Variant report

Variant	nsv607437
Chromosome Location	chr7:70251651-70568354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1664)
CpG islands
(count:2196)
Chromatin interactive
region (count:36)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1664 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:70295432-70295731	HepG2	liver:	n/a	n/a
2	ATF1	chr7:70473461-70473667	K562	blood:	n/a	n/a
3	ATF2	chr7:70294118-70294578	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
5	ATF2	chr7:70258518-70258992	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:70314491-70315160	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:70314522-70315080	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:70321901-70322317	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:70359196-70359849	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:70264860-70265281	GM12878	blood:	n/a	n/a
12	BACH1	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:70384908-70384986	K562	blood:	n/a	n/a
14	BACH1	chr7:70294211-70294569	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr7:70277553-70277731	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr7:70264853-70265265	GM12878	blood:	n/a	n/a
17	BATF	chr7:70264945-70265249	GM12878	blood:	n/a	n/a
18	BATF	chr7:70294231-70294607	GM12878	blood:	n/a	n/a
19	BATF	chr7:70294291-70294547	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:70264916-70265214	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:70264860-70265214	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:70359245-70359587	H1-hESC	embryonic stem cell:	n/a	n/a
23	BHLHE40	chr7:70295491-70295711	HepG2	liver:	n/a	n/a
24	BHLHE40	chr7:70349178-70349357	K562	blood:	n/a	n/a
25	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
26	BHLHE40	chr7:70294194-70294616	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:70482560-70482896	K562	blood:	n/a	n/a
28	BHLHE40	chr7:70498977-70499038	K562	blood:	n/a	n/a
29	BHLHE40	chr7:70470205-70470386	K562	blood:	n/a	n/a
30	BHLHE40	chr7:70294189-70294529	K562	blood:	n/a	n/a
31	BRCA1	chr7:70277589-70277745	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr7:70294156-70294507	H1-hESC	embryonic stem cell:	n/a	n/a
33	CBX3	chr7:70515518-70515757	K562	blood:	n/a	n/a
34	CBX3	chr7:70482488-70483015	K562	blood:	n/a	n/a
35	CBX3	chr7:70538895-70539134	K562	blood:	n/a	n/a
36	CCNT2	chr7:70543176-70543345	K562	blood:	n/a	n/a
37	CEBPB	chr7:70520567-70520872	H1-hESC	embryonic stem cell:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
38	CEBPB	chr7:70426400-70426506	A549	lung:	n/a	n/a
39	CEBPB	chr7:70528726-70528794	K562	blood:	n/a	chr7:70528754-70528765
40	CEBPB	chr7:70473715-70474044	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:70299414-70299733	MCF-7	breast:	n/a	chr7:70299603-70299614
42	CEBPB	chr7:70299440-70299798	HepG2	liver:	n/a	chr7:70299603-70299614
43	CEBPB	chr7:70347542-70347743	HepG2	liver:	n/a	chr7:70347648-70347659
44	CEBPB	chr7:70295428-70295714	HepG2	liver:	n/a	chr7:70295552-70295563
45	CEBPB	chr7:70536265-70536412	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr7:70518584-70518708	A549	lung:	n/a	n/a
47	CEBPB	chr7:70473682-70474054	K562	blood:	n/a	n/a
48	CEBPB	chr7:70520536-70520878	MCF-7	breast:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
49	CEBPB	chr7:70388372-70388507	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:70528739-70528775	H1-hESC	embryonic stem cell:	n/a	chr7:70528754-70528765

(count:2196 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70257960-70258010	HIPEpiC	eye:	n/a
2	chr7:70252448-70252498	HL-60	blood:	n/a
3	chr7:70294511-70294561	U87	brain:	n/a
4	chr7:70256003-70256053	Hepatocyte	liver:	n/a
5	chr7:70359655-70359705	HRPEpiC	eye:	n/a
6	chr7:70252448-70252498	SAEC	small airway:	n/a
7	chr7:70252335-70252385	HNPCEpiC	eye:	n/a
8	chr7:70252953-70253003	AG04450	lung:	fetal
9	chr7:70543320-70543370	HAEpiC	amniotic membrane:	n/a
10	chr7:70417419-70417469	HEK293	kidney:	embryo
11	chr7:70543800-70543850	HCPEpiC	choroid plexus:	n/a
12	chr7:70482771-70482821	BJ	skin:	n/a
13	chr7:70543490-70543540	Caco-2	colon:	n/a
14	chr7:70252282-70252332	T-47D	breast:	n/a
15	chr7:70255210-70255260	AG10803	skin:	n/a
16	chr7:70254810-70254860	HUVEC	blood vessel:	n/a
17	chr7:70311435-70311485	HepG2	liver:	n/a
18	chr7:70417419-70417469	SK-N-SH	brain:	n/a
19	chr7:70257960-70258010	U87	brain:	n/a
20	chr7:70311321-70311371	K562	blood:	n/a
21	chr7:70254810-70254860	SK-N-SH_RA	brain:	n/a
22	chr7:70417419-70417469	K562	blood:	n/a
23	chr7:70294264-70294314	MCF10A-Er-Src	breast:	n/a
24	chr7:70256003-70256053	BJ	skin:	n/a
25	chr7:70543079-70543129	SKMC	muscle:	n/a
26	chr7:70294264-70294314	HMEC	breast:	n/a
27	chr7:70257926-70257976	MCF-7	breast:	n/a
28	chr7:70311435-70311485	MCF-7	breast:	n/a
29	chr7:70543079-70543129	MCF-7	breast:	n/a
30	chr7:70322401-70322451	HNPCEpiC	eye:	n/a
31	chr7:70311532-70311582	GM12878	blood:	n/a
32	chr7:70252662-70252712	GM12891	blood:	n/a
33	chr7:70482891-70482941	GM19239	blood:	n/a
34	chr7:70252571-70252621	NHDF-neo	bronchial:	n/a
35	chr7:70543320-70543370	HCM	heart:	n/a
36	chr7:70258726-70258776	HNPCEpiC	eye:	n/a
37	chr7:70258010-70258060	MCF-7	breast:	n/a
38	chr7:70258010-70258060	NT2-D1	testis:	n/a
39	chr7:70252448-70252498	HEEpiC	esophagus:	n/a
40	chr7:70258753-70258803	BE2_C	brain:	n/a
41	chr7:70543079-70543129	CMK	blood:	n/a
42	chr7:70294511-70294561	HEK293	kidney:	embryo
43	chr7:70252953-70253003	AG10803	skin:	n/a
44	chr7:70255804-70255854	HRCEpiC	kidney:	n/a
45	chr7:70255210-70255260	HepG2	liver:	n/a
46	chr7:70254810-70254860	CMK	blood:	n/a
47	chr7:70482891-70482941	K562	blood:	n/a
48	chr7:70543320-70543370	GM19239	blood:	n/a
49	chr7:70257926-70257976	HL-60	blood:	n/a
50	chr7:70258649-70258699	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
2	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
3	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
4	chr7:70462461..70464194-chr7:70473424..70476009,2	K562	blood:
5	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
6	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
7	chr7:70293870..70294792-chr7:71200529..71201300,6	MCF-7	breast:
8	chr7:70294117..70295302-chr7:71197788..71199575,6	MCF-7	breast:
9	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
10	chr7:70294183..70294797-chr7:71197949..71198693,3	MCF-7	breast:
11	chr7:70321614..70322798-chr7:71200589..71201582,5	MCF-7	breast:
12	chr7:70462545..70464219-chr7:70469088..70471612,2	K562	blood:
13	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
14	chr7:70472764..70475068-chr7:70478258..70480877,2	K562	blood:
15	chr7:70319996..70320657-chr7:71198026..71198561,2	MCF-7	breast:
16	chr7:70255328..70258832-chr7:70260648..70264116,3	K562	blood:
17	chr7:70321617..70322562-chr7:70976561..70977221,2	MCF-7	breast:
18	chr7:70293845..70294790-chr7:71197836..71198902,6	K562	blood:
19	chr7:70244569..70247076-chr7:70250539..70253250,4	K562	blood:
20	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:
21	chr7:70445361..70447643-chr7:70448432..70451410,2	K562	blood:
22	chr7:70321665..70322892-chr7:71197945..71198934,7	MCF-7	breast:
23	chr7:70445361..70447643-chr7:70448432..70451410,2	K562	blood:
24	chr7:70316123..70316992-chr7:71197861..71198674,2	K562	blood:
25	chr7:69997760..70000305-chr7:70252452..70255075,2	MCF-7	breast:
26	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
27	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:
28	chr7:70321651..70322570-chr7:71197952..71198877,7	K562	blood:
29	chr7:70321514..70322440-chr7:71198003..71198947,6	MCF-7	breast:
30	chr5:126205511..126206011-chr7:70301812..70302369,2	MCF-7	breast:
31	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
32	chr7:70472764..70475068-chr7:70478258..70480877,2	K562	blood:
33	chr7:70462545..70464219-chr7:70469088..70471612,2	K562	blood:
34	chr7:70255328..70258832-chr7:70260648..70264116,3	K562	blood:
35	chr7:70462461..70464194-chr7:70473424..70476009,2	K562	blood:
36	chr7:70295507..70296249-chr7:71198004..71198896,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AUTS2-3	chr7:70302724-70302999	NONHSAT121342

No data

Variant related genes	Relation type
ENSG00000236978	TF binding region
ENSG00000236978	CpG island
ENSG00000158321	chromatin interactions

Extended variants
information (count: 9681 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:9681 , 50 per page) page: 1 2 3 4 5 6 7 ... 194

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10499822	chr7:70251651-70251652	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547430229	chr7:70251653-70251654	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs114134849	chr7:70251669-70251670	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs17763090	chr7:70251690-70251691	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs185409175	chr7:70251757-70251758	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368689753	chr7:70251759-70251760	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs370866305	chr7:70251774-70251775	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188422604	chr7:70251783-70251784	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530885485	chr7:70251903-70251904	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs552257479	chr7:70251908-70251909	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2293501	chr7:70251923-70251924	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs534749997	chr7:70251952-70251953	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs547267628	chr7:70251958-70251959	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs59473239	chr7:70251990-70251991	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs568686526	chr7:70252001-70252002	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs536039699	chr7:70252127-70252128	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181817804	chr7:70252147-70252148	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs371118227	chr7:70252167-70252168	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2293500	chr7:70252185-70252186	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs537105723	chr7:70252208-70252209	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs141832494	chr7:70252211-70252212	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs147106727	chr7:70252221-70252222	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs367838374	chr7:70252225-70252226	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs201841605	chr7:70252261-70252262	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs138310814	chr7:70252262-70252263	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs140914046	chr7:70252283-70252284	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs34269381	chr7:70252286-70252287	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372172046	chr7:70252307-70252308	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372882374	chr7:70252335-70252336	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs150219264	chr7:70252336-70252337	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs138800328	chr7:70252346-70252347	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149520335	chr7:70252358-70252359	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201838881	chr7:70252406-70252407	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200188572	chr7:70252409-70252410	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs368191722	chr7:70252433-70252434	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574357735	chr7:70252439-70252440	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs2293499	chr7:70252462-70252463	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541744892	chr7:70252475-70252476	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370404743	chr7:70252488-70252489	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs373876619	chr7:70252489-70252490	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs530626678	chr7:70252523-70252524	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2293498	chr7:70252528-70252529	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536353946	chr7:70252542-70252543	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs80000880	chr7:70252544-70252545	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538071319	chr7:70252571-70252572	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs552243083	chr7:70252587-70252588	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs2293497	chr7:70252588-70252589	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs61424087	chr7:70252596-70252597	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs577853504	chr7:70252633-70252634	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs2293496	chr7:70252645-70252646	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1105 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70222000-70258000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:70226400-70254800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:70227400-70253000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:70228400-70257400	Weak transcription	Right Atrium	heart
5	chr7:70229400-70259600	Strong transcription	Fetal Muscle Trunk	muscle
6	chr7:70229400-70259600	Strong transcription	Rectal Mucosa Donor 29	rectum
7	chr7:70230200-70254000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr7:70230200-70257400	Strong transcription	Rectal Mucosa Donor 31	rectum
9	chr7:70234600-70259600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr7:70235200-70258200	Strong transcription	HSMMtube	muscle
11	chr7:70236400-70257000	Strong transcription	Skeletal Muscle Male	skeletal muscle
12	chr7:70236800-70258200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:70238600-70259600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:70238800-70259600	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr7:70239200-70259400	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr7:70239800-70259400	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr7:70240200-70257000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
18	chr7:70240200-70258000	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr7:70240800-70259200	Strong transcription	Fetal Intestine Small	intestine
20	chr7:70241000-70259200	Strong transcription	Aorta	Aorta
21	chr7:70241200-70257200	Strong transcription	Skeletal Muscle Female	skeletal muscle
22	chr7:70241400-70256400	Strong transcription	Stomach Smooth Muscle	stomach
23	chr7:70241400-70257400	Strong transcription	HSMM	muscle
24	chr7:70241800-70257200	Strong transcription	H9 Cell Line	embryonic stem cell
25	chr7:70241800-70259400	Strong transcription	Duodenum Mucosa	Duodenum
26	chr7:70242000-70252600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:70242000-70257200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:70242200-70259600	Strong transcription	Dnd41	blood
29	chr7:70242200-70259600	Weak transcription	NHDF-Ad	bronchial
30	chr7:70243200-70259600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:70243600-70259600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr7:70243800-70258200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr7:70243800-70258200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr7:70244200-70256000	Strong transcription	Lung	lung
35	chr7:70244200-70256400	Strong transcription	Ovary	ovary
36	chr7:70244800-70259200	Strong transcription	GM12878-XiMat	blood
37	chr7:70245400-70256800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
38	chr7:70245400-70258600	Strong transcription	Fetal Thymus	thymus
39	chr7:70246200-70253000	Strong transcription	Adipose Nuclei	Adipose
40	chr7:70246200-70254400	Strong transcription	NH-A	brain
41	chr7:70246200-70257200	Strong transcription	Thymus	Thymus
42	chr7:70246200-70258400	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr7:70246400-70253000	Strong transcription	Left Ventricle	heart
44	chr7:70246400-70256000	Strong transcription	Gastric	stomach
45	chr7:70246400-70257400	Strong transcription	Esophagus	oesophagus
46	chr7:70246400-70258200	Strong transcription	Fetal Lung	lung
47	chr7:70246400-70259200	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr7:70246600-70252800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:70246600-70256000	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr7:70246600-70257000	Strong transcription	Duodenum Smooth Muscle	Duodenum

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