Variant report

Variant	nsv1061402
Chromosome Location	chr20:719396-896396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3412)
CpG islands
(count:3179)
Chromatin interactive
region (count:134)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3412 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:741674-741770	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:794066-794292	K562	blood:	n/a	n/a
3	ARID3A	chr20:817391-817685	K562	blood:	n/a	n/a
4	ARID3A	chr20:799748-799764	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:796695-796966	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:814187-814420	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:809669-810137	K562	blood:	n/a	n/a
8	ARID3A	chr20:719725-719858	K562	blood:	n/a	n/a
9	ARID3A	chr20:719728-720037	HepG2	liver:	n/a	n/a
10	ARID3A	chr20:746914-747005	HepG2	liver:	n/a	n/a
11	ARID3A	chr20:799025-799096	K562	blood:	n/a	n/a
12	ATF1	chr20:731389-731802	K562	blood:	n/a	n/a
13	ATF1	chr20:806807-806958	K562	blood:	n/a	n/a
14	ATF1	chr20:817307-817664	K562	blood:	n/a	n/a
15	ATF1	chr20:809653-810115	K562	blood:	n/a	n/a
16	ATF1	chr20:750466-750808	K562	blood:	n/a	n/a
17	ATF1	chr20:869910-870110	K562	blood:	n/a	n/a
18	ATF1	chr20:794093-794293	K562	blood:	n/a	n/a
19	ATF2	chr20:814020-814521	GM12878	blood:	n/a	n/a
20	ATF2	chr20:731380-731755	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr20:865629-865937	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr20:741570-741924	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr20:731335-731768	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr20:750526-750853	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr20:731513-731698	K562	blood:	n/a	n/a
26	ATF3	chr20:750522-750750	K562	blood:	n/a	n/a
27	ATF3	chr20:796598-797055	A549	lung:	n/a	n/a
28	ATF3	chr20:726400-726708	K562	blood:	n/a	n/a
29	BACH1	chr20:749353-749495	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr20:814355-814744	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr20:822325-822826	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr20:865721-866064	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr20:741708-741984	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL11A	chr20:814231-814508	GM12878	blood:	n/a	chr20:814382-814391
35	BCL11A	chr20:872390-872700	GM12878	blood:	n/a	n/a
36	BCL11A	chr20:744968-745227	GM12878	blood:	n/a	n/a
37	BCL3	chr20:814181-814710	A549	lung:	n/a	chr20:814382-814391
38	BCLAF1	chr20:814125-814548	GM12878	blood:	n/a	chr20:814382-814391
39	BCLAF1	chr20:827526-828016	GM12878	blood:	n/a	n/a
40	BHLHE40	chr20:741653-741929	HepG2	liver:	n/a	n/a
41	BHLHE40	chr20:827662-827773	GM12878	blood:	n/a	n/a
42	BHLHE40	chr20:872419-872632	GM12878	blood:	n/a	n/a
43	BHLHE40	chr20:814067-814668	K562	blood:	n/a	n/a
44	BHLHE40	chr20:810653-811103	K562	blood:	n/a	n/a
45	BHLHE40	chr20:726935-726995	A549	lung:	n/a	n/a
46	BHLHE40	chr20:741806-741815	GM12878	blood:	n/a	n/a
47	BHLHE40	chr20:749328-749671	K562	blood:	n/a	n/a
48	BHLHE40	chr20:796726-797003	GM12878	blood:	n/a	n/a
49	BHLHE40	chr20:741545-741987	K562	blood:	n/a	n/a
50	BHLHE40	chr20:799729-799886	GM12878	blood:	n/a	n/a

(count:3179 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:821854-821904	HUVEC	blood vessel:	n/a
2	chr20:825798-825848	Jurkat	blood:	n/a
3	chr20:824641-824691	HCPEpiC	choroid plexus:	n/a
4	chr20:865780-865830	AoSMC	blood vessel:	n/a
5	chr20:749148-749198	HRPEpiC	eye:	n/a
6	chr20:826023-826073	PrEC	prostate:	n/a
7	chr20:896349-896399	NT2-D1	testis:	n/a
8	chr20:821854-821904	HUVEC	blood vessel:	n/a
9	chr20:825798-825848	Jurkat	blood:	n/a
10	chr20:824641-824691	HCPEpiC	choroid plexus:	n/a
11	chr20:865780-865830	AoSMC	blood vessel:	n/a
12	chr20:749148-749198	HRPEpiC	eye:	n/a
13	chr20:826023-826073	PrEC	prostate:	n/a
14	chr20:896349-896399	NT2-D1	testis:	n/a
15	chr20:741798-741848	HEK293	kidney:	embryo
16	chr20:825415-825465	ProgFib	skin:	n/a
17	chr20:825052-825102	NHBE	bronchial:	n/a
18	chr20:825489-825539	AG09319	gingival:	n/a
19	chr20:866011-866061	HCPEpiC	choroid plexus:	n/a
20	chr20:824422-824472	SK-N-SH_RA	brain:	n/a
21	chr20:824641-824691	NH-A	brain:	n/a
22	chr20:741049-741099	MCF10A-Er-Src	breast:	n/a
23	chr20:868404-868454	HPAEpiC	pulmonary alveolar:	n/a
24	chr20:819800-819850	HCPEpiC	choroid plexus:	n/a
25	chr20:821854-821904	AG04449	skin:	fetal
26	chr20:896349-896399	CMK	blood:	n/a
27	chr20:819800-819850	PFSK-1	brain:	n/a
28	chr20:825268-825318	Hela-S3	cervix:	n/a
29	chr20:865954-866004	NH-A	brain:	n/a
30	chr20:745857-745907	K562	blood:	n/a
31	chr20:749581-749631	Caco-2	colon:	n/a
32	chr20:865780-865830	PANC-1	pancreas:	n/a
33	chr20:825798-825848	SK-N-SH	brain:	n/a
34	chr20:825155-825205	SK-N-SH_RA	brain:	n/a
35	chr20:819058-819108	HCPEpiC	choroid plexus:	n/a
36	chr20:810805-810855	NB4	blood:	n/a
37	chr20:749452-749502	IMR90	lung:	fetal
38	chr20:749620-749670	Hepatocyte	liver:	n/a
39	chr20:749360-749410	K562	blood:	n/a
40	chr20:828445-828495	NT2-D1	testis:	n/a
41	chr20:749264-749314	HUVEC	blood vessel:	n/a
42	chr20:749148-749198	GM12891	blood:	n/a
43	chr20:749620-749670	Hela-S3	cervix:	n/a
44	chr20:868404-868454	HMEC	breast:	n/a
45	chr20:738228-738278	HL-60	blood:	n/a
46	chr20:741049-741099	CMK	blood:	n/a
47	chr20:825268-825318	IMR90	lung:	fetal
48	chr20:814018-814068	HMEC	breast:	n/a
49	chr20:866011-866061	U87	brain:	n/a
50	chr20:825050-825100	K562	blood:	n/a

(count:134 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr20:275232..277610-chr20:801954..804825,2	MCF-7	breast:
2	chr20:821988..824622-chr20:841989..843992,2	MCF-7	breast:
3	chr20:812809..815721-chr20:816075..817660,2	K562	blood:
4	chr20:837275..840230-chr20:841827..843655,2	K562	blood:
5	chr20:835633..837768-chr20:861494..863421,2	MCF-7	breast:
6	chr20:796367..797247-chr20:1166167..1167087,2	K562	blood:
7	chr20:542088..543085-chr20:719214..720627,6	K562	blood:
8	chr20:819782..827633-chr20:832117..838793,13	MCF-7	breast:
9	chr20:821988..824622-chr20:841989..843992,2	MCF-7	breast:
10	chr20:725665..728031-chr20:732791..734536,2	MCF-7	breast:
11	chr20:827615..829862-chr20:830372..832025,2	K562	blood:
12	chr20:796394..796933-chr20:954059..954656,3	MCF-7	breast:
13	chr20:796433..797362-chr20:934372..935366,3	MCF-7	breast:
14	chr20:814267..817072-chr20:819409..823678,4	K562	blood:
15	chr20:809347..810136-chr20:883815..884702,3	MCF-7	breast:
16	chr20:827615..829862-chr20:830372..832025,2	K562	blood:
17	chr20:755472..758240-chr20:773959..776472,2	K562	blood:
18	chr20:822774..824737-chr20:855647..857303,2	MCF-7	breast:
19	chr20:799309..799872-chr20:1193704..1194207,2	K562	blood:
20	chr20:796451..797739-chr20:936332..938013,6	MCF-7	breast:
21	chr20:859998..862638-chr20:865942..867662,2	MCF-7	breast:
22	chr20:824353..826302-chr20:829157..830739,3	MCF-7	breast:
23	chr20:741861..745276-chr20:746924..750628,4	MCF-7	breast:
24	chr20:727366..729723-chr20:730847..732789,2	MCF-7	breast:
25	chr20:820561..824407-chr20:840052..842078,3	MCF-7	breast:
26	chr20:719552..720453-chr20:748969..749783,5	MCF-7	breast:
27	chr20:822278..824306-chr20:931602..934155,2	MCF-7	breast:
28	chr20:858282..861279-chr20:864400..866707,2	K562	blood:
29	chr20:796973..799654-chr20:935425..937231,3	MCF-7	breast:
30	chr20:826039..828465-chr20:834525..836848,2	MCF-7	breast:
31	chr20:755408..757214-chr20:780386..782814,2	K562	blood:
32	chr20:809172..812066-chr20:1165154..1167156,2	K562	blood:
33	chr20:852716..855499-chr20:860889..862928,2	MCF-7	breast:
34	chr20:725665..728031-chr20:732791..734536,2	MCF-7	breast:
35	chr20:809429..810296-chr20:934002..934836,4	MCF-7	breast:
36	chr20:807439..809063-chr20:811030..813356,2	K562	blood:
37	chr20:766780..768668-chr20:768839..771675,2	K562	blood:
38	chr20:822258..824551-chr20:869597..872027,2	MCF-7	breast:
39	chr20:857198..860086-chr20:873899..876217,2	MCF-7	breast:
40	chr20:807439..809063-chr20:811030..813356,2	K562	blood:
41	chr20:820613..823801-chr20:828835..832638,4	MCF-7	breast:
42	chr20:822774..824737-chr20:855647..857303,2	MCF-7	breast:
43	chr20:837275..840230-chr20:841827..843655,2	K562	blood:
44	chr20:814267..817019-chr20:821778..823678,2	K562	blood:
45	chr20:873612..875715-chr20:890183..892090,2	MCF-7	breast:
46	chr20:633613..634272-chr20:749070..749583,2	MCF-7	breast:
47	chr20:796342..797345-chr20:1193228..1194213,7	K562	blood:
48	chr20:814056..816393-chr20:824842..826846,2	K562	blood:
49	chr20:795971..798592-chr20:1088123..1090467,2	K562	blood:
50	chr20:542038..542591-chr20:719478..720235,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCRT2-1	chr20:748941-749126	NONHSAT078080
2	lnc-ANGPT4-1	chr20:837119-838075	NONHSAT078083
3	lnc-SCRT2-1	chr20:746594-746978	NONHSAT078080

No data

Variant related genes	Relation type
FAM110A	TF binding region
SLC52A3	TF binding region
ENSG00000101278	TF binding region
FAM110A	CpG island
SLC52A3	CpG island
ENSG00000101278	CpG island
ENSG00000101278	chromatin interactions
ENSG00000125898	chromatin interactions
ENSG00000101280	chromatin interactions
ENSG00000101276	chromatin interactions
ENSG00000168066	chromatin interactions
ENSG00000125895	chromatin interactions
ENSG00000271303	chromatin interactions
ENSG00000125818	chromatin interactions

Extended variants
information (count: 7265 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:7265 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551305686	chr20:719421-719422	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs544463281	chr20:719466-719467	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs561252247	chr20:719526-719527	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143293529	chr20:719568-719569	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs558144458	chr20:719577-719578	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188613138	chr20:719588-719589	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs560558733	chr20:719634-719635	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148312224	chr20:719637-719638	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs552435010	chr20:719673-719674	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562857943	chr20:719691-719692	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2317023	chr20:719740-719741	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs531743999	chr20:719741-719742	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs540727814	chr20:719776-719777	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs368555244	chr20:719780-719781	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs548456977	chr20:719821-719822	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568383968	chr20:719852-719853	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs1884639	chr20:719854-719855	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs547552883	chr20:719882-719883	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs1884640	chr20:719883-719884	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs112813069	chr20:719887-719888	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570602675	chr20:719916-719917	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs75987662	chr20:720071-720072	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372796351	chr20:720093-720094	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs377205680	chr20:720104-720105	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs115554221	chr20:720119-720120	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370165907	chr20:720146-720147	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs535106674	chr20:720157-720158	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs561566650	chr20:720177-720178	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs374564670	chr20:720178-720179	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs532029555	chr20:720188-720189	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs55719633	chr20:720218-720219	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575063850	chr20:720222-720223	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs60957781	chr20:720243-720244	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs560732782	chr20:720264-720265	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181324624	chr20:720298-720299	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546236236	chr20:720309-720310	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs141992068	chr20:720313-720314	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs145632637	chr20:720326-720327	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542258396	chr20:720345-720346	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371132334	chr20:720367-720368	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368063478	chr20:720428-720429	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527581114	chr20:720472-720473	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs547415593	chr20:720481-720482	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs185847969	chr20:720494-720495	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs374550171	chr20:720504-720505	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs59488666	chr20:720512-720513	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs56839494	chr20:720518-720519	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs116049467	chr20:720521-720522	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs535210149	chr20:720541-720542	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs76851912	chr20:720558-720559	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	17426248	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3330 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:713600-719400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr20:714400-719400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr20:714800-721400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr20:717800-719400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr20:718200-719400	Weak transcription	Placenta	Placenta
6	chr20:718200-720000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr20:718600-720200	Enhancers	A549	lung
8	chr20:719400-719600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr20:719400-719800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr20:719400-719800	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr20:719400-720200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr20:719400-720200	Enhancers	Brain Angular Gyrus	brain
13	chr20:719400-720800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr20:719400-721400	Enhancers	Fetal Intestine Large	intestine
15	chr20:719400-722400	Enhancers	Placenta	Placenta
16	chr20:719600-719800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr20:719600-719800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
18	chr20:719600-719800	Bivalent Enhancer	HepG2	liver
19	chr20:719600-720000	Enhancers	Brain Germinal Matrix	brain
20	chr20:719600-720000	Enhancers	Ovary	ovary
21	chr20:719600-720200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr20:719600-720200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr20:719600-720200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr20:719600-720200	Enhancers	Fetal Muscle Leg	muscle
25	chr20:719600-720200	Enhancers	K562	blood
26	chr20:719600-720400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr20:719800-720000	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr20:719800-720000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
29	chr20:719800-720200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
30	chr20:719800-720200	Flanking Bivalent TSS/Enh	HepG2	liver
31	chr20:719800-721000	Enhancers	Stomach Mucosa	stomach
32	chr20:720000-721400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr20:720200-720600	Bivalent Enhancer	HepG2	liver
34	chr20:720200-720800	Weak transcription	K562	blood
35	chr20:720400-720800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr20:720400-721000	Enhancers	HMEC	breast
37	chr20:720600-721000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr20:720800-721000	Enhancers	K562	blood
39	chr20:720800-721200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr20:720800-721600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr20:721200-721400	Enhancers	Esophagus	oesophagus
42	chr20:721400-721600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr20:721400-721600	Bivalent Enhancer	Esophagus	oesophagus
44	chr20:728000-735000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr20:730800-731600	Enhancers	Fetal Intestine Small	intestine
46	chr20:731200-731600	Enhancers	Fetal Intestine Large	intestine
47	chr20:731400-731600	Enhancers	Fetal Muscle Leg	muscle
48	chr20:731400-731600	Enhancers	Stomach Mucosa	stomach
49	chr20:731400-731800	Enhancers	Gastric	stomach
50	chr20:731400-732000	Enhancers	K562	blood

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