Variant report

Variant	esv1821275
Chromosome Location	chr2:36991736-37018278
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	ATF1	chr2:37005015-37005196	K562	blood:	n/a	n/a
2	ATF1	chr2:37012380-37012653	K562	blood:	n/a	n/a
3	ATF2	chr2:36997856-36998247	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr2:37012264-37012833	A549	lung:	n/a	n/a
5	ATF3	chr2:37012375-37012760	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:36997827-36998168	K562	blood:	n/a	n/a
7	BHLHE40	chr2:37007503-37007700	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:36997791-36998222	K562	blood:	n/a	n/a
9	BRCA1	chr2:36997868-36998219	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr2:37012480-37012596	HepG2	liver:	n/a	n/a
11	CBX3	chr2:36997838-36998291	K562	blood:	n/a	n/a
12	CBX3	chr2:37012287-37012690	K562	blood:	n/a	n/a
13	CEBPB	chr2:36996292-36996544	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:37007480-37007784	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:36996259-36996565	A549	lung:	n/a	n/a
16	CEBPB	chr2:37000110-37000412	K562	blood:	n/a	chr2:37000128-37000139 chr2:37000126-37000139
17	CEBPB	chr2:37007429-37007807	A549	lung:	n/a	n/a
18	CEBPZ	chr2:37009909-37010041	HepG2	liver:	n/a	n/a
19	CHD1	chr2:36997760-36997996	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr2:37012425-37012647	HepG2	liver:	n/a	n/a
21	CHD2	chr2:36997886-36998068	K562	blood:	n/a	n/a
22	CTCF	chr2:37005076-37005209	HepG2	liver:	n/a	chr2:37005136-37005157 chr2:37005135-37005151 chr2:37005134-37005152
23	CTCF	chr2:36997870-36998210	T-47D	breast:	n/a	chr2:36998027-36998043 chr2:36998083-36998101 chr2:36998026-36998044 chr2:36998028-36998041 chr2:36998028-36998041
24	CTCF	chr2:37013166-37013248	GM19239	blood:	n/a	n/a
25	CTCF	chr2:36997920-36998070	HPF	lung:	n/a	chr2:36998027-36998043 chr2:36998026-36998044 chr2:36998028-36998041 chr2:36998028-36998041
26	CTCF	chr2:37013880-37014030	Caco-2	colon:	n/a	n/a
27	CTCF	chr2:36997980-36998130	SK-N-SH_RA	brain:	n/a	chr2:36998027-36998043 chr2:36998083-36998101 chr2:36998026-36998044 chr2:36998028-36998041 chr2:36998028-36998041
28	CTCF	chr2:37007480-37007630	SAEC	small airway:	n/a	chr2:37007555-37007576 chr2:37007554-37007570 chr2:37007553-37007571
29	CTCF	chr2:36997907-36998172	MCF-7	breast:	n/a	chr2:36998027-36998043 chr2:36998083-36998101 chr2:36998026-36998044 chr2:36998028-36998041 chr2:36998028-36998041
30	CTCF	chr2:37007480-37007630	HUVEC	blood vessel:	n/a	chr2:37007555-37007576 chr2:37007554-37007570 chr2:37007553-37007571
31	CTCF	chr2:37012820-37012970	BJ	skin:	n/a	n/a
32	CTCF	chr2:37012440-37012590	HCPEpiC	choroid plexus:	n/a	chr2:37012503-37012521 chr2:37012510-37012518 chr2:37012505-37012518 chr2:37012504-37012520 chr2:37012498-37012519
33	CTCF	chr2:37007460-37007610	K562	blood:	n/a	chr2:37007555-37007576 chr2:37007554-37007570 chr2:37007553-37007571
34	CTCF	chr2:37012420-37012570	GM12801	blood:	n/a	chr2:37012503-37012521 chr2:37012510-37012518 chr2:37012505-37012518 chr2:37012504-37012520 chr2:37012498-37012519
35	CTCF	chr2:37012368-37012655	GM19238	blood:	n/a	chr2:37012503-37012521 chr2:37012510-37012518 chr2:37012505-37012518 chr2:37012504-37012520 chr2:37012498-37012519
36	CTCF	chr2:37012400-37012550	GM12875	blood:	n/a	chr2:37012503-37012521 chr2:37012510-37012518 chr2:37012505-37012518 chr2:37012504-37012520 chr2:37012498-37012519
37	CTCF	chr2:36997920-36998070	HCT-116	colon:	n/a	chr2:36998027-36998043 chr2:36998026-36998044 chr2:36998028-36998041 chr2:36998028-36998041
38	CTCF	chr2:37007480-37007630	HCFaa	heart:	n/a	chr2:37007555-37007576 chr2:37007554-37007570 chr2:37007553-37007571
39	CTCF	chr2:37012460-37012610	SK-N-SH_RA	brain:	n/a	chr2:37012503-37012521 chr2:37012510-37012518 chr2:37012505-37012518 chr2:37012504-37012520 chr2:37012498-37012519
40	CTCF	chr2:36998000-36998150	HFF	foreskin:	n/a	chr2:36998027-36998043 chr2:36998083-36998101 chr2:36998026-36998044 chr2:36998028-36998041 chr2:36998028-36998041
41	CTCF	chr2:37012385-37012631	GM12891	blood:	n/a	chr2:37012503-37012521 chr2:37012510-37012518 chr2:37012505-37012518 chr2:37012504-37012520 chr2:37012498-37012519
42	CTCF	chr2:37012372-37012668	HUVEC	blood vessel:	n/a	chr2:37012503-37012521 chr2:37012510-37012518 chr2:37012505-37012518 chr2:37012504-37012520 chr2:37012498-37012519
43	CTCF	chr2:37002420-37002570	Caco-2	colon:	n/a	n/a
44	CTCF	chr2:36997960-36998110	GM06990	blood:	n/a	chr2:36998027-36998043 chr2:36998083-36998101 chr2:36998026-36998044 chr2:36998028-36998041 chr2:36998028-36998041
45	CTCF	chr2:37005105-37005220	LNCaP	prostate:	n/a	chr2:37005136-37005157 chr2:37005135-37005151 chr2:37005134-37005152
46	CTCF	chr2:37012131-37012761	MCF-7	breast:	n/a	chr2:37012503-37012521 chr2:37012510-37012518 chr2:37012505-37012518 chr2:37012504-37012520 chr2:37012498-37012519
47	CTCF	chr2:37007440-37007590	HA-sp	spinal cord:	n/a	chr2:37007555-37007576 chr2:37007554-37007570 chr2:37007553-37007571
48	CTCF	chr2:37012460-37012610	GM12868	blood:	n/a	chr2:37012503-37012521 chr2:37012510-37012518 chr2:37012505-37012518 chr2:37012504-37012520 chr2:37012498-37012519
49	CTCF	chr2:37007475-37007528	Fibrobl	skin:	n/a	n/a
50	CTCF	chr2:37007500-37007650	GM12864	blood:	n/a	chr2:37007555-37007576 chr2:37007554-37007570 chr2:37007553-37007571

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37012483-37012533	SK-N-MC	brain:	n/a
2	chr2:37012483-37012533	AG04449	skin:	fetal
3	chr2:37012483-37012533	PFSK-1	brain:	n/a
4	chr2:37012483-37012533	U87	brain:	n/a
5	chr2:37012483-37012533	GM12892	blood:	n/a
6	chr2:37012483-37012533	Jurkat	blood:	n/a
7	chr2:37012483-37012533	HNPCEpiC	eye:	n/a
8	chr2:37012483-37012533	AG09309	skin:	n/a
9	chr2:37012483-37012533	RPTEC	kidney:	n/a
10	chr2:37012483-37012533	Caco-2	colon:	n/a
11	chr2:37012483-37012533	NH-A	brain:	n/a
12	chr2:37012483-37012533	ovcar-3	ovarian:	n/a
13	chr2:37012483-37012533	SAEC	small airway:	n/a
14	chr2:37012483-37012533	HepG2	liver:	n/a
15	chr2:37012483-37012533	AoSMC	blood vessel:	n/a
16	chr2:37012483-37012533	GM12878	blood:	n/a
17	chr2:37012483-37012533	PrEC	prostate:	n/a
18	chr2:37012483-37012533	GM19239	blood:	n/a
19	chr2:37012483-37012533	GM12891	blood:	n/a
20	chr2:37012483-37012533	AG09319	gingival:	n/a
21	chr2:37012483-37012533	ECC-1	luminal epithelium:	n/a
22	chr2:37012483-37012533	HL-60	blood:	n/a
23	chr2:37012483-37012533	BJ	skin:	n/a
24	chr2:37012483-37012533	A549	lung:	n/a
25	chr2:37012483-37012533	NHDF-neo	bronchial:	n/a
26	chr2:37012483-37012533	HCM	heart:	n/a
27	chr2:37012483-37012533	MCF10A-Er-Src	breast:	n/a
28	chr2:37012483-37012533	H1-hESC	embryonic stem cell:	embryo
29	chr2:37012483-37012533	CMK	blood:	n/a
30	chr2:37012483-37012533	HMEC	breast:	n/a
31	chr2:37012483-37012533	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:37012483-37012533	IMR90	lung:	fetal
33	chr2:37012483-37012533	SK-N-SH	brain:	n/a
34	chr2:37012483-37012533	HRE	kidney:	n/a
35	chr2:37012483-37012533	HEEpiC	esophagus:	n/a
36	chr2:37012483-37012533	NB4	blood:	n/a
37	chr2:37012483-37012533	ProgFib	skin:	n/a
38	chr2:37012483-37012533	PANC-1	pancreas:	n/a
39	chr2:37012483-37012533	BE2_C	brain:	n/a
40	chr2:37012483-37012533	NHBE	bronchial:	n/a
41	chr2:37012483-37012533	HRCEpiC	kidney:	n/a
42	chr2:37012483-37012533	HCT-116	colon:	n/a
43	chr2:37012483-37012533	K562	blood:	n/a
44	chr2:37012483-37012533	AG10803	skin:	n/a
45	chr2:37012483-37012533	HCPEpiC	choroid plexus:	n/a
46	chr2:37012483-37012533	HCF	heart:	n/a
47	chr2:37012483-37012533	AG04450	lung:	fetal
48	chr2:37012483-37012533	Hela-S3	cervix:	n/a
49	chr2:37012483-37012533	HAEpiC	amniotic membrane:	n/a
50	chr2:37012483-37012533	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:36928747..36929575-chr2:36997645..36998372,2	MCF-7	breast:
2	chr2:37006258..37010448-chr2:37010681..37014372,3	K562	blood:
3	chr2:37007149..37007661-chr2:37145609..37146127,2	MCF-7	breast:
4	chr2:36932681..36933457-chr2:36997721..36998478,3	MCF-7	breast:
5	chr2:37008165..37009704-chr2:37010243..37012241,2	MCF-7	breast:
6	chr2:36987514..36989270-chr2:36997117..36998900,2	K562	blood:
7	chr2:37007113..37008064-chr2:37231570..37232413,4	MCF-7	breast:
8	chr2:37005141..37008070-chr2:37014842..37017137,3	K562	blood:
9	chr2:36997788..36998511-chr2:37012444..37013096,2	K562	blood:
10	chr2:36922695..36923609-chr2:36997471..36998399,4	MCF-7	breast:
11	chr2:37005478..37008643-chr2:37010810..37013126,3	MCF-7	breast:
12	chr2:37008165..37009704-chr2:37010243..37012241,2	MCF-7	breast:
13	chr2:37005478..37008643-chr2:37010810..37013126,3	MCF-7	breast:
14	chr2:36997788..36998511-chr2:37012444..37013096,2	K562	blood:
15	chr2:37005040..37005587-chr2:37231880..37232793,2	MCF-7	breast:
16	chr2:36579342..36579861-chr2:37012057..37012873,2	K562	blood:
17	chr2:36997612..36998606-chr2:37012147..37012935,3	MCF-7	breast:
18	chr2:36922543..36923508-chr2:37012076..37013001,3	MCF-7	breast:
19	chr2:37011366..37014092-chr2:37310068..37313025,2	K562	blood:
20	chr2:36789668..36791996-chr2:37007136..37008825,2	K562	blood:
21	chr2:36921939..36923848-chr2:36997589..36998532,16	MCF-7	breast:
22	chr2:37000302..37001833-chr2:37006942..37009260,2	K562	blood:
23	chr2:37006258..37010448-chr2:37010681..37014372,3	K562	blood:
24	chr2:36928051..36929243-chr2:36997518..36998542,3	MCF-7	breast:
25	chr2:37005141..37008070-chr2:37014842..37017137,3	K562	blood:
26	chr2:37014502..37017375-chr2:37021178..37022910,2	K562	blood:
27	chr2:36997612..36998606-chr2:37012147..37012935,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CRIM1-2	chr2:36991437-36993016	NONHSAT070090

Variant related genes	Relation type
VIT	TF binding region
VIT	CpG island
ENSG00000152133	chromatin interactions
ENSG00000205221	chromatin interactions
ENSG00000008869	chromatin interactions

Extended variants
information (count: 1218 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1218 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558293329	chr2:36991755-36991756	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs576966196	chr2:36991766-36991767	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs147756448	chr2:36991776-36991777	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs556309335	chr2:36991819-36991820	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs374237171	chr2:36991823-36991824	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs541821841	chr2:36991825-36991826	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs184072628	chr2:36991826-36991827	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs572730421	chr2:36991852-36991853	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs546429380	chr2:36991889-36991890	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs189086165	chr2:36991890-36991891	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs532292126	chr2:36991899-36991900	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs146730714	chr2:36991931-36991932	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs377617473	chr2:36991937-36991938	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs550635745	chr2:36992018-36992019	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs562410297	chr2:36992047-36992048	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs529714823	chr2:36992059-36992060	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs141007155	chr2:36992101-36992102	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs181031333	chr2:36992121-36992122	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs540689629	chr2:36992146-36992147	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs564054993	chr2:36992151-36992152	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs144852489	chr2:36992183-36992184	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs570292850	chr2:36992194-36992195	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs145798763	chr2:36992196-36992197	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs185516234	chr2:36992200-36992201	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs148854739	chr2:36992208-36992209	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs11894158	chr2:36992211-36992212	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs554168587	chr2:36992235-36992236	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs572815700	chr2:36992252-36992253	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs112684658	chr2:36992283-36992284	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs576727305	chr2:36992287-36992288	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs543626647	chr2:36992288-36992289	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs373166462	chr2:36992298-36992299	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs562606934	chr2:36992300-36992301	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs190821999	chr2:36992354-36992355	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs548212369	chr2:36992416-36992417	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs143473563	chr2:36992428-36992429	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs114050435	chr2:36992461-36992462	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs552035382	chr2:36992509-36992510	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs60801682	chr2:36992519-36992520	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs116302963	chr2:36992539-36992540	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs568549744	chr2:36992553-36992554	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs535568705	chr2:36992555-36992556	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs71398212	chr2:36992557-36992558	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs377011128	chr2:36992569-36992570	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs113331161	chr2:36992571-36992572	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs200742628	chr2:36992573-36992574	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs56849075	chr2:36992577-36992578	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs57985843	chr2:36992578-36992579	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs144595357	chr2:36992653-36992654	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs531020867	chr2:36992666-36992667	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	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:260 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36971400-36992600	Weak transcription	Ovary	ovary
2	chr2:36971600-36992600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr2:36982800-36996400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr2:36987000-36992200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr2:36988000-36993000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:36992600-36992800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
7	chr2:36992600-36993200	Strong transcription	Ovary	ovary
8	chr2:36992800-36993000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr2:36993000-36993200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:36993000-37001400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr2:36993200-37007200	Weak transcription	Ovary	ovary
12	chr2:36996200-36996600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr2:36996400-36996800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr2:36997600-36998000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr2:36997800-36998200	Enhancers	HUVEC	blood vessel
16	chr2:37000000-37000400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr2:37001400-37002600	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr2:37002000-37003400	Enhancers	Fetal Brain Male	brain
19	chr2:37002400-37003600	Enhancers	Fetal Brain Female	brain
20	chr2:37002600-37006400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr2:37003400-37007800	Weak transcription	Fetal Brain Male	brain
22	chr2:37003600-37007600	Weak transcription	Fetal Brain Female	brain
23	chr2:37004600-37004800	Enhancers	Fetal Heart	heart
24	chr2:37004800-37005600	Weak transcription	Fetal Heart	heart
25	chr2:37005400-37005600	Enhancers	Right Atrium	heart
26	chr2:37005600-37008200	Enhancers	Fetal Heart	heart
27	chr2:37005800-37006000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr2:37006000-37014600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr2:37006400-37007800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr2:37007000-37007200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr2:37007000-37007200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr2:37007000-37007200	Enhancers	Muscle Satellite Cultured Cells	--
33	chr2:37007000-37007200	Enhancers	NHLF	lung
34	chr2:37007000-37007400	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr2:37007000-37007400	Enhancers	Dnd41	blood
36	chr2:37007000-37007600	Active TSS	Aorta	Aorta
37	chr2:37007000-37007800	Enhancers	Hela-S3	cervix
38	chr2:37007000-37007800	Flanking Active TSS	Osteobl	bone
39	chr2:37007000-37009400	Weak transcription	Right Atrium	heart
40	chr2:37007200-37007400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr2:37007200-37007400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr2:37007200-37007400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr2:37007200-37007400	Active TSS	Brain Hippocampus Middle	brain
44	chr2:37007200-37007400	Enhancers	Duodenum Mucosa	Duodenum
45	chr2:37007200-37007400	Flanking Active TSS	Ovary	ovary
46	chr2:37007200-37007400	Flanking Active TSS	HepG2	liver
47	chr2:37007200-37007400	Enhancers	HUVEC	blood vessel
48	chr2:37007200-37007400	Flanking Active TSS	NHEK	skin
49	chr2:37007200-37007600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:37007200-37007600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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