Variant report

Variant	nsv1006625
Chromosome Location	chr2:99984550-100096371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1213)
CpG islands
(count:611)
Chromatin interactive
region (count:123)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:100019811-100020650	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:99998533-99998986	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:100009947-100010227	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:100040186-100040295	K562	blood:	n/a	n/a
5	ARID3A	chr2:100087382-100087696	K562	blood:	n/a	n/a
6	ARID3A	chr2:100087939-100088495	K562	blood:	n/a	n/a
7	ATF1	chr2:100094906-100095064	K562	blood:	n/a	n/a
8	BACH1	chr2:100006147-100006165	K562	blood:	n/a	n/a
9	BACH1	chr2:100050590-100050689	K562	blood:	n/a	n/a
10	BATF	chr2:99996862-99997132	GM12878	blood:	n/a	n/a
11	BATF	chr2:99996842-99997154	GM12878	blood:	n/a	n/a
12	BCL3	chr2:100016956-100017463	K562	blood:	n/a	n/a
13	BCL3	chr2:100017491-100018041	K562	blood:	n/a	n/a
14	BCL3	chr2:100021759-100023003	K562	blood:	n/a	n/a
15	BCL3	chr2:100018227-100021181	K562	blood:	n/a	chr2:100020827-100020836
16	BHLHE40	chr2:100012277-100012279	K562	blood:	n/a	n/a
17	BHLHE40	chr2:100039074-100039391	GM12878	blood:	n/a	n/a
18	BRCA1	chr2:100077545-100077588	GM12878	blood:	n/a	n/a
19	BRCA1	chr2:100059290-100059314	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr2:100078566-100078907	K562	blood:	n/a	n/a
21	CBX3	chr2:100078443-100078932	K562	blood:	n/a	n/a
22	CBX3	chr2:100087130-100087721	K562	blood:	n/a	n/a
23	CCNT2	chr2:100015472-100015727	K562	blood:	n/a	n/a
24	CEBPB	chr2:100071610-100071886	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:100076824-100076893	HepG2	liver:	n/a	chr2:100076845-100076856
26	CEBPB	chr2:100018689-100018822	K562	blood:	n/a	n/a
27	CEBPB	chr2:99990576-99990702	A549	lung:	n/a	n/a
28	CEBPB	chr2:99990664-99990665	K562	blood:	n/a	n/a
29	CEBPB	chr2:100092398-100092707	HepG2	liver:	n/a	chr2:100092526-100092539 chr2:100092527-100092538 chr2:100092581-100092593
30	CEBPB	chr2:99990511-99990846	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr2:100088813-100089065	A549	lung:	n/a	chr2:100088920-100088931
32	CEBPB	chr2:100088781-100089062	K562	blood:	n/a	chr2:100088920-100088931
33	CEBPB	chr2:100092384-100092690	K562	blood:	n/a	chr2:100092526-100092539 chr2:100092527-100092538 chr2:100092581-100092593
34	CEBPB	chr2:100088782-100088996	IMR90	lung:	n/a	chr2:100088920-100088931
35	CEBPB	chr2:99996270-99996453	H1-hESC	embryonic stem cell:	n/a	chr2:99996373-99996384
36	CEBPB	chr2:100061536-100061845	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:100092434-100092643	A549	lung:	n/a	chr2:100092526-100092539 chr2:100092527-100092538 chr2:100092581-100092593
38	CEBPB	chr2:99990444-99990857	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr2:100074293-100074519	K562	blood:	n/a	n/a
40	CEBPB	chr2:100038053-100038284	K562	blood:	n/a	chr2:100038174-100038187
41	CEBPB	chr2:99996348-99996438	HepG2	liver:	n/a	chr2:99996373-99996384
42	CEBPB	chr2:100036557-100036775	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:100088785-100089079	HepG2	liver:	n/a	chr2:100088920-100088931
44	CEBPB	chr2:100092391-100092685	IMR90	lung:	n/a	chr2:100092526-100092539 chr2:100092527-100092538 chr2:100092581-100092593
45	CEBPB	chr2:100038001-100038342	IMR90	lung:	n/a	chr2:100038174-100038187
46	CEBPB	chr2:100009896-100010175	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:100047421-100047824	IMR90	lung:	n/a	n/a
48	CEBPB	chr2:99990664-99990715	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr2:100088856-100089028	H1-hESC	embryonic stem cell:	n/a	chr2:100088920-100088931
50	CEBPD	chr2:100087372-100087867	K562	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:100061911-100061961	PFSK-1	brain:	n/a
2	chr2:100061911-100061961	PFSK-1	brain:	n/a
3	chr2:100056660-100056710	ProgFib	skin:	n/a
4	chr2:100056660-100056710	AG09319	gingival:	n/a
5	chr2:100056660-100056710	AG04449	skin:	fetal
6	chr2:100038008-100038058	AG09319	gingival:	n/a
7	chr2:99997497-99997547	A549	lung:	n/a
8	chr2:100020390-100020440	GM12891	blood:	n/a
9	chr2:100017168-100017218	NHBE	bronchial:	n/a
10	chr2:100016281-100016331	HEEpiC	esophagus:	n/a
11	chr2:100017168-100017218	HL-60	blood:	n/a
12	chr2:100078174-100078224	LNCaP	prostate:	n/a
13	chr2:100078174-100078224	HRCEpiC	kidney:	n/a
14	chr2:99997497-99997547	HCM	heart:	n/a
15	chr2:99997497-99997547	ECC-1	luminal epithelium:	n/a
16	chr2:100056660-100056710	PrEC	prostate:	n/a
17	chr2:100038008-100038058	ECC-1	luminal epithelium:	n/a
18	chr2:100038008-100038058	AoSMC	blood vessel:	n/a
19	chr2:99997497-99997547	GM19239	blood:	n/a
20	chr2:100038008-100038058	K562	blood:	n/a
21	chr2:100020390-100020440	Jurkat	blood:	n/a
22	chr2:100056660-100056710	NH-A	brain:	n/a
23	chr2:100056660-100056710	T-47D	breast:	n/a
24	chr2:100038008-100038058	HCM	heart:	n/a
25	chr2:100020390-100020440	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:99997497-99997547	GM12878	blood:	n/a
27	chr2:99997497-99997547	K562	blood:	n/a
28	chr2:100089996-100090046	GM12891	blood:	n/a
29	chr2:100017168-100017218	NHDF-neo	bronchial:	n/a
30	chr2:100061911-100061961	K562	blood:	n/a
31	chr2:100017168-100017218	MCF-7	breast:	n/a
32	chr2:100038008-100038058	PFSK-1	brain:	n/a
33	chr2:100017168-100017218	HCPEpiC	choroid plexus:	n/a
34	chr2:99997497-99997547	BE2_C	brain:	n/a
35	chr2:99997497-99997547	NHDF-neo	bronchial:	n/a
36	chr2:100061911-100061961	BE2_C	brain:	n/a
37	chr2:100078174-100078224	ProgFib	skin:	n/a
38	chr2:99997497-99997547	H1-hESC	embryonic stem cell:	embryo
39	chr2:100089996-100090046	LNCaP	prostate:	n/a
40	chr2:99997497-99997547	HRPEpiC	eye:	n/a
41	chr2:100038008-100038058	AG10803	skin:	n/a
42	chr2:100056660-100056710	HRPEpiC	eye:	n/a
43	chr2:100047526-100047576	HCF	heart:	n/a
44	chr2:100089996-100090046	PFSK-1	brain:	n/a
45	chr2:99997497-99997547	HEEpiC	esophagus:	n/a
46	chr2:100016281-100016331	HepG2	liver:	n/a
47	chr2:100020390-100020440	ovcar-3	ovarian:	n/a
48	chr2:100016281-100016331	HCF	heart:	n/a
49	chr2:100047526-100047576	HRCEpiC	kidney:	n/a
50	chr2:100016281-100016331	HRPEpiC	eye:	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:100079142..100082364-chr2:100082502..100085624,3	K562	blood:
2	chr2:100053808..100056700-chr2:100061249..100063281,2	K562	blood:
3	chr2:100045232..100047151-chr2:100053855..100056471,2	MCF-7	breast:
4	chr2:100014826..100019014-chr2:100020376..100023136,4	K562	blood:
5	chr2:100008715..100012637-chr2:100019428..100022260,4	K562	blood:
6	chr2:100066815..100068950-chr2:100081584..100083548,2	K562	blood:
7	chr2:100040044..100044380-chr2:100044487..100048478,6	K562	blood:
8	chr2:100065120..100066698-chr2:100069712..100072523,2	MCF-7	breast:
9	chr2:100072001..100074970-chr2:100080545..100083472,2	MCF-7	breast:
10	chr2:99952493..99955462-chr2:100001894..100004691,2	MCF-7	breast:
11	chr2:100043303..100044815-chr2:100045701..100048091,2	MCF-7	breast:
12	chr2:99984624..99988612-chr2:99989549..99993377,4	MCF-7	breast:
13	chr2:100071675..100073794-chr2:100105117..100106832,2	K562	blood:
14	chr2:100049389..100050894-chr2:100051918..100054292,2	K562	blood:
15	chr2:100020586..100023216-chr2:100029196..100032155,3	MCF-7	breast:
16	chr2:100061358..100063213-chr2:100063988..100066181,2	MCF-7	breast:
17	chr2:100055571..100061199-chr2:100104819..100108042,8	MCF-7	breast:
18	chr2:100028296..100030954-chr2:100031394..100033463,2	MCF-7	breast:
19	chr2:100040660..100042299-chr2:100044487..100046837,3	K562	blood:
20	chr2:100078933..100081024-chr2:100087446..100090857,3	K562	blood:
21	chr2:100038452..100040181-chr2:100105209..100108184,3	MCF-7	breast:
22	chr2:100077312..100079121-chr2:100100989..100102811,2	K562	blood:
23	chr2:100066768..100070769-chr2:100085883..100089135,3	K562	blood:
24	chr14:92505786..92506708-chr2:100018253..100019120,2	NB4	blood:
25	chr2:100088451..100090156-chr2:100093150..100094831,2	MCF-7	breast:
26	chr2:99984624..99988612-chr2:99989549..99993377,4	MCF-7	breast:
27	chr2:100015311..100016881-chr2:100105394..100106940,2	MCF-7	breast:
28	chr2:100064922..100067755-chr2:100103657..100105818,3	MCF-7	breast:
29	chr2:100082529..100085149-chr2:100097513..100099480,2	K562	blood:
30	chr2:99984853..99986736-chr2:99992052..99994926,2	MCF-7	breast:
31	chr2:99998217..100000036-chr2:100003935..100006623,2	K562	blood:
32	chr2:100047306..100048866-chr2:100054752..100056812,2	K562	blood:
33	chr2:100045644..100048567-chr2:100103283..100105124,2	K562	blood:
34	chr2:100087595..100089096-chr2:100090818..100093356,2	K562	blood:
35	chr2:100082191..100084657-chr2:100091943..100094929,2	K562	blood:
36	chr2:100081842..100083413-chr2:100104447..100107377,2	MCF-7	breast:
37	chr2:99950906..99955641-chr2:100018668..100021744,4	MCF-7	breast:
38	chr2:100080735..100084657-chr2:100090928..100093443,3	K562	blood:
39	chr2:100049953..100053253-chr2:100105706..100108759,4	MCF-7	breast:
40	chr2:100091441..100093893-chr2:100095526..100097800,4	K562	blood:
41	chr2:100059471..100059973-chr2:100877276..100877813,2	K562	blood:
42	chr2:100091441..100093893-chr2:100095526..100097800,4	K562	blood:
43	chr2:100086031..100088660-chr2:100104187..100107882,3	MCF-7	breast:
44	chr2:100010012..100012925-chr2:100019306..100020928,2	K562	blood:
45	chr2:100018784..100022368-chr2:100023520..100027749,4	K562	blood:
46	chr2:100065327..100067396-chr2:100072129..100074926,2	K562	blood:
47	chr2:99950527..99953056-chr2:100056612..100059511,2	K562	blood:
48	chr2:100015839..100018219-chr2:100019045..100021443,2	MCF-7	breast:
49	chr2:100068951..100071646-chr2:100081782..100083860,2	K562	blood:
50	chr2:100043076..100046018-chr2:100104970..100106653,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF5B-2	chr2:100021680-100022305	ENSG00000273306.1
2	lnc-TXNDC9-2	chr2:100022787-100022952	NONHSAT072755
3	lnc-TXNDC9-2	chr2:100024491-100024865	NONHSAT072755
4	lnc-TXNDC9-2	chr2:100022546-100022568	NONHSAT072755

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	EIF5B	hsa-miR-16-5p	chr2:100016385-100016407

Variant related genes	Relation type
EIF5B	TF binding region
REV1	TF binding region
ENSG00000273306	TF binding region
EIF5B	CpG island
REV1	CpG island
ENSG00000273306	CpG island
ENSG00000158417	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000100815	chromatin interactions
ENSG00000135945	chromatin interactions
ENSG00000273306	chromatin interactions

Extended variants
information (count: 4066 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4066 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539988662	chr2:99984617-99984618	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs559959724	chr2:99984734-99984735	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532273804	chr2:99984739-99984740	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566758590	chr2:99984751-99984752	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182035524	chr2:99984770-99984771	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149485395	chr2:99984795-99984796	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186988362	chr2:99984804-99984805	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191910117	chr2:99984808-99984809	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183298184	chr2:99984838-99984839	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553594103	chr2:99984858-99984859	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567115660	chr2:99984867-99984868	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538940969	chr2:99984877-99984878	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75885635	chr2:99984893-99984894	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143012269	chr2:99984914-99984915	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376378131	chr2:99984928-99984929	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3205291	chr2:99985017-99985018	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs199551427	chr2:99985029-99985030	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541177514	chr2:99985046-99985047	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554269172	chr2:99985056-99985057	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574151776	chr2:99985065-99985066	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374244254	chr2:99985066-99985067	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79949066	chr2:99985152-99985153	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559896473	chr2:99985241-99985242	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148197801	chr2:99985280-99985281	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545696478	chr2:99985317-99985318	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562775050	chr2:99985397-99985398	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531511952	chr2:99985457-99985458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553918850	chr2:99985489-99985490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550911759	chr2:99985490-99985491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567704112	chr2:99985491-99985492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530214657	chr2:99985507-99985508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565763308	chr2:99985511-99985512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567054397	chr2:99985534-99985535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534020163	chr2:99985591-99985592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200368757	chr2:99985608-99985609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552517019	chr2:99985661-99985662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555244105	chr2:99985670-99985671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188348934	chr2:99985713-99985714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375834698	chr2:99985723-99985724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574125507	chr2:99985745-99985746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533629182	chr2:99985771-99985772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147438767	chr2:99985866-99985867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs199806211	chr2:99985875-99985876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373807627	chr2:99985887-99985888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200710461	chr2:99985946-99985947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190344766	chr2:99985958-99985959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376791708	chr2:99985980-99985981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182609568	chr2:99985988-99985989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186942268	chr2:99986105-99986106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576277550	chr2:99986157-99986158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3618 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99956200-100004800	Weak transcription	Fetal Heart	heart
2	chr2:99957600-99989400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:99975400-100006400	Weak transcription	Stomach Mucosa	stomach
4	chr2:99976000-99989600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr2:99976200-100003800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr2:99976200-100004400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr2:99976400-99988600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:99976400-100003200	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr2:99976600-100002400	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr2:99976600-100004800	Strong transcription	Primary B cells from peripheral blood	blood
11	chr2:99976800-99989600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:99977000-99989200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr2:99977000-99991000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr2:99977000-99996800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr2:99977000-100001000	Strong transcription	Primary B cells from cord blood	blood
16	chr2:99977000-100001400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr2:99977000-100003200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr2:99977000-100003200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr2:99977000-100003600	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr2:99977000-100003800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:99977000-100003800	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr2:99977200-99989600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:99977200-99991000	Strong transcription	Dnd41	blood
24	chr2:99977200-99996200	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr2:99977600-99997000	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr2:99977600-100002200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr2:99977600-100003600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr2:99977800-99989800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr2:99977800-99989800	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr2:99977800-99989800	Strong transcription	Fetal Intestine Large	intestine
31	chr2:99977800-99996800	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr2:99978000-99989000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr2:99978200-99986600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:99978200-99990600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr2:99978200-99997200	Strong transcription	Placenta	Placenta
36	chr2:99978200-100011800	Weak transcription	Esophagus	oesophagus
37	chr2:99978400-99989600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr2:99978400-99989600	Weak transcription	Spleen	Spleen
39	chr2:99978600-99995600	Weak transcription	Small Intestine	intestine
40	chr2:99979200-99987400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr2:99979200-99990600	Strong transcription	Left Ventricle	heart
42	chr2:99979400-99985800	Strong transcription	HepG2	liver
43	chr2:99979400-99986000	Strong transcription	NHDF-Ad	bronchial
44	chr2:99979400-99986200	Strong transcription	K562	blood
45	chr2:99979400-99986600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr2:99979400-99987600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr2:99979400-99990600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
48	chr2:99979400-99991000	Strong transcription	Primary T cells from cord blood	blood
49	chr2:99979400-99999800	Strong transcription	Osteobl	bone
50	chr2:99979400-100001600	Strong transcription	Duodenum Mucosa	Duodenum

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