Variant report

Variant	nsv961868
Chromosome Location	chr2:112012898-112276878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3488)
CpG islands
(count:184)
Chromatin interactive
region (count:7)
LncRNA
region (count:79)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:3488 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:112221794-112221988	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
4	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
5	ARID3A	chr2:112077982-112078035	K562	blood:	n/a	n/a
6	ARID3A	chr2:112078700-112078866	K562	blood:	n/a	n/a
7	ARID3A	chr2:112191601-112191749	K562	blood:	n/a	n/a
8	ATF1	chr2:112252616-112252812	K562	blood:	n/a	n/a
9	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
10	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
11	ATF1	chr2:112174026-112174226	K562	blood:	n/a	n/a
12	ATF1	chr2:112251003-112251203	K562	blood:	n/a	n/a
13	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
14	ATF1	chr2:112191568-112191846	K562	blood:	n/a	n/a
15	ATF1	chr2:112174751-112174909	K562	blood:	n/a	n/a
16	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
17	ATF2	chr2:112183361-112183645	GM12878	blood:	n/a	n/a
18	ATF2	chr2:112236677-112236938	GM12878	blood:	n/a	n/a
19	ATF2	chr2:112183348-112183699	GM12878	blood:	n/a	n/a
20	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
21	BACH1	chr2:112251425-112251440	K562	blood:	n/a	n/a
22	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
23	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
24	BATF	chr2:112220893-112221142	GM12878	blood:	n/a	n/a
25	BATF	chr2:112072847-112073098	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
26	BATF	chr2:112264388-112264857	GM12878	blood:	n/a	n/a
27	BATF	chr2:112049811-112050042	GM12878	blood:	n/a	n/a
28	BATF	chr2:112183252-112183819	GM12878	blood:	n/a	n/a
29	BATF	chr2:112251368-112251781	GM12878	blood:	n/a	chr2:112251535-112251545 chr2:112251573-112251582
30	BATF	chr2:112211976-112212278	GM12878	blood:	n/a	n/a
31	BATF	chr2:112183233-112184090	GM12878	blood:	n/a	n/a
32	BATF	chr2:112188947-112189209	GM12878	blood:	n/a	n/a
33	BATF	chr2:112188889-112189327	GM12878	blood:	n/a	n/a
34	BATF	chr2:112248667-112249139	GM12878	blood:	n/a	n/a
35	BATF	chr2:112240605-112241034	GM12878	blood:	n/a	chr2:112240788-112240798
36	BATF	chr2:112029496-112029836	GM12878	blood:	n/a	chr2:112029663-112029674
37	BATF	chr2:112074557-112074916	GM12878	blood:	n/a	chr2:112074773-112074784
38	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
39	BATF	chr2:112264445-112264864	GM12878	blood:	n/a	n/a
40	BATF	chr2:112037291-112037501	GM12878	blood:	n/a	n/a
41	BATF	chr2:112195246-112195683	GM12878	blood:	n/a	chr2:112195574-112195583
42	BATF	chr2:112072875-112073150	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
43	BATF	chr2:112267135-112267389	GM12878	blood:	n/a	n/a
44	BATF	chr2:112251972-112252940	GM12878	blood:	n/a	chr2:112252692-112252702 chr2:112252678-112252688
45	BATF	chr2:112190573-112190841	GM12878	blood:	n/a	n/a
46	BATF	chr2:112193934-112194446	GM12878	blood:	n/a	chr2:112194264-112194272
47	BATF	chr2:112238764-112238956	GM12878	blood:	n/a	n/a
48	BATF	chr2:112221408-112221914	GM12878	blood:	n/a	n/a
49	BATF	chr2:112195786-112196106	GM12878	blood:	n/a	n/a
50	BATF	chr2:112186898-112187455	GM12878	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112252254-112252304	NH-A	brain:	n/a
2	chr2:112252254-112252304	NH-A	brain:	n/a
3	chr2:112124380-112124430	HEEpiC	esophagus:	n/a
4	chr2:112252254-112252304	HRCEpiC	kidney:	n/a
5	chr2:112124118-112124168	HEEpiC	esophagus:	n/a
6	chr2:112252254-112252304	RPTEC	kidney:	n/a
7	chr2:112124118-112124168	MCF-7	breast:	n/a
8	chr2:112124380-112124430	NH-A	brain:	n/a
9	chr2:112124380-112124430	HL-60	blood:	n/a
10	chr2:112124118-112124168	GM12878	blood:	n/a
11	chr2:112252254-112252304	K562	blood:	n/a
12	chr2:112252254-112252304	GM12892	blood:	n/a
13	chr2:112252254-112252304	GM06990	blood:	n/a
14	chr2:112124380-112124430	PFSK-1	brain:	n/a
15	chr2:112252254-112252304	NB4	blood:	n/a
16	chr2:112252254-112252304	MCF-7	breast:	n/a
17	chr2:112252254-112252304	Hepatocyte	liver:	n/a
18	chr2:112124380-112124430	CMK	blood:	n/a
19	chr2:112124380-112124430	NHBE	bronchial:	n/a
20	chr2:112252254-112252304	HMEC	breast:	n/a
21	chr2:112252254-112252304	AG10803	skin:	n/a
22	chr2:112252254-112252304	HepG2	liver:	n/a
23	chr2:112252254-112252304	HCT-116	colon:	n/a
24	chr2:112124118-112124168	GM12892	blood:	n/a
25	chr2:112124380-112124430	HRPEpiC	eye:	n/a
26	chr2:112252254-112252304	NHBE	bronchial:	n/a
27	chr2:112124380-112124430	IMR90	lung:	fetal
28	chr2:112252254-112252304	U87	brain:	n/a
29	chr2:112124118-112124168	HIPEpiC	eye:	n/a
30	chr2:112252254-112252304	NT2-D1	testis:	n/a
31	chr2:112124118-112124168	AG04450	lung:	fetal
32	chr2:112124118-112124168	Caco-2	colon:	n/a
33	chr2:112124380-112124430	GM06990	blood:	n/a
34	chr2:112124118-112124168	PFSK-1	brain:	n/a
35	chr2:112252254-112252304	PrEC	prostate:	n/a
36	chr2:112124118-112124168	MCF10A-Er-Src	breast:	n/a
37	chr2:112124118-112124168	AG09319	gingival:	n/a
38	chr2:112124380-112124430	HepG2	liver:	n/a
39	chr2:112252254-112252304	HRE	kidney:	n/a
40	chr2:112124380-112124430	ProgFib	skin:	n/a
41	chr2:112124118-112124168	SKMC	muscle:	n/a
42	chr2:112124380-112124430	PrEC	prostate:	n/a
43	chr2:112124118-112124168	HCT-116	colon:	n/a
44	chr2:112124380-112124430	PANC-1	pancreas:	n/a
45	chr2:112252254-112252304	HRPEpiC	eye:	n/a
46	chr2:112124118-112124168	HCF	heart:	n/a
47	chr2:112252254-112252304	HEK293	kidney:	embryo
48	chr2:112124380-112124430	MCF10A-Er-Src	breast:	n/a
49	chr2:112124380-112124430	GM12878	blood:	n/a
50	chr2:112252254-112252304	AoSMC	blood vessel:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:111877393..111879713-chr2:112235053..112237981,2	K562	blood:
2	chr2:112239413..112241217-chr2:112461159..112463413,2	MCF-7	breast:
3	chr2:111878764..111880387-chr2:112231090..112233888,2	MCF-7	breast:
4	chr2:111877705..111880008-chr2:112211679..112213711,2	MCF-7	breast:
5	chr2:111878316..111879893-chr2:112101721..112103928,2	MCF-7	breast:
6	chr2:112158086..112161064-chr8:43095226..43096729,2	MCF-7	breast:
7	chr2:111879395..111881005-chr2:112073345..112075122,2	MCF-7	breast:

(count:79 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
2	lnc-AC108463.1-3	chr2:112101638-112101701	NONHSAT073620
3	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073642
4	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
5	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
6	lnc-AC108463.1-3	chr2:112071889-112072139	ENSG00000172965.6
7	lnc-AC108463.1-3	chr2:112187020-112187197	ENSG00000172965.6
8	lnc-AC108463.1-3	chr2:112237484-112237657	NONHSAT073639
9	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
10	lnc-AC108463.1-3	chr2:112252462-112252625	ENSG00000172965.6
11	lnc-AC108463.1-3	chr2:112199085-112199198	ENSG00000172965.6
12	lnc-AC108463.1-3	chr2:112252462-112252611	ENSG00000172965.6
13	lnc-AC108463.1-3	chr2:112187048-112187197	NONHSAT073639
14	lnc-AC108463.1-3	chr2:112252462-112252597	ENSG00000172965.6
15	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
16	lnc-AC108463.1-3	chr2:112252462-112252602	ENSG00000172965.6
17	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
18	lnc-BCL2L11-3	chr2:112249107-112249838	NONHSAT073654
19	lnc-AC108463.1-3	chr2:112252462-112252540	NONHSAT073639
20	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073622
21	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
22	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
23	lnc-BCL2L11-5	chr2:112085950-112086566	NONHSAT073637
24	lnc-AC108463.1-3	chr2:112252462-112252677	ENSG00000172965.6
25	lnc-AC108463.1-3	chr2:112227364-112227564	ENSG00000172965.6
26	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
27	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
28	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
29	lnc-BCL2L11-8	chr2:112186899-112187197	NONHSAT073647
30	lnc-AC108463.1-3	chr2:112227180-112227564	ENSG00000172965.6
31	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073640
32	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
33	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
34	lnc-AC108463.1-3	chr2:112227215-112227564	ENSG00000172965.6
35	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
36	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
37	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
38	lnc-BCL2L11-5	chr2:112081840-112081972	l_1923_chr2:112081839-112086268_testes
39	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
40	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
41	lnc-BCL2L11-2	chr2:112043757-112044842	XLOC_001624
42	lnc-BCL2L11-6	chr2:112060981-112061323	NONHSAT073618
43	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10
44	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
45	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
46	lnc-AC108463.1-6	chr2:112053206-112053623	NONHSAT073635
47	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
48	lnc-BCL2L11-2	chr2:112037022-112037457	XLOC_001624
49	lnc-AC108463.1-3	chr2:112227364-112227376	NONHSAT073639
50	lnc-AC108463.1-3	chr2:112252462-112252631	ENSG00000172965.6

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4435	chr2:112078638-112078659	MIMAT0018951_1

No data

Variant related genes	Relation type
ENSG00000270190	TF binding region
ENSG00000240350	TF binding region
ENSG00000224959	TF binding region
RPS14P4	TF binding region
MIR4435-1HG	TF binding region
ENSG00000229118	TF binding region
ENSG00000223973	TF binding region
MIR4435-1	TF binding region
ENSG00000270190	CpG island
ENSG00000240350	CpG island
ENSG00000224959	CpG island
RPS14P4	CpG island
MIR4435-1HG	CpG island
ENSG00000229118	CpG island
ENSG00000223973	CpG island
MIR4435-1	CpG island
ENSG00000153094	chromatin interactions
ITSN2	miRNA target sites
KLHL24	miRNA target sites
ASCC3	miRNA target sites

Extended variants
information (count: 6807 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:6807 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200354019	chr2:112012898-112012899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569914204	chr2:112012907-112012908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369632144	chr2:112012989-112012990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs62160426	chr2:112013016-112013017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538803812	chr2:112013062-112013063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533906814	chr2:112013140-112013141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553559711	chr2:112013158-112013159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557443196	chr2:112013164-112013165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570978168	chr2:112013325-112013326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533567699	chr2:112013347-112013348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62160427	chr2:112013373-112013374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201848529	chr2:112013535-112013536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs55778104	chr2:112013606-112013607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149614465	chr2:112013625-112013626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1710483	chr2:112013632-112013633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201338570	chr2:112013747-112013748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576311611	chr2:112013763-112013764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545189732	chr2:112013765-112013766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565399986	chr2:112013838-112013839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527764053	chr2:112014437-112014438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556722926	chr2:112014526-112014527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111243750	chr2:112014693-112014694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541101516	chr2:112014736-112014737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139852707	chr2:112014835-112014836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530374906	chr2:112014869-112014870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550453980	chr2:112014989-112014990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569976530	chr2:112015305-112015306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532585665	chr2:112015306-112015307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190180444	chr2:112015330-112015331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571041872	chr2:112015358-112015359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370415628	chr2:112015362-112015363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374386509	chr2:112015371-112015372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533874709	chr2:112015395-112015396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553532827	chr2:112015446-112015447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567255794	chr2:112015448-112015449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs112439851	chr2:112015449-112015450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535830636	chr2:112015519-112015520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556512171	chr2:112015611-112015612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1706193	chr2:112015653-112015654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576377120	chr2:112015695-112015696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545251388	chr2:112015697-112015698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181029029	chr2:112015700-112015701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs938098	chr2:112015744-112015745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575973790	chr2:112015826-112015827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558769468	chr2:112015857-112015858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572613387	chr2:112015894-112015895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541513237	chr2:112015948-112015949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561179809	chr2:112016172-112016173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530408844	chr2:112016191-112016192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543793747	chr2:112016241-112016242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Breast cancer	22314128	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2477 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112005600-112015800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:112006200-112020200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:112008600-112048600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:112009200-112022600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:112010200-112015400	Weak transcription	HMEC	breast
6	chr2:112010600-112024600	Weak transcription	HSMMtube	muscle
7	chr2:112015400-112016600	Enhancers	HMEC	breast
8	chr2:112015800-112016000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr2:112016000-112016400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:112016000-112016400	Enhancers	NHEK	skin
11	chr2:112016200-112016600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr2:112016400-112016600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:112016600-112029000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr2:112019000-112019200	Enhancers	Ovary	ovary
15	chr2:112019200-112024200	Weak transcription	Ovary	ovary
16	chr2:112019200-112032600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:112020200-112020600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr2:112020200-112020600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:112020200-112020600	Enhancers	Fetal Stomach	stomach
20	chr2:112020200-112020600	Enhancers	NHLF	lung
21	chr2:112020400-112020600	Enhancers	Fetal Muscle Trunk	muscle
22	chr2:112020400-112020600	Enhancers	Lung	lung
23	chr2:112020600-112021800	Weak transcription	NHLF	lung
24	chr2:112020600-112024200	Weak transcription	Lung	lung
25	chr2:112020600-112024600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:112020600-112048000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr2:112022000-112022200	Enhancers	NHLF	lung
28	chr2:112022400-112022600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr2:112022600-112022800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:112022600-112023000	Enhancers	Fetal Muscle Trunk	muscle
31	chr2:112022600-112023400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:112022800-112031200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr2:112023400-112046400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:112024000-112024400	Enhancers	Right Ventricle	heart
35	chr2:112024200-112025000	Enhancers	Lung	lung
36	chr2:112024200-112025200	Enhancers	Fetal Lung	lung
37	chr2:112024200-112025200	Enhancers	Ovary	ovary
38	chr2:112024200-112025200	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr2:112024200-112025200	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr2:112024200-112025400	Enhancers	Pancreas	Pancrea
41	chr2:112024200-112025600	Enhancers	Liver	Liver
42	chr2:112024200-112025600	Enhancers	Fetal Heart	heart
43	chr2:112024400-112025400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr2:112024600-112024800	Enhancers	HSMMtube	muscle
45	chr2:112024600-112025000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr2:112024600-112025000	Enhancers	Gastric	stomach
47	chr2:112024600-112025000	Enhancers	Stomach Mucosa	stomach
48	chr2:112024800-112025000	Enhancers	Fetal Muscle Trunk	muscle
49	chr2:112024800-112026000	Weak transcription	HSMMtube	muscle
50	chr2:112025000-112034400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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