Variant report

Variant	nsv888943
Chromosome Location	chr7:107893695-108058574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1741)
CpG islands
(count:549)
Chromatin interactive
region (count:222)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1741 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:107939809-107940021	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:107998929-107999584	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:107992019-107992880	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:107981410-107981723	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:108025604-108025847	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:108048443-108048485	K562	blood:	n/a	n/a
7	ARID3A	chr7:107940020-107940021	K562	blood:	n/a	n/a
8	ATF1	chr7:108025180-108025769	K562	blood:	n/a	n/a
9	ATF1	chr7:107935160-107935370	K562	blood:	n/a	n/a
10	ATF1	chr7:107915060-107915262	K562	blood:	n/a	n/a
11	ATF1	chr7:108056741-108057052	K562	blood:	n/a	n/a
12	ATF2	chr7:108056158-108056981	GM12878	blood:	n/a	n/a
13	ATF2	chr7:107951706-107952409	GM12878	blood:	n/a	n/a
14	ATF2	chr7:107949317-107949794	GM12878	blood:	n/a	n/a
15	ATF2	chr7:107910793-107911221	GM12878	blood:	n/a	n/a
16	ATF2	chr7:107910685-107911211	GM12878	blood:	n/a	n/a
17	ATF2	chr7:108056128-108057095	GM12878	blood:	n/a	n/a
18	ATF2	chr7:107951874-107952281	GM12878	blood:	n/a	n/a
19	ATF2	chr7:107987995-107988431	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr7:108057568-108057879	K562	blood:	n/a	n/a
21	BATF	chr7:107925297-107925507	GM12878	blood:	n/a	chr7:107925366-107925377
22	BATF	chr7:107951879-107952247	GM12878	blood:	n/a	n/a
23	BATF	chr7:107925241-107925469	GM12878	blood:	n/a	chr7:107925366-107925377
24	BATF	chr7:108016230-108016558	GM12878	blood:	n/a	n/a
25	BATF	chr7:108026544-108026830	GM12878	blood:	n/a	n/a
26	BATF	chr7:107910914-107911171	GM12878	blood:	n/a	n/a
27	BATF	chr7:108016229-108016512	GM12878	blood:	n/a	n/a
28	BATF	chr7:107949364-107949714	GM12878	blood:	n/a	n/a
29	BATF	chr7:108056273-108056541	GM12878	blood:	n/a	n/a
30	BATF	chr7:107951846-107952249	GM12878	blood:	n/a	n/a
31	BATF	chr7:107910852-107911196	GM12878	blood:	n/a	chr7:107910878-107910886
32	BATF	chr7:108056225-108056547	GM12878	blood:	n/a	n/a
33	BATF	chr7:108056724-108056999	GM12878	blood:	n/a	n/a
34	BATF	chr7:107949418-107949714	GM12878	blood:	n/a	n/a
35	BATF	chr7:107948779-107949056	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:107949424-107949695	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:108056224-108056536	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:107925213-107925523	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:107951818-107952231	GM12878	blood:	n/a	chr7:107952166-107952175
40	BCL11A	chr7:108043966-108044249	GM12878	blood:	n/a	n/a
41	BCL3	chr7:107991984-107992629	A549	lung:	n/a	n/a
42	BCL3	chr7:108056161-108056483	GM12878	blood:	n/a	n/a
43	BCL3	chr7:107951878-107952243	GM12878	blood:	n/a	chr7:107952166-107952175
44	BCLAF1	chr7:107951860-107952220	GM12878	blood:	n/a	chr7:107952166-107952175
45	BCLAF1	chr7:108056175-108057045	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:108044299-108044387	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:107998937-107999400	HepG2	liver:	n/a	n/a
48	BHLHE40	chr7:108054598-108054628	K562	blood:	n/a	n/a
49	BHLHE40	chr7:107949515-107949694	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:108056541-108056904	A549	lung:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:107969837-107969887	GM19239	blood:	n/a
2	chr7:107967614-107967664	GM12878	blood:	n/a
3	chr7:107965081-107965131	SK-N-MC	brain:	n/a
4	chr7:107965081-107965131	HL-60	blood:	n/a
5	chr7:108025567-108025617	HCT-116	colon:	n/a
6	chr7:108055705-108055755	T-47D	breast:	n/a
7	chr7:107987769-107987819	A549	lung:	n/a
8	chr7:107967614-107967664	Jurkat	blood:	n/a
9	chr7:107965081-107965131	HRPEpiC	eye:	n/a
10	chr7:108025567-108025617	PANC-1	pancreas:	n/a
11	chr7:107967614-107967664	PFSK-1	brain:	n/a
12	chr7:108055705-108055755	HRCEpiC	kidney:	n/a
13	chr7:107969837-107969887	MCF10A-Er-Src	breast:	n/a
14	chr7:107931294-107931344	MCF-7	breast:	n/a
15	chr7:107950866-107950916	CMK	blood:	n/a
16	chr7:107965081-107965131	AG09319	gingival:	n/a
17	chr7:107967614-107967664	K562	blood:	n/a
18	chr7:107950866-107950916	Hepatocyte	liver:	n/a
19	chr7:107967614-107967664	HCT-116	colon:	n/a
20	chr7:107931294-107931344	BJ	skin:	n/a
21	chr7:107931294-107931344	GM19239	blood:	n/a
22	chr7:108025567-108025617	NHBE	bronchial:	n/a
23	chr7:107948864-107948914	Caco-2	colon:	n/a
24	chr7:107969837-107969887	HUVEC	blood vessel:	n/a
25	chr7:107950866-107950916	SK-N-SH	brain:	n/a
26	chr7:108025567-108025617	GM12878	blood:	n/a
27	chr7:107967614-107967664	PrEC	prostate:	n/a
28	chr7:107967614-107967664	NH-A	brain:	n/a
29	chr7:107969837-107969887	Jurkat	blood:	n/a
30	chr7:108025567-108025617	HRE	kidney:	n/a
31	chr7:107950866-107950916	GM12878	blood:	n/a
32	chr7:107987769-107987819	CMK	blood:	n/a
33	chr7:107950866-107950916	SK-N-SH_RA	brain:	n/a
34	chr7:108025567-108025617	RPTEC	kidney:	n/a
35	chr7:107950866-107950916	BJ	skin:	n/a
36	chr7:107950866-107950916	AoSMC	blood vessel:	n/a
37	chr7:107967614-107967664	HEEpiC	esophagus:	n/a
38	chr7:107967614-107967664	Caco-2	colon:	n/a
39	chr7:107967614-107967664	AoSMC	blood vessel:	n/a
40	chr7:107948864-107948914	AoSMC	blood vessel:	n/a
41	chr7:108025567-108025617	HIPEpiC	eye:	n/a
42	chr7:107967614-107967664	AG10803	skin:	n/a
43	chr7:107948864-107948914	NHBE	bronchial:	n/a
44	chr7:107987769-107987819	MCF-7	breast:	n/a
45	chr7:108025567-108025617	Hepatocyte	liver:	n/a
46	chr7:108055705-108055755	Caco-2	colon:	n/a
47	chr7:107948864-107948914	HCPEpiC	choroid plexus:	n/a
48	chr7:107969837-107969887	SAEC	small airway:	n/a
49	chr7:107931294-107931344	RPTEC	kidney:	n/a
50	chr7:107967614-107967664	CMK	blood:	n/a

(count:222 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr7:108038876..108042615-chr7:108043454..108045817,3	K562	blood:
2	chr7:107923634..107926362-chr7:107928616..107931028,3	MCF-7	breast:
3	chr7:107965337..107967353-chr7:107989055..107990953,2	K562	blood:
4	chr7:107938795..107940686-chr7:107979875..107982816,2	MCF-7	breast:
5	chr7:107946487..107948369-chr7:107949366..107951940,2	K562	blood:
6	chr7:108019480..108021624-chr7:108021812..108023878,2	MCF-7	breast:
7	chr7:107994751..107997423-chr7:108093264..108097218,4	MCF-7	breast:
8	chr7:107991896..107993618-chr7:108006610..108008809,2	MCF-7	breast:
9	chr7:107953333..107956012-chr7:107956153..107957940,2	K562	blood:
10	chr7:107974565..107976099-chr7:108007204..108009580,2	MCF-7	breast:
11	chr7:107943761..107946281-chr7:107950913..107952472,2	MCF-7	breast:
12	chr7:107975728..107977944-chr7:107990404..107993160,3	MCF-7	breast:
13	chr7:107919806..107922501-chr7:107923966..107926073,3	K562	blood:
14	chr7:107934726..107936588-chr7:107945741..107947736,2	K562	blood:
15	chr7:107942489..107944255-chr7:107991552..107993879,2	MCF-7	breast:
16	chr7:107973727..107975875-chr7:107982634..107985172,2	K562	blood:
17	chr7:107940013..107942705-chr7:108208035..108210155,2	K562	blood:
18	chr7:108006500..108008005-chr7:108054331..108056945,2	MCF-7	breast:
19	chr7:108054248..108057900-chr7:108068091..108071582,3	MCF-7	breast:
20	chr7:107945282..107948369-chr7:107949981..107952858,4	K562	blood:
21	chr7:107942231..107944155-chr7:107945358..107947357,2	MCF-7	breast:
22	chr7:107948237..107951019-chr7:107962577..107964592,2	MCF-7	breast:
23	chr7:107974565..107976099-chr7:108007204..108009580,2	MCF-7	breast:
24	chr7:107843916..107845660-chr7:107990160..107992997,2	MCF-7	breast:
25	chr7:107934951..107937063-chr7:108095245..108097236,2	MCF-7	breast:
26	chr7:107923082..107925361-chr7:107930401..107931906,2	K562	blood:
27	chr7:108006947..108010062-chr7:108010245..108014925,5	MCF-7	breast:
28	chr7:107855172..107857535-chr7:107989260..107991457,2	MCF-7	breast:
29	chr7:107962380..107965223-chr7:107965724..107968731,3	K562	blood:
30	chr7:107954604..107957944-chr7:107959964..107962643,4	K562	blood:
31	chr7:107926710..107929161-chr7:107930856..107933186,2	K562	blood:
32	chr7:107997597..108000598-chr7:108005435..108008873,4	MCF-7	breast:
33	chr7:107897446..107900433-chr7:107904725..107906956,2	K562	blood:
34	chr7:107897446..107900433-chr7:107904725..107906956,2	K562	blood:
35	chr7:107930752..107933426-chr7:107936477..107939262,3	MCF-7	breast:
36	chr7:107941830..107944021-chr7:107948605..107950880,3	MCF-7	breast:
37	chr7:108044020..108046145-chr7:108049502..108052110,2	K562	blood:
38	chr7:107988114..107994277-chr7:108093987..108097676,13	MCF-7	breast:
39	chr7:107991286..107993466-chr7:108009431..108011060,2	MCF-7	breast:
40	chr7:107991896..107993618-chr7:108006610..108008809,2	MCF-7	breast:
41	chr7:107988643..107991410-chr7:108016162..108018347,3	MCF-7	breast:
42	chr7:107943761..107946281-chr7:107950913..107952472,2	MCF-7	breast:
43	chr7:107941830..107944021-chr7:107948605..107950880,3	MCF-7	breast:
44	chr7:108044915..108046509-chr7:108049810..108051904,2	MCF-7	breast:
45	chr7:107942489..107944255-chr7:107991552..107993879,2	MCF-7	breast:
46	chr7:108025164..108027464-chr7:108095416..108098539,5	MCF-7	breast:
47	chr7:108049821..108052079-chr7:108053231..108055054,2	MCF-7	breast:
48	chr7:108051946..108054538-chr7:108064091..108066003,2	MCF-7	breast:
49	chr7:107840154..107842979-chr7:107937702..107939902,2	MCF-7	breast:
50	chr7:108016249..108018271-chr7:108046032..108048328,2	MCF-7	breast:

No data

Variant related genes	Relation type
NRCAM	TF binding region
ENSG00000266112	TF binding region
NRCAM	CpG island
ENSG00000266112	CpG island
ENSG00000266112	chromatin interactions
ENSG00000177683	chromatin interactions
ENSG00000091129	chromatin interactions
ENSG00000135241	chromatin interactions
ENSG00000128590	chromatin interactions

Extended variants
information (count: 6086 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:6086 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2111203	chr7:107893695-107893696	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556093872	chr7:107893760-107893761	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs180761095	chr7:107893777-107893778	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs185013760	chr7:107893788-107893789	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs145329460	chr7:107893805-107893806	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs79547888	chr7:107893809-107893810	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs532978802	chr7:107893868-107893869	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs147694897	chr7:107893907-107893908	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs560298552	chr7:107893908-107893909	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs189393318	chr7:107893940-107893941	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs142485052	chr7:107893992-107893993	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs569109253	chr7:107893993-107893994	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs181723972	chr7:107893994-107893995	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs186074070	chr7:107894061-107894062	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs148043232	chr7:107894085-107894086	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs140817889	chr7:107894103-107894104	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs201112968	chr7:107894166-107894167	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs191401401	chr7:107894174-107894175	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs553043341	chr7:107894181-107894182	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs117630356	chr7:107894197-107894198	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs536025913	chr7:107894221-107894222	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs555717266	chr7:107894252-107894253	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs575810734	chr7:107894374-107894375	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs372957456	chr7:107894390-107894391	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs181409670	chr7:107894391-107894392	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs577420335	chr7:107894435-107894436	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs558492437	chr7:107894442-107894443	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs113658118	chr7:107894469-107894470	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs28457047	chr7:107894502-107894503	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs141540338	chr7:107894623-107894624	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs529005224	chr7:107894636-107894637	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs542789162	chr7:107894642-107894643	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs562506892	chr7:107894653-107894654	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs537900059	chr7:107894682-107894683	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs369140951	chr7:107894735-107894736	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs186224568	chr7:107894738-107894739	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs76647201	chr7:107894794-107894795	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs571250803	chr7:107894799-107894800	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs533153292	chr7:107894877-107894878	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146168572	chr7:107894913-107894914	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191118485	chr7:107894957-107894958	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556513130	chr7:107894970-107894971	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs137881405	chr7:107894974-107894975	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs71522863	chr7:107894995-107894996	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373850427	chr7:107894996-107894997	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs60213692	chr7:107894998-107894999	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs75989953	chr7:107894999-107895000	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77437450	chr7:107895003-107895004	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77033509	chr7:107895009-107895010	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs71137620	chr7:107895010-107895011	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
Myxofibrosarcoma	20639860	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:1786 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:107887400-107893800	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:107887400-107894000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:107887400-107925000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr7:107887800-107894000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:107888000-107906800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:107889400-107893800	Weak transcription	HMEC	breast
7	chr7:107889400-107894200	Weak transcription	Osteobl	bone
8	chr7:107891800-107895400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:107892000-107893800	Enhancers	Brain Cingulate Gyrus	brain
10	chr7:107892000-107894000	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr7:107892000-107894000	Enhancers	Brain Angular Gyrus	brain
12	chr7:107892000-107894000	Enhancers	Brain Hippocampus Middle	brain
13	chr7:107892000-107894000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
14	chr7:107892000-107894200	Enhancers	Brain Anterior Caudate	brain
15	chr7:107892000-107894600	Enhancers	K562	blood
16	chr7:107892000-107894800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:107892000-107895200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr7:107892600-107906600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:107892800-107894000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr7:107893000-107893800	Enhancers	Brain Substantia Nigra	brain
21	chr7:107893000-107895000	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr7:107893200-107907400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:107893600-107894000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr7:107893600-107894000	Enhancers	Pancreas	Pancrea
25	chr7:107893600-107894400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr7:107893600-107894800	Flanking Active TSS	A549	lung
27	chr7:107893800-107894400	Enhancers	Fetal Muscle Leg	muscle
28	chr7:107893800-107894400	Enhancers	HMEC	breast
29	chr7:107894000-107894400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:107894000-107894600	Enhancers	Muscle Satellite Cultured Cells	--
31	chr7:107894000-107894800	Enhancers	NH-A	brain
32	chr7:107894000-107895600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:107894000-107898400	Weak transcription	Brain Hippocampus Middle	brain
34	chr7:107894000-107904000	Weak transcription	Pancreas	Pancrea
35	chr7:107894200-107894600	Enhancers	Osteobl	bone
36	chr7:107894400-107898400	Weak transcription	HMEC	breast
37	chr7:107894600-107904200	Weak transcription	K562	blood
38	chr7:107894800-107895400	Enhancers	A549	lung
39	chr7:107895400-107897000	Weak transcription	A549	lung
40	chr7:107895600-107899800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:107897000-107899200	Enhancers	A549	lung
42	chr7:107898400-107898600	Enhancers	Brain Hippocampus Middle	brain
43	chr7:107898400-107898800	Enhancers	HMEC	breast
44	chr7:107899200-107905400	Weak transcription	A549	lung
45	chr7:107901000-107901200	Enhancers	Psoas Muscle	Psoas
46	chr7:107901200-107902200	Weak transcription	Psoas Muscle	Psoas
47	chr7:107901600-107907800	Enhancers	Fetal Muscle Leg	muscle
48	chr7:107902200-107903800	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr7:107902200-107904800	Enhancers	Psoas Muscle	Psoas
50	chr7:107902400-107903400	Enhancers	Skeletal Muscle Male	skeletal muscle

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