132535-chr14:35133653..35135571,2	K562	blood:
22	chr14:35135275..35136944-chr14:35151040..35152580,2	MCF-7	breast:
23	chr14:35146210..35148621-chr14:35155232..35157199,2	MCF-7	breast:
24	chr14:35103930..35106002-chr14:35116842..35119484,2	MCF-7	breast:
25	chr14:35103956..35105473-chr14:35117782..35120594,2	K562	blood:
26	chr14:35118550..35121820-chr14:35125434..35129120,4	MCF-7	breast:
27	chr14:35114358..35116141-chr14:35116901..35120753,3	MCF-7	breast:
28	chr14:35141519..35142408-chr14:35192106..35192849,2	K562	blood:
29	chr14:35098107..35100970-chr14:35116404..35118114,2	MCF-7	breast:
30	chr14:35149549..35152323-chr14:35213699..35215325,2	MCF-7	breast:
31	chr14:35120647..35123453-chr14:35134189..35136107,2	MCF-7	breast:
32	chr14:35150005..35152867-chr14:35168615..35170921,2	MCF-7	breast:
33	chr14:35139329..35142128-chr14:35231474..35234080,2	MCF-7	breast:
34	chr14:35103973..35106509-chr14:35117782..35119447,2	K562	blood:
35	chr14:35130824..35132535-chr14:35133653..35135571,2	K562	blood:
36	chr14:35117978..35120935-chr14:35181287..35183685,2	MCF-7	breast:
37	chr14:35099347..35101109-chr14:35116790..35118482,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRP54-7	chr14:35112786-35113062	uc_372_+
2	lnc-SNX6-1	chr14:35112786-35113062	uc_372_-

No data

Variant related genes	Relation type
RNU6-1261P	TF binding region
RNU6-1261P	CpG island
ENSG00000100916	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000129515	chromatin interactions
ENSG00000165410	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000100883	chromatin interactions

Extended variants
information (count: 1625 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1625 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6571668	chr14:35110512-35110513	Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560629336	chr14:35110567-35110568	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188569892	chr14:35110649-35110650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs72675273	chr14:35110685-35110686	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs547896215	chr14:35110717-35110718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534260505	chr14:35110725-35110726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547155329	chr14:35110727-35110728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530562189	chr14:35110748-35110749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550260246	chr14:35110768-35110769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570167582	chr14:35110814-35110815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145611930	chr14:35110818-35110819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553099990	chr14:35110850-35110851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4424827	chr14:35110857-35110858	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs573722741	chr14:35110860-35110861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377274650	chr14:35110909-35110910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191804537	chr14:35110931-35110932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183051449	chr14:35110936-35110937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140837323	chr14:35110941-35110942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544762157	chr14:35110958-35110959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577734404	chr14:35110959-35110960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs56310586	chr14:35110983-35110984	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs578113705	chr14:35111078-35111079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540483927	chr14:35111117-35111118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs80237122	chr14:35111162-35111163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574289238	chr14:35111187-35111188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560148863	chr14:35111195-35111196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186998851	chr14:35111241-35111242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191525918	chr14:35111242-35111243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150211310	chr14:35111273-35111274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138780629	chr14:35111317-35111318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563856125	chr14:35111320-35111321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532836377	chr14:35111357-35111358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572362844	chr14:35111360-35111361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201510276	chr14:35111391-35111392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs28635844	chr14:35111424-35111425	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs566643650	chr14:35111448-35111449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199794975	chr14:35111449-35111450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542990699	chr14:35111458-35111459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549255846	chr14:35111467-35111468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569125275	chr14:35111485-35111486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183673167	chr14:35111488-35111489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147454761	chr14:35111490-35111491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200720482	chr14:35111492-35111493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs578157103	chr14:35111516-35111517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534274162	chr14:35111529-35111530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570321953	chr14:35111544-35111545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554114043	chr14:35111563-35111564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115439939	chr14:35111568-35111569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4982198	chr14:35111593-35111594	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs562854127	chr14:35111609-35111610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35108200-35111800	Enhancers	Placenta	Placenta
2	chr14:35109000-35117000	Weak transcription	Hela-S3	cervix
3	chr14:35110000-35110800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr14:35110200-35110600	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr14:35110200-35110800	Enhancers	K562	blood
6	chr14:35110200-35110800	Enhancers	Osteobl	bone
7	chr14:35110400-35110800	Enhancers	A549	lung
8	chr14:35110600-35111000	Enhancers	Fetal Muscle Trunk	muscle
9	chr14:35111600-35112800	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr14:35111600-35113200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr14:35111800-35117000	Weak transcription	Placenta	Placenta
12	chr14:35113200-35115400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr14:35115400-35116200	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr14:35115600-35119200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr14:35115800-35116400	Bivalent Enhancer	HepG2	liver
16	chr14:35116000-35116200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:35116000-35116400	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr14:35116200-35116400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr14:35117000-35117600	Bivalent Enhancer	HepG2	liver
20	chr14:35117000-35118000	Enhancers	Hela-S3	cervix
21	chr14:35117000-35121600	Enhancers	Placenta	Placenta
22	chr14:35117600-35117800	Flanking Bivalent TSS/Enh	HepG2	liver
23	chr14:35117600-35118200	Enhancers	A549	lung
24	chr14:35117600-35118200	Enhancers	K562	blood
25	chr14:35117600-35120000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr14:35117800-35118000	Bivalent/Poised TSS	HepG2	liver
27	chr14:35118000-35118200	Enhancers	Muscle Satellite Cultured Cells	--
28	chr14:35118000-35118200	Flanking Active TSS	Hela-S3	cervix
29	chr14:35118000-35118200	Enhancers	Osteobl	bone
30	chr14:35118000-35118400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr14:35118000-35118400	Flanking Bivalent TSS/Enh	HepG2	liver
32	chr14:35118000-35118400	Enhancers	NH-A	brain
33	chr14:35118000-35120600	Enhancers	NHDF-Ad	bronchial
34	chr14:35118000-35120800	Enhancers	NHLF	lung
35	chr14:35118200-35118400	Flanking Active TSS	A549	lung
36	chr14:35118200-35118400	Enhancers	Hela-S3	cervix
37	chr14:35118200-35118400	Flanking Active TSS	K562	blood
38	chr14:35118200-35118600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr14:35118200-35118600	Flanking Active TSS	Osteobl	bone
40	chr14:35118200-35118800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr14:35118200-35119800	Enhancers	HSMM	muscle
42	chr14:35118200-35120200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr14:35118200-35120400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr14:35118200-35120800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr14:35118200-35120800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr14:35118200-35120800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr14:35118200-35120800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr14:35118200-35120800	Enhancers	HUVEC	blood vessel
49	chr14:35118200-35120800	Enhancers	NHEK	skin
50	chr14:35118200-35122400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links