Variant report

Variant	nsv437298
Chromosome Location	chr2:152320118-152356361
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:275)
CpG islands
(count:183)
Chromatin interactive
region (count:21)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:152329594-152329776	K562	blood:	n/a	n/a
2	BACH1	chr2:152321150-152322834	K562	blood:	n/a	n/a
3	BATF	chr2:152338185-152338626	GM12878	blood:	n/a	n/a
4	BATF	chr2:152338242-152338516	GM12878	blood:	n/a	n/a
5	CEBPB	chr2:152338063-152338359	HepG2	liver:	n/a	chr2:152338230-152338239 chr2:152338228-152338239
6	CEBPB	chr2:152332558-152332671	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:152334787-152334886	K562	blood:	n/a	n/a
8	CEBPB	chr2:152338148-152338364	IMR90	lung:	n/a	chr2:152338230-152338239 chr2:152338228-152338239
9	CEBPB	chr2:152332582-152332598	A549	lung:	n/a	n/a
10	CTCF	chr2:152337400-152337550	HFF-Myc	foreskin:	n/a	n/a
11	CTCF	chr2:152353712-152353749	Medullo	brain:	n/a	n/a
12	CTCF	chr2:152342340-152342490	NB4	blood:	n/a	n/a
13	CTCF	chr2:152334461-152334519	GM10266	blood:	n/a	n/a
14	CTCF	chr2:152320404-152320455	GM20000	blood:	n/a	n/a
15	CTCF	chr2:152322683-152322710	K562	blood:	n/a	n/a
16	EBF1	chr2:152338937-152339157	GM12878	blood:	n/a	n/a
17	FAM48A	chr2:152343302-152343452	GM12878	blood:	n/a	n/a
18	FOS	chr2:152334628-152334774	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr2:152334650-152334783	MCF10A-Er-Src	breast:	n/a	n/a
20	FOXA1	chr2:152340486-152340901	HepG2	liver:	n/a	n/a
21	FOXA1	chr2:152340667-152340926	HepG2	liver:	n/a	n/a
22	FOXA1	chr2:152340607-152341035	HepG2	liver:	n/a	n/a
23	FOXA2	chr2:152340624-152340881	HepG2	liver:	n/a	n/a
24	GATA3	chr2:152348629-152348719	SH-SY5Y	brain:	n/a	n/a
25	GATA3	chr2:152321967-152322475	SH-SY5Y	brain:	n/a	n/a
26	IRF1	chr2:152336300-152336476	K562	blood:	n/a	n/a
27	IRF1	chr2:152356287-152356384	K562	blood:	n/a	n/a
28	JUN	chr2:152350353-152350477	H1-hESC	embryonic stem cell:	n/a	n/a
29	JUND	chr2:152334528-152334768	HepG2	liver:	n/a	n/a
30	JUND	chr2:152352179-152352261	H1-hESC	embryonic stem cell:	n/a	n/a
31	MAFF	chr2:152329521-152329840	HepG2	liver:	n/a	chr2:152329686-152329704
32	MAFF	chr2:152329517-152329861	K562	blood:	n/a	chr2:152329686-152329704
33	MAFK	chr2:152329530-152329859	K562	blood:	n/a	chr2:152329688-152329703
34	MAFK	chr2:152329515-152329867	HepG2	liver:	n/a	chr2:152329688-152329703
35	MAFK	chr2:152329582-152329783	Hela-S3	cervix:	n/a	chr2:152329688-152329703
36	MAFK	chr2:152333369-152333527	HepG2	liver:	n/a	n/a
37	MAFK	chr2:152329603-152329845	H1-hESC	embryonic stem cell:	n/a	chr2:152329688-152329703
38	MAFK	chr2:152354701-152354844	HepG2	liver:	n/a	n/a
39	MAFK	chr2:152329512-152329876	IMR90	lung:	n/a	chr2:152329688-152329703
40	MAFK	chr2:152325582-152325751	K562	blood:	n/a	n/a
41	MAFK	chr2:152333436-152333476	HepG2	liver:	n/a	n/a
42	MAFK	chr2:152329524-152329857	HepG2	liver:	n/a	chr2:152329688-152329703
43	MAX	chr2:152331819-152331820	NB4	blood:	n/a	n/a
44	MEF2A	chr2:152338348-152338672	GM12878	blood:	n/a	n/a
45	MXI1	chr2:152327365-152327468	K562	blood:	n/a	n/a
46	MYC	chr2:152330133-152330333	MCF10A-Er-Src	breast:	n/a	n/a
47	MYC	chr2:152339014-152339075	MCF-7	breast:	n/a	n/a
48	NFIC	chr2:152338274-152338667	GM12878	blood:	n/a	n/a
49	NRF1	chr2:152340221-152340251	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr2:152346891-152347047	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:152342216-152342266	HL-60	blood:	n/a
2	chr2:152331806-152331856	HEEpiC	esophagus:	n/a
3	chr2:152342216-152342266	AG09309	skin:	n/a
4	chr2:152331806-152331856	HAEpiC	amniotic membrane:	n/a
5	chr2:152342216-152342266	K562	blood:	n/a
6	chr2:152349105-152349155	IMR90	lung:	fetal
7	chr2:152331806-152331856	K562	blood:	n/a
8	chr2:152349105-152349155	AG09319	gingival:	n/a
9	chr2:152342216-152342266	HMEC	breast:	n/a
10	chr2:152342216-152342266	RPTEC	kidney:	n/a
11	chr2:152331806-152331856	RPTEC	kidney:	n/a
12	chr2:152349105-152349155	HRCEpiC	kidney:	n/a
13	chr2:152349105-152349155	HRPEpiC	eye:	n/a
14	chr2:152331806-152331856	SK-N-MC	brain:	n/a
15	chr2:152342216-152342266	BE2_C	brain:	n/a
16	chr2:152331806-152331856	SAEC	small airway:	n/a
17	chr2:152331806-152331856	HNPCEpiC	eye:	n/a
18	chr2:152342216-152342266	GM06990	blood:	n/a
19	chr2:152342216-152342266	GM12891	blood:	n/a
20	chr2:152331806-152331856	GM19239	blood:	n/a
21	chr2:152349105-152349155	K562	blood:	n/a
22	chr2:152349105-152349155	A549	lung:	n/a
23	chr2:152349105-152349155	PrEC	prostate:	n/a
24	chr2:152331806-152331856	HIPEpiC	eye:	n/a
25	chr2:152349105-152349155	HCM	heart:	n/a
26	chr2:152349105-152349155	H1-hESC	embryonic stem cell:	embryo
27	chr2:152349105-152349155	LNCaP	prostate:	n/a
28	chr2:152331806-152331856	AG09309	skin:	n/a
29	chr2:152349105-152349155	ECC-1	luminal epithelium:	n/a
30	chr2:152349105-152349155	SK-N-SH	brain:	n/a
31	chr2:152342216-152342266	PrEC	prostate:	n/a
32	chr2:152331806-152331856	ovcar-3	ovarian:	n/a
33	chr2:152331806-152331856	PrEC	prostate:	n/a
34	chr2:152342216-152342266	NT2-D1	testis:	n/a
35	chr2:152349105-152349155	HepG2	liver:	n/a
36	chr2:152331806-152331856	GM12878	blood:	n/a
37	chr2:152342216-152342266	HAEpiC	amniotic membrane:	n/a
38	chr2:152331806-152331856	MCF-7	breast:	n/a
39	chr2:152331806-152331856	HMEC	breast:	n/a
40	chr2:152342216-152342266	HUVEC	blood vessel:	n/a
41	chr2:152342216-152342266	PFSK-1	brain:	n/a
42	chr2:152342216-152342266	SAEC	small airway:	n/a
43	chr2:152331806-152331856	HPAEpiC	pulmonary alveolar:	n/a
44	chr2:152331806-152331856	HCM	heart:	n/a
45	chr2:152342216-152342266	U87	brain:	n/a
46	chr2:152349105-152349155	SK-N-SH_RA	brain:	n/a
47	chr2:152331806-152331856	AG10803	skin:	n/a
48	chr2:152331806-152331856	HEK293	kidney:	embryo
49	chr2:152342216-152342266	HCT-116	colon:	n/a
50	chr2:152331806-152331856	Hepatocyte	liver:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:152117786..152119575-chr2:152331132..152333379,2	MCF-7	breast:
2	chr2:152345538..152348326-chr2:152350633..152352626,2	MCF-7	breast:
3	chr2:152343156..152345753-chr2:152361266..152362840,2	K562	blood:
4	chr2:152322769..152325475-chr2:152328124..152330631,2	K562	blood:
5	chr2:152320561..152322132-chr2:152322755..152325305,2	MCF-7	breast:
6	chr2:152344851..152347246-chr2:152350528..152353460,3	K562	blood:
7	chr2:152322769..152325475-chr2:152328124..152330631,2	K562	blood:
8	chr2:152316997..152319818-chr2:152338220..152340859,2	K562	blood:
9	chr2:152319808..152322653-chr2:152331004..152333072,2	K562	blood:
10	chr2:152336512..152339181-chr2:152360323..152362422,2	K562	blood:
11	chr2:152329635..152332984-chr2:152337072..152339089,3	K562	blood:
12	chr2:152329635..152332984-chr2:152337072..152339089,3	K562	blood:
13	chr2:152333499..152335226-chr2:152337769..152339551,2	K562	blood:
14	chr2:152351759..152353707-chr2:152360537..152362140,2	K562	blood:
15	chr2:152333499..152335226-chr2:152337769..152339551,2	K562	blood:
16	chr2:152329723..152332173-chr2:152332317..152334542,2	K562	blood:
17	chr2:152329723..152332173-chr2:152332317..152334542,2	K562	blood:
18	chr2:152355139..152355815-chr2:152882008..152882831,2	K562	blood:
19	chr2:152333590..152335850-chr2:152341846..152344009,2	K562	blood:
20	chr2:152107619..152109429-chr2:152322968..152325434,2	K562	blood:
21	chr2:152347893..152350567-chr2:152361417..152364168,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFAIP6-6	chr2:152342791-152343270	NONHSAT074958
2	lnc-TNFAIP6-6	chr2:152354300-152354729	NONHSAT074959
3	lnc-TNFAIP6-6	chr2:152354300-152354727	NONHSAT074958
4	lnc-TNFAIP6-5	chr2:152332640-152333850	NONHSAT074957
5	lnc-TNFAIP6-6	chr2:152351489-152351840	NONHSAT074959
6	lnc-TNFAIP6-6	chr2:152351743-152351840	NONHSAT074958

No data

Variant related genes	Relation type
RIF1	TF binding region
NEB	TF binding region
RIF1	CpG island
NEB	CpG island
ENSG00000080345	chromatin interactions
ENSG00000183091	chromatin interactions
ENSG00000184898	chromatin interactions

Extended variants
information (count: 1562 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1562 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2123465	chr2:152320118-152320119	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370921071	chr2:152320214-152320215	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs142688397	chr2:152320227-152320228	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs143566263	chr2:152320237-152320238	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs368509274	chr2:152320266-152320267	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs540057492	chr2:152320273-152320274	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs34055759	chr2:152320291-152320292	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs148665312	chr2:152320292-152320293	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs150802512	chr2:152320296-152320297	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs143098880	chr2:152320317-152320318	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs139219411	chr2:152320318-152320319	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs146802065	chr2:152320332-152320333	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs370581551	chr2:152320363-152320364	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs144292917	chr2:152320394-152320395	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs374037751	chr2:152320401-152320402	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs201647082	chr2:152320404-152320405	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs199823030	chr2:152320406-152320407	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs200702180	chr2:152320414-152320415	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs201841036	chr2:152320416-152320417	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs149195123	chr2:152320450-152320451	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs151319999	chr2:152320456-152320457	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs370817713	chr2:152320493-152320494	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs7566841	chr2:152320501-152320502	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs78879803	chr2:152320531-152320532	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs200111568	chr2:152320549-152320550	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs149293885	chr2:152320553-152320554	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs142724873	chr2:152320570-152320571	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs186733365	chr2:152320576-152320577	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs139535635	chr2:152320582-152320583	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs142857822	chr2:152320597-152320598	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs376067163	chr2:152320620-152320621	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs139815683	chr2:152320660-152320661	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs183315754	chr2:152320672-152320673	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs555549721	chr2:152320677-152320678	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200392689	chr2:152320700-152320701	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs141807972	chr2:152320704-152320705	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs536777994	chr2:152320713-152320714	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs540031348	chr2:152320720-152320721	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs553599620	chr2:152320725-152320726	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs576707750	chr2:152320756-152320757	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs147553277	chr2:152320764-152320765	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs200066072	chr2:152320781-152320782	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs562817771	chr2:152320810-152320811	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs34114637	chr2:152320811-152320812	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs373773093	chr2:152320818-152320819	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs370355345	chr2:152320831-152320832	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs147524937	chr2:152320837-152320838	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs143042080	chr2:152320839-152320840	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs541812935	chr2:152320850-152320851	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs148215725	chr2:152320874-152320875	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:49)

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
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	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
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	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:839 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152267600-152379400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:152267800-152340400	Weak transcription	Stomach Mucosa	stomach
3	chr2:152268000-152342800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:152268200-152320800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:152268200-152327800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:152268200-152328400	Strong transcription	H1 Cell Line	embryonic stem cell
7	chr2:152268200-152328600	Strong transcription	Fetal Thymus	thymus
8	chr2:152268400-152327800	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr2:152268600-152326800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr2:152268600-152327800	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr2:152268600-152334400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr2:152268600-152342600	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr2:152268800-152326800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr2:152268800-152327800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:152268800-152327800	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr2:152269400-152327200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:152272400-152327800	Strong transcription	Dnd41	blood
18	chr2:152283800-152334000	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr2:152284200-152327000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr2:152284600-152327800	Strong transcription	HepG2	liver
21	chr2:152285000-152327800	Strong transcription	Placenta	Placenta
22	chr2:152285200-152327600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr2:152285200-152327800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr2:152285200-152331200	Strong transcription	Adipose Nuclei	Adipose
25	chr2:152290600-152323400	Weak transcription	Aorta	Aorta
26	chr2:152291800-152321000	Strong transcription	Duodenum Mucosa	Duodenum
27	chr2:152294400-152321400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr2:152294600-152327800	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr2:152294800-152327800	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr2:152295800-152348400	Weak transcription	Right Ventricle	heart
31	chr2:152298600-152327600	Strong transcription	HUVEC	blood vessel
32	chr2:152300000-152333400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:152300200-152327800	Strong transcription	K562	blood
34	chr2:152301600-152324400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr2:152301800-152343800	Weak transcription	Gastric	stomach
36	chr2:152303200-152325000	Weak transcription	Small Intestine	intestine
37	chr2:152303400-152326400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:152304800-152322800	Strong transcription	Osteobl	bone
39	chr2:152304800-152354000	Weak transcription	Spleen	Spleen
40	chr2:152306200-152322800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr2:152306400-152324800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr2:152306800-152328400	Strong transcription	Fetal Muscle Trunk	muscle
43	chr2:152307000-152328000	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr2:152307600-152327600	Strong transcription	Primary B cells from cord blood	blood
45	chr2:152307600-152327800	Strong transcription	HSMM	muscle
46	chr2:152307600-152328000	Strong transcription	Liver	Liver
47	chr2:152308000-152322000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr2:152309000-152327800	Strong transcription	Fetal Intestine Large	intestine
49	chr2:152310200-152321000	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr2:152311400-152321000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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