Variant report

Variant	nsv1003322
Chromosome Location	chr2:34898412-35216795
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:607)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:44)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:35041098-35041398	K562	blood:	n/a	n/a
2	BACH1	chr2:34989249-34989315	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr2:34902925-34903229	GM12878	blood:	n/a	n/a
4	BATF	chr2:34902921-34903226	GM12878	blood:	n/a	n/a
5	BATF	chr2:34902415-34902679	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:34908833-34908941	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:34930671-34930923	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:35042118-35042381	HepG2	liver:	n/a	n/a
9	BHLHE40	chr2:34963851-34964109	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:35047276-35047302	K562	blood:	n/a	n/a
11	BHLHE40	chr2:35041520-35041884	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:34902255-34902723	GM12878	blood:	n/a	n/a
13	CEBPB	chr2:35175921-35176220	H1-hESC	embryonic stem cell:	n/a	chr2:35176080-35176091
14	CEBPB	chr2:35140749-35141093	HepG2	liver:	n/a	chr2:35140913-35140924 chr2:35140893-35140904
15	CEBPB	chr2:35003237-35003348	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:35157695-35157958	HepG2	liver:	n/a	chr2:35157789-35157800
17	CEBPB	chr2:35174661-35174982	HepG2	liver:	n/a	chr2:35174816-35174827 chr2:35174816-35174829
18	CEBPB	chr2:35157783-35157896	A549	lung:	n/a	chr2:35157789-35157800
19	CEBPB	chr2:35175918-35176267	K562	blood:	n/a	chr2:35176080-35176091
20	CEBPB	chr2:35175897-35176260	IMR90	lung:	n/a	chr2:35176080-35176091
21	CEBPB	chr2:34931219-34931422	HepG2	liver:	n/a	chr2:34931302-34931313
22	CEBPB	chr2:35198711-35198969	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:35100004-35100077	A549	lung:	n/a	n/a
24	CEBPB	chr2:35146505-35146722	HepG2	liver:	n/a	chr2:35146609-35146620 chr2:35146608-35146619
25	CEBPB	chr2:35174670-35174965	A549	lung:	n/a	chr2:35174816-35174827 chr2:35174816-35174829
26	CEBPB	chr2:35080062-35080354	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:35140794-35141058	A549	lung:	n/a	chr2:35140913-35140924 chr2:35140893-35140904
28	CEBPB	chr2:35010577-35010790	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:35175906-35176236	A549	lung:	n/a	chr2:35176080-35176091
30	CEBPB	chr2:34960041-34960126	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:35156794-35157009	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:35175897-35176261	HepG2	liver:	n/a	chr2:35176080-35176091
33	CEBPB	chr2:35175917-35176290	A549	lung:	n/a	chr2:35176080-35176091
34	CEBPB	chr2:34907939-34908176	A549	lung:	n/a	chr2:34908035-34908046
35	CEBPB	chr2:35175907-35176228	Hela-S3	cervix:	n/a	chr2:35176080-35176091
36	CEBPB	chr2:35151291-35151493	HepG2	liver:	n/a	chr2:35151435-35151446 chr2:35151433-35151450
37	CEBPB	chr2:34907924-34908188	HepG2	liver:	n/a	chr2:34908035-34908046
38	CHD1	chr2:34913646-34913857	GM12878	blood:	n/a	n/a
39	CHD1	chr2:34908873-34909006	GM12878	blood:	n/a	n/a
40	CHD1	chr2:34904395-34904596	GM12878	blood:	n/a	n/a
41	CHD1	chr2:34903650-34903710	GM12878	blood:	n/a	n/a
42	CHD1	chr2:35186370-35186423	GM12878	blood:	n/a	n/a
43	CHD1	chr2:34902538-34902913	GM12878	blood:	n/a	n/a
44	CHD2	chr2:35056030-35056177	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr2:34902764-34902800	GM12878	blood:	n/a	n/a
46	CHD2	chr2:35186909-35187241	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr2:34914407-34914412	GM12878	blood:	n/a	n/a
48	CHD2	chr2:34963635-34964103	GM12878	blood:	n/a	n/a
49	CHD2	chr2:34902278-34902563	GM12878	blood:	n/a	n/a
50	CTCF	chr2:34951160-34951310	HRE	kidney:	n/a	chr2:34951208-34951217 chr2:34951206-34951222 chr2:34951205-34951223 chr2:34951210-34951220 chr2:34951196-34951204 chr2:34951207-34951228

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34902113-34902163	BE2_C	brain:	n/a
2	chr2:34902113-34902163	T-47D	breast:	n/a
3	chr2:34902113-34902163	K562	blood:	n/a
4	chr2:34902113-34902163	NHBE	bronchial:	n/a
5	chr2:34902113-34902163	SK-N-SH	brain:	n/a
6	chr2:34902113-34902163	HAEpiC	amniotic membrane:	n/a
7	chr2:34902113-34902163	HCM	heart:	n/a
8	chr2:34902113-34902163	Hepatocyte	liver:	n/a
9	chr2:34902113-34902163	ProgFib	skin:	n/a
10	chr2:34902113-34902163	BJ	skin:	n/a
11	chr2:34902113-34902163	HL-60	blood:	n/a
12	chr2:34902113-34902163	PrEC	prostate:	n/a
13	chr2:34902113-34902163	RPTEC	kidney:	n/a
14	chr2:34902113-34902163	AG09319	gingival:	n/a
15	chr2:34902113-34902163	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:34902113-34902163	GM19239	blood:	n/a
17	chr2:34902113-34902163	IMR90	lung:	fetal
18	chr2:34902113-34902163	GM12892	blood:	n/a
19	chr2:34902113-34902163	AG04449	skin:	fetal
20	chr2:34902113-34902163	SKMC	muscle:	n/a
21	chr2:34902113-34902163	NT2-D1	testis:	n/a
22	chr2:34902113-34902163	A549	lung:	n/a
23	chr2:34902113-34902163	Jurkat	blood:	n/a
24	chr2:34902113-34902163	HMEC	breast:	n/a
25	chr2:34902113-34902163	AG09309	skin:	n/a
26	chr2:34902113-34902163	NHDF-neo	bronchial:	n/a
27	chr2:34902113-34902163	HCPEpiC	choroid plexus:	n/a
28	chr2:34902113-34902163	SK-N-SH_RA	brain:	n/a
29	chr2:34902113-34902163	HEEpiC	esophagus:	n/a
30	chr2:34902113-34902163	CMK	blood:	n/a
31	chr2:34902113-34902163	NB4	blood:	n/a
32	chr2:34902113-34902163	AG10803	skin:	n/a
33	chr2:34902113-34902163	HRCEpiC	kidney:	n/a
34	chr2:34902113-34902163	LNCaP	prostate:	n/a
35	chr2:34902113-34902163	HepG2	liver:	n/a
36	chr2:34902113-34902163	PFSK-1	brain:	n/a
37	chr2:34902113-34902163	HCT-116	colon:	n/a
38	chr2:34902113-34902163	HEK293	kidney:	embryo
39	chr2:34902113-34902163	AoSMC	blood vessel:	n/a
40	chr2:34902113-34902163	PANC-1	pancreas:	n/a
41	chr2:34902113-34902163	AG04450	lung:	fetal
42	chr2:34902113-34902163	U87	brain:	n/a
43	chr2:34902113-34902163	Caco-2	colon:	n/a
44	chr2:34902113-34902163	MCF10A-Er-Src	breast:	n/a
45	chr2:34902113-34902163	GM12878	blood:	n/a
46	chr2:34902113-34902163	MCF-7	breast:	n/a
47	chr2:34902113-34902163	GM06990	blood:	n/a
48	chr2:34902113-34902163	SAEC	small airway:	n/a
49	chr2:34902113-34902163	SK-N-MC	brain:	n/a
50	chr2:34902113-34902163	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:35086981..35089694-chr2:35094487..35097235,2	K562	blood:
2	chr2:35049634..35051232-chr2:35070862..35073503,2	K562	blood:
3	chr2:35130281..35132812-chr2:35144803..35146892,2	K562	blood:
4	chr2:35006274..35008792-chr8:67342394..67345182,2	MCF-7	breast:
5	chr2:34929052..34931868-chr2:34933062..34935710,2	K562	blood:
6	chr2:35152123..35154075-chr2:35162750..35165499,2	K562	blood:
7	chr2:35124308..35126436-chr2:35127473..35129610,2	K562	blood:
8	chr2:35086981..35089694-chr2:35094487..35097235,2	K562	blood:
9	chr2:35152123..35154075-chr2:35162750..35165499,2	K562	blood:
10	chr2:34237581..34238416-chr2:34963443..34964247,2	MCF-7	breast:
11	chr2:35130281..35132812-chr2:35144803..35146892,2	K562	blood:
12	chr2:35130362..35133238-chr2:35148535..35150812,2	K562	blood:
13	chr2:35124308..35126436-chr2:35127473..35129610,2	K562	blood:
14	chr2:35049634..35051232-chr2:35070862..35073503,2	K562	blood:
15	chr2:35130362..35133238-chr2:35148535..35150812,2	K562	blood:
16	chr2:34929052..34931868-chr2:34933062..34935710,2	K562	blood:

(count:44 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-4	chr2:34962148-34962183	NONHSAT070048
2	lnc-RASGRP3-4	chr2:34947066-34947186	ENSG00000228262.4
3	lnc-RASGRP3-4	chr2:34960145-34960753	ENSG00000228262.4
4	lnc-FAM98A-8	chr2:34919267-34919365	ENSG00000272027.1
5	lnc-RASGRP3-4	chr2:34935519-34935571	NONHSAT070044
6	lnc-RASGRP3-4	chr2:34962388-34963298	ENSG00000228262
7	lnc-FAM98A-11	chr2:35078527-35078731	NONHSAT070061
8	lnc-RASGRP3-4	chr2:34957515-34957624	ENSG00000228262.4
9	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
10	lnc-RASGRP3-4	chr2:34935519-34935580	ENSG00000228262.4
11	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
12	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
13	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
14	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
15	lnc-RASGRP3-4	chr2:34938657-34938840	ENSG00000228262.4
16	lnc-RASGRP3-4	chr2:34962388-34962644	ENSG00000228262.4
17	lnc-FAM98A-11	chr2:35076849-35077075	NONHSAT070061
18	lnc-RASGRP3-4	chr2:34947066-34947188	ENSG00000228262.4
19	lnc-FAM98A-8	chr2:34917357-34917552	ENSG00000272027.1
20	lnc-RASGRP3-4	chr2:34962388-34962638	ENSG00000228262.4
21	lnc-RASGRP3-4	chr2:34938657-34938840	ENSG00000228262
22	lnc-CRIM1-1	chr2:35056430-35056559	XLOC_001425
23	lnc-RASGRP3-4	chr2:34959627-34961285	NONHSAT070048
24	lnc-RASGRP3-4	chr2:34957515-34957624	ENSG00000228262
25	lnc-RASGRP3-4	chr2:34938646-34938840	ENSG00000228262.4
26	lnc-CRIM1-1	chr2:35024917-35024966	XLOC_001425
27	lnc-FAM98A-2	chr2:34962148-34962185	ENSG00000232153
28	lnc-RASGRP3-4	chr2:34938646-34938840	ENSG00000228262.4
29	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
30	lnc-RASGRP3-4	chr2:34947066-34947580	ENSG00000228262.4
31	lnc-RASGRP3-4	chr2:34956433-34956605	ENSG00000228262.4
32	lnc-FAM98A-10	chr2:35034320-35034623	NONHSAT070053
33	lnc-RASGRP3-4	chr2:34935518-34935580	NONHSAT070045
34	lnc-RASGRP3-5	chr2:35041549-35041945	XLOC_001426
35	lnc-RASGRP3-4	chr2:34962172-34963510	NONHSAT070051
36	lnc-RASGRP3-4	chr2:34978401-34978447	NONHSAT070051
37	lnc-RASGRP3-4	chr2:34902711-34902994	NONHSAT070044
38	lnc-RASGRP3-4	chr2:34929778-34929989	ENSG00000228262.4
39	lnc-FAM98A-11	chr2:35077532-35077593	NONHSAT070061
40	lnc-RASGRP3-4	chr2:34938646-34938840	NONHSAT070045
41	lnc-RASGRP3-5	chr2:35042159-35042319	XLOC_001426
42	lnc-FAM98A-2	chr2:34960042-34960174	ENSG00000232153
43	lnc-RASGRP3-15	chr2:34909934-34910063	NONHSAT070041
44	lnc-RASGRP3-4	chr2:34947066-34950118	NONHSAT070045

No data

Variant related genes	Relation type
ENSG00000272027	TF binding region
ENSG00000232153	TF binding region
ENSG00000228262	TF binding region
ENSG00000226994	TF binding region
RN7SL602P	TF binding region
ENSG00000272027	CpG island
ENSG00000232153	CpG island
ENSG00000228262	CpG island
ENSG00000226994	CpG island
RN7SL602P	CpG island
ENSG00000147576	chromatin interactions
ENSG00000228262	chromatin interactions
NAP1L1	miRNA target sites

Extended variants
information (count: 8365 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:8365 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185161758	chr2:34901338-34901339	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs576716560	chr2:34901603-34901604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556109675	chr2:34901622-34901623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560669314	chr2:34901640-34901641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529705902	chr2:34901668-34901669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542821351	chr2:34901676-34901677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562695367	chr2:34901683-34901684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534724674	chr2:34901748-34901749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191205570	chr2:34901753-34901754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552034967	chr2:34901758-34901759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370767279	chr2:34901764-34901765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs71449526	chr2:34901765-34901766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377331073	chr2:34901766-34901767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79815808	chr2:34901768-34901769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398104176	chr2:34901769-34901770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368510459	chr2:34901770-34901771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181184962	chr2:34901790-34901791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186906611	chr2:34901795-34901796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147716352	chr2:34901804-34901805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10177777	chr2:34901820-34901821	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs542477084	chr2:34901885-34901886	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs7560410	chr2:34901902-34901903	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs556446722	chr2:34901903-34901904	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs7560419	chr2:34901935-34901936	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs35651537	chr2:34901969-34901970	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs115979877	chr2:34902007-34902008	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs552700895	chr2:34902018-34902019	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs199905577	chr2:34902024-34902025	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs34341706	chr2:34902029-34902030	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs191739765	chr2:34902037-34902038	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs386644712	chr2:34902062-34902063	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs113371860	chr2:34902063-34902064	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs28671161	chr2:34902064-34902065	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs561871224	chr2:34902087-34902088	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs183435466	chr2:34902113-34902114	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs187717118	chr2:34902141-34902142	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs114897594	chr2:34902158-34902159	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs377606281	chr2:34902169-34902170	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs537227801	chr2:34902171-34902172	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs7575839	chr2:34902177-34902178	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs111352817	chr2:34902183-34902184	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs527940222	chr2:34902205-34902206	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs552146517	chr2:34902218-34902219	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs547817911	chr2:34902243-34902244	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs182209862	chr2:34902299-34902300	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs530261852	chr2:34902306-34902307	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs187754985	chr2:34902310-34902311	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs71449527	chr2:34902320-34902321	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs373408390	chr2:34902324-34902325	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs569777085	chr2:34902325-34902326	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34901600-34902400	Enhancers	Liver	Liver
2	chr2:34902400-34902600	Flanking Active TSS	Liver	Liver
3	chr2:34902600-34903000	Enhancers	Pancreas	Pancrea
4	chr2:34902600-34903200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:34902600-34904400	Active TSS	Liver	Liver
6	chr2:34903000-34904200	Active TSS	Fetal Kidney	kidney
7	chr2:34908800-34909400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr2:34919400-34919600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:34919600-34926000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:34926000-34926400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:34926000-34926400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:34926200-34926600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr2:34926400-34927800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:34926400-34957600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:34926600-34927800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr2:34927800-34928200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr2:34927800-34928200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:34927800-34928400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr2:34927800-34928400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr2:34927800-34928400	Enhancers	Pancreas	Pancrea
21	chr2:34928000-34928800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr2:34928200-34929200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:34928200-34929400	Enhancers	Liver	Liver
24	chr2:34929200-34931000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:34929400-34930400	Weak transcription	Liver	Liver
26	chr2:34930400-34930800	Active TSS	Liver	Liver
27	chr2:34930800-34931400	Flanking Active TSS	Liver	Liver
28	chr2:34931000-34931400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:34931400-34931800	Enhancers	Liver	Liver
30	chr2:34931800-34932200	Weak transcription	Liver	Liver
31	chr2:34932200-34932400	Enhancers	Liver	Liver
32	chr2:34932400-34939000	Weak transcription	Liver	Liver
33	chr2:34939000-34939800	Strong transcription	Liver	Liver
34	chr2:34939800-34952800	Weak transcription	Liver	Liver
35	chr2:34941000-34942400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:34942400-34945400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:34942600-34944400	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr2:34942800-34943600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:34942800-34944400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr2:34943000-34944400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr2:34943200-34944000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr2:34943800-34944200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr2:34944000-34944800	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr2:34944800-34945000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
45	chr2:34945000-34946000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr2:34945400-34949800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:34946000-34946400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
48	chr2:34946400-34947400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr2:34949800-34950400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:34951200-34951400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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