Variant report

Variant	esv2760646
Chromosome Location	chr2:87330978-88052330
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7986)
CpG islands
(count:856)
Chromatin interactive
region (count:6)
LncRNA
region (count:52)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:7986 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:87765959-87766268	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:87623758-87624080	K562	blood:	n/a	n/a
3	ARID3A	chr2:87832053-87832224	K562	blood:	n/a	n/a
4	ARID3A	chr2:87812449-87812709	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:87799487-87800222	K562	blood:	n/a	n/a
6	ARID3A	chr2:87903474-87903688	K562	blood:	n/a	n/a
7	ARID3A	chr2:87795618-87796003	K562	blood:	n/a	n/a
8	ARID3A	chr2:87797922-87797977	K562	blood:	n/a	n/a
9	ARID3A	chr2:87623772-87624052	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:87929041-87929371	K562	blood:	n/a	n/a
11	ARID3A	chr2:87816067-87816298	K562	blood:	n/a	n/a
12	ARID3A	chr2:87802514-87802706	K562	blood:	n/a	n/a
13	ARID3A	chr2:87842112-87842471	K562	blood:	n/a	n/a
14	ATF1	chr2:87883958-87884458	K562	blood:	n/a	n/a
15	ATF1	chr2:87929184-87929384	K562	blood:	n/a	n/a
16	ATF1	chr2:87794523-87794820	K562	blood:	n/a	n/a
17	ATF1	chr2:87756399-87756603	K562	blood:	n/a	n/a
18	ATF1	chr2:87816074-87816451	K562	blood:	n/a	n/a
19	ATF1	chr2:87741013-87741231	K562	blood:	n/a	n/a
20	ATF1	chr2:87754798-87755008	K562	blood:	n/a	n/a
21	ATF1	chr2:87842104-87842488	K562	blood:	n/a	n/a
22	ATF1	chr2:87568829-87569093	K562	blood:	n/a	n/a
23	ATF1	chr2:87903372-87903674	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	chr2:87903447-87903666	K562	blood:	n/a	n/a
27	ATF3	chr2:87623739-87624043	A549	lung:	n/a	n/a
28	BACH1	chr2:87754799-87755006	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr2:87770563-87770872	K562	blood:	n/a	n/a
30	BACH1	chr2:87928999-87929447	K562	blood:	n/a	chr2:87929136-87929150
31	BACH1	chr2:87623757-87624094	K562	blood:	n/a	n/a
32	BACH1	chr2:87776227-87776422	K562	blood:	n/a	n/a
33	BACH1	chr2:87929012-87929445	H1-hESC	embryonic stem cell:	n/a	chr2:87929136-87929150
34	BATF	chr2:87932990-87933349	GM12878	blood:	n/a	chr2:87933156-87933167
35	BATF	chr2:88007875-88008242	GM12878	blood:	n/a	n/a
36	BATF	chr2:87742715-87743134	GM12878	blood:	n/a	n/a
37	BATF	chr2:87542193-87542874	GM12878	blood:	n/a	chr2:87542575-87542584
38	BATF	chr2:87848639-87849000	GM12878	blood:	n/a	chr2:87848684-87848694 chr2:87848797-87848808
39	BATF	chr2:87881609-87882132	GM12878	blood:	n/a	n/a
40	BATF	chr2:87785382-87785856	GM12878	blood:	n/a	n/a
41	BATF	chr2:87818560-87818998	GM12878	blood:	n/a	n/a
42	BATF	chr2:87818678-87818940	GM12878	blood:	n/a	n/a
43	BATF	chr2:87563390-87563701	GM12878	blood:	n/a	chr2:87563473-87563482 chr2:87563509-87563520
44	BATF	chr2:87786154-87786403	GM12878	blood:	n/a	n/a
45	BATF	chr2:87797541-87798534	GM12878	blood:	n/a	n/a
46	BATF	chr2:87444879-87445258	GM12878	blood:	n/a	n/a
47	BATF	chr2:87378985-87379249	GM12878	blood:	n/a	n/a
48	BATF	chr2:87749138-87749403	GM12878	blood:	n/a	n/a
49	BATF	chr2:87355904-87356145	GM12878	blood:	n/a	n/a
50	BATF	chr2:87560310-87560572	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	chr2:87420273-87420323	AG04450	lung:	fetal
2	chr2:87576399-87576449	PFSK-1	brain:	n/a
3	chr2:87420273-87420323	AG04450	lung:	fetal
4	chr2:87576399-87576449	PFSK-1	brain:	n/a
5	chr2:87420273-87420323	HEK293	kidney:	embryo
6	chr2:87755371-87755421	GM19239	blood:	n/a
7	chr2:87755371-87755421	HCM	heart:	n/a
8	chr2:87572542-87572592	SAEC	small airway:	n/a
9	chr2:87883547-87883597	HRPEpiC	eye:	n/a
10	chr2:87569447-87569497	HAEpiC	amniotic membrane:	n/a
11	chr2:87883497-87883547	T-47D	breast:	n/a
12	chr2:87569275-87569325	NHBE	bronchial:	n/a
13	chr2:87568958-87569008	AG10803	skin:	n/a
14	chr2:87445161-87445211	HRPEpiC	eye:	n/a
15	chr2:87420273-87420323	PFSK-1	brain:	n/a
16	chr2:87755371-87755421	AG10803	skin:	n/a
17	chr2:87576399-87576449	ECC-1	luminal epithelium:	n/a
18	chr2:87883497-87883547	GM12892	blood:	n/a
19	chr2:87569447-87569497	SK-N-SH	brain:	n/a
20	chr2:87568958-87569008	BJ	skin:	n/a
21	chr2:87576370-87576420	T-47D	breast:	n/a
22	chr2:87569447-87569497	BE2_C	brain:	n/a
23	chr2:87420273-87420323	HCPEpiC	choroid plexus:	n/a
24	chr2:87566763-87566813	NH-A	brain:	n/a
25	chr2:87569142-87569192	HMEC	breast:	n/a
26	chr2:87566763-87566813	Jurkat	blood:	n/a
27	chr2:87569447-87569497	GM12878	blood:	n/a
28	chr2:87566763-87566813	PANC-1	pancreas:	n/a
29	chr2:87445161-87445211	NH-A	brain:	n/a
30	chr2:87445161-87445211	SK-N-SH_RA	brain:	n/a
31	chr2:87420273-87420323	Caco-2	colon:	n/a
32	chr2:87883497-87883547	NH-A	brain:	n/a
33	chr2:87568958-87569008	GM19239	blood:	n/a
34	chr2:87576399-87576449	GM06990	blood:	n/a
35	chr2:87883497-87883547	HEEpiC	esophagus:	n/a
36	chr2:87445161-87445211	ProgFib	skin:	n/a
37	chr2:87572542-87572592	U87	brain:	n/a
38	chr2:87576399-87576449	HIPEpiC	eye:	n/a
39	chr2:87755371-87755421	A549	lung:	n/a
40	chr2:87755371-87755421	SAEC	small airway:	n/a
41	chr2:87883547-87883597	GM06990	blood:	n/a
42	chr2:87572542-87572592	SK-N-MC	brain:	n/a
43	chr2:87569275-87569325	A549	lung:	n/a
44	chr2:87575991-87576041	CMK	blood:	n/a
45	chr2:87575991-87576041	A549	lung:	n/a
46	chr2:87572542-87572592	AG04449	skin:	fetal
47	chr2:87576399-87576449	SK-N-MC	brain:	n/a
48	chr2:87568958-87569008	Hela-S3	cervix:	n/a
49	chr2:87566763-87566813	HPAEpiC	pulmonary alveolar:	n/a
50	chr2:87569275-87569325	T-47D	breast:	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	chr2:87813553..87816546-chr2:111876759..111878642,2	MCF-7	breast:
3	chr2:87472406..87474648-chr2:112477037..112478664,2	MCF-7	breast:
4	chr1:149222733..149224997-chr2:87623931..87625447,2	K562	blood:
5	chr2:87444854..87445468-chr2:112505392..112505911,4	MCF-7	breast:
6	chr2:87431267..87434250-chr2:112516766..112518517,2	MCF-7	breast:

(count:52 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072150
2	lnc-PLGLB2-1	chr2:87820726-87821030	NR_024206
3	lnc-PLGLB1-3	chr2:87405044-87405069	l_1879_chr2:87403978-87405069_thyroid
4	lnc-PLGLB2-1	chr2:87779742-87780126	ENSG00000222041
5	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
6	lnc-PLGLB2-1	chr2:87769669-87769823	ENSG00000222041
7	lnc-PLGLB2-1	chr2:87772259-87772404	NONHSAT072145
8	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072146
9	lnc-PLGLB2-1	chr2:87769669-87769823	ENSG00000222041
10	lnc-PLGLB1-5	chr2:87520158-87520527	l_1881_chr2:87520157-87539624_76bGuttman_hLF
11	lnc-PLGLB2-1	chr2:87779742-87779942	ENSG00000222041
12	lnc-PLGLB2-1	chr2:87755094-87755164	NONHSAT072150
13	lnc-SMYD1-1	chr2:88047115-88047354	XLOC_001560
14	lnc-PLGLB2-1	chr2:87754974-87755164	NONHSAT072145
15	lnc-PLGLB2-1	chr2:87779742-87779942	NONHSAT072146
16	lnc-PLGLB1-5	chr2:87539491-87539624	l_1881_chr2:87520157-87539624_76bGuttman_hLF
17	lnc-PLGLB1-7	chr2:87607003-87607890	NONHSAT072141
18	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
19	lnc-RGPD2-2	chr2:87829755-87831343	NONHSAT072154
20	lnc-RGPD2-1	chr2:87865347-87866283	NONHSAT072155
21	lnc-PLGLB2-1	chr2:87769669-87769823	NONHSAT072150
22	lnc-PLGLB2-1	chr2:87882777-87883000	ENSG00000222041.6
23	lnc-PLGLB1-4	chr2:87448236-87449611	NONHSAT072131
24	lnc-PLGLB2-1	chr2:87880503-87880765	ENSG00000222041.6
25	lnc-PLGLB2-3	chr2:88038283-88038784	NONHSAT072160
26	lnc-PLGLB2-1	chr2:87755061-87755164	ENSG00000222041
27	lnc-PLGLB2-1	chr2:87772259-87772404	ENSG00000222041
28	lnc-PLGLB2-1	chr2:87820726-87821037	ENSG00000222041
29	lnc-PLGLB1-3	chr2:87403979-87404208	l_1879_chr2:87403978-87405069_thyroid
30	lnc-PLGLB2-1	chr2:87755015-87755164	ENSG00000222041
31	lnc-RGPD1-4	chr2:87596356-87596632	NONHSAT072140
32	lnc-PLGLB2-1	chr2:87779742-87779914	NONHSAT072150
33	lnc-PLGLB2-1	chr2:87777641-87777749	NONHSAT072146
34	lnc-PLGLB1-3	chr2:87404223-87404330	l_1879_chr2:87403978-87405069_thyroid
35	lnc-PLGLB2-1	chr2:87772259-87772404	ENSG00000222041
36	lnc-PLGLB2-1	chr2:87882777-87882848	NONHSAT072150
37	lnc-PLGLB2-1	chr2:87777641-87777749	ENSG00000222041
38	lnc-RGPD1-5	chr2:87536124-87536279	ucscGeneNc_uc010fgz_1
39	lnc-PLGLB2-6	chr2:87954409-87954762	NONHSAT072157
40	lnc-PLGLB2-1	chr2:87769469-87769561	ENSG00000222041
41	lnc-PLGLB2-1	chr2:87755024-87755164	ENSG00000222041
42	lnc-PLGLB2-1	chr2:87754974-87755164	NONHSAT072146
43	lnc-PLGLB2-1	chr2:87754998-87755164	ENSG00000222041
44	lnc-RGPD1-2	chr2:87528781-87529374	NONHSAT072132
45	lnc-SMYD1-1	chr2:88045926-88046000	XLOC_001560
46	lnc-RGPD2-3	chr2:87777014-87777553	ENSG00000273445.1
47	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
48	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072145
49	lnc-SMYD1-6	chr2:88050746-88051901	NONHSAT072164
50	lnc-PLGLB2-1	chr2:87754974-87755164	NR_024206

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
ENSG00000234231	TF binding region
IGKV3OR2-268	TF binding region
ENSG00000214354	TF binding region
MIR4771-2	TF binding region
ENSG00000225049	TF binding region
MIR4435-1	TF binding region
PLGLB2	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
ENSG00000234231	CpG island
IGKV3OR2-268	CpG island
ENSG00000214354	CpG island
MIR4771-2	CpG island
ENSG00000225049	CpG island
MIR4435-1	CpG island
PLGLB2	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
ENSG00000153094	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000206737	chromatin interactions
GNA13	miRNA target sites
GLT25D1	miRNA target sites

Extended variants
information (count: 12370 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:12370 , 50 per page) page: 1 2 3 4 5 6 7 ... 248

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549328143	chr2:87330983-87330984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567555744	chr2:87331041-87331042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs202170160	chr2:87331099-87331100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs199650306	chr2:87331108-87331109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78789405	chr2:87331110-87331111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534871440	chr2:87331182-87331183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561100821	chr2:87331342-87331343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571389155	chr2:87331350-87331351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538370096	chr2:87331426-87331427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557002120	chr2:87331505-87331506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574921522	chr2:87331571-87331572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535841223	chr2:87331644-87331645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77908807	chr2:87331686-87331687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573210635	chr2:87331707-87331708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs55662034	chr2:87331735-87331736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540876096	chr2:87331765-87331766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565361474	chr2:87331842-87331843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577335905	chr2:87331885-87331886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544416318	chr2:87331937-87331938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562951299	chr2:87331984-87331985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530155243	chr2:87332003-87332004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548609393	chr2:87332047-87332048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560478339	chr2:87332086-87332087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528415717	chr2:87332108-87332109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376030585	chr2:87332150-87332151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546838314	chr2:87332202-87332203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371386163	chr2:87332435-87332436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371921048	chr2:87332599-87332600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369334460	chr2:87332665-87332666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538804592	chr2:87332692-87332693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550449197	chr2:87332713-87332714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568602162	chr2:87332792-87332793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367685454	chr2:87332980-87332981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535903590	chr2:87332991-87332992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201488396	chr2:87333152-87333153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369388588	chr2:87333153-87333154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192111159	chr2:87333222-87333223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572478792	chr2:87333225-87333226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534241976	chr2:87333233-87333234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559189017	chr2:87333285-87333286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577396626	chr2:87333471-87333472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183365603	chr2:87333490-87333491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563028169	chr2:87333531-87333532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62144429	chr2:87333532-87333533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1116464	chr2:87333607-87333608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142539217	chr2:87333685-87333686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201638700	chr2:87333737-87333738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571529220	chr2:87333816-87333817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527669651	chr2:87333984-87333985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs60846710	chr2:87334042-87334043	Weak transcription	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	23813976	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
Williams Syndrome	20824207	CNVD
Type 1 diabetes	21085585	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:3374 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:87330600-87331000	Weak transcription	Fetal Heart	heart
2	chr2:87331000-87331200	Enhancers	Fetal Heart	heart
3	chr2:87331200-87332000	Weak transcription	Fetal Heart	heart
4	chr2:87332000-87332200	Enhancers	Fetal Heart	heart
5	chr2:87332200-87334200	Weak transcription	Fetal Heart	heart
6	chr2:87333000-87333400	Enhancers	Fetal Lung	lung
7	chr2:87334200-87334400	Enhancers	Fetal Heart	heart
8	chr2:87371800-87372400	Enhancers	Fetal Heart	heart
9	chr2:87373000-87374000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr2:87373600-87374000	Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr2:87373800-87374600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:87374000-87374600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr2:87374600-87374800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr2:87416200-87417000	Enhancers	HUVEC	blood vessel
15	chr2:87418800-87419600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:87425400-87426000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:87431600-87431800	Enhancers	Liver	Liver
18	chr2:87431800-87432200	Flanking Active TSS	Liver	Liver
19	chr2:87447800-87448200	Enhancers	Fetal Heart	heart
20	chr2:87455600-87456400	Enhancers	Fetal Thymus	thymus
21	chr2:87456200-87456800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:87456200-87457000	Enhancers	Rectal Smooth Muscle	rectum
23	chr2:87456200-87457000	Enhancers	Small Intestine	intestine
24	chr2:87456400-87457200	Enhancers	Adipose Nuclei	Adipose
25	chr2:87456600-87457000	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr2:87462000-87462400	Enhancers	Liver	Liver
27	chr2:87462400-87463600	Weak transcription	Liver	Liver
28	chr2:87463600-87463800	Enhancers	Liver	Liver
29	chr2:87464200-87465600	Enhancers	NHEK	skin
30	chr2:87464600-87464800	Enhancers	Hela-S3	cervix
31	chr2:87469400-87469800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:87469400-87469800	Active TSS	Breast Myoepithelial Primary Cells	Breast
33	chr2:87469800-87473200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr2:87473000-87473200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr2:87473200-87473400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:87473200-87473400	Enhancers	Osteobl	bone
37	chr2:87473200-87473600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr2:87473200-87473600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr2:87473200-87473600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr2:87476600-87478200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr2:87477200-87478200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr2:87477400-87478200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr2:87477400-87478200	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr2:87477400-87478200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr2:87477400-87478400	Enhancers	Primary hematopoietic stem cells	blood
46	chr2:87482200-87483000	Enhancers	Primary B cells from peripheral blood	blood
47	chr2:87489600-87489800	Enhancers	HUVEC	blood vessel
48	chr2:87489800-87490000	Enhancers	Right Atrium	heart
49	chr2:87489800-87490800	Weak transcription	HUVEC	blood vessel
50	chr2:87490800-87491200	Enhancers	HUVEC	blood vessel

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