Variant report

Variant	nsv964028
Chromosome Location	chr4:8418957-8430160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8430070-8430295	HepG2	liver:	n/a	n/a
2	ATF1	chr4:8430013-8430812	K562	blood:	n/a	n/a
3	ATF2	chr4:8429909-8430447	GM12878	blood:	n/a	n/a
4	ATF2	chr4:8430055-8430406	GM12878	blood:	n/a	n/a
5	ATF2	chr4:8421093-8421717	GM12878	blood:	n/a	n/a
6	ATF2	chr4:8421154-8421641	GM12878	blood:	n/a	n/a
7	ATF3	chr4:8430143-8430352	GM12878	blood:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
8	ATF3	chr4:8429931-8430553	HepG2	liver:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
9	ATF3	chr4:8430060-8430380	K562	blood:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
10	ATF3	chr4:8430062-8430363	H1-hESC	embryonic stem cell:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
11	ATF3	chr4:8430030-8430439	GM12878	blood:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
12	ATF3	chr4:8430012-8430519	H1-hESC	embryonic stem cell:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
13	ATF3	chr4:8430102-8430422	K562	blood:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
14	ATF3	chr4:8430002-8430420	HepG2	liver:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
15	BACH1	chr4:8421214-8421458	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:8421183-8421487	K562	blood:	n/a	n/a
17	BATF	chr4:8421176-8421733	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:8421129-8421607	GM12878	blood:	n/a	n/a
19	BCL3	chr4:8429932-8430434	A549	lung:	n/a	chr4:8430221-8430234 chr4:8430218-8430227 chr4:8430280-8430293 chr4:8429982-8429995 chr4:8430284-8430297
20	BCL3	chr4:8429841-8430449	GM12878	blood:	n/a	chr4:8430221-8430234 chr4:8430218-8430227 chr4:8430280-8430293 chr4:8429982-8429995 chr4:8430284-8430297
21	BCL3	chr4:8429911-8430529	A549	lung:	n/a	chr4:8430221-8430234 chr4:8430218-8430227 chr4:8430280-8430293 chr4:8429982-8429995 chr4:8430284-8430297
22	BCLAF1	chr4:8429942-8430485	GM12878	blood:	n/a	chr4:8430221-8430234 chr4:8430218-8430227 chr4:8430280-8430293 chr4:8429982-8429995 chr4:8430284-8430297
23	BHLHE40	chr4:8429740-8430403	HepG2	liver:	n/a	n/a
24	BHLHE40	chr4:8429729-8430434	K562	blood:	n/a	n/a
25	BHLHE40	chr4:8429685-8430385	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:8421201-8421716	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:8421192-8421946	K562	blood:	n/a	n/a
28	BHLHE40	chr4:8420591-8420811	K562	blood:	n/a	n/a
29	BRCA1	chr4:8430148-8430413	GM12878	blood:	n/a	n/a
30	BRCA1	chr4:8430048-8430698	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr4:8430058-8430389	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr4:8429722-8429863	GM12878	blood:	n/a	n/a
33	BRCA1	chr4:8430109-8430395	HepG2	liver:	n/a	n/a
34	CBX3	chr4:8428504-8428852	K562	blood:	n/a	n/a
35	CBX3	chr4:8429951-8430427	K562	blood:	n/a	n/a
36	CCNT2	chr4:8429950-8430444	K562	blood:	n/a	n/a
37	CEBPB	chr4:8420105-8420219	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:8430091-8430359	K562	blood:	n/a	n/a
39	CEBPB	chr4:8421010-8421474	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:8430087-8430413	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:8430097-8430356	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:8424067-8424514	MCF-7	breast:	n/a	n/a
43	CEBPB	chr4:8430126-8430357	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:8421056-8421198	K562	blood:	n/a	n/a
45	CEBPB	chr4:8421020-8421447	K562	blood:	n/a	n/a
46	CEBPB	chr4:8424095-8424458	MCF-7	breast:	n/a	n/a
47	CEBPD	chr4:8429950-8430402	HepG2	liver:	n/a	n/a
48	CHD1	chr4:8429596-8430440	GM12878	blood:	n/a	chr4:8430174-8430184
49	CHD2	chr4:8429661-8430448	Hela-S3	cervix:	n/a	chr4:8430174-8430184
50	CHD2	chr4:8430019-8430416	GM12878	blood:	n/a	chr4:8430174-8430184

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8430149-8430199	NHBE	bronchial:	n/a
2	chr4:8426815-8426865	SKMC	muscle:	n/a
3	chr4:8430149-8430199	MCF10A-Er-Src	breast:	n/a
4	chr4:8429229-8429279	SK-N-SH	brain:	n/a
5	chr4:8429930-8429980	PFSK-1	brain:	n/a
6	chr4:8430149-8430199	HMEC	breast:	n/a
7	chr4:8429229-8429279	PrEC	prostate:	n/a
8	chr4:8426815-8426865	Hela-S3	cervix:	n/a
9	chr4:8430149-8430199	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:8429229-8429279	HepG2	liver:	n/a
11	chr4:8426815-8426865	AG09309	skin:	n/a
12	chr4:8429930-8429980	A549	lung:	n/a
13	chr4:8426815-8426865	Jurkat	blood:	n/a
14	chr4:8429930-8429980	Jurkat	blood:	n/a
15	chr4:8426815-8426865	SK-N-SH_RA	brain:	n/a
16	chr4:8430149-8430199	HEEpiC	esophagus:	n/a
17	chr4:8429930-8429980	GM12878	blood:	n/a
18	chr4:8429930-8429980	U87	brain:	n/a
19	chr4:8430149-8430199	HRE	kidney:	n/a
20	chr4:8429229-8429279	HL-60	blood:	n/a
21	chr4:8429930-8429980	NHDF-neo	bronchial:	n/a
22	chr4:8429930-8429980	HEK293	kidney:	embryo
23	chr4:8429229-8429279	U87	brain:	n/a
24	chr4:8429229-8429279	SK-N-SH_RA	brain:	n/a
25	chr4:8426815-8426865	HUVEC	blood vessel:	n/a
26	chr4:8429930-8429980	AG09309	skin:	n/a
27	chr4:8429930-8429980	MCF10A-Er-Src	breast:	n/a
28	chr4:8429229-8429279	SKMC	muscle:	n/a
29	chr4:8429930-8429980	MCF-7	breast:	n/a
30	chr4:8430149-8430199	GM12891	blood:	n/a
31	chr4:8426815-8426865	NHDF-neo	bronchial:	n/a
32	chr4:8426815-8426865	GM12891	blood:	n/a
33	chr4:8426815-8426865	T-47D	breast:	n/a
34	chr4:8429229-8429279	RPTEC	kidney:	n/a
35	chr4:8426815-8426865	NT2-D1	testis:	n/a
36	chr4:8429930-8429980	HepG2	liver:	n/a
37	chr4:8426815-8426865	SK-N-MC	brain:	n/a
38	chr4:8429930-8429980	HNPCEpiC	eye:	n/a
39	chr4:8429229-8429279	T-47D	breast:	n/a
40	chr4:8429229-8429279	MCF10A-Er-Src	breast:	n/a
41	chr4:8430149-8430199	PANC-1	pancreas:	n/a
42	chr4:8430149-8430199	Jurkat	blood:	n/a
43	chr4:8429229-8429279	GM19239	blood:	n/a
44	chr4:8429930-8429980	IMR90	lung:	fetal
45	chr4:8426815-8426865	GM19239	blood:	n/a
46	chr4:8429229-8429279	IMR90	lung:	fetal
47	chr4:8429930-8429980	HCT-116	colon:	n/a
48	chr4:8426815-8426865	SAEC	small airway:	n/a
49	chr4:8426815-8426865	AoSMC	blood vessel:	n/a
50	chr4:8430149-8430199	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:8414211..8417979-chr4:8429248..8432423,3	MCF-7	breast:
2	chr4:8416707..8419298-chr4:8428396..8430193,3	MCF-7	breast:
3	chr4:8428067..8433323-chr4:8440948..8445760,8	K562	blood:
4	chr4:8428810..8430394-chr4:8440724..8444143,3	K562	blood:
5	chr4:8268685..8271204-chr4:8420095..8422355,2	MCF-7	breast:
6	chr4:8419092..8423241-chr4:8430004..8433236,3	MCF-7	breast:
7	chr4:8429725..8430462-chrX:12992795..12993539,2	HCT-116	colon:
8	chr4:8416707..8419298-chr4:8428396..8430193,3	MCF-7	breast:
9	chr4:8429704..8431761-chr4:8439023..8440743,2	MCF-7	breast:
10	chr4:8421637..8423534-chr4:8447080..8448932,2	K562	blood:
11	chr4:8429518..8431924-chr4:8437588..8440150,2	MCF-7	breast:

Variant related genes	Relation type
ACOX3	TF binding region
ACOX3	CpG island
ENSG00000205542	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000155275	chromatin interactions

Extended variants
information (count: 523 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562607895	chr4:8418977-8418978	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs2631765	chr4:8418997-8418998	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs551349161	chr4:8419005-8419006	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572953603	chr4:8419029-8419030	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs533788824	chr4:8419030-8419031	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566582713	chr4:8419045-8419046	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2631764	chr4:8419052-8419053	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs549099155	chr4:8419076-8419077	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs188620979	chr4:8419117-8419118	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373117069	chr4:8419144-8419145	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs538036703	chr4:8419146-8419147	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556829985	chr4:8419147-8419148	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs578164974	chr4:8419180-8419181	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538648155	chr4:8419192-8419193	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs115999866	chr4:8419198-8419199	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11721377	chr4:8419205-8419206	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs542758152	chr4:8419207-8419208	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs143871055	chr4:8419215-8419216	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs561202327	chr4:8419235-8419236	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs10022276	chr4:8419239-8419240	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs145488597	chr4:8419255-8419256	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs145627523	chr4:8419257-8419258	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs143762209	chr4:8419276-8419277	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs562805425	chr4:8419300-8419301	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564845784	chr4:8419333-8419334	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs533223271	chr4:8419358-8419359	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs146854900	chr4:8419388-8419389	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs56727681	chr4:8419424-8419425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs371869029	chr4:8419427-8419428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs561529860	chr4:8419436-8419437	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs527258438	chr4:8419438-8419439	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192996059	chr4:8419471-8419472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541786671	chr4:8419473-8419474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs148845526	chr4:8419498-8419499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs542227838	chr4:8419503-8419504	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs538453778	chr4:8419544-8419545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs142582571	chr4:8419597-8419598	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs28591490	chr4:8419637-8419638	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs538986921	chr4:8419663-8419664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374433030	chr4:8419674-8419675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554040943	chr4:8419698-8419699	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572134473	chr4:8419721-8419722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536229155	chr4:8419757-8419758	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs377009230	chr4:8419785-8419786	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576413280	chr4:8419806-8419807	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544405522	chr4:8419807-8419808	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs370284466	chr4:8419883-8419884	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs560176959	chr4:8419924-8419925	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs562583697	chr4:8420017-8420018	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577912626	chr4:8420035-8420036	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8383800-8419000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr4:8396600-8419400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:8397600-8420400	Weak transcription	NHDF-Ad	bronchial
4	chr4:8399600-8429400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:8403200-8419400	Strong transcription	Fetal Intestine Small	intestine
6	chr4:8404600-8429400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr4:8404800-8420600	Weak transcription	Psoas Muscle	Psoas
8	chr4:8407800-8419200	Weak transcription	Fetal Thymus	thymus
9	chr4:8408800-8422400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:8411000-8419000	Strong transcription	Pancreas	Pancrea
11	chr4:8412400-8421000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr4:8412800-8420600	Weak transcription	K562	blood
13	chr4:8412800-8425600	Weak transcription	Fetal Heart	heart
14	chr4:8413000-8419000	Strong transcription	Fetal Brain Female	brain
15	chr4:8413000-8419200	Strong transcription	Fetal Intestine Large	intestine
16	chr4:8413000-8419400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:8413000-8419400	Strong transcription	Fetal Stomach	stomach
18	chr4:8413000-8423400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr4:8415200-8419000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:8415600-8419400	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr4:8416400-8421400	Weak transcription	HSMM	muscle
22	chr4:8416400-8428000	Weak transcription	Fetal Brain Male	brain
23	chr4:8416800-8419200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:8416800-8421200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:8416800-8421400	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr4:8416800-8429000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr4:8416800-8429000	Weak transcription	Brain Substantia Nigra	brain
28	chr4:8416800-8429000	Weak transcription	Fetal Kidney	kidney
29	chr4:8416800-8429000	Weak transcription	HUVEC	blood vessel
30	chr4:8417000-8419400	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr4:8417000-8420800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:8417000-8421200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr4:8417000-8421600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr4:8417000-8428400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr4:8417000-8429000	Weak transcription	Small Intestine	intestine
36	chr4:8417200-8421200	Weak transcription	NHLF	lung
37	chr4:8417400-8419400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr4:8417600-8428800	Weak transcription	Dnd41	blood
39	chr4:8417800-8419200	Enhancers	Right Atrium	heart
40	chr4:8417800-8420000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr4:8417800-8421200	Weak transcription	Rectal Smooth Muscle	rectum
42	chr4:8417800-8421400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr4:8417800-8421400	Weak transcription	NH-A	brain
44	chr4:8417800-8428400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr4:8417800-8428800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr4:8417800-8428800	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr4:8417800-8429000	Weak transcription	Primary B cells from cord blood	blood
48	chr4:8417800-8429000	Weak transcription	Colonic Mucosa	Colon
49	chr4:8417800-8429000	Weak transcription	HSMMtube	muscle
50	chr4:8417800-8429200	Weak transcription	Fetal Lung	lung

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