Variant report

Variant	nsv1005206
Chromosome Location	chr2:52731518-52781530
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	CEBPB	chr2:52754002-52754143	HepG2	liver:	n/a	chr2:52754025-52754038 chr2:52754025-52754036
2	CEBPB	chr2:52741949-52742162	A549	lung:	n/a	n/a
3	CEBPB	chr2:52779591-52779882	A549	lung:	n/a	chr2:52779731-52779742
4	CEBPB	chr2:52779571-52779911	IMR90	lung:	n/a	chr2:52779731-52779742
5	CEBPB	chr2:52766737-52766993	IMR90	lung:	n/a	n/a
6	CEBPB	chr2:52779693-52779886	HepG2	liver:	n/a	chr2:52779731-52779742
7	CEBPB	chr2:52779600-52779788	K562	blood:	n/a	chr2:52779731-52779742
8	CEBPB	chr2:52779626-52779886	Hela-S3	cervix:	n/a	chr2:52779731-52779742
9	CTCF	chr2:52751960-52752110	GM12875	blood:	n/a	n/a
10	E2F4	chr2:52740249-52740422	MCF10A-Er-Src	breast:	n/a	n/a
11	EP300	chr2:52744039-52744545	T-47D	breast:	n/a	n/a
12	EP300	chr2:52766648-52767467	T-47D	breast:	n/a	chr2:52766962-52766972 chr2:52766715-52766729
13	FOS	chr2:52744156-52744358	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr2:52737672-52737872	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr2:52764103-52764432	MCF10A-Er-Src	breast:	n/a	chr2:52764278-52764286 chr2:52764278-52764285 chr2:52764279-52764290 chr2:52764276-52764288 chr2:52764277-52764286
16	FOS	chr2:52764103-52764447	MCF10A-Er-Src	breast:	n/a	chr2:52764278-52764286 chr2:52764278-52764285 chr2:52764279-52764290 chr2:52764276-52764288 chr2:52764277-52764286
17	FOS	chr2:52744160-52744290	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr2:52737608-52737910	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr2:52764105-52764433	MCF10A-Er-Src	breast:	n/a	chr2:52764278-52764286 chr2:52764278-52764285 chr2:52764279-52764290 chr2:52764276-52764288 chr2:52764277-52764286
20	FOS	chr2:52737672-52737821	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr2:52744087-52744331	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr2:52764107-52764446	MCF10A-Er-Src	breast:	n/a	chr2:52764278-52764286 chr2:52764278-52764285 chr2:52764279-52764290 chr2:52764276-52764288 chr2:52764277-52764286
23	FOXA1	chr2:52744134-52744388	T-47D	breast:	n/a	n/a
24	FOXA1	chr2:52753972-52754152	T-47D	breast:	n/a	n/a
25	FOXA1	chr2:52760908-52761212	T-47D	breast:	n/a	chr2:52761022-52761037
26	FOXA1	chr2:52753873-52754145	T-47D	breast:	n/a	n/a
27	FOXA1	chr2:52767163-52767340	T-47D	breast:	n/a	n/a
28	FOXA1	chr2:52766561-52767471	T-47D	breast:	n/a	n/a
29	FOXA1	chr2:52744072-52744445	T-47D	breast:	n/a	n/a
30	FOXA1	chr2:52766626-52767015	T-47D	breast:	n/a	n/a
31	GABPA	chr2:52743903-52744433	HL-60	blood:	n/a	n/a
32	GATA3	chr2:52767060-52767383	T-47D	breast:	n/a	n/a
33	GATA3	chr2:52766330-52767424	T-47D	breast:	n/a	n/a
34	GATA3	chr2:52766197-52766592	T-47D	breast:	n/a	n/a
35	GATA3	chr2:52744120-52744457	T-47D	breast:	n/a	n/a
36	MAFF	chr2:52764776-52765093	K562	blood:	n/a	chr2:52764917-52764935
37	MAFF	chr2:52764787-52765085	HepG2	liver:	n/a	chr2:52764917-52764935
38	MAFF	chr2:52739940-52740269	K562	blood:	n/a	chr2:52740088-52740106
39	MAFF	chr2:52739943-52740260	HepG2	liver:	n/a	chr2:52740088-52740106
40	MAFK	chr2:52764779-52765066	HepG2	liver:	n/a	chr2:52764918-52764933
41	MAFK	chr2:52739776-52740277	HepG2	liver:	n/a	chr2:52740090-52740105
42	MAFK	chr2:52764754-52765103	HepG2	liver:	n/a	chr2:52764918-52764933
43	MAFK	chr2:52764825-52764933	H1-hESC	embryonic stem cell:	n/a	chr2:52764918-52764933
44	MAFK	chr2:52740041-52740246	K562	blood:	n/a	chr2:52740090-52740105
45	MAFK	chr2:52764755-52765076	K562	blood:	n/a	chr2:52764918-52764933
46	MAFK	chr2:52764738-52765107	IMR90	lung:	n/a	chr2:52764918-52764933
47	MAFK	chr2:52739933-52740283	IMR90	lung:	n/a	chr2:52740090-52740105
48	MAFK	chr2:52764749-52765055	Hela-S3	cervix:	n/a	chr2:52764918-52764933
49	MAFK	chr2:52739917-52740253	HepG2	liver:	n/a	chr2:52740090-52740105
50	MYC	chr2:52764196-52764346	MCF10A-Er-Src	breast:	n/a	chr2:52764278-52764287

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52759434-52759484	AoSMC	blood vessel:	n/a
2	chr2:52759434-52759484	RPTEC	kidney:	n/a
3	chr2:52759434-52759484	NHBE	bronchial:	n/a
4	chr2:52759434-52759484	SK-N-SH	brain:	n/a
5	chr2:52759434-52759484	ProgFib	skin:	n/a
6	chr2:52759434-52759484	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:52759434-52759484	HIPEpiC	eye:	n/a
8	chr2:52759434-52759484	HAEpiC	amniotic membrane:	n/a
9	chr2:52759434-52759484	HL-60	blood:	n/a
10	chr2:52759434-52759484	MCF10A-Er-Src	breast:	n/a
11	chr2:52759434-52759484	HRE	kidney:	n/a
12	chr2:52759434-52759484	AG09319	gingival:	n/a
13	chr2:52759434-52759484	K562	blood:	n/a
14	chr2:52759434-52759484	HepG2	liver:	n/a
15	chr2:52759434-52759484	AG04449	skin:	fetal
16	chr2:52759434-52759484	HCPEpiC	choroid plexus:	n/a
17	chr2:52759434-52759484	AG04450	lung:	fetal
18	chr2:52759434-52759484	HEK293	kidney:	embryo
19	chr2:52759434-52759484	U87	brain:	n/a
20	chr2:52759434-52759484	H1-hESC	embryonic stem cell:	embryo
21	chr2:52759434-52759484	BJ	skin:	n/a
22	chr2:52759434-52759484	Jurkat	blood:	n/a
23	chr2:52759434-52759484	MCF-7	breast:	n/a
24	chr2:52759434-52759484	HNPCEpiC	eye:	n/a
25	chr2:52759434-52759484	Hepatocyte	liver:	n/a
26	chr2:52759434-52759484	PFSK-1	brain:	n/a
27	chr2:52759434-52759484	GM06990	blood:	n/a
28	chr2:52759434-52759484	GM19239	blood:	n/a
29	chr2:52759434-52759484	Caco-2	colon:	n/a
30	chr2:52759434-52759484	AG09309	skin:	n/a
31	chr2:52759434-52759484	HUVEC	blood vessel:	n/a
32	chr2:52759434-52759484	GM12891	blood:	n/a
33	chr2:52759434-52759484	GM12878	blood:	n/a
34	chr2:52759434-52759484	ECC-1	luminal epithelium:	n/a
35	chr2:52759434-52759484	PANC-1	pancreas:	n/a
36	chr2:52759434-52759484	HRCEpiC	kidney:	n/a
37	chr2:52759434-52759484	T-47D	breast:	n/a
38	chr2:52759434-52759484	HMEC	breast:	n/a
39	chr2:52759434-52759484	SK-N-MC	brain:	n/a
40	chr2:52759434-52759484	HCF	heart:	n/a
41	chr2:52759434-52759484	LNCaP	prostate:	n/a
42	chr2:52759434-52759484	HCM	heart:	n/a
43	chr2:52759434-52759484	ovcar-3	ovarian:	n/a
44	chr2:52759434-52759484	HRPEpiC	eye:	n/a
45	chr2:52759434-52759484	NT2-D1	testis:	n/a
46	chr2:52759434-52759484	GM12892	blood:	n/a
47	chr2:52759434-52759484	NHDF-neo	bronchial:	n/a
48	chr2:52759434-52759484	Hela-S3	cervix:	n/a
49	chr2:52759434-52759484	BE2_C	brain:	n/a
50	chr2:52759434-52759484	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:52727791..52731753-chr2:52732140..52733978,3	K562	blood:
2	chr2:52727791..52730786-chr2:52732300..52733978,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB3-9	chr2:52778477-52778840	l_1835_chr2:52771950-52778840_testes
2	lnc-ASB3-9	chr2:52771951-52772275	l_1835_chr2:52771950-52778840_testes

Variant related genes	Relation type
ENSG00000236837	TF binding region
ENSG00000236837	CpG island
ENSG00000236837	chromatin interactions

Extended variants
information (count: 1402 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1402 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548394830	chr2:52731560-52731561	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs72892965	chr2:52731563-52731564	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs531117983	chr2:52731565-52731566	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs1405372	chr2:52731584-52731585	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs34110608	chr2:52731601-52731602	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs182295796	chr2:52731626-52731627	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs376121423	chr2:52731642-52731643	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs78267474	chr2:52731659-52731660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs552185211	chr2:52731698-52731699	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs565795278	chr2:52731703-52731704	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs552222033	chr2:52731990-52731991	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs565640658	chr2:52732033-52732034	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs56775744	chr2:52732048-52732049	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs77751043	chr2:52732064-52732065	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs77468174	chr2:52732075-52732076	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs535406985	chr2:52732101-52732102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs4547561	chr2:52732104-52732105	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs80226670	chr2:52732107-52732108	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs577090387	chr2:52732171-52732172	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs78049738	chr2:52732190-52732191	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs398060187	chr2:52732192-52732193	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539299250	chr2:52732227-52732228	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs140383997	chr2:52732274-52732275	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572938973	chr2:52732332-52732333	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541814529	chr2:52732333-52732334	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs150414029	chr2:52732353-52732354	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs575633266	chr2:52732354-52732355	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs367928278	chr2:52732357-52732358	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575565173	chr2:52732369-52732370	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs544556924	chr2:52732376-52732377	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs544805138	chr2:52732391-52732392	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs117721885	chr2:52732429-52732430	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533688909	chr2:52732430-52732431	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564289677	chr2:52732484-52732485	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs79042076	chr2:52732542-52732543	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs572995526	chr2:52732567-52732568	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs528121908	chr2:52732575-52732576	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548195213	chr2:52732580-52732581	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138146916	chr2:52732598-52732599	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs73931359	chr2:52732665-52732666	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs550755928	chr2:52732696-52732697	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs377685909	chr2:52732705-52732706	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11885229	chr2:52732716-52732717	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs188462075	chr2:52732728-52732729	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs72892969	chr2:52732737-52732738	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs369035677	chr2:52732744-52732745	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs552894129	chr2:52732765-52732766	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs373383999	chr2:52732768-52732769	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs11885258	chr2:52732788-52732789	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs115511211	chr2:52732798-52732799	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	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
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52736400-52736600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr2:52736400-52736600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:52736600-52739800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:52736600-52746600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:52739800-52740200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:52746400-52746600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:52746400-52746800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:52746600-52746800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr2:52746600-52747600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:52746600-52748400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr2:52746800-52747200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr2:52746800-52747200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr2:52746800-52748400	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr2:52747200-52748000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr2:52747200-52748200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr2:52747200-52748400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:52747400-52747800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr2:52747400-52748000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr2:52747600-52748000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:52747600-52748000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr2:52747600-52748400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:52748200-52749200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr2:52748400-52749400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr2:52749200-52749400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr2:52749400-52749600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr2:52754000-52754600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:52754600-52758600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:52758600-52760000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr2:52759400-52760600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:52760000-52760400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:52760400-52761400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:52761400-52764200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:52764200-52764800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:52764400-52764600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr2:52764800-52765800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr2:52764800-52766200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr2:52765800-52766400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:52766000-52766400	Enhancers	Fetal Muscle Trunk	muscle
39	chr2:52766000-52766400	Enhancers	Fetal Muscle Leg	muscle
40	chr2:52766200-52767200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr2:52766400-52767600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr2:52766400-52767800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:52766600-52767200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:52766800-52767400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr2:52766800-52767400	Enhancers	NH-A	brain
46	chr2:52767600-52768000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:52773000-52773400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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