Variant report

Variant	nsv1028692
Chromosome Location	chr7:65673136-65751069
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:605)
CpG islands
(count:489)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:605 , 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	ARID3A	chr7:65703333-65703693	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:65684835-65685020	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:65715845-65716035	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:65736093-65736165	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:65748527-65748807	HepG2	liver:	n/a	n/a
6	ATF1	chr7:65685454-65685541	K562	blood:	n/a	n/a
7	ATF1	chr7:65715748-65716082	K562	blood:	n/a	n/a
8	ATF1	chr7:65730693-65730809	K562	blood:	n/a	n/a
9	ATF3	chr7:65715773-65716055	K562	blood:	n/a	n/a
10	BACH1	chr7:65676558-65676670	K562	blood:	n/a	n/a
11	BACH1	chr7:65746791-65747219	K562	blood:	n/a	n/a
12	BACH1	chr7:65746809-65747168	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr7:65746802-65747232	K562	blood:	n/a	n/a
14	BHLHE40	chr7:65715790-65716031	K562	blood:	n/a	n/a
15	BRCA1	chr7:65737422-65737431	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr7:65715517-65716122	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr7:65746914-65747008	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr7:65712305-65712724	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr7:65722257-65722943	HCT-116	colon:	n/a	n/a
20	CBX3	chr7:65746748-65747246	K562	blood:	n/a	n/a
21	CBX3	chr7:65730531-65731095	HCT-116	colon:	n/a	n/a
22	CBX3	chr7:65730571-65731016	HCT-116	colon:	n/a	n/a
23	CBX3	chr7:65730561-65731007	K562	blood:	n/a	n/a
24	CBX3	chr7:65748436-65748980	HCT-116	colon:	n/a	n/a
25	CBX3	chr7:65730481-65730942	K562	blood:	n/a	n/a
26	CCNT2	chr7:65725931-65725938	K562	blood:	n/a	n/a
27	CCNT2	chr7:65746708-65747132	K562	blood:	n/a	n/a
28	CEBPB	chr7:65748082-65748281	HepG2	liver:	n/a	chr7:65748198-65748209
29	CEBPB	chr7:65715699-65716174	Hela-S3	cervix:	n/a	chr7:65715959-65715970
30	CEBPB	chr7:65720163-65720300	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:65732189-65732689	IMR90	lung:	n/a	chr7:65732554-65732567
32	CEBPB	chr7:65683847-65683992	HepG2	liver:	n/a	chr7:65683923-65683934
33	CEBPB	chr7:65712309-65712781	Hela-S3	cervix:	n/a	chr7:65712715-65712723
34	CEBPB	chr7:65720121-65720467	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:65715701-65716150	IMR90	lung:	n/a	chr7:65715959-65715970
36	CEBPB	chr7:65726087-65726307	HepG2	liver:	n/a	chr7:65726199-65726210
37	CEBPB	chr7:65720075-65720527	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:65676472-65676759	IMR90	lung:	n/a	chr7:65676577-65676588 chr7:65676577-65676588
39	CEBPB	chr7:65726028-65726326	IMR90	lung:	n/a	chr7:65726199-65726210
40	CEBPB	chr7:65726105-65726298	K562	blood:	n/a	chr7:65726199-65726210
41	CEBPB	chr7:65750236-65750482	K562	blood:	n/a	chr7:65750342-65750353
42	CEBPB	chr7:65748079-65748872	Hela-S3	cervix:	n/a	chr7:65748198-65748209
43	CEBPB	chr7:65748104-65748343	A549	lung:	n/a	chr7:65748198-65748209
44	CEBPB	chr7:65715791-65716090	K562	blood:	n/a	chr7:65715959-65715970
45	CEBPB	chr7:65714705-65715024	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:65750241-65750448	IMR90	lung:	n/a	chr7:65750342-65750353
47	CEBPB	chr7:65683795-65684071	IMR90	lung:	n/a	chr7:65683923-65683934
48	CEBPB	chr7:65714619-65714824	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:65712373-65712733	MCF-7	breast:	n/a	chr7:65712715-65712723
50	CEBPB	chr7:65715732-65716108	A549	lung:	n/a	chr7:65715959-65715970

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65705962-65706012	AG04450	lung:	fetal
2	chr7:65705962-65706012	AG04450	lung:	fetal
3	chr7:65695583-65695633	AG09319	gingival:	n/a
4	chr7:65695412-65695462	T-47D	breast:	n/a
5	chr7:65695583-65695633	HMEC	breast:	n/a
6	chr7:65695412-65695462	MCF-7	breast:	n/a
7	chr7:65746852-65746902	AoSMC	blood vessel:	n/a
8	chr7:65733966-65734016	HUVEC	blood vessel:	n/a
9	chr7:65721712-65721762	Caco-2	colon:	n/a
10	chr7:65705962-65706012	HEK293	kidney:	embryo
11	chr7:65695412-65695462	PrEC	prostate:	n/a
12	chr7:65695583-65695633	HUVEC	blood vessel:	n/a
13	chr7:65723664-65723714	AG10803	skin:	n/a
14	chr7:65723664-65723714	RPTEC	kidney:	n/a
15	chr7:65706494-65706544	H1-hESC	embryonic stem cell:	embryo
16	chr7:65706494-65706544	T-47D	breast:	n/a
17	chr7:65733966-65734016	HEEpiC	esophagus:	n/a
18	chr7:65695412-65695462	PFSK-1	brain:	n/a
19	chr7:65695412-65695462	GM12891	blood:	n/a
20	chr7:65695412-65695462	AG09309	skin:	n/a
21	chr7:65705962-65706012	PrEC	prostate:	n/a
22	chr7:65746852-65746902	AG09309	skin:	n/a
23	chr7:65723664-65723714	AG09319	gingival:	n/a
24	chr7:65706494-65706544	HepG2	liver:	n/a
25	chr7:65721712-65721762	Hela-S3	cervix:	n/a
26	chr7:65705962-65706012	HCM	heart:	n/a
27	chr7:65705962-65706012	GM06990	blood:	n/a
28	chr7:65721712-65721762	ProgFib	skin:	n/a
29	chr7:65705962-65706012	MCF-7	breast:	n/a
30	chr7:65721712-65721762	NB4	blood:	n/a
31	chr7:65695583-65695633	AG09309	skin:	n/a
32	chr7:65695583-65695633	BJ	skin:	n/a
33	chr7:65733966-65734016	GM12891	blood:	n/a
34	chr7:65746852-65746902	A549	lung:	n/a
35	chr7:65706494-65706544	HAEpiC	amniotic membrane:	n/a
36	chr7:65706494-65706544	AG04450	lung:	fetal
37	chr7:65733966-65734016	A549	lung:	n/a
38	chr7:65695583-65695633	NHDF-neo	bronchial:	n/a
39	chr7:65695412-65695462	HAEpiC	amniotic membrane:	n/a
40	chr7:65695583-65695633	PrEC	prostate:	n/a
41	chr7:65746852-65746902	Caco-2	colon:	n/a
42	chr7:65721712-65721762	HRCEpiC	kidney:	n/a
43	chr7:65733966-65734016	RPTEC	kidney:	n/a
44	chr7:65695583-65695633	U87	brain:	n/a
45	chr7:65695412-65695462	HepG2	liver:	n/a
46	chr7:65746852-65746902	Hela-S3	cervix:	n/a
47	chr7:65705962-65706012	ECC-1	luminal epithelium:	n/a
48	chr7:65705962-65706012	HRPEpiC	eye:	n/a
49	chr7:65705962-65706012	NHDF-neo	bronchial:	n/a
50	chr7:65746852-65746902	BE2_C	brain:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:65718957..65720490-chr7:65725606..65727154,2	MCF-7	breast:
2	chr7:65723144..65728199-chr7:65728975..65732858,5	K562	blood:
3	chr7:65703885..65706000-chr7:65711760..65714704,2	K562	blood:
4	chr7:65715220..65718095-chr7:65721479..65725150,3	MCF-7	breast:
5	chr7:65715220..65718095-chr7:65721479..65725150,3	MCF-7	breast:
6	chr7:65673531..65675295-chr7:65684693..65686542,2	K562	blood:
7	chr7:65692053..65693924-chr7:65696196..65697706,2	MCF-7	breast:
8	chr7:65703885..65706000-chr7:65711760..65714704,2	K562	blood:
9	chr7:65718957..65720490-chr7:65725606..65727154,2	MCF-7	breast:
10	chr7:65676565..65678528-chr7:65683299..65686041,2	MCF-7	breast:
11	chr7:65680452..65683306-chr7:65691052..65694234,3	MCF-7	breast:
12	chr7:65715302..65717280-chr7:65718267..65720780,2	MCF-7	breast:
13	chr7:65719328..65723355-chr7:65725025..65727882,3	K562	blood:
14	chr7:65728235..65729776-chr7:65732042..65733937,2	MCF-7	breast:
15	chr7:65723144..65728199-chr7:65728975..65732858,5	K562	blood:
16	chr7:65704500..65706480-chr7:65713204..65714741,2	K562	blood:
17	chr7:65685457..65687424-chr7:65688935..65691579,2	K562	blood:
18	chr7:65676565..65678528-chr7:65683299..65686041,2	MCF-7	breast:
19	chr7:65680452..65683306-chr7:65691052..65694234,3	MCF-7	breast:
20	chr7:65705536..65707290-chr7:65707942..65710882,2	K562	blood:
21	chr7:65704500..65706480-chr7:65713204..65714741,2	K562	blood:
22	chr7:65705536..65707290-chr7:65707942..65710882,2	K562	blood:
23	chr7:65673531..65675295-chr7:65684693..65686542,2	K562	blood:
24	chr7:65719328..65723355-chr7:65725025..65727882,3	K562	blood:
25	chr7:65669466..65673274-chr7:65681767..65684284,3	K562	blood:
26	chr7:65715302..65717280-chr7:65718267..65720780,2	MCF-7	breast:
27	chr7:65603533..65606431-chr7:65683250..65685813,2	K562	blood:
28	chr7:65728235..65729776-chr7:65732042..65733937,2	MCF-7	breast:
29	chr7:65669820..65671702-chr7:65672319..65674311,2	MCF-7	breast:
30	chr7:65673035..65675351-chr7:65772228..65774640,2	K562	blood:
31	chr7:65692053..65693924-chr7:65696196..65697706,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CRCP-3	chr7:65705061-65705151	NONHSAT121146

No data

Variant related genes	Relation type
TPST1	TF binding region
TPST1	CpG island
ENSG00000169902	chromatin interactions

Extended variants
information (count: 2684 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2684 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145198139	chr7:65673157-65673158	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs185947750	chr7:65673181-65673182	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147643025	chr7:65673189-65673190	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs530045017	chr7:65673203-65673204	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs546915503	chr7:65673204-65673205	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs534456703	chr7:65673224-65673225	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532333628	chr7:65673338-65673339	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs552319573	chr7:65673367-65673368	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568885426	chr7:65673402-65673403	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs190264042	chr7:65673432-65673433	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs183168178	chr7:65673452-65673453	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200870708	chr7:65673463-65673464	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs567959373	chr7:65673472-65673473	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534534930	chr7:65673529-65673530	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77951319	chr7:65673530-65673531	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs142221219	chr7:65673537-65673538	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs111522924	chr7:65673602-65673603	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs543664639	chr7:65673644-65673645	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs563648411	chr7:65673647-65673648	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12540888	chr7:65673693-65673694	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs576442229	chr7:65673723-65673724	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541950477	chr7:65673724-65673725	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs374854535	chr7:65673736-65673737	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562159992	chr7:65673741-65673742	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs572330093	chr7:65673789-65673790	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs540570277	chr7:65673807-65673808	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560456222	chr7:65673818-65673819	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs532372016	chr7:65673823-65673824	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs369486447	chr7:65673880-65673881	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs546177488	chr7:65673889-65673890	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs562532031	chr7:65673925-65673926	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs186007416	chr7:65673997-65673998	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145453764	chr7:65674015-65674016	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs76562690	chr7:65674051-65674052	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs568080327	chr7:65674069-65674070	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533510373	chr7:65674091-65674092	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs148858235	chr7:65674116-65674117	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550531383	chr7:65674133-65674134	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539654679	chr7:65674174-65674175	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568754541	chr7:65674190-65674191	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535648015	chr7:65674249-65674250	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs117660432	chr7:65674351-65674352	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs576558369	chr7:65674363-65674364	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs190963554	chr7:65674411-65674412	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs555566258	chr7:65674412-65674413	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs183993638	chr7:65674520-65674521	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs145526740	chr7:65674744-65674745	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541412082	chr7:65674794-65674795	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187739575	chr7:65674855-65674856	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529914749	chr7:65674856-65674857	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
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
Hodgkin''s lymphoma	18641027	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
Glioblastoma	21080181	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	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
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Paroxysmal kinesigenic dyskinesia	21940615	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65669400-65673200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:65670000-65673200	Active TSS	NHLF	lung
3	chr7:65670600-65673200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:65670800-65673400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:65671000-65673400	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr7:65671200-65673400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr7:65671200-65673600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:65671400-65674400	Enhancers	Primary B cells from peripheral blood	blood
9	chr7:65671400-65674800	Weak transcription	Fetal Intestine Large	intestine
10	chr7:65671400-65675000	Weak transcription	Esophagus	oesophagus
11	chr7:65671400-65675800	Weak transcription	Lung	lung
12	chr7:65671400-65676200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:65671400-65677000	Weak transcription	Placenta	Placenta
14	chr7:65671400-65678800	Weak transcription	Fetal Muscle Trunk	muscle
15	chr7:65671600-65673200	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr7:65671600-65673400	Enhancers	Fetal Stomach	stomach
17	chr7:65671600-65675000	Weak transcription	Gastric	stomach
18	chr7:65671600-65685400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:65671600-65689000	Weak transcription	Pancreas	Pancrea
20	chr7:65671800-65673200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:65671800-65673400	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr7:65671800-65673400	Enhancers	NHEK	skin
23	chr7:65671800-65673600	Enhancers	Colon Smooth Muscle	Colon
24	chr7:65671800-65674800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr7:65671800-65675200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr7:65671800-65675600	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr7:65671800-65675600	Weak transcription	Stomach Mucosa	stomach
28	chr7:65671800-65677600	Weak transcription	Fetal Muscle Leg	muscle
29	chr7:65671800-65677600	Weak transcription	Spleen	Spleen
30	chr7:65671800-65682200	Weak transcription	Left Ventricle	heart
31	chr7:65672000-65674000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr7:65672000-65677000	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr7:65672200-65673200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr7:65672200-65673200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr7:65672200-65673400	Enhancers	Brain Anterior Caudate	brain
36	chr7:65672200-65677200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr7:65672200-65677400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:65672200-65677600	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr7:65672200-65678000	Weak transcription	HSMM	muscle
40	chr7:65672200-65678800	Weak transcription	HUVEC	blood vessel
41	chr7:65672200-65687400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr7:65672200-65723400	Weak transcription	Right Atrium	heart
43	chr7:65672400-65673200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr7:65672400-65673200	Weak transcription	Ovary	ovary
45	chr7:65672400-65673400	Enhancers	Primary hematopoietic stem cells	blood
46	chr7:65672400-65673400	Enhancers	Brain Cingulate Gyrus	brain
47	chr7:65672400-65673400	Enhancers	Fetal Lung	lung
48	chr7:65672400-65673400	Flanking Active TSS	Osteobl	bone
49	chr7:65672400-65673800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:65672400-65675000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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