Variant report

Variant	nsv883214
Chromosome Location	chr5:177876309-178047217
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2047)
CpG islands
(count:5137)
Chromatin interactive
region (count:121)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2047 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:177888233-177888383	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:177880009-177880448	K562	blood:	n/a	n/a
3	ARID3A	chr5:177875635-177876882	K562	blood:	n/a	n/a
4	ARID3A	chr5:177877562-177878156	K562	blood:	n/a	n/a
5	ATF1	chr5:177993173-177993348	K562	blood:	n/a	n/a
6	ATF1	chr5:177876057-177876633	K562	blood:	n/a	n/a
7	ATF1	chr5:177914943-177915183	K562	blood:	n/a	n/a
8	ATF2	chr5:177982753-177983284	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:177982792-177983283	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:177956139-177956325	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:177920408-177920532	K562	blood:	n/a	n/a
12	BACH1	chr5:177934563-177934814	K562	blood:	n/a	n/a
13	BACH1	chr5:177969361-177969365	K562	blood:	n/a	n/a
14	BACH1	chr5:177986972-177987041	K562	blood:	n/a	n/a
15	BACH1	chr5:177886021-177886090	K562	blood:	n/a	n/a
16	BACH1	chr5:178016908-178018114	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:177876133-177876859	K562	blood:	n/a	n/a
18	BACH1	chr5:177888080-177888450	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr5:177984618-177984625	K562	blood:	n/a	n/a
20	BACH1	chr5:177982556-177983199	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr5:178003565-178003761	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr5:178016327-178016499	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr5:178012458-178012770	GM12878	blood:	n/a	n/a
24	BCLAF1	chr5:177876134-177876491	K562	blood:	n/a	n/a
25	BHLHE40	chr5:177956208-177956472	K562	blood:	n/a	n/a
26	BHLHE40	chr5:178045118-178045154	K562	blood:	n/a	n/a
27	BHLHE40	chr5:177929771-177930071	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:178012519-178012877	K562	blood:	n/a	n/a
29	BHLHE40	chr5:178013403-178013420	K562	blood:	n/a	n/a
30	BHLHE40	chr5:177910645-177910908	K562	blood:	n/a	n/a
31	BHLHE40	chr5:177918301-177918460	K562	blood:	n/a	chr5:177918370-177918383
32	BHLHE40	chr5:177930090-177930416	K562	blood:	n/a	n/a
33	BHLHE40	chr5:177880099-177880651	K562	blood:	n/a	n/a
34	BHLHE40	chr5:177895932-177896151	K562	blood:	n/a	n/a
35	BHLHE40	chr5:177974306-177974548	K562	blood:	n/a	n/a
36	BHLHE40	chr5:177962319-177962548	K562	blood:	n/a	n/a
37	BHLHE40	chr5:177910649-177910918	GM12878	blood:	n/a	n/a
38	BHLHE40	chr5:177876113-177877870	K562	blood:	n/a	n/a
39	BHLHE40	chr5:177980034-177980313	K562	blood:	n/a	n/a
40	BHLHE40	chr5:177984564-177984758	K562	blood:	n/a	n/a
41	BHLHE40	chr5:178017646-178018069	K562	blood:	n/a	n/a
42	BHLHE40	chr5:178007428-178007484	K562	blood:	n/a	n/a
43	BHLHE40	chr5:177956283-177956517	GM12878	blood:	n/a	n/a
44	BHLHE40	chr5:177981768-177982464	K562	blood:	n/a	n/a
45	BHLHE40	chr5:178017213-178017413	K562	blood:	n/a	n/a
46	BHLHE40	chr5:177921213-177921579	K562	blood:	n/a	n/a
47	BHLHE40	chr5:177888120-177888558	K562	blood:	n/a	n/a
48	BHLHE40	chr5:177934517-177934717	K562	blood:	n/a	n/a
49	BRCA1	chr5:177888202-177888501	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr5:178012520-178012716	GM12878	blood:	n/a	n/a

(count:5137 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177895047-177895097	CMK	blood:	n/a
2	chr5:178046262-178046312	LNCaP	prostate:	n/a
3	chr5:178017578-178017628	ProgFib	skin:	n/a
4	chr5:178017376-178017426	GM06990	blood:	n/a
5	chr5:177964789-177964839	NHBE	bronchial:	n/a
6	chr5:177890816-177890866	GM12891	blood:	n/a
7	chr5:177947425-177947475	Caco-2	colon:	n/a
8	chr5:177876863-177876913	ProgFib	skin:	n/a
9	chr5:178014801-178014851	NH-A	brain:	n/a
10	chr5:177956199-177956249	GM19239	blood:	n/a
11	chr5:177942856-177942906	HepG2	liver:	n/a
12	chr5:177889945-177889995	HCF	heart:	n/a
13	chr5:177947425-177947475	HEEpiC	esophagus:	n/a
14	chr5:177895047-177895097	CMK	blood:	n/a
15	chr5:178046262-178046312	LNCaP	prostate:	n/a
16	chr5:178017578-178017628	ProgFib	skin:	n/a
17	chr5:178017376-178017426	GM06990	blood:	n/a
18	chr5:177964789-177964839	NHBE	bronchial:	n/a
19	chr5:177890816-177890866	GM12891	blood:	n/a
20	chr5:177947425-177947475	Caco-2	colon:	n/a
21	chr5:177876863-177876913	ProgFib	skin:	n/a
22	chr5:178014801-178014851	NH-A	brain:	n/a
23	chr5:177956199-177956249	GM19239	blood:	n/a
24	chr5:177942856-177942906	HepG2	liver:	n/a
25	chr5:177889945-177889995	HCF	heart:	n/a
26	chr5:177947425-177947475	HEEpiC	esophagus:	n/a
27	chr5:177952737-177952787	MCF10A-Er-Src	breast:	n/a
28	chr5:178017879-178017929	PFSK-1	brain:	n/a
29	chr5:177947425-177947475	BE2_C	brain:	n/a
30	chr5:177952737-177952787	ProgFib	skin:	n/a
31	chr5:178017669-178017719	IMR90	lung:	fetal
32	chr5:178014801-178014851	HCF	heart:	n/a
33	chr5:177916395-177916445	NHBE	bronchial:	n/a
34	chr5:177952711-177952761	HRE	kidney:	n/a
35	chr5:178017578-178017628	AG09319	gingival:	n/a
36	chr5:178004685-178004735	NHBE	bronchial:	n/a
37	chr5:177986696-177986746	PrEC	prostate:	n/a
38	chr5:177951909-177951959	SK-N-SH	brain:	n/a
39	chr5:177876863-177876913	RPTEC	kidney:	n/a
40	chr5:178004012-178004062	HEEpiC	esophagus:	n/a
41	chr5:177952059-177952109	HIPEpiC	eye:	n/a
42	chr5:177949147-177949197	HEK293	kidney:	embryo
43	chr5:178004091-178004141	HIPEpiC	eye:	n/a
44	chr5:177950666-177950716	RPTEC	kidney:	n/a
45	chr5:178017827-178017877	AG09319	gingival:	n/a
46	chr5:177987724-177987774	HCF	heart:	n/a
47	chr5:177953742-177953792	RPTEC	kidney:	n/a
48	chr5:178018968-178019018	NH-A	brain:	n/a
49	chr5:178018015-178018065	NB4	blood:	n/a
50	chr5:177991670-177991720	HEK293	kidney:	embryo

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:177894292..177896063-chr5:177897258..177899224,2	K562	blood:
2	chr5:178039032..178042525-chr5:178047298..178050527,4	K562	blood:
3	chr5:178034097..178036598-chr5:178052522..178054162,2	MCF-7	breast:
4	chr5:177957278..177960312-chr5:177962305..177965618,3	MCF-7	breast:
5	chr5:177629964..177631778-chr5:178045699..178047442,2	K562	blood:
6	chr5:177876265..177878231-chr5:177880241..177881910,2	K562	blood:
7	chr5:178006099..178008478-chr5:178010854..178012707,2	MCF-7	breast:
8	chr5:177894292..177896063-chr5:177897258..177899224,2	K562	blood:
9	chr5:177888252..177888759-chr5:177978244..177978784,2	K562	blood:
10	chr5:178029796..178032282-chr5:178045188..178047536,2	K562	blood:
11	chr5:177888015..177888839-chr5:177977833..177978735,3	MCF-7	breast:
12	chr5:177876012..177877743-chr5:177880216..177882479,2	MCF-7	breast:
13	chr5:178035905..178038376-chr5:178039304..178042820,3	K562	blood:
14	chr5:178039292..178042196-chr5:178044380..178046432,3	K562	blood:
15	chr5:177882178..177883994-chr5:177886180..177888676,2	K562	blood:
16	chr5:177892314..177894580-chr5:177899757..177901738,2	K562	blood:
17	chr5:177876012..177877743-chr5:177880216..177882479,2	MCF-7	breast:
18	chr5:178035506..178039480-chr5:178042939..178045569,4	MCF-7	breast:
19	chr5:177865902..177866648-chr5:177887888..177888885,2	K562	blood:
20	chr5:177706688..177707297-chr5:177977028..177977867,2	MCF-7	breast:
21	chr5:177887719..177888721-chr5:177977307..177978270,3	MCF-7	breast:
22	chr5:177879886..177881970-chr5:177890471..177892015,2	K562	blood:
23	chr5:178022246..178024591-chr5:178025333..178028233,2	MCF-7	breast:
24	chr5:177876786..177879529-chr5:177883377..177886367,2	K562	blood:
25	chr5:177706996..177707580-chr5:177887844..177888573,2	K562	blood:
26	chr5:178022246..178024591-chr5:178025333..178028233,2	MCF-7	breast:
27	chr5:177861655..177863245-chr5:177875652..177877153,2	K562	blood:
28	chr5:177995855..177997941-chr5:178001993..178004774,2	K562	blood:
29	chr5:177888015..177888839-chr5:177977833..177978735,3	MCF-7	breast:
30	chr5:177912045..177914389-chr5:177919098..177921696,2	MCF-7	breast:
31	chr5:178029713..178031440-chr5:178034410..178036578,2	K562	blood:
32	chr5:177767131..177770109-chr5:178047191..178050111,2	MCF-7	breast:
33	chr5:178006099..178008478-chr5:178010854..178012707,2	MCF-7	breast:
34	chr5:178035433..178037862-chr5:178050507..178052447,2	K562	blood:
35	chr5:177871515..177874034-chr5:177875821..177877688,2	MCF-7	breast:
36	chr5:177879706..177881386-chr5:177883345..177884930,2	K562	blood:
37	chr5:178042530..178044673-chr5:178156858..178158969,2	MCF-7	breast:
38	chr5:177768665..177770480-chr5:177878843..177880879,2	K562	blood:
39	chr5:177957278..177960312-chr5:177962305..177965618,3	MCF-7	breast:
40	chr5:177995855..177997941-chr5:178001993..178004774,2	K562	blood:
41	chr5:177915163..177917911-chr5:177920254..177922621,2	K562	blood:
42	chr5:177893036..177895122-chr5:177964444..177967291,2	K562	blood:
43	chr5:177876786..177879529-chr5:177883377..177886367,2	K562	blood:
44	chr5:178001407..178003756-chr5:178005377..178007780,2	K562	blood:
45	chr5:177881991..177885625-chr5:177886030..177888202,3	MCF-7	breast:
46	chr5:178035905..178038376-chr5:178039304..178042820,3	K562	blood:
47	chr5:177633748..177635466-chr5:177877015..177878524,2	K562	blood:
48	chr5:178026410..178028805-chr5:178033864..178036012,2	K562	blood:
49	chr5:177997965..178000895-chr5:178002250..178003802,2	MCF-7	breast:
50	chr5:177892314..177894580-chr5:177899757..177901738,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLK4-2	chr5:177950506-177950714	NONHSAT105537
2	lnc-COL23A1-2	chr5:178046729-178046999	NONHSAT105542
3	lnc-CLK4-2	chr5:177989599-177989727	NONHSAT105537
4	lnc-CLK4-2	chr5:177988845-177989007	NONHSAT105537
5	lnc-CLK4-2	chr5:177987683-177987749	NONHSAT105537

No data

Variant related genes	Relation type
RN7SKP70	TF binding region
COL23A1	TF binding region
CLK4	TF binding region
RN7SKP70	CpG island
COL23A1	CpG island
CLK4	CpG island
ENSG00000169131	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000175309	chromatin interactions
ENSG00000050767	chromatin interactions
ENSG00000252464	chromatin interactions
ENSG00000113240	chromatin interactions

Extended variants
information (count: 7272 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:7272 , 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	rs4976725	chr5:177876309-177876310	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141297777	chr5:177876383-177876384	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs562130084	chr5:177876427-177876428	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs574093482	chr5:177876431-177876432	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs541391568	chr5:177876437-177876438	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs375481583	chr5:177876470-177876471	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs559486619	chr5:177876479-177876480	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs554802726	chr5:177876487-177876488	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs368923460	chr5:177876501-177876502	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs533723282	chr5:177876526-177876527	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs13169031	chr5:177876545-177876546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs560251987	chr5:177876652-177876653	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs146992439	chr5:177876653-177876654	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs548681505	chr5:177876658-177876659	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs116280064	chr5:177876659-177876660	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs7709839	chr5:177876692-177876693	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs369575575	chr5:177876717-177876718	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs187350906	chr5:177876721-177876722	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs546234800	chr5:177876737-177876738	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs138371875	chr5:177876745-177876746	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs76944622	chr5:177876779-177876780	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs556953584	chr5:177876785-177876786	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs370591643	chr5:177876805-177876806	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs7709174	chr5:177876814-177876815	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs192251637	chr5:177876820-177876821	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs555901871	chr5:177876834-177876835	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs574233943	chr5:177876866-177876867	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs541528883	chr5:177876903-177876904	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs6885012	chr5:177876928-177876929	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs577938128	chr5:177876941-177876942	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs545708171	chr5:177876972-177876973	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs372898936	chr5:177877068-177877069	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
33	rs562711441	chr5:177877078-177877079	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
34	rs377620803	chr5:177877111-177877112	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
35	rs78194337	chr5:177877132-177877133	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs531016767	chr5:177877137-177877138	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs184359203	chr5:177877156-177877157	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs188445996	chr5:177877169-177877170	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs532045586	chr5:177877214-177877215	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs192740202	chr5:177877241-177877242	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
41	rs9329147	chr5:177877249-177877250	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs546362437	chr5:177877250-177877251	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
43	rs113413013	chr5:177877258-177877259	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
44	rs535144894	chr5:177877259-177877260	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
45	rs531984087	chr5:177877263-177877264	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
46	rs76765801	chr5:177877325-177877326	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
47	rs58925950	chr5:177877330-177877331	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs184416015	chr5:177877336-177877337	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
49	rs554845904	chr5:177877337-177877338	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs566656760	chr5:177877402-177877403	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	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
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2853 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177856800-177887200	Weak transcription	Right Atrium	heart
2	chr5:177871800-177880600	Weak transcription	Fetal Thymus	thymus
3	chr5:177874600-177888200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:177875600-177876400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr5:177875600-177876400	Enhancers	Right Ventricle	heart
6	chr5:177876200-177876400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:177876200-177876400	Active TSS	Brain Cingulate Gyrus	brain
8	chr5:177876200-177876400	Enhancers	Brain Hippocampus Middle	brain
9	chr5:177876200-177876400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr5:177876200-177876400	Bivalent Enhancer	Placenta	Placenta
11	chr5:177876200-177876400	Active TSS	K562	blood
12	chr5:177876200-177876400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
13	chr5:177876200-177876600	Enhancers	Brain Angular Gyrus	brain
14	chr5:177876200-177876800	Bivalent Enhancer	Primary B cells from cord blood	blood
15	chr5:177876200-177877000	Enhancers	Left Ventricle	heart
16	chr5:177876200-177877400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr5:177876200-177877600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr5:177876200-177877600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr5:177876200-177877600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:177876200-177877600	Enhancers	Gastric	stomach
21	chr5:177876200-177877600	Enhancers	Spleen	Spleen
22	chr5:177876200-177877800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr5:177876200-177877800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr5:177876200-177878000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr5:177876400-177876600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:177876400-177876600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr5:177876400-177876600	Flanking Active TSS	Brain Cingulate Gyrus	brain
28	chr5:177876400-177876600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
29	chr5:177876400-177876800	Active TSS	Brain Hippocampus Middle	brain
30	chr5:177876400-177877000	Bivalent Enhancer	Stomach Mucosa	stomach
31	chr5:177876400-177877200	Enhancers	Fetal Heart	heart
32	chr5:177876400-177877400	Weak transcription	Right Ventricle	heart
33	chr5:177876400-177877800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr5:177876400-177877800	Flanking Active TSS	K562	blood
35	chr5:177876600-177876800	Active TSS	Brain Cingulate Gyrus	brain
36	chr5:177876600-177877000	Flanking Active TSS	Brain Angular Gyrus	brain
37	chr5:177876600-177877200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
38	chr5:177876800-177877000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr5:177876800-177877000	Flanking Active TSS	Brain Cingulate Gyrus	brain
40	chr5:177876800-177877000	Flanking Active TSS	Brain Hippocampus Middle	brain
41	chr5:177876800-177877200	Enhancers	Primary hematopoietic stem cells	blood
42	chr5:177876800-177877200	Enhancers	Brain Substantia Nigra	brain
43	chr5:177876800-177877400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
44	chr5:177876800-177877400	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr5:177876800-177877600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr5:177876800-177877800	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr5:177877000-177877200	Enhancers	Brain Angular Gyrus	brain
48	chr5:177877000-177877200	Enhancers	Brain Cingulate Gyrus	brain
49	chr5:177877000-177877200	Enhancers	Brain Hippocampus Middle	brain
50	chr5:177877000-177877200	Flanking Bivalent TSS/Enh	Stomach Mucosa	stomach

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