Variant report

Variant	nsv535707
Chromosome Location	chr2:51166993-51396921
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	chr2:51330523-51330544	HepG2	liver:	n/a	n/a
2	ATF2	chr2:51259020-51259511	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:51259057-51259636	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:51246247-51246255	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:51240144-51240458	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:51330505-51330576	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr2:51330297-51330702	HepG2	liver:	n/a	n/a
8	BRCA1	chr2:51214813-51214934	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr2:51179768-51180665	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr2:51185262-51185455	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr2:51330435-51330474	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr2:51259605-51259656	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr2:51240017-51240569	HCT-116	colon:	n/a	n/a
14	CEBPB	chr2:51229696-51229991	IMR90	lung:	n/a	chr2:51229820-51229831
15	CEBPB	chr2:51180120-51180462	HepG2	liver:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
16	CEBPB	chr2:51325500-51325735	H1-hESC	embryonic stem cell:	n/a	chr2:51325594-51325607
17	CEBPB	chr2:51184080-51184410	A549	lung:	n/a	chr2:51184131-51184142
18	CEBPB	chr2:51256026-51256305	HepG2	liver:	n/a	chr2:51256172-51256183
19	CEBPB	chr2:51282778-51283040	IMR90	lung:	n/a	chr2:51282886-51282897
20	CEBPB	chr2:51185023-51185436	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
21	CEBPB	chr2:51328029-51328351	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr2:51185072-51185406	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
23	CEBPB	chr2:51185008-51185377	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
24	CEBPB	chr2:51376877-51377106	A549	lung:	n/a	n/a
25	CEBPB	chr2:51240147-51240542	MCF-7	breast:	n/a	n/a
26	CEBPB	chr2:51255980-51256366	H1-hESC	embryonic stem cell:	n/a	chr2:51256172-51256183
27	CEBPB	chr2:51392868-51393388	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:51335948-51336306	IMR90	lung:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
29	CEBPB	chr2:51184010-51184263	HepG2	liver:	n/a	chr2:51184131-51184142
30	CEBPB	chr2:51184978-51185335	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
31	CEBPB	chr2:51259207-51259533	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:51282756-51283052	HepG2	liver:	n/a	chr2:51282886-51282897
33	CEBPB	chr2:51185014-51185411	Hela-S3	cervix:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
34	CEBPB	chr2:51185035-51185357	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
35	CEBPB	chr2:51256004-51256330	K562	blood:	n/a	chr2:51256172-51256183
36	CEBPB	chr2:51196131-51196377	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:51272267-51272564	A549	lung:	n/a	chr2:51272397-51272408 chr2:51272396-51272409
38	CEBPB	chr2:51196305-51196335	K562	blood:	n/a	n/a
39	CEBPB	chr2:51256005-51256373	Hela-S3	cervix:	n/a	chr2:51256172-51256183
40	CEBPB	chr2:51330315-51330732	IMR90	lung:	n/a	n/a
41	CEBPB	chr2:51185077-51185269	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185201-51185210 chr2:51185201-51185210
42	CEBPB	chr2:51255964-51256336	MCF-7	breast:	n/a	chr2:51256172-51256183
43	CEBPB	chr2:51196130-51196480	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:51330496-51330704	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:51335993-51336283	H1-hESC	embryonic stem cell:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
46	CEBPB	chr2:51335948-51336305	HepG2	liver:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
47	CEBPB	chr2:51185019-51185391	H1-hESC	embryonic stem cell:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
48	CEBPB	chr2:51180081-51180588	ECC-1	luminal epithelium:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
49	CEBPB	chr2:51392842-51393189	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr2:51335991-51336268	Hela-S3	cervix:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51218880-51218930	Hepatocyte	liver:	n/a
2	chr2:51260399-51260449	NB4	blood:	n/a
3	chr2:51259697-51259747	ProgFib	skin:	n/a
4	chr2:51254823-51254873	SKMC	muscle:	n/a
5	chr2:51218880-51218930	Hepatocyte	liver:	n/a
6	chr2:51260399-51260449	NB4	blood:	n/a
7	chr2:51259697-51259747	ProgFib	skin:	n/a
8	chr2:51254823-51254873	SKMC	muscle:	n/a
9	chr2:51259786-51259836	HRCEpiC	kidney:	n/a
10	chr2:51255306-51255356	ProgFib	skin:	n/a
11	chr2:51259693-51259743	HCT-116	colon:	n/a
12	chr2:51259786-51259836	HUVEC	blood vessel:	n/a
13	chr2:51254102-51254152	NHDF-neo	bronchial:	n/a
14	chr2:51378948-51378998	ProgFib	skin:	n/a
15	chr2:51231649-51231699	AG04450	lung:	fetal
16	chr2:51259703-51259753	AG09309	skin:	n/a
17	chr2:51259697-51259747	AG10803	skin:	n/a
18	chr2:51259552-51259602	Caco-2	colon:	n/a
19	chr2:51259703-51259753	SK-N-SH_RA	brain:	n/a
20	chr2:51259786-51259836	AG10803	skin:	n/a
21	chr2:51255324-51255374	ovcar-3	ovarian:	n/a
22	chr2:51231649-51231699	SAEC	small airway:	n/a
23	chr2:51259552-51259602	PrEC	prostate:	n/a
24	chr2:51259786-51259836	NHBE	bronchial:	n/a
25	chr2:51228125-51228175	BE2_C	brain:	n/a
26	chr2:51254102-51254152	Hela-S3	cervix:	n/a
27	chr2:51255306-51255356	RPTEC	kidney:	n/a
28	chr2:51259693-51259743	MCF-7	breast:	n/a
29	chr2:51254021-51254071	AG10803	skin:	n/a
30	chr2:51254102-51254152	HRCEpiC	kidney:	n/a
31	chr2:51255627-51255677	GM12891	blood:	n/a
32	chr2:51254132-51254182	HPAEpiC	pulmonary alveolar:	n/a
33	chr2:51255627-51255677	H1-hESC	embryonic stem cell:	embryo
34	chr2:51254132-51254182	SK-N-SH_RA	brain:	n/a
35	chr2:51218880-51218930	GM06990	blood:	n/a
36	chr2:51260399-51260449	GM12892	blood:	n/a
37	chr2:51260399-51260449	HRE	kidney:	n/a
38	chr2:51228125-51228175	AG09319	gingival:	n/a
39	chr2:51240310-51240360	HRCEpiC	kidney:	n/a
40	chr2:51259697-51259747	SK-N-SH_RA	brain:	n/a
41	chr2:51259697-51259747	AG04449	skin:	fetal
42	chr2:51378948-51378998	SKMC	muscle:	n/a
43	chr2:51254132-51254182	GM12891	blood:	n/a
44	chr2:51260399-51260449	AG04449	skin:	fetal
45	chr2:51228125-51228175	HUVEC	blood vessel:	n/a
46	chr2:51259493-51259543	GM12892	blood:	n/a
47	chr2:51259807-51259857	T-47D	breast:	n/a
48	chr2:51259786-51259836	HL-60	blood:	n/a
49	chr2:51231649-51231699	ECC-1	luminal epithelium:	n/a
50	chr2:51255306-51255356	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
2	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
3	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
4	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
5	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
6	chr2:51288072..51290967-chr2:232569534..232571521,2	MCF-7	breast:
7	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
8	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
9	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
10	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-4	chr2:51279495-51279592	ENSG00000231918.1
2	lnc-NRXN1-3	chr2:51283633-51283791	NONHSAT070652
3	lnc-NRXN1-3	chr2:51302314-51302406	NONHSAT070652
4	lnc-NRXN1-3	chr2:51294575-51294743	l_1833_chr2:51283578-51306188_testes
5	lnc-NRXN1-3	chr2:51283579-51283793	l_1833_chr2:51283578-51306188_testes
6	lnc-CHAC2-4	chr2:51259739-51260154	ENSG00000231918.1
7	lnc-NRXN1-3	chr2:51306149-51306209	l_1833_chr2:51283578-51306188_testes
8	lnc-NRXN1-3	chr2:51302313-51302437	l_1833_chr2:51283578-51306188_testes
9	lnc-NRXN1-3	chr2:51282723-51282956	NONHSAT070652

Variant related genes	Relation type
NRXN1	TF binding region
ENSG00000216011	TF binding region
ENSG00000272385	TF binding region
ENSG00000231918	TF binding region
NRXN1	CpG island
ENSG00000216011	CpG island
ENSG00000272385	CpG island
ENSG00000231918	CpG island

Extended variants
information (count: 6642 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:6642 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184155958	chr2:51167004-51167005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75998786	chr2:51167061-51167062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560068106	chr2:51167095-51167096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188504282	chr2:51167104-51167105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192232609	chr2:51167118-51167119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570505413	chr2:51167128-51167129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556471057	chr2:51167157-51167158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530865866	chr2:51167193-51167194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184258981	chr2:51167197-51167198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553122620	chr2:51167240-51167241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570521780	chr2:51167274-51167275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528312707	chr2:51167341-51167342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546421135	chr2:51167345-51167346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568003081	chr2:51167360-51167361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535403409	chr2:51167372-51167373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556491364	chr2:51167380-51167381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572811952	chr2:51167386-51167387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190130157	chr2:51167387-51167388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116522762	chr2:51167396-51167397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557855882	chr2:51167400-51167401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572880651	chr2:51167401-51167402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541599160	chr2:51167411-51167412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553643894	chr2:51167418-51167419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575206839	chr2:51167439-51167440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6752095	chr2:51167441-51167442	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs11685581	chr2:51167442-51167443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182172354	chr2:51167450-51167451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11680442	chr2:51167464-51167465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11680475	chr2:51167481-51167482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11674665	chr2:51167493-51167494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144043714	chr2:51167494-51167495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545955791	chr2:51167539-51167540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564586974	chr2:51167548-51167549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528617535	chr2:51167600-51167601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575201019	chr2:51167623-51167624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112617505	chr2:51167624-51167625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79271329	chr2:51167645-51167646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550477163	chr2:51167649-51167650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs80017183	chr2:51167663-51167664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539396371	chr2:51167679-51167680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113337873	chr2:51167720-51167721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187213628	chr2:51167721-51167722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150950152	chr2:51167723-51167724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140837491	chr2:51167751-51167752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150149383	chr2:51167752-51167753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189177838	chr2:51167753-51167754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536125236	chr2:51167770-51167771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557710132	chr2:51167777-51167778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575879395	chr2:51167799-51167800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368894645	chr2:51167801-51167802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
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
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	17989066	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1018 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51158200-51171000	Weak transcription	Fetal Brain Male	brain
2	chr2:51167000-51168000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:51168000-51168400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:51168000-51169800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:51168200-51171000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
6	chr2:51168400-51178000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:51169000-51169600	ZNF genes & repeats	Fetal Brain Female	brain
8	chr2:51169200-51170800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr2:51169800-51170000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr2:51170800-51175600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr2:51171000-51171600	Enhancers	Fetal Brain Male	brain
12	chr2:51171000-51175000	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr2:51173800-51174000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:51174200-51177000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:51174800-51177400	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr2:51175000-51177400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr2:51175400-51176200	Enhancers	Brain Germinal Matrix	brain
18	chr2:51175600-51176000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:51175600-51177000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:51175800-51176000	Enhancers	Brain Substantia Nigra	brain
21	chr2:51176000-51176200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr2:51176000-51176600	Weak transcription	Brain Substantia Nigra	brain
23	chr2:51176000-51178200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:51176200-51181400	Weak transcription	Brain Germinal Matrix	brain
25	chr2:51176400-51190600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr2:51176600-51177200	Enhancers	Brain Substantia Nigra	brain
27	chr2:51177000-51177200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr2:51177200-51178200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:51177200-51181800	Weak transcription	Brain Substantia Nigra	brain
30	chr2:51177400-51179600	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr2:51177400-51182400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr2:51177800-51179800	Enhancers	Hela-S3	cervix
33	chr2:51178000-51178600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr2:51178000-51180000	Enhancers	HMEC	breast
35	chr2:51178200-51178600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:51178200-51178600	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr2:51178200-51178600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr2:51178200-51178800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr2:51178200-51179000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:51178200-51179600	Enhancers	NHEK	skin
41	chr2:51178400-51178600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr2:51178400-51178600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr2:51178400-51178600	Enhancers	Osteobl	bone
44	chr2:51178400-51178800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:51178400-51179000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr2:51178400-51179600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:51178400-51180400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr2:51178600-51179600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr2:51178600-51179600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr2:51178600-51179600	Weak transcription	Osteobl	bone

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