Variant report

Variant	nsv1007588
Chromosome Location	chr2:87322042-87960588
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7583)
CpG islands
(count:856)
Chromatin interactive
region (count:6)
LncRNA
region (count:48)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:7583 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:87816067-87816298	K562	blood:	n/a	n/a
2	ARID3A	chr2:87623772-87624052	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:87799487-87800222	K562	blood:	n/a	n/a
4	ARID3A	chr2:87832053-87832224	K562	blood:	n/a	n/a
5	ARID3A	chr2:87802514-87802706	K562	blood:	n/a	n/a
6	ARID3A	chr2:87797922-87797977	K562	blood:	n/a	n/a
7	ARID3A	chr2:87929041-87929371	K562	blood:	n/a	n/a
8	ARID3A	chr2:87903474-87903688	K562	blood:	n/a	n/a
9	ARID3A	chr2:87765959-87766268	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:87842112-87842471	K562	blood:	n/a	n/a
11	ARID3A	chr2:87812449-87812709	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:87623758-87624080	K562	blood:	n/a	n/a
13	ARID3A	chr2:87795618-87796003	K562	blood:	n/a	n/a
14	ATF1	chr2:87903372-87903674	K562	blood:	n/a	n/a
15	ATF1	chr2:87568829-87569093	K562	blood:	n/a	n/a
16	ATF1	chr2:87754798-87755008	K562	blood:	n/a	n/a
17	ATF1	chr2:87883958-87884458	K562	blood:	n/a	n/a
18	ATF1	chr2:87741013-87741231	K562	blood:	n/a	n/a
19	ATF1	chr2:87756399-87756603	K562	blood:	n/a	n/a
20	ATF1	chr2:87842104-87842488	K562	blood:	n/a	n/a
21	ATF1	chr2:87794523-87794820	K562	blood:	n/a	n/a
22	ATF1	chr2:87816074-87816451	K562	blood:	n/a	n/a
23	ATF1	chr2:87929184-87929384	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	chr2:87928999-87929447	K562	blood:	n/a	chr2:87929136-87929150
29	BACH1	chr2:87770563-87770872	K562	blood:	n/a	n/a
30	BACH1	chr2:87929012-87929445	H1-hESC	embryonic stem cell:	n/a	chr2:87929136-87929150
31	BACH1	chr2:87623757-87624094	K562	blood:	n/a	n/a
32	BACH1	chr2:87754799-87755006	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr2:87776227-87776422	K562	blood:	n/a	n/a
34	BATF	chr2:87820433-87820990	GM12878	blood:	n/a	n/a
35	BATF	chr2:87565968-87566380	GM12878	blood:	n/a	n/a
36	BATF	chr2:87557578-87557976	GM12878	blood:	n/a	chr2:87557756-87557767
37	BATF	chr2:87600918-87601134	GM12878	blood:	n/a	n/a
38	BATF	chr2:87740183-87740443	GM12878	blood:	n/a	n/a
39	BATF	chr2:87811814-87812101	GM12878	blood:	n/a	n/a
40	BATF	chr2:87563390-87563701	GM12878	blood:	n/a	chr2:87563473-87563482 chr2:87563509-87563520
41	BATF	chr2:87785404-87785776	GM12878	blood:	n/a	n/a
42	BATF	chr2:87749138-87749403	GM12878	blood:	n/a	n/a
43	BATF	chr2:87811725-87812163	GM12878	blood:	n/a	n/a
44	BATF	chr2:87837872-87838066	GM12878	blood:	n/a	chr2:87837994-87838005
45	BATF	chr2:87766299-87766672	GM12878	blood:	n/a	chr2:87766502-87766512
46	BATF	chr2:87881609-87882132	GM12878	blood:	n/a	n/a
47	BATF	chr2:87797541-87798534	GM12878	blood:	n/a	n/a
48	BATF	chr2:87565969-87566353	GM12878	blood:	n/a	n/a
49	BATF	chr2:87612582-87612810	GM12878	blood:	n/a	n/a
50	BATF	chr2:87355904-87356145	GM12878	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:87569275-87569325	MCF10A-Er-Src	breast:	n/a
2	chr2:87883547-87883597	Hela-S3	cervix:	n/a
3	chr2:87569275-87569325	MCF10A-Er-Src	breast:	n/a
4	chr2:87883547-87883597	Hela-S3	cervix:	n/a
5	chr2:87883497-87883547	SK-N-SH	brain:	n/a
6	chr2:87445161-87445211	H1-hESC	embryonic stem cell:	embryo
7	chr2:87420273-87420323	HL-60	blood:	n/a
8	chr2:87568958-87569008	U87	brain:	n/a
9	chr2:87445161-87445211	PFSK-1	brain:	n/a
10	chr2:87883547-87883597	ProgFib	skin:	n/a
11	chr2:87420273-87420323	AG04450	lung:	fetal
12	chr2:87569275-87569325	AG10803	skin:	n/a
13	chr2:87445161-87445211	K562	blood:	n/a
14	chr2:87572542-87572592	NHBE	bronchial:	n/a
15	chr2:87569142-87569192	HRCEpiC	kidney:	n/a
16	chr2:87576370-87576420	HEK293	kidney:	embryo
17	chr2:87569275-87569325	AG04450	lung:	fetal
18	chr2:87883497-87883547	PFSK-1	brain:	n/a
19	chr2:87566763-87566813	K562	blood:	n/a
20	chr2:87569142-87569192	IMR90	lung:	fetal
21	chr2:87569275-87569325	U87	brain:	n/a
22	chr2:87883497-87883547	Jurkat	blood:	n/a
23	chr2:87420273-87420323	AG09309	skin:	n/a
24	chr2:87572542-87572592	RPTEC	kidney:	n/a
25	chr2:87572542-87572592	AG10803	skin:	n/a
26	chr2:87568958-87569008	SKMC	muscle:	n/a
27	chr2:87883547-87883597	CMK	blood:	n/a
28	chr2:87755371-87755421	SK-N-SH	brain:	n/a
29	chr2:87572542-87572592	SAEC	small airway:	n/a
30	chr2:87568958-87569008	ovcar-3	ovarian:	n/a
31	chr2:87576370-87576420	K562	blood:	n/a
32	chr2:87755371-87755421	HIPEpiC	eye:	n/a
33	chr2:87420273-87420323	A549	lung:	n/a
34	chr2:87883547-87883597	HL-60	blood:	n/a
35	chr2:87576399-87576449	NHBE	bronchial:	n/a
36	chr2:87572542-87572592	MCF10A-Er-Src	breast:	n/a
37	chr2:87883547-87883597	NHDF-neo	bronchial:	n/a
38	chr2:87569275-87569325	PFSK-1	brain:	n/a
39	chr2:87445161-87445211	HCM	heart:	n/a
40	chr2:87883547-87883597	BE2_C	brain:	n/a
41	chr2:87569275-87569325	Hela-S3	cervix:	n/a
42	chr2:87883547-87883597	HRCEpiC	kidney:	n/a
43	chr2:87569447-87569497	AG09309	skin:	n/a
44	chr2:87572542-87572592	HRPEpiC	eye:	n/a
45	chr2:87445161-87445211	IMR90	lung:	fetal
46	chr2:87883497-87883547	PrEC	prostate:	n/a
47	chr2:87883497-87883547	SK-N-SH_RA	brain:	n/a
48	chr2:87445161-87445211	NHDF-neo	bronchial:	n/a
49	chr2:87569275-87569325	HUVEC	blood vessel:	n/a
50	chr2:87576370-87576420	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:87794607..87797367-chr2:88315602..88317365,2	K562	blood:
2	chr2:87431267..87434250-chr2:112516766..112518517,2	MCF-7	breast:
3	chr2:87813553..87816546-chr2:111876759..111878642,2	MCF-7	breast:
4	chr2:87472406..87474648-chr2:112477037..112478664,2	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:48 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLGLB2-1	chr2:87882777-87882848	NONHSAT072150
2	lnc-PLGLB2-1	chr2:87882777-87883000	ENSG00000222041.6
3	lnc-PLGLB2-1	chr2:87779742-87780126	ENSG00000222041
4	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072150
5	lnc-PLGLB1-7	chr2:87607003-87607890	NONHSAT072141
6	lnc-RGPD2-3	chr2:87777014-87777553	ENSG00000273445.1
7	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
8	lnc-PLGLB2-1	chr2:87772259-87772404	ENSG00000222041
9	lnc-PLGLB2-1	chr2:87779742-87779914	NONHSAT072150
10	lnc-PLGLB2-1	chr2:87754998-87755164	ENSG00000222041
11	lnc-RGPD1-5	chr2:87601841-87602143	ucscGeneNc_uc010fgz_1
12	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
13	lnc-PLGLB1-3	chr2:87405044-87405069	l_1879_chr2:87403978-87405069_thyroid
14	lnc-PLGLB2-1	chr2:87772259-87772404	ENSG00000222041
15	lnc-RGPD2-2	chr2:87829755-87831343	NONHSAT072154
16	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
17	lnc-PLGLB1-3	chr2:87403979-87404208	l_1879_chr2:87403978-87405069_thyroid
18	lnc-PLGLB2-1	chr2:87754974-87755164	NR_024206
19	lnc-PLGLB2-1	chr2:87754974-87755164	NONHSAT072146
20	lnc-PLGLB2-1	chr2:87755094-87755164	NONHSAT072150
21	lnc-PLGLB2-1	chr2:87820726-87821030	NR_024206
22	lnc-PLGLB2-1	chr2:87769669-87769823	ENSG00000222041
23	lnc-PLGLB2-1	chr2:87769469-87769561	ENSG00000222041
24	lnc-RGPD1-5	chr2:87536124-87536279	ucscGeneNc_uc010fgz_1
25	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072146
26	lnc-PLGLB2-1	chr2:87755061-87755164	ENSG00000222041
27	lnc-PLGLB2-1	chr2:87777641-87777749	ENSG00000222041
28	lnc-PLGLB1-3	chr2:87404223-87404330	l_1879_chr2:87403978-87405069_thyroid
29	lnc-PLGLB2-1	chr2:87755015-87755164	ENSG00000222041
30	lnc-PLGLB2-1	chr2:87769669-87769823	NONHSAT072150
31	lnc-PLGLB2-1	chr2:87820726-87821037	ENSG00000222041
32	lnc-RGPD1-2	chr2:87528781-87529374	NONHSAT072132
33	lnc-PLGLB2-1	chr2:87779742-87780211	ENSG00000222041
34	lnc-RGPD1-4	chr2:87596356-87596632	NONHSAT072140
35	lnc-PLGLB2-1	chr2:87777641-87777749	NONHSAT072146
36	lnc-RGPD2-1	chr2:87865347-87866283	NONHSAT072155
37	lnc-PLGLB2-1	chr2:87880503-87880765	ENSG00000222041.6
38	lnc-PLGLB2-1	chr2:87772259-87772404	NONHSAT072145
39	lnc-PLGLB2-1	chr2:87779742-87779942	ENSG00000222041
40	lnc-PLGLB2-1	chr2:87754974-87755164	NONHSAT072145
41	lnc-PLGLB1-5	chr2:87539491-87539624	l_1881_chr2:87520157-87539624_76bGuttman_hLF
42	lnc-PLGLB2-1	chr2:87769669-87769823	ENSG00000222041
43	lnc-PLGLB2-1	chr2:87779742-87779942	NONHSAT072146
44	lnc-PLGLB2-6	chr2:87954409-87954762	NONHSAT072157
45	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072145
46	lnc-PLGLB1-4	chr2:87448236-87449611	NONHSAT072131
47	lnc-PLGLB2-1	chr2:87755024-87755164	ENSG00000222041
48	lnc-PLGLB1-5	chr2:87520158-87520527	l_1881_chr2:87520157-87539624_76bGuttman_hLF

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

No data

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

Extended variants
information (count: 10973 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:10973 , 50 per page) page: 1 2 3 4 5 6 7 ... 220

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181197916	chr2:87330311-87330312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2887047	chr2:87330312-87330313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185804325	chr2:87330322-87330323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2887048	chr2:87330370-87330371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569186069	chr2:87330371-87330372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2887049	chr2:87330405-87330406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537367024	chr2:87330423-87330424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2367685	chr2:87330433-87330434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2887050	chr2:87330437-87330438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555669444	chr2:87330439-87330440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371102893	chr2:87330481-87330482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567506141	chr2:87330506-87330507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534805847	chr2:87330564-87330565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553069698	chr2:87330609-87330610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191555644	chr2:87330621-87330622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577672979	chr2:87330627-87330628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2887051	chr2:87330633-87330634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545040060	chr2:87330654-87330655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115247827	chr2:87330667-87330668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556704096	chr2:87330681-87330682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2367686	chr2:87330682-87330683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182134036	chr2:87330724-87330725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369722484	chr2:87330736-87330737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563335576	chr2:87330756-87330757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530641494	chr2:87330760-87330761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561223733	chr2:87330790-87330791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186802419	chr2:87330806-87330807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373215710	chr2:87330807-87330808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540461597	chr2:87330841-87330842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565437922	chr2:87330860-87330861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367597653	chr2:87330901-87330902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532503510	chr2:87330928-87330929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551028042	chr2:87330939-87330940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569175329	chr2:87330958-87330959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530103758	chr2:87330975-87330976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549328143	chr2:87330983-87330984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567555744	chr2:87331041-87331042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs202170160	chr2:87331099-87331100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199650306	chr2:87331108-87331109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78789405	chr2:87331110-87331111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534871440	chr2:87331182-87331183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561100821	chr2:87331342-87331343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571389155	chr2:87331350-87331351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538370096	chr2:87331426-87331427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557002120	chr2:87331505-87331506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574921522	chr2:87331571-87331572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535841223	chr2:87331644-87331645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77908807	chr2:87331686-87331687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573210635	chr2:87331707-87331708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs55662034	chr2:87331735-87331736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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	23813976	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	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
Williams Syndrome	20824207	CNVD
Type 1 diabetes	21085585	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:3277 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:87330200-87330600	Enhancers	Fetal Heart	heart
2	chr2:87330600-87331000	Weak transcription	Fetal Heart	heart
3	chr2:87331000-87331200	Enhancers	Fetal Heart	heart
4	chr2:87331200-87332000	Weak transcription	Fetal Heart	heart
5	chr2:87332000-87332200	Enhancers	Fetal Heart	heart
6	chr2:87332200-87334200	Weak transcription	Fetal Heart	heart
7	chr2:87333000-87333400	Enhancers	Fetal Lung	lung
8	chr2:87334200-87334400	Enhancers	Fetal Heart	heart
9	chr2:87371800-87372400	Enhancers	Fetal Heart	heart
10	chr2:87373000-87374000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:87373600-87374000	Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr2:87373800-87374600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr2:87374000-87374600	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr2:87374600-87374800	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr2:87416200-87417000	Enhancers	HUVEC	blood vessel
16	chr2:87418800-87419600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr2:87425400-87426000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr2:87431600-87431800	Enhancers	Liver	Liver
19	chr2:87431800-87432200	Flanking Active TSS	Liver	Liver
20	chr2:87447800-87448200	Enhancers	Fetal Heart	heart
21	chr2:87455600-87456400	Enhancers	Fetal Thymus	thymus
22	chr2:87456200-87456800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:87456200-87457000	Enhancers	Rectal Smooth Muscle	rectum
24	chr2:87456200-87457000	Enhancers	Small Intestine	intestine
25	chr2:87456400-87457200	Enhancers	Adipose Nuclei	Adipose
26	chr2:87456600-87457000	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr2:87462000-87462400	Enhancers	Liver	Liver
28	chr2:87462400-87463600	Weak transcription	Liver	Liver
29	chr2:87463600-87463800	Enhancers	Liver	Liver
30	chr2:87464200-87465600	Enhancers	NHEK	skin
31	chr2:87464600-87464800	Enhancers	Hela-S3	cervix
32	chr2:87469400-87469800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:87469400-87469800	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr2:87469800-87473200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:87473000-87473200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:87473200-87473400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:87473200-87473400	Enhancers	Osteobl	bone
38	chr2:87473200-87473600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:87473200-87473600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr2:87473200-87473600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:87476600-87478200	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr2:87477200-87478200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr2:87477400-87478200	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr2:87477400-87478200	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr2:87477400-87478200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:87477400-87478400	Enhancers	Primary hematopoietic stem cells	blood
47	chr2:87482200-87483000	Enhancers	Primary B cells from peripheral blood	blood
48	chr2:87489600-87489800	Enhancers	HUVEC	blood vessel
49	chr2:87489800-87490000	Enhancers	Right Atrium	heart
50	chr2:87489800-87490800	Weak transcription	HUVEC	blood vessel

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