Variant report

Variant	nsv1009977
Chromosome Location	chr2:50826820-51067628
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	BACH1	chr2:50955596-50955702	K562	blood:	n/a	n/a
2	BCL11A	chr2:50842488-50842720	H1-hESC	embryonic stem cell:	n/a	chr2:50842539-50842548
3	CEBPB	chr2:50854196-50854476	IMR90	lung:	n/a	chr2:50854319-50854330 chr2:50854320-50854331 chr2:50854319-50854332
4	CEBPB	chr2:50858684-50858994	HepG2	liver:	n/a	chr2:50858808-50858817 chr2:50858807-50858818 chr2:50858808-50858817 chr2:50858808-50858817 chr2:50858806-50858817 chr2:50858808-50858817
5	CEBPB	chr2:50890728-50891191	HepG2	liver:	n/a	chr2:50890749-50890760 chr2:50891044-50891055
6	CEBPB	chr2:50854171-50854480	A549	lung:	n/a	chr2:50854319-50854330 chr2:50854320-50854331 chr2:50854319-50854332
7	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
10	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
11	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:50839136-50839812	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
14	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
15	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
16	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
17	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
20	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
22	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:50842436-50842646	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:50854209-50854495	HepG2	liver:	n/a	chr2:50854319-50854330 chr2:50854320-50854331 chr2:50854319-50854332
25	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
27	CTCF	chr2:50902080-50902230	GM12869	blood:	n/a	n/a
28	CTCF	chr2:50973732-50973938	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50902100-50902250	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr2:50973740-50973890	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:51013578-51013819	Medullo	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
32	CTCF	chr2:50907104-50907160	GM20000	blood:	n/a	n/a
33	CTCF	chr2:50973746-50973953	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973733-50973956	GM13977	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50833940-50834090	HCM	heart:	n/a	n/a
36	CTCF	chr2:51009680-51009830	HRE	kidney:	n/a	n/a
37	CTCF	chr2:50902197-50902266	Medullo	brain:	n/a	n/a
38	CTCF	chr2:50834360-50834510	HRE	kidney:	n/a	n/a
39	CTCF	chr2:50902100-50902250	K562	blood:	n/a	n/a
40	CTCF	chr2:50902140-50902290	NB4	blood:	n/a	n/a
41	CTCF	chr2:50973720-50973870	GM12868	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:51056731-51056889	GM20000	blood:	n/a	n/a
43	CTCF	chr2:50902120-50902270	HepG2	liver:	n/a	n/a
44	CTCF	chr2:50848080-50848230	HCT-116	colon:	n/a	n/a
45	CTCF	chr2:50848100-50848250	HEK293	kidney:	n/a	n/a
46	CTCF	chr2:50834002-50834176	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr2:50902140-50902290	GM12865	blood:	n/a	n/a
48	CTCF	chr2:50973780-50973930	GM12874	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50889598-50889668	NHEK	skin:	n/a	n/a
50	CTCF	chr2:50973760-50973910	GM12875	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51057548-51057598	GM12892	blood:	n/a
2	chr2:50884252-50884302	MCF10A-Er-Src	breast:	n/a
3	chr2:50992829-50992879	PFSK-1	brain:	n/a
4	chr2:51056822-51056872	AG09309	skin:	n/a
5	chr2:50956659-50956709	MCF10A-Er-Src	breast:	n/a
6	chr2:51057218-51057268	PFSK-1	brain:	n/a
7	chr2:50876837-50876887	LNCaP	prostate:	n/a
8	chr2:51001003-51001053	HAEpiC	amniotic membrane:	n/a
9	chr2:51001003-51001053	GM12892	blood:	n/a
10	chr2:51001003-51001053	AoSMC	blood vessel:	n/a
11	chr2:51065673-51065723	A549	lung:	n/a
12	chr2:50852209-50852259	SKMC	muscle:	n/a
13	chr2:51056822-51056872	Hepatocyte	liver:	n/a
14	chr2:50884693-50884743	HMEC	breast:	n/a
15	chr2:50884252-50884302	NH-A	brain:	n/a
16	chr2:50884252-50884302	T-47D	breast:	n/a
17	chr2:50884693-50884743	SK-N-SH	brain:	n/a
18	chr2:51057548-51057598	AoSMC	blood vessel:	n/a
19	chr2:50884252-50884302	PANC-1	pancreas:	n/a
20	chr2:51056822-51056872	HMEC	breast:	n/a
21	chr2:50863603-50863653	GM06990	blood:	n/a
22	chr2:50876837-50876887	AG09319	gingival:	n/a
23	chr2:51057548-51057598	ECC-1	luminal epithelium:	n/a
24	chr2:51056822-51056872	HCF	heart:	n/a
25	chr2:50863603-50863653	HRE	kidney:	n/a
26	chr2:50863603-50863653	AG04450	lung:	fetal
27	chr2:51065673-51065723	MCF-7	breast:	n/a
28	chr2:51057548-51057598	GM12878	blood:	n/a
29	chr2:50884693-50884743	MCF10A-Er-Src	breast:	n/a
30	chr2:50992829-50992879	BJ	skin:	n/a
31	chr2:50992829-50992879	GM19239	blood:	n/a
32	chr2:51057218-51057268	GM12892	blood:	n/a
33	chr2:50884693-50884743	H1-hESC	embryonic stem cell:	embryo
34	chr2:50863603-50863653	GM12878	blood:	n/a
35	chr2:51056884-51056934	HepG2	liver:	n/a
36	chr2:50852209-50852259	HEK293	kidney:	embryo
37	chr2:51065673-51065723	SK-N-SH_RA	brain:	n/a
38	chr2:50992829-50992879	HCT-116	colon:	n/a
39	chr2:50992829-50992879	GM12892	blood:	n/a
40	chr2:50956659-50956709	Jurkat	blood:	n/a
41	chr2:50863603-50863653	HIPEpiC	eye:	n/a
42	chr2:50956659-50956709	CMK	blood:	n/a
43	chr2:51065673-51065723	ECC-1	luminal epithelium:	n/a
44	chr2:50992829-50992879	HRE	kidney:	n/a
45	chr2:50884252-50884302	SK-N-MC	brain:	n/a
46	chr2:51056884-51056934	T-47D	breast:	n/a
47	chr2:50852209-50852259	HRCEpiC	kidney:	n/a
48	chr2:51057218-51057268	GM06990	blood:	n/a
49	chr2:51057218-51057268	NHBE	bronchial:	n/a
50	chr2:50876837-50876887	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
2	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
3	chr2:50883231..50884999-chr2:50887642..50889397,2	MCF-7	breast:
4	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
5	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
6	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
7	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
8	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
9	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
10	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
11	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
12	chr2:50814373..50817124-chr2:50829622..50831513,2	MCF-7	breast:
13	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
14	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
15	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
16	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
17	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STON1-GTF2A1L-4	chr2:50851950-50852041	NONHSAT070645
2	lnc-FSHR-5	chr2:51056580-51056816	NONHSAT070648
3	lnc-STON1-GTF2A1L-4	chr2:50859486-50859749	NONHSAT070645
4	lnc-STON1-GTF2A1L-4	chr2:50858415-50858521	NONHSAT070645

Variant related genes	Relation type
ENSG00000216191	TF binding region
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
NRXN1	TF binding region
ENSG00000216191	CpG island
ENSG00000238165	CpG island
ENSG00000215968	CpG island
NRXN1	CpG island
ENSG00000216191	chromatin interactions
ENSG00000230327	chromatin interactions
ENSG00000179915	chromatin interactions

Extended variants
information (count: 8761 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:8761 , 50 per page) page: 1 2 3 4 5 6 7 ... 176

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60788817	chr2:50826828-50826829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571147170	chr2:50826899-50826900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140365858	chr2:50826927-50826928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs202104241	chr2:50826929-50826930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150408615	chr2:50826944-50826945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547216154	chr2:50826963-50826964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185770062	chr2:50826965-50826966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114258444	chr2:50826975-50826976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114447774	chr2:50826979-50826980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568788004	chr2:50827012-50827013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539438885	chr2:50827041-50827042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557433565	chr2:50827072-50827073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188820364	chr2:50827122-50827123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4971684	chr2:50827138-50827139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs373598199	chr2:50827142-50827143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138118165	chr2:50827148-50827149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377026794	chr2:50827174-50827175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573492201	chr2:50827232-50827233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181194488	chr2:50827243-50827244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4971685	chr2:50827276-50827277	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs59198531	chr2:50827304-50827305	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs546196258	chr2:50827350-50827351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142446204	chr2:50827377-50827378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564457896	chr2:50827414-50827415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372622104	chr2:50827415-50827416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74861058	chr2:50827443-50827444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573446572	chr2:50827460-50827461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74506990	chr2:50827478-50827479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372327284	chr2:50827492-50827493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375348372	chr2:50827526-50827527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528839143	chr2:50827531-50827532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112780367	chr2:50827533-50827534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562300167	chr2:50827539-50827540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537770945	chr2:50827541-50827542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369668507	chr2:50827555-50827556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377010355	chr2:50827557-50827558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2351769	chr2:50827582-50827583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146645214	chr2:50827588-50827589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139139920	chr2:50827607-50827608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191657247	chr2:50827608-50827609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373110936	chr2:50827620-50827621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143239187	chr2:50827623-50827624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533874460	chr2:50827624-50827625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555227113	chr2:50827647-50827648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375442405	chr2:50827665-50827666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183878866	chr2:50827702-50827703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556051962	chr2:50827715-50827716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371988778	chr2:50827732-50827733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575705114	chr2:50827755-50827756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527460701	chr2:50827776-50827777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
small cell lung cancer	20016488	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
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	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
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Psychiatric disorder	19734545	CNVD
Autism	20844286	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Autism	19218893	CNVD
Autism	22209245	CNVD
Neuropsychiatric disorder	21827697	CNVD
Schizophrenia	22118685	CNVD
Autism	20663923	CNVD
Schizophrenia	21285140	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Schizophrenia	22885689	CNVD
Autism	20964600	CNVD
Schizophrenia	19521646	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Mental retardation	19896112	CNVD
Acute myeloid leukemia	20729466	CNVD
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:910 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50802600-50832400	Weak transcription	Fetal Brain Female	brain
2	chr2:50812400-50827200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:50820000-50833400	Weak transcription	Brain Germinal Matrix	brain
4	chr2:50820600-50834200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:50828200-50829000	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr2:50830400-50830600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:50831400-50832600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:50832400-50832800	Enhancers	Fetal Brain Female	brain
9	chr2:50832600-50833800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:50832800-50838400	Weak transcription	Fetal Brain Female	brain
11	chr2:50833000-50834200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr2:50833400-50833600	Enhancers	Brain Germinal Matrix	brain
13	chr2:50833400-50834200	Enhancers	Hela-S3	cervix
14	chr2:50833600-50834200	Weak transcription	Brain Germinal Matrix	brain
15	chr2:50833800-50834200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr2:50834000-50834600	Enhancers	Brain Cingulate Gyrus	brain
17	chr2:50834200-50834600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr2:50834200-50834600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr2:50834200-50834800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr2:50834200-50835200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:50834200-50835200	Enhancers	Brain Germinal Matrix	brain
22	chr2:50834200-50835200	Enhancers	Fetal Stomach	stomach
23	chr2:50834200-50838200	Weak transcription	Hela-S3	cervix
24	chr2:50834200-50838600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr2:50834400-50835400	Enhancers	Fetal Muscle Leg	muscle
26	chr2:50834600-50838800	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr2:50835200-50847200	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr2:50835200-50848600	Weak transcription	Brain Germinal Matrix	brain
29	chr2:50835400-50838400	Weak transcription	Fetal Muscle Leg	muscle
30	chr2:50838200-50841400	Enhancers	Hela-S3	cervix
31	chr2:50838400-50838800	Enhancers	Fetal Brain Female	brain
32	chr2:50838400-50838800	Enhancers	Fetal Muscle Leg	muscle
33	chr2:50838400-50840200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:50838600-50839000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:50838600-50840000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr2:50838800-50839000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr2:50838800-50839400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr2:50838800-50849400	Weak transcription	Fetal Brain Female	brain
39	chr2:50839000-50839400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr2:50839000-50851800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr2:50839200-50841400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr2:50839400-50840000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:50839400-50841600	Enhancers	NHEK	skin
44	chr2:50839400-50842000	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr2:50839600-50841600	Enhancers	HMEC	breast
46	chr2:50839800-50841600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:50839800-50841600	Enhancers	NH-A	brain
48	chr2:50840000-50842000	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr2:50840000-50847800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr2:50840600-50841400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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