Variant report

Variant	nsv895366
Chromosome Location	chr10:49299274-49576454
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3256)
CpG islands
(count:1772)
Chromatin interactive
region (count:187)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3256 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:49499283-49499420	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:49402930-49403171	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:49517762-49518319	K562	blood:	n/a	n/a
4	ARID3A	chr10:49571602-49572216	K562	blood:	n/a	n/a
5	ARID3A	chr10:49517881-49518317	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:49568402-49569571	K562	blood:	n/a	chr10:49569138-49569154
7	ARID3A	chr10:49571652-49572193	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:49514425-49514517	K562	blood:	n/a	n/a
9	ARID3A	chr10:49572586-49573103	HepG2	liver:	n/a	n/a
10	ARID3A	chr10:49395850-49396192	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:49514699-49514899	HepG2	liver:	n/a	n/a
12	ATF1	chr10:49540982-49541199	K562	blood:	n/a	n/a
13	ATF1	chr10:49568436-49568787	K562	blood:	n/a	n/a
14	ATF1	chr10:49433149-49433416	K562	blood:	n/a	n/a
15	ATF1	chr10:49499290-49499629	K562	blood:	n/a	n/a
16	ATF1	chr10:49497714-49498043	K562	blood:	n/a	n/a
17	ATF2	chr10:49486941-49487901	GM12878	blood:	n/a	n/a
18	ATF2	chr10:49493627-49494187	GM12878	blood:	n/a	n/a
19	ATF2	chr10:49486865-49488015	GM12878	blood:	n/a	n/a
20	ATF2	chr10:49544824-49545622	GM12878	blood:	n/a	n/a
21	ATF2	chr10:49497434-49498032	GM12878	blood:	n/a	n/a
22	ATF2	chr10:49544810-49545603	GM12878	blood:	n/a	n/a
23	ATF2	chr10:49493624-49494189	GM12878	blood:	n/a	n/a
24	ATF2	chr10:49439298-49440117	GM12878	blood:	n/a	n/a
25	ATF2	chr10:49490835-49491395	GM12878	blood:	n/a	n/a
26	ATF2	chr10:49497607-49498044	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr10:49490829-49491340	GM12878	blood:	n/a	n/a
28	ATF2	chr10:49495897-49496410	GM12878	blood:	n/a	n/a
29	ATF3	chr10:49514255-49514895	K562	blood:	n/a	n/a
30	BACH1	chr10:49515040-49515249	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr10:49547080-49547086	K562	blood:	n/a	n/a
32	BATF	chr10:49487504-49487868	GM12878	blood:	n/a	n/a
33	BATF	chr10:49544991-49545441	GM12878	blood:	n/a	chr10:49545213-49545224
34	BATF	chr10:49414070-49414325	GM12878	blood:	n/a	chr10:49414164-49414174
35	BATF	chr10:49495976-49496300	GM12878	blood:	n/a	n/a
36	BATF	chr10:49480801-49481052	GM12878	blood:	n/a	n/a
37	BATF	chr10:49495983-49496331	GM12878	blood:	n/a	n/a
38	BATF	chr10:49539529-49539813	GM12878	blood:	n/a	n/a
39	BATF	chr10:49474596-49474854	GM12878	blood:	n/a	n/a
40	BATF	chr10:49493773-49494002	GM12878	blood:	n/a	n/a
41	BATF	chr10:49490920-49491270	GM12878	blood:	n/a	n/a
42	BATF	chr10:49439308-49439566	GM12878	blood:	n/a	n/a
43	BATF	chr10:49544894-49545460	GM12878	blood:	n/a	chr10:49545213-49545224
44	BATF	chr10:49493745-49494164	GM12878	blood:	n/a	n/a
45	BATF	chr10:49517737-49518300	GM12878	blood:	n/a	n/a
46	BATF	chr10:49532622-49532924	GM12878	blood:	n/a	chr10:49532764-49532775 chr10:49532765-49532775
47	BATF	chr10:49517766-49518251	GM12878	blood:	n/a	n/a
48	BATF	chr10:49474491-49474913	GM12878	blood:	n/a	n/a
49	BATF	chr10:49417399-49417601	GM12878	blood:	n/a	n/a
50	BATF	chr10:49486980-49487476	GM12878	blood:	n/a	n/a

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49365197-49365247	HCM	heart:	n/a
2	chr10:49381591-49381641	HRCEpiC	kidney:	n/a
3	chr10:49459800-49459850	NH-A	brain:	n/a
4	chr10:49365197-49365247	HCM	heart:	n/a
5	chr10:49381591-49381641	HRCEpiC	kidney:	n/a
6	chr10:49459800-49459850	NH-A	brain:	n/a
7	chr10:49482826-49482876	HRE	kidney:	n/a
8	chr10:49381591-49381641	HEEpiC	esophagus:	n/a
9	chr10:49482723-49482773	HMEC	breast:	n/a
10	chr10:49514530-49514580	PFSK-1	brain:	n/a
11	chr10:49348564-49348614	HEK293	kidney:	embryo
12	chr10:49387924-49387974	HEEpiC	esophagus:	n/a
13	chr10:49365197-49365247	A549	lung:	n/a
14	chr10:49483356-49483406	PrEC	prostate:	n/a
15	chr10:49514530-49514580	AG04450	lung:	fetal
16	chr10:49517767-49517817	T-47D	breast:	n/a
17	chr10:49517767-49517817	NT2-D1	testis:	n/a
18	chr10:49482871-49482921	AG09309	skin:	n/a
19	chr10:49348564-49348614	AoSMC	blood vessel:	n/a
20	chr10:49460154-49460204	ProgFib	skin:	n/a
21	chr10:49348564-49348614	PANC-1	pancreas:	n/a
22	chr10:49515028-49515078	T-47D	breast:	n/a
23	chr10:49459949-49459999	HNPCEpiC	eye:	n/a
24	chr10:49482767-49482817	HCF	heart:	n/a
25	chr10:49516634-49516684	AoSMC	blood vessel:	n/a
26	chr10:49348564-49348614	LNCaP	prostate:	n/a
27	chr10:49482826-49482876	T-47D	breast:	n/a
28	chr10:49460154-49460204	GM12878	blood:	n/a
29	chr10:49482826-49482876	NH-A	brain:	n/a
30	chr10:49483700-49483750	HNPCEpiC	eye:	n/a
31	chr10:49388054-49388104	BE2_C	brain:	n/a
32	chr10:49514273-49514323	HCT-116	colon:	n/a
33	chr10:49460249-49460299	HRE	kidney:	n/a
34	chr10:49483700-49483750	AG09319	gingival:	n/a
35	chr10:49514337-49514387	U87	brain:	n/a
36	chr10:49514337-49514387	HCM	heart:	n/a
37	chr10:49515028-49515078	PFSK-1	brain:	n/a
38	chr10:49459800-49459850	HEEpiC	esophagus:	n/a
39	chr10:49444466-49444516	HRCEpiC	kidney:	n/a
40	chr10:49483700-49483750	GM12891	blood:	n/a
41	chr10:49348564-49348614	PFSK-1	brain:	n/a
42	chr10:49514337-49514387	HEK293	kidney:	embryo
43	chr10:49483356-49483406	HUVEC	blood vessel:	n/a
44	chr10:49571897-49571947	MCF10A-Er-Src	breast:	n/a
45	chr10:49514273-49514323	NH-A	brain:	n/a
46	chr10:49483700-49483750	K562	blood:	n/a
47	chr10:49460249-49460299	GM19239	blood:	n/a
48	chr10:49482767-49482817	SKMC	muscle:	n/a
49	chr10:49459800-49459850	AG09319	gingival:	n/a
50	chr10:49514337-49514387	PrEC	prostate:	n/a

(count:187 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr10:49423588..49424151-chr10:49714065..49715162,3	MCF-7	breast:
2	chr10:49498367..49502317-chr10:49513526..49516072,3	MCF-7	breast:
3	chr10:49451828..49454602-chr10:49458352..49460279,2	K562	blood:
4	chr10:49514705..49518265-chr10:49536043..49538219,3	K562	blood:
5	chr10:49423310..49424126-chr10:49540299..49540827,2	MCF-7	breast:
6	chr10:49423144..49424160-chr10:49497116..49498379,10	MCF-7	breast:
7	chr10:49518947..49521091-chr10:49533089..49535117,2	K562	blood:
8	chr10:49528331..49530432-chr10:49537117..49539235,2	K562	blood:
9	chr10:49433973..49437325-chr10:49440787..49445569,4	K562	blood:
10	chr10:49570196..49573404-chr10:49729951..49734102,5	K562	blood:
11	chr10:49569844..49571916-chr17:59471462..59473939,2	MCF-7	breast:
12	chr10:49571145..49574084-chr10:49715215..49717894,2	MCF-7	breast:
13	chr10:49489462..49491590-chr10:49496144..49498930,2	MCF-7	breast:
14	chr10:49497874..49500351-chr10:49502359..49504964,2	MCF-7	breast:
15	chr10:49495690..49496196-chr10:51547486..51547990,2	MCF-7	breast:
16	chr10:49521352..49523336-chr10:49525109..49528054,2	MCF-7	breast:
17	chr10:49507404..49509732-chr10:49510277..49512510,2	K562	blood:
18	chr10:49460728..49464367-chr10:49465892..49469453,3	K562	blood:
19	chr10:49517027..49519236-chr10:49642083..49643882,2	K562	blood:
20	chr10:49414750..49417091-chr10:49417343..49420422,3	K562	blood:
21	chr10:49430760..49432504-chr10:49497937..49500737,2	K562	blood:
22	chr10:49571319..49572300-chr10:49717652..49718657,4	MCF-7	breast:
23	chr10:49525969..49527721-chr10:49529565..49532271,2	K562	blood:
24	chr10:49544127..49546033-chr10:49548139..49550800,2	K562	blood:
25	chr10:49518153..49519864-chr10:49521781..49524737,2	MCF-7	breast:
26	chr10:49488285..49491107-chr10:49498371..49500631,2	MCF-7	breast:
27	chr10:49391985..49393913-chr10:49401403..49403869,2	K562	blood:
28	chr10:49423127..49424126-chr10:49497102..49498218,5	MCF-7	breast:
29	chr10:49540878..49543802-chr10:49546206..49547724,2	K562	blood:
30	chr10:49540944..49543155-chr10:49549106..49551548,2	MCF-7	breast:
31	chr10:49415578..49417989-chr16:3671827..3674383,2	MCF-7	breast:
32	chr10:49513964..49516103-chr10:49525788..49528265,2	MCF-7	breast:
33	chr10:49527138..49528910-chr10:49653802..49655584,2	K562	blood:
34	chr10:49517657..49518610-chr10:49713350..49714126,2	MCF-7	breast:
35	chr10:49455241..49456959-chr10:49462949..49465290,2	MCF-7	breast:
36	chr10:49423481..49424232-chr10:49497847..49498349,2	K562	blood:
37	chr10:49423144..49424160-chr10:49497116..49498379,10	MCF-7	breast:
38	chr10:49489462..49491590-chr10:49496144..49498930,2	MCF-7	breast:
39	chr10:49496582..49501262-chr10:49513244..49517429,4	K562	blood:
40	chr10:49538148..49542508-chr10:49545021..49547777,3	K562	blood:
41	chr10:49574821..49576525-chr10:49722125..49725054,2	K562	blood:
42	chr10:49506365..49508904-chr10:49509611..49511777,2	K562	blood:
43	chr10:49516332..49518147-chr10:49551001..49553402,2	MCF-7	breast:
44	chr10:49414468..49418793-chr10:49423679..49426769,3	K562	blood:
45	chr10:49575086..49577260-chr10:49608077..49611007,2	K562	blood:
46	chr10:49572362..49572988-chr10:49851740..49852675,2	K562	blood:
47	chr10:49504955..49507590-chr10:49509692..49512990,3	MCF-7	breast:
48	chr10:49464368..49465891-chr10:49470466..49472102,2	MCF-7	breast:
49	chr10:49390312..49393030-chr10:49413165..49415155,2	K562	blood:
50	chr10:49423548..49424230-chr10:49863873..49864448,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRMPD2-2	chr10:49550355-49550475	NONHSAT013265
2	lnc-MAPK8-4	chr10:49456119-49456389	NONHSAT013262
3	lnc-PTPN20C-3	chr10:49357092-49357245	ucscGeneNc_uc001jgw_2
4	lnc-PTPN20C-2	chr10:49407711-49407889	ENSG00000248306.1
5	lnc-PTPN20C-6	chr10:49387910-49389727	ucscGeneNc_uc001jgx_1
6	lnc-PTPN20C-7	chr10:49456586-49457221	NONHSAT013263
7	lnc-MAPK8-4	chr10:49455216-49455941	NONHSAT013262
8	lnc-PTPN20C-7	chr10:49459609-49459654	NONHSAT013263
9	lnc-MAPK8-6	chr10:49313937-49314716	expReg_chr10_2502_+
10	lnc-MAPK8-5	chr10:49316927-49317254	expReg_chr10_2514_+
11	lnc-PTPN20C-3	chr10:49346057-49347865	ucscGeneNc_uc001jgw_2
12	lnc-PTPN20C-1	chr10:49364136-49364177	ENSG00000232462.1
13	lnc-MAPK8-3	chr10:49500742-49501460	NONHSAT013264
14	lnc-FRMPD2-2	chr10:49542250-49542463	NONHSAT013265
15	lnc-PTPN20C-1	chr10:49363368-49363746	ENSG00000232462.1
16	lnc-PTPN20C-2	chr10:49409271-49409697	ENSG00000248306.1

No data

Variant related genes	Relation type
PTPN20CP	TF binding region
MAPK8	TF binding region
ENSG00000232462	TF binding region
FRMPD2	TF binding region
ENSG00000225482	TF binding region
PTPN20CP	CpG island
MAPK8	CpG island
ENSG00000232462	CpG island
FRMPD2	CpG island
ENSG00000225482	CpG island
ENSG00000187742	chromatin interactions
ENSG00000128805	chromatin interactions
ENSG00000225482	chromatin interactions
ENSG00000111371	chromatin interactions
ENSG00000107643	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000248682	chromatin interactions
ENSG00000113407	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000170324	chromatin interactions

Extended variants
information (count: 7806 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:7806 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138195894	chr10:49310509-49310510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185504229	chr10:49310590-49310591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191579497	chr10:49310598-49310599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558449027	chr10:49310648-49310649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143098719	chr10:49310649-49310650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544165530	chr10:49310739-49310740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562733244	chr10:49310782-49310783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529844001	chr10:49311107-49311108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543145062	chr10:49311127-49311128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561324246	chr10:49311144-49311145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565306225	chr10:49314146-49314147	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs182558120	chr10:49314191-49314192	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs551266185	chr10:49314321-49314322	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs569405478	chr10:49314373-49314374	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs530340159	chr10:49314399-49314400	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs548342006	chr10:49314407-49314408	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs187976247	chr10:49314452-49314453	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs536401310	chr10:49314453-49314454	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs533672368	chr10:49314526-49314527	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs558230079	chr10:49314537-49314538	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs570464759	chr10:49314613-49314614	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs199855129	chr10:49318679-49318680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540777286	chr10:49318817-49318818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565338595	chr10:49318856-49318857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577172848	chr10:49318868-49318869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2652370	chr10:49318884-49318885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs369804133	chr10:49318978-49318979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150013691	chr10:49319300-49319301	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
29	rs151200482	chr10:49319323-49319324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs556133196	chr10:49319921-49319922	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs983721	chr10:49319933-49319934	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs183414315	chr10:49319942-49319943	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs983722	chr10:49319950-49319951	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs544679057	chr10:49320027-49320028	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs562773805	chr10:49320031-49320032	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs374071451	chr10:49320144-49320145	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs574775850	chr10:49320146-49320147	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs572454053	chr10:49320207-49320208	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs367989472	chr10:49320287-49320288	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs199613641	chr10:49320822-49320823	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs542161028	chr10:49320960-49320961	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs560371583	chr10:49321040-49321041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs527880328	chr10:49321042-49321043	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs552322880	chr10:49321379-49321380	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs564220810	chr10:49321530-49321531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs371567115	chr10:49321604-49321605	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs368501799	chr10:49321634-49321635	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs371434469	chr10:49321774-49321775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs531339673	chr10:49321782-49321783	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs549824394	chr10:49321818-49321819	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
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
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
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
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2354 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49310400-49310800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr10:49310400-49310800	Enhancers	Fetal Thymus	thymus
3	chr10:49310400-49311200	Enhancers	Dnd41	blood
4	chr10:49318600-49319000	Enhancers	Dnd41	blood
5	chr10:49356400-49357000	Enhancers	Dnd41	blood
6	chr10:49361000-49361200	Enhancers	Fetal Thymus	thymus
7	chr10:49361200-49362200	Weak transcription	Fetal Thymus	thymus
8	chr10:49362200-49363000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:49362200-49363200	Enhancers	Fetal Thymus	thymus
10	chr10:49362800-49363600	Enhancers	Dnd41	blood
11	chr10:49378400-49379000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr10:49379000-49380400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr10:49380400-49381000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr10:49380400-49381800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr10:49380600-49381000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr10:49380600-49381000	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr10:49380800-49381000	Enhancers	Brain Substantia Nigra	brain
18	chr10:49381000-49390400	Weak transcription	Brain Substantia Nigra	brain
19	chr10:49390400-49390800	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr10:49390400-49391000	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr10:49390400-49391200	Enhancers	Brain Substantia Nigra	brain
22	chr10:49390400-49391400	Enhancers	Brain Anterior Caudate	brain
23	chr10:49390600-49390800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr10:49390600-49391000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr10:49390600-49391200	Enhancers	Brain Hippocampus Middle	brain
26	chr10:49390800-49391000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr10:49390800-49395800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr10:49391000-49396200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr10:49393600-49393800	Enhancers	Fetal Brain Male	brain
30	chr10:49393800-49400000	Weak transcription	Fetal Brain Male	brain
31	chr10:49394200-49395800	Weak transcription	Brain Anterior Caudate	brain
32	chr10:49394600-49394800	Bivalent/Poised TSS	K562	blood
33	chr10:49394800-49395000	Flanking Bivalent TSS/Enh	K562	blood
34	chr10:49394800-49398000	Enhancers	Fetal Intestine Large	intestine
35	chr10:49395000-49395400	Flanking Active TSS	K562	blood
36	chr10:49395000-49395800	Enhancers	HepG2	liver
37	chr10:49395200-49396000	Enhancers	Right Atrium	heart
38	chr10:49395200-49397000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr10:49395200-49398000	Enhancers	Fetal Intestine Small	intestine
40	chr10:49395400-49396000	Enhancers	K562	blood
41	chr10:49395800-49396000	Enhancers	Brain Anterior Caudate	brain
42	chr10:49395800-49396400	Enhancers	Fetal Lung	lung
43	chr10:49395800-49396600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr10:49395800-49396600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr10:49395800-49396600	Enhancers	Fetal Muscle Leg	muscle
46	chr10:49395800-49396600	Enhancers	Left Ventricle	heart
47	chr10:49395800-49397000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr10:49395800-49397000	Flanking Active TSS	HepG2	liver
49	chr10:49396000-49396600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr10:49396000-49396800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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