Variant report

Variant	nsv833892
Chromosome Location	chr2:40188785-40363480
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:716)
CpG islands
(count:366)
Chromatin interactive
region (count:15)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:716 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:40223765-40224372	K562	blood:	n/a	n/a
2	ATF1	chr2:40217162-40217725	K562	blood:	n/a	n/a
3	ATF1	chr2:40222613-40222712	K562	blood:	n/a	n/a
4	BACH1	chr2:40351612-40351729	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:40208471-40208655	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr2:40323608-40323787	HepG2	liver:	n/a	n/a
7	CBX3	chr2:40223784-40224393	HCT-116	colon:	n/a	n/a
8	CCNT2	chr2:40279953-40280153	K562	blood:	n/a	n/a
9	CCNT2	chr2:40224014-40224213	K562	blood:	n/a	n/a
10	CEBPB	chr2:40351972-40352202	A549	lung:	n/a	chr2:40352104-40352115 chr2:40352074-40352087 chr2:40352102-40352113 chr2:40352102-40352115
11	CEBPB	chr2:40194970-40195037	K562	blood:	n/a	chr2:40195008-40195019
12	CEBPB	chr2:40330290-40330603	H1-hESC	embryonic stem cell:	n/a	chr2:40330437-40330448 chr2:40330438-40330447
13	CEBPB	chr2:40258067-40258360	K562	blood:	n/a	chr2:40258206-40258217
14	CEBPB	chr2:40218547-40218785	A549	lung:	n/a	chr2:40218674-40218685
15	CEBPB	chr2:40339221-40339389	Hela-S3	cervix:	n/a	chr2:40339272-40339283 chr2:40339274-40339283 chr2:40339274-40339285
16	CEBPB	chr2:40194850-40195177	HepG2	liver:	n/a	chr2:40195008-40195019
17	CEBPB	chr2:40330341-40330569	A549	lung:	n/a	chr2:40330437-40330448 chr2:40330438-40330447
18	CEBPB	chr2:40324745-40325354	A549	lung:	n/a	n/a
19	CEBPB	chr2:40330231-40331193	IMR90	lung:	n/a	chr2:40330437-40330448 chr2:40330438-40330447
20	CEBPB	chr2:40258064-40258380	A549	lung:	n/a	chr2:40258206-40258217
21	CEBPB	chr2:40286576-40286696	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:40319866-40319890	HepG2	liver:	n/a	chr2:40319879-40319890
23	CEBPB	chr2:40329747-40329985	H1-hESC	embryonic stem cell:	n/a	chr2:40329843-40329856
24	CEBPB	chr2:40324645-40325431	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:40194890-40195200	A549	lung:	n/a	chr2:40195008-40195019
26	CEBPB	chr2:40218494-40218859	IMR90	lung:	n/a	chr2:40218674-40218685
27	CEBPB	chr2:40324907-40325147	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:40223962-40224177	A549	lung:	n/a	n/a
29	CEBPB	chr2:40355036-40355623	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:40266300-40266894	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:40258083-40258389	HepG2	liver:	n/a	chr2:40258206-40258217
32	CEBPB	chr2:40288200-40288530	HepG2	liver:	n/a	chr2:40288341-40288352
33	CEBPB	chr2:40243495-40243987	IMR90	lung:	n/a	chr2:40243790-40243803 chr2:40243792-40243803
34	CEBPB	chr2:40218557-40218771	H1-hESC	embryonic stem cell:	n/a	chr2:40218674-40218685
35	CEBPB	chr2:40319735-40319825	A549	lung:	n/a	n/a
36	CEBPB	chr2:40339184-40339384	A549	lung:	n/a	chr2:40339272-40339283 chr2:40339274-40339283 chr2:40339274-40339285
37	CEBPB	chr2:40330267-40330599	Hela-S3	cervix:	n/a	chr2:40330437-40330448 chr2:40330438-40330447
38	CEBPB	chr2:40324822-40325151	A549	lung:	n/a	n/a
39	CEBPB	chr2:40339108-40339410	IMR90	lung:	n/a	chr2:40339272-40339283 chr2:40339274-40339283 chr2:40339274-40339285
40	CEBPB	chr2:40221391-40221660	IMR90	lung:	n/a	n/a
41	CEBPB	chr2:40339141-40339430	HepG2	liver:	n/a	chr2:40339272-40339283 chr2:40339274-40339283 chr2:40339274-40339285
42	CEBPB	chr2:40259963-40260548	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:40223752-40224243	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:40269113-40269506	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:40351937-40352262	MCF-7	breast:	n/a	chr2:40352104-40352115 chr2:40352074-40352087 chr2:40352102-40352113 chr2:40352102-40352115
46	CEBPB	chr2:40223859-40224267	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr2:40288194-40288467	IMR90	lung:	n/a	chr2:40288341-40288352
48	CEBPB	chr2:40330299-40330611	HepG2	liver:	n/a	chr2:40330437-40330448 chr2:40330438-40330447
49	CEBPB	chr2:40351880-40352226	MCF-7	breast:	n/a	chr2:40352104-40352115 chr2:40352074-40352087 chr2:40352102-40352113 chr2:40352102-40352115
50	CEBPB	chr2:40223865-40224375	HCT-116	colon:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40356782-40356832	IMR90	lung:	fetal
2	chr2:40356782-40356832	GM12891	blood:	n/a
3	chr2:40260498-40260548	HCPEpiC	choroid plexus:	n/a
4	chr2:40260498-40260548	PrEC	prostate:	n/a
5	chr2:40351367-40351417	GM19239	blood:	n/a
6	chr2:40266366-40266416	AG10803	skin:	n/a
7	chr2:40203342-40203392	Jurkat	blood:	n/a
8	chr2:40266366-40266416	HEK293	kidney:	embryo
9	chr2:40203342-40203392	HRE	kidney:	n/a
10	chr2:40266366-40266416	ovcar-3	ovarian:	n/a
11	chr2:40260498-40260548	ECC-1	luminal epithelium:	n/a
12	chr2:40342248-40342298	SK-N-SH	brain:	n/a
13	chr2:40203342-40203392	SAEC	small airway:	n/a
14	chr2:40266366-40266416	LNCaP	prostate:	n/a
15	chr2:40266366-40266416	AG09309	skin:	n/a
16	chr2:40356782-40356832	HNPCEpiC	eye:	n/a
17	chr2:40351367-40351417	AG09319	gingival:	n/a
18	chr2:40266366-40266416	RPTEC	kidney:	n/a
19	chr2:40356782-40356832	HepG2	liver:	n/a
20	chr2:40351367-40351417	Jurkat	blood:	n/a
21	chr2:40260498-40260548	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:40203342-40203392	HEK293	kidney:	embryo
23	chr2:40356782-40356832	LNCaP	prostate:	n/a
24	chr2:40356782-40356832	HCM	heart:	n/a
25	chr2:40342248-40342298	AoSMC	blood vessel:	n/a
26	chr2:40351367-40351417	Caco-2	colon:	n/a
27	chr2:40356782-40356832	NB4	blood:	n/a
28	chr2:40260498-40260548	HRE	kidney:	n/a
29	chr2:40266366-40266416	Jurkat	blood:	n/a
30	chr2:40351367-40351417	ovcar-3	ovarian:	n/a
31	chr2:40203342-40203392	SK-N-MC	brain:	n/a
32	chr2:40260498-40260548	AG10803	skin:	n/a
33	chr2:40342248-40342298	NB4	blood:	n/a
34	chr2:40351367-40351417	HCT-116	colon:	n/a
35	chr2:40203342-40203392	GM12892	blood:	n/a
36	chr2:40356782-40356832	U87	brain:	n/a
37	chr2:40260498-40260548	HEEpiC	esophagus:	n/a
38	chr2:40266366-40266416	AG09319	gingival:	n/a
39	chr2:40266366-40266416	HRCEpiC	kidney:	n/a
40	chr2:40342248-40342298	MCF10A-Er-Src	breast:	n/a
41	chr2:40260498-40260548	AG04450	lung:	fetal
42	chr2:40342248-40342298	HEK293	kidney:	embryo
43	chr2:40266366-40266416	BJ	skin:	n/a
44	chr2:40260498-40260548	MCF10A-Er-Src	breast:	n/a
45	chr2:40260498-40260548	BE2_C	brain:	n/a
46	chr2:40203342-40203392	K562	blood:	n/a
47	chr2:40351367-40351417	GM12891	blood:	n/a
48	chr2:40351367-40351417	GM06990	blood:	n/a
49	chr2:40203342-40203392	HCT-116	colon:	n/a
50	chr2:40260498-40260548	HRCEpiC	kidney:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:40322332..40325510-chr2:40329886..40332730,3	MCF-7	breast:
2	chr2:40334175..40336560-chr2:40339727..40341466,2	MCF-7	breast:
3	chr2:40358658..40360428-chr2:40361170..40364164,2	MCF-7	breast:
4	chr2:40340588..40343446-chr2:40344341..40345880,2	K562	blood:
5	chr2:40358744..40360269-chr2:40362071..40363765,2	K562	blood:
6	chr2:40358658..40360428-chr2:40361170..40364164,2	MCF-7	breast:
7	chr2:40319121..40321528-chr2:40332638..40334554,2	K562	blood:
8	chr2:40319121..40321528-chr2:40332638..40334554,2	K562	blood:
9	chr2:40248216..40251072-chr2:40272085..40274359,2	K562	blood:
10	chr2:40334175..40336560-chr2:40339727..40341466,2	MCF-7	breast:
11	chr2:40254887..40256636-chr2:40272268..40275019,2	K562	blood:
12	chr2:40317100..40319815-chr2:40339611..40341990,2	MCF-7	breast:
13	chr2:40254887..40256636-chr2:40272268..40275019,2	K562	blood:
14	chr2:40358744..40360269-chr2:40362071..40363765,2	K562	blood:
15	chr2:40248216..40251072-chr2:40272085..40274359,2	K562	blood:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
2	lnc-TMEM178-2	chr2:40341142-40341243	ENSG00000227028.2
3	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
4	lnc-TMEM178-2	chr2:40345452-40345645	ENSG00000227028.2
5	lnc-TMEM178-2	chr2:40341142-40341243	ENSG00000227028.2
6	lnc-TMEM178-2	chr2:40335064-40335843	ucscGeneNc_uc002rrw_2
7	lnc-TMEM178-2	chr2:40314104-40314153	ENSG00000227028.2
8	lnc-TMEM178-2	chr2:40314104-40314153	ENSG00000227028.2
9	lnc-TMEM178-2	chr2:40341142-40341243	ENSG00000227028.2
10	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
11	lnc-TMEM178-2	chr2:40292487-40292995	ENSG00000227028.2
12	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
13	lnc-TMEM178-2	chr2:40328301-40328397	ENSG00000227028.2
14	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
15	lnc-TMEM178-2	chr2:40350286-40350414	ENSG00000227028.2
16	lnc-TMEM178-2	chr2:40345529-40345645	ENSG00000227028.2
17	lnc-TMEM178-2	chr2:40299893-40300140	ENSG00000227028.2
18	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.1
19	lnc-TMEM178-2	chr2:40341678-40342293	ENSG00000227028.2
20	lnc-TMEM178-2	chr2:40342075-40342293	ENSG00000227028.2
21	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.1
22	lnc-TMEM178-2	chr2:40332328-40332418	ucscGeneNc_uc002rrw_2
23	lnc-TMEM178-2	chr2:40269490-40269613	ENSG00000227028.1
24	lnc-TMEM178-2	chr2:40341142-40341243	ENSG00000227028.2
25	lnc-TMEM178-2	chr2:40332301-40332562	ENSG00000227028.1
26	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
27	lnc-TMEM178-2	chr2:40332049-40332102	NONHSAT070261
28	lnc-TMEM178-2	chr2:40332049-40332461	ENSG00000227028.1
29	lnc-TMEM178-2	chr2:40270558-40270682	ENSG00000227028.1
30	lnc-SLC8A1-1	chr2:40324916-40328505	NONHSAT070272
31	lnc-TMEM178-2	chr2:40332049-40332102	ENSG00000227028.2
32	lnc-TMEM178-2	chr2:40350286-40350414	ENSG00000227028.2
33	lnc-TMEM178-2	chr2:40314104-40314153	ENSG00000227028.2
34	lnc-TMEM178-2	chr2:40314104-40314153	ENSG00000227028.2
35	lnc-TMEM178-2	chr2:40332049-40332102	NONHSAT070263
36	lnc-TMEM178-2	chr2:40342169-40342293	ENSG00000227028.1
37	lnc-TMEM178-2	chr2:40347844-40347940	ENSG00000227028.2
38	lnc-TMEM178-2	chr2:40292493-40292612	ENSG00000227028.2

No data

Variant related genes	Relation type
SLC8A1-AS1	TF binding region
SLC8A1-AS1	CpG island
ENSG00000227028	chromatin interactions

Extended variants
information (count: 8917 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:8917 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544923663	chr2:40188793-40188794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182322895	chr2:40188798-40188799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185040882	chr2:40188799-40188800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188190667	chr2:40188804-40188805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181038466	chr2:40188809-40188810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528083956	chr2:40188822-40188823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546665689	chr2:40188823-40188824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571300070	chr2:40188837-40188838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117436136	chr2:40188849-40188850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551722262	chr2:40188855-40188856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552633095	chr2:40188868-40188869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140356063	chr2:40188885-40188886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111750813	chr2:40188895-40188896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556100107	chr2:40188920-40188921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565253821	chr2:40188928-40188929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574044755	chr2:40188947-40188948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185559296	chr2:40188950-40188951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553431318	chr2:40188965-40188966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs13391265	chr2:40188969-40188970	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs545497618	chr2:40189007-40189008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2080298	chr2:40189011-40189012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs113334894	chr2:40189051-40189052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542469616	chr2:40189061-40189062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191447581	chr2:40189098-40189099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2080297	chr2:40189109-40189110	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546305530	chr2:40189121-40189122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564977196	chr2:40189131-40189132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144622042	chr2:40189141-40189142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550674526	chr2:40189151-40189152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539956720	chr2:40189194-40189195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138438917	chr2:40189195-40189196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549691086	chr2:40189244-40189245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149283365	chr2:40189253-40189254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144313195	chr2:40189266-40189267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148772788	chr2:40189270-40189271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554915896	chr2:40189315-40189316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577986225	chr2:40189317-40189318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538709823	chr2:40189356-40189357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183604429	chr2:40189445-40189446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575085559	chr2:40189465-40189466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186894941	chr2:40189496-40189497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192285915	chr2:40189522-40189523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573535484	chr2:40189525-40189526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544230161	chr2:40189530-40189531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573088073	chr2:40189534-40189535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540536915	chr2:40189554-40189555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564699861	chr2:40189571-40189572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141557295	chr2:40189624-40189625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78490122	chr2:40189626-40189627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544284461	chr2:40189627-40189628	Weak transcription	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
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
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	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	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	21364760	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40176200-40195200	Weak transcription	HSMM	muscle
2	chr2:40182000-40218000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:40194000-40194600	Enhancers	NHDF-Ad	bronchial
4	chr2:40194000-40196400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:40195200-40195400	ZNF genes & repeats	HSMM	muscle
6	chr2:40195400-40199200	Weak transcription	HSMM	muscle
7	chr2:40202400-40203800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:40202600-40203400	Enhancers	Dnd41	blood
9	chr2:40202600-40203800	Enhancers	Fetal Stomach	stomach
10	chr2:40202600-40204600	Enhancers	Ovary	ovary
11	chr2:40203000-40203400	Enhancers	Fetal Lung	lung
12	chr2:40203400-40204200	Weak transcription	Dnd41	blood
13	chr2:40203800-40209000	Weak transcription	Fetal Stomach	stomach
14	chr2:40204200-40204400	Enhancers	Dnd41	blood
15	chr2:40204400-40206200	Weak transcription	Dnd41	blood
16	chr2:40204600-40209000	Weak transcription	Ovary	ovary
17	chr2:40208400-40209000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:40208400-40209200	Enhancers	Stomach Smooth Muscle	stomach
19	chr2:40208400-40210000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr2:40208600-40209800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr2:40208800-40209000	Enhancers	NHDF-Ad	bronchial
22	chr2:40208800-40209200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr2:40208800-40209800	Enhancers	Colon Smooth Muscle	Colon
24	chr2:40209000-40209400	Enhancers	Fetal Muscle Leg	muscle
25	chr2:40209000-40209600	Enhancers	Fetal Stomach	stomach
26	chr2:40209000-40209600	Enhancers	Ovary	ovary
27	chr2:40209600-40209800	Enhancers	NHDF-Ad	bronchial
28	chr2:40216800-40218200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr2:40217000-40219200	Enhancers	Osteobl	bone
30	chr2:40217200-40218200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:40217200-40219400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:40217400-40217600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:40217400-40219400	Enhancers	HSMM	muscle
34	chr2:40217600-40218600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:40217800-40219000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:40217800-40219200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr2:40217800-40219200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr2:40217800-40219400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr2:40218000-40218400	Enhancers	HSMMtube	muscle
40	chr2:40218000-40219000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr2:40218000-40219400	Enhancers	NHDF-Ad	bronchial
42	chr2:40218200-40221000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr2:40218200-40222600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr2:40218400-40218800	Weak transcription	HSMMtube	muscle
45	chr2:40218400-40219000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr2:40218400-40225200	Weak transcription	Fetal Kidney	kidney
47	chr2:40218600-40219000	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr2:40218600-40219000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr2:40218600-40220000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:40218800-40219000	Enhancers	HSMMtube	muscle

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