Variant report

Variant	nsv1042408
Chromosome Location	chr14:36693910-36810554
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1317)
CpG islands
(count:976)
Chromatin interactive
region (count:80)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1317 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:36769601-36770046	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:36784635-36784815	K562	blood:	n/a	n/a
3	ARID3A	chr14:36789353-36790203	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:36789827-36789998	K562	blood:	n/a	n/a
5	ARID3A	chr14:36733302-36734246	K562	blood:	n/a	n/a
6	ARID3A	chr14:36725743-36725753	K562	blood:	n/a	n/a
7	ARID3A	chr14:36730001-36730419	K562	blood:	n/a	n/a
8	ARID3A	chr14:36785526-36785702	K562	blood:	n/a	n/a
9	ARID3A	chr14:36786874-36787050	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:36723506-36723776	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:36754518-36754696	K562	blood:	n/a	n/a
12	ARID3A	chr14:36740785-36740980	K562	blood:	n/a	n/a
13	ARID3A	chr14:36710498-36710696	K562	blood:	n/a	n/a
14	ARID3A	chr14:36754429-36754629	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:36787931-36788470	HepG2	liver:	n/a	n/a
16	ATF1	chr14:36789684-36790159	K562	blood:	n/a	n/a
17	ATF1	chr14:36707940-36708121	K562	blood:	n/a	n/a
18	ATF1	chr14:36733817-36734157	K562	blood:	n/a	n/a
19	ATF2	chr14:36769592-36769971	GM12878	blood:	n/a	n/a
20	ATF2	chr14:36789693-36790117	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr14:36789725-36790108	GM12878	blood:	n/a	n/a
22	ATF2	chr14:36789612-36790132	GM12878	blood:	n/a	n/a
23	ATF2	chr14:36769598-36769998	GM12878	blood:	n/a	n/a
24	ATF3	chr14:36789765-36789985	GM12878	blood:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
25	ATF3	chr14:36789736-36790012	K562	blood:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
26	ATF3	chr14:36789354-36790107	HepG2	liver:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
27	ATF3	chr14:36789635-36790064	H1-hESC	embryonic stem cell:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
28	BACH1	chr14:36723518-36723757	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr14:36764628-36764681	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr14:36784705-36785059	GM12878	blood:	n/a	chr14:36784842-36784853
31	BATF	chr14:36769541-36769888	GM12878	blood:	n/a	chr14:36769803-36769813
32	BATF	chr14:36784726-36785054	GM12878	blood:	n/a	chr14:36784842-36784853
33	BCL11A	chr14:36769496-36769723	GM12878	blood:	n/a	n/a
34	BCL3	chr14:36789549-36790347	A549	lung:	n/a	n/a
35	BCL3	chr14:36784682-36784987	GM12878	blood:	n/a	chr14:36784811-36784820
36	BHLHE40	chr14:36784748-36785137	GM12878	blood:	n/a	n/a
37	BHLHE40	chr14:36754810-36755151	K562	blood:	n/a	n/a
38	BHLHE40	chr14:36733661-36734189	K562	blood:	n/a	n/a
39	BHLHE40	chr14:36789595-36790169	K562	blood:	n/a	n/a
40	BHLHE40	chr14:36707944-36708015	K562	blood:	n/a	n/a
41	BRCA1	chr14:36789668-36790245	HepG2	liver:	n/a	n/a
42	BRCA1	chr14:36789033-36790188	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr14:36788746-36788783	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr14:36750501-36750838	K562	blood:	n/a	n/a
45	CBX3	chr14:36733668-36734157	K562	blood:	n/a	n/a
46	CBX3	chr14:36789680-36790403	K562	blood:	n/a	n/a
47	CCNT2	chr14:36733614-36734251	K562	blood:	n/a	n/a
48	CCNT2	chr14:36789394-36790044	K562	blood:	n/a	chr14:36789846-36789855
49	CCNT2	chr14:36730207-36730528	K562	blood:	n/a	n/a
50	CEBPB	chr14:36722395-36722595	HepG2	liver:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:36741794-36741844	HL-60	blood:	n/a
2	chr14:36789810-36789860	HIPEpiC	eye:	n/a
3	chr14:36695421-36695471	NHDF-neo	bronchial:	n/a
4	chr14:36789886-36789936	HRPEpiC	eye:	n/a
5	chr14:36741794-36741844	AG10803	skin:	n/a
6	chr14:36698832-36698882	HIPEpiC	eye:	n/a
7	chr14:36743725-36743775	HepG2	liver:	n/a
8	chr14:36711182-36711232	A549	lung:	n/a
9	chr14:36790242-36790292	HPAEpiC	pulmonary alveolar:	n/a
10	chr14:36741645-36741695	U87	brain:	n/a
11	chr14:36790242-36790292	HRPEpiC	eye:	n/a
12	chr14:36789985-36790035	PFSK-1	brain:	n/a
13	chr14:36789985-36790035	NT2-D1	testis:	n/a
14	chr14:36789691-36789741	GM06990	blood:	n/a
15	chr14:36708508-36708558	SK-N-SH	brain:	n/a
16	chr14:36789886-36789936	GM12892	blood:	n/a
17	chr14:36711182-36711232	NHBE	bronchial:	n/a
18	chr14:36789488-36789538	MCF-7	breast:	n/a
19	chr14:36765887-36765937	NH-A	brain:	n/a
20	chr14:36741645-36741695	ProgFib	skin:	n/a
21	chr14:36708508-36708558	BE2_C	brain:	n/a
22	chr14:36711182-36711232	LNCaP	prostate:	n/a
23	chr14:36789691-36789741	Caco-2	colon:	n/a
24	chr14:36790242-36790292	A549	lung:	n/a
25	chr14:36743725-36743775	HRCEpiC	kidney:	n/a
26	chr14:36698832-36698882	AG10803	skin:	n/a
27	chr14:36765887-36765937	HIPEpiC	eye:	n/a
28	chr14:36789488-36789538	A549	lung:	n/a
29	chr14:36741794-36741844	PrEC	prostate:	n/a
30	chr14:36789810-36789860	IMR90	lung:	fetal
31	chr14:36741794-36741844	NHBE	bronchial:	n/a
32	chr14:36789488-36789538	BE2_C	brain:	n/a
33	chr14:36789810-36789860	AG09309	skin:	n/a
34	chr14:36743725-36743775	IMR90	lung:	fetal
35	chr14:36741794-36741844	GM12892	blood:	n/a
36	chr14:36765887-36765937	Hela-S3	cervix:	n/a
37	chr14:36789810-36789860	RPTEC	kidney:	n/a
38	chr14:36743725-36743775	HAEpiC	amniotic membrane:	n/a
39	chr14:36711182-36711232	HRPEpiC	eye:	n/a
40	chr14:36789985-36790035	Caco-2	colon:	n/a
41	chr14:36789488-36789538	GM19239	blood:	n/a
42	chr14:36743725-36743775	RPTEC	kidney:	n/a
43	chr14:36783435-36783485	HAEpiC	amniotic membrane:	n/a
44	chr14:36789488-36789538	U87	brain:	n/a
45	chr14:36708508-36708558	ECC-1	luminal epithelium:	n/a
46	chr14:36743725-36743775	HUVEC	blood vessel:	n/a
47	chr14:36789691-36789741	HMEC	breast:	n/a
48	chr14:36737696-36737746	HepG2	liver:	n/a
49	chr14:36789985-36790035	GM19239	blood:	n/a
50	chr14:36789691-36789741	SK-N-SH	brain:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:36745048..36746882-chr14:36747424..36749342,2	K562	blood:
2	chr14:36726358..36728728-chr14:36730369..36733275,2	MCF-7	breast:
3	chr14:36763341..36766160-chr14:36772206..36774961,2	K562	blood:
4	chr14:36733892..36735443-chr14:36737409..36739659,2	K562	blood:
5	chr14:36692567..36694676-chr14:36694678..36697500,2	MCF-7	breast:
6	chr14:36774640..36776851-chr14:36779144..36781211,2	K562	blood:
7	chr14:36797776..36799754-chr14:36805074..36807804,2	MCF-7	breast:
8	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
9	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:
10	chr14:36774640..36777657-chr14:36778032..36780826,3	K562	blood:
11	chr14:36789374..36789875-chr8:119123638..119124514,2	Hela-S3	cervix:
12	chr14:36778847..36780826-chr14:36784208..36786054,2	MCF-7	breast:
13	chr14:36538483..36541249-chr14:36788541..36791272,2	MCF-7	breast:
14	chr1:53308102..53308983-chr14:36776394..36777212,2	MCF-7	breast:
15	chr14:36760298..36763164-chr14:36770896..36773643,2	K562	blood:
16	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:
17	chr14:36750490..36753269-chr14:36756385..36758922,2	K562	blood:
18	chr14:36745048..36746882-chr14:36747424..36749342,2	K562	blood:
19	chr14:36784989..36787450-chr14:36787865..36790918,4	K562	blood:
20	chr14:36747888..36750635-chr14:36759343..36761098,2	K562	blood:
21	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
22	chr14:36757907..36759500-chr14:36766689..36768870,2	MCF-7	breast:
23	chr10:69141438..69142223-chr14:36735859..36736731,2	MCF-7	breast:
24	chr14:36539398..36539927-chr14:36782854..36783534,2	MCF-7	breast:
25	chr14:36710168..36711061-chr14:36843146..36843702,2	MCF-7	breast:
26	chr14:36752607..36756130-chr14:36756602..36759411,3	K562	blood:
27	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:
28	chr14:36747753..36750130-chr14:36837234..36840040,2	K562	blood:
29	chr14:36781444..36784031-chr14:36790836..36792756,2	K562	blood:
30	chr14:36763341..36766160-chr14:36772206..36774961,2	K562	blood:
31	chr14:36777999..36779910-chr14:36780693..36782263,2	K562	blood:
32	chr14:36744330..36746505-chr14:36753051..36754941,2	MCF-7	breast:
33	chr14:36726599..36728699-chr14:36730093..36731782,2	K562	blood:
34	chr14:36772767..36774449-chr14:36777469..36780447,2	K562	blood:
35	chr14:36739666..36742566-chr14:36744671..36747415,2	K562	blood:
36	chr14:36788593..36791761-chr14:36792192..36795536,3	K562	blood:
37	chr14:36797776..36799754-chr14:36805074..36807804,2	MCF-7	breast:
38	chr14:36733892..36736595-chr14:36737409..36740158,4	K562	blood:
39	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
40	chr14:36733094..36734657-chr14:36742759..36745467,2	K562	blood:
41	chr14:36723640..36727122-chr14:36730351..36734194,3	MCF-7	breast:
42	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
43	chr14:36757907..36759500-chr14:36766689..36768870,2	MCF-7	breast:
44	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:
45	chr14:36759414..36761344-chr14:36764422..36766950,2	MCF-7	breast:
46	chr14:36723640..36727122-chr14:36730351..36734194,3	MCF-7	breast:
47	chr14:36682051..36684620-chr14:36711169..36712893,2	K562	blood:
48	chr14:36733094..36734657-chr14:36742759..36745467,2	K562	blood:
49	chr14:36739666..36742566-chr14:36744671..36747415,2	K562	blood:
50	chr14:36747888..36750635-chr14:36759343..36761098,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SFTA3-2	chr14:36785664-36785887	uc_374_-
2	lnc-MBIP-1	chr14:36741625-36742658	XLOC_010997
3	lnc-MBIP-1	chr14:36738278-36738517	XLOC_010997
4	lnc-BRMS1L-4	chr14:36758889-36759236	XLOC_010799
5	lnc-MBIP-4	chr14:36700761-36700980	NONHSAT036424
6	lnc-PAX9-10	chr14:36785664-36785887	uc_374_+
7	lnc-BRMS1L-4	chr14:36747208-36747276	XLOC_010799
8	lnc-BRMS1L-3	chr14:36704530-36704814	ENSG00000258844
9	lnc-BRMS1L-4	chr14:36741574-36742599	XLOC_010799
10	lnc-BRMS1L-3	chr14:36704526-36704816	XLOC_010798

No data

Variant related genes	Relation type
RN7SKP21	TF binding region
MBIP	TF binding region
RN7SKP21	CpG island
MBIP	CpG island
ENSG00000203995	chromatin interactions
ENSG00000258844	chromatin interactions
ENSG00000257585	chromatin interactions
ENSG00000151332	chromatin interactions
ENSG00000182197	chromatin interactions
SNAI2	miRNA target sites

Extended variants
information (count: 3573 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3573 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577589278	chr14:36693932-36693933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149938732	chr14:36693936-36693937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560275860	chr14:36693956-36693957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572801003	chr14:36693980-36693981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1755778	chr14:36693991-36693992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs559736955	chr14:36693993-36693994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548860093	chr14:36694035-36694036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184786350	chr14:36694036-36694037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115625122	chr14:36694051-36694052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114364225	chr14:36694087-36694088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530227347	chr14:36694156-36694157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533864125	chr14:36694181-36694182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1766141	chr14:36694219-36694220	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs188224432	chr14:36694235-36694236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560775531	chr14:36694276-36694277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369530627	chr14:36694299-36694300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556851028	chr14:36694313-36694314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576516261	chr14:36694326-36694327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545390057	chr14:36694327-36694328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563605507	chr14:36694480-36694481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146478907	chr14:36694506-36694507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141307587	chr14:36694552-36694553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180790337	chr14:36694553-36694554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529036516	chr14:36694562-36694563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532689186	chr14:36694564-36694565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562408927	chr14:36694571-36694572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541905791	chr14:36694594-36694595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115674679	chr14:36694603-36694604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79857012	chr14:36694616-36694617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1755779	chr14:36694638-36694639	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs547467011	chr14:36694681-36694682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567768145	chr14:36694686-36694687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536815333	chr14:36694701-36694702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536130086	chr14:36694712-36694713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556914426	chr14:36694716-36694717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368861176	chr14:36694782-36694783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552242647	chr14:36694815-36694816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs56357420	chr14:36694822-36694823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs66606098	chr14:36694823-36694824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372063108	chr14:36694828-36694829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74772804	chr14:36694847-36694848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370923848	chr14:36694863-36694864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376396145	chr14:36694885-36694886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552478603	chr14:36694921-36694922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528621700	chr14:36694989-36694990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199703917	chr14:36695072-36695073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534808814	chr14:36695079-36695080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528287674	chr14:36695090-36695091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555006551	chr14:36695107-36695108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573768584	chr14:36695110-36695111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:1907 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:36687600-36695600	Weak transcription	NHEK	skin
2	chr14:36690800-36699000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:36692600-36695000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr14:36692600-36697400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr14:36692600-36697800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr14:36692600-36698600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr14:36692600-36698600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr14:36692600-36704000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr14:36692800-36698600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr14:36693000-36694400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr14:36693000-36696800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr14:36693200-36695400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr14:36695000-36697600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr14:36695400-36695800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr14:36695600-36695800	Enhancers	HMEC	breast
16	chr14:36695600-36696200	Enhancers	NHEK	skin
17	chr14:36695800-36697200	Weak transcription	HMEC	breast
18	chr14:36696200-36696800	Weak transcription	NHEK	skin
19	chr14:36696400-36697600	Enhancers	Hela-S3	cervix
20	chr14:36696400-36698000	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr14:36696600-36697800	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr14:36696800-36697400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr14:36696800-36697800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr14:36696800-36697800	Enhancers	Fetal Intestine Large	intestine
25	chr14:36696800-36698000	Enhancers	NHEK	skin
26	chr14:36696800-36698200	Enhancers	HUVEC	blood vessel
27	chr14:36697200-36697800	Enhancers	HMEC	breast
28	chr14:36697200-36698200	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr14:36697200-36698800	Enhancers	H9 Cell Line	embryonic stem cell
30	chr14:36697400-36698000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr14:36697400-36698600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr14:36697800-36699400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr14:36698000-36698400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr14:36698400-36699000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr14:36698400-36699000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr14:36698600-36699000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr14:36698600-36699200	Enhancers	H1 Cell Line	embryonic stem cell
38	chr14:36698600-36699200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr14:36698600-36699200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr14:36698800-36699000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr14:36698800-36711800	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr14:36699000-36699400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr14:36699000-36711800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr14:36699200-36699400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr14:36699400-36711800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr14:36702400-36702800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:36702800-36711800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr14:36704000-36704400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr14:36706600-36707200	Enhancers	Liver	Liver
50	chr14:36706600-36707200	Bivalent Enhancer	HepG2	liver

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