Variant report

Variant	nsv1039369
Chromosome Location	chr14:21499054-21530301
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:670)
CpG islands
(count:1406)
Chromatin interactive
region (count:57)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:670 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21522047-21523246	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:21530276-21530613	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:21529043-21529502	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:21523653-21524323	HepG2	liver:	n/a	n/a
5	BCL11A	chr14:21518841-21519050	GM12878	blood:	n/a	n/a
6	BHLHE40	chr14:21508373-21508593	HepG2	liver:	n/a	n/a
7	BHLHE40	chr14:21522242-21522904	HepG2	liver:	n/a	n/a
8	BHLHE40	chr14:21500543-21500699	K562	blood:	n/a	chr14:21500615-21500636 chr14:21500619-21500632
9	BHLHE40	chr14:21509838-21510149	K562	blood:	n/a	n/a
10	BHLHE40	chr14:21512219-21512759	K562	blood:	n/a	n/a
11	BRCA1	chr14:21525979-21526127	HepG2	liver:	n/a	n/a
12	BRCA1	chr14:21512112-21512596	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr14:21522460-21522517	HepG2	liver:	n/a	n/a
14	CCNT2	chr14:21512465-21512745	K562	blood:	n/a	n/a
15	CEBPB	chr14:21522515-21522941	HepG2	liver:	n/a	n/a
16	CEBPB	chr14:21512073-21512450	IMR90	lung:	n/a	chr14:21512257-21512268
17	CEBPB	chr14:21512111-21512420	H1-hESC	embryonic stem cell:	n/a	chr14:21512257-21512268
18	CEBPB	chr14:21522179-21522962	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:21512042-21512785	MCF-7	breast:	n/a	chr14:21512257-21512268
20	CEBPB	chr14:21512120-21512387	K562	blood:	n/a	chr14:21512257-21512268
21	CEBPB	chr14:21512027-21512847	Hela-S3	cervix:	n/a	chr14:21512257-21512268
22	CEBPB	chr14:21522186-21522964	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:21512058-21512505	K562	blood:	n/a	chr14:21512257-21512268
24	CEBPB	chr14:21512064-21512509	HepG2	liver:	n/a	chr14:21512257-21512268
25	CEBPB	chr14:21522191-21522994	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:21512028-21512500	HCT-116	colon:	n/a	chr14:21512257-21512268
27	CEBPB	chr14:21529299-21529508	HepG2	liver:	n/a	n/a
28	CEBPB	chr14:21512112-21512509	HepG2	liver:	n/a	chr14:21512257-21512268
29	CEBPB	chr14:21512086-21512445	A549	lung:	n/a	chr14:21512257-21512268
30	CEBPB	chr14:21512114-21512444	ECC-1	luminal epithelium:	n/a	chr14:21512257-21512268
31	CEBPB	chr14:21512128-21512398	HepG2	liver:	n/a	chr14:21512257-21512268
32	CEBPB	chr14:21507284-21507468	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:21529206-21529570	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:21511992-21512412	K562	blood:	n/a	chr14:21512257-21512268
35	CEBPB	chr14:21511971-21512576	MCF-7	breast:	n/a	chr14:21512257-21512268
36	CEBPB	chr14:21515603-21515711	HepG2	liver:	n/a	chr14:21515626-21515637
37	CEBPB	chr14:21512078-21512447	HepG2	liver:	n/a	chr14:21512257-21512268
38	CEBPB	chr14:21512087-21512457	ECC-1	luminal epithelium:	n/a	chr14:21512257-21512268
39	CEBPB	chr14:21529265-21529573	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:21506163-21506284	HepG2	liver:	n/a	n/a
41	CEBPD	chr14:21523695-21524180	HepG2	liver:	n/a	n/a
42	CEBPD	chr14:21522639-21522983	HepG2	liver:	n/a	n/a
43	CEBPD	chr14:21522516-21522881	HepG2	liver:	n/a	n/a
44	CEBPD	chr14:21512170-21512386	HepG2	liver:	n/a	n/a
45	CEBPD	chr14:21512109-21512413	HepG2	liver:	n/a	n/a
46	CEBPD	chr14:21529264-21529511	HepG2	liver:	n/a	n/a
47	CHD2	chr14:21507273-21507427	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr14:21522540-21522821	HepG2	liver:	n/a	n/a
49	CHD2	chr14:21508195-21508473	HepG2	liver:	n/a	n/a
50	CHD2	chr14:21507215-21507423	HepG2	liver:	n/a	n/a

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21511112-21511162	NHDF-neo	bronchial:	n/a
2	chr14:21504131-21504181	SAEC	small airway:	n/a
3	chr14:21510323-21510373	HCM	heart:	n/a
4	chr14:21511112-21511162	NHDF-neo	bronchial:	n/a
5	chr14:21504131-21504181	SAEC	small airway:	n/a
6	chr14:21510323-21510373	HCM	heart:	n/a
7	chr14:21511112-21511162	SKMC	muscle:	n/a
8	chr14:21511501-21511551	PANC-1	pancreas:	n/a
9	chr14:21504190-21504240	NHDF-neo	bronchial:	n/a
10	chr14:21525319-21525369	CMK	blood:	n/a
11	chr14:21511676-21511726	MCF-7	breast:	n/a
12	chr14:21504190-21504240	HCF	heart:	n/a
13	chr14:21510479-21510529	PFSK-1	brain:	n/a
14	chr14:21511112-21511162	GM12892	blood:	n/a
15	chr14:21508371-21508421	LNCaP	prostate:	n/a
16	chr14:21504131-21504181	SKMC	muscle:	n/a
17	chr14:21525319-21525369	GM19239	blood:	n/a
18	chr14:21504190-21504240	HL-60	blood:	n/a
19	chr14:21511112-21511162	HUVEC	blood vessel:	n/a
20	chr14:21526267-21526317	IMR90	lung:	fetal
21	chr14:21509062-21509112	ovcar-3	ovarian:	n/a
22	chr14:21525131-21525181	HRCEpiC	kidney:	n/a
23	chr14:21504131-21504181	PFSK-1	brain:	n/a
24	chr14:21510479-21510529	NH-A	brain:	n/a
25	chr14:21510056-21510106	RPTEC	kidney:	n/a
26	chr14:21511112-21511162	PFSK-1	brain:	n/a
27	chr14:21510323-21510373	HL-60	blood:	n/a
28	chr14:21510479-21510529	MCF10A-Er-Src	breast:	n/a
29	chr14:21509062-21509112	SK-N-SH	brain:	n/a
30	chr14:21501986-21502036	HCT-116	colon:	n/a
31	chr14:21503521-21503571	BE2_C	brain:	n/a
32	chr14:21510479-21510529	GM06990	blood:	n/a
33	chr14:21510384-21510434	HMEC	breast:	n/a
34	chr14:21525319-21525369	HAEpiC	amniotic membrane:	n/a
35	chr14:21509062-21509112	ProgFib	skin:	n/a
36	chr14:21509062-21509112	HIPEpiC	eye:	n/a
37	chr14:21501764-21501814	AG09309	skin:	n/a
38	chr14:21509062-21509112	AG04449	skin:	fetal
39	chr14:21511676-21511726	GM12878	blood:	n/a
40	chr14:21511676-21511726	HIPEpiC	eye:	n/a
41	chr14:21510479-21510529	BE2_C	brain:	n/a
42	chr14:21525131-21525181	U87	brain:	n/a
43	chr14:21510056-21510106	HRCEpiC	kidney:	n/a
44	chr14:21524938-21524988	MCF-7	breast:	n/a
45	chr14:21503144-21503194	PrEC	prostate:	n/a
46	chr14:21509062-21509112	HL-60	blood:	n/a
47	chr14:21508979-21509029	NHBE	bronchial:	n/a
48	chr14:21509062-21509112	GM19239	blood:	n/a
49	chr14:21525131-21525181	SK-N-SH	brain:	n/a
50	chr14:21511676-21511726	BJ	skin:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:21502672..21505742-chr14:21506739..21508583,3	K562	blood:
2	chr14:21482631..21484066-chr14:21507957..21508944,12	K562	blood:
3	chr14:21498286..21500648-chr14:21502338..21505596,3	K562	blood:
4	chr14:21492029..21495068-chr14:21497147..21502990,6	K562	blood:
5	chr14:21502778..21505418-chr14:21509371..21512527,3	K562	blood:
6	chr14:21500318..21502814-chr14:21570831..21572874,2	MCF-7	breast:
7	chr14:21487890..21490586-chr14:21498522..21500630,2	K562	blood:
8	chr14:21507601..21509614-chr14:21519216..21521001,2	MCF-7	breast:
9	chr14:21520666..21522460-chr17:57913642..57916296,2	MCF-7	breast:
10	chr14:21519022..21522273-chr14:21527508..21531812,4	MCF-7	breast:
11	chr14:21507601..21509614-chr14:21519216..21521001,2	MCF-7	breast:
12	chr14:21522361..21524775-chr14:21533789..21535927,2	K562	blood:
13	chr14:21492535..21494592-chr14:21505376..21508450,3	MCF-7	breast:
14	chr14:21492507..21494609-chr14:21507224..21509507,2	K562	blood:
15	chr14:21503364..21505418-chr14:21509371..21512241,2	K562	blood:
16	chr14:21481135..21484032-chr14:21528367..21530840,3	K562	blood:
17	chr14:21509178..21511087-chr14:21512780..21515097,2	K562	blood:
18	chr14:21490493..21493487-chr14:21503206..21505661,2	MCF-7	breast:
19	chr14:21491425..21493645-chr14:21500297..21503030,2	MCF-7	breast:
20	chr14:21510788..21513106-chr14:21516290..21517988,2	K562	blood:
21	chr14:21456794..21459241-chr14:21511016..21512746,2	MCF-7	breast:
22	chr14:21482863..21483660-chr14:21507269..21507782,2	K562	blood:
23	chr14:21529316..21532303-chr14:21535271..21538305,3	MCF-7	breast:
24	chr14:21517395..21519655-chr14:21567580..21570511,2	MCF-7	breast:
25	chr14:21507927..21508724-chr14:21539605..21540435,2	K562	blood:
26	chr14:21490682..21493075-chr14:21505531..21508369,2	K562	blood:
27	chr14:21515628..21517908-chr14:21517949..21520341,2	MCF-7	breast:
28	chr14:21325086..21326530-chr14:21507784..21508853,5	MCF-7	breast:
29	chr14:21492571..21495097-chr14:21514382..21516574,2	K562	blood:
30	chr14:21520181..21522093-chr14:21562731..21565529,2	MCF-7	breast:
31	chr14:21481135..21483868-chr14:21528367..21530840,2	K562	blood:
32	chr14:21508218..21509211-chr14:21549174..21549907,2	K562	blood:
33	chr14:21492682..21495124-chr14:21516936..21518759,2	MCF-7	breast:
34	chr14:21518226..21520349-chr14:21522564..21524134,2	MCF-7	breast:
35	chr14:21519022..21522273-chr14:21527508..21531812,4	MCF-7	breast:
36	chr14:21458581..21460223-chr14:21499152..21500713,2	MCF-7	breast:
37	chr14:21518226..21520349-chr14:21522564..21524134,2	MCF-7	breast:
38	chr14:21521893..21523709-chr14:21667067..21669493,2	K562	blood:
39	chr14:21498286..21500648-chr14:21502338..21505596,3	K562	blood:
40	chr14:21482658..21483556-chr14:21503623..21504131,2	MCF-7	breast:
41	chr14:21518131..21520316-chr14:21538706..21541230,2	K562	blood:
42	chr14:21529965..21532217-chr14:21564746..21566795,2	MCF-7	breast:
43	chr14:21529710..21531813-chr14:21532415..21535311,2	MCF-7	breast:
44	chr14:21439378..21440166-chr14:21507981..21508704,3	K562	blood:
45	chr14:21482549..21483464-chr14:21507965..21508939,9	MCF-7	breast:
46	chr14:21498205..21499188-chr14:21507409..21508017,2	K562	blood:
47	chr14:21492771..21495041-chr14:21522458..21525106,2	K562	blood:
48	chr14:21508340..21508948-chr14:21560393..21561249,2	K562	blood:
49	chr14:21502778..21505418-chr14:21509371..21512527,3	K562	blood:
50	chr14:21482504..21484085-chr14:21507966..21509030,20	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASE13-1	chr14:21510241-21510531	NONHSAT035645
2	lnc-RNASE13-1	chr14:21511528-21514097	NONHSAT035645
3	lnc-RNASE13-1	chr14:21510241-21510517	ENSG00000258523
4	lnc-RNASE13-1	chr14:21511515-21514097	ENSG00000258523
5	lnc-ARHGEF40-2	chr14:21529469-21529822	NONHSAT035647

No data

Variant related genes	Relation type
RNASE8	TF binding region
TPPP2	TF binding region
ENSG00000255472	TF binding region
RNASE7	TF binding region
NDRG2	TF binding region
RNASE13	TF binding region
RNASE8	CpG island
TPPP2	CpG island
ENSG00000255472	CpG island
RNASE7	CpG island
NDRG2	CpG island
RNASE13	CpG island
ENSG00000062716	chromatin interactions
ENSG00000165792	chromatin interactions
ENSG00000165795	chromatin interactions
ENSG00000232070	chromatin interactions
ENSG00000178107	chromatin interactions
ENSG00000165799	chromatin interactions
ENSG00000206150	chromatin interactions
ENSG00000165804	chromatin interactions
ENSG00000258604	chromatin interactions
ENSG00000179636	chromatin interactions

Extended variants
information (count: 1337 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1337 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1243459	chr14:21499054-21499055	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146609024	chr14:21499061-21499062	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs2282035	chr14:21499072-21499073	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs545611679	chr14:21499078-21499079	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs201159300	chr14:21499111-21499112	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs192487205	chr14:21499117-21499118	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs372513527	chr14:21499134-21499135	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs202091704	chr14:21499180-21499181	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs143975728	chr14:21499181-21499182	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs185684452	chr14:21499185-21499186	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs561585406	chr14:21499204-21499205	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs374336364	chr14:21499224-21499225	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs188573795	chr14:21499226-21499227	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs375701695	chr14:21499230-21499231	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs565764016	chr14:21499238-21499239	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs148606055	chr14:21499276-21499277	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs369707582	chr14:21499292-21499293	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs373475785	chr14:21499301-21499302	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs528214749	chr14:21499303-21499304	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs375716775	chr14:21499305-21499306	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs142073310	chr14:21499317-21499318	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs112271660	chr14:21499319-21499320	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs201559716	chr14:21499342-21499343	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs374666914	chr14:21499350-21499351	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs543485522	chr14:21499371-21499372	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs75127364	chr14:21499427-21499428	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs188571201	chr14:21499428-21499429	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs79270812	chr14:21499439-21499440	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs552298846	chr14:21499511-21499512	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs541370774	chr14:21499523-21499524	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs375035778	chr14:21499555-21499556	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs539166280	chr14:21499557-21499558	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs1243460	chr14:21499561-21499562	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs180675343	chr14:21499591-21499592	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs544832025	chr14:21499647-21499648	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs561582057	chr14:21499679-21499680	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs374891965	chr14:21499690-21499691	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs575079613	chr14:21499718-21499719	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs534597165	chr14:21499727-21499728	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs542599115	chr14:21499744-21499745	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs183605100	chr14:21499750-21499751	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs201639170	chr14:21499769-21499770	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs141400462	chr14:21499813-21499814	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs376895888	chr14:21499827-21499828	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs145171972	chr14:21499871-21499872	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs564653708	chr14:21499873-21499874	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs1243461	chr14:21499884-21499885	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs375813729	chr14:21499889-21499890	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs77107395	chr14:21499891-21499892	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs188321875	chr14:21499896-21499897	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21494400-21500000	Weak transcription	Esophagus	oesophagus
2	chr14:21495400-21500000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr14:21495400-21501600	Weak transcription	Fetal Muscle Trunk	muscle
4	chr14:21495400-21505200	Weak transcription	Spleen	Spleen
5	chr14:21495400-21514200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:21495600-21499600	Weak transcription	Fetal Muscle Leg	muscle
7	chr14:21495600-21500800	Weak transcription	Right Ventricle	heart
8	chr14:21496000-21499400	Weak transcription	HepG2	liver
9	chr14:21496000-21500000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr14:21496000-21500200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr14:21496200-21499600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr14:21496200-21499600	Weak transcription	K562	blood
13	chr14:21496200-21499800	Weak transcription	Brain Hippocampus Middle	brain
14	chr14:21496200-21499800	Weak transcription	Brain Substantia Nigra	brain
15	chr14:21496200-21500000	Weak transcription	Brain Anterior Caudate	brain
16	chr14:21496200-21500800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr14:21496400-21499800	Weak transcription	Ovary	ovary
18	chr14:21496800-21500600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr14:21497000-21500600	Strong transcription	Liver	Liver
20	chr14:21498600-21499800	Weak transcription	Psoas Muscle	Psoas
21	chr14:21498600-21500200	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr14:21499000-21500200	Enhancers	Fetal Kidney	kidney
23	chr14:21499400-21499600	Enhancers	HepG2	liver
24	chr14:21499600-21500200	Enhancers	Brain Cingulate Gyrus	brain
25	chr14:21499600-21500600	Enhancers	K562	blood
26	chr14:21499600-21503400	Enhancers	Fetal Muscle Leg	muscle
27	chr14:21499800-21500600	Enhancers	Psoas Muscle	Psoas
28	chr14:21499800-21501000	Enhancers	Ovary	ovary
29	chr14:21499800-21501800	Enhancers	Brain Substantia Nigra	brain
30	chr14:21499800-21502800	Enhancers	Brain Hippocampus Middle	brain
31	chr14:21500000-21500200	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr14:21500000-21501200	Enhancers	Brain Anterior Caudate	brain
33	chr14:21500000-21501200	Enhancers	Esophagus	oesophagus
34	chr14:21500000-21501200	Enhancers	Placenta Amnion	Placenta Amnion
35	chr14:21500200-21500400	Enhancers	Brain Angular Gyrus	brain
36	chr14:21500200-21500400	Enhancers	Fetal Stomach	stomach
37	chr14:21500200-21500600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr14:21500200-21501200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr14:21500200-21502000	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr14:21500200-21503000	Weak transcription	Brain Cingulate Gyrus	brain
41	chr14:21500400-21501600	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr14:21500400-21505000	Weak transcription	Brain Angular Gyrus	brain
43	chr14:21500600-21500800	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr14:21500600-21501200	Weak transcription	Psoas Muscle	Psoas
45	chr14:21500600-21501600	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr14:21500600-21501800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:21500600-21502200	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr14:21500600-21506000	Weak transcription	Liver	Liver
49	chr14:21500800-21501000	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr14:21500800-21501200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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