Variant report

Variant	esv1802718
Chromosome Location	chr14:35400075-35429777
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	CEBPB	chr14:35404663-35404976	HepG2	liver:	n/a	chr14:35404786-35404797
2	CEBPB	chr14:35424166-35424264	HepG2	liver:	n/a	n/a
3	CEBPB	chr14:35420541-35420728	HepG2	liver:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
4	CEBPB	chr14:35420493-35420854	IMR90	lung:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
5	CEBPB	chr14:35417192-35417509	HepG2	liver:	n/a	chr14:35417352-35417365 chr14:35417353-35417364
6	CEBPB	chr14:35420425-35420947	MCF-7	breast:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
7	CEBPB	chr14:35420358-35420886	MCF-7	breast:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682 chr14:35420422-35420430
8	CEBPB	chr14:35420557-35420750	Hela-S3	cervix:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
9	CEBPB	chr14:35420615-35420711	K562	blood:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
10	CTCF	chr14:35411360-35411510	MCF-7	breast:	n/a	n/a
11	CTCF	chr14:35406828-35406971	GM12878	blood:	n/a	n/a
12	CTCF	chr14:35411289-35411384	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr14:35411240-35411390	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr14:35411220-35411370	MCF-7	breast:	n/a	n/a
15	E2F4	chr14:35404253-35404288	MCF10A-Er-Src	breast:	n/a	n/a
16	FAM48A	chr14:35428930-35429105	GM12878	blood:	n/a	n/a
17	FOSL2	chr14:35416440-35416810	HepG2	liver:	n/a	n/a
18	FOSL2	chr14:35417523-35418268	HepG2	liver:	n/a	n/a
19	GATA1	chr14:35426247-35426586	PBDE	blood:	n/a	n/a
20	GATA3	chr14:35420359-35420956	MCF-7	breast:	n/a	n/a
21	JUN	chr14:35411161-35411371	HepG2	liver:	n/a	chr14:35411230-35411243
22	MAFF	chr14:35426119-35426455	HepG2	liver:	n/a	chr14:35426287-35426305
23	MAFF	chr14:35405357-35405778	HepG2	liver:	n/a	chr14:35405469-35405487
24	MAFF	chr14:35415925-35416280	HepG2	liver:	n/a	chr14:35416105-35416123
25	MAFF	chr14:35399801-35400095	HepG2	liver:	n/a	chr14:35399928-35399946
26	MAFF	chr14:35415959-35416263	K562	blood:	n/a	chr14:35416105-35416123
27	MAFF	chr14:35424020-35424214	HepG2	liver:	n/a	n/a
28	MAFK	chr14:35415972-35416202	K562	blood:	n/a	chr14:35416111-35416122 chr14:35416109-35416123 chr14:35416106-35416121 chr14:35416110-35416121 chr14:35416106-35416122 chr14:35416111-35416122
29	MAFK	chr14:35415925-35416284	HepG2	liver:	n/a	chr14:35416111-35416122 chr14:35416109-35416123 chr14:35416106-35416121 chr14:35416110-35416121 chr14:35416106-35416122 chr14:35416111-35416122
30	MAFK	chr14:35399782-35400095	HepG2	liver:	n/a	chr14:35399931-35399942 chr14:35399930-35399945 chr14:35399929-35399943 chr14:35399931-35399942 chr14:35399930-35399946 chr14:35399930-35399941 chr14:35399850-35399865 chr14:35399930-35399941
31	MAFK	chr14:35404640-35404959	HepG2	liver:	n/a	n/a
32	MAFK	chr14:35426224-35426458	HepG2	liver:	n/a	chr14:35426289-35426304
33	MAFK	chr14:35415935-35416277	IMR90	lung:	n/a	chr14:35416111-35416122 chr14:35416109-35416123 chr14:35416106-35416121 chr14:35416110-35416121 chr14:35416106-35416122 chr14:35416111-35416122
34	MAFK	chr14:35426240-35426327	IMR90	lung:	n/a	chr14:35426289-35426304
35	MAFK	chr14:35404655-35404927	HepG2	liver:	n/a	n/a
36	MAFK	chr14:35416060-35416195	H1-hESC	embryonic stem cell:	n/a	chr14:35416111-35416122 chr14:35416109-35416123 chr14:35416106-35416121 chr14:35416110-35416121 chr14:35416106-35416122 chr14:35416111-35416122
37	MAFK	chr14:35399796-35400099	HepG2	liver:	n/a	chr14:35399931-35399942 chr14:35399930-35399945 chr14:35399929-35399943 chr14:35399931-35399942 chr14:35399930-35399946 chr14:35399930-35399941 chr14:35399850-35399865 chr14:35399930-35399941
38	MAFK	chr14:35415925-35416296	HepG2	liver:	n/a	chr14:35416111-35416122 chr14:35416109-35416123 chr14:35416106-35416121 chr14:35416110-35416121 chr14:35416106-35416122 chr14:35416111-35416122
39	MAFK	chr14:35405356-35405767	HepG2	liver:	n/a	chr14:35405707-35405716 chr14:35405706-35405716
40	MAFK	chr14:35405357-35405654	IMR90	lung:	n/a	n/a
41	MAFK	chr14:35405320-35405820	HepG2	liver:	n/a	chr14:35405707-35405716 chr14:35405706-35405716
42	MAFK	chr14:35423966-35424282	HepG2	liver:	n/a	chr14:35424109-35424120 chr14:35424109-35424120
43	MAFK	chr14:35423964-35424249	HepG2	liver:	n/a	chr14:35424109-35424120 chr14:35424109-35424120
44	MAFK	chr14:35415971-35416226	Hela-S3	cervix:	n/a	chr14:35416111-35416122 chr14:35416109-35416123 chr14:35416106-35416121 chr14:35416110-35416121 chr14:35416106-35416122 chr14:35416111-35416122
45	MAFK	chr14:35426122-35426460	HepG2	liver:	n/a	chr14:35426289-35426304
46	MAX	chr14:35427205-35427239	NB4	blood:	n/a	n/a
47	MYC	chr14:35414685-35414798	MCF10A-Er-Src	breast:	n/a	n/a
48	MYC	chr14:35403825-35403924	MCF-7	breast:	n/a	n/a
49	NFIC	chr14:35399997-35400570	GM12878	blood:	n/a	n/a
50	NR2F2	chr14:35420019-35420958	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35409083-35409133	PrEC	prostate:	n/a
2	chr14:35408569-35408619	PFSK-1	brain:	n/a
3	chr14:35409083-35409133	HepG2	liver:	n/a
4	chr14:35409083-35409133	MCF10A-Er-Src	breast:	n/a
5	chr14:35408689-35408739	AoSMC	blood vessel:	n/a
6	chr14:35408569-35408619	NHBE	bronchial:	n/a
7	chr14:35409641-35409691	ProgFib	skin:	n/a
8	chr14:35409641-35409691	HUVEC	blood vessel:	n/a
9	chr14:35408689-35408739	NHDF-neo	bronchial:	n/a
10	chr14:35409641-35409691	Caco-2	colon:	n/a
11	chr14:35409641-35409691	NT2-D1	testis:	n/a
12	chr14:35408689-35408739	GM12891	blood:	n/a
13	chr14:35408689-35408739	CMK	blood:	n/a
14	chr14:35409083-35409133	BE2_C	brain:	n/a
15	chr14:35409641-35409691	GM19239	blood:	n/a
16	chr14:35408689-35408739	SK-N-MC	brain:	n/a
17	chr14:35409641-35409691	SK-N-SH_RA	brain:	n/a
18	chr14:35409641-35409691	RPTEC	kidney:	n/a
19	chr14:35408689-35408739	AG09309	skin:	n/a
20	chr14:35408689-35408739	SK-N-SH_RA	brain:	n/a
21	chr14:35408569-35408619	HCT-116	colon:	n/a
22	chr14:35408569-35408619	SK-N-MC	brain:	n/a
23	chr14:35409641-35409691	HCT-116	colon:	n/a
24	chr14:35409641-35409691	AG04449	skin:	fetal
25	chr14:35409641-35409691	HMEC	breast:	n/a
26	chr14:35409083-35409133	GM12891	blood:	n/a
27	chr14:35408569-35408619	HPAEpiC	pulmonary alveolar:	n/a
28	chr14:35409083-35409133	T-47D	breast:	n/a
29	chr14:35408569-35408619	Jurkat	blood:	n/a
30	chr14:35409083-35409133	AoSMC	blood vessel:	n/a
31	chr14:35408569-35408619	NH-A	brain:	n/a
32	chr14:35408689-35408739	ECC-1	luminal epithelium:	n/a
33	chr14:35408689-35408739	PFSK-1	brain:	n/a
34	chr14:35408569-35408619	AG09309	skin:	n/a
35	chr14:35409641-35409691	HIPEpiC	eye:	n/a
36	chr14:35409083-35409133	LNCaP	prostate:	n/a
37	chr14:35408569-35408619	AoSMC	blood vessel:	n/a
38	chr14:35408689-35408739	HAEpiC	amniotic membrane:	n/a
39	chr14:35408689-35408739	AG09319	gingival:	n/a
40	chr14:35408569-35408619	BJ	skin:	n/a
41	chr14:35409641-35409691	K562	blood:	n/a
42	chr14:35409083-35409133	HCPEpiC	choroid plexus:	n/a
43	chr14:35408569-35408619	ProgFib	skin:	n/a
44	chr14:35408689-35408739	Jurkat	blood:	n/a
45	chr14:35408569-35408619	K562	blood:	n/a
46	chr14:35409641-35409691	H1-hESC	embryonic stem cell:	embryo
47	chr14:35408569-35408619	GM12878	blood:	n/a
48	chr14:35408689-35408739	SK-N-SH	brain:	n/a
49	chr14:35409641-35409691	SK-N-MC	brain:	n/a
50	chr14:35409641-35409691	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:35393659..35395682-chr14:35403132..35405921,2	K562	blood:
2	chr14:35342877..35345707-chr14:35420662..35422275,2	MCF-7	breast:
3	chr14:35342311..35345634-chr14:35398849..35401832,3	MCF-7	breast:
4	chr14:35424726..35426528-chr14:35427204..35429694,2	K562	blood:
5	chr14:35343121..35345679-chr14:35426875..35428541,2	K562	blood:
6	chr14:35405852..35407525-chr14:35456925..35458489,2	K562	blood:
7	chr14:35397975..35400662-chr14:35403521..35405781,3	K562	blood:
8	chr14:35397975..35400662-chr14:35403521..35405781,3	K562	blood:
9	chr14:35426260..35429015-chr14:35450690..35452638,2	K562	blood:
10	chr14:35424726..35426528-chr14:35427204..35429694,2	K562	blood:
11	chr14:35347443..35349212-chr14:35398653..35401635,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRP54-5	chr14:35409128-35409702	NR_002937

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

Extended variants
information (count: 1088 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1088 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1712349	chr14:35400075-35400076	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546521264	chr14:35400082-35400083	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs191616551	chr14:35400166-35400167	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs150150875	chr14:35400194-35400195	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs149009040	chr14:35400198-35400199	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs71204283	chr14:35400223-35400224	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs61100068	chr14:35400232-35400233	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs932473	chr14:35400282-35400283	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs529355001	chr14:35400306-35400307	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs5807802	chr14:35400312-35400313	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs567044959	chr14:35400325-35400326	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs531562530	chr14:35400348-35400349	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs112334659	chr14:35400363-35400364	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs535811530	chr14:35400372-35400373	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555750208	chr14:35400387-35400388	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs1517546	chr14:35400392-35400393	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs189067275	chr14:35400396-35400397	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs35892093	chr14:35400409-35400410	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs558467016	chr14:35400527-35400528	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs75745145	chr14:35400534-35400535	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs180816185	chr14:35400535-35400536	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs541142203	chr14:35400614-35400615	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs561336328	chr14:35400638-35400639	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs151082266	chr14:35400755-35400756	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs543796875	chr14:35400801-35400802	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535453176	chr14:35400866-35400867	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs141052384	chr14:35400909-35400910	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs551095395	chr14:35400920-35400921	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs568954685	chr14:35400921-35400922	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs150312647	chr14:35401050-35401051	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs34189886	chr14:35401087-35401088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs559675328	chr14:35401109-35401110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs146454399	chr14:35401124-35401125	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs111819968	chr14:35401139-35401140	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs566983912	chr14:35401152-35401153	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs187364338	chr14:35401158-35401159	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs551349368	chr14:35401200-35401201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs111624054	chr14:35401241-35401242	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs201264265	chr14:35401256-35401257	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs538544368	chr14:35401277-35401278	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs533518757	chr14:35401331-35401332	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs549797109	chr14:35401346-35401347	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144627191	chr14:35401388-35401389	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs572269095	chr14:35401414-35401415	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs534779218	chr14:35401415-35401416	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs554811156	chr14:35401416-35401417	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs574936922	chr14:35401421-35401422	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs9944134	chr14:35401492-35401493	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs56756157	chr14:35401716-35401717	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs369783372	chr14:35401717-35401718	Weak transcription Enhancers	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:466 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35381400-35412200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:35389600-35411400	Weak transcription	Aorta	Aorta
3	chr14:35390000-35412600	Weak transcription	Ovary	ovary
4	chr14:35390200-35400600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr14:35393000-35404400	Weak transcription	Left Ventricle	heart
6	chr14:35394600-35424000	Weak transcription	Fetal Lung	lung
7	chr14:35396000-35400400	Weak transcription	A549	lung
8	chr14:35396400-35400200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr14:35396400-35400400	Weak transcription	Osteobl	bone
10	chr14:35396400-35425200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr14:35396600-35424800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr14:35397200-35412800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr14:35397800-35420600	Weak transcription	Thymus	Thymus
14	chr14:35398000-35408200	Weak transcription	Liver	Liver
15	chr14:35398200-35400800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr14:35398400-35401000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr14:35398400-35401200	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr14:35398800-35410600	Weak transcription	Fetal Brain Male	brain
19	chr14:35399000-35412200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr14:35399200-35400800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
21	chr14:35399400-35400600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
22	chr14:35399400-35400800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr14:35399400-35402200	Weak transcription	HepG2	liver
24	chr14:35399400-35406800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr14:35399600-35400400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
26	chr14:35399600-35400600	Enhancers	Primary hematopoietic stem cells	blood
27	chr14:35399600-35401000	Enhancers	HUVEC	blood vessel
28	chr14:35399600-35412200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr14:35399800-35400200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
30	chr14:35399800-35400400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr14:35399800-35400400	Enhancers	GM12878-XiMat	blood
32	chr14:35399800-35400800	Enhancers	Primary B cells from peripheral blood	blood
33	chr14:35399800-35400800	Flanking Active TSS	Primary T cells from cord blood	blood
34	chr14:35399800-35400800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr14:35399800-35400800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr14:35399800-35400800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr14:35399800-35400800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
38	chr14:35399800-35400800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr14:35399800-35400800	Enhancers	Adipose Nuclei	Adipose
40	chr14:35399800-35400800	Enhancers	Duodenum Mucosa	Duodenum
41	chr14:35399800-35400800	Enhancers	Rectal Mucosa Donor 29	rectum
42	chr14:35399800-35400800	Enhancers	Small Intestine	intestine
43	chr14:35399800-35400800	Enhancers	Dnd41	blood
44	chr14:35399800-35400800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr14:35399800-35401400	Enhancers	Stomach Mucosa	stomach
46	chr14:35399800-35404400	Weak transcription	Fetal Intestine Small	intestine
47	chr14:35400000-35400800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr14:35400000-35400800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr14:35400200-35401000	Enhancers	Muscle Satellite Cultured Cells	--
50	chr14:35400200-35401400	Enhancers	Primary T cells fromperipheralblood	blood

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