Variant report

Variant	nsv829583
Chromosome Location	chr2:101031032-101038750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:332)
CpG islands
(count:490)
Chromatin interactive
region (count:12)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:101033612-101034385	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:101034692-101034706	K562	blood:	n/a	n/a
3	BHLHE40	chr2:101034948-101035203	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:101033917-101034421	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:101035096-101035114	K562	blood:	n/a	n/a
6	BHLHE40	chr2:101033247-101034118	K562	blood:	n/a	n/a
7	BHLHE40	chr2:101035046-101035246	HepG2	liver:	n/a	n/a
8	BRCA1	chr2:101033607-101033884	HepG2	liver:	n/a	n/a
9	CCNT2	chr2:101033708-101034334	K562	blood:	n/a	n/a
10	CEBPB	chr2:101033502-101033779	HepG2	liver:	n/a	chr2:101033641-101033652
11	CEBPB	chr2:101036462-101036663	A549	lung:	n/a	chr2:101036556-101036567
12	CEBPB	chr2:101036370-101036735	HepG2	liver:	n/a	chr2:101036556-101036567
13	CEBPB	chr2:101033449-101033839	IMR90	lung:	n/a	chr2:101033641-101033652
14	CEBPB	chr2:101036433-101036634	Hela-S3	cervix:	n/a	chr2:101036556-101036567
15	CEBPB	chr2:101033398-101033814	A549	lung:	n/a	chr2:101033641-101033652
16	CEBPB	chr2:101033477-101034018	HepG2	liver:	n/a	chr2:101033641-101033652
17	CEBPB	chr2:101036408-101036623	H1-hESC	embryonic stem cell:	n/a	chr2:101036556-101036567
18	CEBPB	chr2:101036397-101036723	IMR90	lung:	n/a	chr2:101036556-101036567
19	CEBPB	chr2:101033294-101034009	A549	lung:	n/a	chr2:101033641-101033652
20	CEBPB	chr2:101036360-101036727	K562	blood:	n/a	chr2:101036556-101036567
21	CEBPB	chr2:101033380-101033849	MCF-7	breast:	n/a	chr2:101033641-101033652
22	CEBPB	chr2:101033310-101033846	K562	blood:	n/a	chr2:101033641-101033652
23	CEBPB	chr2:101033431-101033873	ECC-1	luminal epithelium:	n/a	chr2:101033641-101033652
24	CEBPB	chr2:101033451-101033816	Hela-S3	cervix:	n/a	chr2:101033641-101033652
25	CEBPB	chr2:101033451-101033773	ECC-1	luminal epithelium:	n/a	chr2:101033641-101033652
26	CEBPB	chr2:101036454-101036677	HepG2	liver:	n/a	chr2:101036556-101036567
27	CEBPB	chr2:101036305-101036750	HepG2	liver:	n/a	chr2:101036556-101036567
28	CEBPB	chr2:101033458-101033835	H1-hESC	embryonic stem cell:	n/a	chr2:101033641-101033652
29	CEBPB	chr2:101033417-101033942	MCF-7	breast:	n/a	chr2:101033641-101033652
30	CEBPB	chr2:101033484-101033815	A549	lung:	n/a	chr2:101033641-101033652
31	CEBPB	chr2:101033108-101033842	K562	blood:	n/a	chr2:101033641-101033652
32	CEBPB	chr2:101033554-101033705	K562	blood:	n/a	chr2:101033641-101033652
33	CEBPB	chr2:101033462-101033833	HepG2	liver:	n/a	chr2:101033641-101033652
34	CEBPD	chr2:101033542-101034194	HepG2	liver:	n/a	chr2:101033642-101033653
35	CHD1	chr2:101034203-101034394	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr2:101033543-101033752	K562	blood:	n/a	n/a
37	CHD2	chr2:101033531-101034032	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr2:101033570-101033847	HepG2	liver:	n/a	n/a
39	CHD2	chr2:101033169-101033434	GM12878	blood:	n/a	n/a
40	CHD2	chr2:101034712-101034731	GM12878	blood:	n/a	n/a
41	CREB1	chr2:101033815-101034299	A549	lung:	n/a	n/a
42	CTCF	chr2:101038749-101039164	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr2:101033940-101034090	GM12868	blood:	n/a	n/a
44	CTCF	chr2:101038582-101039370	SK-N-SH	brain:	n/a	n/a
45	CTCF	chr2:101033413-101033490	Fibrobl	skin:	n/a	n/a
46	CTCF	chr2:101038750-101039153	A549	lung:	n/a	n/a
47	CTCF	chr2:101037900-101038050	RPTEC	kidney:	n/a	n/a
48	CTCF	chr2:101038700-101038850	SAEC	small airway:	n/a	n/a
49	CTCF	chr2:101033708-101033920	GM12878	blood:	n/a	n/a
50	CTCF	chr2:101033660-101033810	HUVEC	blood vessel:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:101033747-101033797	NHDF-neo	bronchial:	n/a
2	chr2:101034270-101034320	HMEC	breast:	n/a
3	chr2:101033747-101033797	NHDF-neo	bronchial:	n/a
4	chr2:101034270-101034320	HMEC	breast:	n/a
5	chr2:101034279-101034329	AG04450	lung:	fetal
6	chr2:101038262-101038312	NB4	blood:	n/a
7	chr2:101035456-101035506	ProgFib	skin:	n/a
8	chr2:101034257-101034307	AG04450	lung:	fetal
9	chr2:101034825-101034875	HMEC	breast:	n/a
10	chr2:101034279-101034329	NT2-D1	testis:	n/a
11	chr2:101035456-101035506	NT2-D1	testis:	n/a
12	chr2:101034825-101034875	NHDF-neo	bronchial:	n/a
13	chr2:101034825-101034875	Hepatocyte	liver:	n/a
14	chr2:101034825-101034875	GM19239	blood:	n/a
15	chr2:101033546-101033596	AG04450	lung:	fetal
16	chr2:101034279-101034329	GM12891	blood:	n/a
17	chr2:101035456-101035506	GM12891	blood:	n/a
18	chr2:101033546-101033596	AG04449	skin:	fetal
19	chr2:101034257-101034307	K562	blood:	n/a
20	chr2:101034279-101034329	LNCaP	prostate:	n/a
21	chr2:101034270-101034320	SK-N-SH	brain:	n/a
22	chr2:101033546-101033596	Jurkat	blood:	n/a
23	chr2:101035456-101035506	HCT-116	colon:	n/a
24	chr2:101034270-101034320	AoSMC	blood vessel:	n/a
25	chr2:101033747-101033797	HRPEpiC	eye:	n/a
26	chr2:101034825-101034875	HCT-116	colon:	n/a
27	chr2:101035456-101035506	SAEC	small airway:	n/a
28	chr2:101034825-101034875	HUVEC	blood vessel:	n/a
29	chr2:101034825-101034875	AG09309	skin:	n/a
30	chr2:101034825-101034875	PrEC	prostate:	n/a
31	chr2:101033546-101033596	HAEpiC	amniotic membrane:	n/a
32	chr2:101035456-101035506	MCF-7	breast:	n/a
33	chr2:101038262-101038312	AG09309	skin:	n/a
34	chr2:101034257-101034307	NB4	blood:	n/a
35	chr2:101038262-101038312	SK-N-SH	brain:	n/a
36	chr2:101034825-101034875	Jurkat	blood:	n/a
37	chr2:101034279-101034329	HIPEpiC	eye:	n/a
38	chr2:101034270-101034320	NT2-D1	testis:	n/a
39	chr2:101033546-101033596	HEEpiC	esophagus:	n/a
40	chr2:101034825-101034875	GM12891	blood:	n/a
41	chr2:101034270-101034320	GM06990	blood:	n/a
42	chr2:101033546-101033596	Caco-2	colon:	n/a
43	chr2:101033546-101033596	ProgFib	skin:	n/a
44	chr2:101034825-101034875	HEK293	kidney:	embryo
45	chr2:101038262-101038312	HRE	kidney:	n/a
46	chr2:101034825-101034875	MCF10A-Er-Src	breast:	n/a
47	chr2:101038262-101038312	ECC-1	luminal epithelium:	n/a
48	chr2:101034825-101034875	BJ	skin:	n/a
49	chr2:101033747-101033797	Hepatocyte	liver:	n/a
50	chr2:101033546-101033596	SKMC	muscle:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:101032545..101035627-chr2:101179557..101182939,4	K562	blood:
2	chr2:100907128..100908845-chr2:101037649..101040314,2	MCF-7	breast:
3	chr2:100937085..100941836-chr2:101033510..101036438,4	MCF-7	breast:
4	chr2:100876984..100878779-chr2:101034439..101036226,2	K562	blood:
5	chr2:100879489..100880003-chr2:101038489..101039474,2	K562	blood:
6	chr2:100882939..100884943-chr2:101037829..101040208,2	MCF-7	breast:
7	chr2:101032643..101036022-chr2:101036491..101040981,5	K562	blood:
8	chr2:101029935..101035569-chr2:101035669..101041059,9	MCF-7	breast:
9	chr2:100936794..100939483-chr2:101033248..101035645,2	K562	blood:
10	chr2:101033038..101035627-chr2:101178228..101182939,5	K562	blood:
11	chr2:100940073..100942309-chr2:101029977..101032288,2	K562	blood:
12	chr2:101002203..101003708-chr2:101029202..101031443,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LONRF2-1	chr2:101031503-101031573	NONHSAT072776
2	lnc-LONRF2-1	chr2:101031503-101031573	NONHSAT072777
3	lnc-LONRF2-1	chr2:101031515-101031573	NONHSAT072778
4	lnc-LONRF2-1	chr2:101032685-101032987	NONHSAT072778
5	lnc-LONRF2-1	chr2:101033593-101033717	NONHSAT072778
6	lnc-LONRF2-1	chr2:101033836-101033873	NONHSAT072777
7	lnc-LONRF2-1	chr2:101033836-101034076	NONHSAT072776

No data

Variant related genes	Relation type
CHST10	TF binding region
ENSG00000238029	TF binding region
CHST10	CpG island
ENSG00000238029	CpG island
ENSG00000115526	chromatin interactions
ENSG00000115539	chromatin interactions
ENSG00000170500	chromatin interactions

Extended variants
information (count: 270 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568999058	chr2:101031044-101031045	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs374348511	chr2:101031081-101031082	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs114679683	chr2:101031086-101031087	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs372760691	chr2:101031105-101031106	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs377676484	chr2:101031111-101031112	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs536680407	chr2:101031138-101031139	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs553383286	chr2:101031141-101031142	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs573481675	chr2:101031145-101031146	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs376020881	chr2:101031172-101031173	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs533451114	chr2:101031176-101031177	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs551713531	chr2:101031193-101031194	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs186174115	chr2:101031201-101031202	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs569968058	chr2:101031223-101031224	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs189038328	chr2:101031334-101031335	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs57305094	chr2:101031347-101031348	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs207462105	chr2:101031422-101031423	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs560687661	chr2:101031427-101031428	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs574177140	chr2:101031450-101031451	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs370608495	chr2:101031474-101031475	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs560065502	chr2:101031498-101031499	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs567453291	chr2:101031499-101031500	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs146735593	chr2:101031512-101031513	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
23	rs140321683	chr2:101031518-101031519	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
24	rs181993153	chr2:101031524-101031525	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
25	rs72552256	chr2:101031528-101031529	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
26	rs143278882	chr2:101031529-101031530	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
27	rs567187190	chr2:101031537-101031538	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
28	rs3828193	chr2:101031561-101031562	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs75042666	chr2:101031574-101031575	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs536718418	chr2:101031589-101031590	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs553302172	chr2:101031691-101031692	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs145697214	chr2:101031693-101031694	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs4149508	chr2:101031740-101031741	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs140908155	chr2:101031765-101031766	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs3791358	chr2:101031865-101031866	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs559246124	chr2:101031877-101031878	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575836677	chr2:101031953-101031954	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs186175544	chr2:101031954-101031955	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs190692387	chr2:101031991-101031992	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs376528979	chr2:101032021-101032022	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs539906614	chr2:101032058-101032059	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs538943386	chr2:101032077-101032078	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs182863706	chr2:101032085-101032086	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs138188405	chr2:101032090-101032091	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs57710676	chr2:101032092-101032093	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs78342084	chr2:101032113-101032114	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs548428199	chr2:101032172-101032173	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs185716494	chr2:101032199-101032200	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs75446912	chr2:101032219-101032220	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs573883808	chr2:101032252-101032253	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	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
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:101005600-101032800	Weak transcription	HUVEC	blood vessel
2	chr2:101005800-101033000	Weak transcription	Duodenum Mucosa	Duodenum
3	chr2:101006600-101031600	Strong transcription	Fetal Stomach	stomach
4	chr2:101007200-101032000	Weak transcription	NHDF-Ad	bronchial
5	chr2:101008000-101033000	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr2:101010200-101032800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr2:101013200-101033000	Weak transcription	Fetal Intestine Large	intestine
8	chr2:101014400-101033200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr2:101014800-101032400	Weak transcription	Hela-S3	cervix
10	chr2:101015600-101033000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr2:101016400-101032600	Weak transcription	HSMM	muscle
12	chr2:101017000-101032800	Weak transcription	Osteobl	bone
13	chr2:101018400-101033000	Weak transcription	Primary B cells from cord blood	blood
14	chr2:101019000-101032800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:101021000-101033200	Weak transcription	Colonic Mucosa	Colon
16	chr2:101022200-101033000	Weak transcription	HSMMtube	muscle
17	chr2:101022600-101032200	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr2:101022800-101032200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr2:101022800-101032400	Weak transcription	Colon Smooth Muscle	Colon
20	chr2:101022800-101033000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr2:101022800-101033000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr2:101023200-101032800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:101023200-101033000	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr2:101023200-101033000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr2:101023200-101033000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr2:101023200-101033000	Weak transcription	Fetal Thymus	thymus
27	chr2:101023400-101032600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr2:101023400-101033000	Weak transcription	Fetal Kidney	kidney
29	chr2:101023600-101031800	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr2:101023600-101032800	Weak transcription	Primary B cells from peripheral blood	blood
31	chr2:101023800-101032200	Weak transcription	Ovary	ovary
32	chr2:101023800-101032800	Weak transcription	Psoas Muscle	Psoas
33	chr2:101024000-101031400	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr2:101024000-101033000	Weak transcription	Fetal Intestine Small	intestine
35	chr2:101024200-101032000	Weak transcription	Primary T cells from cord blood	blood
36	chr2:101024200-101032400	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr2:101024200-101032800	Weak transcription	Adipose Nuclei	Adipose
38	chr2:101024200-101033000	Weak transcription	Gastric	stomach
39	chr2:101024400-101033000	Weak transcription	Spleen	Spleen
40	chr2:101025000-101033000	Weak transcription	Pancreas	Pancrea
41	chr2:101025600-101032400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr2:101025800-101032200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr2:101027000-101033000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:101027000-101033000	Weak transcription	Placenta	Placenta
45	chr2:101027000-101033000	Weak transcription	Left Ventricle	heart
46	chr2:101027000-101033000	Weak transcription	Lung	lung
47	chr2:101027000-101033000	Weak transcription	Right Ventricle	heart
48	chr2:101027000-101033200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr2:101027400-101032000	Weak transcription	Fetal Heart	heart
50	chr2:101027800-101032800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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