Variant report

Variant	nsv895078
Chromosome Location	chr10:43467392-43524522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:428)
CpG islands
(count:244)
Chromatin interactive
region (count:100)
LncRNA
region (count:9)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:43474055-43474377	K562	blood:	n/a	n/a
2	ATF1	chr10:43474747-43475125	K562	blood:	n/a	n/a
3	BACH1	chr10:43521962-43522259	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:43508437-43508606	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr10:43484487-43484837	K562	blood:	n/a	n/a
6	BHLHE40	chr10:43476829-43477169	K562	blood:	n/a	chr10:43476970-43476986
7	CCNT2	chr10:43476863-43477053	K562	blood:	n/a	n/a
8	CEBPB	chr10:43474862-43474980	K562	blood:	n/a	n/a
9	CEBPB	chr10:43468469-43468786	HepG2	liver:	n/a	chr10:43468625-43468636 chr10:43468624-43468637
10	CEBPB	chr10:43468559-43468690	K562	blood:	n/a	chr10:43468625-43468636 chr10:43468624-43468637
11	CEBPB	chr10:43467355-43467475	IMR90	lung:	n/a	n/a
12	CEBPB	chr10:43477134-43477208	K562	blood:	n/a	n/a
13	CHD2	chr10:43471209-43471243	HepG2	liver:	n/a	n/a
14	CHD2	chr10:43522101-43522438	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr10:43471240-43471390	HEK293	kidney:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
16	CTCF	chr10:43471200-43471350	SK-N-SH_RA	brain:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
17	CTCF	chr10:43471059-43471454	HCT-116	colon:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
18	CTCF	chr10:43471200-43471350	GM12865	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
19	CTCF	chr10:43471200-43471350	GM06990	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
20	CTCF	chr10:43471200-43471350	Hela-S3	cervix:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
21	CTCF	chr10:43471260-43471410	GM12864	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
22	CTCF	chr10:43471180-43471330	NHEK	skin:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
23	CTCF	chr10:43471167-43471341	GM12891	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
24	CTCF	chr10:43471180-43471330	GM12864	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
25	CTCF	chr10:43517980-43518130	Caco-2	colon:	n/a	chr10:43518112-43518130 chr10:43518115-43518123 chr10:43518115-43518128
26	CTCF	chr10:43471141-43471338	HepG2	liver:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
27	CTCF	chr10:43494840-43494900	K562	blood:	n/a	n/a
28	CTCF	chr10:43475960-43476110	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr10:43518137-43518139	MCF-7	breast:	n/a	n/a
30	CTCF	chr10:43471160-43471310	GM12878	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
31	CTCF	chr10:43471198-43471318	GM19240	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
32	CTCF	chr10:43471220-43471370	BE2_C	brain:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
33	CTCF	chr10:43471040-43471190	GM12869	blood:	n/a	n/a
34	CTCF	chr10:43471200-43471350	NB4	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
35	CTCF	chr10:43471120-43471270	GM06990	blood:	n/a	n/a
36	CTCF	chr10:43471140-43471290	AG04449	skin:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
37	CTCF	chr10:43490594-43490694	GM20000	blood:	n/a	n/a
38	CTCF	chr10:43471144-43471346	A549	lung:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
39	CTCF	chr10:43514879-43514928	GM13976	blood:	n/a	n/a
40	CTCF	chr10:43471091-43471404	MCF-7	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
41	CTCF	chr10:43471200-43471350	MCF-7	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
42	CTCF	chr10:43471320-43471470	A549	lung:	n/a	n/a
43	CTCF	chr10:43471192-43471328	GM19238	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
44	CTCF	chr10:43524180-43524330	HMEC	breast:	n/a	n/a
45	CTCF	chr10:43475300-43475530	BE2_C	brain:	n/a	n/a
46	CTCF	chr10:43471117-43471401	MCF-7	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
47	CTCF	chr10:43471180-43471330	MCF-7	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
48	CTCF	chr10:43471180-43471330	AG04449	skin:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
49	CTCF	chr10:43471180-43471330	WERI-Rb-1	eye:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
50	CTCF	chr10:43471400-43471550	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43522343-43522393	SAEC	small airway:	n/a
2	chr10:43522190-43522240	PrEC	prostate:	n/a
3	chr10:43522143-43522193	HEK293	kidney:	embryo
4	chr10:43507407-43507457	GM06990	blood:	n/a
5	chr10:43507407-43507457	ProgFib	skin:	n/a
6	chr10:43522143-43522193	HNPCEpiC	eye:	n/a
7	chr10:43507407-43507457	NH-A	brain:	n/a
8	chr10:43507407-43507457	SAEC	small airway:	n/a
9	chr10:43522343-43522393	GM12891	blood:	n/a
10	chr10:43507407-43507457	HUVEC	blood vessel:	n/a
11	chr10:43522343-43522393	NHDF-neo	bronchial:	n/a
12	chr10:43522343-43522393	AoSMC	blood vessel:	n/a
13	chr10:43522143-43522193	NHBE	bronchial:	n/a
14	chr10:43522143-43522193	SK-N-SH_RA	brain:	n/a
15	chr10:43522143-43522193	HCPEpiC	choroid plexus:	n/a
16	chr10:43522343-43522393	HUVEC	blood vessel:	n/a
17	chr10:43507407-43507457	HCF	heart:	n/a
18	chr10:43507407-43507457	CMK	blood:	n/a
19	chr10:43522143-43522193	AoSMC	blood vessel:	n/a
20	chr10:43522343-43522393	SK-N-MC	brain:	n/a
21	chr10:43522190-43522240	HRCEpiC	kidney:	n/a
22	chr10:43522343-43522393	HCF	heart:	n/a
23	chr10:43522143-43522193	AG04449	skin:	fetal
24	chr10:43522343-43522393	LNCaP	prostate:	n/a
25	chr10:43522143-43522193	HRCEpiC	kidney:	n/a
26	chr10:43507407-43507457	HEEpiC	esophagus:	n/a
27	chr10:43507407-43507457	H1-hESC	embryonic stem cell:	embryo
28	chr10:43522343-43522393	HPAEpiC	pulmonary alveolar:	n/a
29	chr10:43522190-43522240	U87	brain:	n/a
30	chr10:43522343-43522393	NH-A	brain:	n/a
31	chr10:43522190-43522240	HepG2	liver:	n/a
32	chr10:43522190-43522240	T-47D	breast:	n/a
33	chr10:43522190-43522240	Jurkat	blood:	n/a
34	chr10:43522143-43522193	NB4	blood:	n/a
35	chr10:43522143-43522193	HCM	heart:	n/a
36	chr10:43522343-43522393	PrEC	prostate:	n/a
37	chr10:43522190-43522240	RPTEC	kidney:	n/a
38	chr10:43507407-43507457	A549	lung:	n/a
39	chr10:43522143-43522193	NT2-D1	testis:	n/a
40	chr10:43522143-43522193	ovcar-3	ovarian:	n/a
41	chr10:43522190-43522240	HEEpiC	esophagus:	n/a
42	chr10:43507407-43507457	IMR90	lung:	fetal
43	chr10:43522143-43522193	HCT-116	colon:	n/a
44	chr10:43507407-43507457	GM12891	blood:	n/a
45	chr10:43507407-43507457	HL-60	blood:	n/a
46	chr10:43522343-43522393	GM19239	blood:	n/a
47	chr10:43522343-43522393	NHBE	bronchial:	n/a
48	chr10:43507407-43507457	SKMC	muscle:	n/a
49	chr10:43522343-43522393	AG09309	skin:	n/a
50	chr10:43522143-43522193	PrEC	prostate:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:43521853..43522545-chr10:43539851..43540728,3	MCF-7	breast:
2	chr10:43494956..43496475-chr10:43498262..43500423,2	K562	blood:
3	chr10:43522082..43523941-chr10:43632029..43633686,2	MCF-7	breast:
4	chr10:43452048..43454806-chr10:43520323..43522084,2	MCF-7	breast:
5	chr10:43477135..43480872-chr10:43482623..43485089,4	MCF-7	breast:
6	chr10:43521558..43522630-chr10:43533126..43534073,11	MCF-7	breast:
7	chr10:43476360..43477727-chr10:43521597..43522461,10	MCF-7	breast:
8	chr10:43520913..43524676-chr10:43563115..43566179,5	MCF-7	breast:
9	chr10:43509037..43511424-chr10:43519957..43522490,2	MCF-7	breast:
10	chr10:43450408..43453024-chr10:43497080..43499917,2	K562	blood:
11	chr10:43365921..43366623-chr10:43521643..43522303,3	MCF-7	breast:
12	chr10:43470043..43470710-chr4:7069530..7070337,2	NB4	blood:
13	chr10:43472378..43475581-chr10:43520718..43522410,3	MCF-7	breast:
14	chr10:43476496..43477680-chr10:43521631..43522494,5	MCF-7	breast:
15	chr10:43364281..43367091-chr10:43516077..43518838,2	MCF-7	breast:
16	chr10:43517701..43518324-chr10:43573585..43574127,2	MCF-7	breast:
17	chr10:43471587..43474099-chr10:43476210..43479281,3	MCF-7	breast:
18	chr10:43465926..43467640-chr10:43469651..43471316,2	K562	blood:
19	chr10:43521524..43522456-chr10:43605890..43606964,14	MCF-7	breast:
20	chr10:43369343..43371320-chr10:43469616..43472165,2	MCF-7	breast:
21	chr10:43516622..43519495-chr10:43560494..43562660,2	MCF-7	breast:
22	chr10:43472378..43475581-chr10:43520718..43522410,3	MCF-7	breast:
23	chr10:43521557..43522557-chr10:43605823..43606953,34	MCF-7	breast:
24	chr10:43523482..43525302-chr10:43587306..43589145,2	MCF-7	breast:
25	chr10:43521977..43523730-chr10:43523968..43526061,2	MCF-7	breast:
26	chr10:43521470..43522630-chr10:43533126..43534089,18	MCF-7	breast:
27	chr10:43517249..43519024-chr10:43519060..43521993,5	MCF-7	breast:
28	chr10:43494122..43496846-chr10:43520768..43523139,2	MCF-7	breast:
29	chr10:43484291..43485932-chr10:43488466..43491187,2	MCF-7	breast:
30	chr10:43494122..43496846-chr10:43520768..43523139,2	MCF-7	breast:
31	chr10:43361867..43362389-chr10:43470791..43471531,2	K562	blood:
32	chr10:43521617..43522540-chr10:43581453..43582423,6	MCF-7	breast:
33	chr10:43482866..43485744-chr10:43490374..43493373,2	K562	blood:
34	chr10:43520674..43522630-chr10:43627624..43629272,2	MCF-7	breast:
35	chr10:43521578..43522089-chr10:51547030..51547754,2	MCF-7	breast:
36	chr10:43472744..43475645-chr10:43482853..43485433,2	K562	blood:
37	chr10:43511982..43514503-chr10:43520094..43521790,2	MCF-7	breast:
38	chr10:43486095..43489357-chr10:43490017..43492485,3	MCF-7	breast:
39	chr10:43522999..43525382-chr10:43554403..43557112,2	MCF-7	breast:
40	chr10:43516002..43526594-chr10:43563705..43585824,64	MCF-7	breast:
41	chr10:43481086..43483555-chr10:43520776..43523098,2	MCF-7	breast:
42	chr10:43365868..43366659-chr10:43470638..43471752,5	MCF-7	breast:
43	chr10:43521534..43522099-chr10:43595175..43595724,2	MCF-7	breast:
44	chr10:43521500..43522685-chr10:43605254..43606963,53	MCF-7	breast:
45	chr10:43521937..43524113-chr10:43534529..43536882,2	MCF-7	breast:
46	chr10:43469169..43471779-chr10:43471792..43473949,2	K562	blood:
47	chr10:43442278..43444933-chr10:43480874..43482921,2	K562	blood:
48	chr10:43469610..43472857-chr10:43520371..43524809,5	MCF-7	breast:
49	chr10:43474536..43476774-chr10:43520389..43522895,3	MCF-7	breast:
50	chr10:43511982..43514503-chr10:43520094..43521790,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RET-2	chr10:43482124-43482459	NONHSAT012938
2	lnc-RASGEF1A-1	chr10:43476816-43476955	XLOC_008790
3	lnc-RET-3	chr10:43489288-43490153	ucscGeneNc_uc001jba_2
4	lnc-RET-3	chr10:43487172-43487532	ucscGeneNc_uc001jba_2
5	lnc-RASGEF1A-1	chr10:43475731-43476007	XLOC_008790
6	lnc-RASGEF1A-1	chr10:43474465-43474547	XLOC_008790
7	lnc-RET-2	chr10:43481122-43481247	NONHSAT012938
8	lnc-RET-3	chr10:43486575-43486975	ucscGeneNc_uc001jba_2
9	lnc-RET-3	chr10:43487762-43487899	ucscGeneNc_uc001jba_2

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5100	chr10:43493078-43493099	MIMAT0022259

No data

Variant related genes	Relation type
MIR5100	TF binding region
ENSG00000229630	TF binding region
MIR5100	CpG island
ENSG00000229630	CpG island
ENSG00000138780	chromatin interactions
ENSG00000136059	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000234944	chromatin interactions
ENSG00000229630	chromatin interactions
ENSG00000110330	chromatin interactions
ENSG00000263795	chromatin interactions
ENSG00000138785	chromatin interactions
ENSG00000109519	chromatin interactions

Extended variants
information (count: 2333 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2333 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17431892	chr10:43467392-43467393	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188448583	chr10:43467397-43467398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559955061	chr10:43467417-43467418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527289144	chr10:43467459-43467460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs193204863	chr10:43467486-43467487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115687775	chr10:43467496-43467497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111414750	chr10:43467514-43467515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138093040	chr10:43467533-43467534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149109122	chr10:43467606-43467607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183267149	chr10:43467631-43467632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs375673627	chr10:43467668-43467669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547386626	chr10:43467669-43467670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573538002	chr10:43467680-43467681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116603883	chr10:43467691-43467692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539472251	chr10:43467724-43467725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143680737	chr10:43467815-43467816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569701927	chr10:43467826-43467827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376137893	chr10:43467836-43467837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2995398	chr10:43467875-43467876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs148081076	chr10:43467886-43467887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs115939156	chr10:43467952-43467953	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs186617026	chr10:43467981-43467982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553410202	chr10:43468008-43468009	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs143931160	chr10:43468028-43468029	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563471572	chr10:43468060-43468061	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs191458425	chr10:43468101-43468102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs35621984	chr10:43468152-43468153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538646799	chr10:43468159-43468160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs74709238	chr10:43468172-43468173	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs377362008	chr10:43468193-43468194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs147275968	chr10:43468220-43468221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs529081591	chr10:43468235-43468236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577254572	chr10:43468252-43468253	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs73260394	chr10:43468269-43468270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs189975640	chr10:43468276-43468277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551242147	chr10:43468336-43468337	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs546119833	chr10:43468337-43468338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569764258	chr10:43468339-43468340	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs537005440	chr10:43468375-43468376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs549210343	chr10:43468378-43468379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs567719735	chr10:43468382-43468383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs72779312	chr10:43468387-43468388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs78296233	chr10:43468395-43468396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs185167546	chr10:43468406-43468407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs139109986	chr10:43468432-43468433	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371517839	chr10:43468439-43468440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs374457225	chr10:43468440-43468441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs373033423	chr10:43468441-43468442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557677259	chr10:43468510-43468511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs576117517	chr10:43468584-43468585	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43465800-43471200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr10:43465800-43471400	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr10:43466000-43471200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr10:43466600-43470200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:43466600-43470400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:43466600-43470800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr10:43466800-43470200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:43467000-43471000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:43468200-43469000	Enhancers	Liver	Liver
10	chr10:43469400-43470000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr10:43469600-43470200	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr10:43470200-43471000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr10:43470200-43471600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr10:43470400-43470600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr10:43470400-43471000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:43470400-43471200	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr10:43470400-43471400	Enhancers	Placenta	Placenta
18	chr10:43470800-43471200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr10:43471000-43471400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr10:43471000-43474800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr10:43471200-43474800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr10:43471600-43474600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr10:43474000-43474200	Bivalent/Poised TSS	Fetal Lung	lung
24	chr10:43474200-43474400	Bivalent Enhancer	Fetal Brain Male	brain
25	chr10:43474200-43474600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr10:43474200-43474600	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr10:43474200-43475000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr10:43474400-43475000	Enhancers	Fetal Brain Male	brain
29	chr10:43474600-43474800	Enhancers	Gastric	stomach
30	chr10:43474600-43475000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr10:43474600-43475400	Enhancers	Brain Germinal Matrix	brain
32	chr10:43474800-43475000	Enhancers	K562	blood
33	chr10:43474800-43475200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr10:43474800-43475200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr10:43474800-43475200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr10:43474800-43475400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr10:43474800-43475400	Weak transcription	Gastric	stomach
38	chr10:43474800-43476000	Enhancers	Pancreas	Pancrea
39	chr10:43475000-43475200	Enhancers	Stomach Mucosa	stomach
40	chr10:43475000-43477200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr10:43475200-43475600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr10:43475200-43475600	Enhancers	Dnd41	blood
43	chr10:43475400-43475600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr10:43475400-43475600	Bivalent Enhancer	Fetal Stomach	stomach
45	chr10:43475400-43476600	Weak transcription	Stomach Mucosa	stomach
46	chr10:43475400-43477600	Enhancers	Gastric	stomach
47	chr10:43475600-43477800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr10:43476000-43476200	Weak transcription	Pancreas	Pancrea
49	chr10:43476000-43476200	Active TSS	Spleen	Spleen
50	chr10:43476000-43479000	Enhancers	Fetal Intestine Small	intestine

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