Variant report

Variant	nsv1011449
Chromosome Location	chr2:53894529-53947781
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	chr2:53928413-53928764	K562	blood:	n/a	n/a
2	ARID3A	chr2:53942779-53943047	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:53895440-53896413	K562	blood:	n/a	n/a
4	ATF1	chr2:53895683-53896356	K562	blood:	n/a	n/a
5	ATF3	chr2:53895648-53896172	K562	blood:	n/a	chr2:53895893-53895908
6	BACH1	chr2:53928536-53928700	K562	blood:	n/a	n/a
7	BACH1	chr2:53896184-53896206	K562	blood:	n/a	n/a
8	BHLHE40	chr2:53895735-53896261	K562	blood:	n/a	n/a
9	CBX3	chr2:53936100-53936437	K562	blood:	n/a	n/a
10	CBX3	chr2:53936090-53936485	K562	blood:	n/a	n/a
11	CBX3	chr2:53895593-53896202	K562	blood:	n/a	n/a
12	CBX3	chr2:53895662-53896060	K562	blood:	n/a	n/a
13	CCNT2	chr2:53895460-53896251	K562	blood:	n/a	chr2:53895829-53895849
14	CEBPB	chr2:53895592-53896355	K562	blood:	n/a	chr2:53895934-53895945
15	CEBPB	chr2:53940521-53940567	K562	blood:	n/a	n/a
16	CEBPB	chr2:53895621-53896236	K562	blood:	n/a	chr2:53895934-53895945
17	CEBPB	chr2:53923351-53923501	A549	lung:	n/a	n/a
18	CEBPB	chr2:53895732-53895946	K562	blood:	n/a	chr2:53895934-53895945
19	CEBPB	chr2:53896884-53897403	K562	blood:	n/a	n/a
20	CEBPD	chr2:53895593-53896339	K562	blood:	n/a	n/a
21	CEBPD	chr2:53895590-53896274	K562	blood:	n/a	n/a
22	CREB1	chr2:53895503-53896336	K562	blood:	n/a	chr2:53895894-53895907
23	CREB1	chr2:53895692-53896220	K562	blood:	n/a	chr2:53895894-53895907
24	CTCF	chr2:53942720-53942870	BE2_C	brain:	n/a	n/a
25	CTCF	chr2:53942820-53942970	GM12865	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
26	CTCF	chr2:53942740-53942890	HVMF	connective:	n/a	n/a
27	CTCF	chr2:53942820-53943008	LNCaP	prostate:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
28	CTCF	chr2:53942800-53942950	NHDF-neo	bronchial:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
29	CTCF	chr2:53942200-53942350	HCM	heart:	n/a	n/a
30	CTCF	chr2:53942840-53942990	GM12878	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
31	CTCF	chr2:53942780-53942930	GM12865	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
32	CTCF	chr2:53942820-53942970	NHDF-neo	bronchial:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
33	CTCF	chr2:53942783-53942943	SK-N-SH_RA	brain:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
34	CTCF	chr2:53942800-53942950	GM12878	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
35	CTCF	chr2:53942800-53942950	AG09319	gingival:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
36	CTCF	chr2:53942820-53942970	AG09319	gingival:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
37	CTCF	chr2:53943338-53943355	GM10248	blood:	n/a	n/a
38	CTCF	chr2:53942800-53942950	GM12872	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
39	CTCF	chr2:53936100-53936250	HepG2	liver:	n/a	n/a
40	CTCF	chr2:53942722-53943101	K562	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
41	CTCF	chr2:53942860-53943010	GM12872	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
42	CTCF	chr2:53942815-53943011	K562	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
43	CTCF	chr2:53942774-53942971	H1-hESC	embryonic stem cell:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
44	CTCF	chr2:53942940-53943090	HCT-116	colon:	n/a	n/a
45	CTCF	chr2:53942800-53942950	SAEC	small airway:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
46	CTCF	chr2:53942860-53943010	GM12864	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
47	CTCF	chr2:53942860-53943010	HMEC	breast:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
48	CTCF	chr2:53942840-53942990	MCF-7	breast:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
49	CTCF	chr2:53942820-53942970	GM12869	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
50	CTCF	chr2:53942840-53942990	BJ	skin:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53898063-53898113	SK-N-MC	brain:	n/a
2	chr2:53898063-53898113	RPTEC	kidney:	n/a
3	chr2:53898063-53898113	HRE	kidney:	n/a
4	chr2:53898063-53898113	NH-A	brain:	n/a
5	chr2:53898063-53898113	HUVEC	blood vessel:	n/a
6	chr2:53898063-53898113	BE2_C	brain:	n/a
7	chr2:53898063-53898113	AG10803	skin:	n/a
8	chr2:53898063-53898113	Caco-2	colon:	n/a
9	chr2:53898063-53898113	HAEpiC	amniotic membrane:	n/a
10	chr2:53898063-53898113	GM12892	blood:	n/a
11	chr2:53898063-53898113	Jurkat	blood:	n/a
12	chr2:53898063-53898113	GM12878	blood:	n/a
13	chr2:53898063-53898113	SKMC	muscle:	n/a
14	chr2:53898063-53898113	NB4	blood:	n/a
15	chr2:53898063-53898113	SK-N-SH_RA	brain:	n/a
16	chr2:53898063-53898113	LNCaP	prostate:	n/a
17	chr2:53898063-53898113	MCF10A-Er-Src	breast:	n/a
18	chr2:53898063-53898113	K562	blood:	n/a
19	chr2:53898063-53898113	ECC-1	luminal epithelium:	n/a
20	chr2:53898063-53898113	HL-60	blood:	n/a
21	chr2:53898063-53898113	PANC-1	pancreas:	n/a
22	chr2:53898063-53898113	HCT-116	colon:	n/a
23	chr2:53898063-53898113	A549	lung:	n/a
24	chr2:53898063-53898113	GM12891	blood:	n/a
25	chr2:53898063-53898113	HRCEpiC	kidney:	n/a
26	chr2:53898063-53898113	HepG2	liver:	n/a
27	chr2:53898063-53898113	NHBE	bronchial:	n/a
28	chr2:53898063-53898113	GM19239	blood:	n/a
29	chr2:53898063-53898113	AG09319	gingival:	n/a
30	chr2:53898063-53898113	NT2-D1	testis:	n/a
31	chr2:53898063-53898113	HNPCEpiC	eye:	n/a
32	chr2:53898063-53898113	HPAEpiC	pulmonary alveolar:	n/a
33	chr2:53898063-53898113	Hepatocyte	liver:	n/a
34	chr2:53898063-53898113	SK-N-SH	brain:	n/a
35	chr2:53898063-53898113	HMEC	breast:	n/a
36	chr2:53898063-53898113	GM06990	blood:	n/a
37	chr2:53898063-53898113	T-47D	breast:	n/a
38	chr2:53898063-53898113	MCF-7	breast:	n/a
39	chr2:53898063-53898113	IMR90	lung:	fetal
40	chr2:53898063-53898113	ProgFib	skin:	n/a
41	chr2:53898063-53898113	ovcar-3	ovarian:	n/a
42	chr2:53898063-53898113	AG09309	skin:	n/a
43	chr2:53898063-53898113	U87	brain:	n/a
44	chr2:53898063-53898113	H1-hESC	embryonic stem cell:	embryo
45	chr2:53898063-53898113	AoSMC	blood vessel:	n/a
46	chr2:53898063-53898113	PFSK-1	brain:	n/a
47	chr2:53898063-53898113	HCPEpiC	choroid plexus:	n/a
48	chr2:53898063-53898113	PrEC	prostate:	n/a
49	chr2:53898063-53898113	HEK293	kidney:	embryo
50	chr2:53898063-53898113	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:53931144..53933214-chr2:53937294..53940246,2	K562	blood:
2	chr17:70758626..70759130-chr2:53924202..53924904,2	MCF-7	breast:
3	chr2:53926842..53929678-chr2:54004293..54006164,2	K562	blood:
4	chr2:53927372..53929338-chr2:53931727..53933877,2	K562	blood:
5	chr2:53901787..53904265-chr2:53994019..53996587,2	K562	blood:
6	chr2:53931144..53933214-chr2:53937294..53940246,2	K562	blood:
7	chr1:11966927..11968808-chr2:53945839..53947359,4	MCF-7	breast:
8	chr2:53925981..53927589-chr2:53940700..53943084,2	K562	blood:
9	chr2:53894424..53897447-chr2:53898122..53902216,4	K562	blood:
10	chr2:53920239..53922188-chr2:53922712..53925505,2	K562	blood:
11	chr2:53926965..53929338-chr2:53930911..53933227,2	K562	blood:
12	chr1:11967949..11968659-chr2:53945359..53946359,5	MCF-7	breast:
13	chr2:53669933..53670563-chr2:53942920..53943446,2	MCF-7	breast:
14	chr2:53894424..53897447-chr2:53898122..53902216,4	K562	blood:
15	chr2:53687389..53688064-chr2:53942616..53943230,2	MCF-7	breast:
16	chr1:11967940..11968599-chr2:53945834..53946359,2	MCF-7	breast:
17	chr2:53925981..53927589-chr2:53940700..53943084,2	K562	blood:
18	chr1:11966902..11969473-chr2:53944359..53947359,6	MCF-7	breast:
19	chr2:53926965..53929338-chr2:53930911..53933227,2	K562	blood:
20	chr2:53927372..53929338-chr2:53931727..53933877,2	K562	blood:
21	chr2:53938900..53941731-chr2:54013134..54015288,2	K562	blood:
22	chr2:53887538..53889702-chr2:53894811..53897627,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-5	chr2:53941521-53941719	NONHSAT070694
2	lnc-CHAC2-5	chr2:53927406-53927679	NONHSAT070694

Variant related genes	Relation type
GPR75-ASB3	TF binding region
GPR75-ASB3	CpG island
ENSG00000143942	chromatin interactions
ENSG00000115239	chromatin interactions
ENSG00000068912	chromatin interactions
ENSG00000199347	chromatin interactions

Extended variants
information (count: 2476 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2476 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188270619	chr2:53894537-53894538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs111687695	chr2:53894538-53894539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569209064	chr2:53894566-53894567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538155851	chr2:53894571-53894572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559666006	chr2:53894596-53894597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182375862	chr2:53894630-53894631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533613261	chr2:53894642-53894643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs13394137	chr2:53894646-53894647	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs187811840	chr2:53894655-53894656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542845733	chr2:53894711-53894712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547609573	chr2:53894727-53894728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs137918753	chr2:53894732-53894733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576298635	chr2:53894764-53894765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13394147	chr2:53894772-53894773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113796879	chr2:53894779-53894780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536779331	chr2:53894787-53894788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552209106	chr2:53894801-53894802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201284096	chr2:53894806-53894807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374859292	chr2:53894817-53894818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375912958	chr2:53894820-53894821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377515387	chr2:53894822-53894823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs60043375	chr2:53894856-53894857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565091727	chr2:53894860-53894861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62139784	chr2:53894884-53894885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527725108	chr2:53894887-53894888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372622611	chr2:53894895-53894896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541162811	chr2:53894897-53894898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561462591	chr2:53894945-53894946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192625590	chr2:53894970-53894971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35039987	chr2:53894978-53894979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549166519	chr2:53894981-53894982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569096348	chr2:53895013-53895014	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574749526	chr2:53895030-53895031	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184510058	chr2:53895073-53895074	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571148924	chr2:53895074-53895075	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372923137	chr2:53895082-53895083	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139303394	chr2:53895088-53895089	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567317641	chr2:53895089-53895090	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556401483	chr2:53895090-53895091	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188575094	chr2:53895117-53895118	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193159942	chr2:53895119-53895120	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184593160	chr2:53895124-53895125	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75760748	chr2:53895131-53895132	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545285641	chr2:53895173-53895174	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189899221	chr2:53895189-53895190	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs180733628	chr2:53895194-53895195	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541354224	chr2:53895210-53895211	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375786816	chr2:53895241-53895242	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183715033	chr2:53895245-53895246	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189261810	chr2:53895256-53895257	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
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
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1105 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53874200-53935000	Weak transcription	Pancreas	Pancrea
2	chr2:53879400-53895600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr2:53881200-53895800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr2:53881400-53934400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr2:53881800-53896400	Weak transcription	Aorta	Aorta
6	chr2:53882800-53895600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr2:53883200-53897800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr2:53883600-53896600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:53885000-53895800	Weak transcription	Dnd41	blood
10	chr2:53885600-53925000	Weak transcription	Fetal Intestine Small	intestine
11	chr2:53885800-53911800	Weak transcription	Adipose Nuclei	Adipose
12	chr2:53886600-53896400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:53887000-53895400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:53887000-53898000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:53887800-53899800	Weak transcription	Primary B cells from cord blood	blood
16	chr2:53888200-53934200	Weak transcription	Lung	lung
17	chr2:53888400-53896000	Weak transcription	Primary T cells from cord blood	blood
18	chr2:53888400-53935200	Weak transcription	Fetal Brain Male	brain
19	chr2:53888600-53897200	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr2:53888600-53935200	Weak transcription	Hela-S3	cervix
21	chr2:53889000-53935800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr2:53889400-53895800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr2:53889400-53896800	Weak transcription	Fetal Lung	lung
24	chr2:53889800-53895800	Weak transcription	Primary hematopoietic stem cells	blood
25	chr2:53891600-53900000	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr2:53892600-53902600	Weak transcription	Rectal Smooth Muscle	rectum
27	chr2:53892600-53918800	Weak transcription	Left Ventricle	heart
28	chr2:53893400-53915200	Weak transcription	Ovary	ovary
29	chr2:53893800-53926800	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr2:53894000-53895600	Weak transcription	Fetal Brain Female	brain
31	chr2:53894200-53895800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr2:53894200-53895800	Weak transcription	Fetal Thymus	thymus
33	chr2:53894200-53920800	Weak transcription	Duodenum Mucosa	Duodenum
34	chr2:53894400-53896000	Weak transcription	HepG2	liver
35	chr2:53894400-53900400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr2:53894400-53912200	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr2:53894400-53914400	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr2:53894400-53925000	Weak transcription	Fetal Muscle Trunk	muscle
39	chr2:53894400-53933800	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr2:53894600-53895000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:53894600-53900000	Weak transcription	Stomach Mucosa	stomach
42	chr2:53894600-53911200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr2:53894800-53900000	Weak transcription	Brain Hippocampus Middle	brain
44	chr2:53895000-53895200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:53895000-53896000	Enhancers	K562	blood
46	chr2:53895000-53900200	Weak transcription	Brain Substantia Nigra	brain
47	chr2:53895000-53911800	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr2:53895200-53896000	ZNF genes & repeats	Fetal Muscle Leg	muscle
49	chr2:53895200-53898000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr2:53895400-53896000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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