Variant report

Variant	nsv1009608
Chromosome Location	chr2:148897348-149133718
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:939)
CpG islands
(count:244)
Chromatin interactive
region (count:33)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:939 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:148959061-148959356	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:148920439-148920729	K562	blood:	n/a	n/a
3	ARID3A	chr2:148968850-148969044	HepG2	liver:	n/a	chr2:148969017-148969033
4	ARID3A	chr2:149002017-149002569	HepG2	liver:	n/a	chr2:149002050-149002066
5	ARID3A	chr2:149009605-149009760	HepG2	liver:	n/a	n/a
6	ATF1	chr2:149017285-149017419	K562	blood:	n/a	n/a
7	ATF1	chr2:148967322-148967474	K562	blood:	n/a	n/a
8	BACH1	chr2:149017398-149017543	K562	blood:	n/a	n/a
9	BACH1	chr2:149017369-149017502	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:148936476-148936481	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:149030956-149031246	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr2:149002150-149002345	HepG2	liver:	n/a	n/a
13	BHLHE40	chr2:149017230-149017473	K562	blood:	n/a	n/a
14	BHLHE40	chr2:149011302-149011613	K562	blood:	n/a	n/a
15	CBX3	chr2:149017230-149017609	K562	blood:	n/a	n/a
16	CBX3	chr2:149011246-149011697	HCT-116	colon:	n/a	n/a
17	CBX3	chr2:149011244-149011646	K562	blood:	n/a	n/a
18	CBX3	chr2:148958977-148959378	K562	blood:	n/a	n/a
19	CEBPB	chr2:149017292-149017407	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:149036906-149037097	H1-hESC	embryonic stem cell:	n/a	chr2:149036949-149036960
21	CEBPB	chr2:148975993-148976472	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:148915403-148915653	K562	blood:	n/a	n/a
23	CEBPB	chr2:149036854-149037024	HepG2	liver:	n/a	chr2:149036949-149036960
24	CEBPB	chr2:149063181-149063185	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:148916321-148916417	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:149038725-149038955	HepG2	liver:	n/a	chr2:149038862-149038873
27	CEBPB	chr2:149038733-149038964	H1-hESC	embryonic stem cell:	n/a	chr2:149038862-149038873
28	CEBPB	chr2:149017197-149017491	A549	lung:	n/a	n/a
29	CEBPB	chr2:149017219-149017602	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr2:149017156-149017589	MCF-7	breast:	n/a	n/a
31	CEBPB	chr2:149036772-149037160	MCF-7	breast:	n/a	chr2:149036949-149036960
32	CEBPB	chr2:148987418-148987618	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:148958857-148959275	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:148928096-148928358	IMR90	lung:	n/a	chr2:148928214-148928227 chr2:148928214-148928225
35	CEBPB	chr2:149013459-149013924	MCF-7	breast:	n/a	chr2:149013700-149013711
36	CEBPB	chr2:148958865-148959261	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:149017206-149017525	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr2:149013595-149013834	H1-hESC	embryonic stem cell:	n/a	chr2:149013700-149013711
39	CEBPB	chr2:149017187-149017476	K562	blood:	n/a	n/a
40	CEBPB	chr2:149013365-149013868	Hela-S3	cervix:	n/a	chr2:149013700-149013711
41	CEBPB	chr2:149045883-149046183	IMR90	lung:	n/a	n/a
42	CEBPB	chr2:149013272-149013893	IMR90	lung:	n/a	chr2:149013700-149013711
43	CEBPB	chr2:149002296-149002654	IMR90	lung:	n/a	chr2:149002570-149002581
44	CEBPB	chr2:149002111-149002276	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:149013233-149013884	A549	lung:	n/a	chr2:149013700-149013711
46	CEBPB	chr2:149017246-149017540	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr2:149118753-149118918	HepG2	liver:	n/a	chr2:149118869-149118880
48	CEBPB	chr2:149108389-149108611	A549	lung:	n/a	chr2:149108533-149108546 chr2:149108534-149108545 chr2:149108533-149108546 chr2:149108533-149108544 chr2:149108533-149108546
49	CEBPB	chr2:148977101-148977398	IMR90	lung:	n/a	chr2:148977256-148977267
50	CEBPB	chr2:149017261-149017445	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:149041060-149041110	GM19239	blood:	n/a
2	chr2:149063092-149063142	HUVEC	blood vessel:	n/a
3	chr2:149041060-149041110	HCT-116	colon:	n/a
4	chr2:148976109-148976159	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:148976109-148976159	SK-N-MC	brain:	n/a
6	chr2:148976109-148976159	Hepatocyte	liver:	n/a
7	chr2:149041060-149041110	Hela-S3	cervix:	n/a
8	chr2:149063092-149063142	HEEpiC	esophagus:	n/a
9	chr2:149041060-149041110	U87	brain:	n/a
10	chr2:149041060-149041110	AG10803	skin:	n/a
11	chr2:148976109-148976159	H1-hESC	embryonic stem cell:	embryo
12	chr2:149063092-149063142	HRE	kidney:	n/a
13	chr2:149063092-149063142	BJ	skin:	n/a
14	chr2:148976109-148976159	AG10803	skin:	n/a
15	chr2:149096527-149096577	HCM	heart:	n/a
16	chr2:148976109-148976159	Caco-2	colon:	n/a
17	chr2:148976109-148976159	SKMC	muscle:	n/a
18	chr2:149096527-149096577	A549	lung:	n/a
19	chr2:149096527-149096577	AoSMC	blood vessel:	n/a
20	chr2:149096527-149096577	CMK	blood:	n/a
21	chr2:149063092-149063142	Hela-S3	cervix:	n/a
22	chr2:149096527-149096577	MCF-7	breast:	n/a
23	chr2:148976109-148976159	PrEC	prostate:	n/a
24	chr2:149063092-149063142	PANC-1	pancreas:	n/a
25	chr2:149063092-149063142	HCPEpiC	choroid plexus:	n/a
26	chr2:149096527-149096577	AG09309	skin:	n/a
27	chr2:149096527-149096577	HMEC	breast:	n/a
28	chr2:149063092-149063142	HepG2	liver:	n/a
29	chr2:149041060-149041110	HRCEpiC	kidney:	n/a
30	chr2:149041060-149041110	ECC-1	luminal epithelium:	n/a
31	chr2:148976109-148976159	RPTEC	kidney:	n/a
32	chr2:149041060-149041110	T-47D	breast:	n/a
33	chr2:148976109-148976159	IMR90	lung:	fetal
34	chr2:149041060-149041110	GM12892	blood:	n/a
35	chr2:149041060-149041110	SK-N-SH_RA	brain:	n/a
36	chr2:149096527-149096577	U87	brain:	n/a
37	chr2:148976109-148976159	K562	blood:	n/a
38	chr2:149063092-149063142	GM19239	blood:	n/a
39	chr2:149041060-149041110	ProgFib	skin:	n/a
40	chr2:149041060-149041110	NH-A	brain:	n/a
41	chr2:148976109-148976159	HCPEpiC	choroid plexus:	n/a
42	chr2:148976109-148976159	HRCEpiC	kidney:	n/a
43	chr2:148976109-148976159	HEK293	kidney:	embryo
44	chr2:149041060-149041110	SK-N-MC	brain:	n/a
45	chr2:149063092-149063142	MCF-7	breast:	n/a
46	chr2:149063092-149063142	NHBE	bronchial:	n/a
47	chr2:149096527-149096577	Hela-S3	cervix:	n/a
48	chr2:149096527-149096577	BJ	skin:	n/a
49	chr2:149096527-149096577	IMR90	lung:	fetal
50	chr2:149096527-149096577	HCT-116	colon:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:148931889..148933794-chr2:148936353..148939104,2	K562	blood:
2	chr2:149075837..149077502-chr2:149078187..149080957,2	K562	blood:
3	chr2:148925257..148925927-chr2:149266799..149267551,3	MCF-7	breast:
4	chr17:56707748..56709669-chr2:149007960..149010940,5	MCF-7	breast:
5	chr2:148976677..148978352-chr2:149006227..149008013,2	MCF-7	breast:
6	chr2:148976677..148978352-chr2:149006227..149008013,2	MCF-7	breast:
7	chr2:148996066..148998300-chr2:149002088..149004966,2	K562	blood:
8	chr2:148995742..148998637-chr2:149000873..149004003,3	MCF-7	breast:
9	chr2:148951330..148953430-chr2:148956133..148959129,2	K562	blood:
10	chr2:149130660..149131621-chr21:9826960..9827638,2	MCF-7	breast:
11	chr2:148951330..148953430-chr2:148956133..148959129,2	K562	blood:
12	chr17:56707733..56709409-chr2:149007940..149009460,7	MCF-7	breast:
13	chr17:56708724..56710145-chr2:149008940..149009960,20	MCF-7	breast:
14	chr2:148892318..148894319-chr2:148896559..148898244,2	MCF-7	breast:
15	chr2:148924504..148926944-chr2:148937289..148939887,2	MCF-7	breast:
16	chr17:56707881..56710421-chr2:149007960..149010940,2	K562	blood:
17	chr2:148960078..148961760-chr2:148963590..148966098,2	MCF-7	breast:
18	chr2:148994771..148998300-chr2:149002088..149006299,3	K562	blood:
19	chr2:148995742..148998637-chr2:149000873..149004003,3	MCF-7	breast:
20	chr17:56708470..56709572-chr2:149008937..149009960,15	MCF-7	breast:
21	chr2:148964117..148966027-chr2:148967186..148969154,2	MCF-7	breast:
22	chr2:149075837..149077502-chr2:149078187..149080957,2	K562	blood:
23	chr2:148931889..148933794-chr2:148936353..148939104,2	K562	blood:
24	chr2:148695045..148696010-chr2:148958677..148959570,5	K562	blood:
25	chr2:148924504..148926944-chr2:148937289..148939887,2	MCF-7	breast:
26	chr2:148746466..148747928-chr2:148959011..148960040,7	MCF-7	breast:
27	chr2:148960078..148961760-chr2:148963590..148966098,2	MCF-7	breast:
28	chr2:148994771..148998300-chr2:149002088..149006299,3	K562	blood:
29	chr2:148996066..148998300-chr2:149002088..149004966,2	K562	blood:
30	chr2:149098190..149099193-chr8:103870990..103871561,3	MCF-7	breast:
31	chr2:148964117..148966027-chr2:148967186..148969154,2	MCF-7	breast:
32	chr2:148967081..148967666-chr2:149266757..149267493,2	MCF-7	breast:
33	chr2:148777816..148780257-chr2:148961269..148962957,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074871
2	lnc-ORC4-3	chr2:149053225-149054248	NONHSAT074880
3	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074872
4	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074872
5	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074878
6	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074871
7	lnc-MBD5-1	chr2:148977516-148977602	NONHSAT074878
8	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074878
9	lnc-MBD5-1	chr2:148990814-148990964	NONHSAT074878
10	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074875
11	lnc-MBD5-1	chr2:148990814-148990964	NONHSAT074872
12	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074874
13	lnc-MBD5-1	chr2:148990814-148990896	NONHSAT074874

No data

Variant related genes	Relation type
ENSG00000212181	TF binding region
ENSG00000224007	TF binding region
ENSG00000212181	CpG island
ENSG00000224007	CpG island
ENSG00000115947	chromatin interactions
ENSG00000204406	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 8367 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:8367 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561821283	chr2:148897348-148897349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573826344	chr2:148897380-148897381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540813948	chr2:148897406-148897407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559542789	chr2:148897433-148897434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139660429	chr2:148897451-148897452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181944107	chr2:148897562-148897563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546751421	chr2:148897564-148897565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541519789	chr2:148897607-148897608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561545202	chr2:148897631-148897632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149744606	chr2:148897688-148897689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562061500	chr2:148897690-148897691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549019611	chr2:148897709-148897710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529533704	chr2:148897735-148897736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567346764	chr2:148897739-148897740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6430294	chr2:148897773-148897774	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs6430295	chr2:148897781-148897782	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs10195846	chr2:148897868-148897869	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs79715381	chr2:148897874-148897875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374366418	chr2:148897893-148897894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547475935	chr2:148897907-148897908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539655543	chr2:148897926-148897927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543370916	chr2:148897954-148897955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558397112	chr2:148897995-148897996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35235556	chr2:148897996-148897997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186445121	chr2:148898014-148898015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537028127	chr2:148898019-148898020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78052877	chr2:148898065-148898066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531781551	chr2:148898094-148898095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188960776	chr2:148898385-148898386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147779090	chr2:148898432-148898433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577723946	chr2:148898439-148898440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533092351	chr2:148898458-148898459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544889323	chr2:148898491-148898492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374960250	chr2:148898492-148898493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530852979	chr2:148898508-148898509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542628882	chr2:148898535-148898536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10209751	chr2:148898550-148898551	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs529384656	chr2:148898551-148898552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139417296	chr2:148898572-148898573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571271900	chr2:148898576-148898577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533542821	chr2:148898616-148898617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145154242	chr2:148898632-148898633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542881850	chr2:148898640-148898641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570315388	chr2:148898661-148898662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566528316	chr2:148898781-148898782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371885314	chr2:148898796-148898797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370359791	chr2:148898822-148898823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533983728	chr2:148898825-148898826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555341779	chr2:148898875-148898876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555565251	chr2:148898921-148898922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
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	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	19904302	CNVD
Intellectual disability	19904302	CNVD
Microcephaly	19904302	CNVD
severe speech impairment	19904302	CNVD
Mental retardation	20152051	CNVD
2q23.1 microdeletion syndrome	18812405	CNVD
Mental retardation	19809484	CNVD
Autism	21981781	CNVD
Breast cancer	22522925	CNVD
Mental retardation	17847001	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Autism	21865298	CNVD

Chromatin state (count:1934 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148855800-148901000	Weak transcription	Fetal Intestine Small	intestine
2	chr2:148877400-148901200	Weak transcription	Primary B cells from cord blood	blood
3	chr2:148880800-148900400	Weak transcription	HSMM	muscle
4	chr2:148882200-148905400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:148891000-148902200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:148893800-148900200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:148895600-148898200	Weak transcription	Primary T cells from cord blood	blood
8	chr2:148903000-148905200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr2:148904400-148906800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr2:148905000-148906200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr2:148905200-148905600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
12	chr2:148905400-148906000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:148905800-148906000	ZNF genes & repeats	Ovary	ovary
14	chr2:148906000-148906800	Weak transcription	Ovary	ovary
15	chr2:148906000-148937000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr2:148911000-148916000	Weak transcription	Primary T cells from cord blood	blood
17	chr2:148911400-148942400	Weak transcription	Ovary	ovary
18	chr2:148912200-148913000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr2:148912800-148913000	Enhancers	Aorta	Aorta
20	chr2:148912800-148913000	Enhancers	Left Ventricle	heart
21	chr2:148913000-148916800	Weak transcription	Fetal Stomach	stomach
22	chr2:148913000-148919400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:148913000-148919600	Weak transcription	Left Ventricle	heart
24	chr2:148913000-148977600	Weak transcription	Aorta	Aorta
25	chr2:148913200-148916600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr2:148913400-148930400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:148913600-148923200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr2:148914000-148914200	Enhancers	Fetal Kidney	kidney
29	chr2:148914200-148923800	Weak transcription	Fetal Kidney	kidney
30	chr2:148914600-148917800	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr2:148914800-148936000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:148915000-148937000	Weak transcription	Adipose Nuclei	Adipose
33	chr2:148915200-148929600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:148915400-148918000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr2:148915400-148929600	Weak transcription	Fetal Intestine Small	intestine
36	chr2:148915600-148920800	Weak transcription	Lung	lung
37	chr2:148916000-148917200	Strong transcription	Primary T cells from cord blood	blood
38	chr2:148916600-148917000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr2:148916800-148917200	Strong transcription	Fetal Stomach	stomach
40	chr2:148916800-148938600	Weak transcription	Primary B cells from cord blood	blood
41	chr2:148917000-148919200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr2:148917200-148928400	Weak transcription	Primary T cells from cord blood	blood
43	chr2:148917200-148929400	Weak transcription	Fetal Stomach	stomach
44	chr2:148917400-148917600	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr2:148917800-148937200	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr2:148918800-148938000	Weak transcription	Fetal Lung	lung
47	chr2:148919200-148920000	Enhancers	Brain Germinal Matrix	brain
48	chr2:148919400-148919800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:148919400-148919800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:148919400-148919800	Enhancers	HUES48 Cell Line	embryonic stem cell

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