Variant report

Variant	nsv533591
Chromosome Location	chr2:52706226-52781440
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	chr2:52766737-52766993	IMR90	lung:	n/a	n/a
2	CEBPB	chr2:52779571-52779911	IMR90	lung:	n/a	chr2:52779731-52779742
3	CEBPB	chr2:52779600-52779788	K562	blood:	n/a	chr2:52779731-52779742
4	CEBPB	chr2:52754002-52754143	HepG2	liver:	n/a	chr2:52754025-52754038 chr2:52754025-52754036
5	CEBPB	chr2:52779693-52779886	HepG2	liver:	n/a	chr2:52779731-52779742
6	CEBPB	chr2:52779626-52779886	Hela-S3	cervix:	n/a	chr2:52779731-52779742
7	CEBPB	chr2:52741949-52742162	A549	lung:	n/a	n/a
8	CEBPB	chr2:52779591-52779882	A549	lung:	n/a	chr2:52779731-52779742
9	CTCF	chr2:52706319-52706404	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr2:52706386-52706414	Medullo	brain:	n/a	n/a
11	CTCF	chr2:52706320-52706470	SK-N-SH_RA	brain:	n/a	n/a
12	CTCF	chr2:52706340-52706490	AG04450	lung:	n/a	n/a
13	CTCF	chr2:52706289-52706362	Medullo	brain:	n/a	n/a
14	CTCF	chr2:52706300-52706450	HMF	breast:	n/a	n/a
15	CTCF	chr2:52706200-52706350	HCT-116	colon:	n/a	n/a
16	CTCF	chr2:52706240-52706390	HCFaa	heart:	n/a	n/a
17	CTCF	chr2:52706200-52706350	HPF	lung:	n/a	n/a
18	CTCF	chr2:52751960-52752110	GM12875	blood:	n/a	n/a
19	CTCF	chr2:52706560-52706710	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr2:52706340-52706490	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr2:52706320-52706470	NHEK	skin:	n/a	n/a
22	CTCF	chr2:52706240-52706390	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr2:52706260-52706410	HCT-116	colon:	n/a	n/a
24	E2F4	chr2:52740249-52740422	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr2:52716051-52716210	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr2:52726538-52726745	MCF10A-Er-Src	breast:	n/a	n/a
27	EP300	chr2:52744039-52744545	T-47D	breast:	n/a	n/a
28	EP300	chr2:52725664-52725727	GM12878	blood:	n/a	n/a
29	EP300	chr2:52766648-52767467	T-47D	breast:	n/a	chr2:52766962-52766972 chr2:52766715-52766729
30	FOS	chr2:52737608-52737910	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr2:52737672-52737872	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr2:52744160-52744290	MCF10A-Er-Src	breast:	n/a	n/a
33	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
34	FOS	chr2:52737672-52737821	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr2:52744156-52744358	MCF10A-Er-Src	breast:	n/a	n/a
36	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
37	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
38	FOS	chr2:52744087-52744331	MCF10A-Er-Src	breast:	n/a	n/a
39	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
40	FOXA1	chr2:52766561-52767471	T-47D	breast:	n/a	n/a
41	FOXA1	chr2:52753972-52754152	T-47D	breast:	n/a	n/a
42	FOXA1	chr2:52744134-52744388	T-47D	breast:	n/a	n/a
43	FOXA1	chr2:52753873-52754145	T-47D	breast:	n/a	n/a
44	FOXA1	chr2:52760908-52761212	T-47D	breast:	n/a	chr2:52761022-52761037
45	FOXA1	chr2:52766626-52767015	T-47D	breast:	n/a	n/a
46	FOXA1	chr2:52767163-52767340	T-47D	breast:	n/a	n/a
47	FOXA1	chr2:52744072-52744445	T-47D	breast:	n/a	n/a
48	GABPA	chr2:52743903-52744433	HL-60	blood:	n/a	n/a
49	GATA3	chr2:52766197-52766592	T-47D	breast:	n/a	n/a
50	GATA3	chr2:52767060-52767383	T-47D	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52759434-52759484	IMR90	lung:	fetal
2	chr2:52759434-52759484	NHDF-neo	bronchial:	n/a
3	chr2:52759434-52759484	HEEpiC	esophagus:	n/a
4	chr2:52759434-52759484	NHBE	bronchial:	n/a
5	chr2:52759434-52759484	MCF10A-Er-Src	breast:	n/a
6	chr2:52759434-52759484	AG10803	skin:	n/a
7	chr2:52759434-52759484	RPTEC	kidney:	n/a
8	chr2:52759434-52759484	AoSMC	blood vessel:	n/a
9	chr2:52759434-52759484	SKMC	muscle:	n/a
10	chr2:52759434-52759484	HCF	heart:	n/a
11	chr2:52759434-52759484	HEK293	kidney:	embryo
12	chr2:52759434-52759484	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:52759434-52759484	HepG2	liver:	n/a
14	chr2:52759434-52759484	PANC-1	pancreas:	n/a
15	chr2:52759434-52759484	Hela-S3	cervix:	n/a
16	chr2:52759434-52759484	NT2-D1	testis:	n/a
17	chr2:52759434-52759484	CMK	blood:	n/a
18	chr2:52759434-52759484	GM06990	blood:	n/a
19	chr2:52759434-52759484	MCF-7	breast:	n/a
20	chr2:52759434-52759484	HRCEpiC	kidney:	n/a
21	chr2:52759434-52759484	BE2_C	brain:	n/a
22	chr2:52759434-52759484	HCM	heart:	n/a
23	chr2:52759434-52759484	Hepatocyte	liver:	n/a
24	chr2:52759434-52759484	AG04450	lung:	fetal
25	chr2:52759434-52759484	PrEC	prostate:	n/a
26	chr2:52759434-52759484	HCPEpiC	choroid plexus:	n/a
27	chr2:52759434-52759484	GM19239	blood:	n/a
28	chr2:52759434-52759484	Caco-2	colon:	n/a
29	chr2:52759434-52759484	HUVEC	blood vessel:	n/a
30	chr2:52759434-52759484	PFSK-1	brain:	n/a
31	chr2:52759434-52759484	HCT-116	colon:	n/a
32	chr2:52759434-52759484	SK-N-SH_RA	brain:	n/a
33	chr2:52759434-52759484	SK-N-MC	brain:	n/a
34	chr2:52759434-52759484	HL-60	blood:	n/a
35	chr2:52759434-52759484	ECC-1	luminal epithelium:	n/a
36	chr2:52759434-52759484	T-47D	breast:	n/a
37	chr2:52759434-52759484	HIPEpiC	eye:	n/a
38	chr2:52759434-52759484	HNPCEpiC	eye:	n/a
39	chr2:52759434-52759484	A549	lung:	n/a
40	chr2:52759434-52759484	HRE	kidney:	n/a
41	chr2:52759434-52759484	HRPEpiC	eye:	n/a
42	chr2:52759434-52759484	AG04449	skin:	fetal
43	chr2:52759434-52759484	ovcar-3	ovarian:	n/a
44	chr2:52759434-52759484	ProgFib	skin:	n/a
45	chr2:52759434-52759484	U87	brain:	n/a
46	chr2:52759434-52759484	GM12891	blood:	n/a
47	chr2:52759434-52759484	BJ	skin:	n/a
48	chr2:52759434-52759484	HAEpiC	amniotic membrane:	n/a
49	chr2:52759434-52759484	H1-hESC	embryonic stem cell:	embryo
50	chr2:52759434-52759484	NB4	blood:	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	chr2:52771951-52772275	l_1835_chr2:52771950-52778840_testes
2	lnc-ASB3-3	chr2:52722903-52722974	XLOC_002095
3	lnc-ASB3-3	chr2:52727682-52727890	XLOC_002095
4	lnc-ASB3-3	chr2:52725741-52725923	XLOC_002095
5	lnc-ASB3-3	chr2:52721826-52722000	XLOC_002095
6	lnc-ASB3-9	chr2:52778477-52778840	l_1835_chr2:52771950-52778840_testes

Variant related genes	Relation type
ENSG00000225842	TF binding region
ENSG00000236837	TF binding region
ENSG00000225842	CpG island
ENSG00000236837	CpG island
ENSG00000236837	chromatin interactions
RABEP1	miRNA target sites
RAB9B	miRNA target sites
RAD23B	miRNA target sites

Extended variants
information (count: 1841 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1841 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562404913	chr2:52706243-52706244	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs13406808	chr2:52706261-52706262	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs551409920	chr2:52706281-52706282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs571298502	chr2:52706290-52706291	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs34379797	chr2:52706332-52706333	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs527821067	chr2:52706347-52706348	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs56391076	chr2:52706394-52706395	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs374480960	chr2:52706457-52706458	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs567864804	chr2:52706480-52706481	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs13407104	chr2:52706489-52706490	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs369055629	chr2:52706494-52706495	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs373487791	chr2:52706498-52706499	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs548140973	chr2:52706542-52706543	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs6760658	chr2:52721889-52721890	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs183134793	chr2:52721891-52721892	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs373846948	chr2:52721898-52721899	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs548303190	chr2:52721926-52721927	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs187124321	chr2:52721936-52721937	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs570235571	chr2:52721991-52721992	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs528365748	chr2:52722806-52722807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548326664	chr2:52722815-52722816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116495765	chr2:52722817-52722818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141406683	chr2:52722833-52722834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs4971836	chr2:52722835-52722836	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs145282772	chr2:52722849-52722850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185616967	chr2:52722864-52722865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs72892924	chr2:52722885-52722886	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs368269216	chr2:52722886-52722887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146421197	chr2:52722894-52722895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571222732	chr2:52722898-52722899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536113717	chr2:52722902-52722903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552900930	chr2:52722922-52722923	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs574440522	chr2:52722932-52722933	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs527392277	chr2:52722934-52722935	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs548989745	chr2:52722971-52722972	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs17043033	chr2:52722976-52722977	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs190487733	chr2:52722981-52722982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117953477	chr2:52722988-52722989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375246615	chr2:52722996-52722997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs72892927	chr2:52723020-52723021	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs114628095	chr2:52723026-52723027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4971606	chr2:52723031-52723032	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs542078364	chr2:52723068-52723069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561939286	chr2:52723109-52723110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140955476	chr2:52723112-52723113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544188847	chr2:52723128-52723129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570963693	chr2:52723147-52723148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368789731	chr2:52723155-52723156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538418837	chr2:52723163-52723164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150415195	chr2:52723198-52723199	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52722800-52723800	Enhancers	Liver	Liver
2	chr2:52723800-52724600	Weak transcription	Liver	Liver
3	chr2:52724600-52725800	ZNF genes & repeats	Liver	Liver
4	chr2:52725800-52727200	Weak transcription	Liver	Liver
5	chr2:52727200-52730600	Enhancers	Liver	Liver
6	chr2:52727400-52729600	Enhancers	Fetal Heart	heart
7	chr2:52727600-52728600	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr2:52727600-52729800	Enhancers	Fetal Lung	lung
9	chr2:52727800-52728000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr2:52728000-52728600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr2:52728600-52729400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:52728800-52729600	Enhancers	Fetal Intestine Small	intestine
13	chr2:52728800-52729600	Enhancers	Left Ventricle	heart
14	chr2:52728800-52729600	Enhancers	Pancreas	Pancrea
15	chr2:52728800-52730400	Enhancers	Fetal Intestine Large	intestine
16	chr2:52736400-52736600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr2:52736400-52736600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr2:52736600-52739800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr2:52736600-52746600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:52739800-52740200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:52746400-52746600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:52746400-52746800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr2:52746600-52746800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr2:52746600-52747600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:52746600-52748400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr2:52746800-52747200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr2:52746800-52747200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:52746800-52748400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr2:52747200-52748000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:52747200-52748200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr2:52747200-52748400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:52747400-52747800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr2:52747400-52748000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:52747600-52748000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr2:52747600-52748000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:52747600-52748400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr2:52748200-52749200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr2:52748400-52749400	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr2:52749200-52749400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr2:52749400-52749600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr2:52754000-52754600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr2:52754600-52758600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:52758600-52760000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr2:52759400-52760600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr2:52760000-52760400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr2:52760400-52761400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:52761400-52764200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:52764200-52764800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:52764400-52764600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr2:52764800-52765800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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