Variant report

Variant	nsv1012193
Chromosome Location	chr2:211684524-212072213
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1928)
CpG islands
(count:61)
Chromatin interactive
region (count:46)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1928 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:211898514-211898839	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:211828150-211828564	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:212022640-212022955	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:211763832-211764099	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:211926380-211926665	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:211958451-211958883	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:211900278-211900659	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:211879134-211879533	HepG2	liver:	n/a	chr2:211879336-211879344
9	ARID3A	chr2:211949808-211950164	HepG2	liver:	n/a	n/a
10	ATF2	chr2:211898510-211898902	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr2:211898445-211898900	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr2:211711877-211711882	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr2:212008796-212009176	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:212008822-212009185	K562	blood:	n/a	n/a
15	BCL11A	chr2:211777520-211777739	GM12878	blood:	n/a	n/a
16	BCL3	chr2:211990245-211990455	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:211879099-211879458	HepG2	liver:	n/a	n/a
18	BRCA1	chr2:212038171-212038226	HepG2	liver:	n/a	n/a
19	BRCA1	chr2:212069501-212070462	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr2:211900288-211900548	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr2:211763857-211764342	HCT-116	colon:	n/a	n/a
22	CBX3	chr2:211889909-211890138	K562	blood:	n/a	n/a
23	CEBPB	chr2:212012498-212012839	HepG2	liver:	n/a	chr2:212012667-212012678 chr2:212012666-212012677 chr2:212012666-212012679
24	CEBPB	chr2:211927814-211927993	HepG2	liver:	n/a	chr2:211927924-211927935
25	CEBPB	chr2:211822757-211823102	HepG2	liver:	n/a	chr2:211822922-211822933 chr2:211822922-211822935 chr2:211822924-211822935
26	CEBPB	chr2:211982668-211982985	Hela-S3	cervix:	n/a	chr2:211982801-211982812 chr2:211982799-211982812 chr2:211982799-211982810 chr2:211982799-211982812 chr2:211982801-211982810
27	CEBPB	chr2:212008824-212009539	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:211859368-211859431	HepG2	liver:	n/a	chr2:211859394-211859405
29	CEBPB	chr2:212062696-212062950	HepG2	liver:	n/a	chr2:212062782-212062793 chr2:212062764-212062775
30	CEBPB	chr2:211862083-211862424	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:212041242-212041442	A549	lung:	n/a	chr2:212041322-212041333
32	CEBPB	chr2:211927826-211928093	MCF-7	breast:	n/a	chr2:211927924-211927935
33	CEBPB	chr2:211956669-211956869	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:211826932-211827209	A549	lung:	n/a	n/a
35	CEBPB	chr2:212008816-212009250	MCF-7	breast:	n/a	n/a
36	CEBPB	chr2:212032861-212033194	Hela-S3	cervix:	n/a	chr2:212033014-212033025
37	CEBPB	chr2:211901523-211901829	HepG2	liver:	n/a	chr2:211901660-211901673 chr2:211901660-211901673 chr2:211901661-211901672 chr2:211901659-211901676
38	CEBPB	chr2:212008809-212009294	HCT-116	colon:	n/a	n/a
39	CEBPB	chr2:211898572-211898832	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:211942142-211942342	HepG2	liver:	n/a	chr2:211942290-211942301
41	CEBPB	chr2:212008873-212009210	HCT-116	colon:	n/a	n/a
42	CEBPB	chr2:211898551-211898852	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr2:211830169-211830551	Hela-S3	cervix:	n/a	chr2:211830267-211830278 chr2:211830351-211830362 chr2:211830351-211830364 chr2:211830265-211830278 chr2:211830353-211830362 chr2:211830353-211830362 chr2:211830265-211830278 chr2:211830350-211830367 chr2:211830353-211830362
44	CEBPB	chr2:211860485-211860723	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr2:211822921-211822949	Hela-S3	cervix:	n/a	chr2:211822922-211822933 chr2:211822922-211822935 chr2:211822924-211822935
46	CEBPB	chr2:211898557-211898853	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr2:211989455-211989654	HepG2	liver:	n/a	chr2:211989481-211989492
48	CEBPB	chr2:211997327-211997736	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr2:211820406-211820702	IMR90	lung:	n/a	chr2:211820451-211820463
50	CEBPB	chr2:211927791-211928102	A549	lung:	n/a	chr2:211927924-211927935

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:211698619-211698669	NB4	blood:	n/a
2	chr2:211698619-211698669	HEEpiC	esophagus:	n/a
3	chr2:211698619-211698669	GM06990	blood:	n/a
4	chr2:211698619-211698669	SKMC	muscle:	n/a
5	chr2:211698619-211698669	MCF10A-Er-Src	breast:	n/a
6	chr2:211698619-211698669	AG10803	skin:	n/a
7	chr2:211698619-211698669	GM12878	blood:	n/a
8	chr2:211698619-211698669	ECC-1	luminal epithelium:	n/a
9	chr2:211698619-211698669	AG04450	lung:	fetal
10	chr2:211698619-211698669	Hepatocyte	liver:	n/a
11	chr2:211698619-211698669	AoSMC	blood vessel:	n/a
12	chr2:211698619-211698669	HCM	heart:	n/a
13	chr2:211698619-211698669	GM12892	blood:	n/a
14	chr2:211698619-211698669	BE2_C	brain:	n/a
15	chr2:211698619-211698669	HCF	heart:	n/a
16	chr2:211698619-211698669	T-47D	breast:	n/a
17	chr2:211698619-211698669	GM12891	blood:	n/a
18	chr2:211698619-211698669	HRE	kidney:	n/a
19	chr2:211698619-211698669	HIPEpiC	eye:	n/a
20	chr2:211698619-211698669	ProgFib	skin:	n/a
21	chr2:211698619-211698669	RPTEC	kidney:	n/a
22	chr2:211698619-211698669	IMR90	lung:	fetal
23	chr2:211698619-211698669	PrEC	prostate:	n/a
24	chr2:211698619-211698669	HRCEpiC	kidney:	n/a
25	chr2:211698619-211698669	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:211698619-211698669	A549	lung:	n/a
27	chr2:211698619-211698669	AG04449	skin:	fetal
28	chr2:211698619-211698669	K562	blood:	n/a
29	chr2:211698619-211698669	AG09309	skin:	n/a
30	chr2:211698619-211698669	HCPEpiC	choroid plexus:	n/a
31	chr2:211698619-211698669	HCT-116	colon:	n/a
32	chr2:211698619-211698669	MCF-7	breast:	n/a
33	chr2:211698619-211698669	U87	brain:	n/a
34	chr2:211698619-211698669	CMK	blood:	n/a
35	chr2:211698619-211698669	Caco-2	colon:	n/a
36	chr2:211698619-211698669	HUVEC	blood vessel:	n/a
37	chr2:211698619-211698669	HMEC	breast:	n/a
38	chr2:211698619-211698669	NT2-D1	testis:	n/a
39	chr2:211698619-211698669	PFSK-1	brain:	n/a
40	chr2:211698619-211698669	PANC-1	pancreas:	n/a
41	chr2:211698619-211698669	H1-hESC	embryonic stem cell:	embryo
42	chr2:211698619-211698669	HL-60	blood:	n/a
43	chr2:211698619-211698669	GM19239	blood:	n/a
44	chr2:211698619-211698669	BJ	skin:	n/a
45	chr2:211698619-211698669	HRPEpiC	eye:	n/a
46	chr2:211698619-211698669	AG09319	gingival:	n/a
47	chr2:211698619-211698669	SK-N-MC	brain:	n/a
48	chr2:211698619-211698669	SK-N-SH_RA	brain:	n/a
49	chr2:211698619-211698669	HepG2	liver:	n/a
50	chr2:211698619-211698669	NH-A	brain:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:211527997..211528722-chr2:211900005..211900896,3	MCF-7	breast:
2	chr2:211482310..211483112-chr2:212022669..212023186,2	MCF-7	breast:
3	chr2:211676043..211678802-chr2:211682762..211685242,2	K562	blood:
4	chr2:211863806..211866464-chr2:211874254..211876730,2	MCF-7	breast:
5	chr2:211949706..211950500-chr2:212022258..212023250,2	MCF-7	breast:
6	chr2:212042472..212044097-chr2:212046243..212049125,2	K562	blood:
7	chr2:211528012..211528782-chr2:211919888..211920455,2	MCF-7	breast:
8	chr2:212048363..212050986-chr2:212055468..212057547,3	K562	blood:
9	chr2:211482589..211483492-chr2:211899977..211900599,3	MCF-7	breast:
10	chr2:212048363..212050986-chr2:212055897..212057547,2	K562	blood:
11	chr2:211527941..211528689-chr2:211896794..211897496,2	MCF-7	breast:
12	chr2:211527960..211528912-chr2:211899983..211901271,6	MCF-7	breast:
13	chr2:211912454..211914426-chr2:211915786..211917883,2	K562	blood:
14	chr2:211958444..211959027-chr2:212022593..212023191,2	MCF-7	breast:
15	chr2:211920134..211920765-chr2:211949746..211950414,2	MCF-7	breast:
16	chr2:212042472..212044097-chr2:212046243..212049125,2	K562	blood:
17	chr2:212055110..212056655-chr2:212069046..212071730,2	MCF-7	breast:
18	chr2:212022878..212025223-chr2:212045457..212047124,2	K562	blood:
19	chr2:211951231..211952004-chr2:212022300..212022853,2	MCF-7	breast:
20	chr2:211949726..211950394-chr2:212022355..212023014,3	MCF-7	breast:
21	chr2:211898222..211899132-chr2:211949475..211950082,2	MCF-7	breast:
22	chr2:211951231..211952004-chr2:212022300..212022853,2	MCF-7	breast:
23	chr2:211898222..211899132-chr2:211949475..211950082,2	MCF-7	breast:
24	chr2:211918949..211922416-chr2:211922605..211926396,3	MCF-7	breast:
25	chr2:211920134..211920765-chr2:211949746..211950414,2	MCF-7	breast:
26	chr2:212048363..212050986-chr2:212055468..212057547,3	K562	blood:
27	chr2:211949706..211950500-chr2:212022258..212023250,2	MCF-7	breast:
28	chr2:211918949..211922416-chr2:211922605..211926396,3	MCF-7	breast:
29	chr2:212022243..212024951-chr2:212075273..212077446,2	MCF-7	breast:
30	chr2:212022878..212025223-chr2:212045457..212047124,2	K562	blood:
31	chr2:211442263..211442919-chr2:211898314..211899126,2	MCF-7	breast:
32	chr17:57922098..57924197-chr2:211699892..211701526,2	MCF-7	breast:
33	chr2:212048363..212050986-chr2:212055897..212057547,2	K562	blood:
34	chr2:211958444..211959027-chr2:212022593..212023191,2	MCF-7	breast:
35	chr2:211826156..211830730-chr2:211835135..211838762,5	MCF-7	breast:
36	chr2:212055110..212056655-chr2:212069046..212071730,2	MCF-7	breast:
37	chr2:211826156..211830730-chr2:211835135..211838762,5	MCF-7	breast:
38	chr2:211979527..211981470-chr2:211988454..211991128,2	MCF-7	breast:
39	chr2:211912454..211914426-chr2:211915786..211917883,2	K562	blood:
40	chr2:211979527..211981470-chr2:211988454..211991128,2	MCF-7	breast:
41	chr2:211949726..211950394-chr2:212022355..212023014,3	MCF-7	breast:
42	chr2:211863806..211866464-chr2:211874254..211876730,2	MCF-7	breast:
43	chr2:211949622..211950636-chr2:213412760..213413513,3	MCF-7	breast:
44	chr2:211989762..211992437-chr2:211995215..211997517,2	MCF-7	breast:
45	chr2:211989762..211992437-chr2:211995215..211997517,2	MCF-7	breast:
46	chr2:211112989..211113918-chr2:211900038..211900547,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPS1-3	chr2:211969658-211970456	NONHSAT076684

No data

Variant related genes	Relation type
ENSG00000271074	TF binding region
ENSG00000271074	CpG island

Extended variants
information (count: 6737 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6737 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2542924	chr2:211698206-211698207	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545967886	chr2:211698297-211698298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35063095	chr2:211698301-211698302	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs531427768	chr2:211698390-211698391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6757069	chr2:211698420-211698421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568051771	chr2:211698444-211698445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527243477	chr2:211698452-211698453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547729731	chr2:211698499-211698500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142187010	chr2:211698503-211698504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369903751	chr2:211698506-211698507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4673562	chr2:211698511-211698512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182346087	chr2:211698548-211698549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375753461	chr2:211698568-211698569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548013243	chr2:211698574-211698575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538339735	chr2:211698583-211698584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34052153	chr2:211698612-211698613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554722691	chr2:211698679-211698680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574790103	chr2:211698700-211698701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540204062	chr2:211698717-211698718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373016961	chr2:211698769-211698770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs56294429	chr2:211698800-211698801	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs566128972	chr2:211698807-211698808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577108450	chr2:211698816-211698817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546031115	chr2:211698848-211698849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563095889	chr2:211698868-211698869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531767463	chr2:211698870-211698871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541919014	chr2:211698874-211698875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73987018	chr2:211698887-211698888	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs527305932	chr2:211698891-211698892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs151061542	chr2:211698922-211698923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564413587	chr2:211698928-211698929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140817683	chr2:211698957-211698958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549762248	chr2:211698974-211698975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144582257	chr2:211698992-211698993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs7607199	chr2:211704032-211704033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2542923	chr2:211704083-211704084	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs145329897	chr2:211704109-211704110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572804268	chr2:211704132-211704133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181197083	chr2:211704133-211704134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539228215	chr2:211704165-211704166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552666922	chr2:211704203-211704204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76718077	chr2:211704242-211704243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533505361	chr2:211704271-211704272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537889405	chr2:211704316-211704317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554537625	chr2:211704334-211704335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1016403	chr2:211704356-211704357	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs534228992	chr2:211704392-211704393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114917845	chr2:211704416-211704417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577391302	chr2:211704422-211704423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546060277	chr2:211704446-211704447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	17661082	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211698200-211698600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:211698200-211699000	Enhancers	H9 Cell Line	embryonic stem cell
3	chr2:211704000-211704400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:211704400-211707400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:211707200-211707600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr2:211707200-211707600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr2:211707200-211707800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr2:211707200-211707800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr2:211707200-211708000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr2:211707200-211708000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:211707400-211707800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:211707400-211707800	Enhancers	Brain Germinal Matrix	brain
13	chr2:211707400-211708000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr2:211707400-211708200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:211707800-211710400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr2:211707800-211712400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr2:211708000-211711000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr2:211708200-211708800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:211708800-211709000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:211710400-211710800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr2:211710600-211711000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr2:211710800-211714400	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr2:211714200-211714800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr2:211714400-211714800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr2:211714400-211715000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr2:211714400-211715000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr2:211714600-211715000	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr2:211722400-211723000	Enhancers	HUVEC	blood vessel
29	chr2:211722800-211725000	Weak transcription	Brain Germinal Matrix	brain
30	chr2:211723000-211723600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr2:211723000-211728000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:211723000-211728000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr2:211723200-211723400	Enhancers	H1 Cell Line	embryonic stem cell
34	chr2:211723200-211723400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr2:211723200-211725000	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr2:211723200-211728200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr2:211723400-211724200	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr2:211723400-211726000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr2:211723600-211724000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr2:211723600-211725800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr2:211723800-211727000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:211724000-211724200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr2:211724000-211727400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr2:211724200-211724400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:211724200-211724400	Enhancers	H9 Cell Line	embryonic stem cell
46	chr2:211724200-211724400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr2:211724200-211726400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr2:211724400-211725200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:211724400-211725200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr2:211724400-211726800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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