Variant report

Variant	nsv456363
Chromosome Location	chr2:37109281-37235324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1537)
CpG islands
(count:671)
Chromatin interactive
region (count:106)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1537 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37118711-37118749	K562	blood:	n/a	n/a
2	ARID3A	chr2:37116978-37117164	K562	blood:	n/a	n/a
3	ARID3A	chr2:37194875-37195389	K562	blood:	n/a	n/a
4	ARID3A	chr2:37215196-37215467	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:37199752-37199774	K562	blood:	n/a	n/a
6	ARID3A	chr2:37194557-37195345	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:37193591-37194171	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:37158400-37158403	K562	blood:	n/a	n/a
9	ARID3A	chr2:37200534-37200833	K562	blood:	n/a	n/a
10	ARID3A	chr2:37192499-37192734	K562	blood:	n/a	n/a
11	ATF1	chr2:37193621-37194184	K562	blood:	n/a	n/a
12	ATF1	chr2:37200535-37200833	K562	blood:	n/a	n/a
13	ATF1	chr2:37169144-37169386	K562	blood:	n/a	n/a
14	ATF2	chr2:37193513-37194453	GM12878	blood:	n/a	n/a
15	ATF2	chr2:37190162-37190643	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr2:37193657-37194244	GM12878	blood:	n/a	n/a
17	ATF2	chr2:37232207-37232802	GM12878	blood:	n/a	n/a
18	ATF3	chr2:37193339-37193621	HepG2	liver:	n/a	n/a
19	ATF3	chr2:37193618-37193918	K562	blood:	n/a	chr2:37193733-37193742
20	BACH1	chr2:37146461-37146584	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr2:37193057-37193778	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr2:37193979-37194421	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr2:37117338-37117348	K562	blood:	n/a	n/a
24	BATF	chr2:37153306-37153657	GM12878	blood:	n/a	chr2:37153454-37153465
25	BATF	chr2:37186112-37186421	GM12878	blood:	n/a	n/a
26	BATF	chr2:37186153-37186547	GM12878	blood:	n/a	n/a
27	BATF	chr2:37153366-37153641	GM12878	blood:	n/a	chr2:37153454-37153465
28	BCL3	chr2:37193785-37194419	A549	lung:	n/a	chr2:37194170-37194183
29	BCLAF1	chr2:37193449-37194144	K562	blood:	n/a	chr2:37193645-37193654 chr2:37193640-37193653 chr2:37193633-37193646 chr2:37193686-37193695
30	BCLAF1	chr2:37193440-37194364	GM12878	blood:	n/a	chr2:37193645-37193654 chr2:37194170-37194183 chr2:37193640-37193653 chr2:37193633-37193646 chr2:37193686-37193695
31	BCLAF1	chr2:37232209-37232835	GM12878	blood:	n/a	n/a
32	BCLAF1	chr2:37193508-37194370	K562	blood:	n/a	chr2:37193645-37193654 chr2:37194170-37194183 chr2:37193640-37193653 chr2:37193633-37193646 chr2:37193686-37193695
33	BHLHE40	chr2:37195124-37195308	K562	blood:	n/a	n/a
34	BHLHE40	chr2:37200552-37200885	K562	blood:	n/a	n/a
35	BHLHE40	chr2:37192822-37193156	K562	blood:	n/a	n/a
36	BHLHE40	chr2:37193589-37194382	HepG2	liver:	n/a	chr2:37193635-37193651
37	BHLHE40	chr2:37232378-37232794	GM12878	blood:	n/a	n/a
38	BHLHE40	chr2:37192887-37193122	GM12878	blood:	n/a	n/a
39	BHLHE40	chr2:37194689-37195186	HepG2	liver:	n/a	n/a
40	BHLHE40	chr2:37193393-37194433	GM12878	blood:	n/a	chr2:37193635-37193651
41	BHLHE40	chr2:37193439-37194400	K562	blood:	n/a	chr2:37193635-37193651
42	BRCA1	chr2:37193601-37193856	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr2:37184112-37184121	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr2:37164518-37164872	K562	blood:	n/a	n/a
45	CBX3	chr2:37191711-37192242	K562	blood:	n/a	n/a
46	CBX3	chr2:37194631-37196191	K562	blood:	n/a	n/a
47	CBX3	chr2:37193501-37194576	K562	blood:	n/a	n/a
48	CCNT2	chr2:37118857-37119094	K562	blood:	n/a	n/a
49	CCNT2	chr2:37193342-37194335	K562	blood:	n/a	n/a
50	CCNT2	chr2:37200436-37200844	K562	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37193481-37193531	BE2_C	brain:	n/a
2	chr2:37194356-37194406	HRCEpiC	kidney:	n/a
3	chr2:37193060-37193110	NH-A	brain:	n/a
4	chr2:37193690-37193740	HCPEpiC	choroid plexus:	n/a
5	chr2:37194071-37194121	MCF-7	breast:	n/a
6	chr2:37179041-37179091	HCF	heart:	n/a
7	chr2:37193060-37193110	HCPEpiC	choroid plexus:	n/a
8	chr2:37193481-37193531	SK-N-MC	brain:	n/a
9	chr2:37190024-37190074	SKMC	muscle:	n/a
10	chr2:37193358-37193408	HIPEpiC	eye:	n/a
11	chr2:37190024-37190074	MCF-7	breast:	n/a
12	chr2:37193481-37193531	PrEC	prostate:	n/a
13	chr2:37193690-37193740	NHBE	bronchial:	n/a
14	chr2:37193481-37193531	HCF	heart:	n/a
15	chr2:37145953-37146003	H1-hESC	embryonic stem cell:	embryo
16	chr2:37194155-37194205	LNCaP	prostate:	n/a
17	chr2:37193358-37193408	ProgFib	skin:	n/a
18	chr2:37145953-37146003	HCPEpiC	choroid plexus:	n/a
19	chr2:37194356-37194406	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:37192797-37192847	GM12891	blood:	n/a
21	chr2:37193060-37193110	CMK	blood:	n/a
22	chr2:37145953-37146003	IMR90	lung:	fetal
23	chr2:37193060-37193110	HEK293	kidney:	embryo
24	chr2:37194356-37194406	NH-A	brain:	n/a
25	chr2:37190024-37190074	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:37192797-37192847	GM12892	blood:	n/a
27	chr2:37179041-37179091	AG09319	gingival:	n/a
28	chr2:37194155-37194205	Caco-2	colon:	n/a
29	chr2:37193690-37193740	Hepatocyte	liver:	n/a
30	chr2:37193060-37193110	AoSMC	blood vessel:	n/a
31	chr2:37190024-37190074	IMR90	lung:	fetal
32	chr2:37179041-37179091	GM12891	blood:	n/a
33	chr2:37190024-37190074	GM19239	blood:	n/a
34	chr2:37193358-37193408	HepG2	liver:	n/a
35	chr2:37194071-37194121	GM12891	blood:	n/a
36	chr2:37194071-37194121	BE2_C	brain:	n/a
37	chr2:37192797-37192847	PrEC	prostate:	n/a
38	chr2:37194155-37194205	HUVEC	blood vessel:	n/a
39	chr2:37194155-37194205	HRPEpiC	eye:	n/a
40	chr2:37192797-37192847	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:37194356-37194406	HCF	heart:	n/a
42	chr2:37145953-37146003	HCF	heart:	n/a
43	chr2:37194155-37194205	HAEpiC	amniotic membrane:	n/a
44	chr2:37194071-37194121	IMR90	lung:	fetal
45	chr2:37194155-37194205	MCF10A-Er-Src	breast:	n/a
46	chr2:37190024-37190074	T-47D	breast:	n/a
47	chr2:37179041-37179091	NB4	blood:	n/a
48	chr2:37145953-37146003	U87	brain:	n/a
49	chr2:37193690-37193740	SK-N-SH_RA	brain:	n/a
50	chr2:37193358-37193408	AG09319	gingival:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:37194247..37196675-chr2:37203224..37205629,3	K562	blood:
2	chr18:77438103..77438604-chr2:37191695..37192195,2	Hela-S3	cervix:
3	chr2:37190637..37196620-chr2:37200622..37205629,7	K562	blood:
4	chr2:37193759..37194604-chr6:30294819..30295525,2	Hela-S3	cervix:
5	chr2:37102067..37105059-chr2:37110141..37111787,2	K562	blood:
6	chr2:37204760..37206841-chr2:37210799..37212478,2	K562	blood:
7	chr2:37138982..37142311-chr2:37143440..37145643,3	K562	blood:
8	chr2:37135486..37138382-chr2:37141654..37143991,3	K562	blood:
9	chr2:37170595..37172882-chr2:37190992..37193264,2	K562	blood:
10	chr2:37193543..37195604-chr2:37419400..37421969,2	K562	blood:
11	chr2:37172866..37175406-chr2:37175824..37179648,3	K562	blood:
12	chr2:37181946..37184586-chr2:37193992..37195533,2	K562	blood:
13	chr2:37111890..37113424-chr2:37118017..37119870,2	K562	blood:
14	chr2:37186145..37190956-chr2:37191183..37194668,5	K562	blood:
15	chr2:37114816..37116390-chr2:37191550..37193356,2	MCF-7	breast:
16	chr2:37193659..37195188-chr2:37231958..37233613,2	MCF-7	breast:
17	chr2:37114816..37116390-chr2:37191550..37193356,2	MCF-7	breast:
18	chr2:37087369..37088984-chr2:37161141..37163056,2	K562	blood:
19	chr2:37184337..37185980-chr2:37189673..37191731,2	MCF-7	breast:
20	chr2:37181739..37184063-chr2:37191720..37193711,2	K562	blood:
21	chr2:37176203..37178213-chr2:37192124..37194925,2	MCF-7	breast:
22	chr2:37135486..37138382-chr2:37141654..37143991,3	K562	blood:
23	chr2:37112252..37114608-chr2:37115570..37119781,3	MCF-7	breast:
24	chr2:37179298..37181482-chr2:37191385..37194374,2	K562	blood:
25	chr2:37218150..37220358-chr2:37221248..37224159,2	K562	blood:
26	chr2:37138982..37142311-chr2:37143440..37145643,3	K562	blood:
27	chr2:37178708..37180301-chr2:37186224..37188629,2	MCF-7	breast:
28	chr2:37182696..37184565-chr2:37185219..37186794,2	K562	blood:
29	chr2:37218150..37220358-chr2:37221248..37224159,2	K562	blood:
30	chr2:37116050..37118229-chr2:37119836..37122372,2	K562	blood:
31	chr2:37183661..37187179-chr2:37192061..37194972,3	MCF-7	breast:
32	chr2:37194014..37195839-chr2:37202260..37204776,2	MCF-7	breast:
33	chr2:37108584..37111533-chr2:37117079..37119450,3	K562	blood:
34	chr2:37194014..37195839-chr2:37202260..37204776,2	MCF-7	breast:
35	chr2:37183461..37185242-chr2:37187560..37189178,2	MCF-7	breast:
36	chr2:37110942..37112649-chr2:37193437..37195294,2	MCF-7	breast:
37	chr2:37194557..37197275-chr2:37197696..37199511,3	K562	blood:
38	chr2:37108584..37111603-chr2:37116874..37118803,4	K562	blood:
39	chr2:37219829..37222181-chr2:37235362..37237238,2	K562	blood:
40	chr2:37194557..37197275-chr2:37197696..37199511,3	K562	blood:
41	chr2:37119952..37122407-chr2:37130124..37132171,2	MCF-7	breast:
42	chr2:37046287..37047005-chr2:37145243..37146052,3	MCF-7	breast:
43	chr2:37007113..37008064-chr2:37231570..37232413,4	MCF-7	breast:
44	chr2:37129384..37131644-chr2:37135815..37138378,2	MCF-7	breast:
45	chr2:37194252..37196693-chr2:37198973..37200836,2	MCF-7	breast:
46	chr2:37108584..37111603-chr2:37116874..37118803,4	K562	blood:
47	chr2:37214250..37217213-chr2:37218281..37220281,2	K562	blood:
48	chr2:37119952..37122407-chr2:37130124..37132171,2	MCF-7	breast:
49	chr2:37177111..37181482-chr2:37191828..37195720,6	K562	blood:
50	chr2:37212231..37214849-chr2:37242255..37244987,2	K562	blood:

No data

Variant related genes	Relation type
HEATR5B	TF binding region
STRN	TF binding region
RNU6-846P	TF binding region
HEATR5B	CpG island
STRN	CpG island
RNU6-846P	CpG island
ENSG00000133466	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000231074	chromatin interactions
ENSG00000233159	chromatin interactions
ENSG00000252518	chromatin interactions
ENSG00000175505	chromatin interactions
ENSG00000066654	chromatin interactions
ENSG00000152133	chromatin interactions
ENSG00000204599	chromatin interactions
ENSG00000115808	chromatin interactions
ENSG00000008869	chromatin interactions

Extended variants
information (count: 5614 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:5614 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1019311	chr2:37109281-37109282	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562917267	chr2:37109330-37109331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574876628	chr2:37109343-37109344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs36064902	chr2:37109349-37109350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184934566	chr2:37109382-37109383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546169210	chr2:37109391-37109392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538071338	chr2:37109400-37109401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556153869	chr2:37109422-37109423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs57884362	chr2:37109424-37109425	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs541417977	chr2:37109426-37109427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115837881	chr2:37109450-37109451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528784331	chr2:37109465-37109466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79300848	chr2:37109528-37109529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186636862	chr2:37109532-37109533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377579877	chr2:37109585-37109586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116490242	chr2:37109600-37109601	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370551589	chr2:37109647-37109648	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562204142	chr2:37109672-37109673	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371738739	chr2:37109678-37109679	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556371230	chr2:37109701-37109702	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115833449	chr2:37109714-37109715	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547732053	chr2:37109727-37109728	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2717519	chr2:37109744-37109745	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs539481085	chr2:37109821-37109822	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141271837	chr2:37109839-37109840	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569834468	chr2:37109846-37109847	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537605929	chr2:37109868-37109869	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553344115	chr2:37109869-37109870	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574596424	chr2:37110028-37110029	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191092516	chr2:37110035-37110036	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78370830	chr2:37110071-37110072	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376884293	chr2:37110072-37110073	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370194498	chr2:37110089-37110090	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145783875	chr2:37110102-37110103	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551121592	chr2:37110104-37110105	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150760011	chr2:37110105-37110106	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369097089	chr2:37110119-37110120	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183642619	chr2:37110213-37110214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545838142	chr2:37110230-37110231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564135957	chr2:37110253-37110254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372942595	chr2:37110264-37110265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571093603	chr2:37110266-37110267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576096799	chr2:37110310-37110311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543606832	chr2:37110326-37110327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562305430	chr2:37110352-37110353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529502755	chr2:37110365-37110366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375605891	chr2:37110374-37110375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537413924	chr2:37110382-37110383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547667400	chr2:37110384-37110385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559648502	chr2:37110396-37110397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:3026 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37067600-37146200	Weak transcription	Psoas Muscle	Psoas
2	chr2:37075600-37139200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:37076800-37111600	Weak transcription	Brain Germinal Matrix	brain
4	chr2:37077000-37116200	Weak transcription	Hela-S3	cervix
5	chr2:37077000-37116200	Weak transcription	NHLF	lung
6	chr2:37077200-37144400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr2:37077400-37136600	Weak transcription	Colon Smooth Muscle	Colon
8	chr2:37078200-37118400	Weak transcription	Fetal Brain Male	brain
9	chr2:37079200-37111000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr2:37082200-37115600	Weak transcription	Stomach Mucosa	stomach
11	chr2:37087400-37146200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:37090800-37114200	Strong transcription	Primary B cells from peripheral blood	blood
13	chr2:37091000-37114000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:37091200-37114400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr2:37092800-37115600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr2:37094200-37113400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr2:37094400-37110400	Weak transcription	NH-A	brain
18	chr2:37094400-37154200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr2:37095800-37112600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr2:37096000-37111200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:37096400-37110800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr2:37096400-37117000	Weak transcription	K562	blood
23	chr2:37096400-37143800	Weak transcription	Fetal Kidney	kidney
24	chr2:37096800-37154400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr2:37098000-37112400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr2:37098400-37109800	Strong transcription	Primary T cells from cord blood	blood
27	chr2:37099000-37116800	Weak transcription	A549	lung
28	chr2:37099200-37112000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr2:37099200-37140200	Weak transcription	Colonic Mucosa	Colon
30	chr2:37099600-37109800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr2:37099600-37112400	Weak transcription	HUVEC	blood vessel
32	chr2:37100000-37110800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr2:37100400-37116800	Weak transcription	Brain Cingulate Gyrus	brain
34	chr2:37101200-37111200	Strong transcription	Liver	Liver
35	chr2:37101800-37119200	Weak transcription	GM12878-XiMat	blood
36	chr2:37102400-37114200	Weak transcription	NHDF-Ad	bronchial
37	chr2:37102600-37112200	Weak transcription	Fetal Heart	heart
38	chr2:37103400-37109600	Weak transcription	Gastric	stomach
39	chr2:37103400-37109800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:37103800-37113400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:37103800-37117200	Weak transcription	HSMMtube	muscle
42	chr2:37103800-37121400	Weak transcription	Small Intestine	intestine
43	chr2:37103800-37146200	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr2:37104200-37117800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr2:37104600-37109600	Weak transcription	Osteobl	bone
46	chr2:37105000-37152600	Weak transcription	Rectal Smooth Muscle	rectum
47	chr2:37105000-37164600	Weak transcription	Lung	lung
48	chr2:37105200-37109600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr2:37105200-37109600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr2:37105200-37109600	Weak transcription	Adipose Nuclei	Adipose

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