Variant report

Variant	nsv581978
Chromosome Location	chr2:53091691-53227749
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	chr2:53161835-53161893	HepG2	liver:	n/a	n/a
2	ATF2	chr2:53161624-53162186	GM12878	blood:	n/a	n/a
3	ATF2	chr2:53124799-53125218	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr2:53161550-53162230	GM12878	blood:	n/a	n/a
5	ATF3	chr2:53161366-53162095	HCT-116	colon:	n/a	n/a
6	BATF	chr2:53161569-53162046	GM12878	blood:	n/a	chr2:53161802-53161813 chr2:53161799-53161809 chr2:53161784-53161795
7	BATF	chr2:53166348-53166822	GM12878	blood:	n/a	n/a
8	BATF	chr2:53161603-53162043	GM12878	blood:	n/a	chr2:53161802-53161813 chr2:53161799-53161809 chr2:53161784-53161795
9	BCL11A	chr2:53152851-53153076	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:53166415-53166672	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:53161550-53162089	GM12878	blood:	n/a	chr2:53161787-53161796 chr2:53161788-53161797 chr2:53161801-53161810 chr2:53161802-53161811
12	BCL11A	chr2:53158346-53158507	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:53161743-53162072	GM12878	blood:	n/a	chr2:53161787-53161796 chr2:53161788-53161797 chr2:53161801-53161810 chr2:53161802-53161811
14	BCL3	chr2:53108842-53109038	GM12878	blood:	n/a	chr2:53108968-53108977
15	BCL3	chr2:53161702-53162170	GM12878	blood:	n/a	chr2:53161787-53161796 chr2:53161788-53161797 chr2:53161801-53161810 chr2:53161802-53161811
16	BHLHE40	chr2:53161740-53162175	GM12878	blood:	n/a	n/a
17	BRCA1	chr2:53160924-53162066	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr2:53161249-53162217	HCT-116	colon:	n/a	chr2:53162199-53162210
19	CBX3	chr2:53161275-53162160	HCT-116	colon:	n/a	n/a
20	CBX3	chr2:53108658-53109304	HCT-116	colon:	n/a	n/a
21	CEBPB	chr2:53131722-53132000	Hela-S3	cervix:	n/a	chr2:53131973-53131984
22	CEBPB	chr2:53161558-53162223	GM12878	blood:	n/a	chr2:53161857-53161869
23	CEBPB	chr2:53160531-53162111	Hela-S3	cervix:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
24	CEBPB	chr2:53155376-53155506	A549	lung:	n/a	n/a
25	CEBPB	chr2:53160427-53162176	HCT-116	colon:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
26	CEBPB	chr2:53122020-53122313	A549	lung:	n/a	chr2:53122180-53122191
27	CEBPB	chr2:53122154-53122200	Hela-S3	cervix:	n/a	chr2:53122180-53122191
28	CEBPB	chr2:53191978-53192295	IMR90	lung:	n/a	chr2:53192135-53192146 chr2:53192133-53192144 chr2:53192133-53192146
29	CEBPB	chr2:53104947-53105036	A549	lung:	n/a	n/a
30	CEBPB	chr2:53191991-53192268	Hela-S3	cervix:	n/a	chr2:53192135-53192146 chr2:53192133-53192144 chr2:53192133-53192146
31	CEBPB	chr2:53122010-53122340	HepG2	liver:	n/a	chr2:53122180-53122191
32	CEBPB	chr2:53161339-53161782	ECC-1	luminal epithelium:	n/a	chr2:53161529-53161540 chr2:53161549-53161560
33	CEBPB	chr2:53183276-53183632	IMR90	lung:	n/a	chr2:53183413-53183424 chr2:53183449-53183460
34	CEBPB	chr2:53161347-53161796	A549	lung:	n/a	chr2:53161529-53161540 chr2:53161549-53161560
35	CEBPB	chr2:53161204-53162173	HCT-116	colon:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
36	CEBPB	chr2:53161220-53162079	IMR90	lung:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
37	CEBPB	chr2:53122149-53122189	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:53108848-53109174	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:53191970-53192319	A549	lung:	n/a	chr2:53192135-53192146 chr2:53192133-53192144 chr2:53192133-53192146
40	CEBPB	chr2:53123918-53124240	A549	lung:	n/a	chr2:53124077-53124088 chr2:53124075-53124088 chr2:53124075-53124086
41	CEBPB	chr2:53123913-53124233	HepG2	liver:	n/a	chr2:53124077-53124088 chr2:53124075-53124088 chr2:53124075-53124086
42	CEBPB	chr2:53177429-53177688	HepG2	liver:	n/a	chr2:53177576-53177587
43	CEBPB	chr2:53183277-53183618	Hela-S3	cervix:	n/a	chr2:53183413-53183424 chr2:53183449-53183460
44	CEBPB	chr2:53145768-53146137	Hela-S3	cervix:	n/a	chr2:53145956-53145969
45	CEBPB	chr2:53145642-53146180	IMR90	lung:	n/a	chr2:53145956-53145969
46	CEBPB	chr2:53191959-53192336	H1-hESC	embryonic stem cell:	n/a	chr2:53192135-53192146 chr2:53192133-53192144 chr2:53192133-53192146
47	CEBPB	chr2:53161364-53161728	HepG2	liver:	n/a	chr2:53161529-53161540 chr2:53161549-53161560
48	CEBPB	chr2:53094201-53094581	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:53191950-53192305	HepG2	liver:	n/a	chr2:53192135-53192146 chr2:53192133-53192144 chr2:53192133-53192146
50	CEBPB	chr2:53183274-53183631	HepG2	liver:	n/a	chr2:53183413-53183424 chr2:53183449-53183460

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53107842-53107892	LNCaP	prostate:	n/a
2	chr2:53160678-53160728	HRPEpiC	eye:	n/a
3	chr2:53094222-53094272	PANC-1	pancreas:	n/a
4	chr2:53105695-53105745	CMK	blood:	n/a
5	chr2:53094222-53094272	LNCaP	prostate:	n/a
6	chr2:53160678-53160728	GM12892	blood:	n/a
7	chr2:53094222-53094272	HRCEpiC	kidney:	n/a
8	chr2:53107842-53107892	HL-60	blood:	n/a
9	chr2:53160678-53160728	H1-hESC	embryonic stem cell:	embryo
10	chr2:53105695-53105745	Caco-2	colon:	n/a
11	chr2:53107842-53107892	Hepatocyte	liver:	n/a
12	chr2:53160678-53160728	RPTEC	kidney:	n/a
13	chr2:53094222-53094272	HEEpiC	esophagus:	n/a
14	chr2:53094222-53094272	GM12892	blood:	n/a
15	chr2:53160678-53160728	GM19239	blood:	n/a
16	chr2:53192311-53192361	SK-N-SH	brain:	n/a
17	chr2:53160678-53160728	ProgFib	skin:	n/a
18	chr2:53107842-53107892	SAEC	small airway:	n/a
19	chr2:53107842-53107892	CMK	blood:	n/a
20	chr2:53160678-53160728	HCM	heart:	n/a
21	chr2:53192311-53192361	ovcar-3	ovarian:	n/a
22	chr2:53094222-53094272	NT2-D1	testis:	n/a
23	chr2:53192311-53192361	NB4	blood:	n/a
24	chr2:53107842-53107892	AoSMC	blood vessel:	n/a
25	chr2:53105695-53105745	ovcar-3	ovarian:	n/a
26	chr2:53160678-53160728	NB4	blood:	n/a
27	chr2:53105695-53105745	SKMC	muscle:	n/a
28	chr2:53094222-53094272	HepG2	liver:	n/a
29	chr2:53192311-53192361	HEEpiC	esophagus:	n/a
30	chr2:53160678-53160728	IMR90	lung:	fetal
31	chr2:53094222-53094272	NHDF-neo	bronchial:	n/a
32	chr2:53105695-53105745	SK-N-MC	brain:	n/a
33	chr2:53192311-53192361	HRCEpiC	kidney:	n/a
34	chr2:53160678-53160728	PFSK-1	brain:	n/a
35	chr2:53105695-53105745	SK-N-SH_RA	brain:	n/a
36	chr2:53094222-53094272	NH-A	brain:	n/a
37	chr2:53107842-53107892	U87	brain:	n/a
38	chr2:53160678-53160728	GM12891	blood:	n/a
39	chr2:53094222-53094272	H1-hESC	embryonic stem cell:	embryo
40	chr2:53107842-53107892	AG09309	skin:	n/a
41	chr2:53192311-53192361	Hepatocyte	liver:	n/a
42	chr2:53094222-53094272	U87	brain:	n/a
43	chr2:53105695-53105745	PFSK-1	brain:	n/a
44	chr2:53105695-53105745	PANC-1	pancreas:	n/a
45	chr2:53105695-53105745	NHBE	bronchial:	n/a
46	chr2:53192311-53192361	HUVEC	blood vessel:	n/a
47	chr2:53107842-53107892	HCM	heart:	n/a
48	chr2:53160678-53160728	HUVEC	blood vessel:	n/a
49	chr2:53105695-53105745	SK-N-SH	brain:	n/a
50	chr2:53192311-53192361	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:53198477..53200410-chr2:53204167..53206396,2	K562	blood:
2	chr2:53103066..53106486-chr2:53106611..53109718,3	MCF-7	breast:
3	chr2:53048846..53049807-chr2:53183875..53184416,2	MCF-7	breast:
4	chr2:53037286..53038157-chr2:53203093..53203814,3	MCF-7	breast:
5	chr2:53115077..53117448-chr2:53686034..53688851,2	MCF-7	breast:
6	chr2:53132852..53133808-chr20:52198265..52198765,2	MCF-7	breast:
7	chr2:53103066..53106486-chr2:53106611..53109718,3	MCF-7	breast:
8	chr2:53198477..53200410-chr2:53204167..53206396,2	K562	blood:
9	chr2:53203292..53203812-chr2:53700344..53701275,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB3-1	chr2:53124381-53124442	ENSG00000228033
2	lnc-ASB3-1	chr2:53137102-53137158	ENSG00000228033
3	lnc-ASB3-1	chr2:53137102-53137158	ENSG00000228033
4	lnc-CHAC2-1	chr2:53093519-53093769	XLOC_001470
5	lnc-ASB3-1	chr2:53124381-53124442	ENSG00000228033
6	lnc-CHAC2-6	chr2:53110381-53110593	NONHSAT070683

Variant related genes	Relation type
ENSG00000228033	TF binding region
ENSG00000232668	TF binding region
ENSG00000228033	CpG island
ENSG00000232668	CpG island

Extended variants
information (count: 5055 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5055 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12618983	chr2:53091691-53091692	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572607831	chr2:53091766-53091767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530725075	chr2:53091798-53091799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541396216	chr2:53091799-53091800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147310437	chr2:53091805-53091806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377441290	chr2:53091806-53091807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs70944108	chr2:53091836-53091837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554956790	chr2:53091841-53091842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531648925	chr2:53091905-53091906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574928166	chr2:53091981-53091982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544127836	chr2:53092075-53092076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79811678	chr2:53092076-53092077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564267612	chr2:53092078-53092079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4672031	chr2:53092094-53092095	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs546702881	chr2:53092098-53092099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540060672	chr2:53092107-53092108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376352658	chr2:53092151-53092152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533924900	chr2:53092190-53092191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566497757	chr2:53092225-53092226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529277775	chr2:53092251-53092252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112980238	chr2:53092267-53092268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150561968	chr2:53092318-53092319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529424491	chr2:53092348-53092349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549535683	chr2:53092383-53092384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112209759	chr2:53092447-53092448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs70944109	chr2:53092449-53092450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569490366	chr2:53092467-53092468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375369776	chr2:53092492-53092493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs180962626	chr2:53092504-53092505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187247266	chr2:53092506-53092507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552041142	chr2:53092551-53092552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571858335	chr2:53092573-53092574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189508217	chr2:53092584-53092585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547694767	chr2:53092591-53092592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1451456	chr2:53092604-53092605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs372235470	chr2:53092618-53092619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78531685	chr2:53092688-53092689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181447531	chr2:53092695-53092696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139592356	chr2:53092710-53092711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs17039473	chr2:53092740-53092741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557989521	chr2:53092764-53092765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144707599	chr2:53092792-53092793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs17504530	chr2:53092800-53092801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs372862695	chr2:53092831-53092832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186279604	chr2:53092866-53092867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539512796	chr2:53092877-53092878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543143374	chr2:53092905-53092906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190205254	chr2:53092909-53092910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531691296	chr2:53092958-53092959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367781764	chr2:53092985-53092986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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

Chromatin state (count:211 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53090200-53093600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr2:53090400-53091800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:53090400-53096200	Weak transcription	NHDF-Ad	bronchial
4	chr2:53091600-53095600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr2:53091800-53092600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:53092600-53093400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:53093400-53094400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:53093400-53095000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:53093600-53094200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr2:53093600-53095000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:53093600-53095200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr2:53094000-53094400	Enhancers	Fetal Lung	lung
13	chr2:53094400-53094800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr2:53094400-53108600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:53095000-53096000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:53095800-53096400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr2:53096000-53096400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr2:53096000-53096600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr2:53096200-53096400	Enhancers	NHDF-Ad	bronchial
20	chr2:53101800-53102600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:53102600-53108200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:53104000-53104200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr2:53104200-53104600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:53104400-53107200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:53104600-53104800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr2:53104600-53105600	Enhancers	Fetal Stomach	stomach
27	chr2:53104600-53105600	Enhancers	Pancreas	Pancrea
28	chr2:53104600-53105600	Enhancers	Stomach Smooth Muscle	stomach
29	chr2:53104600-53105600	Enhancers	A549	lung
30	chr2:53105400-53107600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:53105600-53108200	Weak transcription	A549	lung
32	chr2:53105600-53121800	Weak transcription	Pancreas	Pancrea
33	chr2:53106800-53107000	Enhancers	Colon Smooth Muscle	Colon
34	chr2:53107200-53109000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:53107400-53107800	Enhancers	Colon Smooth Muscle	Colon
36	chr2:53107600-53108200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:53107600-53108200	Enhancers	Fetal Heart	heart
38	chr2:53107600-53109000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr2:53107800-53109000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:53107800-53109200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr2:53108200-53108400	Enhancers	A549	lung
42	chr2:53108200-53109200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr2:53108200-53119800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr2:53108400-53108800	Weak transcription	A549	lung
45	chr2:53108600-53109400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:53108600-53109400	Enhancers	Hela-S3	cervix
47	chr2:53108800-53109200	Enhancers	A549	lung
48	chr2:53108800-53109600	Enhancers	HMEC	breast
49	chr2:53109000-53109200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:53109200-53110400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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