Variant report

Variant	nsv522217
Chromosome Location	chr7:6189780-6212656
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:6201433-6201909	GM12878	blood:	n/a	n/a
2	BACH1	chr7:6199913-6200132	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:6204016-6204358	H1-hESC	embryonic stem cell:	n/a	n/a
4	CCNT2	chr7:6200018-6200134	K562	blood:	n/a	n/a
5	CCNT2	chr7:6194167-6194449	K562	blood:	n/a	n/a
6	CEBPB	chr7:6200666-6201009	IMR90	lung:	n/a	chr7:6200829-6200840
7	CEBPB	chr7:6200710-6200995	HepG2	liver:	n/a	chr7:6200829-6200840
8	CHD2	chr7:6196841-6196885	HepG2	liver:	n/a	n/a
9	CHD2	chr7:6198047-6198084	K562	blood:	n/a	n/a
10	CHD2	chr7:6204212-6204322	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr7:6211312-6211829	H1-hESC	embryonic stem cell:	n/a	chr7:6211548-6211558
12	CTCF	chr7:6199880-6200030	HCFaa	heart:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
13	CTCF	chr7:6199920-6200070	GM12873	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
14	CTCF	chr7:6204160-6204310	MCF-7	breast:	n/a	n/a
15	CTCF	chr7:6204160-6204310	GM12868	blood:	n/a	n/a
16	CTCF	chr7:6199960-6200110	HEEpiC	esophagus:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
17	CTCF	chr7:6199920-6200070	AG09319	gingival:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
18	CTCF	chr7:6199878-6200102	Pancreas_OC	pancreas:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
19	CTCF	chr7:6199728-6200219	H1-hESC	embryonic stem cell:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
20	CTCF	chr7:6195237-6195339	MCF-7	breast:	n/a	n/a
21	CTCF	chr7:6199722-6200148	MCF-7	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
22	CTCF	chr7:6204180-6204330	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr7:6199839-6200216	K562	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
24	CTCF	chr7:6204200-6204350	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr7:6199880-6200030	AG04449	skin:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
26	CTCF	chr7:6199860-6200010	BJ	skin:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
27	CTCF	chr7:6199898-6200077	GM10266	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
28	CTCF	chr7:6204200-6204350	GM12866	blood:	n/a	n/a
29	CTCF	chr7:6199832-6200106	HUVEC	blood vessel:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
30	CTCF	chr7:6204160-6204310	HMF	breast:	n/a	n/a
31	CTCF	chr7:6199860-6200010	GM12875	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
32	CTCF	chr7:6199853-6200115	MCF-7	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
33	CTCF	chr7:6199717-6200212	T-47D	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
34	CTCF	chr7:6199872-6200104	GM12891	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
35	CTCF	chr7:6199880-6200030	AG09309	skin:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
36	CTCF	chr7:6204140-6204290	HAc	cerebellar:	n/a	n/a
37	CTCF	chr7:6199907-6200016	GM10248	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
38	CTCF	chr7:6199764-6200216	A549	lung:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
39	CTCF	chr7:6204140-6204290	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:6199920-6200070	HEK293	kidney:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
41	CTCF	chr7:6205340-6205490	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr7:6199900-6200050	AG04450	lung:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
43	CTCF	chr7:6199840-6199990	GM12868	blood:	n/a	n/a
44	CTCF	chr7:6204140-6204290	HVMF	connective:	n/a	n/a
45	CTCF	chr7:6199920-6200070	HBMEC	blood vessel:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
46	CTCF	chr7:6204120-6204270	HMF	breast:	n/a	n/a
47	CTCF	chr7:6199712-6200295	MCF-7	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
48	CTCF	chr7:6204180-6204330	BE2_C	brain:	n/a	n/a
49	CTCF	chr7:6199852-6200120	Spleen_OC	spleen:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
50	CTCF	chr7:6199880-6200030	BJ	skin:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6198846-6198896	GM12891	blood:	n/a
2	chr7:6192000-6192050	SK-N-SH	brain:	n/a
3	chr7:6212481-6212531	SKMC	muscle:	n/a
4	chr7:6212576-6212626	GM19239	blood:	n/a
5	chr7:6198846-6198896	GM12891	blood:	n/a
6	chr7:6192000-6192050	SK-N-SH	brain:	n/a
7	chr7:6212481-6212531	SKMC	muscle:	n/a
8	chr7:6212576-6212626	GM19239	blood:	n/a
9	chr7:6212481-6212531	PFSK-1	brain:	n/a
10	chr7:6199980-6200030	K562	blood:	n/a
11	chr7:6209326-6209376	T-47D	breast:	n/a
12	chr7:6205417-6205467	HRE	kidney:	n/a
13	chr7:6197576-6197626	MCF10A-Er-Src	breast:	n/a
14	chr7:6204863-6204913	SKMC	muscle:	n/a
15	chr7:6204863-6204913	K562	blood:	n/a
16	chr7:6204302-6204352	HCT-116	colon:	n/a
17	chr7:6203267-6203317	NB4	blood:	n/a
18	chr7:6197678-6197728	T-47D	breast:	n/a
19	chr7:6204863-6204913	BE2_C	brain:	n/a
20	chr7:6198604-6198654	HIPEpiC	eye:	n/a
21	chr7:6200886-6200936	HCM	heart:	n/a
22	chr7:6208213-6208263	AG10803	skin:	n/a
23	chr7:6199980-6200030	GM12891	blood:	n/a
24	chr7:6210667-6210717	HepG2	liver:	n/a
25	chr7:6198496-6198546	BE2_C	brain:	n/a
26	chr7:6191780-6191830	K562	blood:	n/a
27	chr7:6204983-6205033	LNCaP	prostate:	n/a
28	chr7:6204863-6204913	NHDF-neo	bronchial:	n/a
29	chr7:6198846-6198896	NHDF-neo	bronchial:	n/a
30	chr7:6203267-6203317	K562	blood:	n/a
31	chr7:6204863-6204913	SK-N-MC	brain:	n/a
32	chr7:6203389-6203439	HMEC	breast:	n/a
33	chr7:6209326-6209376	ECC-1	luminal epithelium:	n/a
34	chr7:6197678-6197728	HUVEC	blood vessel:	n/a
35	chr7:6199437-6199487	HCT-116	colon:	n/a
36	chr7:6200116-6200166	A549	lung:	n/a
37	chr7:6209931-6209981	HRE	kidney:	n/a
38	chr7:6197514-6197564	HIPEpiC	eye:	n/a
39	chr7:6197576-6197626	A549	lung:	n/a
40	chr7:6197576-6197626	HIPEpiC	eye:	n/a
41	chr7:6198496-6198546	PANC-1	pancreas:	n/a
42	chr7:6194677-6194727	AG04450	lung:	fetal
43	chr7:6199437-6199487	HNPCEpiC	eye:	n/a
44	chr7:6197678-6197728	HIPEpiC	eye:	n/a
45	chr7:6197678-6197728	ovcar-3	ovarian:	n/a
46	chr7:6198004-6198054	GM12878	blood:	n/a
47	chr7:6198703-6198753	SK-N-MC	brain:	n/a
48	chr7:6212576-6212626	GM12878	blood:	n/a
49	chr7:6209326-6209376	PFSK-1	brain:	n/a
50	chr7:6204774-6204824	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6205893..6207874-chr7:6209038..6211442,3	K562	blood:
2	chr7:6202248..6204197-chr7:6205375..6207619,2	K562	blood:
3	chr7:6197102..6199080-chr7:6201748..6203601,2	K562	blood:
4	chr7:6198247..6199856-chr7:6202022..6204046,2	MCF-7	breast:
5	chr7:6195312..6197722-chr7:6310990..6313470,2	K562	blood:
6	chr7:6198247..6199856-chr7:6202022..6204046,2	MCF-7	breast:
7	chr7:6185367..6187227-chr7:6188994..6190699,2	MCF-7	breast:
8	chr7:6199470..6202116-chr7:6204941..6208439,5	K562	blood:
9	chr7:6047355..6050049-chr7:6209625..6211423,2	MCF-7	breast:
10	chr7:6200618..6201665-chr7:6361362..6362302,3	K562	blood:
11	chr7:6199039..6200525-chr7:6362284..6363316,17	MCF-7	breast:
12	chr7:6198597..6201773-chr7:6386005..6390187,3	MCF-7	breast:
13	chr7:6199470..6202116-chr7:6204941..6208439,5	K562	blood:
14	chr7:6183038..6185913-chr7:6186874..6189877,3	K562	blood:
15	chr7:6203205..6205349-chr7:6208114..6211098,2	K562	blood:
16	chr7:6199867..6200929-chr7:6475011..6475738,3	MCF-7	breast:
17	chr7:6197102..6199080-chr7:6201748..6203601,2	K562	blood:
18	chr7:6206063..6207710-chr7:6310368..6312250,2	MCF-7	breast:
19	chr7:6189338..6192083-chr7:6192220..6194410,2	K562	blood:
20	chr7:6194450..6196699-chr7:6202081..6204089,2	MCF-7	breast:
21	chr7:6202248..6204197-chr7:6205375..6207619,2	K562	blood:
22	chr7:6204362..6204955-chr7:51756969..51757469,2	Hela-S3	cervix:
23	chr7:6064779..6066813-chr7:6192306..6194117,2	MCF-7	breast:
24	chr7:6186873..6189164-chr7:6206563..6209171,2	K562	blood:
25	chr7:6196482..6198122-chr7:6199857..6201667,2	K562	blood:
26	chr7:6194593..6196125-chr7:6200629..6202167,2	K562	blood:
27	chr7:6199558..6200447-chr7:6362313..6363284,3	MCF-7	breast:
28	chr7:6196482..6198122-chr7:6199857..6201667,2	K562	blood:
29	chr7:6189338..6192083-chr7:6192220..6194410,2	K562	blood:
30	chr7:6194593..6196125-chr7:6200629..6202167,2	K562	blood:
31	chr7:6204442..6207336-chr7:6209471..6212385,2	MCF-7	breast:
32	chr7:6208105..6209788-chr7:6212799..6214937,2	K562	blood:
33	chr7:6194450..6196699-chr7:6202081..6204089,2	MCF-7	breast:
34	chr7:6142710..6146060-chr7:6197801..6200881,4	MCF-7	breast:
35	chr7:6195894..6198040-chr7:6361741..6363493,2	MCF-7	breast:
36	chr7:6203849..6207393-chr7:6209598..6212801,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2AK1-3	chr7:6210757-6210945	NONHSAT118988
2	lnc-EIF2AK1-3	chr7:6212362-6212706	NONHSAT118988

No.	miRNA target gene	miRNA name	Chromosome Location
1	USP42	hsa-miR-16-5p	chr7:6199383-6199389
2	USP42	hsa-miR-103a-3p	chr7:6200427-6200450
3	USP42	hsa-miR-103a-3p	chr7:6199382-6199388
4	CYTH3	hsa-miR-320a	chr7:6202808-6202802
5	USP42	hsa-miR-320a	chr7:6200204-6200226
6	USP42	hsa-miR-16-5p	chr7:6200429-6200451

Variant related genes	Relation type
CYTH3	TF binding region
CYTH3	CpG island
ENSG00000008256	chromatin interactions
ENSG00000238534	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000086232	chromatin interactions
ENSG00000178397	chromatin interactions

Extended variants
information (count: 1317 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1317 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3764814	chr7:6189780-6189781	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546255931	chr7:6189801-6189802	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530604176	chr7:6189805-6189806	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200418298	chr7:6189823-6189824	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61752591	chr7:6189843-6189844	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs200429464	chr7:6189853-6189854	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369332625	chr7:6189872-6189873	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572277214	chr7:6189890-6189891	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558262584	chr7:6189899-6189900	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201342208	chr7:6189919-6189920	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375648875	chr7:6189943-6189944	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369951067	chr7:6189944-6189945	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370179651	chr7:6189949-6189950	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563893341	chr7:6189958-6189959	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150612440	chr7:6189970-6189971	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373489451	chr7:6189976-6189977	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376378452	chr7:6189982-6189983	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202090545	chr7:6190005-6190006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201264431	chr7:6190009-6190010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374438551	chr7:6190014-6190015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529503554	chr7:6190093-6190094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376617636	chr7:6190104-6190105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547723082	chr7:6190110-6190111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199521734	chr7:6190119-6190120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374947317	chr7:6190122-6190123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117155332	chr7:6190125-6190126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3815216	chr7:6190126-6190127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376195442	chr7:6190129-6190130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368694025	chr7:6190131-6190132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372021498	chr7:6190135-6190136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200910208	chr7:6190143-6190144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376440635	chr7:6190163-6190164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569666661	chr7:6190277-6190278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558871135	chr7:6190278-6190279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577496769	chr7:6190281-6190282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566345	chr7:6190289-6190290	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs368359490	chr7:6190340-6190341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141727339	chr7:6190366-6190367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567467273	chr7:6190387-6190388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535249063	chr7:6190416-6190417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553718132	chr7:6190419-6190420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189735953	chr7:6190466-6190467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572221349	chr7:6190499-6190500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74540684	chr7:6190528-6190529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180986269	chr7:6190541-6190542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78817497	chr7:6190560-6190561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543484947	chr7:6190564-6190565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28496021	chr7:6190576-6190577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150574619	chr7:6190587-6190588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545482304	chr7:6190589-6190590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6146800-6218200	Weak transcription	Stomach Mucosa	stomach
2	chr7:6160600-6201800	Strong transcription	Fetal Thymus	thymus
3	chr7:6161400-6199600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:6161400-6202200	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr7:6161600-6192000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:6164000-6192400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:6164200-6199400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr7:6167400-6205600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr7:6172800-6202600	Strong transcription	Dnd41	blood
10	chr7:6173200-6192600	Strong transcription	Fetal Muscle Trunk	muscle
11	chr7:6173200-6204800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:6173800-6192200	Strong transcription	Primary B cells from cord blood	blood
13	chr7:6173800-6205000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:6174000-6193400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr7:6174200-6204800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr7:6174400-6190800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr7:6174400-6200600	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr7:6174600-6202200	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr7:6174800-6200000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:6175200-6199200	Strong transcription	Cortex derived primary cultured neurospheres	brain
21	chr7:6175400-6193200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:6175400-6204200	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr7:6175600-6198800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:6175800-6193600	Strong transcription	Fetal Intestine Large	intestine
25	chr7:6176000-6198200	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr7:6177000-6199400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:6177600-6199600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:6177600-6202400	Strong transcription	Primary B cells from peripheral blood	blood
29	chr7:6178000-6190200	Strong transcription	Hela-S3	cervix
30	chr7:6178000-6197800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:6178000-6198800	Strong transcription	Fetal Muscle Leg	muscle
32	chr7:6178200-6192600	Strong transcription	HepG2	liver
33	chr7:6178200-6194800	Strong transcription	Colonic Mucosa	Colon
34	chr7:6178200-6199200	Strong transcription	Brain Germinal Matrix	brain
35	chr7:6178200-6201800	Strong transcription	Liver	Liver
36	chr7:6178200-6204600	Strong transcription	Thymus	Thymus
37	chr7:6178400-6198800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr7:6178600-6192200	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr7:6178600-6192600	Strong transcription	NH-A	brain
40	chr7:6178600-6192800	Strong transcription	Fetal Lung	lung
41	chr7:6178600-6196800	Strong transcription	Muscle Satellite Cultured Cells	--
42	chr7:6178600-6198400	Strong transcription	Fetal Brain Female	brain
43	chr7:6178600-6199200	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr7:6178600-6199800	Strong transcription	H1 Cell Line	embryonic stem cell
45	chr7:6178800-6198600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:6180200-6204800	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr7:6181200-6199200	Strong transcription	Skeletal Muscle Male	skeletal muscle
48	chr7:6181200-6199600	Strong transcription	Primary T cells from cord blood	blood
49	chr7:6181200-6205400	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr7:6181200-6211800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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