Variant report

Variant	nsv887427
Chromosome Location	chr7:6190126-6213396
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	chr7:6194167-6194449	K562	blood:	n/a	n/a
5	CCNT2	chr7:6200018-6200134	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	chr7:6198047-6198084	K562	blood:	n/a	n/a
9	CHD2	chr7:6211312-6211829	H1-hESC	embryonic stem cell:	n/a	chr7:6211548-6211558
10	CHD2	chr7:6204212-6204322	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr7:6196841-6196885	HepG2	liver:	n/a	n/a
12	CTCF	chr7:6199907-6200016	GM10248	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
13	CTCF	chr7:6199950-6199957	GM20000	blood:	n/a	n/a
14	CTCF	chr7:6199900-6200050	BE2_C	brain:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
15	CTCF	chr7:6199842-6200092	A549	lung:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
16	CTCF	chr7:6204160-6204310	RPTEC	kidney:	n/a	n/a
17	CTCF	chr7:6199960-6200110	HCT-116	colon:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
18	CTCF	chr7:6199080-6199230	BJ	skin:	n/a	n/a
19	CTCF	chr7:6199840-6200152	MCF-7	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
20	CTCF	chr7:6199940-6200090	AG09319	gingival:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
21	CTCF	chr7:6199920-6200070	HepG2	liver:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
22	CTCF	chr7:6200120-6200270	GM12872	blood:	n/a	n/a
23	CTCF	chr7:6199920-6200070	BE2_C	brain:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
24	CTCF	chr7:6199460-6199610	BJ	skin:	n/a	chr7:6199553-6199566
25	CTCF	chr7:6199940-6200090	HPF	lung:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
26	CTCF	chr7:6199851-6200131	MCF-7	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
27	CTCF	chr7:6199829-6200116	Lung_OC	lung:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
28	CTCF	chr7:6199900-6200050	HBMEC	blood vessel:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
29	CTCF	chr7:6199836-6200161	A549	lung:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
30	CTCF	chr7:6199920-6200070	AG10803	skin:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
31	CTCF	chr7:6204180-6204330	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr7:6204200-6204350	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr7:6199728-6200219	H1-hESC	embryonic stem cell:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
34	CTCF	chr7:6199940-6200090	HRPEpiC	eye:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
35	CTCF	chr7:6204166-6204315	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr7:6199860-6200010	HMEC	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
37	CTCF	chr7:6199920-6200070	HVMF	connective:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
38	CTCF	chr7:6199900-6200050	HRPEpiC	eye:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
39	CTCF	chr7:6204126-6204364	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr7:6199980-6200130	A549	lung:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
41	CTCF	chr7:6204200-6204350	BJ	skin:	n/a	n/a
42	CTCF	chr7:6204139-6204326	K562	blood:	n/a	n/a
43	CTCF	chr7:6199400-6199550	WI-38	lung:	n/a	n/a
44	CTCF	chr7:6199872-6200108	GM19238	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
45	CTCF	chr7:6204080-6204230	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr7:6199940-6200090	MCF-7	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
47	CTCF	chr7:6204095-6204418	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr7:6204200-6204350	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr7:6204180-6204330	HCFaa	heart:	n/a	n/a
50	CTCF	chr7:6199920-6200070	HUVEC	blood vessel:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6204185-6204235	GM12891	blood:	n/a
2	chr7:6205492-6205542	PFSK-1	brain:	n/a
3	chr7:6191921-6191971	HIPEpiC	eye:	n/a
4	chr7:6197576-6197626	SKMC	muscle:	n/a
5	chr7:6204185-6204235	GM12891	blood:	n/a
6	chr7:6205492-6205542	PFSK-1	brain:	n/a
7	chr7:6191921-6191971	HIPEpiC	eye:	n/a
8	chr7:6197576-6197626	SKMC	muscle:	n/a
9	chr7:6198496-6198546	LNCaP	prostate:	n/a
10	chr7:6197576-6197626	HepG2	liver:	n/a
11	chr7:6197576-6197626	LNCaP	prostate:	n/a
12	chr7:6209417-6209467	SK-N-MC	brain:	n/a
13	chr7:6209326-6209376	T-47D	breast:	n/a
14	chr7:6204983-6205033	NB4	blood:	n/a
15	chr7:6204302-6204352	H1-hESC	embryonic stem cell:	embryo
16	chr7:6203156-6203206	HUVEC	blood vessel:	n/a
17	chr7:6199437-6199487	NT2-D1	testis:	n/a
18	chr7:6191807-6191857	HL-60	blood:	n/a
19	chr7:6196591-6196641	GM06990	blood:	n/a
20	chr7:6194677-6194727	K562	blood:	n/a
21	chr7:6204302-6204352	HIPEpiC	eye:	n/a
22	chr7:6192000-6192050	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:6197890-6197940	HCF	heart:	n/a
24	chr7:6194677-6194727	CMK	blood:	n/a
25	chr7:6200886-6200936	NH-A	brain:	n/a
26	chr7:6212775-6212825	GM19239	blood:	n/a
27	chr7:6210667-6210717	HNPCEpiC	eye:	n/a
28	chr7:6199472-6199522	HIPEpiC	eye:	n/a
29	chr7:6199472-6199522	HCM	heart:	n/a
30	chr7:6208213-6208263	AoSMC	blood vessel:	n/a
31	chr7:6203267-6203317	SKMC	muscle:	n/a
32	chr7:6197576-6197626	SK-N-MC	brain:	n/a
33	chr7:6209417-6209467	HRE	kidney:	n/a
34	chr7:6210236-6210286	Caco-2	colon:	n/a
35	chr7:6191780-6191830	T-47D	breast:	n/a
36	chr7:6204521-6204571	GM12878	blood:	n/a
37	chr7:6197514-6197564	AoSMC	blood vessel:	n/a
38	chr7:6203389-6203439	HUVEC	blood vessel:	n/a
39	chr7:6199472-6199522	Hela-S3	cervix:	n/a
40	chr7:6203267-6203317	GM12878	blood:	n/a
41	chr7:6208128-6208178	SKMC	muscle:	n/a
42	chr7:6212481-6212531	T-47D	breast:	n/a
43	chr7:6199472-6199522	T-47D	breast:	n/a
44	chr7:6199980-6200030	AG09309	skin:	n/a
45	chr7:6212576-6212626	IMR90	lung:	fetal
46	chr7:6204302-6204352	CMK	blood:	n/a
47	chr7:6197890-6197940	HIPEpiC	eye:	n/a
48	chr7:6199980-6200030	HL-60	blood:	n/a
49	chr7:6204302-6204352	PFSK-1	brain:	n/a
50	chr7:6197576-6197626	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6200618..6201665-chr7:6361362..6362302,3	K562	blood:
2	chr7:6194450..6196699-chr7:6202081..6204089,2	MCF-7	breast:
3	chr7:6142710..6146060-chr7:6197801..6200881,4	MCF-7	breast:
4	chr7:6195894..6198040-chr7:6361741..6363493,2	MCF-7	breast:
5	chr7:6197102..6199080-chr7:6201748..6203601,2	K562	blood:
6	chr7:6202248..6204197-chr7:6205375..6207619,2	K562	blood:
7	chr7:6204442..6207336-chr7:6209471..6212385,2	MCF-7	breast:
8	chr7:6199867..6200929-chr7:6475011..6475738,3	MCF-7	breast:
9	chr7:6186873..6189164-chr7:6206563..6209171,2	K562	blood:
10	chr7:6199470..6202116-chr7:6204941..6208439,5	K562	blood:
11	chr7:6194593..6196125-chr7:6200629..6202167,2	K562	blood:
12	chr7:6197102..6199080-chr7:6201748..6203601,2	K562	blood:
13	chr7:6195312..6197722-chr7:6310990..6313470,2	K562	blood:
14	chr7:6196482..6198122-chr7:6199857..6201667,2	K562	blood:
15	chr7:6204362..6204955-chr7:51756969..51757469,2	Hela-S3	cervix:
16	chr7:6194450..6196699-chr7:6202081..6204089,2	MCF-7	breast:
17	chr7:6198247..6199856-chr7:6202022..6204046,2	MCF-7	breast:
18	chr7:6203205..6205349-chr7:6208114..6211098,2	K562	blood:
19	chr7:6208105..6209788-chr7:6212799..6214937,2	K562	blood:
20	chr7:6064779..6066813-chr7:6192306..6194117,2	MCF-7	breast:
21	chr7:6205893..6207874-chr7:6209038..6211442,3	K562	blood:
22	chr7:6199470..6202116-chr7:6204941..6208439,5	K562	blood:
23	chr7:6189338..6192083-chr7:6192220..6194410,2	K562	blood:
24	chr7:6206063..6207710-chr7:6310368..6312250,2	MCF-7	breast:
25	chr7:6199039..6200525-chr7:6362284..6363316,17	MCF-7	breast:
26	chr7:6047355..6050049-chr7:6209625..6211423,2	MCF-7	breast:
27	chr7:6198247..6199856-chr7:6202022..6204046,2	MCF-7	breast:
28	chr7:6199558..6200447-chr7:6362313..6363284,3	MCF-7	breast:
29	chr7:6185367..6187227-chr7:6188994..6190699,2	MCF-7	breast:
30	chr7:6196482..6198122-chr7:6199857..6201667,2	K562	blood:
31	chr7:6194593..6196125-chr7:6200629..6202167,2	K562	blood:
32	chr7:6189338..6192083-chr7:6192220..6194410,2	K562	blood:
33	chr7:6203849..6207393-chr7:6209598..6212801,3	K562	blood:
34	chr7:6198597..6201773-chr7:6386005..6390187,3	MCF-7	breast:
35	chr7:6202248..6204197-chr7:6205375..6207619,2	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-320a	chr7:6200204-6200226
2	CYTH3	hsa-miR-320a	chr7:6202808-6202802
3	USP42	hsa-miR-103a-3p	chr7:6199382-6199388
4	USP42	hsa-miR-16-5p	chr7:6200429-6200451
5	USP42	hsa-miR-103a-3p	chr7:6200427-6200450
6	USP42	hsa-miR-16-5p	chr7:6199383-6199389

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

Extended variants
information (count: 1334 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1334 , 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	rs3815216	chr7:6190126-6190127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376195442	chr7:6190129-6190130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368694025	chr7:6190131-6190132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372021498	chr7:6190135-6190136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200910208	chr7:6190143-6190144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376440635	chr7:6190163-6190164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569666661	chr7:6190277-6190278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558871135	chr7:6190278-6190279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577496769	chr7:6190281-6190282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566345	chr7:6190289-6190290	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs368359490	chr7:6190340-6190341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141727339	chr7:6190366-6190367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567467273	chr7:6190387-6190388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535249063	chr7:6190416-6190417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553718132	chr7:6190419-6190420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189735953	chr7:6190466-6190467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572221349	chr7:6190499-6190500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74540684	chr7:6190528-6190529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs180986269	chr7:6190541-6190542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78817497	chr7:6190560-6190561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543484947	chr7:6190564-6190565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28496021	chr7:6190576-6190577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150574619	chr7:6190587-6190588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545482304	chr7:6190589-6190590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559659877	chr7:6190646-6190647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533572496	chr7:6190676-6190677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs59122532	chr7:6190677-6190678	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs190567081	chr7:6190697-6190698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112245957	chr7:6190700-6190701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138638823	chr7:6190705-6190706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181928850	chr7:6190744-6190745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186301821	chr7:6190764-6190765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370260557	chr7:6190766-6190767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574451925	chr7:6190798-6190799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148854249	chr7:6190829-6190830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190696685	chr7:6190860-6190861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550988498	chr7:6190874-6190875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547093035	chr7:6190882-6190883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368591682	chr7:6190896-6190897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368118267	chr7:6190905-6190906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530631394	chr7:6190925-6190926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541924407	chr7:6190945-6190946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10249786	chr7:6190946-6190947	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs576453100	chr7:6190986-6190987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374991376	chr7:6191062-6191063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530594135	chr7:6191068-6191069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77098901	chr7:6191077-6191078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573698925	chr7:6191138-6191139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149313256	chr7:6191206-6191207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564097746	chr7:6191217-6191218	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:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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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