Variant report

Variant	esv2761847
Chromosome Location	chr14:81392124-81453137
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1219)
CpG islands
(count:1648)
Chromatin interactive
region (count:42)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1219 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:81408108-81408383	K562	blood:	n/a	n/a
2	ARID3A	chr14:81407660-81407725	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:81421155-81421357	K562	blood:	n/a	n/a
4	ARID3A	chr14:81408038-81408468	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:81421092-81421441	HepG2	liver:	n/a	n/a
6	ATF1	chr14:81397207-81397512	K562	blood:	n/a	n/a
7	ATF2	chr14:81397008-81397875	GM12878	blood:	n/a	n/a
8	ATF2	chr14:81425656-81426351	GM12878	blood:	n/a	n/a
9	ATF2	chr14:81425667-81426340	GM12878	blood:	n/a	n/a
10	ATF2	chr14:81397108-81397920	GM12878	blood:	n/a	n/a
11	ATF3	chr14:81397162-81397461	K562	blood:	n/a	n/a
12	BACH1	chr14:81407866-81408111	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:81407987-81408051	K562	blood:	n/a	n/a
14	BACH1	chr14:81421226-81421524	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr14:81422602-81422695	K562	blood:	n/a	n/a
16	BACH1	chr14:81421988-81422007	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr14:81396449-81396747	GM12878	blood:	n/a	chr14:81396581-81396592
18	BATF	chr14:81396399-81396771	GM12878	blood:	n/a	chr14:81396581-81396592
19	BATF	chr14:81425713-81426251	GM12878	blood:	n/a	n/a
20	BATF	chr14:81425702-81426242	GM12878	blood:	n/a	n/a
21	BATF	chr14:81397048-81397838	GM12878	blood:	n/a	n/a
22	BATF	chr14:81397314-81397799	GM12878	blood:	n/a	n/a
23	BATF	chr14:81406533-81406767	GM12878	blood:	n/a	chr14:81406669-81406679 chr14:81406668-81406679
24	BCL11A	chr14:81397382-81397717	GM12878	blood:	n/a	n/a
25	BCL11A	chr14:81425794-81426232	GM12878	blood:	n/a	chr14:81425939-81425948 chr14:81426062-81426070
26	BCL11A	chr14:81396986-81397858	GM12878	blood:	n/a	n/a
27	BCL11A	chr14:81425717-81426288	GM12878	blood:	n/a	chr14:81425939-81425948 chr14:81426062-81426070
28	BCL11A	chr14:81396984-81397264	GM12878	blood:	n/a	n/a
29	BCL3	chr14:81397207-81397791	GM12878	blood:	n/a	n/a
30	BCL3	chr14:81397382-81397705	GM12878	blood:	n/a	n/a
31	BCLAF1	chr14:81397245-81397849	GM12878	blood:	n/a	n/a
32	BCLAF1	chr14:81407906-81408368	GM12878	blood:	n/a	n/a
33	BCLAF1	chr14:81397335-81397813	GM12878	blood:	n/a	n/a
34	BCLAF1	chr14:81425680-81426248	GM12878	blood:	n/a	chr14:81425939-81425948 chr14:81426062-81426070
35	BCLAF1	chr14:81407837-81408461	GM12878	blood:	n/a	n/a
36	BCLAF1	chr14:81421043-81421453	GM12878	blood:	n/a	chr14:81421296-81421309
37	BCLAF1	chr14:81425756-81426310	GM12878	blood:	n/a	chr14:81425939-81425948 chr14:81426062-81426070
38	BHLHE40	chr14:81407612-81408380	K562	blood:	n/a	n/a
39	BHLHE40	chr14:81397131-81397461	K562	blood:	n/a	n/a
40	BHLHE40	chr14:81425723-81426256	GM12878	blood:	n/a	n/a
41	BHLHE40	chr14:81397115-81397778	GM12878	blood:	n/a	n/a
42	BHLHE40	chr14:81407974-81408354	GM12878	blood:	n/a	n/a
43	BHLHE40	chr14:81421148-81421499	K562	blood:	n/a	chr14:81421348-81421364
44	BHLHE40	chr14:81408033-81408295	HepG2	liver:	n/a	n/a
45	BRCA1	chr14:81407519-81408600	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr14:81407957-81408768	GM12878	blood:	n/a	n/a
47	BRCA1	chr14:81421111-81421414	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr14:81408192-81408491	HepG2	liver:	n/a	n/a
49	CBX3	chr14:81397142-81397629	HCT-116	colon:	n/a	n/a
50	CCNT2	chr14:81421175-81421533	K562	blood:	n/a	n/a

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81407087-81407137	HL-60	blood:	n/a
2	chr14:81407087-81407137	HL-60	blood:	n/a
3	chr14:81407988-81408038	SKMC	muscle:	n/a
4	chr14:81421508-81421558	AG09319	gingival:	n/a
5	chr14:81421989-81422039	K562	blood:	n/a
6	chr14:81421403-81421453	HCM	heart:	n/a
7	chr14:81426234-81426284	PFSK-1	brain:	n/a
8	chr14:81421989-81422039	LNCaP	prostate:	n/a
9	chr14:81421322-81421372	AG09309	skin:	n/a
10	chr14:81408086-81408136	GM12878	blood:	n/a
11	chr14:81421297-81421347	LNCaP	prostate:	n/a
12	chr14:81407988-81408038	Hepatocyte	liver:	n/a
13	chr14:81424527-81424577	K562	blood:	n/a
14	chr14:81407087-81407137	GM12892	blood:	n/a
15	chr14:81424527-81424577	Hepatocyte	liver:	n/a
16	chr14:81421322-81421372	Jurkat	blood:	n/a
17	chr14:81407087-81407137	NHDF-neo	bronchial:	n/a
18	chr14:81425912-81425962	ECC-1	luminal epithelium:	n/a
19	chr14:81421508-81421558	BE2_C	brain:	n/a
20	chr14:81407711-81407761	BJ	skin:	n/a
21	chr14:81426577-81426627	HRPEpiC	eye:	n/a
22	chr14:81407988-81408038	SK-N-SH	brain:	n/a
23	chr14:81422160-81422210	NHDF-neo	bronchial:	n/a
24	chr14:81421403-81421453	HRPEpiC	eye:	n/a
25	chr14:81426234-81426284	PrEC	prostate:	n/a
26	chr14:81392851-81392901	PrEC	prostate:	n/a
27	chr14:81408086-81408136	GM06990	blood:	n/a
28	chr14:81421600-81421650	ovcar-3	ovarian:	n/a
29	chr14:81405846-81405896	AG09309	skin:	n/a
30	chr14:81407711-81407761	AG09309	skin:	n/a
31	chr14:81407988-81408038	HCT-116	colon:	n/a
32	chr14:81422111-81422161	GM06990	blood:	n/a
33	chr14:81421983-81422033	ProgFib	skin:	n/a
34	chr14:81422098-81422148	AG10803	skin:	n/a
35	chr14:81425912-81425962	HL-60	blood:	n/a
36	chr14:81424527-81424577	HEEpiC	esophagus:	n/a
37	chr14:81407711-81407761	HAEpiC	amniotic membrane:	n/a
38	chr14:81422160-81422210	HepG2	liver:	n/a
39	chr14:81404956-81405006	GM12891	blood:	n/a
40	chr14:81421508-81421558	AG04449	skin:	fetal
41	chr14:81421322-81421372	HRCEpiC	kidney:	n/a
42	chr14:81421600-81421650	GM12891	blood:	n/a
43	chr14:81422160-81422210	HCF	heart:	n/a
44	chr14:81422111-81422161	ProgFib	skin:	n/a
45	chr14:81404956-81405006	RPTEC	kidney:	n/a
46	chr14:81404956-81405006	HEEpiC	esophagus:	n/a
47	chr14:81421983-81422033	HNPCEpiC	eye:	n/a
48	chr14:81421403-81421453	AG09319	gingival:	n/a
49	chr14:81426015-81426065	AG09309	skin:	n/a
50	chr14:81426012-81426062	GM06990	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:81420793..81423189-chr14:81424553..81427836,4	MCF-7	breast:
2	chr14:81429469..81431335-chr14:81685731..81687718,2	K562	blood:
3	chr14:81397911..81402411-chr14:81683829..81688491,5	K562	blood:
4	chr14:81401790..81404001-chr14:81408260..81409826,2	K562	blood:
5	chr14:81437706..81439686-chr14:81442892..81444755,2	MCF-7	breast:
6	chr14:81388857..81391378-chr14:81393034..81394576,2	K562	blood:
7	chr14:81447196..81448849-chr14:81635444..81638287,2	MCF-7	breast:
8	chr14:81443218..81445707-chr14:81448649..81450326,2	K562	blood:
9	chr14:81429871..81432242-chr14:81433461..81436310,2	MCF-7	breast:
10	chr14:81420793..81423189-chr14:81424553..81427836,4	MCF-7	breast:
11	chr14:81432696..81434242-chr14:81439337..81441996,2	MCF-7	breast:
12	chr14:81401790..81404001-chr14:81408260..81409826,2	K562	blood:
13	chr14:81397350..81398918-chr14:81404330..81405953,2	MCF-7	breast:
14	chr14:81442891..81446024-chr14:81447547..81451295,3	K562	blood:
15	chr14:81413969..81417033-chr14:81418099..81421076,3	K562	blood:
16	chr14:81401530..81405637-chr14:81405681..81409826,5	K562	blood:
17	chr14:81443218..81445707-chr14:81448649..81450326,2	K562	blood:
18	chr14:81413969..81417033-chr14:81418099..81421076,3	K562	blood:
19	chr14:81421633..81424276-chr14:81426151..81427849,2	K562	blood:
20	chr14:81427260..81428823-chr14:81430386..81432233,2	MCF-7	breast:
21	chr14:81396050..81399080-chr14:81399956..81402754,3	K562	blood:
22	chr14:81400340..81402827-chr14:81422342..81424603,2	K562	blood:
23	chr14:81396675..81399080-chr14:81400094..81402837,4	K562	blood:
24	chr14:81400340..81402827-chr14:81422342..81424603,2	K562	blood:
25	chr14:81432696..81434242-chr14:81439337..81441996,2	MCF-7	breast:
26	chr14:81427260..81428823-chr14:81430386..81432233,2	MCF-7	breast:
27	chr14:81429871..81432242-chr14:81433461..81436310,2	MCF-7	breast:
28	chr14:81421283..81423197-chr14:81423259..81426025,2	K562	blood:
29	chr14:81405070..81407655-chr14:81893214..81894963,2	K562	blood:
30	chr14:81437706..81439686-chr14:81442892..81444755,2	MCF-7	breast:
31	chr14:81420764..81421641-chr14:81452541..81453280,3	MCF-7	breast:
32	chr14:81421307..81423560-chr14:81685821..81687772,2	MCF-7	breast:
33	chr14:81389769..81391378-chr14:81393076..81395517,2	K562	blood:
34	chr14:81405781..81407858-chr14:81414654..81417606,2	K562	blood:
35	chr14:81406001..81408090-chr14:81684696..81687286,2	MCF-7	breast:
36	chr14:81409086..81412079-chr14:81684654..81686943,2	K562	blood:
37	chr14:81396675..81399080-chr14:81400094..81402837,4	K562	blood:
38	chr14:81421283..81423197-chr14:81423259..81426025,2	K562	blood:
39	chr14:81434370..81436740-chr14:81683438..81686246,2	MCF-7	breast:
40	chr14:81427520..81429022-chr14:81432254..81434626,2	K562	blood:
41	chr14:81427520..81429022-chr14:81432254..81434626,2	K562	blood:
42	chr14:81396050..81399080-chr14:81399956..81402754,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP128-1	chr14:81424142-81424629	NONHSAT038045
2	lnc-NRXN3-4	chr14:81448332-81449982	NONHSAT038046
3	lnc-CEP128-1	chr14:81425776-81425861	NONHSAT038042
4	lnc-CEP128-1	chr14:81425776-81425850	NONHSAT038045
5	lnc-CEP128-1	chr14:81411900-81412111	NONHSAT038042
6	lnc-CEP128-1	chr14:81424522-81424629	NONHSAT038042

No data

Variant related genes	Relation type
TSHR	TF binding region
CEP128	TF binding region
ENSG00000258915	TF binding region
TSHR	CpG island
CEP128	CpG island
ENSG00000258915	CpG island
ENSG00000100629	chromatin interactions
ENSG00000258999	chromatin interactions
ENSG00000140022	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000258915	chromatin interactions
ENSG00000165409	chromatin interactions

Extended variants
information (count: 2267 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2267 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4903948	chr14:81392124-81392125	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569146762	chr14:81392133-81392134	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573446391	chr14:81392185-81392186	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540449244	chr14:81392253-81392254	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536683392	chr14:81392277-81392278	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114363971	chr14:81392282-81392283	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529552395	chr14:81392441-81392442	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548216688	chr14:81392452-81392453	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563092494	chr14:81392458-81392459	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184924086	chr14:81392468-81392469	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116875278	chr14:81392483-81392484	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573501346	chr14:81392484-81392485	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10132220	chr14:81392502-81392503	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs4903949	chr14:81392513-81392514	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs568387849	chr14:81392527-81392528	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535341349	chr14:81392542-81392543	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372207378	chr14:81392557-81392558	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117857224	chr14:81392561-81392562	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144074292	chr14:81392591-81392592	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539961301	chr14:81392605-81392606	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79860425	chr14:81392609-81392610	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573359788	chr14:81392685-81392686	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540863735	chr14:81392693-81392694	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558955738	chr14:81392722-81392723	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139688687	chr14:81392761-81392762	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529638152	chr14:81392806-81392807	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373190771	chr14:81392807-81392808	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149800429	chr14:81392810-81392811	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368869286	chr14:81392852-81392853	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78060889	chr14:81392888-81392889	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374840983	chr14:81392927-81392928	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562963811	chr14:81392943-81392944	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144706923	chr14:81392976-81392977	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545375829	chr14:81392994-81392995	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189916320	chr14:81393032-81393033	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112329130	chr14:81393088-81393089	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528130685	chr14:81393096-81393097	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs118124229	chr14:81393115-81393116	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75118096	chr14:81393118-81393119	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527590528	chr14:81393139-81393140	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181533460	chr14:81393151-81393152	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542700317	chr14:81393237-81393238	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117088913	chr14:81393247-81393248	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147918289	chr14:81393297-81393298	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375865844	chr14:81393329-81393330	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572935366	chr14:81393384-81393385	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs36102034	chr14:81393404-81393405	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs569145539	chr14:81393473-81393474	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs2371456	chr14:81393496-81393497	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs558141955	chr14:81393505-81393506	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81351400-81398400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr14:81357800-81392600	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr14:81358000-81396600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr14:81359400-81406000	Weak transcription	A549	lung
5	chr14:81359800-81396200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr14:81359800-81407200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:81360200-81393800	Weak transcription	HMEC	breast
8	chr14:81362200-81392600	Weak transcription	NH-A	brain
9	chr14:81362200-81392800	Weak transcription	Fetal Muscle Leg	muscle
10	chr14:81364400-81395800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr14:81364400-81395800	Weak transcription	GM12878-XiMat	blood
12	chr14:81365200-81393000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr14:81369600-81397200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr14:81370400-81393600	Weak transcription	NHEK	skin
15	chr14:81371600-81392800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:81373600-81392600	Weak transcription	Esophagus	oesophagus
17	chr14:81373800-81392200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr14:81375400-81407600	Weak transcription	Gastric	stomach
19	chr14:81375800-81392800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr14:81379200-81392400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr14:81379400-81407400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr14:81380000-81392600	Weak transcription	Right Ventricle	heart
23	chr14:81380800-81392800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr14:81382600-81392400	Weak transcription	HSMM	muscle
25	chr14:81382600-81392600	Weak transcription	Left Ventricle	heart
26	chr14:81382600-81393200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr14:81382600-81406400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr14:81382800-81396000	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr14:81382800-81396200	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr14:81382800-81396800	Weak transcription	Primary B cells from cord blood	blood
31	chr14:81382800-81397200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr14:81382800-81397200	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr14:81383000-81392200	Weak transcription	Thymus	Thymus
34	chr14:81383400-81393600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr14:81384600-81392800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr14:81386800-81392200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr14:81387800-81407200	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr14:81388200-81393600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr14:81390000-81392200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr14:81390000-81405000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr14:81390000-81407200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr14:81391000-81392600	Weak transcription	Fetal Thymus	thymus
43	chr14:81391200-81392600	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr14:81391200-81393600	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr14:81391400-81392200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr14:81391800-81392200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr14:81391800-81392400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr14:81391800-81393000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
49	chr14:81392000-81392600	ZNF genes & repeats	Fetal Stomach	stomach
50	chr14:81392000-81392800	Enhancers	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links