Variant report

Variant	nsv1004841
Chromosome Location	chr2:133124355-133350008
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1930)
CpG islands
(count:2018)
Chromatin interactive
region (count:87)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1930 , 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	chr2:133182024-133182468	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:133174024-133174324	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:133304875-133304890	K562	blood:	n/a	n/a
4	ARID3A	chr2:133197370-133197703	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:133206471-133206700	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:133304775-133304963	HepG2	liver:	n/a	n/a
7	ATF3	chr2:133196210-133196622	A549	lung:	n/a	n/a
8	ATF3	chr2:133173868-133174360	A549	lung:	n/a	n/a
9	BACH1	chr2:133173941-133174219	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr2:133151603-133151834	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:133151626-133151809	GM12878	blood:	n/a	n/a
12	BCL3	chr2:133196055-133196767	A549	lung:	n/a	chr2:133196462-133196471
13	BCL3	chr2:133173475-133174583	A549	lung:	n/a	chr2:133174091-133174104 chr2:133174016-133174025 chr2:133174107-133174120 chr2:133173569-133173578
14	BCL3	chr2:133173786-133174427	A549	lung:	n/a	chr2:133174091-133174104 chr2:133174016-133174025 chr2:133174107-133174120
15	BCL3	chr2:133196228-133196753	A549	lung:	n/a	chr2:133196462-133196471
16	BHLHE40	chr2:133175471-133175541	K562	blood:	n/a	n/a
17	BHLHE40	chr2:133173885-133174262	HepG2	liver:	n/a	chr2:133173990-133174006 chr2:133173975-133173991
18	BHLHE40	chr2:133174899-133175021	K562	blood:	n/a	n/a
19	BHLHE40	chr2:133174028-133174155	K562	blood:	n/a	n/a
20	BHLHE40	chr2:133141777-133141786	K562	blood:	n/a	n/a
21	BHLHE40	chr2:133187043-133187166	K562	blood:	n/a	n/a
22	BHLHE40	chr2:133197341-133197721	HepG2	liver:	n/a	n/a
23	BRCA1	chr2:133174120-133174267	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr2:133196024-133196837	HCT-116	colon:	n/a	n/a
25	CEBPB	chr2:133157682-133158096	IMR90	lung:	n/a	chr2:133157953-133157964 chr2:133157953-133157964 chr2:133157953-133157966
26	CEBPB	chr2:133325933-133326035	IMR90	lung:	n/a	chr2:133325967-133325978
27	CEBPB	chr2:133333363-133333495	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:133157731-133157997	K562	blood:	n/a	chr2:133157953-133157964 chr2:133157953-133157964 chr2:133157953-133157966
29	CEBPB	chr2:133172696-133173266	A549	lung:	n/a	chr2:133173034-133173045
30	CEBPB	chr2:133142766-133142903	HepG2	liver:	n/a	chr2:133142768-133142781 chr2:133142769-133142780
31	CEBPB	chr2:133195547-133195632	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:133200719-133201049	IMR90	lung:	n/a	chr2:133200853-133200864
33	CEBPB	chr2:133172679-133173262	IMR90	lung:	n/a	chr2:133173034-133173045
34	CEBPB	chr2:133319880-133320042	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:133200725-133201046	HepG2	liver:	n/a	chr2:133200853-133200864
36	CEBPB	chr2:133333292-133333484	A549	lung:	n/a	n/a
37	CEBPB	chr2:133196084-133196752	A549	lung:	n/a	n/a
38	CEBPB	chr2:133172939-133173163	H1-hESC	embryonic stem cell:	n/a	chr2:133173034-133173045
39	CEBPB	chr2:133157636-133158145	K562	blood:	n/a	chr2:133157953-133157964 chr2:133157953-133157964 chr2:133157953-133157966
40	CEBPB	chr2:133347693-133347799	IMR90	lung:	n/a	n/a
41	CEBPB	chr2:133131693-133131961	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr2:133189784-133190098	HepG2	liver:	n/a	chr2:133189927-133189938
43	CEBPB	chr2:133200681-133201013	A549	lung:	n/a	chr2:133200853-133200864
44	CEBPB	chr2:133231795-133231925	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:133173813-133174515	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr2:133204426-133204623	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:133197407-133197648	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:133325882-133326055	HepG2	liver:	n/a	chr2:133325967-133325978
49	CEBPB	chr2:133189883-133190087	IMR90	lung:	n/a	chr2:133189927-133189938
50	CEBPB	chr2:133173960-133174204	IMR90	lung:	n/a	n/a

(count:2018 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133197577-133197627	NHDF-neo	bronchial:	n/a
2	chr2:133343628-133343678	SK-N-MC	brain:	n/a
3	chr2:133173533-133173583	HAEpiC	amniotic membrane:	n/a
4	chr2:133342286-133342336	HRPEpiC	eye:	n/a
5	chr2:133342286-133342336	GM12891	blood:	n/a
6	chr2:133197577-133197627	NHDF-neo	bronchial:	n/a
7	chr2:133343628-133343678	SK-N-MC	brain:	n/a
8	chr2:133173533-133173583	HAEpiC	amniotic membrane:	n/a
9	chr2:133342286-133342336	HRPEpiC	eye:	n/a
10	chr2:133342286-133342336	GM12891	blood:	n/a
11	chr2:133174042-133174092	HAEpiC	amniotic membrane:	n/a
12	chr2:133343115-133343165	PrEC	prostate:	n/a
13	chr2:133189699-133189749	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:133174136-133174186	Hepatocyte	liver:	n/a
15	chr2:133343618-133343668	AoSMC	blood vessel:	n/a
16	chr2:133175382-133175432	ovcar-3	ovarian:	n/a
17	chr2:133346858-133346908	HAEpiC	amniotic membrane:	n/a
18	chr2:133176249-133176299	NHDF-neo	bronchial:	n/a
19	chr2:133343274-133343324	HEEpiC	esophagus:	n/a
20	chr2:133174635-133174685	ovcar-3	ovarian:	n/a
21	chr2:133343657-133343707	HEK293	kidney:	embryo
22	chr2:133175382-133175432	HUVEC	blood vessel:	n/a
23	chr2:133346858-133346908	Jurkat	blood:	n/a
24	chr2:133173533-133173583	SK-N-SH	brain:	n/a
25	chr2:133342838-133342888	HRPEpiC	eye:	n/a
26	chr2:133178190-133178240	NHBE	bronchial:	n/a
27	chr2:133175397-133175447	AG10803	skin:	n/a
28	chr2:133346858-133346908	AG04450	lung:	fetal
29	chr2:133171941-133171991	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:133189699-133189749	A549	lung:	n/a
31	chr2:133339746-133339796	HUVEC	blood vessel:	n/a
32	chr2:133343657-133343707	PrEC	prostate:	n/a
33	chr2:133189699-133189749	HRCEpiC	kidney:	n/a
34	chr2:133173433-133173483	IMR90	lung:	fetal
35	chr2:133175382-133175432	MCF10A-Er-Src	breast:	n/a
36	chr2:133171381-133171431	HepG2	liver:	n/a
37	chr2:133171941-133171991	MCF-7	breast:	n/a
38	chr2:133342838-133342888	AoSMC	blood vessel:	n/a
39	chr2:133174168-133174218	BE2_C	brain:	n/a
40	chr2:133174168-133174218	HCT-116	colon:	n/a
41	chr2:133173433-133173483	GM06990	blood:	n/a
42	chr2:133176249-133176299	HEEpiC	esophagus:	n/a
43	chr2:133175382-133175432	SAEC	small airway:	n/a
44	chr2:133343308-133343358	CMK	blood:	n/a
45	chr2:133342286-133342336	HRCEpiC	kidney:	n/a
46	chr2:133339746-133339796	HCPEpiC	choroid plexus:	n/a
47	chr2:133343373-133343423	CMK	blood:	n/a
48	chr2:133343628-133343678	GM19239	blood:	n/a
49	chr2:133339746-133339796	CMK	blood:	n/a
50	chr2:133342838-133342888	AG10803	skin:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:133104010..133106361-chr2:133176429..133178884,2	MCF-7	breast:
2	chr2:133180532..133182214-chr2:133186789..133189602,2	MCF-7	breast:
3	chr2:133106413..133107377-chr2:133181739..133182675,3	MCF-7	breast:
4	chr2:133340082..133340612-chr2:133355931..133356931,2	MCF-7	breast:
5	chr2:133166126..133168437-chr2:133171121..133175253,4	MCF-7	breast:
6	chr2:133171742..133175089-chr2:133186181..133188508,3	MCF-7	breast:
7	chr2:133339726..133340597-chr2:133369688..133370670,9	MCF-7	breast:
8	chr2:133304762..133308062-chr2:133425978..133429369,3	MCF-7	breast:
9	chr2:133136843..133139726-chr2:133171493..133174059,2	MCF-7	breast:
10	chr2:133228178..133229976-chr2:133230852..133233408,2	MCF-7	breast:
11	chr2:133339726..133340368-chr2:133369767..133370722,4	MCF-7	breast:
12	chr2:133335745..133337645-chr2:133340420..133342351,2	K562	blood:
13	chr2:133123487..133125732-chr2:133126959..133129500,2	K562	blood:
14	chr2:133173744..133175513-chr2:133427199..133429009,2	MCF-7	breast:
15	chr2:133272961..133273729-chr2:133339881..133340586,2	MCF-7	breast:
16	chr2:133108792..133112199-chr2:133172607..133174892,3	MCF-7	breast:
17	chr2:133184307..133187012-chr2:133200888..133203786,2	MCF-7	breast:
18	chr2:133304640..133305382-chr2:133928983..133929651,2	MCF-7	breast:
19	chr2:133153165..133154899-chr2:133171288..133174191,2	MCF-7	breast:
20	chr2:133339634..133341724-chr2:133426515..133429384,4	MCF-7	breast:
21	chr2:133304259..133305229-chr2:133647133..133647703,2	MCF-7	breast:
22	chr2:133152507..133155415-chr2:133160169..133163042,2	MCF-7	breast:
23	chr2:133312121..133314029-chr2:133316957..133319082,2	K562	blood:
24	chr2:133171122..133175666-chr2:133177374..133180650,5	MCF-7	breast:
25	chr2:133308087..133308889-chr2:133339718..133340292,2	MCF-7	breast:
26	chr2:133195794..133199100-chr2:133203040..133205652,3	MCF-7	breast:
27	chr2:133136843..133139726-chr2:133171493..133174059,2	MCF-7	breast:
28	chr2:133129464..133129981-chr2:133206123..133207082,2	MCF-7	breast:
29	chr2:133230048..133232279-chr2:133233399..133234934,2	MCF-7	breast:
30	chr2:133133601..133135526-chr2:133136954..133139569,2	MCF-7	breast:
31	chr2:133183645..133185687-chr2:133186251..133189764,3	MCF-7	breast:
32	chr2:133174216..133177088-chr2:133183800..133185718,2	MCF-7	breast:
33	chr2:133106447..133107306-chr2:133173079..133174146,3	MCF-7	breast:
34	chr2:133124752..133127513-chr2:133337164..133339818,2	MCF-7	breast:
35	chr2:133152507..133155415-chr2:133160169..133163042,2	MCF-7	breast:
36	chr2:133189109..133191436-chr2:133194344..133196000,2	MCF-7	breast:
37	chr2:133312121..133314029-chr2:133316957..133319082,2	K562	blood:
38	chr2:133164142..133169602-chr2:133170573..133175419,7	MCF-7	breast:
39	chr2:133129464..133129981-chr2:133206123..133207082,2	MCF-7	breast:
40	chr2:133108915..133111457-chr2:133172343..133174834,3	MCF-7	breast:
41	chr2:133218783..133221422-chr2:133221426..133223420,2	MCF-7	breast:
42	chr2:133339903..133340611-chr2:134262125..134263083,2	MCF-7	breast:
43	chr2:133180532..133182214-chr2:133186789..133189602,2	MCF-7	breast:
44	chr2:133174816..133177571-chr2:133199085..133201866,2	MCF-7	breast:
45	chr2:133274387..133277041-chr2:133279166..133281960,2	MCF-7	breast:
46	chr2:133335745..133337645-chr2:133340420..133342351,2	K562	blood:
47	chr2:133339874..133340573-chr2:133634427..133635308,3	MCF-7	breast:
48	chr2:133174816..133177571-chr2:133199085..133201866,2	MCF-7	breast:
49	chr2:133189109..133191436-chr2:133194344..133196000,2	MCF-7	breast:
50	chr2:133164142..133169602-chr2:133170573..133175419,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYPD1-3	chr2:133246127-133246661	NONHSAT074536
2	lnc-C2orf27A-10	chr2:133281190-133281509	NONHSAT074537

No data

Variant related genes	Relation type
YBX1P7	TF binding region
GPR39	TF binding region
RNU6-175P	TF binding region
ENSG00000221142	TF binding region
RN7SKP103	TF binding region
YBX1P7	CpG island
GPR39	CpG island
RNU6-175P	CpG island
ENSG00000221142	CpG island
RN7SKP103	CpG island
ENSG00000150551	chromatin interactions
ENSG00000230992	chromatin interactions
ENSG00000183840	chromatin interactions
ENSG00000272769	chromatin interactions
ENSG00000200718	chromatin interactions
ENSG00000252705	chromatin interactions
ENSG00000221142	chromatin interactions

Extended variants
information (count: 8840 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:8840 , 50 per page) page: 1 2 3 4 5 6 7 ... 177

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371095384	chr2:133124441-133124442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562470567	chr2:133124466-133124467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373847616	chr2:133124493-133124494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533055645	chr2:133124526-133124527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112660746	chr2:133124557-133124558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114649391	chr2:133124586-133124587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560306314	chr2:133124598-133124599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs527446969	chr2:133124701-133124702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549082357	chr2:133124776-133124777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567334664	chr2:133124810-133124811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184451273	chr2:133124843-133124844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549777860	chr2:133124924-133124925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs151257140	chr2:133124926-133124927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2315373	chr2:133124929-133124930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77152684	chr2:133124944-133124945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114756422	chr2:133124978-133124979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572624804	chr2:133124989-133124990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536413831	chr2:133124991-133124992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554680593	chr2:133124995-133124996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558582555	chr2:133125835-133125836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs4954321	chr2:133125851-133125852	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs73955628	chr2:133125878-133125879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542522691	chr2:133125927-133125928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181152388	chr2:133125932-133125933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145967707	chr2:133125996-133125997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138587753	chr2:133126023-133126024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186654039	chr2:133126036-133126037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561051483	chr2:133126058-133126059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75971178	chr2:133126126-133126127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs116121970	chr2:133126169-133126170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369997697	chr2:133126171-133126172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191300936	chr2:133126174-133126175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535214334	chr2:133126601-133126602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116236192	chr2:133126603-133126604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572345067	chr2:133126609-133126610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542951837	chr2:133126624-133126625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191032668	chr2:133126634-133126635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571077168	chr2:133126653-133126654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115428596	chr2:133126725-133126726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78849873	chr2:133126726-133126727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142372517	chr2:133126744-133126745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557860850	chr2:133126802-133126803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535788505	chr2:133126818-133126819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560517135	chr2:133126896-133126897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541062071	chr2:133126920-133126921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559098021	chr2:133126940-133126941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183390455	chr2:133127061-133127062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs56377781	chr2:133127069-133127070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12691770	chr2:133127075-133127076	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs145929444	chr2:133127090-133127091	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	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
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	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1739 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133124400-133125000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr2:133125800-133126200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:133125800-133126200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr2:133126600-133127000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:133126600-133127400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr2:133126800-133127000	Enhancers	Fetal Muscle Leg	muscle
7	chr2:133127400-133130800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:133128000-133128200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:133129000-133129600	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr2:133129000-133131000	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr2:133129600-133130200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr2:133129800-133130200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr2:133130200-133132200	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr2:133130600-133131400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:133130800-133131400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:133130800-133132800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:133131200-133131400	Enhancers	Brain Anterior Caudate	brain
18	chr2:133131200-133132200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:133131200-133132600	Enhancers	Placenta Amnion	Placenta Amnion
20	chr2:133131400-133132000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:133131400-133132000	Weak transcription	Brain Anterior Caudate	brain
22	chr2:133131400-133132400	Enhancers	Fetal Intestine Small	intestine
23	chr2:133131400-133134000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr2:133131600-133131800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr2:133131600-133131800	Active TSS	Rectal Mucosa Donor 29	rectum
26	chr2:133131600-133132600	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr2:133131600-133132800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:133131800-133132000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:133131800-133132200	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr2:133131800-133132400	Enhancers	Fetal Intestine Large	intestine
31	chr2:133132000-133132400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:133132000-133132600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:133132000-133132800	Enhancers	Brain Anterior Caudate	brain
34	chr2:133132200-133132400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
35	chr2:133132200-133132800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:133132200-133132800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr2:133132200-133132800	Enhancers	Brain Substantia Nigra	brain
38	chr2:133132200-133132800	Enhancers	Colon Smooth Muscle	Colon
39	chr2:133132200-133132800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr2:133132200-133133000	Enhancers	Brain Hippocampus Middle	brain
41	chr2:133132400-133132600	Flanking Active TSS	NHDF-Ad	bronchial
42	chr2:133132400-133132800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:133132400-133132800	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr2:133132600-133133000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:133132800-133133000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:133132800-133134200	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr2:133132800-133136400	Weak transcription	Brain Substantia Nigra	brain
48	chr2:133132800-133138000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr2:133136800-133137000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr2:133138400-133138800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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