Variant report

Variant	esv1828600
Chromosome Location	chr16:70500809-70515355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:760)
CpG islands
(count:551)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70504903-70504937	HepG2	liver:	n/a	n/a
2	ATF2	chr16:70510276-70511074	GM12878	blood:	n/a	n/a
3	ATF2	chr16:70510238-70511043	GM12878	blood:	n/a	n/a
4	BATF	chr16:70510415-70510895	GM12878	blood:	n/a	chr16:70510644-70510655 chr16:70510645-70510655
5	BATF	chr16:70510353-70511022	GM12878	blood:	n/a	chr16:70510644-70510655 chr16:70510645-70510655
6	BCL11A	chr16:70510390-70510925	GM12878	blood:	n/a	n/a
7	BCL11A	chr16:70510348-70510966	GM12878	blood:	n/a	chr16:70510357-70510366
8	BCL3	chr16:70510406-70510869	GM12878	blood:	n/a	n/a
9	BCL3	chr16:70510307-70510906	GM12878	blood:	n/a	chr16:70510357-70510366
10	BCLAF1	chr16:70510362-70511056	GM12878	blood:	n/a	n/a
11	BCLAF1	chr16:70510199-70511054	GM12878	blood:	n/a	chr16:70510357-70510366
12	BHLHE40	chr16:70510344-70511014	GM12878	blood:	n/a	n/a
13	BHLHE40	chr16:70504880-70505067	K562	blood:	n/a	n/a
14	BHLHE40	chr16:70504789-70505092	HepG2	liver:	n/a	n/a
15	BRCA1	chr16:70510334-70510892	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr16:70504894-70505145	K562	blood:	n/a	n/a
17	CEBPB	chr16:70505679-70505879	K562	blood:	n/a	n/a
18	CEBPB	chr16:70510182-70511138	GM12878	blood:	n/a	n/a
19	CEBPB	chr16:70505488-70505933	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr16:70504819-70505000	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr16:70510400-70510765	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr16:70505753-70505832	A549	lung:	n/a	n/a
23	CEBPB	chr16:70509610-70509813	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr16:70504933-70504983	HepG2	liver:	n/a	n/a
25	CHD2	chr16:70504973-70505004	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr16:70510300-70511008	GM12878	blood:	n/a	n/a
27	CHD2	chr16:70510216-70510745	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr16:70504847-70505131	Pancreas_OC	pancreas:	n/a	chr16:70504851-70504864
29	CTCF	chr16:70501080-70501230	GM12869	blood:	n/a	n/a
30	CTCF	chr16:70510460-70510610	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr16:70504840-70504990	HEEpiC	esophagus:	n/a	chr16:70504851-70504864
32	CTCF	chr16:70504900-70505050	SAEC	small airway:	n/a	n/a
33	CTCF	chr16:70507720-70507870	HepG2	liver:	n/a	n/a
34	CTCF	chr16:70504783-70505150	K562	blood:	n/a	chr16:70504851-70504864
35	CTCF	chr16:70501120-70501270	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr16:70504769-70505171	A549	lung:	n/a	chr16:70504851-70504864
37	CTCF	chr16:70504880-70505030	BJ	skin:	n/a	n/a
38	CTCF	chr16:70501139-70501282	GM19240	blood:	n/a	n/a
39	CTCF	chr16:70507760-70507910	GM12864	blood:	n/a	n/a
40	CTCF	chr16:70504846-70505108	MCF-7	breast:	n/a	chr16:70504851-70504864
41	CTCF	chr16:70504890-70505062	GM10248	blood:	n/a	n/a
42	CTCF	chr16:70501080-70501230	GM12872	blood:	n/a	n/a
43	CTCF	chr16:70507775-70507892	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr16:70504626-70505221	K562	blood:	n/a	chr16:70504851-70504864
45	CTCF	chr16:70507760-70507910	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr16:70504696-70505144	HepG2	liver:	n/a	chr16:70504851-70504864
47	CTCF	chr16:70504900-70505050	HMEC	breast:	n/a	n/a
48	CTCF	chr16:70501020-70501170	GM12871	blood:	n/a	n/a
49	CTCF	chr16:70507740-70507890	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr16:70507769-70507920	GM12891	blood:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70508086-70508136	SK-N-MC	brain:	n/a
2	chr16:70514664-70514714	Caco-2	colon:	n/a
3	chr16:70508086-70508136	SK-N-MC	brain:	n/a
4	chr16:70514664-70514714	Caco-2	colon:	n/a
5	chr16:70514664-70514714	HCM	heart:	n/a
6	chr16:70505196-70505246	A549	lung:	n/a
7	chr16:70507104-70507154	HepG2	liver:	n/a
8	chr16:70507115-70507165	HNPCEpiC	eye:	n/a
9	chr16:70513830-70513880	SK-N-SH	brain:	n/a
10	chr16:70510663-70510713	HMEC	breast:	n/a
11	chr16:70510663-70510713	H1-hESC	embryonic stem cell:	embryo
12	chr16:70507104-70507154	T-47D	breast:	n/a
13	chr16:70514664-70514714	AoSMC	blood vessel:	n/a
14	chr16:70505196-70505246	HCPEpiC	choroid plexus:	n/a
15	chr16:70513830-70513880	GM12878	blood:	n/a
16	chr16:70504393-70504443	T-47D	breast:	n/a
17	chr16:70510663-70510713	AG10803	skin:	n/a
18	chr16:70507094-70507144	PANC-1	pancreas:	n/a
19	chr16:70504393-70504443	AG10803	skin:	n/a
20	chr16:70505196-70505246	SAEC	small airway:	n/a
21	chr16:70510663-70510713	GM19239	blood:	n/a
22	chr16:70504393-70504443	NH-A	brain:	n/a
23	chr16:70513830-70513880	NHDF-neo	bronchial:	n/a
24	chr16:70507115-70507165	HRE	kidney:	n/a
25	chr16:70507104-70507154	SK-N-SH_RA	brain:	n/a
26	chr16:70510663-70510713	HUVEC	blood vessel:	n/a
27	chr16:70505196-70505246	H1-hESC	embryonic stem cell:	embryo
28	chr16:70507104-70507154	HCT-116	colon:	n/a
29	chr16:70507115-70507165	SKMC	muscle:	n/a
30	chr16:70507115-70507165	HAEpiC	amniotic membrane:	n/a
31	chr16:70505196-70505246	AG09319	gingival:	n/a
32	chr16:70507094-70507144	HRCEpiC	kidney:	n/a
33	chr16:70510663-70510713	BJ	skin:	n/a
34	chr16:70507104-70507154	U87	brain:	n/a
35	chr16:70508086-70508136	GM06990	blood:	n/a
36	chr16:70510663-70510713	HEEpiC	esophagus:	n/a
37	chr16:70508086-70508136	HMEC	breast:	n/a
38	chr16:70513830-70513880	ProgFib	skin:	n/a
39	chr16:70510663-70510713	PANC-1	pancreas:	n/a
40	chr16:70510663-70510713	HCT-116	colon:	n/a
41	chr16:70507094-70507144	AG09309	skin:	n/a
42	chr16:70510663-70510713	HRCEpiC	kidney:	n/a
43	chr16:70510663-70510713	ovcar-3	ovarian:	n/a
44	chr16:70508086-70508136	Jurkat	blood:	n/a
45	chr16:70507094-70507144	GM12891	blood:	n/a
46	chr16:70505196-70505246	SK-N-SH	brain:	n/a
47	chr16:70514664-70514714	MCF-7	breast:	n/a
48	chr16:70510663-70510713	Hela-S3	cervix:	n/a
49	chr16:70507094-70507144	GM12892	blood:	n/a
50	chr16:70507115-70507165	HepG2	liver:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70413009..70414536-chr16:70505272..70507294,2	MCF-7	breast:
2	chr16:70487960..70489638-chr16:70506359..70508682,2	MCF-7	breast:
3	chr16:70513484..70515449-chr16:70517366..70519641,2	K562	blood:
4	chr16:70504816..70506986-chr16:70508068..70510563,2	MCF-7	breast:
5	chr16:70515238..70517748-chr16:70555099..70558723,4	MCF-7	breast:
6	chr16:70509867..70512688-chr16:70534872..70536534,2	K562	blood:
7	chr16:70411449..70413987-chr16:70507586..70509151,2	MCF-7	breast:
8	chr16:70495605..70497210-chr16:70502567..70505009,2	K562	blood:
9	chr16:70504177..70506838-chr16:70507916..70509706,2	K562	blood:
10	chr16:70408425..70412469-chr16:70501223..70503201,4	MCF-7	breast:
11	chr16:70413020..70418181-chr16:70497448..70510572,26	MCF-7	breast:
12	chr16:70414709..70415539-chr16:70504523..70505445,2	MCF-7	breast:
13	chr16:70412596..70415415-chr16:70513984..70516318,3	MCF-7	breast:
14	chr16:70510715..70512361-chr16:70515275..70517741,2	MCF-7	breast:
15	chr16:70499787..70501643-chr16:70507798..70509638,2	K562	blood:
16	chr16:70430256..70430847-chr16:70504861..70505385,2	MCF-7	breast:
17	chr16:70428887..70429566-chr16:70504906..70505567,3	MCF-7	breast:
18	chr16:70510715..70512361-chr16:70515275..70517741,2	MCF-7	breast:
19	chr16:70406308..70408837-chr16:70511303..70514267,2	MCF-7	breast:
20	chr16:70381919..70383634-chr16:70512388..70514213,2	K562	blood:
21	chr16:70429294..70430017-chr16:70504194..70504760,2	MCF-7	breast:
22	chr16:70424507..70425403-chr16:70504469..70505365,3	MCF-7	breast:
23	chr16:70429376..70429898-chr16:70504488..70505417,3	K562	blood:
24	chr16:70487135..70489570-chr16:70502867..70505697,3	MCF-7	breast:
25	chr16:70507044..70509667-chr16:70557071..70558921,2	MCF-7	breast:
26	chr16:70495074..70498358-chr16:70501504..70504908,3	MCF-7	breast:
27	chr16:70503633..70506860-chr16:70556143..70558862,3	MCF-7	breast:
28	chr16:70503488..70506383-chr16:70517357..70519879,2	MCF-7	breast:
29	chr16:70505499..70507933-chr16:70517566..70519175,2	MCF-7	breast:
30	chr16:70495439..70497105-chr16:70502567..70504359,2	K562	blood:
31	chr16:70507845..70510277-chr16:70513994..70516516,2	K562	blood:
32	chr16:70503433..70505616-chr16:70512228..70514633,3	K562	blood:
33	chr16:70428972..70429950-chr16:70504540..70505471,10	MCF-7	breast:
34	chr16:70510287..70517781-chr16:70555054..70559513,7	MCF-7	breast:
35	chr16:70503433..70505616-chr16:70512228..70514633,3	K562	blood:
36	chr16:70498553..70500148-chr16:70504235..70506069,2	K562	blood:

No data

Variant related genes	Relation type
FUK	TF binding region
FUK	CpG island
ENSG00000189091	chromatin interactions
ENSG00000260111	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000157353	chromatin interactions

Extended variants
information (count: 743 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17881323	chr16:70500809-70500810	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531073690	chr16:70500811-70500812	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs375426430	chr16:70500826-70500827	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368046961	chr16:70500829-70500830	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs144507237	chr16:70500830-70500831	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs35319442	chr16:70500839-70500840	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs35269698	chr16:70500853-70500854	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs56366805	chr16:70500875-70500876	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs183873641	chr16:70500878-70500879	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546703084	chr16:70500883-70500884	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs571376277	chr16:70500884-70500885	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368981551	chr16:70500891-70500892	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373227415	chr16:70500892-70500893	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs556896712	chr16:70500954-70500955	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs569224522	chr16:70500955-70500956	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs17882726	chr16:70500969-70500970	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs555615636	chr16:70500999-70501000	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs573789272	chr16:70501004-70501005	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs541192547	chr16:70501053-70501054	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs550076291	chr16:70501062-70501063	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs553126297	chr16:70501150-70501151	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs188597379	chr16:70501156-70501157	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs180693403	chr16:70501187-70501188	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs545034932	chr16:70501189-70501190	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs563609257	chr16:70501193-70501194	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs185102649	chr16:70501217-70501218	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs371941048	chr16:70501226-70501227	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs376738855	chr16:70501242-70501243	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs369776864	chr16:70501255-70501256	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs376683810	chr16:70501277-70501278	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs370681598	chr16:70501297-70501298	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs372937279	chr16:70501307-70501308	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs35036235	chr16:70501314-70501315	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs546740302	chr16:70501331-70501332	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs370283040	chr16:70501332-70501333	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532510018	chr16:70501348-70501349	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs373589147	chr16:70501354-70501355	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs552110451	chr16:70501389-70501390	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs17883840	chr16:70501390-70501391	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs569184921	chr16:70501395-70501396	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs17884111	chr16:70501400-70501401	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs368476051	chr16:70501401-70501402	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs199518013	chr16:70501412-70501413	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs566079647	chr16:70501433-70501434	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs534816410	chr16:70501437-70501438	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs374648976	chr16:70501443-70501444	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs17879684	chr16:70501465-70501466	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs577904648	chr16:70501477-70501478	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs190383706	chr16:70501507-70501508	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs538788212	chr16:70501519-70501520	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:653 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70489200-70506000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr16:70489200-70508800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr16:70489400-70504600	Weak transcription	A549	lung
4	chr16:70489400-70508800	Weak transcription	HMEC	breast
5	chr16:70489400-70509000	Weak transcription	NHEK	skin
6	chr16:70489400-70509400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr16:70489400-70510600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr16:70489400-70511800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr16:70489400-70512000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr16:70489400-70513000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr16:70489400-70513400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr16:70489400-70513800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr16:70489400-70513800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr16:70489400-70514200	Weak transcription	Small Intestine	intestine
15	chr16:70489400-70556400	Weak transcription	Stomach Mucosa	stomach
16	chr16:70490200-70504400	Weak transcription	Hela-S3	cervix
17	chr16:70490200-70514400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr16:70490600-70505600	Weak transcription	K562	blood
19	chr16:70495000-70504600	Weak transcription	HepG2	liver
20	chr16:70495000-70519000	Strong transcription	Primary T cells from cord blood	blood
21	chr16:70495200-70510200	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr16:70495200-70510200	Weak transcription	Osteobl	bone
23	chr16:70495400-70506800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr16:70495400-70507000	Weak transcription	Fetal Brain Female	brain
25	chr16:70495400-70508800	Weak transcription	GM12878-XiMat	blood
26	chr16:70495400-70510200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr16:70495400-70510200	Weak transcription	HSMM	muscle
28	chr16:70495400-70510400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr16:70495600-70504400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr16:70495800-70512800	Weak transcription	Right Atrium	heart
31	chr16:70496800-70501800	Strong transcription	Adipose Nuclei	Adipose
32	chr16:70496800-70502000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr16:70497000-70501600	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr16:70497000-70501800	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr16:70497000-70502000	Strong transcription	Liver	Liver
36	chr16:70497000-70502000	Strong transcription	Spleen	Spleen
37	chr16:70497000-70503400	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr16:70497000-70507800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr16:70497000-70510200	Strong transcription	Duodenum Mucosa	Duodenum
40	chr16:70497200-70501000	Strong transcription	Aorta	Aorta
41	chr16:70497200-70501200	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr16:70497200-70501200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr16:70497200-70501600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr16:70497200-70501800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr16:70497200-70501800	Strong transcription	Brain Cingulate Gyrus	brain
46	chr16:70497200-70502000	Strong transcription	Right Ventricle	heart
47	chr16:70497200-70503200	Strong transcription	Pancreas	Pancrea
48	chr16:70497200-70503600	Strong transcription	Sigmoid Colon	Sigmoid Colon
49	chr16:70497200-70504400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr16:70497200-70504800	Strong transcription	Stomach Smooth Muscle	stomach

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