Variant report

Variant	nsv491906
Chromosome Location	chr2:110783236-110964737
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2500)
CpG islands
(count:1835)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 3)
miRNA target
sites (count:0)

(count:2500 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:110955152-110955153	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:110962555-110963074	K562	blood:	n/a	n/a
3	ARID3A	chr2:110859522-110859666	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:110871867-110871999	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:110903443-110904181	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:110914785-110915086	K562	blood:	n/a	n/a
7	ARID3A	chr2:110907344-110907902	K562	blood:	n/a	n/a
8	ARID3A	chr2:110962422-110963251	HepG2	liver:	n/a	n/a
9	ATF1	chr2:110962363-110962896	K562	blood:	n/a	n/a
10	ATF1	chr2:110929088-110929321	K562	blood:	n/a	n/a
11	ATF3	chr2:110962327-110962949	HepG2	liver:	n/a	chr2:110962598-110962618 chr2:110962608-110962619 chr2:110962606-110962621 chr2:110962609-110962629
12	ATF3	chr2:110962420-110962802	K562	blood:	n/a	chr2:110962598-110962618 chr2:110962608-110962619 chr2:110962606-110962621 chr2:110962609-110962629
13	ATF3	chr2:110962400-110962806	K562	blood:	n/a	chr2:110962598-110962618 chr2:110962608-110962619 chr2:110962606-110962621 chr2:110962609-110962629
14	ATF3	chr2:110962365-110962828	HepG2	liver:	n/a	chr2:110962598-110962618 chr2:110962608-110962619 chr2:110962606-110962621 chr2:110962609-110962629
15	ATF3	chr2:110863282-110864651	A549	lung:	n/a	n/a
16	ATF3	chr2:110858605-110859874	A549	lung:	n/a	n/a
17	ATF3	chr2:110863340-110864704	A549	lung:	n/a	n/a
18	ATF3	chr2:110962474-110962794	H1-hESC	embryonic stem cell:	n/a	chr2:110962598-110962618 chr2:110962608-110962619 chr2:110962606-110962621 chr2:110962609-110962629
19	ATF3	chr2:110962515-110962730	GM12878	blood:	n/a	chr2:110962598-110962618 chr2:110962608-110962619 chr2:110962606-110962621 chr2:110962609-110962629
20	ATF3	chr2:110858656-110859426	A549	lung:	n/a	n/a
21	ATF3	chr2:110962346-110962841	GM12878	blood:	n/a	chr2:110962598-110962618 chr2:110962608-110962619 chr2:110962606-110962621 chr2:110962609-110962629
22	ATF3	chr2:110962470-110962819	H1-hESC	embryonic stem cell:	n/a	chr2:110962598-110962618 chr2:110962608-110962619 chr2:110962606-110962621 chr2:110962609-110962629
23	BACH1	chr2:110962493-110963081	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr2:110962546-110962912	K562	blood:	n/a	n/a
25	BACH1	chr2:110890558-110890583	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr2:110937562-110937683	K562	blood:	n/a	n/a
27	BATF	chr2:110859621-110859879	GM12878	blood:	n/a	n/a
28	BATF	chr2:110901676-110901865	GM12878	blood:	n/a	n/a
29	BATF	chr2:110901606-110901868	GM12878	blood:	n/a	n/a
30	BATF	chr2:110829579-110829796	GM12878	blood:	n/a	n/a
31	BCL3	chr2:110858636-110860316	A549	lung:	n/a	chr2:110859557-110859566 chr2:110859688-110859697 chr2:110859202-110859211
32	BCL3	chr2:110861855-110862496	A549	lung:	n/a	n/a
33	BCL3	chr2:110871502-110872812	A549	lung:	n/a	n/a
34	BCL3	chr2:110863085-110865362	A549	lung:	n/a	chr2:110863098-110863107
35	BCL3	chr2:110871334-110872613	A549	lung:	n/a	n/a
36	BCL3	chr2:110863087-110865215	A549	lung:	n/a	chr2:110863098-110863107
37	BCL3	chr2:110873303-110874494	A549	lung:	n/a	chr2:110873394-110873407 chr2:110873542-110873555
38	BCL3	chr2:110962153-110963143	A549	lung:	n/a	n/a
39	BCL3	chr2:110858630-110860176	A549	lung:	n/a	chr2:110859557-110859566 chr2:110859688-110859697 chr2:110859202-110859211
40	BCL3	chr2:110861718-110862627	A549	lung:	n/a	n/a
41	BHLHE40	chr2:110914808-110915073	K562	blood:	n/a	n/a
42	BHLHE40	chr2:110873755-110873774	K562	blood:	n/a	n/a
43	BHLHE40	chr2:110874089-110874236	K562	blood:	n/a	n/a
44	BHLHE40	chr2:110858774-110859754	A549	lung:	n/a	n/a
45	BHLHE40	chr2:110863718-110864150	A549	lung:	n/a	n/a
46	BHLHE40	chr2:110829505-110829790	HepG2	liver:	n/a	n/a
47	BHLHE40	chr2:110962217-110963241	K562	blood:	n/a	chr2:110962412-110962428 chr2:110962420-110962436
48	BHLHE40	chr2:110863741-110864010	HepG2	liver:	n/a	n/a
49	BHLHE40	chr2:110871580-110872256	HepG2	liver:	n/a	n/a
50	BHLHE40	chr2:110858908-110858916	K562	blood:	n/a	n/a

(count:1835 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:110833739-110833789	Jurkat	blood:	n/a
2	chr2:110863886-110863936	AG04450	lung:	fetal
3	chr2:110875551-110875601	SK-N-SH_RA	brain:	n/a
4	chr2:110863886-110863936	HCM	heart:	n/a
5	chr2:110959266-110959316	SK-N-SH_RA	brain:	n/a
6	chr2:110833739-110833789	Jurkat	blood:	n/a
7	chr2:110863886-110863936	AG04450	lung:	fetal
8	chr2:110875551-110875601	SK-N-SH_RA	brain:	n/a
9	chr2:110863886-110863936	HCM	heart:	n/a
10	chr2:110959266-110959316	SK-N-SH_RA	brain:	n/a
11	chr2:110925418-110925468	HEEpiC	esophagus:	n/a
12	chr2:110872620-110872670	Hepatocyte	liver:	n/a
13	chr2:110872620-110872670	SAEC	small airway:	n/a
14	chr2:110872655-110872705	HRPEpiC	eye:	n/a
15	chr2:110872655-110872705	NB4	blood:	n/a
16	chr2:110963774-110963824	PFSK-1	brain:	n/a
17	chr2:110863886-110863936	HEK293	kidney:	embryo
18	chr2:110962741-110962791	HRE	kidney:	n/a
19	chr2:110962626-110962676	HCM	heart:	n/a
20	chr2:110873031-110873081	SK-N-SH	brain:	n/a
21	chr2:110873396-110873446	HAEpiC	amniotic membrane:	n/a
22	chr2:110872655-110872705	HCM	heart:	n/a
23	chr2:110962626-110962676	AG04449	skin:	fetal
24	chr2:110859091-110859141	HMEC	breast:	n/a
25	chr2:110962429-110962479	T-47D	breast:	n/a
26	chr2:110863886-110863936	NB4	blood:	n/a
27	chr2:110963774-110963824	IMR90	lung:	fetal
28	chr2:110872620-110872670	T-47D	breast:	n/a
29	chr2:110962741-110962791	AoSMC	blood vessel:	n/a
30	chr2:110925418-110925468	A549	lung:	n/a
31	chr2:110962429-110962479	AG09309	skin:	n/a
32	chr2:110874360-110874410	HepG2	liver:	n/a
33	chr2:110875551-110875601	Hepatocyte	liver:	n/a
34	chr2:110959266-110959316	IMR90	lung:	fetal
35	chr2:110876674-110876724	SK-N-SH	brain:	n/a
36	chr2:110872655-110872705	HepG2	liver:	n/a
37	chr2:110962429-110962479	BJ	skin:	n/a
38	chr2:110875551-110875601	BE2_C	brain:	n/a
39	chr2:110959266-110959316	HL-60	blood:	n/a
40	chr2:110962741-110962791	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:110829661-110829711	T-47D	breast:	n/a
42	chr2:110873031-110873081	BJ	skin:	n/a
43	chr2:110833739-110833789	HNPCEpiC	eye:	n/a
44	chr2:110827645-110827695	CMK	blood:	n/a
45	chr2:110827645-110827695	NHBE	bronchial:	n/a
46	chr2:110874344-110874394	HCT-116	colon:	n/a
47	chr2:110962594-110962644	GM19239	blood:	n/a
48	chr2:110959266-110959316	HRPEpiC	eye:	n/a
49	chr2:110962687-110962737	HL-60	blood:	n/a
50	chr2:110871644-110871694	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:110876469..110878609-chr2:110902842..110905689,2	MCF-7	breast:
2	chr2:110855709..110858865-chr2:110862093..110865475,3	MCF-7	breast:
3	chr2:110922454..110925211-chr2:110926455..110929229,2	MCF-7	breast:
4	chr2:110859680..110861955-chr2:110862122..110864189,2	MCF-7	breast:
5	chr2:110935898..110937753-chr2:110970388..110973084,2	MCF-7	breast:
6	chr2:110871483..110872172-chr2:110914465..110915379,4	MCF-7	breast:
7	chr2:110873870..110875390-chr2:110887506..110889173,2	MCF-7	breast:
8	chr2:110857583..110859746-chr2:110914068..110916196,2	MCF-7	breast:
9	chr2:110922454..110925211-chr2:110926455..110929229,2	MCF-7	breast:
10	chr2:110857860..110860963-chr2:110860996..110866153,6	MCF-7	breast:
11	chr2:110857583..110859746-chr2:110914068..110916196,2	MCF-7	breast:
12	chr2:110863205..110865655-chr2:110910127..110912316,2	MCF-7	breast:
13	chr2:110855709..110858865-chr2:110862093..110865475,3	MCF-7	breast:
14	chr2:110859680..110861955-chr2:110862122..110864189,2	MCF-7	breast:
15	chr2:110876653..110878314-chr2:110879309..110881722,2	K562	blood:
16	chr2:110869904..110873579-chr2:110876521..110879513,4	MCF-7	breast:
17	chr2:110960357..110966320-chr2:110966517..110974106,19	K562	blood:
18	chr2:110873716..110875965-chr2:110877265..110879197,2	MCF-7	breast:
19	chr16:74700318..74701202-chr2:110873506..110874030,2	HCT-116	colon:
20	chr2:110871483..110872172-chr2:110914465..110915379,4	MCF-7	breast:
21	chr2:110881943..110884295-chr2:110888302..110890520,2	MCF-7	breast:
22	chr2:110862148..110865580-chr2:110871176..110875147,4	MCF-7	breast:
23	chr2:110880610..110883092-chr2:110962084..110964585,2	MCF-7	breast:
24	chr2:110881943..110884295-chr2:110888302..110890520,2	MCF-7	breast:
25	chr2:110858332..110860187-chr2:110869577..110871663,2	MCF-7	breast:
26	chr2:110870665..110876483-chr2:110879456..110884042,6	MCF-7	breast:
27	chr2:110882795..110884830-chr2:110896939..110900233,3	MCF-7	breast:
28	chr2:110926060..110928547-chr2:110928935..110931419,2	MCF-7	breast:
29	chr2:110855266..110858639-chr2:110858645..110861501,3	MCF-7	breast:
30	chr2:110857860..110860963-chr2:110860996..110866153,6	MCF-7	breast:
31	chr2:110859324..110861924-chr2:110871252..110875012,4	MCF-7	breast:
32	chr2:110876469..110878609-chr2:110902842..110905689,2	MCF-7	breast:
33	chr2:110873456..110876325-chr2:110905236..110907102,2	MCF-7	breast:
34	chr2:110925820..110928862-chr2:110966345..110968999,3	K562	blood:
35	chr2:110876653..110878314-chr2:110879309..110881722,2	K562	blood:
36	chr2:110873447..110874172-chr3:14443659..14444526,2	HCT-116	colon:
37	chr2:110863346..110864881-chr2:110906381..110908081,2	MCF-7	breast:
38	chr2:110855266..110858639-chr2:110858645..110861501,3	MCF-7	breast:
39	chr2:110904402..110906403-chr2:110923344..110925858,2	MCF-7	breast:
40	chr2:110875117..110876760-chr2:110880549..110882080,2	MCF-7	breast:
41	chr2:110875117..110876760-chr2:110880549..110882080,2	MCF-7	breast:
42	chr2:110878722..110881260-chr2:110966564..110969008,2	MCF-7	breast:
43	chr2:110859259..110860018-chr7:26239929..26240470,2	Hela-S3	cervix:
44	chr2:110863205..110865655-chr2:110910127..110912316,2	MCF-7	breast:
45	chr2:110872387..110874922-chr2:110875122..110878209,5	MCF-7	breast:
46	chr2:110926060..110928547-chr2:110928935..110931419,2	MCF-7	breast:
47	chr2:110863346..110864881-chr2:110906381..110908081,2	MCF-7	breast:
48	chr2:110858332..110860187-chr2:110869577..110871663,2	MCF-7	breast:
49	chr2:110904402..110906403-chr2:110923344..110925858,2	MCF-7	breast:
50	chr2:110864486..110867223-chr2:110872239..110874303,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4267	chr2:110827594-110827609	MIMAT0016893
hsa-miR-4436b-5p	chr2:110844067-110844088	MIMAT0019940
hsa-miR-4436b-3p	chr2:110844020-110844041	MIMAT0019941

No data

Variant related genes	Relation type
MIR4436B1	TF binding region
MALL	TF binding region
NPHP1	TF binding region
MIR4267	TF binding region
ENSG00000212091	TF binding region
ENSG00000233370	TF binding region
MIR4436B1	CpG island
MALL	CpG island
NPHP1	CpG island
MIR4267	CpG island
ENSG00000212091	CpG island
ENSG00000233370	CpG island
ENSG00000131389	chromatin interactions
ENSG00000175701	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000144061	chromatin interactions
ENSG00000144063	chromatin interactions
ENSG00000212091	chromatin interactions
ENSG00000168411	chromatin interactions

Extended variants
information (count: 4110 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4110 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565180888	chr2:110783876-110783877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1972810	chr2:110783884-110783885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577318078	chr2:110783915-110783916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539970087	chr2:110784109-110784110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141473006	chr2:110784119-110784120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559701968	chr2:110784128-110784129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528898543	chr2:110784139-110784140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371847735	chr2:110784160-110784161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376854971	chr2:110784183-110784184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368696583	chr2:110784206-110784207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546688534	chr2:110784207-110784208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs406115	chr2:110784224-110784225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549233318	chr2:110784305-110784306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562644349	chr2:110784309-110784310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113660456	chr2:110784377-110784378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370164758	chr2:110784380-110784381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373168391	chr2:110784523-110784524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571510723	chr2:110784545-110784546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534261562	chr2:110785548-110785549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547945701	chr2:110785566-110785567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146681801	chr2:110785634-110785635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536271763	chr2:110785674-110785675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556768588	chr2:110785676-110785677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576655433	chr2:110785690-110785691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539367379	chr2:110785694-110785695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558705337	chr2:110785711-110785712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572339410	chr2:110785721-110785722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539908978	chr2:110785750-110785751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559839391	chr2:110785777-110785778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201533161	chr2:110785796-110785797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143984605	chr2:110785805-110785806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542265895	chr2:110785810-110785811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562543760	chr2:110785827-110785828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531501378	chr2:110785839-110785840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545347773	chr2:110785870-110785871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565058085	chr2:110785872-110785873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527497641	chr2:110785923-110785924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547882918	chr2:110785973-110785974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567656530	chr2:110786003-110786004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs336776	chr2:110786008-110786009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549905422	chr2:110786010-110786011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs62160479	chr2:110786078-110786079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570060545	chr2:110786104-110786105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538931735	chr2:110786107-110786108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558842186	chr2:110786118-110786119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565909541	chr2:110786132-110786133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534894184	chr2:110786134-110786135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553413284	chr2:110786152-110786153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573642652	chr2:110786252-110786253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542752375	chr2:110786254-110786255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Breast cancer	22522925	CNVD

Chromatin state (count:2030 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:110783800-110784000	Enhancers	Fetal Intestine Large	intestine
2	chr2:110783800-110786000	Weak transcription	Pancreas	Pancrea
3	chr2:110785800-110792600	Weak transcription	Fetal Intestine Large	intestine
4	chr2:110786000-110786400	Enhancers	Fetal Muscle Trunk	muscle
5	chr2:110792600-110793000	Enhancers	Pancreas	Pancrea
6	chr2:110805800-110806600	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr2:110805800-110806600	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr2:110806000-110806600	Enhancers	Pancreas	Pancrea
9	chr2:110806000-110807600	Enhancers	Fetal Muscle Trunk	muscle
10	chr2:110806000-110807600	Enhancers	HepG2	liver
11	chr2:110806200-110806600	Enhancers	HSMMtube	muscle
12	chr2:110806400-110807000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr2:110810400-110811000	Enhancers	HUVEC	blood vessel
14	chr2:110810600-110810800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr2:110810600-110810800	Enhancers	Fetal Heart	heart
16	chr2:110810600-110810800	Enhancers	A549	lung
17	chr2:110810600-110810800	Enhancers	NHEK	skin
18	chr2:110810600-110811000	Enhancers	Fetal Lung	lung
19	chr2:110810600-110811000	Enhancers	Dnd41	blood
20	chr2:110811000-110812000	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr2:110811000-110812000	Weak transcription	Fetal Heart	heart
22	chr2:110811000-110812000	Weak transcription	Fetal Lung	lung
23	chr2:110811000-110812000	Weak transcription	A549	lung
24	chr2:110811000-110812000	Weak transcription	HUVEC	blood vessel
25	chr2:110811000-110812000	Weak transcription	NHEK	skin
26	chr2:110812000-110812200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr2:110812000-110812200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr2:110812000-110812200	Enhancers	Fetal Brain Male	brain
29	chr2:110812000-110812200	Enhancers	Fetal Lung	lung
30	chr2:110812000-110812400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr2:110812000-110812400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr2:110812000-110812400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:110812000-110812400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:110812000-110812400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:110812000-110812400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:110812000-110812400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:110812000-110812400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr2:110812000-110812400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:110812000-110812400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr2:110812000-110812400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr2:110812000-110812400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr2:110812000-110812400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr2:110812000-110812400	Enhancers	Brain Hippocampus Middle	brain
44	chr2:110812000-110812400	Enhancers	Fetal Heart	heart
45	chr2:110812000-110812400	Enhancers	Fetal Intestine Large	intestine
46	chr2:110812000-110812400	Enhancers	Fetal Intestine Small	intestine
47	chr2:110812000-110812400	Enhancers	Fetal Stomach	stomach
48	chr2:110812000-110812400	Enhancers	Left Ventricle	heart
49	chr2:110812000-110812400	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr2:110812000-110812400	Enhancers	A549	lung

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