Variant report

Variant	nsv873780
Chromosome Location	chr2:32626617-32725022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:597)
CpG islands
(count:123)
Chromatin interactive
region (count:63)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:32678784-32679113	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:32667025-32667589	HepG2	liver:	n/a	chr2:32667295-32667311
3	ARID3A	chr2:32704957-32705557	K562	blood:	n/a	n/a
4	ATF1	chr2:32661286-32661606	K562	blood:	n/a	n/a
5	ATF1	chr2:32710011-32710380	K562	blood:	n/a	n/a
6	ATF3	chr2:32709931-32710256	K562	blood:	n/a	n/a
7	BHLHE40	chr2:32644064-32644202	A549	lung:	n/a	n/a
8	BHLHE40	chr2:32705137-32705435	K562	blood:	n/a	n/a
9	BHLHE40	chr2:32653232-32653458	K562	blood:	n/a	n/a
10	BRCA1	chr2:32650791-32650795	GM12878	blood:	n/a	n/a
11	CBX3	chr2:32671924-32672171	K562	blood:	n/a	n/a
12	CCNT2	chr2:32660641-32660742	K562	blood:	n/a	n/a
13	CCNT2	chr2:32705210-32705391	K562	blood:	n/a	n/a
14	CEBPB	chr2:32644019-32644201	A549	lung:	n/a	chr2:32644124-32644137
15	CEBPB	chr2:32671365-32671769	IMR90	lung:	n/a	chr2:32671441-32671452 chr2:32671441-32671454
16	CEBPB	chr2:32721700-32721999	IMR90	lung:	n/a	chr2:32721819-32721830
17	CEBPB	chr2:32721692-32721985	K562	blood:	n/a	chr2:32721819-32721830
18	CEBPB	chr2:32642671-32643145	A549	lung:	n/a	chr2:32642903-32642914
19	CEBPB	chr2:32711557-32711710	A549	lung:	n/a	chr2:32711640-32711653
20	CEBPB	chr2:32671329-32671776	HepG2	liver:	n/a	chr2:32671441-32671452 chr2:32671441-32671454
21	CEBPB	chr2:32671453-32671753	K562	blood:	n/a	n/a
22	CEBPB	chr2:32684932-32685189	HepG2	liver:	n/a	chr2:32685049-32685060
23	CEBPB	chr2:32721671-32721990	A549	lung:	n/a	chr2:32721819-32721830
24	CEBPB	chr2:32642715-32643066	K562	blood:	n/a	chr2:32642903-32642914
25	CEBPB	chr2:32647670-32647801	A549	lung:	n/a	n/a
26	CEBPB	chr2:32721668-32721984	HepG2	liver:	n/a	chr2:32721819-32721830
27	CEBPB	chr2:32642717-32643094	HepG2	liver:	n/a	chr2:32642903-32642914
28	CEBPB	chr2:32642712-32643097	K562	blood:	n/a	chr2:32642903-32642914
29	CEBPB	chr2:32711519-32711711	K562	blood:	n/a	chr2:32711640-32711653
30	CEBPB	chr2:32709838-32710480	A549	lung:	n/a	n/a
31	CEBPB	chr2:32642784-32643015	K562	blood:	n/a	chr2:32642903-32642914
32	CEBPB	chr2:32710090-32710290	K562	blood:	n/a	n/a
33	CEBPB	chr2:32671493-32671720	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:32642752-32643064	ECC-1	luminal epithelium:	n/a	chr2:32642903-32642914
35	CEBPB	chr2:32671440-32671756	H1-hESC	embryonic stem cell:	n/a	chr2:32671441-32671452 chr2:32671441-32671454
36	CEBPB	chr2:32721724-32721984	Hela-S3	cervix:	n/a	chr2:32721819-32721830
37	CEBPB	chr2:32684929-32685182	IMR90	lung:	n/a	chr2:32685049-32685060
38	CEBPB	chr2:32709884-32710595	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:32721659-32722010	H1-hESC	embryonic stem cell:	n/a	chr2:32721819-32721830
40	CEBPB	chr2:32642702-32643059	MCF-7	breast:	n/a	chr2:32642903-32642914
41	CEBPB	chr2:32671499-32671661	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:32671379-32671750	MCF-7	breast:	n/a	chr2:32671441-32671452 chr2:32671441-32671454
43	CEBPB	chr2:32709980-32710446	HCT-116	colon:	n/a	n/a
44	CEBPB	chr2:32684883-32685163	K562	blood:	n/a	chr2:32685049-32685060
45	CEBPB	chr2:32671329-32671767	A549	lung:	n/a	chr2:32671441-32671452 chr2:32671441-32671454
46	CEBPB	chr2:32642759-32643080	H1-hESC	embryonic stem cell:	n/a	chr2:32642903-32642914
47	CEBPB	chr2:32678741-32679160	HepG2	liver:	n/a	chr2:32679093-32679104 chr2:32679001-32679012
48	CEBPB	chr2:32642719-32643099	IMR90	lung:	n/a	chr2:32642903-32642914
49	CEBPB	chr2:32684998-32685159	A549	lung:	n/a	chr2:32685049-32685060
50	CEBPB	chr2:32642678-32643145	MCF-7	breast:	n/a	chr2:32642903-32642914

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:32673206-32673256	HMEC	breast:	n/a
2	chr2:32673206-32673256	HMEC	breast:	n/a
3	chr2:32678846-32678896	PrEC	prostate:	n/a
4	chr2:32678846-32678896	AG09319	gingival:	n/a
5	chr2:32673206-32673256	AG09319	gingival:	n/a
6	chr2:32673206-32673256	HUVEC	blood vessel:	n/a
7	chr2:32673206-32673256	AG04450	lung:	fetal
8	chr2:32678846-32678896	AG04450	lung:	fetal
9	chr2:32678846-32678896	HRCEpiC	kidney:	n/a
10	chr2:32673206-32673256	HCT-116	colon:	n/a
11	chr2:32678846-32678896	AG09309	skin:	n/a
12	chr2:32673206-32673256	HRPEpiC	eye:	n/a
13	chr2:32678846-32678896	PFSK-1	brain:	n/a
14	chr2:32678846-32678896	HEK293	kidney:	embryo
15	chr2:32678846-32678896	SAEC	small airway:	n/a
16	chr2:32678846-32678896	NHBE	bronchial:	n/a
17	chr2:32678846-32678896	GM19239	blood:	n/a
18	chr2:32673206-32673256	U87	brain:	n/a
19	chr2:32673206-32673256	NHBE	bronchial:	n/a
20	chr2:32673206-32673256	GM19239	blood:	n/a
21	chr2:32673206-32673256	AG10803	skin:	n/a
22	chr2:32673206-32673256	PrEC	prostate:	n/a
23	chr2:32673206-32673256	Hepatocyte	liver:	n/a
24	chr2:32673206-32673256	CMK	blood:	n/a
25	chr2:32678846-32678896	SK-N-MC	brain:	n/a
26	chr2:32678846-32678896	HCM	heart:	n/a
27	chr2:32673206-32673256	HEK293	kidney:	embryo
28	chr2:32678846-32678896	HNPCEpiC	eye:	n/a
29	chr2:32678846-32678896	GM12891	blood:	n/a
30	chr2:32678846-32678896	HEEpiC	esophagus:	n/a
31	chr2:32678846-32678896	T-47D	breast:	n/a
32	chr2:32673206-32673256	HRCEpiC	kidney:	n/a
33	chr2:32678846-32678896	HCPEpiC	choroid plexus:	n/a
34	chr2:32678846-32678896	HepG2	liver:	n/a
35	chr2:32673206-32673256	HL-60	blood:	n/a
36	chr2:32678846-32678896	MCF-7	breast:	n/a
37	chr2:32673206-32673256	NT2-D1	testis:	n/a
38	chr2:32673206-32673256	HepG2	liver:	n/a
39	chr2:32673206-32673256	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:32673206-32673256	HCM	heart:	n/a
41	chr2:32673206-32673256	HEEpiC	esophagus:	n/a
42	chr2:32678846-32678896	HL-60	blood:	n/a
43	chr2:32678846-32678896	A549	lung:	n/a
44	chr2:32678846-32678896	HAEpiC	amniotic membrane:	n/a
45	chr2:32678846-32678896	BJ	skin:	n/a
46	chr2:32678846-32678896	GM06990	blood:	n/a
47	chr2:32673206-32673256	A549	lung:	n/a
48	chr2:32673206-32673256	SK-N-MC	brain:	n/a
49	chr2:32678846-32678896	U87	brain:	n/a
50	chr2:32673206-32673256	PANC-1	pancreas:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:32651894..32653691-chr2:32654473..32656959,2	K562	blood:
2	chr2:32634859..32637266-chr2:32638497..32641278,2	MCF-7	breast:
3	chr2:32710721..32712306-chr2:32712654..32714495,2	MCF-7	breast:
4	chr2:32696181..32697686-chr2:32703369..32704888,2	MCF-7	breast:
5	chr2:32581170..32583606-chr2:32648522..32652057,4	MCF-7	breast:
6	chr2:32705619..32707758-chr2:32716833..32718434,2	K562	blood:
7	chr2:32628910..32631702-chr2:32651764..32653919,2	MCF-7	breast:
8	chr2:32666229..32669442-chr2:32676026..32679242,3	K562	blood:
9	chr2:32580833..32585262-chr2:32639494..32642748,4	MCF-7	breast:
10	chr2:32642567..32646471-chr2:32648839..32652679,3	K562	blood:
11	chr2:32695471..32697894-chr2:32707788..32710174,2	MCF-7	breast:
12	chr2:32631333..32634011-chr2:32636154..32637762,2	K562	blood:
13	chr2:32655375..32657837-chr2:32663152..32664844,2	K562	blood:
14	chr2:32648680..32650262-chr2:32651820..32653321,2	MCF-7	breast:
15	chr2:32611734..32613914-chr2:32643255..32645038,2	K562	blood:
16	chr2:32705619..32707758-chr2:32716833..32718434,2	K562	blood:
17	chr2:32631333..32634011-chr2:32636154..32637762,2	K562	blood:
18	chr2:32697674..32700411-chr2:32709724..32712334,2	MCF-7	breast:
19	chr2:32648680..32650262-chr2:32651820..32653321,2	MCF-7	breast:
20	chr2:32584914..32587228-chr2:32703630..32705353,2	K562	blood:
21	chr2:32638863..32640718-chr2:32652115..32654346,2	MCF-7	breast:
22	chr2:32692267..32694137-chr2:32700993..32702587,2	MCF-7	breast:
23	chr2:32650702..32653420-chr2:32683411..32685638,2	MCF-7	breast:
24	chr2:32694400..32696081-chr2:32747755..32749936,2	K562	blood:
25	chr2:32642567..32646471-chr2:32648839..32652679,3	K562	blood:
26	chr2:32638863..32640718-chr2:32652115..32654346,2	MCF-7	breast:
27	chr2:32713396..32715355-chr2:32717113..32719991,2	K562	blood:
28	chr2:32582006..32583703-chr2:32658464..32660440,2	K562	blood:
29	chr2:32635540..32637140-chr2:32639058..32641939,2	K562	blood:
30	chr2:32661395..32664058-chr2:32665882..32669007,3	MCF-7	breast:
31	chr2:32713396..32715355-chr2:32717113..32719991,2	K562	blood:
32	chr2:32649820..32653520-chr2:32656022..32658272,3	K562	blood:
33	chr2:32655375..32657837-chr2:32663152..32664844,2	K562	blood:
34	chr2:32655316..32658127-chr2:32662690..32665444,3	K562	blood:
35	chr2:32663362..32665357-chr2:32667579..32669468,2	K562	blood:
36	chr2:32710721..32712306-chr2:32712654..32714495,2	MCF-7	breast:
37	chr2:32655530..32658471-chr2:32661173..32663842,2	MCF-7	breast:
38	chr2:32675460..32677596-chr2:32681562..32684315,2	MCF-7	breast:
39	chr2:32655316..32658127-chr2:32662690..32665444,3	K562	blood:
40	chr2:32580654..32583565-chr2:32680156..32681675,2	K562	blood:
41	chr2:32658851..32660649-chr2:32708053..32709653,2	K562	blood:
42	chr2:32582274..32583881-chr2:32678469..32681108,2	MCF-7	breast:
43	chr2:32658851..32660649-chr2:32708053..32709653,2	K562	blood:
44	chr2:32690803..32693344-chr2:32695188..32697337,2	K562	blood:
45	chr2:32601960..32603780-chr2:32628492..32630204,2	MCF-7	breast:
46	chr2:32692267..32694137-chr2:32700993..32702587,2	MCF-7	breast:
47	chr2:32704912..32707758-chr2:32715954..32718434,3	K562	blood:
48	chr2:32649820..32653520-chr2:32656022..32658272,3	K562	blood:
49	chr2:32696181..32697686-chr2:32703369..32704888,2	MCF-7	breast:
50	chr2:32650702..32653420-chr2:32683411..32685638,2	MCF-7	breast:

No data

Variant related genes	Relation type
BIRC6	TF binding region
BIRC6	CpG island
ENSG00000115760	chromatin interactions
ENSG00000185608	chromatin interactions

Extended variants
information (count: 3931 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3931 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13033581	chr2:32626617-32626618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs139494254	chr2:32626625-32626626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201426570	chr2:32626689-32626690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370670186	chr2:32626721-32626722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115882868	chr2:32626722-32626723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199598287	chr2:32626723-32626724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200691665	chr2:32626741-32626742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568997793	chr2:32626789-32626790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537823403	chr2:32626793-32626794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569421445	chr2:32626795-32626796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551433069	chr2:32626823-32626824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533804594	chr2:32626875-32626876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150864876	chr2:32626925-32626926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554456574	chr2:32626928-32626929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574116176	chr2:32626939-32626940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs36003874	chr2:32626951-32626952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536871574	chr2:32626966-32626967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556362291	chr2:32626974-32626975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200017375	chr2:32627001-32627002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138407768	chr2:32627018-32627019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573724174	chr2:32627038-32627039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs55788900	chr2:32627064-32627065	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs564985262	chr2:32627066-32627067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572113984	chr2:32627082-32627083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143102008	chr2:32627083-32627084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560414175	chr2:32627136-32627137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529052982	chr2:32627172-32627173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs58534020	chr2:32627190-32627191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566932633	chr2:32627241-32627242	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549192667	chr2:32627292-32627293	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562558982	chr2:32627400-32627401	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531477837	chr2:32627401-32627402	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551501889	chr2:32627409-32627410	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571221470	chr2:32627575-32627576	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376904035	chr2:32627641-32627642	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs76427095	chr2:32627707-32627708	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139827594	chr2:32627708-32627709	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78111477	chr2:32627740-32627741	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372490790	chr2:32627784-32627785	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs62136279	chr2:32627808-32627809	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs149659187	chr2:32627844-32627845	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576124998	chr2:32627845-32627846	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538700783	chr2:32627890-32627891	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs78232568	chr2:32627893-32627894	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572077546	chr2:32627913-32627914	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555883615	chr2:32627929-32627930	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541439600	chr2:32627972-32627973	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560167588	chr2:32628004-32628005	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573917734	chr2:32628011-32628012	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542451899	chr2:32628021-32628022	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	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
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Neurocytoma	17123091	CNVD
Breast cancer	22522925	CNVD
Autism	22549408	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3011 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:32583600-32653200	Weak transcription	Gastric	stomach
2	chr2:32583800-32649000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:32602000-32653000	Weak transcription	Stomach Mucosa	stomach
4	chr2:32604600-32635000	Strong transcription	Fetal Thymus	thymus
5	chr2:32604600-32635200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr2:32604600-32637200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:32604800-32635600	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr2:32605200-32635400	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr2:32605200-32637200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:32605400-32652800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr2:32605800-32634000	Strong transcription	Duodenum Mucosa	Duodenum
12	chr2:32606800-32636800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:32607000-32636200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:32607200-32650600	Weak transcription	Fetal Heart	heart
15	chr2:32607600-32627600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr2:32607600-32639800	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr2:32607800-32634000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr2:32607800-32637800	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr2:32607800-32640200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:32609000-32632200	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr2:32609800-32637400	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr2:32613400-32627400	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr2:32613800-32645400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:32617000-32627600	Strong transcription	Fetal Muscle Trunk	muscle
25	chr2:32617200-32627400	Strong transcription	Sigmoid Colon	Sigmoid Colon
26	chr2:32617400-32632200	Weak transcription	Colon Smooth Muscle	Colon
27	chr2:32617800-32650800	Weak transcription	Right Ventricle	heart
28	chr2:32618000-32640400	Weak transcription	Small Intestine	intestine
29	chr2:32618000-32650800	Weak transcription	Psoas Muscle	Psoas
30	chr2:32618600-32644800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr2:32618800-32640000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr2:32619000-32629000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:32620200-32650600	Weak transcription	Aorta	Aorta
34	chr2:32621000-32631600	Weak transcription	Hela-S3	cervix
35	chr2:32621000-32669800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr2:32621200-32664600	Weak transcription	Fetal Brain Male	brain
37	chr2:32621400-32640000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr2:32621600-32693400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr2:32621800-32626800	Strong transcription	Fetal Intestine Small	intestine
40	chr2:32621800-32630600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr2:32621800-32639800	Weak transcription	Brain Anterior Caudate	brain
42	chr2:32621800-32639800	Weak transcription	Brain Cingulate Gyrus	brain
43	chr2:32622000-32629000	Weak transcription	Primary hematopoietic stem cells	blood
44	chr2:32622000-32639800	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr2:32622000-32640200	Weak transcription	Rectal Smooth Muscle	rectum
46	chr2:32622200-32627200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr2:32622200-32640000	Weak transcription	Brain Substantia Nigra	brain
48	chr2:32622200-32640000	Weak transcription	Ovary	ovary
49	chr2:32622400-32629400	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr2:32622400-32639800	Weak transcription	NHLF	lung

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