Variant report

Variant	nsv874265
Chromosome Location	chr2:72789764-72982609
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1738)
CpG islands
(count:428)
Chromatin interactive
region (count:62)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1738 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:72950763-72951325	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:72908532-72909035	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:72982071-72982343	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:72923696-72923927	K562	blood:	n/a	n/a
5	ARID3A	chr2:72900432-72900756	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:72972848-72973270	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:72832983-72833344	K562	blood:	n/a	n/a
8	ARID3A	chr2:72980625-72980790	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:72921982-72922407	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:72806734-72807017	K562	blood:	n/a	n/a
11	ARID3A	chr2:72949745-72950229	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:72970722-72970959	HepG2	liver:	n/a	n/a
13	ATF1	chr2:72922027-72922420	K562	blood:	n/a	n/a
14	ATF1	chr2:72978362-72978374	K562	blood:	n/a	n/a
15	ATF1	chr2:72789723-72789889	K562	blood:	n/a	n/a
16	BACH1	chr2:72972705-72973151	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:72830811-72830958	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr2:72799244-72799541	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr2:72799526-72800263	A549	lung:	n/a	chr2:72800173-72800182
20	BCL3	chr2:72903221-72904242	A549	lung:	n/a	n/a
21	BCL3	chr2:72896221-72896737	A549	lung:	n/a	n/a
22	BCL3	chr2:72908492-72909148	A549	lung:	n/a	chr2:72908913-72908922
23	BHLHE40	chr2:72922098-72922370	K562	blood:	n/a	n/a
24	BHLHE40	chr2:72897717-72897722	GM12878	blood:	n/a	n/a
25	BHLHE40	chr2:72973005-72973171	GM12878	blood:	n/a	n/a
26	BRCA1	chr2:72797514-72798113	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr2:72788911-72790074	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr2:72799610-72800067	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr2:72843536-72843844	K562	blood:	n/a	n/a
30	CBX3	chr2:72923767-72924122	K562	blood:	n/a	n/a
31	CBX3	chr2:72923636-72924137	K562	blood:	n/a	n/a
32	CCNT2	chr2:72789641-72789857	K562	blood:	n/a	n/a
33	CEBPB	chr2:72895824-72896705	Hela-S3	cervix:	n/a	chr2:72895994-72896005
34	CEBPB	chr2:72974368-72974871	A549	lung:	n/a	chr2:72974631-72974642
35	CEBPB	chr2:72800323-72800834	IMR90	lung:	n/a	chr2:72800505-72800516 chr2:72800506-72800515 chr2:72800504-72800515
36	CEBPB	chr2:72800335-72800692	HepG2	liver:	n/a	chr2:72800505-72800516 chr2:72800506-72800515 chr2:72800504-72800515
37	CEBPB	chr2:72788839-72790247	Hela-S3	cervix:	n/a	chr2:72789733-72789745
38	CEBPB	chr2:72879229-72879314	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:72895806-72896225	A549	lung:	n/a	chr2:72895994-72896005
40	CEBPB	chr2:72800451-72800575	H1-hESC	embryonic stem cell:	n/a	chr2:72800505-72800516 chr2:72800506-72800515 chr2:72800504-72800515
41	CEBPB	chr2:72908630-72908990	A549	lung:	n/a	chr2:72908937-72908954
42	CEBPB	chr2:72974543-72974876	Hela-S3	cervix:	n/a	chr2:72974631-72974642
43	CEBPB	chr2:72799588-72800901	Hela-S3	cervix:	n/a	chr2:72800505-72800516 chr2:72800506-72800515 chr2:72800504-72800515
44	CEBPB	chr2:72973958-72973980	A549	lung:	n/a	n/a
45	CEBPB	chr2:72935402-72935735	IMR90	lung:	n/a	chr2:72935568-72935579
46	CEBPB	chr2:72955163-72955164	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr2:72895812-72896775	A549	lung:	n/a	chr2:72895994-72896005
48	CEBPB	chr2:72867124-72867270	A549	lung:	n/a	n/a
49	CEBPB	chr2:72974472-72974805	K562	blood:	n/a	chr2:72974631-72974642
50	CEBPB	chr2:72895810-72896601	IMR90	lung:	n/a	chr2:72895994-72896005

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:72980252-72980302	BJ	skin:	n/a
2	chr2:72980252-72980302	BJ	skin:	n/a
3	chr2:72837980-72838030	NB4	blood:	n/a
4	chr2:72980252-72980302	MCF10A-Er-Src	breast:	n/a
5	chr2:72830705-72830755	NHDF-neo	bronchial:	n/a
6	chr2:72977657-72977707	HRCEpiC	kidney:	n/a
7	chr2:72922245-72922295	AG09319	gingival:	n/a
8	chr2:72977657-72977707	RPTEC	kidney:	n/a
9	chr2:72946664-72946714	Jurkat	blood:	n/a
10	chr2:72837980-72838030	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:72977657-72977707	HRPEpiC	eye:	n/a
12	chr2:72980252-72980302	HIPEpiC	eye:	n/a
13	chr2:72837980-72838030	MCF-7	breast:	n/a
14	chr2:72946664-72946714	GM12891	blood:	n/a
15	chr2:72980252-72980302	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:72980252-72980302	HL-60	blood:	n/a
17	chr2:72946664-72946714	HL-60	blood:	n/a
18	chr2:72980252-72980302	AoSMC	blood vessel:	n/a
19	chr2:72946664-72946714	LNCaP	prostate:	n/a
20	chr2:72977657-72977707	ProgFib	skin:	n/a
21	chr2:72830705-72830755	HL-60	blood:	n/a
22	chr2:72977657-72977707	PANC-1	pancreas:	n/a
23	chr2:72837980-72838030	HL-60	blood:	n/a
24	chr2:72904298-72904348	SK-N-SH	brain:	n/a
25	chr2:72922245-72922295	HCPEpiC	choroid plexus:	n/a
26	chr2:72977657-72977707	HepG2	liver:	n/a
27	chr2:72977657-72977707	AG09319	gingival:	n/a
28	chr2:72830705-72830755	AG04449	skin:	fetal
29	chr2:72922245-72922295	NHDF-neo	bronchial:	n/a
30	chr2:72946664-72946714	NHBE	bronchial:	n/a
31	chr2:72922245-72922295	MCF10A-Er-Src	breast:	n/a
32	chr2:72977657-72977707	LNCaP	prostate:	n/a
33	chr2:72977657-72977707	HEEpiC	esophagus:	n/a
34	chr2:72904298-72904348	HCT-116	colon:	n/a
35	chr2:72904298-72904348	HRE	kidney:	n/a
36	chr2:72837980-72838030	IMR90	lung:	fetal
37	chr2:72830705-72830755	PrEC	prostate:	n/a
38	chr2:72837980-72838030	HNPCEpiC	eye:	n/a
39	chr2:72922245-72922295	HEK293	kidney:	embryo
40	chr2:72922245-72922295	LNCaP	prostate:	n/a
41	chr2:72946664-72946714	ECC-1	luminal epithelium:	n/a
42	chr2:72980252-72980302	Caco-2	colon:	n/a
43	chr2:72830705-72830755	Jurkat	blood:	n/a
44	chr2:72980252-72980302	NH-A	brain:	n/a
45	chr2:72904298-72904348	RPTEC	kidney:	n/a
46	chr2:72977657-72977707	IMR90	lung:	fetal
47	chr2:72946664-72946714	HNPCEpiC	eye:	n/a
48	chr2:72946664-72946714	GM19239	blood:	n/a
49	chr2:72980252-72980302	Jurkat	blood:	n/a
50	chr2:72922245-72922295	HRCEpiC	kidney:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:72377620..72378560-chr2:72972635..72973309,3	MCF-7	breast:
2	chr2:71757607..71758363-chr2:72806520..72807337,2	K562	blood:
3	chr2:72949375..72951848-chr2:72956840..72958572,2	K562	blood:
4	chr2:72844116..72846713-chr2:72857224..72859116,2	MCF-7	breast:
5	chr2:72901546..72903873-chr2:72916111..72918469,2	MCF-7	breast:
6	chr2:72914545..72916052-chr2:72918627..72920937,2	K562	blood:
7	chr2:72909548..72911648-chr2:72914521..72916177,2	K562	blood:
8	chr2:72849584..72851851-chr20:21361364..21363747,2	MCF-7	breast:
9	chr2:72981525..72984417-chr2:72997552..72999644,2	MCF-7	breast:
10	chr2:72909548..72911648-chr2:72914521..72916177,2	K562	blood:
11	chr2:72798438..72800996-chr2:72804039..72807217,3	K562	blood:
12	chr2:72797499..72799587-chr2:72800647..72803483,4	MCF-7	breast:
13	chr2:72975058..72976959-chr2:72978477..72981008,2	MCF-7	breast:
14	chr2:72341454..72343292-chr2:72805755..72808480,2	MCF-7	breast:
15	chr2:72357423..72359989-chr2:72817889..72819964,2	MCF-7	breast:
16	chr2:72975058..72976959-chr2:72978477..72981008,2	MCF-7	breast:
17	chr2:72375894..72377452-chr2:72802054..72803816,2	MCF-7	breast:
18	chr2:72850658..72853261-chr2:72859580..72861953,2	MCF-7	breast:
19	chr2:72914545..72916052-chr2:72918627..72920937,2	K562	blood:
20	chr2:72806388..72806936-chr2:72972660..72973356,2	MCF-7	breast:
21	chr2:72971179..72973717-chr2:72974748..72977332,2	K562	blood:
22	chr2:72856670..72859423-chr2:72860463..72863012,2	K562	blood:
23	chr2:72949375..72951848-chr2:72956840..72958572,2	K562	blood:
24	chr2:72973191..72975509-chr2:72979303..72982247,2	MCF-7	breast:
25	chr2:72827697..72829477-chr2:72834836..72837419,2	K562	blood:
26	chr2:72904382..72907029-chr2:72919984..72921758,2	MCF-7	breast:
27	chr2:72150772..72151702-chr2:72972617..72973142,2	K562	blood:
28	chr2:72035085..72037146-chr2:72806344..72808508,2	MCF-7	breast:
29	chr2:72948613..72949596-chr3:73160073..73160623,2	Hela-S3	cervix:
30	chr2:72901546..72903873-chr2:72916111..72918469,2	MCF-7	breast:
31	chr2:72884841..72886353-chr2:72887986..72890423,2	K562	blood:
32	chr2:72818726..72821056-chr2:72834950..72837136,2	MCF-7	breast:
33	chr2:72034767..72037407-chr2:72950731..72952275,2	MCF-7	breast:
34	chr2:72378019..72378538-chr2:72806122..72806836,2	MCF-7	breast:
35	chr2:72884841..72886353-chr2:72887986..72890423,2	K562	blood:
36	chr2:72818726..72821056-chr2:72834950..72837136,2	MCF-7	breast:
37	chr2:72377339..72378675-chr2:72806432..72807386,5	MCF-7	breast:
38	chr2:72844116..72846713-chr2:72857224..72859116,2	MCF-7	breast:
39	chr2:72151219..72151757-chr2:72806441..72806991,2	K562	blood:
40	chr2:72903226..72905209-chr2:72919789..72921712,2	MCF-7	breast:
41	chr2:72971179..72973717-chr2:72974748..72977332,2	K562	blood:
42	chr2:72827697..72829477-chr2:72834836..72837419,2	K562	blood:
43	chr2:72798438..72800996-chr2:72804039..72807217,3	K562	blood:
44	chr2:72806388..72806936-chr2:72972660..72973356,2	MCF-7	breast:
45	chr2:72802770..72805375-chr2:72805450..72807796,2	MCF-7	breast:
46	chr2:72425556..72426522-chr2:72806538..72807121,3	MCF-7	breast:
47	chr2:72790315..72792488-chr2:72796199..72797805,2	K562	blood:
48	chr2:72830279..72832470-chr2:72845355..72847337,2	K562	blood:
49	chr2:72783993..72785922-chr2:72791174..72793181,2	K562	blood:
50	chr2:72850658..72853261-chr2:72859580..72861953,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU2-39P	TF binding region
RNU2-39P	CpG island
ENSG00000223247	chromatin interactions

Extended variants
information (count: 6182 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:6182 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12471312	chr2:72789764-72789765	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532798983	chr2:72789797-72789798	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs547773399	chr2:72789799-72789800	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs566061927	chr2:72789806-72789807	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs186615449	chr2:72789824-72789825	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs527242925	chr2:72789842-72789843	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs547600356	chr2:72789933-72789934	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs567491434	chr2:72789936-72789937	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs549455294	chr2:72789953-72789954	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116198497	chr2:72789970-72789971	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs139804926	chr2:72789971-72789972	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs146192370	chr2:72789980-72789981	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs537153728	chr2:72790043-72790044	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs114220814	chr2:72790049-72790050	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs571346453	chr2:72790054-72790055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs143128749	chr2:72790066-72790067	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs554085117	chr2:72790068-72790069	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs549989073	chr2:72790120-72790121	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs560819182	chr2:72790207-72790208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113895217	chr2:72790276-72790277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538660531	chr2:72790277-72790278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111541553	chr2:72790312-72790313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558872206	chr2:72790335-72790336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183627267	chr2:72790384-72790385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576039361	chr2:72790387-72790388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543159945	chr2:72790448-72790449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145523809	chr2:72790483-72790484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532577055	chr2:72790575-72790576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148416532	chr2:72790716-72790717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142638910	chr2:72790720-72790721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35641394	chr2:72790769-72790770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187632205	chr2:72790854-72790855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561631616	chr2:72790864-72790865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73943201	chr2:72790933-72790934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs112710945	chr2:72790977-72790978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548132266	chr2:72790991-72790992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569961470	chr2:72791048-72791049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530975540	chr2:72791056-72791057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116076012	chr2:72791064-72791065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7340484	chr2:72791189-72791190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193113731	chr2:72791230-72791231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538439954	chr2:72791275-72791276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554833332	chr2:72791280-72791281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs80228559	chr2:72791322-72791323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10182863	chr2:72791357-72791358	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs536551402	chr2:72791384-72791385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147842090	chr2:72791402-72791403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575936014	chr2:72791407-72791408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537080205	chr2:72791429-72791430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558355512	chr2:72791455-72791456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
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
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	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
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	23813976	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1582 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:72775000-72808800	Weak transcription	Ovary	ovary
2	chr2:72783400-72792200	Weak transcription	Left Ventricle	heart
3	chr2:72783600-72793600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr2:72784000-72800800	Weak transcription	Placenta	Placenta
5	chr2:72784200-72799600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:72786000-72803800	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr2:72787600-72791000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr2:72788000-72789800	Enhancers	Rectal Smooth Muscle	rectum
9	chr2:72788000-72790600	Enhancers	Hela-S3	cervix
10	chr2:72788200-72790000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:72788600-72789800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:72788600-72789800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:72788600-72789800	Enhancers	NHDF-Ad	bronchial
14	chr2:72788600-72790000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:72788600-72790000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr2:72788600-72790000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr2:72788600-72790000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:72788600-72790000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:72788600-72790000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr2:72788600-72790000	Enhancers	Fetal Heart	heart
21	chr2:72788600-72790000	Enhancers	HSMM	muscle
22	chr2:72788600-72790200	Enhancers	Aorta	Aorta
23	chr2:72788600-72790200	Enhancers	Brain Hippocampus Middle	brain
24	chr2:72788600-72790200	Enhancers	NHLF	lung
25	chr2:72788600-72790600	Enhancers	NH-A	brain
26	chr2:72788800-72789800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:72788800-72789800	Enhancers	Brain Cingulate Gyrus	brain
28	chr2:72788800-72789800	Flanking Active TSS	HUVEC	blood vessel
29	chr2:72788800-72790000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:72788800-72790000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr2:72788800-72790000	Enhancers	Placenta Amnion	Placenta Amnion
32	chr2:72788800-72790000	Flanking Active TSS	A549	lung
33	chr2:72788800-72790000	Enhancers	HMEC	breast
34	chr2:72788800-72790400	Enhancers	Colon Smooth Muscle	Colon
35	chr2:72788800-72790400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr2:72789000-72789800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr2:72789000-72789800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:72789000-72789800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:72789000-72789800	Enhancers	Brain Angular Gyrus	brain
40	chr2:72789000-72789800	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr2:72789000-72790000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr2:72789000-72792200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr2:72789200-72789800	Enhancers	K562	blood
44	chr2:72789200-72789800	Enhancers	NHEK	skin
45	chr2:72789200-72790000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr2:72789200-72790000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr2:72789200-72790200	Enhancers	Brain Substantia Nigra	brain
48	chr2:72789200-72790600	Enhancers	Primary hematopoietic stem cells	blood
49	chr2:72789200-72790600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr2:72789200-72803600	Weak transcription	Duodenum Smooth Muscle	Duodenum

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