Variant report

Variant	nsv999465
Chromosome Location	chr2:37029347-37095895
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37046300-37046538	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:37085943-37086690	HepG2	liver:	n/a	n/a
3	BATF	chr2:37085614-37086030	GM12878	blood:	n/a	n/a
4	BATF	chr2:37032793-37033069	GM12878	blood:	n/a	n/a
5	BATF	chr2:37032861-37033028	GM12878	blood:	n/a	n/a
6	BATF	chr2:37085647-37086223	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:37085805-37086219	GM12878	blood:	n/a	n/a
8	CCNT2	chr2:37095797-37095899	K562	blood:	n/a	n/a
9	CEBPB	chr2:37076424-37076775	K562	blood:	n/a	chr2:37076591-37076602
10	CEBPB	chr2:37080365-37080533	HepG2	liver:	n/a	chr2:37080443-37080454
11	CEBPB	chr2:37083150-37083407	IMR90	lung:	n/a	chr2:37083249-37083260
12	CEBPB	chr2:37083111-37083424	HepG2	liver:	n/a	chr2:37083249-37083260
13	CEBPB	chr2:37083205-37083311	H1-hESC	embryonic stem cell:	n/a	chr2:37083249-37083260
14	CEBPB	chr2:37076417-37076769	IMR90	lung:	n/a	chr2:37076591-37076602
15	CEBPB	chr2:37076410-37076778	A549	lung:	n/a	chr2:37076591-37076602
16	CEBPB	chr2:37076514-37076754	H1-hESC	embryonic stem cell:	n/a	chr2:37076591-37076602
17	CEBPB	chr2:37076415-37076767	HepG2	liver:	n/a	chr2:37076591-37076602
18	CEBPB	chr2:37083147-37083378	A549	lung:	n/a	chr2:37083249-37083260
19	CEBPB	chr2:37087867-37087986	HepG2	liver:	n/a	chr2:37087939-37087950
20	CHD1	chr2:37051473-37051475	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr2:37051405-37051727	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr2:37085596-37086176	GM12878	blood:	n/a	n/a
23	CHD2	chr2:37039443-37039715	H1-hESC	embryonic stem cell:	n/a	chr2:37039457-37039467
24	CTCF	chr2:37039420-37039570	HUVEC	blood vessel:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
25	CTCF	chr2:37039480-37039630	A549	lung:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
26	CTCF	chr2:37046600-37046750	A549	lung:	n/a	n/a
27	CTCF	chr2:37039460-37039610	HEK293	kidney:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
28	CTCF	chr2:37039500-37039650	HCPEpiC	choroid plexus:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
29	CTCF	chr2:37039100-37039250	HCT-116	colon:	n/a	n/a
30	CTCF	chr2:37039480-37039630	HBMEC	blood vessel:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
31	CTCF	chr2:37039460-37039610	HMEC	breast:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
32	CTCF	chr2:37085022-37085161	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:37046582-37046735	A549	lung:	n/a	n/a
34	CTCF	chr2:37039380-37039530	BJ	skin:	n/a	n/a
35	CTCF	chr2:37039355-37039651	K562	blood:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
36	CTCF	chr2:37039460-37039610	GM12874	blood:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
37	CTCF	chr2:37085038-37085161	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:37039270-37039686	K562	blood:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
39	CTCF	chr2:37039452-37039613	SK-N-SH_RA	brain:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
40	CTCF	chr2:37046520-37046670	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:37039480-37039630	HRE	kidney:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
42	CTCF	chr2:37061155-37061191	LNCaP	prostate:	n/a	n/a
43	CTCF	chr2:37039435-37039611	IMR90	lung:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
44	CTCF	chr2:37085052-37085103	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr2:37039500-37039650	WI-38	lung:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
46	CTCF	chr2:37039460-37039610	GM12878	blood:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
47	CTCF	chr2:37039460-37039610	GM12871	blood:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
48	CTCF	chr2:37039438-37039642	GM19240	blood:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
49	CTCF	chr2:37039426-37039637	GM12891	blood:	n/a	chr2:37039539-37039560 chr2:37039537-37039555 chr2:37039540-37039553
50	CTCF	chr2:37046540-37046690	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37035865-37035915	HCPEpiC	choroid plexus:	n/a
2	chr2:37035865-37035915	HCPEpiC	choroid plexus:	n/a
3	chr2:37061797-37061847	BJ	skin:	n/a
4	chr2:37035539-37035589	K562	blood:	n/a
5	chr2:37041582-37041632	HUVEC	blood vessel:	n/a
6	chr2:37035539-37035589	GM19239	blood:	n/a
7	chr2:37039119-37039169	LNCaP	prostate:	n/a
8	chr2:37075592-37075642	AG10803	skin:	n/a
9	chr2:37035650-37035700	GM12878	blood:	n/a
10	chr2:37041582-37041632	HRPEpiC	eye:	n/a
11	chr2:37035539-37035589	IMR90	lung:	fetal
12	chr2:37035539-37035589	GM06990	blood:	n/a
13	chr2:37032102-37032152	HNPCEpiC	eye:	n/a
14	chr2:37032102-37032152	HEEpiC	esophagus:	n/a
15	chr2:37070005-37070055	BE2_C	brain:	n/a
16	chr2:37035650-37035700	IMR90	lung:	fetal
17	chr2:37061797-37061847	GM12878	blood:	n/a
18	chr2:37039119-37039169	IMR90	lung:	fetal
19	chr2:37035865-37035915	SK-N-SH_RA	brain:	n/a
20	chr2:37035539-37035589	HMEC	breast:	n/a
21	chr2:37035809-37035859	Caco-2	colon:	n/a
22	chr2:37070005-37070055	PFSK-1	brain:	n/a
23	chr2:37061797-37061847	HEEpiC	esophagus:	n/a
24	chr2:37035707-37035757	HCT-116	colon:	n/a
25	chr2:37075592-37075642	SAEC	small airway:	n/a
26	chr2:37035707-37035757	SK-N-SH_RA	brain:	n/a
27	chr2:37035865-37035915	NT2-D1	testis:	n/a
28	chr2:37070005-37070055	HIPEpiC	eye:	n/a
29	chr2:37035539-37035589	Hepatocyte	liver:	n/a
30	chr2:37035539-37035589	ProgFib	skin:	n/a
31	chr2:37070005-37070055	AG10803	skin:	n/a
32	chr2:37041582-37041632	SK-N-SH	brain:	n/a
33	chr2:37032102-37032152	ECC-1	luminal epithelium:	n/a
34	chr2:37075592-37075642	NHDF-neo	bronchial:	n/a
35	chr2:37075592-37075642	RPTEC	kidney:	n/a
36	chr2:37070005-37070055	GM06990	blood:	n/a
37	chr2:37039119-37039169	CMK	blood:	n/a
38	chr2:37035650-37035700	T-47D	breast:	n/a
39	chr2:37041582-37041632	MCF10A-Er-Src	breast:	n/a
40	chr2:37032102-37032152	AG09309	skin:	n/a
41	chr2:37039119-37039169	MCF-7	breast:	n/a
42	chr2:37039119-37039169	MCF10A-Er-Src	breast:	n/a
43	chr2:37061797-37061847	Jurkat	blood:	n/a
44	chr2:37035809-37035859	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:37032102-37032152	HCPEpiC	choroid plexus:	n/a
46	chr2:37035539-37035589	HCT-116	colon:	n/a
47	chr2:37035809-37035859	SK-N-SH	brain:	n/a
48	chr2:37039119-37039169	K562	blood:	n/a
49	chr2:37039119-37039169	ECC-1	luminal epithelium:	n/a
50	chr2:37035865-37035915	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:37053268..37055932-chr2:37062190..37065035,2	MCF-7	breast:
2	chr2:37029593..37034563-chr2:37035958..37037760,4	K562	blood:
3	chr2:37047490..37050281-chr2:37192919..37195129,2	K562	blood:
4	chr2:37029593..37034563-chr2:37035958..37037760,4	K562	blood:
5	chr2:37077524..37079091-chr2:37080598..37082395,2	MCF-7	breast:
6	chr2:37046380..37047296-chr2:37232183..37232895,3	MCF-7	breast:
7	chr2:37068151..37070389-chr2:37071740..37074179,2	K562	blood:
8	chr2:37095568..37097536-chr2:37100134..37102065,2	K562	blood:
9	chr2:37070373..37072769-chr2:37080148..37082605,2	K562	blood:
10	chr2:37070518..37072329-chr2:37074111..37076172,2	K562	blood:
11	chr2:37026211..37031295-chr2:37031745..37037130,6	MCF-7	breast:
12	chr2:37048381..37050442-chr2:37052103..37054094,2	MCF-7	breast:
13	chr2:37070468..37072403-chr2:37075217..37077956,2	MCF-7	breast:
14	chr2:37083137..37085335-chr2:37192988..37194551,2	MCF-7	breast:
15	chr2:37038416..37040674-chr2:37042878..37045165,2	MCF-7	breast:
16	chr2:37026042..37027658-chr2:37028263..37030381,2	K562	blood:
17	chr2:37038416..37040674-chr2:37042878..37045165,2	MCF-7	breast:
18	chr2:37026211..37031295-chr2:37031745..37037130,6	MCF-7	breast:
19	chr2:37053268..37055932-chr2:37062190..37065035,2	MCF-7	breast:
20	chr2:37080118..37082736-chr2:37085866..37087782,3	K562	blood:
21	chr2:37038445..37041439-chr2:37044172..37046404,2	MCF-7	breast:
22	chr2:37070518..37072329-chr2:37074111..37076172,2	K562	blood:
23	chr2:37087369..37088984-chr2:37161141..37163056,2	K562	blood:
24	chr2:37080118..37082736-chr2:37085866..37087782,2	K562	blood:
25	chr2:37080118..37082736-chr2:37085866..37087782,2	K562	blood:
26	chr2:37068889..37071543-chr2:37072679..37074601,2	K562	blood:
27	chr2:37073507..37075966-chr2:37080375..37082990,2	MCF-7	breast:
28	chr2:37080118..37082736-chr2:37085866..37087782,3	K562	blood:
29	chr2:37068889..37071543-chr2:37072679..37074601,2	K562	blood:
30	chr2:37048381..37050442-chr2:37052103..37054094,2	MCF-7	breast:
31	chr2:37070468..37072403-chr2:37075217..37077956,2	MCF-7	breast:
32	chr2:37077524..37079091-chr2:37080598..37082395,2	MCF-7	breast:
33	chr2:37045354..37047713-chr2:37230824..37232867,2	MCF-7	breast:
34	chr2:37073507..37075966-chr2:37080375..37082990,2	MCF-7	breast:
35	chr2:37046287..37047005-chr2:37145243..37146052,3	MCF-7	breast:
36	chr2:37034700..37036255-chr2:37423104..37425586,2	K562	blood:
37	chr2:37038445..37041439-chr2:37044172..37046404,2	MCF-7	breast:
38	chr2:37070373..37072769-chr2:37080148..37082605,2	K562	blood:
39	chr2:37082616..37084189-chr2:37192203..37194544,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STRN-1	chr2:37066146-37066788	NONHSAT070091
2	lnc-STRN-1	chr2:37070934-37071545	NONHSAT070091
3	lnc-STRN-1	chr2:37071730-37073048	NONHSAT070091
4	lnc-STRN-1	chr2:37067534-37069337	NONHSAT070091
5	lnc-STRN-1	chr2:37073062-37073286	NONHSAT070091

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	STRN	hsa-miR-342-3p	chr2:37073734-37073728
2	STRN	hsa-miR-342-3p	chr2:37071389-37071383

Variant related genes	Relation type
RNU6-577P	TF binding region
ENSG00000268688	TF binding region
RNU6-577P	CpG island
ENSG00000268688	CpG island
ENSG00000138068	chromatin interactions
ENSG00000218739	chromatin interactions
ENSG00000268688	chromatin interactions
ENSG00000115808	chromatin interactions

Extended variants
information (count: 3179 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3179 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7578335	chr2:37029347-37029348	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375311416	chr2:37029352-37029353	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560209996	chr2:37029375-37029376	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527264125	chr2:37029380-37029381	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184874872	chr2:37029388-37029389	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541681949	chr2:37029437-37029438	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564371947	chr2:37029438-37029439	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369283107	chr2:37029445-37029446	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7578448	chr2:37029446-37029447	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150493106	chr2:37029473-37029474	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536266615	chr2:37029476-37029477	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376942686	chr2:37029504-37029505	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188077074	chr2:37029548-37029549	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11891319	chr2:37029573-37029574	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs114167860	chr2:37029580-37029581	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558076850	chr2:37029604-37029605	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570002528	chr2:37029608-37029609	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537303976	chr2:37029611-37029612	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553367598	chr2:37029635-37029636	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371342963	chr2:37029639-37029640	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574122249	chr2:37029659-37029660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192518853	chr2:37029725-37029726	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541945367	chr2:37029747-37029748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138468340	chr2:37029767-37029768	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567286425	chr2:37029786-37029787	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553883124	chr2:37029854-37029855	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572120615	chr2:37029863-37029864	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142985592	chr2:37029864-37029865	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575127459	chr2:37029889-37029890	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146113332	chr2:37029903-37029904	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184370315	chr2:37029926-37029927	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138602012	chr2:37029952-37029953	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542440269	chr2:37029962-37029963	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375566196	chr2:37030023-37030024	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565829853	chr2:37030056-37030057	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73924905	chr2:37030145-37030146	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs149260223	chr2:37030146-37030147	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569667027	chr2:37030149-37030150	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537770132	chr2:37030159-37030160	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555747889	chr2:37030247-37030248	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144444219	chr2:37030273-37030274	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs62132487	chr2:37030296-37030297	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs563774754	chr2:37030297-37030298	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74760820	chr2:37030325-37030326	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs371742067	chr2:37030340-37030341	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539495331	chr2:37030343-37030344	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78043350	chr2:37030351-37030352	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190040567	chr2:37030356-37030357	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543733418	chr2:37030367-37030368	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148415473	chr2:37030384-37030385	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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	22737080	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:1057 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37013000-37033000	Weak transcription	Ovary	ovary
2	chr2:37024400-37033800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr2:37025200-37033000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:37027400-37044200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:37027600-37036200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:37028200-37030800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr2:37028400-37029400	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr2:37029200-37030200	Enhancers	Stomach Mucosa	stomach
9	chr2:37029400-37030000	Enhancers	HepG2	liver
10	chr2:37029400-37034200	Enhancers	Primary T cells fromperipheralblood	blood
11	chr2:37030200-37032800	Weak transcription	Stomach Mucosa	stomach
12	chr2:37030800-37031600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr2:37031400-37031600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr2:37031600-37032200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:37031600-37032800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr2:37031600-37035400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr2:37032400-37033000	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr2:37032400-37033800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:37032800-37033400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr2:37032800-37033400	Enhancers	Stomach Mucosa	stomach
21	chr2:37033000-37033400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr2:37033000-37034200	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr2:37033000-37034400	Active TSS	Rectal Mucosa Donor 29	rectum
24	chr2:37033000-37034600	Strong transcription	Ovary	ovary
25	chr2:37033200-37033400	Flanking Active TSS	K562	blood
26	chr2:37033400-37033600	Flanking Active TSS	Stomach Mucosa	stomach
27	chr2:37033600-37033800	Enhancers	Stomach Mucosa	stomach
28	chr2:37033800-37034200	Active TSS	Stomach Mucosa	stomach
29	chr2:37033800-37034400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:37033800-37035400	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr2:37034000-37034800	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr2:37034200-37034400	Flanking Active TSS	Stomach Mucosa	stomach
33	chr2:37034200-37034600	Active TSS	Colonic Mucosa	Colon
34	chr2:37034200-37034600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
35	chr2:37034200-37034600	Active TSS	Rectal Smooth Muscle	rectum
36	chr2:37034200-37035200	Enhancers	Duodenum Mucosa	Duodenum
37	chr2:37034200-37035600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:37034400-37034600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:37034400-37034800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
40	chr2:37034400-37035800	Enhancers	Stomach Mucosa	stomach
41	chr2:37034600-37035200	Weak transcription	Colonic Mucosa	Colon
42	chr2:37034600-37036200	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr2:37034600-37042800	Weak transcription	Ovary	ovary
44	chr2:37034800-37035400	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr2:37034800-37036200	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr2:37034800-37036400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr2:37035200-37035800	Enhancers	Colonic Mucosa	Colon
48	chr2:37035400-37035600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr2:37035400-37036000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr2:37035400-37036000	Strong transcription	Placenta Amnion	Placenta Amnion

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