Variant report

Variant	nsv1009615
Chromosome Location	chr2:87337957-87951698
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7433)
CpG islands
(count:855)
Chromatin interactive
region (count:6)
LncRNA
region (count:47)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:7433 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:87903474-87903688	K562	blood:	n/a	n/a
2	ARID3A	chr2:87802514-87802706	K562	blood:	n/a	n/a
3	ARID3A	chr2:87623758-87624080	K562	blood:	n/a	n/a
4	ARID3A	chr2:87799487-87800222	K562	blood:	n/a	n/a
5	ARID3A	chr2:87623772-87624052	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:87812449-87812709	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:87797922-87797977	K562	blood:	n/a	n/a
8	ARID3A	chr2:87795618-87796003	K562	blood:	n/a	n/a
9	ARID3A	chr2:87765959-87766268	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:87929041-87929371	K562	blood:	n/a	n/a
11	ARID3A	chr2:87842112-87842471	K562	blood:	n/a	n/a
12	ARID3A	chr2:87816067-87816298	K562	blood:	n/a	n/a
13	ARID3A	chr2:87832053-87832224	K562	blood:	n/a	n/a
14	ATF1	chr2:87754798-87755008	K562	blood:	n/a	n/a
15	ATF1	chr2:87756399-87756603	K562	blood:	n/a	n/a
16	ATF1	chr2:87929184-87929384	K562	blood:	n/a	n/a
17	ATF1	chr2:87816074-87816451	K562	blood:	n/a	n/a
18	ATF1	chr2:87903372-87903674	K562	blood:	n/a	n/a
19	ATF1	chr2:87842104-87842488	K562	blood:	n/a	n/a
20	ATF1	chr2:87568829-87569093	K562	blood:	n/a	n/a
21	ATF1	chr2:87741013-87741231	K562	blood:	n/a	n/a
22	ATF1	chr2:87883958-87884458	K562	blood:	n/a	n/a
23	ATF1	chr2:87794523-87794820	K562	blood:	n/a	n/a
24	ATF2	chr2:87770596-87770855	GM12878	blood:	n/a	n/a
25	ATF2	chr2:87770617-87770892	GM12878	blood:	n/a	n/a
26	ATF3	chr2:87623739-87624043	A549	lung:	n/a	n/a
27	ATF3	chr2:87903447-87903666	K562	blood:	n/a	n/a
28	BACH1	chr2:87623757-87624094	K562	blood:	n/a	n/a
29	BACH1	chr2:87754799-87755006	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr2:87770563-87770872	K562	blood:	n/a	n/a
31	BACH1	chr2:87928999-87929447	K562	blood:	n/a	chr2:87929136-87929150
32	BACH1	chr2:87929012-87929445	H1-hESC	embryonic stem cell:	n/a	chr2:87929136-87929150
33	BACH1	chr2:87776227-87776422	K562	blood:	n/a	n/a
34	BATF	chr2:87795654-87795929	GM12878	blood:	n/a	n/a
35	BATF	chr2:87758196-87759003	GM12878	blood:	n/a	n/a
36	BATF	chr2:87540572-87540863	GM12878	blood:	n/a	chr2:87540719-87540729 chr2:87540723-87540733 chr2:87540722-87540733
37	BATF	chr2:87809533-87809865	GM12878	blood:	n/a	n/a
38	BATF	chr2:87607684-87607939	GM12878	blood:	n/a	n/a
39	BATF	chr2:87797541-87798534	GM12878	blood:	n/a	n/a
40	BATF	chr2:87770154-87770752	GM12878	blood:	n/a	n/a
41	BATF	chr2:87785382-87785856	GM12878	blood:	n/a	n/a
42	BATF	chr2:87755810-87756214	GM12878	blood:	n/a	chr2:87756080-87756090 chr2:87756043-87756052
43	BATF	chr2:87820486-87820924	GM12878	blood:	n/a	n/a
44	BATF	chr2:87359765-87360029	GM12878	blood:	n/a	n/a
45	BATF	chr2:87444976-87445145	GM12878	blood:	n/a	n/a
46	BATF	chr2:87785404-87785776	GM12878	blood:	n/a	n/a
47	BATF	chr2:87818678-87818940	GM12878	blood:	n/a	n/a
48	BATF	chr2:87560256-87560538	GM12878	blood:	n/a	n/a
49	BATF	chr2:87518026-87518413	GM12878	blood:	n/a	n/a
50	BATF	chr2:87837872-87838066	GM12878	blood:	n/a	chr2:87837994-87838005

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:87576399-87576449	GM12878	blood:	n/a
2	chr2:87576399-87576449	GM12878	blood:	n/a
3	chr2:87568958-87569008	AG04449	skin:	fetal
4	chr2:87568958-87569008	RPTEC	kidney:	n/a
5	chr2:87576370-87576420	GM12878	blood:	n/a
6	chr2:87572542-87572592	HCT-116	colon:	n/a
7	chr2:87572542-87572592	ovcar-3	ovarian:	n/a
8	chr2:87883547-87883597	Caco-2	colon:	n/a
9	chr2:87755371-87755421	HRE	kidney:	n/a
10	chr2:87576399-87576449	AoSMC	blood vessel:	n/a
11	chr2:87568958-87569008	HAEpiC	amniotic membrane:	n/a
12	chr2:87569275-87569325	HCPEpiC	choroid plexus:	n/a
13	chr2:87883497-87883547	A549	lung:	n/a
14	chr2:87576370-87576420	SK-N-MC	brain:	n/a
15	chr2:87572542-87572592	AoSMC	blood vessel:	n/a
16	chr2:87420273-87420323	GM06990	blood:	n/a
17	chr2:87576370-87576420	HRE	kidney:	n/a
18	chr2:87569447-87569497	Caco-2	colon:	n/a
19	chr2:87576399-87576449	SK-N-MC	brain:	n/a
20	chr2:87575991-87576041	HCPEpiC	choroid plexus:	n/a
21	chr2:87576370-87576420	U87	brain:	n/a
22	chr2:87575991-87576041	HNPCEpiC	eye:	n/a
23	chr2:87566763-87566813	LNCaP	prostate:	n/a
24	chr2:87566763-87566813	GM12878	blood:	n/a
25	chr2:87569142-87569192	GM19239	blood:	n/a
26	chr2:87883497-87883547	AG09309	skin:	n/a
27	chr2:87569275-87569325	MCF10A-Er-Src	breast:	n/a
28	chr2:87568958-87569008	Jurkat	blood:	n/a
29	chr2:87566763-87566813	PrEC	prostate:	n/a
30	chr2:87755371-87755421	BJ	skin:	n/a
31	chr2:87568958-87569008	SK-N-SH	brain:	n/a
32	chr2:87575991-87576041	HEK293	kidney:	embryo
33	chr2:87566763-87566813	HCM	heart:	n/a
34	chr2:87883547-87883597	NT2-D1	testis:	n/a
35	chr2:87568958-87569008	NT2-D1	testis:	n/a
36	chr2:87576370-87576420	RPTEC	kidney:	n/a
37	chr2:87755371-87755421	Caco-2	colon:	n/a
38	chr2:87420273-87420323	HCT-116	colon:	n/a
39	chr2:87572542-87572592	GM12891	blood:	n/a
40	chr2:87575991-87576041	Jurkat	blood:	n/a
41	chr2:87883497-87883547	HCM	heart:	n/a
42	chr2:87569447-87569497	MCF-7	breast:	n/a
43	chr2:87569275-87569325	HAEpiC	amniotic membrane:	n/a
44	chr2:87575991-87576041	AG10803	skin:	n/a
45	chr2:87576370-87576420	AG09309	skin:	n/a
46	chr2:87569447-87569497	NH-A	brain:	n/a
47	chr2:87576399-87576449	AG10803	skin:	n/a
48	chr2:87569142-87569192	T-47D	breast:	n/a
49	chr2:87445161-87445211	HMEC	breast:	n/a
50	chr2:87883497-87883547	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:87813553..87816546-chr2:111876759..111878642,2	MCF-7	breast:
2	chr2:87472406..87474648-chr2:112477037..112478664,2	MCF-7	breast:
3	chr2:87794607..87797367-chr2:88315602..88317365,2	K562	blood:
4	chr2:87431267..87434250-chr2:112516766..112518517,2	MCF-7	breast:
5	chr2:87444854..87445468-chr2:112505392..112505911,4	MCF-7	breast:
6	chr1:149222733..149224997-chr2:87623931..87625447,2	K562	blood:

(count:47 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLGLB2-1	chr2:87772259-87772404	ENSG00000222041
2	lnc-PLGLB2-1	chr2:87769669-87769823	NONHSAT072150
3	lnc-RGPD2-3	chr2:87777014-87777553	ENSG00000273445.1
4	lnc-PLGLB2-1	chr2:87754974-87755164	NONHSAT072145
5	lnc-RGPD2-1	chr2:87865347-87866283	NONHSAT072155
6	lnc-PLGLB2-1	chr2:87769669-87769823	ENSG00000222041
7	lnc-RGPD1-4	chr2:87596356-87596632	NONHSAT072140
8	lnc-RGPD1-5	chr2:87536124-87536279	ucscGeneNc_uc010fgz_1
9	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072145
10	lnc-PLGLB2-1	chr2:87777641-87777749	NONHSAT072146
11	lnc-PLGLB2-1	chr2:87769469-87769561	ENSG00000222041
12	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072146
13	lnc-PLGLB2-1	chr2:87755094-87755164	NONHSAT072150
14	lnc-PLGLB1-3	chr2:87404223-87404330	l_1879_chr2:87403978-87405069_thyroid
15	lnc-PLGLB2-1	chr2:87882777-87883000	ENSG00000222041.6
16	lnc-PLGLB1-3	chr2:87405044-87405069	l_1879_chr2:87403978-87405069_thyroid
17	lnc-PLGLB2-1	chr2:87754974-87755164	NONHSAT072146
18	lnc-RGPD1-2	chr2:87528781-87529374	NONHSAT072132
19	lnc-PLGLB2-1	chr2:87754974-87755164	NR_024206
20	lnc-PLGLB2-1	chr2:87769669-87769823	ENSG00000222041
21	lnc-PLGLB2-1	chr2:87755061-87755164	ENSG00000222041
22	lnc-PLGLB2-1	chr2:87772259-87772404	ENSG00000222041
23	lnc-PLGLB2-1	chr2:87779742-87780211	ENSG00000222041
24	lnc-PLGLB2-1	chr2:87880503-87880765	ENSG00000222041.6
25	lnc-PLGLB2-1	chr2:87779742-87779942	ENSG00000222041
26	lnc-RGPD1-5	chr2:87601841-87602143	ucscGeneNc_uc010fgz_1
27	lnc-PLGLB2-1	chr2:87779742-87779942	NONHSAT072146
28	lnc-PLGLB1-3	chr2:87403979-87404208	l_1879_chr2:87403978-87405069_thyroid
29	lnc-PLGLB2-1	chr2:87754998-87755164	ENSG00000222041
30	lnc-PLGLB2-1	chr2:87755015-87755164	ENSG00000222041
31	lnc-PLGLB2-1	chr2:87820726-87821030	NR_024206
32	lnc-PLGLB2-1	chr2:87779742-87779914	NONHSAT072150
33	lnc-PLGLB2-1	chr2:87755024-87755164	ENSG00000222041
34	lnc-PLGLB2-1	chr2:87820726-87821037	ENSG00000222041
35	lnc-PLGLB2-1	chr2:87777641-87777749	ENSG00000222041
36	lnc-PLGLB2-1	chr2:87779742-87780126	ENSG00000222041
37	lnc-PLGLB1-5	chr2:87520158-87520527	l_1881_chr2:87520157-87539624_76bGuttman_hLF
38	lnc-PLGLB1-5	chr2:87539491-87539624	l_1881_chr2:87520157-87539624_76bGuttman_hLF
39	lnc-PLGLB2-1	chr2:87882777-87882848	NONHSAT072150
40	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072150
41	lnc-PLGLB1-4	chr2:87448236-87449611	NONHSAT072131
42	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
43	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
44	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
45	lnc-RGPD2-2	chr2:87829755-87831343	NONHSAT072154
46	lnc-PLGLB2-1	chr2:87772259-87772404	NONHSAT072145
47	lnc-PLGLB1-7	chr2:87607003-87607890	NONHSAT072141

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4435	chr2:87929283-87929304	MIMAT0018951
hsa-miR-4771	chr2:87421953-87421973	MIMAT0019925

No data

Variant related genes	Relation type
IGKV3OR2-268	TF binding region
ENSG00000214354	TF binding region
MIR4771-2	TF binding region
ENSG00000225049	TF binding region
MIR4435-1	TF binding region
ENSG00000273445	TF binding region
ENSG00000213375	TF binding region
ENSG00000224881	TF binding region
LINC00152	TF binding region
ENSG00000225933	TF binding region
ENSG00000230395	TF binding region
ENSG00000204745	TF binding region
ENSG00000271097	TF binding region
ENSG00000233671	TF binding region
IGKV3OR2-268	CpG island
ENSG00000214354	CpG island
MIR4771-2	CpG island
ENSG00000225049	CpG island
MIR4435-1	CpG island
ENSG00000273445	CpG island
ENSG00000213375	CpG island
ENSG00000224881	CpG island
LINC00152	CpG island
ENSG00000225933	CpG island
ENSG00000230395	CpG island
ENSG00000204745	CpG island
ENSG00000271097	CpG island
ENSG00000233671	CpG island
ENSG00000222724	chromatin interactions
ENSG00000153094	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 10610 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:10610 , 50 per page) page: 1 2 3 4 5 6 7 ... 213

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202048070	chr2:87347862-87347863	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs377213779	chr2:87347895-87347896	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs528404887	chr2:87347929-87347930	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs540129091	chr2:87348169-87348170	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs564766057	chr2:87348196-87348197	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs201037623	chr2:87350079-87350080	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs373165744	chr2:87350325-87350326	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs554334803	chr2:87350341-87350342	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs534527062	chr2:87350352-87350353	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs188592416	chr2:87350360-87350361	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs571087124	chr2:87350372-87350373	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs538440632	chr2:87350386-87350387	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs556750853	chr2:87350414-87350415	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs538501526	chr2:87351724-87351725	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs192269070	chr2:87351726-87351727	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs374255303	chr2:87351732-87351733	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs568642486	chr2:87351773-87351774	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs535973716	chr2:87351791-87351792	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs553960060	chr2:87351966-87351967	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs62144435	chr2:87351980-87351981	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs572443870	chr2:87352118-87352119	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs201250802	chr2:87352314-87352315	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs562361694	chr2:87352346-87352347	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs574522926	chr2:87352367-87352368	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs74575721	chr2:87352393-87352394	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs541939569	chr2:87352394-87352395	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs60179502	chr2:87371833-87371834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs36125102	chr2:87371859-87371860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs34922646	chr2:87371880-87371881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35541059	chr2:87371886-87371887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2969576	chr2:87371921-87371922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34288489	chr2:87371925-87371926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529315567	chr2:87371932-87371933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2367688	chr2:87371967-87371968	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs565713177	chr2:87371969-87371970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2926670	chr2:87371980-87371981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77519047	chr2:87372004-87372005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552435701	chr2:87372032-87372033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199879200	chr2:87372033-87372034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538048502	chr2:87372034-87372035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146949268	chr2:87372055-87372056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35933635	chr2:87372071-87372072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574599960	chr2:87372074-87372075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146811331	chr2:87372088-87372089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540600998	chr2:87372101-87372102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535513299	chr2:87372110-87372111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553838263	chr2:87372183-87372184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375291760	chr2:87372188-87372189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572061419	chr2:87372217-87372218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374135072	chr2:87372244-87372245	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Schizophrenia	23813976	CNVD
Williams Syndrome	20824207	CNVD
Type 1 diabetes	21085585	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:3242 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:87371800-87372400	Enhancers	Fetal Heart	heart
2	chr2:87373000-87374000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr2:87373600-87374000	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr2:87373800-87374600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:87374000-87374600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:87374600-87374800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr2:87416200-87417000	Enhancers	HUVEC	blood vessel
8	chr2:87418800-87419600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr2:87425400-87426000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:87431600-87431800	Enhancers	Liver	Liver
11	chr2:87431800-87432200	Flanking Active TSS	Liver	Liver
12	chr2:87447800-87448200	Enhancers	Fetal Heart	heart
13	chr2:87455600-87456400	Enhancers	Fetal Thymus	thymus
14	chr2:87456200-87456800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr2:87456200-87457000	Enhancers	Rectal Smooth Muscle	rectum
16	chr2:87456200-87457000	Enhancers	Small Intestine	intestine
17	chr2:87456400-87457200	Enhancers	Adipose Nuclei	Adipose
18	chr2:87456600-87457000	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr2:87462000-87462400	Enhancers	Liver	Liver
20	chr2:87462400-87463600	Weak transcription	Liver	Liver
21	chr2:87463600-87463800	Enhancers	Liver	Liver
22	chr2:87464200-87465600	Enhancers	NHEK	skin
23	chr2:87464600-87464800	Enhancers	Hela-S3	cervix
24	chr2:87469400-87469800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:87469400-87469800	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr2:87469800-87473200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:87473000-87473200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr2:87473200-87473400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr2:87473200-87473400	Enhancers	Osteobl	bone
30	chr2:87473200-87473600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr2:87473200-87473600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:87473200-87473600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:87476600-87478200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr2:87477200-87478200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:87477400-87478200	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr2:87477400-87478200	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr2:87477400-87478200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr2:87477400-87478400	Enhancers	Primary hematopoietic stem cells	blood
39	chr2:87482200-87483000	Enhancers	Primary B cells from peripheral blood	blood
40	chr2:87489600-87489800	Enhancers	HUVEC	blood vessel
41	chr2:87489800-87490000	Enhancers	Right Atrium	heart
42	chr2:87489800-87490800	Weak transcription	HUVEC	blood vessel
43	chr2:87490800-87491200	Enhancers	HUVEC	blood vessel
44	chr2:87502000-87502400	Enhancers	Liver	Liver
45	chr2:87502400-87502800	Weak transcription	Liver	Liver
46	chr2:87502800-87503800	Enhancers	Liver	Liver
47	chr2:87503000-87504200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:87503200-87503600	Enhancers	Left Ventricle	heart
49	chr2:87503200-87503600	Enhancers	Psoas Muscle	Psoas
50	chr2:87503200-87503600	Enhancers	Right Atrium	heart

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