Variant report

Variant	nsv874133
Chromosome Location	chr2:52910065-53023825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:151)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:151 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr2:52944119-52944258	A549	lung:	n/a	n/a
2	CEBPB	chr2:52922799-52922999	HepG2	liver:	n/a	chr2:52922910-52922921
3	CEBPB	chr2:53005825-53006043	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr2:52972320-52972582	K562	blood:	n/a	chr2:52972476-52972487
5	CEBPB	chr2:52972311-52972651	IMR90	lung:	n/a	chr2:52972476-52972487
6	CEBPB	chr2:53010829-53011118	IMR90	lung:	n/a	n/a
7	CEBPB	chr2:52990621-52990931	HepG2	liver:	n/a	chr2:52990766-52990777 chr2:52990767-52990778 chr2:52990768-52990777
8	CEBPB	chr2:53002901-53003198	A549	lung:	n/a	n/a
9	CEBPB	chr2:52976955-52977240	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:52990470-52990921	IMR90	lung:	n/a	chr2:52990766-52990777 chr2:52990767-52990778 chr2:52990768-52990777
11	CEBPB	chr2:52989878-52990124	HepG2	liver:	n/a	chr2:52990014-52990025
12	CEBPB	chr2:52920883-52921124	HepG2	liver:	n/a	chr2:52921007-52921018 chr2:52921028-52921041 chr2:52921006-52921019
13	CEBPB	chr2:53002959-53003131	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr2:53005783-53005972	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:52972350-52972653	A549	lung:	n/a	chr2:52972476-52972487
16	CEBPB	chr2:52972339-52972663	HepG2	liver:	n/a	chr2:52972476-52972487
17	CEBPB	chr2:52914095-52914425	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:52922787-52923136	IMR90	lung:	n/a	chr2:52922910-52922921
19	CEBPB	chr2:53002978-53003223	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:52934308-52934550	HepG2	liver:	n/a	chr2:52934413-52934424 chr2:52934415-52934426
21	CEBPB	chr2:53002930-53003243	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:53016681-53016865	HepG2	liver:	n/a	chr2:53016744-53016755
23	CEBPB	chr2:52972338-52972613	H1-hESC	embryonic stem cell:	n/a	chr2:52972476-52972487
24	CEBPB	chr2:52976939-52977247	A549	lung:	n/a	n/a
25	CEBPB	chr2:52954006-52954024	A549	lung:	n/a	n/a
26	CTCF	chr2:53016048-53016084	Lung_OC	lung:	n/a	n/a
27	CTCF	chr2:52935246-52935558	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr2:53016121-53016185	GM13976	blood:	n/a	n/a
29	CTCF	chr2:52972106-52972192	Lung_OC	lung:	n/a	n/a
30	CTCF	chr2:52935340-52935490	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr2:52916633-52916679	K562	blood:	n/a	n/a
32	CTCF	chr2:52991020-52991170	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr2:52935320-52935470	MCF-7	breast:	n/a	n/a
34	CTCF	chr2:52991700-52991850	HepG2	liver:	n/a	n/a
35	E2F4	chr2:52933953-52934153	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr2:52963721-52963902	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr2:53022285-53022485	MCF10A-Er-Src	breast:	n/a	n/a
38	EBF1	chr2:52927636-52927870	GM12878	blood:	n/a	chr2:52927777-52927788
39	FAM48A	chr2:52946139-52946333	GM12878	blood:	n/a	n/a
40	FOS	chr2:52990411-52990670	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr2:53003795-53003955	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr2:52914134-52914413	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr2:52931883-52932244	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr2:52914149-52914439	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr2:52931974-52932245	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr2:52914139-52914412	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr2:52990429-52990719	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr2:52931947-52932240	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr2:52990443-52990719	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr2:52931859-52932254	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53004359-53004409	HIPEpiC	eye:	n/a
2	chr2:53004359-53004409	GM12891	blood:	n/a
3	chr2:53004359-53004409	SAEC	small airway:	n/a
4	chr2:53004359-53004409	HMEC	breast:	n/a
5	chr2:53004359-53004409	HNPCEpiC	eye:	n/a
6	chr2:53004359-53004409	AG10803	skin:	n/a
7	chr2:53004359-53004409	NT2-D1	testis:	n/a
8	chr2:53004359-53004409	GM06990	blood:	n/a
9	chr2:53004359-53004409	HRE	kidney:	n/a
10	chr2:53004359-53004409	ovcar-3	ovarian:	n/a
11	chr2:53004359-53004409	SKMC	muscle:	n/a
12	chr2:53004359-53004409	AG04450	lung:	fetal
13	chr2:53004359-53004409	HUVEC	blood vessel:	n/a
14	chr2:53004359-53004409	HAEpiC	amniotic membrane:	n/a
15	chr2:53004359-53004409	LNCaP	prostate:	n/a
16	chr2:53004359-53004409	NB4	blood:	n/a
17	chr2:53004359-53004409	NHDF-neo	bronchial:	n/a
18	chr2:53004359-53004409	NHBE	bronchial:	n/a
19	chr2:53004359-53004409	H1-hESC	embryonic stem cell:	embryo
20	chr2:53004359-53004409	PrEC	prostate:	n/a
21	chr2:53004359-53004409	PANC-1	pancreas:	n/a
22	chr2:53004359-53004409	Caco-2	colon:	n/a
23	chr2:53004359-53004409	PFSK-1	brain:	n/a
24	chr2:53004359-53004409	A549	lung:	n/a
25	chr2:53004359-53004409	HCF	heart:	n/a
26	chr2:53004359-53004409	MCF-7	breast:	n/a
27	chr2:53004359-53004409	IMR90	lung:	fetal
28	chr2:53004359-53004409	BE2_C	brain:	n/a
29	chr2:53004359-53004409	T-47D	breast:	n/a
30	chr2:53004359-53004409	HCM	heart:	n/a
31	chr2:53004359-53004409	GM19239	blood:	n/a
32	chr2:53004359-53004409	SK-N-MC	brain:	n/a
33	chr2:53004359-53004409	HEK293	kidney:	embryo
34	chr2:53004359-53004409	HL-60	blood:	n/a
35	chr2:53004359-53004409	AG09319	gingival:	n/a
36	chr2:53004359-53004409	HCPEpiC	choroid plexus:	n/a
37	chr2:53004359-53004409	GM12878	blood:	n/a
38	chr2:53004359-53004409	MCF10A-Er-Src	breast:	n/a
39	chr2:53004359-53004409	AG09309	skin:	n/a
40	chr2:53004359-53004409	AG04449	skin:	fetal
41	chr2:53004359-53004409	K562	blood:	n/a
42	chr2:53004359-53004409	GM12892	blood:	n/a
43	chr2:53004359-53004409	SK-N-SH	brain:	n/a
44	chr2:53004359-53004409	U87	brain:	n/a
45	chr2:53004359-53004409	HEEpiC	esophagus:	n/a
46	chr2:53004359-53004409	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:53004359-53004409	NH-A	brain:	n/a
48	chr2:53004359-53004409	HCT-116	colon:	n/a
49	chr2:53004359-53004409	Jurkat	blood:	n/a
50	chr2:53004359-53004409	SK-N-SH_RA	brain:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:52917899..52919786-chr20:52823528..52826131,2	MCF-7	breast:
2	chr2:52948968..52951484-chr2:52953850..52956784,2	MCF-7	breast:
3	chr2:52948968..52951484-chr2:52953850..52956784,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-7	chr2:52947023-52947273	NONHSAT070679
2	lnc-ASB3-1	chr2:52949815-52950001	ENSG00000228033
3	lnc-ASB3-1	chr2:52953810-52953956	ENSG00000228033
4	lnc-CHAC2-7	chr2:52944877-52944958	NONHSAT070679
5	lnc-ASB3-2	chr2:52924973-52925210	XLOC_002096
6	lnc-ASB3-2	chr2:52918447-52918771	XLOC_002096
7	lnc-ASB3-1	chr2:52949815-52950001	ENSG00000228033
8	lnc-ASB3-1	chr2:52953810-52953956	ENSG00000228033
9	lnc-ASB3-1	chr2:52959880-52959915	ENSG00000228033

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4431	chr2:52929726-52929747	MIMAT0018947

No data

Variant related genes	Relation type
MIR4431	TF binding region
MIR4431	CpG island
ENSG00000101132	chromatin interactions
MAP3K1	miRNA target sites

Extended variants
information (count: 838 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:838 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370952765	chr2:52917924-52917925	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs573742373	chr2:52917968-52917969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs13426132	chr2:52917971-52917972	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs532502067	chr2:52917977-52917978	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562662550	chr2:52917991-52917992	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs531590959	chr2:52918011-52918012	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551810253	chr2:52918079-52918080	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs190499246	chr2:52918080-52918081	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs527813571	chr2:52918085-52918086	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183754675	chr2:52918123-52918124	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs62126963	chr2:52918171-52918172	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370043340	chr2:52918173-52918174	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188489454	chr2:52918182-52918183	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs368330122	chr2:52918207-52918208	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs373834039	chr2:52918211-52918212	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570020696	chr2:52918238-52918239	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs116929347	chr2:52918268-52918269	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557379476	chr2:52918270-52918271	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs528685142	chr2:52918288-52918289	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577198070	chr2:52918302-52918303	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs533925322	chr2:52918345-52918346	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs538600229	chr2:52918352-52918353	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553604487	chr2:52918369-52918370	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs573653421	chr2:52918377-52918378	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371600641	chr2:52918402-52918403	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78005812	chr2:52918427-52918428	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs116620294	chr2:52918447-52918448	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs144801079	chr2:52918448-52918449	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs576446848	chr2:52918451-52918452	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs150883621	chr2:52918468-52918469	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs565312303	chr2:52918488-52918489	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs558528564	chr2:52918542-52918543	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs541388462	chr2:52918561-52918562	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs561226541	chr2:52918567-52918568	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs192881245	chr2:52918574-52918575	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs184964326	chr2:52918595-52918596	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs2279346	chr2:52918600-52918601	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs139494654	chr2:52918625-52918626	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs149693924	chr2:52918630-52918631	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs1454381	chr2:52918674-52918675	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs186471242	chr2:52918691-52918692	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs536337072	chr2:52918762-52918763	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs191322761	chr2:52918775-52918776	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375769957	chr2:52918787-52918788	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576286551	chr2:52918821-52918822	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545189733	chr2:52918871-52918872	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs375386309	chr2:52918891-52918892	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs368562694	chr2:52918895-52918896	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115748978	chr2:52918898-52918899	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140230194	chr2:52918918-52918919	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52925600-52926000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:52925600-52926400	Enhancers	Ovary	ovary
3	chr2:52926200-52926600	Enhancers	Fetal Brain Male	brain
4	chr2:52929600-52929800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr2:52929600-52930000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:52929600-52932000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:52929800-52930400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr2:52929800-52930400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:52929800-52930400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr2:52929800-52930600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr2:52929800-52932000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr2:52930000-52930800	Enhancers	Rectal Smooth Muscle	rectum
13	chr2:52930200-52930600	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr2:52930400-52931000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr2:52930600-52931600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr2:52930600-52931800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr2:52931000-52931800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr2:52938200-52938600	Enhancers	Fetal Brain Female	brain
19	chr2:52938400-52939000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr2:52944200-52944400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr2:52944400-52945000	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr2:52944800-52945200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:52945000-52945200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr2:52945200-52946000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr2:52951000-52951400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr2:52951400-52952200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:52951800-52952200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr2:52951800-52952200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr2:52952200-52952400	Enhancers	Brain Hippocampus Middle	brain
30	chr2:52959800-52960600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:52959800-52961200	Enhancers	Stomach Mucosa	stomach
32	chr2:52960000-52960400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr2:52960000-52960400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr2:52960000-52960400	Enhancers	Spleen	Spleen
35	chr2:52960000-52960600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr2:52960000-52960600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr2:52960200-52960600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr2:52960200-52960600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr2:52960600-52961600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr2:52961200-52961600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:52961600-52961800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr2:52968200-52968800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:52972800-52973400	Active TSS	Fetal Heart	heart
44	chr2:53003600-53004200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr2:53003800-53004200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:53004200-53006400	Enhancers	Fetal Intestine Large	intestine
47	chr2:53021800-53022200	Enhancers	Adipose Nuclei	Adipose

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