Variant report

Variant	nsv1003896
Chromosome Location	chr2:40094081-40231585
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	chr2:40140743-40141194	HepG2	liver:	n/a	n/a
2	ATF1	chr2:40217162-40217725	K562	blood:	n/a	n/a
3	ATF1	chr2:40223765-40224372	K562	blood:	n/a	n/a
4	ATF1	chr2:40222613-40222712	K562	blood:	n/a	n/a
5	BACH1	chr2:40208471-40208655	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:40149983-40150021	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr2:40140740-40141114	GM12878	blood:	n/a	n/a
8	CBX3	chr2:40223784-40224393	HCT-116	colon:	n/a	n/a
9	CCNT2	chr2:40224014-40224213	K562	blood:	n/a	n/a
10	CEBPB	chr2:40223679-40224438	HCT-116	colon:	n/a	n/a
11	CEBPB	chr2:40218547-40218785	A549	lung:	n/a	chr2:40218674-40218685
12	CEBPB	chr2:40140745-40141199	MCF-7	breast:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
13	CEBPB	chr2:40223962-40224177	A549	lung:	n/a	n/a
14	CEBPB	chr2:40140766-40141153	MCF-7	breast:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
15	CEBPB	chr2:40109129-40109399	HepG2	liver:	n/a	chr2:40109315-40109326
16	CEBPB	chr2:40140785-40141280	IMR90	lung:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
17	CEBPB	chr2:40140765-40141163	H1-hESC	embryonic stem cell:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
18	CEBPB	chr2:40102298-40102797	A549	lung:	n/a	n/a
19	CEBPB	chr2:40194909-40195167	H1-hESC	embryonic stem cell:	n/a	chr2:40195008-40195019
20	CEBPB	chr2:40157413-40157574	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:40218557-40218771	H1-hESC	embryonic stem cell:	n/a	chr2:40218674-40218685
22	CEBPB	chr2:40223752-40224243	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:40221391-40221660	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:40099919-40100201	A549	lung:	n/a	chr2:40100075-40100086 chr2:40100077-40100086 chr2:40100075-40100088 chr2:40100076-40100087
25	CEBPB	chr2:40103180-40103257	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:40099988-40100193	IMR90	lung:	n/a	chr2:40100075-40100086 chr2:40100077-40100086 chr2:40100075-40100088 chr2:40100076-40100087
27	CEBPB	chr2:40132841-40132864	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:40140744-40141140	Hela-S3	cervix:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
29	CEBPB	chr2:40099903-40100249	HepG2	liver:	n/a	chr2:40100075-40100086 chr2:40100077-40100086 chr2:40100075-40100088 chr2:40100076-40100087
30	CEBPB	chr2:40102314-40103169	IMR90	lung:	n/a	chr2:40102862-40102870 chr2:40102918-40102929
31	CEBPB	chr2:40102341-40102721	MCF-7	breast:	n/a	n/a
32	CEBPB	chr2:40103034-40103345	MCF-7	breast:	n/a	n/a
33	CEBPB	chr2:40102210-40102846	A549	lung:	n/a	n/a
34	CEBPB	chr2:40140795-40141098	K562	blood:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
35	CEBPB	chr2:40187092-40187228	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr2:40223859-40224267	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:40223865-40224375	HCT-116	colon:	n/a	n/a
38	CEBPB	chr2:40102344-40103213	A549	lung:	n/a	chr2:40102862-40102870 chr2:40102918-40102929
39	CEBPB	chr2:40101859-40102061	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:40099920-40100158	K562	blood:	n/a	chr2:40100075-40100086 chr2:40100077-40100086 chr2:40100075-40100088 chr2:40100076-40100087
41	CEBPB	chr2:40194850-40195177	HepG2	liver:	n/a	chr2:40195008-40195019
42	CEBPB	chr2:40099979-40100144	H1-hESC	embryonic stem cell:	n/a	chr2:40100075-40100086 chr2:40100077-40100086 chr2:40100075-40100088 chr2:40100076-40100087
43	CEBPB	chr2:40187059-40187300	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:40218494-40218859	IMR90	lung:	n/a	chr2:40218674-40218685
45	CEBPB	chr2:40109105-40109372	A549	lung:	n/a	chr2:40109315-40109326
46	CEBPB	chr2:40218529-40218785	HepG2	liver:	n/a	chr2:40218674-40218685
47	CEBPB	chr2:40144232-40144363	A549	lung:	n/a	n/a
48	CEBPB	chr2:40194890-40195200	A549	lung:	n/a	chr2:40195008-40195019
49	CEBPB	chr2:40194970-40195037	K562	blood:	n/a	chr2:40195008-40195019
50	CEBPB	chr2:40140796-40141140	A549	lung:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40102810-40102860	K562	blood:	n/a
2	chr2:40147801-40147851	NH-A	brain:	n/a
3	chr2:40140929-40140979	AG10803	skin:	n/a
4	chr2:40097661-40097711	GM12892	blood:	n/a
5	chr2:40149258-40149308	U87	brain:	n/a
6	chr2:40165558-40165608	PrEC	prostate:	n/a
7	chr2:40149258-40149308	GM19239	blood:	n/a
8	chr2:40097661-40097711	GM06990	blood:	n/a
9	chr2:40097661-40097711	HMEC	breast:	n/a
10	chr2:40097661-40097711	MCF10A-Er-Src	breast:	n/a
11	chr2:40203342-40203392	HMEC	breast:	n/a
12	chr2:40140929-40140979	AG04449	skin:	fetal
13	chr2:40149258-40149308	HUVEC	blood vessel:	n/a
14	chr2:40097661-40097711	SK-N-SH_RA	brain:	n/a
15	chr2:40147801-40147851	Hepatocyte	liver:	n/a
16	chr2:40203342-40203392	HUVEC	blood vessel:	n/a
17	chr2:40102810-40102860	U87	brain:	n/a
18	chr2:40140929-40140979	AG09309	skin:	n/a
19	chr2:40149258-40149308	SK-N-MC	brain:	n/a
20	chr2:40147801-40147851	SAEC	small airway:	n/a
21	chr2:40165558-40165608	NHDF-neo	bronchial:	n/a
22	chr2:40203342-40203392	BJ	skin:	n/a
23	chr2:40097661-40097711	PFSK-1	brain:	n/a
24	chr2:40149258-40149308	GM12891	blood:	n/a
25	chr2:40147801-40147851	HCM	heart:	n/a
26	chr2:40203342-40203392	Hela-S3	cervix:	n/a
27	chr2:40147801-40147851	HCF	heart:	n/a
28	chr2:40165558-40165608	HEEpiC	esophagus:	n/a
29	chr2:40165558-40165608	RPTEC	kidney:	n/a
30	chr2:40149258-40149308	Hela-S3	cervix:	n/a
31	chr2:40140929-40140979	HCPEpiC	choroid plexus:	n/a
32	chr2:40140929-40140979	AG04450	lung:	fetal
33	chr2:40147801-40147851	CMK	blood:	n/a
34	chr2:40203342-40203392	HNPCEpiC	eye:	n/a
35	chr2:40147801-40147851	MCF-7	breast:	n/a
36	chr2:40097661-40097711	HCT-116	colon:	n/a
37	chr2:40165558-40165608	GM12891	blood:	n/a
38	chr2:40140929-40140979	MCF10A-Er-Src	breast:	n/a
39	chr2:40165558-40165608	AG09309	skin:	n/a
40	chr2:40165558-40165608	HCPEpiC	choroid plexus:	n/a
41	chr2:40149258-40149308	HRCEpiC	kidney:	n/a
42	chr2:40140929-40140979	HEEpiC	esophagus:	n/a
43	chr2:40140929-40140979	HRPEpiC	eye:	n/a
44	chr2:40203342-40203392	HepG2	liver:	n/a
45	chr2:40102810-40102860	SK-N-SH_RA	brain:	n/a
46	chr2:40165558-40165608	GM12892	blood:	n/a
47	chr2:40140929-40140979	RPTEC	kidney:	n/a
48	chr2:40147801-40147851	GM12878	blood:	n/a
49	chr2:40102810-40102860	HMEC	breast:	n/a
50	chr2:40165558-40165608	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:
2	chr2:40004496..40006686-chr2:40138159..40140367,2	MCF-7	breast:
3	chr2:40140445..40141319-chr2:41925707..41926458,2	K562	blood:
4	chr2:40140455..40141410-chr2:40986765..40987805,5	MCF-7	breast:
5	chr2:40127848..40131758-chr2:40131769..40134520,3	K562	blood:
6	chr2:40100537..40101165-chr2:40112091..40112603,2	MCF-7	breast:
7	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:
8	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
9	chr2:40140472..40141253-chr2:40471871..40472400,2	MCF-7	breast:
10	chr2:39991894..39993577-chr2:40151910..40153730,2	K562	blood:
11	chr2:40127848..40131758-chr2:40131769..40134520,3	K562	blood:
12	chr2:40140709..40141329-chr2:40986882..40987436,2	MCF-7	breast:
13	chr2:40140525..40141334-chr2:42009019..42009970,2	K562	blood:
14	chr2:40100537..40101165-chr2:40112091..40112603,2	MCF-7	breast:
15	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
16	chr2:40140915..40141986-chr2:40781509..40782393,3	MCF-7	breast:
17	chr2:40081608..40083244-chr2:40101423..40104022,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40185553-40185606	ucscGeneNc_uc002rrw_2
2	lnc-TMEM178-2	chr2:40144774-40144799	NONHSAT070261
3	lnc-TMEM178-2	chr2:40146833-40146923	ENSG00000227028.1
4	lnc-TMEM178-2	chr2:40149990-40150029	NONHSAT070263
5	lnc-TMEM178-2	chr2:40149989-40150029	ENSG00000227028.1
6	lnc-TMEM178-2	chr2:40149989-40150029	NONHSAT070261

Variant related genes	Relation type
ENSG00000235653	TF binding region
SLC8A1-AS1	TF binding region
ENSG00000235653	CpG island
SLC8A1-AS1	CpG island
ENSG00000138050	chromatin interactions

Extended variants
information (count: 6450 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:6450 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12475386	chr2:40094081-40094082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145271738	chr2:40094082-40094083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150591418	chr2:40094119-40094120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139444268	chr2:40094151-40094152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565554198	chr2:40094168-40094169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115821718	chr2:40094170-40094171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528580663	chr2:40094176-40094177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531449173	chr2:40094191-40094192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532874373	chr2:40094199-40094200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550689870	chr2:40094218-40094219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569280107	chr2:40094245-40094246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34712279	chr2:40094252-40094253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs398080196	chr2:40094253-40094254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs397870583	chr2:40094254-40094255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536308997	chr2:40094334-40094335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375300840	chr2:40094356-40094357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548293268	chr2:40094368-40094369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369965530	chr2:40094393-40094394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533717500	chr2:40094441-40094442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571419273	chr2:40094447-40094448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149672108	chr2:40094459-40094460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555585706	chr2:40094483-40094484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538188267	chr2:40094519-40094520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555841344	chr2:40094529-40094530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574381469	chr2:40094534-40094535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183991047	chr2:40094555-40094556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375384564	chr2:40094613-40094614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188773291	chr2:40094614-40094615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372522571	chr2:40094656-40094657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569827231	chr2:40094675-40094676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540814101	chr2:40094680-40094681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6751368	chr2:40094708-40094709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs181667068	chr2:40094735-40094736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145474675	chr2:40094790-40094791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs17480400	chr2:40094801-40094802	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
36	rs140279234	chr2:40094816-40094817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185115834	chr2:40094836-40094837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113851980	chr2:40094864-40094865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369255224	chr2:40094876-40094877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146845334	chr2:40094906-40094907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140667322	chr2:40094921-40094922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528366819	chr2:40094925-40094926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550970022	chr2:40094927-40094928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533008305	chr2:40094992-40094993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555358284	chr2:40094994-40094995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567430955	chr2:40095017-40095018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199783687	chr2:40095037-40095038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373380329	chr2:40095045-40095046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556435276	chr2:40095058-40095059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567933195	chr2:40095060-40095061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:574 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40093200-40097200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:40093600-40097200	Weak transcription	HMEC	breast
3	chr2:40094000-40098400	Weak transcription	Dnd41	blood
4	chr2:40097000-40098800	Enhancers	Fetal Stomach	stomach
5	chr2:40097200-40097400	Enhancers	Brain Anterior Caudate	brain
6	chr2:40097200-40098400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr2:40097200-40098600	Enhancers	HSMMtube	muscle
8	chr2:40097200-40098800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr2:40097200-40098800	Enhancers	NHLF	lung
10	chr2:40097200-40099200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:40097200-40099200	Enhancers	HMEC	breast
12	chr2:40097200-40099200	Enhancers	NHEK	skin
13	chr2:40097400-40097800	Enhancers	Fetal Heart	heart
14	chr2:40097400-40098000	Weak transcription	Brain Anterior Caudate	brain
15	chr2:40097400-40098400	Enhancers	Stomach Smooth Muscle	stomach
16	chr2:40097400-40099200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr2:40097400-40099200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr2:40097400-40099200	Enhancers	NH-A	brain
19	chr2:40097400-40099200	Enhancers	NHDF-Ad	bronchial
20	chr2:40097400-40099200	Enhancers	Osteobl	bone
21	chr2:40097400-40099400	Enhancers	HSMM	muscle
22	chr2:40097600-40098200	Enhancers	Muscle Satellite Cultured Cells	--
23	chr2:40097600-40098400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr2:40097600-40099000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr2:40097600-40099400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:40098000-40098600	Enhancers	Brain Anterior Caudate	brain
27	chr2:40098000-40098600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr2:40098000-40099200	Enhancers	Fetal Muscle Leg	muscle
29	chr2:40098200-40098800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:40098200-40098800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
31	chr2:40098200-40098800	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr2:40098200-40098800	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr2:40098400-40098600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr2:40098400-40098600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr2:40098400-40098800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr2:40098400-40098800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr2:40098400-40098800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr2:40098400-40098800	Enhancers	Dnd41	blood
39	chr2:40098400-40099000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:40098400-40099000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr2:40098400-40099000	Enhancers	Colon Smooth Muscle	Colon
42	chr2:40098400-40102200	Weak transcription	Stomach Smooth Muscle	stomach
43	chr2:40098600-40099000	Enhancers	Fetal Brain Female	brain
44	chr2:40098600-40099200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:40098600-40099200	Flanking Active TSS	HSMMtube	muscle
46	chr2:40098600-40102400	Weak transcription	Brain Anterior Caudate	brain
47	chr2:40098600-40102400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr2:40098800-40099400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr2:40098800-40099400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr2:40098800-40101400	Weak transcription	NHLF	lung

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