Variant report

Variant	esv2830192
Chromosome Location	chr2:134259612-134311713
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	BCL11A	chr2:134260874-134261163	GM12878	blood:	n/a	chr2:134261092-134261101
2	BHLHE40	chr2:134260882-134261211	GM12878	blood:	n/a	n/a
3	CEBPB	chr2:134274199-134274578	HepG2	liver:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
4	CEBPB	chr2:134278939-134279168	A549	lung:	n/a	n/a
5	CEBPB	chr2:134294344-134294544	IMR90	lung:	n/a	chr2:134294444-134294455
6	CEBPB	chr2:134274206-134274547	HepG2	liver:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
7	CEBPB	chr2:134274175-134274591	MCF-7	breast:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
8	CEBPB	chr2:134274241-134274513	H1-hESC	embryonic stem cell:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
9	CEBPB	chr2:134274231-134274564	K562	blood:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
10	CEBPB	chr2:134290437-134290854	A549	lung:	n/a	n/a
11	CEBPB	chr2:134278915-134279223	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:134274219-134274616	ECC-1	luminal epithelium:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
13	CEBPB	chr2:134284059-134284192	Hela-S3	cervix:	n/a	chr2:134284125-134284136
14	CEBPB	chr2:134292626-134292826	A549	lung:	n/a	n/a
15	CEBPB	chr2:134290470-134290695	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:134294307-134294503	HepG2	liver:	n/a	chr2:134294444-134294455
17	CEBPB	chr2:134274252-134274573	MCF-7	breast:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
18	CEBPB	chr2:134274141-134274573	A549	lung:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
19	CEBPB	chr2:134274209-134274574	Hela-S3	cervix:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
20	CEBPB	chr2:134290389-134290949	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:134274227-134274600	ECC-1	luminal epithelium:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
22	CEBPB	chr2:134284002-134284292	HepG2	liver:	n/a	chr2:134284125-134284136
23	CEBPB	chr2:134274191-134274616	A549	lung:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
24	CEBPB	chr2:134274201-134274569	A549	lung:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
25	CEBPB	chr2:134283964-134284305	IMR90	lung:	n/a	chr2:134284125-134284136
26	CEBPB	chr2:134278932-134279258	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:134274205-134274581	IMR90	lung:	n/a	chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274387-134274396 chr2:134274385-134274396
28	CEBPB	chr2:134290425-134290851	IMR90	lung:	n/a	n/a
29	CHD2	chr2:134260606-134261303	GM12878	blood:	n/a	n/a
30	CHD2	chr2:134290515-134290896	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr2:134277400-134277550	SAEC	small airway:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
32	CTCF	chr2:134277380-134277530	HepG2	liver:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
33	CTCF	chr2:134290620-134290770	AG04450	lung:	n/a	n/a
34	CTCF	chr2:134273854-134273914	ProgFib	skin:	n/a	n/a
35	CTCF	chr2:134271879-134271922	LNCaP	prostate:	n/a	n/a
36	CTCF	chr2:134277175-134277570	MCF-7	breast:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
37	CTCF	chr2:134277200-134277350	A549	lung:	n/a	n/a
38	CTCF	chr2:134277206-134277541	HepG2	liver:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
39	CTCF	chr2:134277320-134277470	HEK293	kidney:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
40	CTCF	chr2:134277340-134277490	BJ	skin:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
41	CTCF	chr2:134277340-134277490	NHDF-neo	bronchial:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
42	CTCF	chr2:134290500-134290650	HFF	foreskin:	n/a	n/a
43	CTCF	chr2:134277340-134277490	GM06990	blood:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
44	CTCF	chr2:134277393-134277552	Fibrobl	skin:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
45	CTCF	chr2:134277220-134277370	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr2:134277300-134277450	HL-60	blood:	n/a	n/a
47	CTCF	chr2:134277388-134277495	Pancreas_OC	pancreas:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
48	CTCF	chr2:134277340-134277490	HCM	heart:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
49	CTCF	chr2:134277320-134277470	HMF	breast:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458
50	CTCF	chr2:134277360-134277510	NHLF	lung:	n/a	chr2:134277447-134277465 chr2:134277450-134277463 chr2:134277449-134277470 chr2:134277450-134277458

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:134304653-134304703	GM19239	blood:	n/a
2	chr2:134282102-134282152	MCF-7	breast:	n/a
3	chr2:134304653-134304703	NHBE	bronchial:	n/a
4	chr2:134304756-134304806	H1-hESC	embryonic stem cell:	embryo
5	chr2:134272244-134272294	PFSK-1	brain:	n/a
6	chr2:134272244-134272294	A549	lung:	n/a
7	chr2:134304653-134304703	LNCaP	prostate:	n/a
8	chr2:134304653-134304703	U87	brain:	n/a
9	chr2:134272244-134272294	HCF	heart:	n/a
10	chr2:134282102-134282152	GM12891	blood:	n/a
11	chr2:134272244-134272294	CMK	blood:	n/a
12	chr2:134282102-134282152	SK-N-SH_RA	brain:	n/a
13	chr2:134304653-134304703	K562	blood:	n/a
14	chr2:134304756-134304806	BE2_C	brain:	n/a
15	chr2:134282102-134282152	SAEC	small airway:	n/a
16	chr2:134304653-134304703	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:134304653-134304703	AG09309	skin:	n/a
18	chr2:134304653-134304703	BE2_C	brain:	n/a
19	chr2:134282102-134282152	K562	blood:	n/a
20	chr2:134282102-134282152	Hela-S3	cervix:	n/a
21	chr2:134272244-134272294	HepG2	liver:	n/a
22	chr2:134272244-134272294	MCF-7	breast:	n/a
23	chr2:134304756-134304806	BJ	skin:	n/a
24	chr2:134272244-134272294	PANC-1	pancreas:	n/a
25	chr2:134272244-134272294	ProgFib	skin:	n/a
26	chr2:134282102-134282152	HL-60	blood:	n/a
27	chr2:134304653-134304703	ovcar-3	ovarian:	n/a
28	chr2:134304756-134304806	IMR90	lung:	fetal
29	chr2:134282102-134282152	HRPEpiC	eye:	n/a
30	chr2:134272244-134272294	AG09309	skin:	n/a
31	chr2:134304756-134304806	Caco-2	colon:	n/a
32	chr2:134272244-134272294	H1-hESC	embryonic stem cell:	embryo
33	chr2:134282102-134282152	AG09309	skin:	n/a
34	chr2:134304653-134304703	AG09319	gingival:	n/a
35	chr2:134304653-134304703	GM06990	blood:	n/a
36	chr2:134304653-134304703	HL-60	blood:	n/a
37	chr2:134304653-134304703	HepG2	liver:	n/a
38	chr2:134304653-134304703	SAEC	small airway:	n/a
39	chr2:134304653-134304703	GM12892	blood:	n/a
40	chr2:134272244-134272294	NHBE	bronchial:	n/a
41	chr2:134304756-134304806	HRCEpiC	kidney:	n/a
42	chr2:134272244-134272294	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:134304756-134304806	LNCaP	prostate:	n/a
44	chr2:134272244-134272294	AG09319	gingival:	n/a
45	chr2:134304653-134304703	RPTEC	kidney:	n/a
46	chr2:134282102-134282152	GM06990	blood:	n/a
47	chr2:134282102-134282152	NH-A	brain:	n/a
48	chr2:134304756-134304806	GM12892	blood:	n/a
49	chr2:134304653-134304703	NB4	blood:	n/a
50	chr2:134282102-134282152	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:134250271..134251246-chr2:134262119..134262954,2	MCF-7	breast:
2	chr2:134083491..134086031-chr2:134262913..134265457,2	MCF-7	breast:
3	chr2:134253868..134259578-chr2:134259579..134266138,12	MCF-7	breast:
4	chr2:134089345..134089856-chr2:134262223..134263005,2	MCF-7	breast:
5	chr2:134193206..134195489-chr2:134262827..134264976,2	MCF-7	breast:
6	chr2:134262296..134264688-chr2:134267619..134270356,2	MCF-7	breast:
7	chr2:133339903..133340611-chr2:134262125..134263083,2	MCF-7	breast:
8	chr2:134265911..134268884-chr2:134269496..134274997,4	MCF-7	breast:
9	chr2:134288676..134290659-chr2:134294672..134296438,2	MCF-7	breast:
10	chr2:134279989..134282547-chr2:134284755..134287346,3	K562	blood:
11	chr2:134250215..134251119-chr2:134262111..134263140,7	MCF-7	breast:
12	chr2:72206068..72206655-chr2:134299699..134300454,2	MCF-7	breast:
13	chr2:134288676..134290659-chr2:134294672..134296438,2	MCF-7	breast:
14	chr2:134263749..134265675-chr2:134399274..134401241,2	MCF-7	breast:
15	chr2:134277436..134277987-chr2:134537073..134537950,2	MCF-7	breast:
16	chr2:134089010..134089877-chr2:134262426..134263057,3	MCF-7	breast:
17	chr2:134019056..134021492-chr2:134262374..134264487,2	MCF-7	breast:
18	chr2:133428056..133430073-chr2:134262695..134265949,3	MCF-7	breast:
19	chr2:134250274..134251222-chr2:134262111..134262982,5	MCF-7	breast:
20	chr2:134257170..134260161-chr2:134313651..134315459,2	MCF-7	breast:
21	chr2:134265911..134268884-chr2:134269496..134274997,4	MCF-7	breast:
22	chr2:134262296..134264688-chr2:134267619..134270356,2	MCF-7	breast:
23	chr2:134250267..134251079-chr2:134262506..134263278,3	MCF-7	breast:
24	chr2:134277466..134278009-chr2:134318355..134319063,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000223430	TF binding region
NCKAP5	TF binding region
ENSG00000223430	CpG island
NCKAP5	CpG island
ENSG00000150551	chromatin interactions
ENSG00000176771	chromatin interactions

Extended variants
information (count: 2018 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2018 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2163654	chr2:134259612-134259613	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575533353	chr2:134259621-134259622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568718759	chr2:134259623-134259624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537098204	chr2:134259626-134259627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558671603	chr2:134259628-134259629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115562664	chr2:134259640-134259641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143534200	chr2:134259676-134259677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6749346	chr2:134259684-134259685	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs573391370	chr2:134259899-134259900	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148013450	chr2:134259921-134259922	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112219682	chr2:134259926-134259927	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143502016	chr2:134259944-134259945	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562260227	chr2:134259982-134259983	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546575342	chr2:134260042-134260043	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112885802	chr2:134260055-134260056	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374054173	chr2:134260099-134260100	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529658252	chr2:134260102-134260103	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189562433	chr2:134260111-134260112	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575957130	chr2:134260120-134260121	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541305300	chr2:134260147-134260148	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545905542	chr2:134260209-134260210	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564242605	chr2:134260227-134260228	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528055513	chr2:134260268-134260269	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145804433	chr2:134260315-134260316	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2163655	chr2:134260318-134260319	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561547684	chr2:134260329-134260330	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs59817257	chr2:134260359-134260360	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576557129	chr2:134260366-134260367	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138651541	chr2:134260379-134260380	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371927855	chr2:134260380-134260381	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532998107	chr2:134260383-134260384	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs56949683	chr2:134260409-134260410	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs180792170	chr2:134260424-134260425	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142670923	chr2:134260431-134260432	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546938628	chr2:134260440-134260441	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368942717	chr2:134260442-134260443	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531820308	chr2:134260447-134260448	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs386650772	chr2:134260458-134260459	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78015341	chr2:134260459-134260460	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557728317	chr2:134260465-134260466	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575892864	chr2:134260496-134260497	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150695060	chr2:134260508-134260509	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558093522	chr2:134260518-134260519	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572863670	chr2:134260605-134260606	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112032390	chr2:134260606-134260607	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs36064721	chr2:134260612-134260613	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570404791	chr2:134260614-134260615	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528279353	chr2:134260620-134260621	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139950816	chr2:134260635-134260636	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11886344	chr2:134260660-134260661	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:134240000-134262400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:134246400-134262400	Weak transcription	Gastric	stomach
3	chr2:134248000-134262000	Weak transcription	NHLF	lung
4	chr2:134251600-134261400	Weak transcription	Right Atrium	heart
5	chr2:134255400-134259800	Weak transcription	Left Ventricle	heart
6	chr2:134255400-134261800	Weak transcription	Brain Anterior Caudate	brain
7	chr2:134255400-134261800	Weak transcription	Brain Cingulate Gyrus	brain
8	chr2:134255400-134262000	Weak transcription	Brain Angular Gyrus	brain
9	chr2:134255400-134262200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:134255600-134260400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr2:134255800-134260200	Weak transcription	Brain Hippocampus Middle	brain
12	chr2:134255800-134260400	Weak transcription	Liver	Liver
13	chr2:134255800-134260600	Weak transcription	Brain Substantia Nigra	brain
14	chr2:134256600-134261800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:134256600-134262000	Weak transcription	Fetal Lung	lung
16	chr2:134256600-134262200	Weak transcription	Fetal Stomach	stomach
17	chr2:134256600-134262400	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr2:134256800-134261200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr2:134256800-134262200	Weak transcription	Fetal Brain Male	brain
20	chr2:134257000-134260400	Weak transcription	Small Intestine	intestine
21	chr2:134257000-134261400	Weak transcription	Fetal Brain Female	brain
22	chr2:134257000-134262000	Weak transcription	Fetal Kidney	kidney
23	chr2:134257200-134259800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:134257200-134260200	Weak transcription	Fetal Intestine Small	intestine
25	chr2:134257200-134260400	Weak transcription	Stomach Mucosa	stomach
26	chr2:134257200-134262000	Weak transcription	Brain Germinal Matrix	brain
27	chr2:134257200-134262400	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr2:134257400-134262400	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr2:134257600-134260400	Weak transcription	Fetal Intestine Large	intestine
30	chr2:134258000-134261400	Weak transcription	NHDF-Ad	bronchial
31	chr2:134258200-134261400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr2:134258200-134261400	Weak transcription	HMEC	breast
33	chr2:134258200-134261800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:134258800-134261400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr2:134258800-134262000	Weak transcription	NHEK	skin
36	chr2:134259000-134261600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr2:134259000-134265600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:134259600-134261400	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr2:134259800-134260600	Enhancers	Left Ventricle	heart
40	chr2:134259800-134261400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:134260000-134260400	Weak transcription	Right Ventricle	heart
42	chr2:134260200-134262600	Enhancers	Fetal Intestine Small	intestine
43	chr2:134260200-134263800	Enhancers	Brain Hippocampus Middle	brain
44	chr2:134260400-134260600	Enhancers	Fetal Muscle Trunk	muscle
45	chr2:134260400-134260600	Enhancers	Pancreas	Pancrea
46	chr2:134260400-134260600	Enhancers	Right Ventricle	heart
47	chr2:134260400-134260600	Enhancers	GM12878-XiMat	blood
48	chr2:134260400-134261400	Enhancers	Stomach Mucosa	stomach
49	chr2:134260400-134261600	Enhancers	Small Intestine	intestine
50	chr2:134260400-134262400	Enhancers	Fetal Intestine Large	intestine

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