Variant report

Variant	nsv873891
Chromosome Location	chr2:40046658-40173905
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	chr2:40063976-40064113	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:40048059-40048309	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:40140743-40141194	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:40065069-40065346	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:40064934-40065232	K562	blood:	n/a	n/a
6	ATF1	chr2:40061595-40061892	K562	blood:	n/a	n/a
7	BACH1	chr2:40149983-40150021	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:40081958-40081966	K562	blood:	n/a	n/a
9	BCLAF1	chr2:40140740-40141114	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:40065039-40065357	K562	blood:	n/a	n/a
11	BHLHE40	chr2:40065052-40065398	HepG2	liver:	n/a	n/a
12	CBX3	chr2:40072443-40073031	HCT-116	colon:	n/a	n/a
13	CBX3	chr2:40063705-40064135	HCT-116	colon:	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	chr2:40144232-40144363	A549	lung:	n/a	n/a
16	CEBPB	chr2:40109105-40109372	A549	lung:	n/a	chr2:40109315-40109326
17	CEBPB	chr2:40099979-40100144	H1-hESC	embryonic stem cell:	n/a	chr2:40100075-40100086 chr2:40100077-40100086 chr2:40100075-40100088 chr2:40100076-40100087
18	CEBPB	chr2:40103034-40103345	MCF-7	breast:	n/a	n/a
19	CEBPB	chr2:40102344-40103213	A549	lung:	n/a	chr2:40102862-40102870 chr2:40102918-40102929
20	CEBPB	chr2:40109129-40109399	HepG2	liver:	n/a	chr2:40109315-40109326
21	CEBPB	chr2:40099920-40100158	K562	blood:	n/a	chr2:40100075-40100086 chr2:40100077-40100086 chr2:40100075-40100088 chr2:40100076-40100087
22	CEBPB	chr2:40140785-40141280	IMR90	lung:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
23	CEBPB	chr2:40073005-40073172	A549	lung:	n/a	n/a
24	CEBPB	chr2:40157413-40157574	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:40103180-40103257	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:40102210-40102846	A549	lung:	n/a	n/a
27	CEBPB	chr2:40140744-40141140	Hela-S3	cervix:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
28	CEBPB	chr2:40099903-40100249	HepG2	liver:	n/a	chr2:40100075-40100086 chr2:40100077-40100086 chr2:40100075-40100088 chr2:40100076-40100087
29	CEBPB	chr2:40102298-40102797	A549	lung:	n/a	n/a
30	CEBPB	chr2:40101859-40102061	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:40140796-40141140	A549	lung:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
32	CEBPB	chr2:40099919-40100201	A549	lung:	n/a	chr2:40100075-40100086 chr2:40100077-40100086 chr2:40100075-40100088 chr2:40100076-40100087
33	CEBPB	chr2:40140745-40141199	MCF-7	breast:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
34	CEBPB	chr2:40073533-40073760	A549	lung:	n/a	n/a
35	CEBPB	chr2:40140795-40141098	K562	blood:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
36	CEBPB	chr2:40102314-40103169	IMR90	lung:	n/a	chr2:40102862-40102870 chr2:40102918-40102929
37	CEBPB	chr2:40140765-40141163	H1-hESC	embryonic stem cell:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
38	CEBPB	chr2:40132841-40132864	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:40102341-40102721	MCF-7	breast:	n/a	n/a
40	CEBPB	chr2:40099988-40100193	IMR90	lung:	n/a	chr2:40100075-40100086 chr2:40100077-40100086 chr2:40100075-40100088 chr2:40100076-40100087
41	CHD1	chr2:40140686-40141899	IMR90	lung:	n/a	n/a
42	CTCF	chr2:40079140-40079290	MCF-7	breast:	n/a	chr2:40079196-40079217
43	CTCF	chr2:40140793-40140983	LNCaP	prostate:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
44	CTCF	chr2:40140800-40140950	WERI-Rb-1	eye:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
45	CTCF	chr2:40065420-40065570	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr2:40065404-40065476	GM12891	blood:	n/a	n/a
47	CTCF	chr2:40140820-40140970	HUVEC	blood vessel:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
48	CTCF	chr2:40079100-40079250	HVMF	connective:	n/a	chr2:40079196-40079217
49	CTCF	chr2:40065007-40065443	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:40140740-40141042	HepG2	liver:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40140929-40140979	LNCaP	prostate:	n/a
2	chr2:40140929-40140979	LNCaP	prostate:	n/a
3	chr2:40102810-40102860	K562	blood:	n/a
4	chr2:40140929-40140979	ProgFib	skin:	n/a
5	chr2:40165558-40165608	HRE	kidney:	n/a
6	chr2:40147801-40147851	HepG2	liver:	n/a
7	chr2:40097661-40097711	Hepatocyte	liver:	n/a
8	chr2:40102810-40102860	HNPCEpiC	eye:	n/a
9	chr2:40097661-40097711	HIPEpiC	eye:	n/a
10	chr2:40147801-40147851	CMK	blood:	n/a
11	chr2:40102810-40102860	SK-N-MC	brain:	n/a
12	chr2:40147801-40147851	K562	blood:	n/a
13	chr2:40147801-40147851	ECC-1	luminal epithelium:	n/a
14	chr2:40149258-40149308	HIPEpiC	eye:	n/a
15	chr2:40165558-40165608	Jurkat	blood:	n/a
16	chr2:40149258-40149308	NB4	blood:	n/a
17	chr2:40165558-40165608	ECC-1	luminal epithelium:	n/a
18	chr2:40140929-40140979	NB4	blood:	n/a
19	chr2:40165558-40165608	BJ	skin:	n/a
20	chr2:40102810-40102860	T-47D	breast:	n/a
21	chr2:40102810-40102860	NB4	blood:	n/a
22	chr2:40147801-40147851	SK-N-SH	brain:	n/a
23	chr2:40149258-40149308	AG09309	skin:	n/a
24	chr2:40102810-40102860	A549	lung:	n/a
25	chr2:40097661-40097711	HCPEpiC	choroid plexus:	n/a
26	chr2:40097661-40097711	SKMC	muscle:	n/a
27	chr2:40165558-40165608	HepG2	liver:	n/a
28	chr2:40147801-40147851	MCF-7	breast:	n/a
29	chr2:40147801-40147851	RPTEC	kidney:	n/a
30	chr2:40102810-40102860	HRPEpiC	eye:	n/a
31	chr2:40097661-40097711	HNPCEpiC	eye:	n/a
32	chr2:40165558-40165608	HIPEpiC	eye:	n/a
33	chr2:40140929-40140979	HRE	kidney:	n/a
34	chr2:40147801-40147851	Jurkat	blood:	n/a
35	chr2:40097661-40097711	AG10803	skin:	n/a
36	chr2:40140929-40140979	HUVEC	blood vessel:	n/a
37	chr2:40097661-40097711	NH-A	brain:	n/a
38	chr2:40140929-40140979	T-47D	breast:	n/a
39	chr2:40165558-40165608	K562	blood:	n/a
40	chr2:40149258-40149308	HUVEC	blood vessel:	n/a
41	chr2:40165558-40165608	GM12892	blood:	n/a
42	chr2:40102810-40102860	HCM	heart:	n/a
43	chr2:40097661-40097711	K562	blood:	n/a
44	chr2:40147801-40147851	HIPEpiC	eye:	n/a
45	chr2:40097661-40097711	HUVEC	blood vessel:	n/a
46	chr2:40147801-40147851	Hela-S3	cervix:	n/a
47	chr2:40165558-40165608	Hela-S3	cervix:	n/a
48	chr2:40097661-40097711	HRCEpiC	kidney:	n/a
49	chr2:40140929-40140979	K562	blood:	n/a
50	chr2:40149258-40149308	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:40140445..40141319-chr2:41925707..41926458,2	K562	blood:
2	chr2:40140525..40141334-chr2:42009019..42009970,2	K562	blood:
3	chr2:40039211..40041944-chr2:40045536..40047144,2	MCF-7	breast:
4	chr2:40081608..40083244-chr2:40101423..40104022,3	MCF-7	breast:
5	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
6	chr2:39991894..39993577-chr2:40151910..40153730,2	K562	blood:
7	chr2:40140472..40141253-chr2:40471871..40472400,2	MCF-7	breast:
8	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
9	chr2:39996683..39999283-chr2:40048598..40050382,2	K562	blood:
10	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:
11	chr2:40064756..40065596-chr2:40082708..40083242,2	MCF-7	breast:
12	chr2:40127848..40131758-chr2:40131769..40134520,3	K562	blood:
13	chr2:40071382..40074146-chr2:40078508..40080014,2	MCF-7	breast:
14	chr2:40004496..40006686-chr2:40138159..40140367,2	MCF-7	breast:
15	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:
16	chr2:39606937..39607476-chr2:40065093..40065933,2	MCF-7	breast:
17	chr2:40140455..40141410-chr2:40986765..40987805,5	MCF-7	breast:
18	chr2:40071382..40074146-chr2:40078508..40080014,2	MCF-7	breast:
19	chr2:40140709..40141329-chr2:40986882..40987436,2	MCF-7	breast:
20	chr2:40100537..40101165-chr2:40112091..40112603,2	MCF-7	breast:
21	chr2:40064756..40065596-chr2:40082708..40083242,2	MCF-7	breast:
22	chr2:40127848..40131758-chr2:40131769..40134520,3	K562	blood:
23	chr2:40100537..40101165-chr2:40112091..40112603,2	MCF-7	breast:
24	chr2:40081608..40083244-chr2:40101423..40104022,3	MCF-7	breast:
25	chr2:40140915..40141986-chr2:40781509..40782393,3	MCF-7	breast:

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

Variant related genes	Relation type
ENSG00000235653	TF binding region
SLC8A1-AS1	TF binding region
ENSG00000235653	CpG island
SLC8A1-AS1	CpG island
ENSG00000138050	chromatin interactions
ENSG00000011566	chromatin interactions

Extended variants
information (count: 4431 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4431 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544408771	chr2:40048010-40048011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs79031264	chr2:40048031-40048032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574649775	chr2:40048037-40048038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555350514	chr2:40048049-40048050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80037550	chr2:40048052-40048053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150406628	chr2:40048167-40048168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527272919	chr2:40048171-40048172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76485987	chr2:40048173-40048174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544316059	chr2:40048192-40048193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563829639	chr2:40048215-40048216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531316327	chr2:40048229-40048230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550716459	chr2:40048244-40048245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149159015	chr2:40048257-40048258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143307210	chr2:40048270-40048271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548583712	chr2:40048321-40048322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189210073	chr2:40048335-40048336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190611157	chr2:40048341-40048342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138666685	chr2:40048344-40048345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115073654	chr2:40048367-40048368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs77143907	chr2:40048626-40048627	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs79475690	chr2:40048631-40048632	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs115520788	chr2:40048635-40048636	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545353635	chr2:40048724-40048725	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563744159	chr2:40048754-40048755	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs145519105	chr2:40048773-40048774	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs541289156	chr2:40048783-40048784	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543128193	chr2:40048813-40048814	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182208488	chr2:40048842-40048843	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs561855613	chr2:40048898-40048899	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs13035930	chr2:40048923-40048924	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs138142375	chr2:40048994-40048995	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs186895396	chr2:40049022-40049023	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs532781362	chr2:40049052-40049053	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548807843	chr2:40049059-40049060	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs72789110	chr2:40049066-40049067	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7601124	chr2:40049067-40049068	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs117743394	chr2:40049072-40049073	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552556884	chr2:40049097-40049098	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529739523	chr2:40049098-40049099	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs141615563	chr2:40049140-40049141	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538279167	chr2:40049146-40049147	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs73924993	chr2:40049201-40049202	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs568590498	chr2:40049228-40049229	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs4670971	chr2:40049301-40049302	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546638607	chr2:40049323-40049324	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs191742803	chr2:40049343-40049344	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs57881063	chr2:40049367-40049368	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs530524602	chr2:40049418-40049419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184109278	chr2:40049427-40049428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs557295503	chr2:40049463-40049464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40048000-40048400	Enhancers	Liver	Liver
2	chr2:40048800-40049400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr2:40048800-40049400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr2:40048800-40049400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:40049000-40049800	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr2:40049400-40050600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:40050600-40050800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:40057600-40058200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr2:40057600-40058400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr2:40057600-40058400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr2:40057600-40058400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:40057800-40058000	Enhancers	Esophagus	oesophagus
13	chr2:40057800-40058400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr2:40058000-40058200	Active TSS	Esophagus	oesophagus
15	chr2:40058000-40058400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:40058200-40058400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:40058200-40058400	Bivalent/Poised TSS	Esophagus	oesophagus
18	chr2:40058400-40058600	Bivalent Enhancer	Esophagus	oesophagus
19	chr2:40061200-40062000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr2:40065200-40065400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:40065200-40066000	Enhancers	K562	blood
22	chr2:40065200-40066400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:40065200-40067200	Enhancers	Fetal Thymus	thymus
24	chr2:40065400-40066000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:40065400-40066600	Enhancers	Esophagus	oesophagus
26	chr2:40065600-40067200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr2:40066000-40066200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr2:40066200-40066400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr2:40066200-40067000	Enhancers	GM12878-XiMat	blood
30	chr2:40066400-40066600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr2:40070800-40071600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr2:40072000-40073600	Enhancers	HMEC	breast
33	chr2:40072200-40072600	Enhancers	Placenta Amnion	Placenta Amnion
34	chr2:40072200-40073400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr2:40072200-40073400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:40072400-40073400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr2:40072400-40073800	Enhancers	NHEK	skin
38	chr2:40073200-40074400	Enhancers	Dnd41	blood
39	chr2:40073400-40077000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:40073400-40077800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr2:40073400-40078200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr2:40073600-40077000	Weak transcription	HMEC	breast
43	chr2:40074400-40074800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr2:40074400-40076400	Weak transcription	Dnd41	blood
45	chr2:40076200-40076400	Enhancers	Fetal Kidney	kidney
46	chr2:40076200-40080000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr2:40076400-40076600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr2:40076400-40076600	Enhancers	HSMMtube	muscle
49	chr2:40076400-40079000	Enhancers	Dnd41	blood
50	chr2:40076600-40077200	Weak transcription	HSMMtube	muscle

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