Variant report

Variant	nsv1003361
Chromosome Location	chr2:34746445-35202302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1054)
CpG islands
(count:122)
Chromatin interactive
region (count:25)
LncRNA
region (count:58)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1054 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:34814574-34814687	K562	blood:	n/a	n/a
2	ATF1	chr2:35041098-35041398	K562	blood:	n/a	n/a
3	BACH1	chr2:34989249-34989315	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:34881803-34882061	GM12878	blood:	n/a	n/a
5	BATF	chr2:34902921-34903226	GM12878	blood:	n/a	n/a
6	BATF	chr2:34902415-34902679	GM12878	blood:	n/a	n/a
7	BATF	chr2:34902925-34903229	GM12878	blood:	n/a	n/a
8	BCL3	chr2:34803709-34804015	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:35047276-35047302	K562	blood:	n/a	n/a
10	BHLHE40	chr2:34891473-34891834	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:34963851-34964109	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:35042118-35042381	HepG2	liver:	n/a	n/a
13	BHLHE40	chr2:34902255-34902723	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:34908833-34908941	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:34795688-34795858	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:34827333-34827668	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:34930671-34930923	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:35041520-35041884	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:34759877-34760165	K562	blood:	n/a	chr2:34759972-34759985
20	CEBPB	chr2:34759886-34760188	MCF-7	breast:	n/a	chr2:34759972-34759985
21	CEBPB	chr2:35010577-35010790	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:34960041-34960126	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:34840044-34840132	A549	lung:	n/a	n/a
24	CEBPB	chr2:34788007-34788119	K562	blood:	n/a	chr2:34788088-34788101 chr2:34788090-34788101 chr2:34788088-34788101 chr2:34788090-34788101
25	CEBPB	chr2:35175918-35176267	K562	blood:	n/a	chr2:35176080-35176091
26	CEBPB	chr2:34876038-34876081	K562	blood:	n/a	n/a
27	CEBPB	chr2:34795632-34795901	MCF-7	breast:	n/a	n/a
28	CEBPB	chr2:34850841-34851040	A549	lung:	n/a	chr2:34850939-34850950 chr2:34850903-34850914
29	CEBPB	chr2:35080062-35080354	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:35175906-35176236	A549	lung:	n/a	chr2:35176080-35176091
31	CEBPB	chr2:34931219-34931422	HepG2	liver:	n/a	chr2:34931302-34931313
32	CEBPB	chr2:35175917-35176290	A549	lung:	n/a	chr2:35176080-35176091
33	CEBPB	chr2:35003237-35003348	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:35100004-35100077	A549	lung:	n/a	n/a
35	CEBPB	chr2:35175897-35176261	HepG2	liver:	n/a	chr2:35176080-35176091
36	CEBPB	chr2:34759033-34759047	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:35157695-35157958	HepG2	liver:	n/a	chr2:35157789-35157800
38	CEBPB	chr2:35140749-35141093	HepG2	liver:	n/a	chr2:35140913-35140924 chr2:35140893-35140904
39	CEBPB	chr2:34907939-34908176	A549	lung:	n/a	chr2:34908035-34908046
40	CEBPB	chr2:35198711-35198969	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:35175921-35176220	H1-hESC	embryonic stem cell:	n/a	chr2:35176080-35176091
42	CEBPB	chr2:34850814-34851079	HepG2	liver:	n/a	chr2:34850939-34850950 chr2:34850903-34850914
43	CEBPB	chr2:35140794-35141058	A549	lung:	n/a	chr2:35140913-35140924 chr2:35140893-35140904
44	CEBPB	chr2:34907924-34908188	HepG2	liver:	n/a	chr2:34908035-34908046
45	CEBPB	chr2:35151291-35151493	HepG2	liver:	n/a	chr2:35151435-35151446 chr2:35151433-35151450
46	CEBPB	chr2:35175897-35176260	IMR90	lung:	n/a	chr2:35176080-35176091
47	CEBPB	chr2:35157783-35157896	A549	lung:	n/a	chr2:35157789-35157800
48	CEBPB	chr2:34793002-34793270	HepG2	liver:	n/a	chr2:34793159-34793170 chr2:34793159-34793172 chr2:34793160-34793171
49	CEBPB	chr2:34759749-34759988	HepG2	liver:	n/a	chr2:34759832-34759845 chr2:34759832-34759843 chr2:34759972-34759985
50	CEBPB	chr2:35174661-35174982	HepG2	liver:	n/a	chr2:35174816-35174827 chr2:35174816-35174829

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34852273-34852323	GM12891	blood:	n/a
2	chr2:34852273-34852323	NT2-D1	testis:	n/a
3	chr2:34902113-34902163	HUVEC	blood vessel:	n/a
4	chr2:34852273-34852323	HCF	heart:	n/a
5	chr2:34852273-34852323	AG10803	skin:	n/a
6	chr2:34852273-34852323	CMK	blood:	n/a
7	chr2:34902113-34902163	LNCaP	prostate:	n/a
8	chr2:34852273-34852323	Caco-2	colon:	n/a
9	chr2:34902113-34902163	CMK	blood:	n/a
10	chr2:34902113-34902163	HRPEpiC	eye:	n/a
11	chr2:34902113-34902163	Hepatocyte	liver:	n/a
12	chr2:34852273-34852323	ProgFib	skin:	n/a
13	chr2:34902113-34902163	HAEpiC	amniotic membrane:	n/a
14	chr2:34902113-34902163	RPTEC	kidney:	n/a
15	chr2:34902113-34902163	NHDF-neo	bronchial:	n/a
16	chr2:34852273-34852323	ovcar-3	ovarian:	n/a
17	chr2:34852273-34852323	HCPEpiC	choroid plexus:	n/a
18	chr2:34852273-34852323	HCM	heart:	n/a
19	chr2:34852273-34852323	HAEpiC	amniotic membrane:	n/a
20	chr2:34852273-34852323	GM19239	blood:	n/a
21	chr2:34902113-34902163	PANC-1	pancreas:	n/a
22	chr2:34852273-34852323	GM12892	blood:	n/a
23	chr2:34902113-34902163	IMR90	lung:	fetal
24	chr2:34852273-34852323	NH-A	brain:	n/a
25	chr2:34852273-34852323	PrEC	prostate:	n/a
26	chr2:34902113-34902163	HepG2	liver:	n/a
27	chr2:34902113-34902163	MCF10A-Er-Src	breast:	n/a
28	chr2:34902113-34902163	HRE	kidney:	n/a
29	chr2:34852273-34852323	H1-hESC	embryonic stem cell:	embryo
30	chr2:34852273-34852323	IMR90	lung:	fetal
31	chr2:34902113-34902163	AG04449	skin:	fetal
32	chr2:34902113-34902163	ECC-1	luminal epithelium:	n/a
33	chr2:34902113-34902163	HMEC	breast:	n/a
34	chr2:34852273-34852323	U87	brain:	n/a
35	chr2:34852273-34852323	AG04449	skin:	fetal
36	chr2:34902113-34902163	GM12891	blood:	n/a
37	chr2:34902113-34902163	AG04450	lung:	fetal
38	chr2:34902113-34902163	HCM	heart:	n/a
39	chr2:34852273-34852323	Hepatocyte	liver:	n/a
40	chr2:34852273-34852323	SKMC	muscle:	n/a
41	chr2:34902113-34902163	SK-N-SH_RA	brain:	n/a
42	chr2:34852273-34852323	HepG2	liver:	n/a
43	chr2:34852273-34852323	MCF10A-Er-Src	breast:	n/a
44	chr2:34902113-34902163	SK-N-MC	brain:	n/a
45	chr2:34902113-34902163	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:34902113-34902163	AG09319	gingival:	n/a
47	chr2:34852273-34852323	HUVEC	blood vessel:	n/a
48	chr2:34902113-34902163	HRCEpiC	kidney:	n/a
49	chr2:34852273-34852323	NB4	blood:	n/a
50	chr2:34902113-34902163	HL-60	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:34795663..34796225-chr8:85142407..85143298,2	MCF-7	breast:
2	chr2:35152123..35154075-chr2:35162750..35165499,2	K562	blood:
3	chr2:35124308..35126436-chr2:35127473..35129610,2	K562	blood:
4	chr2:35086981..35089694-chr2:35094487..35097235,2	K562	blood:
5	chr2:34876891..34879240-chr2:34886043..34888561,2	K562	blood:
6	chr2:35130362..35133238-chr2:35148535..35150812,2	K562	blood:
7	chr2:35049634..35051232-chr2:35070862..35073503,2	K562	blood:
8	chr2:34237681..34238401-chr2:34795339..34796232,5	MCF-7	breast:
9	chr2:35086981..35089694-chr2:35094487..35097235,2	K562	blood:
10	chr2:34929052..34931868-chr2:34933062..34935710,2	K562	blood:
11	chr2:35124308..35126436-chr2:35127473..35129610,2	K562	blood:
12	chr2:35006274..35008792-chr8:67342394..67345182,2	MCF-7	breast:
13	chr2:33906151..33906814-chr2:34795262..34796206,5	MCF-7	breast:
14	chr2:34321381..34322557-chr2:34795669..34796275,5	MCF-7	breast:
15	chr2:35152123..35154075-chr2:35162750..35165499,2	K562	blood:
16	chr17:76778253..76778888-chr2:34769758..34770277,2	MCF-7	breast:
17	chr2:34929052..34931868-chr2:34933062..34935710,2	K562	blood:
18	chr2:34321239..34322372-chr2:34772370..34773083,4	MCF-7	breast:
19	chr2:34237581..34238416-chr2:34963443..34964247,2	MCF-7	breast:
20	chr2:35049634..35051232-chr2:35070862..35073503,2	K562	blood:
21	chr2:35130281..35132812-chr2:35144803..35146892,2	K562	blood:
22	chr2:35130281..35132812-chr2:35144803..35146892,2	K562	blood:
23	chr2:35130362..35133238-chr2:35148535..35150812,2	K562	blood:
24	chr2:34237506..34238447-chr2:34795265..34796658,5	MCF-7	breast:
25	chr2:34876891..34879240-chr2:34886043..34888561,2	K562	blood:

(count:58 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-5	chr2:35041549-35041945	XLOC_001426
2	lnc-FAM98A-11	chr2:35076849-35077075	NONHSAT070061
3	lnc-RASGRP3-4	chr2:34962172-34963510	NONHSAT070051
4	lnc-RASGRP3-15	chr2:34909934-34910063	NONHSAT070041
5	lnc-RASGRP3-4	chr2:34929778-34929989	ENSG00000228262.4
6	lnc-RASGRP3-4	chr2:34978401-34978447	NONHSAT070051
7	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
8	lnc-RASGRP3-4	chr2:34959627-34961285	NONHSAT070048
9	lnc-RASGRP3-4	chr2:34962388-34962644	ENSG00000228262.4
10	lnc-RASGRP3-4	chr2:34947066-34947186	ENSG00000228262.4
11	lnc-RASGRP3-15	chr2:34878421-34878470	NONHSAT070041
12	lnc-RASGRP3-4	chr2:34938657-34938840	ENSG00000228262
13	lnc-RASGRP3-4	chr2:34938646-34938840	ENSG00000228262.4
14	lnc-FAM98A-11	chr2:35077532-35077593	NONHSAT070061
15	lnc-RASGRP3-4	chr2:34947066-34950118	NONHSAT070045
16	lnc-FAM98A-2	chr2:34960042-34960174	ENSG00000232153
17	lnc-FAM98A-7	chr2:34823138-34823205	NONHSAT070038
18	lnc-RASGRP3-4	chr2:34938646-34938840	NONHSAT070045
19	lnc-RASGRP3-4	chr2:34935519-34935580	ENSG00000228262.4
20	lnc-CRIM1-1	chr2:35056430-35056559	XLOC_001425
21	lnc-RASGRP3-4	chr2:34947066-34947188	ENSG00000228262.4
22	lnc-RASGRP3-5	chr2:35042159-35042319	XLOC_001426
23	lnc-RASGRP3-4	chr2:34938657-34938840	ENSG00000228262.4
24	lnc-FAM98A-8	chr2:34917357-34917552	ENSG00000272027.1
25	lnc-FAM98A-11	chr2:35078527-35078731	NONHSAT070061
26	lnc-RASGRP3-14	chr2:34800570-34801134	NONHSAT070037
27	lnc-RASGRP3-14	chr2:34792147-34792344	l_1807_chr2:34789043-34803561_liver
28	lnc-RASGRP3-4	chr2:34957515-34957624	ENSG00000228262
29	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
30	lnc-RASGRP3-14	chr2:34815892-34816802	NONHSAT070039
31	lnc-RASGRP3-4	chr2:34938646-34938840	ENSG00000228262.4
32	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
33	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
34	lnc-FAM98A-10	chr2:35034320-35034623	NONHSAT070053
35	lnc-FAM98A-7	chr2:34787656-34787849	NONHSAT070038
36	lnc-RASGRP3-3	chr2:34860316-34860407	ENSG00000226785
37	lnc-FAM98A-2	chr2:34962148-34962185	ENSG00000232153
38	lnc-RASGRP3-4	chr2:34935519-34935571	NONHSAT070044
39	lnc-RASGRP3-14	chr2:34811019-34811128	NONHSAT070039
40	lnc-RASGRP3-4	chr2:34962388-34962638	ENSG00000228262.4
41	lnc-RASGRP3-14	chr2:34756150-34756498	NONHSAT070037
42	lnc-CRIM1-1	chr2:35056445-35056559	ENSG00000226994.3
43	lnc-RASGRP3-4	chr2:34935518-34935580	NONHSAT070045
44	lnc-RASGRP3-14	chr2:34792150-34792344	NONHSAT070037
45	lnc-RASGRP3-14	chr2:34789044-34789084	l_1807_chr2:34789043-34803561_liver
46	lnc-FAM98A-8	chr2:34919267-34919365	ENSG00000272027.1
47	lnc-RASGRP3-4	chr2:34902711-34902994	NONHSAT070044
48	lnc-RASGRP3-4	chr2:34947066-34947580	ENSG00000228262.4
49	lnc-RASGRP3-4	chr2:34956433-34956605	ENSG00000228262.4
50	lnc-RASGRP3-4	chr2:34962148-34962183	NONHSAT070048

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
ENSG00000108669	chromatin interactions
NAP1L1	miRNA target sites

Extended variants
information (count: 9605 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:9605 , 50 per page) page: 1 2 3 4 5 6 7 ... 193

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35457498	chr2:34749203-34749204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs75263533	chr2:34749226-34749227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539221457	chr2:34749235-34749236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559322484	chr2:34749242-34749243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566214999	chr2:34749250-34749251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192159257	chr2:34749253-34749254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554620833	chr2:34749277-34749278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143930613	chr2:34749296-34749297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563697219	chr2:34749299-34749300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs116210328	chr2:34749367-34749368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557017783	chr2:34749385-34749386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542985394	chr2:34749399-34749400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7602247	chr2:34749420-34749421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188877624	chr2:34749437-34749438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145100299	chr2:34749456-34749457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs193247720	chr2:34749500-34749501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531713387	chr2:34749520-34749521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150395217	chr2:34749586-34749587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115998537	chr2:34749637-34749638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530511487	chr2:34749639-34749640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550731530	chr2:34749641-34749642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564149896	chr2:34749663-34749664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184506778	chr2:34749679-34749680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138156940	chr2:34749680-34749681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189485327	chr2:34749758-34749759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191325168	chr2:34749779-34749780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540271595	chr2:34752209-34752210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190019874	chr2:34752237-34752238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568303926	chr2:34752244-34752245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200176497	chr2:34752287-34752288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143714421	chr2:34752293-34752294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs151023784	chr2:34752294-34752295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183039824	chr2:34752317-34752318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188610736	chr2:34752329-34752330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531552158	chr2:34752345-34752346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551560390	chr2:34752372-34752373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550633141	chr2:34752438-34752439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571452380	chr2:34752451-34752452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140933435	chr2:34752463-34752464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576894944	chr2:34752487-34752488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555590693	chr2:34752491-34752492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547363662	chr2:34752536-34752537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111420778	chr2:34752580-34752581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77023883	chr2:34752582-34752583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75828331	chr2:34752608-34752609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575697916	chr2:34752615-34752616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146447319	chr2:34752701-34752702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374691782	chr2:34752704-34752705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558284356	chr2:34752806-34752807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs578108317	chr2:34752849-34752850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34749200-34749600	Enhancers	NHEK	skin
2	chr2:34749200-34749800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr2:34752200-34752400	Enhancers	Fetal Kidney	kidney
4	chr2:34752400-34753200	Weak transcription	Fetal Kidney	kidney
5	chr2:34752800-34753200	Enhancers	Fetal Intestine Large	intestine
6	chr2:34753200-34753600	Enhancers	Fetal Intestine Small	intestine
7	chr2:34753200-34753600	Enhancers	Fetal Kidney	kidney
8	chr2:34753400-34753800	Enhancers	Fetal Intestine Large	intestine
9	chr2:34753600-34758800	Weak transcription	Fetal Kidney	kidney
10	chr2:34753600-34759000	Weak transcription	Fetal Intestine Small	intestine
11	chr2:34758800-34759200	Enhancers	Fetal Kidney	kidney
12	chr2:34758800-34760600	Enhancers	Fetal Lung	lung
13	chr2:34759000-34760600	Enhancers	Fetal Intestine Small	intestine
14	chr2:34759200-34759400	Weak transcription	Fetal Kidney	kidney
15	chr2:34759200-34761400	Enhancers	Fetal Intestine Large	intestine
16	chr2:34759400-34759800	Enhancers	Fetal Kidney	kidney
17	chr2:34761200-34761600	Enhancers	Pancreas	Pancrea
18	chr2:34770400-34771000	Enhancers	Fetal Muscle Trunk	muscle
19	chr2:34772200-34772400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:34772400-34773000	Enhancers	Pancreas	Pancrea
21	chr2:34772400-34774200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr2:34773000-34773400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:34774000-34775000	Enhancers	NHEK	skin
24	chr2:34774200-34775400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr2:34774200-34775400	Enhancers	HMEC	breast
26	chr2:34774400-34775000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:34775000-34775400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr2:34775000-34775400	Flanking Active TSS	NHEK	skin
29	chr2:34792200-34792600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr2:34809400-34810200	Enhancers	Fetal Lung	lung
31	chr2:34829200-34829600	Enhancers	Brain Germinal Matrix	brain
32	chr2:34829400-34829600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr2:34842200-34842800	Enhancers	Fetal Lung	lung
34	chr2:34860400-34861000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:34875600-34875800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr2:34881800-34882600	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr2:34884400-34890200	Weak transcription	Right Atrium	heart
38	chr2:34885200-34885600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr2:34885800-34886200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr2:34885800-34886200	Enhancers	Fetal Lung	lung
41	chr2:34889000-34890600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:34890600-34892000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:34891600-34892400	Enhancers	Brain Germinal Matrix	brain
44	chr2:34892000-34892200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:34892200-34892600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:34892600-34893600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:34895400-34895600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:34901600-34902400	Enhancers	Liver	Liver
49	chr2:34902400-34902600	Flanking Active TSS	Liver	Liver
50	chr2:34902600-34903000	Enhancers	Pancreas	Pancrea

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