Variant report

Variant	nsv998957
Chromosome Location	chr1:161353351-161398414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2218)
CpG islands
(count:1404)
Chromatin interactive
region (count:145)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2218 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:161368906-161369722	K562	blood:	n/a	n/a
2	ARID3A	chr1:161367773-161368224	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:161359358-161359744	K562	blood:	n/a	n/a
4	ARID3A	chr1:161391697-161392047	K562	blood:	n/a	n/a
5	ARID3A	chr1:161360027-161360191	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:161368722-161369741	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:161373912-161374076	K562	blood:	n/a	n/a
8	ATF1	chr1:161397773-161398450	K562	blood:	n/a	n/a
9	ATF1	chr1:161368885-161369639	K562	blood:	n/a	n/a
10	ATF1	chr1:161377600-161377723	K562	blood:	n/a	n/a
11	ATF1	chr1:161359492-161360173	K562	blood:	n/a	n/a
12	ATF2	chr1:161397531-161398339	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr1:161368588-161369854	GM12878	blood:	n/a	n/a
14	ATF2	chr1:161379562-161380002	GM12878	blood:	n/a	n/a
15	ATF2	chr1:161391588-161392093	GM12878	blood:	n/a	n/a
16	ATF2	chr1:161368808-161369999	GM12878	blood:	n/a	n/a
17	ATF2	chr1:161391699-161392081	GM12878	blood:	n/a	n/a
18	ATF2	chr1:161368726-161369802	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr1:161397660-161398232	GM12878	blood:	n/a	n/a
20	ATF2	chr1:161391572-161392109	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr1:161397685-161398197	GM12878	blood:	n/a	n/a
22	ATF2	chr1:161397569-161398247	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr1:161368954-161369981	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr1:161368766-161370153	A549	lung:	n/a	n/a
25	ATF3	chr1:161397299-161398505	A549	lung:	n/a	n/a
26	ATF3	chr1:161368812-161370029	A549	lung:	n/a	n/a
27	ATF3	chr1:161391517-161392131	HCT-116	colon:	n/a	n/a
28	ATF3	chr1:161390468-161390994	A549	lung:	n/a	n/a
29	ATF3	chr1:161397507-161398223	K562	blood:	n/a	n/a
30	ATF3	chr1:161391480-161392128	A549	lung:	n/a	n/a
31	ATF3	chr1:161367806-161368317	A549	lung:	n/a	n/a
32	ATF3	chr1:161397463-161398306	A549	lung:	n/a	n/a
33	ATF3	chr1:161391379-161392139	A549	lung:	n/a	n/a
34	ATF3	chr1:161391569-161392148	HCT-116	colon:	n/a	n/a
35	ATF3	chr1:161390522-161390920	A549	lung:	n/a	n/a
36	ATF3	chr1:161397566-161398331	HCT-116	colon:	n/a	n/a
37	ATF3	chr1:161397443-161398363	HCT-116	colon:	n/a	n/a
38	ATF3	chr1:161370191-161370550	K562	blood:	n/a	n/a
39	ATF3	chr1:161391531-161392126	K562	blood:	n/a	n/a
40	ATF3	chr1:161390543-161390879	K562	blood:	n/a	n/a
41	ATF3	chr1:161368795-161369869	K562	blood:	n/a	n/a
42	BACH1	chr1:161391803-161392018	K562	blood:	n/a	n/a
43	BACH1	chr1:161359378-161360271	H1-hESC	embryonic stem cell:	n/a	chr1:161359766-161359780
44	BACH1	chr1:161369264-161369832	K562	blood:	n/a	n/a
45	BACH1	chr1:161368853-161370143	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr1:161368021-161368210	K562	blood:	n/a	n/a
47	BATF	chr1:161379614-161379994	GM12878	blood:	n/a	n/a
48	BATF	chr1:161379655-161380102	GM12878	blood:	n/a	n/a
49	BATF	chr1:161397697-161398141	GM12878	blood:	n/a	n/a
50	BATF	chr1:161369304-161369914	GM12878	blood:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:161369931-161369981	AG10803	skin:	n/a
2	chr1:161369931-161369981	AG10803	skin:	n/a
3	chr1:161360101-161360151	HCF	heart:	n/a
4	chr1:161359705-161359755	Hepatocyte	liver:	n/a
5	chr1:161359705-161359755	GM12892	blood:	n/a
6	chr1:161369648-161369698	HEK293	kidney:	embryo
7	chr1:161375390-161375440	BE2_C	brain:	n/a
8	chr1:161362084-161362134	HEK293	kidney:	embryo
9	chr1:161362084-161362134	NHDF-neo	bronchial:	n/a
10	chr1:161358133-161358183	HepG2	liver:	n/a
11	chr1:161362084-161362134	Caco-2	colon:	n/a
12	chr1:161373646-161373696	HRPEpiC	eye:	n/a
13	chr1:161360101-161360151	Hela-S3	cervix:	n/a
14	chr1:161369009-161369059	ProgFib	skin:	n/a
15	chr1:161369277-161369327	Jurkat	blood:	n/a
16	chr1:161355643-161355693	RPTEC	kidney:	n/a
17	chr1:161358133-161358183	HCF	heart:	n/a
18	chr1:161391807-161391857	AG09309	skin:	n/a
19	chr1:161369725-161369775	A549	lung:	n/a
20	chr1:161359705-161359755	SK-N-SH_RA	brain:	n/a
21	chr1:161355643-161355693	HCM	heart:	n/a
22	chr1:161358133-161358183	BE2_C	brain:	n/a
23	chr1:161359506-161359556	HAEpiC	amniotic membrane:	n/a
24	chr1:161369970-161370020	NHDF-neo	bronchial:	n/a
25	chr1:161375390-161375440	GM06990	blood:	n/a
26	chr1:161369725-161369775	HepG2	liver:	n/a
27	chr1:161362188-161362238	H1-hESC	embryonic stem cell:	embryo
28	chr1:161359705-161359755	GM06990	blood:	n/a
29	chr1:161369725-161369775	SAEC	small airway:	n/a
30	chr1:161369931-161369981	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:161369277-161369327	Hepatocyte	liver:	n/a
32	chr1:161359705-161359755	HCPEpiC	choroid plexus:	n/a
33	chr1:161368947-161368997	NB4	blood:	n/a
34	chr1:161369931-161369981	NH-A	brain:	n/a
35	chr1:161360266-161360316	GM06990	blood:	n/a
36	chr1:161362188-161362238	K562	blood:	n/a
37	chr1:161369970-161370020	HUVEC	blood vessel:	n/a
38	chr1:161391807-161391857	T-47D	breast:	n/a
39	chr1:161355643-161355693	BJ	skin:	n/a
40	chr1:161359705-161359755	HCM	heart:	n/a
41	chr1:161375390-161375440	GM12891	blood:	n/a
42	chr1:161369277-161369327	PANC-1	pancreas:	n/a
43	chr1:161369648-161369698	PrEC	prostate:	n/a
44	chr1:161373646-161373696	HCPEpiC	choroid plexus:	n/a
45	chr1:161373646-161373696	BJ	skin:	n/a
46	chr1:161368947-161368997	PFSK-1	brain:	n/a
47	chr1:161369009-161369059	AG10803	skin:	n/a
48	chr1:161359784-161359834	ovcar-3	ovarian:	n/a
49	chr1:161362084-161362134	NB4	blood:	n/a
50	chr1:161360266-161360316	HCT-116	colon:	n/a

(count:145 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:161372330..161375943-chr1:161377177..161380756,5	K562	blood:
2	chr1:161134865..161137183-chr1:161358550..161360077,2	K562	blood:
3	chr1:161352053..161353728-chr1:161407304..161409972,2	K562	blood:
4	chr1:161369557..161370167-chr21:44865534..44866035,2	Hela-S3	cervix:
5	chr1:161396356..161400063-chr1:161401364..161404724,5	K562	blood:
6	chr1:161358508..161360458-chr1:161366457..161368829,2	MCF-7	breast:
7	chr1:161358861..161359510-chr7:102984199..102985144,2	Hela-S3	cervix:
8	chr1:161134675..161137547-chr1:161367639..161370796,3	MCF-7	breast:
9	chr1:161368637..161369445-chr7:32534785..32535506,2	Hela-S3	cervix:
10	chr1:161391115..161393084-chr1:161396926..161398763,2	MCF-7	breast:
11	chr1:161341445..161342945-chr1:161357890..161360001,2	K562	blood:
12	chr1:161367170..161369307-chr1:161718494..161721063,2	MCF-7	breast:
13	chr1:161357605..161359788-chr1:161389913..161391867,2	K562	blood:
14	chr1:161370061..161375696-chr1:161394134..161399507,5	K562	blood:
15	chr1:161357437..161366069-chr1:161366187..161371309,27	K562	blood:
16	chr1:161362735..161364411-chr1:161396215..161399022,2	K562	blood:
17	chr1:161371806..161374700-chr1:161382431..161384803,2	MCF-7	breast:
18	chr1:161283233..161286394-chr1:161358272..161361598,5	K562	blood:
19	chr1:161195417..161197356-chr1:161369111..161371418,2	MCF-7	breast:
20	chr1:161379123..161382070-chr1:161387001..161390523,3	K562	blood:
21	chr1:161351090..161356215-chr1:161358922..161361757,5	MCF-7	breast:
22	chr1:161358247..161360860-chr1:161371655..161373907,3	K562	blood:
23	chr1:161163886..161166683-chr1:161359884..161361575,2	K562	blood:
24	chr1:161368901..161369511-chr12:57913791..57914555,2	Hela-S3	cervix:
25	chr1:161391834..161393520-chr1:161394976..161397393,2	K562	blood:
26	chr1:161369089..161369854-chr2:88927297..88927921,2	Hela-S3	cervix:
27	chr1:161358508..161360458-chr1:161366457..161368829,2	MCF-7	breast:
28	chr1:161367523..161369303-chr1:161373719..161375547,2	MCF-7	breast:
29	chr1:161367523..161369303-chr1:161373719..161375547,2	MCF-7	breast:
30	chr1:161358757..161360406-chr1:161361978..161363939,2	K562	blood:
31	chr1:161369732..161370315-chr1:161409694..161410275,2	MCF-7	breast:
32	chr1:161367430..161368932-chr1:161384466..161386892,2	MCF-7	breast:
33	chr1:161390100..161392594-chr1:161405039..161407945,2	K562	blood:
34	chr1:161170434..161172328-chr1:161378596..161380361,2	K562	blood:
35	chr1:161169854..161174151-chr1:161367669..161371061,6	K562	blood:
36	chr1:161339110..161342306-chr1:161354763..161357671,3	K562	blood:
37	chr1:161145759..161147740-chr1:161357028..161358969,2	K562	blood:
38	chr1:161354244..161356268-chr1:161357860..161359450,2	K562	blood:
39	chr1:161371806..161374700-chr1:161382431..161384803,2	MCF-7	breast:
40	chr1:161359596..161364953-chr1:161367894..161371258,10	MCF-7	breast:
41	chr1:110949781..110950700-chr1:161368976..161369850,2	Hela-S3	cervix:
42	chr1:161194802..161197493-chr1:161358344..161361187,2	MCF-7	breast:
43	chr1:161354244..161356268-chr1:161357860..161359450,2	K562	blood:
44	chr1:161358757..161360406-chr1:161361978..161363939,2	K562	blood:
45	chr1:161373435..161375369-chr1:161381940..161384249,4	K562	blood:
46	chr1:161360479..161362170-chr1:161367532..161370441,2	MCF-7	breast:
47	chr1:161367820..161369576-chr1:173836178..173838599,2	MCF-7	breast:
48	chr1:161374486..161376275-chr1:161385955..161388750,2	K562	blood:
49	chr1:161385881..161387506-chr1:161389116..161391807,2	K562	blood:
50	chr1:161273676..161276435-chr1:161357253..161360044,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1orf192-1	chr1:161389333-161389678	XLOC_001066
2	lnc-C1orf192-1	chr1:161390013-161390169	XLOC_001066

No data

Variant related genes	Relation type
RNU6-481P	TF binding region
RRM2P2	TF binding region
ENSG00000215840	TF binding region
RNU6-481P	CpG island
RRM2P2	CpG island
ENSG00000215840	CpG island
ENSG00000081721	chromatin interactions
ENSG00000143252	chromatin interactions
ENSG00000162910	chromatin interactions
ENSG00000143257	chromatin interactions
ENSG00000234028	chromatin interactions
ENSG00000224699	chromatin interactions
ENSG00000206921	chromatin interactions
ENSG00000248485	chromatin interactions
ENSG00000235477	chromatin interactions
ENSG00000161057	chromatin interactions
ENSG00000143224	chromatin interactions
ENSG00000175197	chromatin interactions
ENSG00000158887	chromatin interactions
ENSG00000134248	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000134186	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000261202	chromatin interactions
ENSG00000188931	chromatin interactions
ENSG00000215840	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000158850	chromatin interactions
ENSG00000158882	chromatin interactions
ENSG00000166987	chromatin interactions
ENSG00000143258	chromatin interactions
ENSG00000158773	chromatin interactions
ENSG00000143222	chromatin interactions
ENSG00000100354	chromatin interactions
ENSG00000263548	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000197483	chromatin interactions
ENSG00000106355	chromatin interactions
ENSG00000205084	chromatin interactions
ENSG00000158864	chromatin interactions
ENSG00000165119	chromatin interactions
ENSG00000158859	chromatin interactions
ENSG00000105821	chromatin interactions
ENSG00000105778	chromatin interactions
ENSG00000158869	chromatin interactions

Extended variants
information (count: 1704 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1704 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185245021	chr1:161353383-161353384	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs115850603	chr1:161353390-161353391	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs561340943	chr1:161353463-161353464	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs542279008	chr1:161353511-161353512	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs561591534	chr1:161353573-161353574	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs562224727	chr1:161353623-161353624	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs190099495	chr1:161353628-161353629	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs75316625	chr1:161353685-161353686	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
9	rs201630655	chr1:161353798-161353799	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs543929128	chr1:161353830-161353831	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs547247065	chr1:161353867-161353868	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs564659070	chr1:161353874-161353875	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs533350856	chr1:161353908-161353909	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs77404951	chr1:161353919-161353920	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs551825411	chr1:161353968-161353969	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs568626333	chr1:161354006-161354007	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs537431812	chr1:161354021-161354022	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548196090	chr1:161354025-161354026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs568261119	chr1:161354060-161354061	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534053535	chr1:161354061-161354062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570437473	chr1:161354093-161354094	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs377063918	chr1:161354100-161354101	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs199893558	chr1:161354103-161354104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576941565	chr1:161354130-161354131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs55996762	chr1:161354148-161354149	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs556681282	chr1:161354149-161354150	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576640138	chr1:161354153-161354154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs151244188	chr1:161354192-161354193	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549549211	chr1:161354253-161354254	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562155766	chr1:161354260-161354261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs35876806	chr1:161354299-161354300	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs373495481	chr1:161354337-161354338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140467497	chr1:161354369-161354370	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564646049	chr1:161354376-161354377	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs56169917	chr1:161354380-161354381	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs549994993	chr1:161354416-161354417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs182245810	chr1:161354422-161354423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs535243820	chr1:161354451-161354452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531350694	chr1:161354457-161354458	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs187464502	chr1:161354485-161354486	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547867573	chr1:161354555-161354556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs16832911	chr1:161354580-161354581	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs572638608	chr1:161354604-161354605	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527310943	chr1:161354646-161354647	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs547636348	chr1:161354663-161354664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs570796031	chr1:161354706-161354707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539624396	chr1:161354714-161354715	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs12027347	chr1:161354717-161354718	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186252584	chr1:161354775-161354776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189881667	chr1:161354867-161354868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1452 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161328400-161359000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:161328600-161359000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:161335000-161356000	Weak transcription	K562	blood
4	chr1:161337800-161356200	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr1:161338000-161356000	Weak transcription	GM12878-XiMat	blood
6	chr1:161349200-161358600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:161351600-161353600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:161351600-161353800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr1:161351800-161358800	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr1:161352000-161353400	Enhancers	Adipose Nuclei	Adipose
11	chr1:161352200-161353400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:161352400-161355600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr1:161352400-161358600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:161352400-161358800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr1:161352600-161359200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr1:161352600-161359200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr1:161352800-161353400	Enhancers	A549	lung
18	chr1:161352800-161353400	Enhancers	Osteobl	bone
19	chr1:161352800-161353800	Enhancers	Muscle Satellite Cultured Cells	--
20	chr1:161352800-161353800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:161352800-161353800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:161352800-161353800	Enhancers	Hela-S3	cervix
23	chr1:161352800-161353800	Enhancers	HMEC	breast
24	chr1:161352800-161356000	Weak transcription	HepG2	liver
25	chr1:161352800-161359200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr1:161353000-161353800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:161353000-161354000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:161353000-161359200	Weak transcription	HUVEC	blood vessel
29	chr1:161353000-161359200	Weak transcription	NHLF	lung
30	chr1:161353200-161354000	Enhancers	NHEK	skin
31	chr1:161353400-161354600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:161353400-161356200	Weak transcription	A549	lung
33	chr1:161353400-161359000	Weak transcription	Adipose Nuclei	Adipose
34	chr1:161353400-161359200	Weak transcription	Osteobl	bone
35	chr1:161353800-161356200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr1:161353800-161358600	Weak transcription	Hela-S3	cervix
37	chr1:161353800-161358800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:161353800-161358800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr1:161353800-161358800	Weak transcription	HMEC	breast
40	chr1:161353800-161359200	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr1:161354000-161358600	Weak transcription	NHEK	skin
42	chr1:161354000-161359200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:161354600-161359200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:161355200-161356400	Weak transcription	Liver	Liver
45	chr1:161355600-161357400	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr1:161355600-161357600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr1:161356000-161356400	Enhancers	Primary T cells fromperipheralblood	blood
48	chr1:161356000-161356400	Enhancers	K562	blood
49	chr1:161356000-161356800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr1:161356000-161357000	Enhancers	HepG2	liver

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