Variant report

Variant	nsv901959
Chromosome Location	chr14:55853724-55916225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2086)
CpG islands
(count:1831)
Chromatin interactive
region (count:75)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2086 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:55896954-55897161	K562	blood:	n/a	n/a
2	ARID3A	chr14:55912933-55913378	K562	blood:	n/a	n/a
3	ARID3A	chr14:55897005-55897180	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:55901366-55901865	HepG2	liver:	n/a	chr14:55901771-55901787
5	ARID3A	chr14:55912857-55913179	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:55886501-55886594	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:55884839-55884914	K562	blood:	n/a	n/a
8	ARID3A	chr14:55865349-55865785	K562	blood:	n/a	n/a
9	ARID3A	chr14:55878445-55878842	HepG2	liver:	n/a	n/a
10	ATF1	chr14:55865401-55865745	K562	blood:	n/a	n/a
11	ATF2	chr14:55878330-55878770	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr14:55878289-55878963	GM12878	blood:	n/a	n/a
13	ATF2	chr14:55878367-55878784	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr14:55878444-55878902	GM12878	blood:	n/a	n/a
15	ATF2	chr14:55896755-55897141	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr14:55878444-55878620	GM12878	blood:	n/a	n/a
17	ATF3	chr14:55878356-55878801	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr14:55878392-55878727	HepG2	liver:	n/a	n/a
19	ATF3	chr14:55878236-55878771	GM12878	blood:	n/a	n/a
20	ATF3	chr14:55878386-55878648	K562	blood:	n/a	n/a
21	ATF3	chr14:55878254-55878821	A549	lung:	n/a	n/a
22	ATF3	chr14:55878343-55878649	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr14:55896818-55897008	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL3	chr14:55878288-55879012	A549	lung:	n/a	chr14:55878658-55878667 chr14:55878655-55878664
25	BCL3	chr14:55914719-55915425	A549	lung:	n/a	chr14:55915028-55915037 chr14:55914868-55914876
26	BCLAF1	chr14:55878283-55878822	GM12878	blood:	n/a	chr14:55878658-55878667 chr14:55878655-55878664
27	BHLHE40	chr14:55878390-55879136	K562	blood:	n/a	n/a
28	BHLHE40	chr14:55865467-55865799	A549	lung:	n/a	n/a
29	BHLHE40	chr14:55865345-55865808	K562	blood:	n/a	n/a
30	BHLHE40	chr14:55893630-55893941	K562	blood:	n/a	n/a
31	BHLHE40	chr14:55912882-55913119	GM12878	blood:	n/a	n/a
32	BHLHE40	chr14:55878402-55878729	HepG2	liver:	n/a	n/a
33	BHLHE40	chr14:55878367-55878849	GM12878	blood:	n/a	n/a
34	BHLHE40	chr14:55877793-55877817	HepG2	liver:	n/a	n/a
35	BHLHE40	chr14:55882151-55882265	GM12878	blood:	n/a	n/a
36	BRCA1	chr14:55878519-55878849	HepG2	liver:	n/a	n/a
37	BRCA1	chr14:55894056-55894479	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr14:55878481-55878734	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr14:55914803-55915381	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr14:55865520-55865897	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr14:55896897-55897056	H1-hESC	embryonic stem cell:	n/a	n/a
42	CBX3	chr14:55865270-55865882	HCT-116	colon:	n/a	chr14:55865731-55865742
43	CBX3	chr14:55894048-55894670	HCT-116	colon:	n/a	chr14:55894509-55894520
44	CBX3	chr14:55914606-55915523	HCT-116	colon:	n/a	n/a
45	CBX3	chr14:55914460-55915611	HCT-116	colon:	n/a	n/a
46	CCNT2	chr14:55878338-55878808	K562	blood:	n/a	n/a
47	CEBPB	chr14:55904270-55904420	IMR90	lung:	n/a	chr14:55904331-55904344 chr14:55904332-55904343 chr14:55904348-55904361 chr14:55904349-55904360 chr14:55904331-55904342
48	CEBPB	chr14:55904235-55904496	Hela-S3	cervix:	n/a	chr14:55904331-55904344 chr14:55904332-55904343 chr14:55904348-55904361 chr14:55904349-55904360 chr14:55904331-55904342
49	CEBPB	chr14:55865473-55865783	IMR90	lung:	n/a	n/a
50	CEBPB	chr14:55914668-55915621	HCT-116	colon:	n/a	chr14:55915316-55915329 chr14:55915316-55915328

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:55907007-55907057	SK-N-MC	brain:	n/a
2	chr14:55907007-55907057	SK-N-MC	brain:	n/a
3	chr14:55875634-55875684	PFSK-1	brain:	n/a
4	chr14:55907299-55907349	HCT-116	colon:	n/a
5	chr14:55878649-55878699	AG09319	gingival:	n/a
6	chr14:55878758-55878808	U87	brain:	n/a
7	chr14:55879046-55879096	HL-60	blood:	n/a
8	chr14:55908301-55908351	HMEC	breast:	n/a
9	chr14:55907007-55907057	GM12878	blood:	n/a
10	chr14:55878649-55878699	GM06990	blood:	n/a
11	chr14:55878680-55878730	HCF	heart:	n/a
12	chr14:55910650-55910700	GM19239	blood:	n/a
13	chr14:55907385-55907435	SKMC	muscle:	n/a
14	chr14:55907460-55907510	HMEC	breast:	n/a
15	chr14:55907460-55907510	AG09309	skin:	n/a
16	chr14:55908301-55908351	T-47D	breast:	n/a
17	chr14:55907198-55907248	Hela-S3	cervix:	n/a
18	chr14:55907417-55907467	IMR90	lung:	fetal
19	chr14:55908301-55908351	LNCaP	prostate:	n/a
20	chr14:55907198-55907248	IMR90	lung:	fetal
21	chr14:55878303-55878353	PFSK-1	brain:	n/a
22	chr14:55907460-55907510	HCT-116	colon:	n/a
23	chr14:55878235-55878285	HEEpiC	esophagus:	n/a
24	chr14:55878235-55878285	ovcar-3	ovarian:	n/a
25	chr14:55855938-55855988	HEK293	kidney:	embryo
26	chr14:55907417-55907467	T-47D	breast:	n/a
27	chr14:55878303-55878353	SK-N-SH	brain:	n/a
28	chr14:55878235-55878285	HCT-116	colon:	n/a
29	chr14:55907417-55907467	HUVEC	blood vessel:	n/a
30	chr14:55907198-55907248	HAEpiC	amniotic membrane:	n/a
31	chr14:55905105-55905155	SKMC	muscle:	n/a
32	chr14:55879046-55879096	AG09319	gingival:	n/a
33	chr14:55908365-55908415	T-47D	breast:	n/a
34	chr14:55878649-55878699	NHDF-neo	bronchial:	n/a
35	chr14:55907007-55907057	CMK	blood:	n/a
36	chr14:55907299-55907349	AG04450	lung:	fetal
37	chr14:55907299-55907349	RPTEC	kidney:	n/a
38	chr14:55907385-55907435	HEK293	kidney:	embryo
39	chr14:55907501-55907551	MCF-7	breast:	n/a
40	chr14:55878799-55878849	K562	blood:	n/a
41	chr14:55879046-55879096	HRPEpiC	eye:	n/a
42	chr14:55907385-55907435	MCF10A-Er-Src	breast:	n/a
43	chr14:55878649-55878699	HRPEpiC	eye:	n/a
44	chr14:55907007-55907057	ECC-1	luminal epithelium:	n/a
45	chr14:55907122-55907172	HRE	kidney:	n/a
46	chr14:55907385-55907435	SK-N-MC	brain:	n/a
47	chr14:55907374-55907424	U87	brain:	n/a
48	chr14:55907385-55907435	Hela-S3	cervix:	n/a
49	chr14:55907460-55907510	H1-hESC	embryonic stem cell:	embryo
50	chr14:55907122-55907172	SAEC	small airway:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:55736665..55740457-chr14:55875135..55883763,10	K562	blood:
2	chr14:55863838..55865668-chr14:55871049..55872578,2	K562	blood:
3	chr14:55912884..55915003-chr14:55916118..55918746,2	K562	blood:
4	chr14:55862301..55864393-chr14:55864806..55866499,2	K562	blood:
5	chr14:55737932..55740165-chr14:55894081..55895808,2	MCF-7	breast:
6	chr14:55851517..55854050-chr14:55862955..55864558,2	K562	blood:
7	chr14:55873181..55876141-chr14:55896106..55898564,2	K562	blood:
8	chr14:55736801..55739826-chr14:55895387..55899212,3	K562	blood:
9	chr14:55913503..55916476-chr14:55916660..55918746,2	K562	blood:
10	chr14:55851134..55854346-chr14:55857455..55859971,3	K562	blood:
11	chr14:55863036..55866300-chr14:55870450..55873492,4	K562	blood:
12	chr14:55911475..55914836-chr14:55916178..55919121,4	MCF-7	breast:
13	chr14:55877783..55881962-chr14:55882620..55887567,10	MCF-7	breast:
14	chr14:55863726..55865438-chr14:55877995..55880631,2	MCF-7	breast:
15	chr14:55873181..55876141-chr14:55896106..55898564,2	K562	blood:
16	chr14:55910738..55912957-chr14:56045973..56048447,2	MCF-7	breast:
17	chr14:55868160..55871360-chr14:55872388..55874705,3	K562	blood:
18	chr14:55870951..55872840-chr14:55874953..55876700,2	K562	blood:
19	chr14:55877097..55882120-chr14:55890369..55898508,8	MCF-7	breast:
20	chr14:55869644..55873537-chr14:55877661..55881822,3	K562	blood:
21	chr14:55736998..55739504-chr14:55895479..55898305,3	MCF-7	breast:
22	chr14:55883538..55884193-chr14:55896578..55897445,2	MCF-7	breast:
23	chr14:55882209..55883793-chr14:55889649..55891588,2	K562	blood:
24	chr14:55736296..55738259-chr14:55878149..55880015,2	MCF-7	breast:
25	chr14:55878684..55880292-chr14:55881926..55883661,2	K562	blood:
26	chr14:55851395..55854155-chr14:55863478..55865665,2	MCF-7	breast:
27	chr14:55868020..55869750-chr14:55873508..55875755,2	MCF-7	breast:
28	chr14:55890007..55892259-chr14:56172820..56174391,2	K562	blood:
29	chr14:55913599..55916759-chr14:56004997..56009666,4	MCF-7	breast:
30	chr14:55904613..55905202-chr14:56806452..56807250,2	MCF-7	breast:
31	chr14:55878199..55878800-chr7:128170749..128171703,2	NB4	blood:
32	chr14:55831903..55834657-chr14:55852806..55855439,2	MCF-7	breast:
33	chr14:55870132..55872485-chr14:55876302..55878951,2	MCF-7	breast:
34	chr14:55883538..55884193-chr14:55896578..55897445,2	MCF-7	breast:
35	chr14:55877415..55882128-chr14:55883755..55887346,6	K562	blood:
36	chr14:55870951..55872840-chr14:55874953..55876700,2	K562	blood:
37	chr14:55905450..55907568-chr14:56045550..56047292,2	MCF-7	breast:
38	chr14:55832794..55835676-chr14:55852395..55854057,2	K562	blood:
39	chr14:55851395..55854155-chr14:55863478..55865665,2	MCF-7	breast:
40	chr14:55888467..55890762-chr14:55899523..55901753,2	K562	blood:
41	chr14:55912628..55913132-chr14:56940932..56941697,2	MCF-7	breast:
42	chr14:55888145..55889967-chr14:55899523..55902153,2	K562	blood:
43	chr14:55832090..55833883-chr14:55878712..55880700,2	MCF-7	breast:
44	chr14:55904524..55905404-chr14:56941095..56941735,2	MCF-7	breast:
45	chr14:55882209..55883793-chr14:55889649..55891588,2	K562	blood:
46	chr14:55738462..55740457-chr14:55876208..55878548,3	K562	blood:
47	chr14:55737969..55739630-chr14:55884088..55886762,2	K562	blood:
48	chr14:55889778..55893394-chr14:55894134..55896526,3	K562	blood:
49	chr14:55878417..55880292-chr14:55881684..55883661,2	K562	blood:
50	chr14:55654827..55657243-chr14:55881202..55883542,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG14-2	chr14:55880274-55880777	NONHSAT037009
2	lnc-TBPL2-2	chr14:55861658-55861951	NONHSAT037008

No data

Variant related genes	Relation type
ATG14	TF binding region
TBPL2	TF binding region
RPL21P6	TF binding region
ENSG00000259318	TF binding region
ATG14	CpG island
TBPL2	CpG island
RPL21P6	CpG island
ENSG00000259318	CpG island
ENSG00000197568	chromatin interactions
ENSG00000239199	chromatin interactions
ENSG00000258413	chromatin interactions
ENSG00000273270	chromatin interactions
ENSG00000126777	chromatin interactions
ENSG00000126775	chromatin interactions
ENSG00000186615	chromatin interactions
ENSG00000118454	chromatin interactions
ENSG00000178974	chromatin interactions

Extended variants
information (count: 2567 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2567 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17742621	chr14:55853724-55853725	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537196371	chr14:55853745-55853746	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs534131857	chr14:55853751-55853752	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181386620	chr14:55853754-55853755	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs113716510	chr14:55853799-55853800	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs79816457	chr14:55853810-55853811	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs112917786	chr14:55853829-55853830	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185672648	chr14:55853892-55853893	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558815977	chr14:55853911-55853912	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs113399172	chr14:55853921-55853922	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373781407	chr14:55853932-55853933	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs572103106	chr14:55853963-55853964	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141471232	chr14:55853983-55853984	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565284527	chr14:55853984-55853985	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553898029	chr14:55854001-55854002	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs73280917	chr14:55854163-55854164	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs150864054	chr14:55854186-55854187	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs3783652	chr14:55854208-55854209	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs188468294	chr14:55854233-55854234	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs10149420	chr14:55854257-55854258	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs79187445	chr14:55854292-55854293	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs74053904	chr14:55854398-55854399	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs139612464	chr14:55854409-55854410	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12892465	chr14:55854417-55854418	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs144223903	chr14:55854418-55854419	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs180683835	chr14:55854430-55854431	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12892493	chr14:55854453-55854454	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146540288	chr14:55854472-55854473	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577139149	chr14:55854474-55854475	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576558150	chr14:55854479-55854480	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537691664	chr14:55854671-55854672	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558736211	chr14:55854735-55854736	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187426720	chr14:55854742-55854743	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551640375	chr14:55854760-55854761	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564622478	chr14:55854801-55854802	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs56042503	chr14:55854803-55854804	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs368778313	chr14:55854810-55854811	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191845784	chr14:55854821-55854822	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116871487	chr14:55854842-55854843	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145818046	chr14:55854877-55854878	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs72717748	chr14:55854891-55854892	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs528823356	chr14:55854907-55854908	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111917922	chr14:55854975-55854976	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549959573	chr14:55854993-55854994	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs3783653	chr14:55855007-55855008	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs72717749	chr14:55855035-55855036	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs148968412	chr14:55855038-55855039	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs75494610	chr14:55855057-55855058	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs143760689	chr14:55855058-55855059	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs112146878	chr14:55855088-55855089	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD

Chromatin state (count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55808800-55865200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:55818200-55877600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:55818400-55858800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:55819400-55855200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr14:55821400-55865200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr14:55831000-55859400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr14:55831800-55858000	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr14:55832400-55857800	Strong transcription	Liver	Liver
9	chr14:55836800-55877800	Weak transcription	Esophagus	oesophagus
10	chr14:55839400-55859200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr14:55839600-55858600	Strong transcription	Primary B cells from peripheral blood	blood
12	chr14:55840200-55858800	Strong transcription	Primary B cells from cord blood	blood
13	chr14:55840400-55856600	Strong transcription	Fetal Intestine Large	intestine
14	chr14:55840400-55856800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr14:55840600-55854200	Strong transcription	Brain Cingulate Gyrus	brain
16	chr14:55841000-55859000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr14:55841800-55855000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr14:55842000-55856200	Strong transcription	Fetal Muscle Leg	muscle
19	chr14:55842200-55856400	Strong transcription	Placenta	Placenta
20	chr14:55842400-55854200	Strong transcription	Brain Hippocampus Middle	brain
21	chr14:55842400-55855400	Strong transcription	Fetal Stomach	stomach
22	chr14:55843600-55855000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr14:55844000-55854800	Weak transcription	Fetal Brain Male	brain
24	chr14:55845000-55855200	Strong transcription	Fetal Intestine Small	intestine
25	chr14:55846000-55854800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr14:55847200-55855400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr14:55847200-55856800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr14:55848600-55856200	Strong transcription	HepG2	liver
29	chr14:55848600-55876600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr14:55848800-55854800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr14:55848800-55855000	Weak transcription	HMEC	breast
32	chr14:55848800-55855800	Weak transcription	Brain Angular Gyrus	brain
33	chr14:55848800-55861000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr14:55848800-55861200	Weak transcription	Small Intestine	intestine
35	chr14:55848800-55861800	Weak transcription	HUVEC	blood vessel
36	chr14:55848800-55864600	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr14:55848800-55865000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr14:55849000-55855000	Weak transcription	NHDF-Ad	bronchial
39	chr14:55849000-55856000	Weak transcription	Primary hematopoietic stem cells	blood
40	chr14:55849200-55876600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr14:55849200-55878000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr14:55849600-55855800	Weak transcription	Fetal Lung	lung
43	chr14:55849800-55865200	Weak transcription	A549	lung
44	chr14:55850000-55868400	Weak transcription	Right Ventricle	heart
45	chr14:55850200-55853800	Weak transcription	Brain Anterior Caudate	brain
46	chr14:55850200-55855000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr14:55850400-55856200	Strong transcription	Ovary	ovary
48	chr14:55850400-55856600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr14:55850400-55856600	Strong transcription	Fetal Brain Female	brain
50	chr14:55850400-55857000	Strong transcription	Primary T cells from cord blood	blood

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