Variant report

Variant	nsv482316
Chromosome Location	chr4:48151953-48338746
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3453)
CpG islands
(count:1587)
Chromatin interactive
region (count:182)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3453 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48308510-48308668	K562	blood:	n/a	n/a
2	ARID3A	chr4:48199618-48200001	K562	blood:	n/a	n/a
3	ARID3A	chr4:48260893-48260896	K562	blood:	n/a	n/a
4	ARID3A	chr4:48214291-48214523	K562	blood:	n/a	n/a
5	ARID3A	chr4:48318058-48318358	K562	blood:	n/a	n/a
6	ARID3A	chr4:48292311-48292743	K562	blood:	n/a	n/a
7	ARID3A	chr4:48236621-48236842	K562	blood:	n/a	n/a
8	ARID3A	chr4:48331307-48331648	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:48307560-48307777	K562	blood:	n/a	n/a
10	ARID3A	chr4:48318112-48318426	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:48271978-48272494	K562	blood:	n/a	n/a
12	ARID3A	chr4:48189758-48190105	K562	blood:	n/a	n/a
13	ARID3A	chr4:48245400-48245848	K562	blood:	n/a	n/a
14	ARID3A	chr4:48164388-48164498	K562	blood:	n/a	n/a
15	ARID3A	chr4:48231013-48231317	K562	blood:	n/a	n/a
16	ARID3A	chr4:48271156-48271462	K562	blood:	n/a	n/a
17	ARID3A	chr4:48205747-48206212	K562	blood:	n/a	n/a
18	ARID3A	chr4:48249420-48249934	K562	blood:	n/a	n/a
19	ARID3A	chr4:48277272-48277623	K562	blood:	n/a	n/a
20	ATF1	chr4:48189913-48190232	K562	blood:	n/a	n/a
21	ATF1	chr4:48336827-48337337	K562	blood:	n/a	n/a
22	ATF1	chr4:48221517-48221791	K562	blood:	n/a	n/a
23	ATF1	chr4:48245408-48245828	K562	blood:	n/a	n/a
24	ATF1	chr4:48249224-48249377	K562	blood:	n/a	n/a
25	ATF1	chr4:48272999-48273508	K562	blood:	n/a	n/a
26	ATF1	chr4:48214196-48214612	K562	blood:	n/a	n/a
27	ATF1	chr4:48231005-48231283	K562	blood:	n/a	n/a
28	ATF1	chr4:48332142-48332339	K562	blood:	n/a	n/a
29	ATF1	chr4:48240069-48240358	K562	blood:	n/a	n/a
30	ATF1	chr4:48254522-48254801	K562	blood:	n/a	n/a
31	ATF1	chr4:48257322-48257741	K562	blood:	n/a	n/a
32	ATF1	chr4:48205774-48206215	K562	blood:	n/a	n/a
33	ATF1	chr4:48318081-48318455	K562	blood:	n/a	n/a
34	ATF2	chr4:48271260-48271747	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr4:48249067-48249653	GM12878	blood:	n/a	n/a
36	ATF2	chr4:48175511-48176214	GM12878	blood:	n/a	n/a
37	ATF2	chr4:48205320-48205690	GM12878	blood:	n/a	n/a
38	ATF2	chr4:48198537-48199201	GM12878	blood:	n/a	n/a
39	ATF2	chr4:48155708-48156417	GM12878	blood:	n/a	n/a
40	ATF2	chr4:48213476-48214744	GM12878	blood:	n/a	n/a
41	ATF2	chr4:48175444-48176110	GM12878	blood:	n/a	n/a
42	ATF2	chr4:48214100-48214829	GM12878	blood:	n/a	n/a
43	ATF2	chr4:48197230-48199822	GM12878	blood:	n/a	n/a
44	ATF2	chr4:48271888-48272435	GM12878	blood:	n/a	n/a
45	ATF2	chr4:48205274-48206233	GM12878	blood:	n/a	n/a
46	ATF2	chr4:48272043-48272668	GM12878	blood:	n/a	n/a
47	ATF2	chr4:48271289-48271867	GM12878	blood:	n/a	n/a
48	ATF2	chr4:48155652-48156227	GM12878	blood:	n/a	n/a
49	ATF2	chr4:48212319-48212836	GM12878	blood:	n/a	n/a
50	ATF3	chr4:48205452-48205645	GM12878	blood:	n/a	n/a

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48271893-48271943	HCPEpiC	choroid plexus:	n/a
2	chr4:48271893-48271943	HCPEpiC	choroid plexus:	n/a
3	chr4:48188522-48188572	HEEpiC	esophagus:	n/a
4	chr4:48231543-48231593	NHDF-neo	bronchial:	n/a
5	chr4:48271835-48271885	HRCEpiC	kidney:	n/a
6	chr4:48271835-48271885	A549	lung:	n/a
7	chr4:48272059-48272109	HRPEpiC	eye:	n/a
8	chr4:48231543-48231593	HNPCEpiC	eye:	n/a
9	chr4:48271072-48271122	AoSMC	blood vessel:	n/a
10	chr4:48271072-48271122	HIPEpiC	eye:	n/a
11	chr4:48271923-48271973	T-47D	breast:	n/a
12	chr4:48257144-48257194	MCF-7	breast:	n/a
13	chr4:48271826-48271876	HRE	kidney:	n/a
14	chr4:48271072-48271122	T-47D	breast:	n/a
15	chr4:48271893-48271943	ProgFib	skin:	n/a
16	chr4:48176413-48176463	MCF-7	breast:	n/a
17	chr4:48273240-48273290	NB4	blood:	n/a
18	chr4:48271942-48271992	A549	lung:	n/a
19	chr4:48271149-48271199	HCF	heart:	n/a
20	chr4:48271149-48271199	HIPEpiC	eye:	n/a
21	chr4:48271893-48271943	PFSK-1	brain:	n/a
22	chr4:48271942-48271992	NHDF-neo	bronchial:	n/a
23	chr4:48272059-48272109	MCF-7	breast:	n/a
24	chr4:48271107-48271157	BE2_C	brain:	n/a
25	chr4:48272513-48272563	PFSK-1	brain:	n/a
26	chr4:48271149-48271199	BE2_C	brain:	n/a
27	chr4:48271893-48271943	NH-A	brain:	n/a
28	chr4:48272077-48272127	GM19239	blood:	n/a
29	chr4:48271121-48271171	HIPEpiC	eye:	n/a
30	chr4:48271149-48271199	HMEC	breast:	n/a
31	chr4:48271149-48271199	HRCEpiC	kidney:	n/a
32	chr4:48271918-48271968	NB4	blood:	n/a
33	chr4:48188143-48188193	T-47D	breast:	n/a
34	chr4:48272059-48272109	AG09309	skin:	n/a
35	chr4:48271826-48271876	SK-N-MC	brain:	n/a
36	chr4:48272266-48272316	HRCEpiC	kidney:	n/a
37	chr4:48271918-48271968	HepG2	liver:	n/a
38	chr4:48272266-48272316	LNCaP	prostate:	n/a
39	chr4:48271893-48271943	Caco-2	colon:	n/a
40	chr4:48231543-48231593	HMEC	breast:	n/a
41	chr4:48257144-48257194	ECC-1	luminal epithelium:	n/a
42	chr4:48175353-48175403	Jurkat	blood:	n/a
43	chr4:48271923-48271973	HRPEpiC	eye:	n/a
44	chr4:48273240-48273290	Hela-S3	cervix:	n/a
45	chr4:48269743-48269793	MCF-7	breast:	n/a
46	chr4:48271121-48271171	NHDF-neo	bronchial:	n/a
47	chr4:48301717-48301767	H1-hESC	embryonic stem cell:	embryo
48	chr4:48188522-48188572	T-47D	breast:	n/a
49	chr4:48271121-48271171	HCPEpiC	choroid plexus:	n/a
50	chr4:48272513-48272563	HRPEpiC	eye:	n/a

(count:182 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:48222033..48225544-chr4:48235946..48240353,4	K562	blood:
2	chr4:48128237..48129739-chr4:48292379..48294258,2	K562	blood:
3	chr4:48248411..48250691-chr4:48255149..48257827,3	K562	blood:
4	chr4:48270643..48273355-chr4:48275449..48277966,4	K562	blood:
5	chr4:48295312..48297676-chr4:48299825..48301786,2	MCF-7	breast:
6	chr4:48171039..48173617-chr4:48175205..48177661,3	MCF-7	breast:
7	chr4:48322582..48327982-chr4:48329571..48333922,4	K562	blood:
8	chr4:48222033..48225544-chr4:48235946..48240353,4	K562	blood:
9	chr4:48184426..48187348-chr4:48194025..48197135,3	K562	blood:
10	chr4:48164755..48167571-chr4:48169298..48171997,3	MCF-7	breast:
11	chr4:48251770..48253352-chr4:48260141..48262130,2	K562	blood:
12	chr4:48255711..48257883-chr4:48270489..48272038,2	MCF-7	breast:
13	chr2:96873932..96874574-chr4:48271406..48272081,2	Hela-S3	cervix:
14	chr4:48173393..48175271-chr4:48298166..48300256,2	K562	blood:
15	chr4:48274201..48276645-chr4:48276828..48280429,3	K562	blood:
16	chr4:48171039..48173617-chr4:48175205..48177661,3	MCF-7	breast:
17	chr4:48214281..48216760-chr4:48261228..48263562,2	K562	blood:
18	chr4:48238892..48241068-chr4:48247777..48249287,2	K562	blood:
19	chr4:48190967..48193401-chr4:48269923..48272696,2	K562	blood:
20	chr4:48214281..48216760-chr4:48261228..48263562,2	K562	blood:
21	chr4:48262092..48265166-chr4:48265573..48268015,3	K562	blood:
22	chr4:48294874..48299158-chr4:48300568..48304359,7	K562	blood:
23	chr4:48250701..48254731-chr4:48255352..48259390,5	K562	blood:
24	chr4:48256167..48259627-chr4:48260322..48264297,6	K562	blood:
25	chr17:74448509..74449477-chr4:48271558..48272150,2	Hela-S3	cervix:
26	chr4:48239378..48241079-chr4:48271387..48273021,2	MCF-7	breast:
27	chr4:48174022..48176386-chr4:48181420..48183923,2	K562	blood:
28	chr4:48248891..48252665-chr4:48270333..48273467,3	MCF-7	breast:
29	chr4:48211265..48214247-chr4:48216270..48217913,2	K562	blood:
30	chr4:48258706..48261232-chr4:48269979..48272552,2	MCF-7	breast:
31	chr4:48238807..48240507-chr4:48244867..48247720,2	K562	blood:
32	chr4:48206028..48209307-chr4:48238256..48241207,3	K562	blood:
33	chr4:48238892..48241068-chr4:48247777..48249287,2	K562	blood:
34	chr4:48168015..48170294-chr4:48173927..48176191,2	K562	blood:
35	chr4:48214305..48216308-chr4:48218289..48220414,2	K562	blood:
36	chr4:48322582..48325559-chr4:48331467..48333922,2	K562	blood:
37	chr4:48270379..48272614-chr4:48278296..48280074,2	K562	blood:
38	chr4:48204459..48206911-chr4:48210318..48213685,3	K562	blood:
39	chr4:48169322..48172122-chr4:48178324..48180864,2	K562	blood:
40	chr4:48129602..48130429-chr4:48277151..48277985,3	MCF-7	breast:
41	chr4:48238606..48240406-chr4:48242704..48244753,3	K562	blood:
42	chr4:48175263..48177129-chr4:48197621..48199593,2	K562	blood:
43	chr4:48250701..48254731-chr4:48255352..48259390,5	K562	blood:
44	chr4:48169322..48172122-chr4:48178324..48180864,2	K562	blood:
45	chr4:48238807..48240507-chr4:48244867..48247720,2	K562	blood:
46	chr4:48222218..48225128-chr4:48229730..48232280,2	K562	blood:
47	chr2:33218746..33219424-chr4:48292388..48293103,2	MCF-7	breast:
48	chr4:48260906..48263782-chr4:48270701..48272361,2	K562	blood:
49	chr4:48214305..48216308-chr4:48218289..48220414,2	K562	blood:
50	chr4:48191298..48193401-chr4:48269923..48271820,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TEC-1	chr4:48304519-48305067	NONHSAT096284

No data

Variant related genes	Relation type
TEC	TF binding region
SLAIN2	TF binding region
ENSG00000202014	TF binding region
TEC	CpG island
SLAIN2	CpG island
ENSG00000202014	CpG island
ENSG00000163659	chromatin interactions
ENSG00000108312	chromatin interactions
ENSG00000129673	chromatin interactions
ENSG00000127948	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000204685	chromatin interactions
ENSG00000109171	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000084090	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000175931	chromatin interactions
ENSG00000092853	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000243926	chromatin interactions
ENSG00000202014	chromatin interactions
ENSG00000197019	chromatin interactions
ENSG00000145248	chromatin interactions
ENSG00000135605	chromatin interactions
ENSG00000265020	chromatin interactions
ENSG00000163281	chromatin interactions
ENSG00000182831	chromatin interactions
ENSG00000065135	chromatin interactions

Extended variants
information (count: 6255 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:6255 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566063247	chr4:48151971-48151972	Weak transcription Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs16861067	chr4:48152006-48152007	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs557694877	chr4:48152053-48152054	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs576401249	chr4:48152092-48152093	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537383178	chr4:48152131-48152132	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs183572055	chr4:48152163-48152164	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs1156798	chr4:48152195-48152196	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs527292830	chr4:48152197-48152198	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs187444748	chr4:48152200-48152201	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534529655	chr4:48152221-48152222	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs10938522	chr4:48152256-48152257	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs73814677	chr4:48152264-48152265	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs143420941	chr4:48152359-48152360	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs75130319	chr4:48152377-48152378	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs564388874	chr4:48152383-48152384	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs531876743	chr4:48152415-48152416	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs192354426	chr4:48152424-48152425	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs562049154	chr4:48152430-48152431	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs150770724	chr4:48152485-48152486	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs547490435	chr4:48152585-48152586	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184738010	chr4:48152806-48152807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539593190	chr4:48152808-48152809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200628097	chr4:48152854-48152855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375270524	chr4:48152856-48152857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2271175	chr4:48152862-48152863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372899880	chr4:48152870-48152871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150273344	chr4:48152912-48152913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76959651	chr4:48152921-48152922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376360760	chr4:48152936-48152937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201762999	chr4:48152983-48152984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2251240	chr4:48153010-48153011	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs139802691	chr4:48153012-48153013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534593057	chr4:48153065-48153066	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs552724932	chr4:48153109-48153110	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs546417532	chr4:48153138-48153139	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs577666085	chr4:48153155-48153156	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs369893108	chr4:48153223-48153224	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs544820405	chr4:48153257-48153258	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs563055235	chr4:48153504-48153505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552196553	chr4:48153629-48153630	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2661535	chr4:48153654-48153655	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs7654182	chr4:48153706-48153707	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs149793609	chr4:48153752-48153753	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371856050	chr4:48153783-48153784	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547765570	chr4:48153824-48153825	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145716765	chr4:48153841-48153842	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187963585	chr4:48153853-48153854	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148724733	chr4:48153879-48153880	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551851473	chr4:48153892-48153893	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570182513	chr4:48153918-48153919	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	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
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2182 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48129800-48157400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:48130400-48152200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:48130400-48155400	Weak transcription	Psoas Muscle	Psoas
4	chr4:48130400-48156200	Weak transcription	Adipose Nuclei	Adipose
5	chr4:48130400-48156800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr4:48130400-48157600	Weak transcription	Colonic Mucosa	Colon
7	chr4:48132000-48157000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:48132000-48157200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr4:48133000-48153000	Weak transcription	Placenta	Placenta
10	chr4:48137800-48153600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:48138400-48157400	Weak transcription	Aorta	Aorta
12	chr4:48138600-48155800	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr4:48139200-48154600	Weak transcription	Fetal Intestine Small	intestine
14	chr4:48139200-48155600	Weak transcription	Fetal Intestine Large	intestine
15	chr4:48139200-48157600	Weak transcription	Gastric	stomach
16	chr4:48139200-48159000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr4:48139800-48155400	Weak transcription	Spleen	Spleen
18	chr4:48139800-48155800	Weak transcription	Lung	lung
19	chr4:48140200-48157400	Weak transcription	Pancreas	Pancrea
20	chr4:48141000-48152200	Weak transcription	Left Ventricle	heart
21	chr4:48141000-48155800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr4:48141200-48155400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr4:48141800-48155600	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr4:48142400-48155600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr4:48142600-48155400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr4:48142800-48152200	Strong transcription	GM12878-XiMat	blood
27	chr4:48143000-48152200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr4:48143000-48155800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr4:48143000-48157600	Weak transcription	Fetal Thymus	thymus
30	chr4:48143000-48157600	Weak transcription	Thymus	Thymus
31	chr4:48143200-48155600	Weak transcription	Primary T cells from cord blood	blood
32	chr4:48144000-48155400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:48144400-48155800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr4:48144800-48157200	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr4:48146600-48156000	Strong transcription	Primary hematopoietic stem cells	blood
36	chr4:48147600-48155600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr4:48147600-48155600	Weak transcription	Esophagus	oesophagus
38	chr4:48147800-48153000	Weak transcription	Primary B cells from peripheral blood	blood
39	chr4:48147800-48155600	Weak transcription	Duodenum Mucosa	Duodenum
40	chr4:48148000-48155600	Weak transcription	Primary B cells from cord blood	blood
41	chr4:48150000-48164000	Weak transcription	Hela-S3	cervix
42	chr4:48150400-48152600	Strong transcription	Liver	Liver
43	chr4:48151400-48152600	Enhancers	HSMMtube	muscle
44	chr4:48151400-48152600	Strong transcription	K562	blood
45	chr4:48151400-48155800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr4:48151600-48152000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:48151600-48152200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr4:48151600-48152400	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr4:48151600-48152400	Enhancers	Fetal Heart	heart
50	chr4:48151600-48152600	Strong transcription	Rectal Mucosa Donor 29	rectum

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