Variant report

Variant	nsv580973
Chromosome Location	chr2:11864946-11898931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2266)
CpG islands
(count:1283)
Chromatin interactive
region (count:48)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2266 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:11885337-11885557	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:11878746-11878837	K562	blood:	n/a	n/a
3	ARID3A	chr2:11875899-11876054	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:11884041-11884638	K562	blood:	n/a	n/a
5	ARID3A	chr2:11886470-11886670	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:11896311-11896484	K562	blood:	n/a	n/a
7	ARID3A	chr2:11884128-11884621	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:11885849-11885951	K562	blood:	n/a	n/a
9	ARID3A	chr2:11893708-11894050	K562	blood:	n/a	n/a
10	ARID3A	chr2:11886593-11886619	K562	blood:	n/a	n/a
11	ATF1	chr2:11884089-11884582	K562	blood:	n/a	n/a
12	ATF1	chr2:11893642-11894295	K562	blood:	n/a	n/a
13	ATF2	chr2:11889831-11890411	GM12878	blood:	n/a	n/a
14	ATF2	chr2:11884038-11884673	GM12878	blood:	n/a	n/a
15	ATF2	chr2:11889745-11891404	GM12878	blood:	n/a	n/a
16	ATF2	chr2:11883996-11884600	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr2:11893357-11894827	GM12878	blood:	n/a	n/a
18	ATF2	chr2:11890416-11891493	GM12878	blood:	n/a	n/a
19	ATF2	chr2:11883995-11884589	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr2:11883900-11884645	GM12878	blood:	n/a	n/a
21	ATF2	chr2:11893373-11894172	GM12878	blood:	n/a	n/a
22	ATF3	chr2:11884155-11884520	K562	blood:	n/a	n/a
23	ATF3	chr2:11883851-11884683	A549	lung:	n/a	n/a
24	ATF3	chr2:11886568-11886953	K562	blood:	n/a	n/a
25	ATF3	chr2:11884071-11884600	K562	blood:	n/a	n/a
26	ATF3	chr2:11883896-11884621	A549	lung:	n/a	n/a
27	BACH1	chr2:11884114-11884607	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr2:11886479-11887426	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr2:11884073-11884566	K562	blood:	n/a	n/a
30	BATF	chr2:11894257-11894698	GM12878	blood:	n/a	n/a
31	BATF	chr2:11884163-11884501	GM12878	blood:	n/a	chr2:11884301-11884312
32	BATF	chr2:11893468-11894141	GM12878	blood:	n/a	n/a
33	BATF	chr2:11893594-11894120	GM12878	blood:	n/a	n/a
34	BATF	chr2:11884063-11884582	GM12878	blood:	n/a	chr2:11884301-11884312
35	BATF	chr2:11889954-11890298	GM12878	blood:	n/a	n/a
36	BCL11A	chr2:11889970-11890340	GM12878	blood:	n/a	n/a
37	BCL11A	chr2:11889931-11890311	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:11893449-11894214	GM12878	blood:	n/a	chr2:11893912-11893921
39	BCL11A	chr2:11894285-11894584	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:11891045-11891457	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:11884071-11884592	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:11893524-11893942	GM12878	blood:	n/a	chr2:11893912-11893921
43	BCL11A	chr2:11894789-11895070	GM12878	blood:	n/a	n/a
44	BCL3	chr2:11882447-11882803	GM12878	blood:	n/a	chr2:11882642-11882651
45	BCL3	chr2:11893491-11893968	GM12878	blood:	n/a	chr2:11893912-11893921
46	BCL3	chr2:11884163-11884463	GM12878	blood:	n/a	n/a
47	BCL3	chr2:11886333-11886874	A549	lung:	n/a	chr2:11886745-11886758 chr2:11886834-11886847
48	BCL3	chr2:11883899-11885397	A549	lung:	n/a	n/a
49	BCL3	chr2:11883942-11884601	GM12878	blood:	n/a	n/a
50	BCL3	chr2:11883883-11884682	A549	lung:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:11886589-11886639	HepG2	liver:	n/a
2	chr2:11885266-11885316	T-47D	breast:	n/a
3	chr2:11886589-11886639	HepG2	liver:	n/a
4	chr2:11885266-11885316	T-47D	breast:	n/a
5	chr2:11867801-11867851	NHDF-neo	bronchial:	n/a
6	chr2:11885266-11885316	ProgFib	skin:	n/a
7	chr2:11890700-11890750	AG10803	skin:	n/a
8	chr2:11888753-11888803	Hela-S3	cervix:	n/a
9	chr2:11878864-11878914	GM12891	blood:	n/a
10	chr2:11886400-11886450	NH-A	brain:	n/a
11	chr2:11881420-11881470	SK-N-MC	brain:	n/a
12	chr2:11881225-11881275	LNCaP	prostate:	n/a
13	chr2:11881462-11881512	SKMC	muscle:	n/a
14	chr2:11887120-11887170	GM12891	blood:	n/a
15	chr2:11888753-11888803	AG09319	gingival:	n/a
16	chr2:11881338-11881388	T-47D	breast:	n/a
17	chr2:11886253-11886303	GM12891	blood:	n/a
18	chr2:11885560-11885610	HepG2	liver:	n/a
19	chr2:11881338-11881388	PANC-1	pancreas:	n/a
20	chr2:11878864-11878914	U87	brain:	n/a
21	chr2:11883947-11883997	HNPCEpiC	eye:	n/a
22	chr2:11883947-11883997	ECC-1	luminal epithelium:	n/a
23	chr2:11867801-11867851	HCF	heart:	n/a
24	chr2:11885266-11885316	SK-N-SH_RA	brain:	n/a
25	chr2:11886589-11886639	HCM	heart:	n/a
26	chr2:11890700-11890750	A549	lung:	n/a
27	chr2:11886253-11886303	HepG2	liver:	n/a
28	chr2:11885321-11885371	GM12892	blood:	n/a
29	chr2:11887322-11887372	HEK293	kidney:	embryo
30	chr2:11890700-11890750	H1-hESC	embryonic stem cell:	embryo
31	chr2:11881225-11881275	SAEC	small airway:	n/a
32	chr2:11894464-11894514	AG04450	lung:	fetal
33	chr2:11884333-11884383	GM12878	blood:	n/a
34	chr2:11887322-11887372	MCF-7	breast:	n/a
35	chr2:11878864-11878914	HCT-116	colon:	n/a
36	chr2:11878864-11878914	SKMC	muscle:	n/a
37	chr2:11887322-11887372	HCPEpiC	choroid plexus:	n/a
38	chr2:11887120-11887170	AG04449	skin:	fetal
39	chr2:11890700-11890750	HL-60	blood:	n/a
40	chr2:11886253-11886303	NB4	blood:	n/a
41	chr2:11881420-11881470	HMEC	breast:	n/a
42	chr2:11885560-11885610	HEEpiC	esophagus:	n/a
43	chr2:11886400-11886450	ECC-1	luminal epithelium:	n/a
44	chr2:11888753-11888803	HCPEpiC	choroid plexus:	n/a
45	chr2:11885266-11885316	CMK	blood:	n/a
46	chr2:11883947-11883997	Hela-S3	cervix:	n/a
47	chr2:11878864-11878914	A549	lung:	n/a
48	chr2:11887120-11887170	SK-N-MC	brain:	n/a
49	chr2:11881462-11881512	PFSK-1	brain:	n/a
50	chr2:11885266-11885316	GM06990	blood:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:11885383..11891655-chr2:11894666..11900002,13	K562	blood:
2	chr2:11881178..11885762-chr2:11886043..11889477,7	MCF-7	breast:
3	chr2:11894229..11895862-chr2:11899704..11901384,2	K562	blood:
4	chr2:11875528..11877148-chr2:11877418..11878938,2	MCF-7	breast:
5	chr2:11604833..11608003-chr2:11882353..11886330,4	K562	blood:
6	chr2:11864143..11867018-chr2:11871062..11872663,2	K562	blood:
7	chr2:11893238..11895926-chr2:11901659..11904630,2	MCF-7	breast:
8	chr2:11869912..11872464-chr2:11874565..11877057,2	K562	blood:
9	chr2:11885343..11888558-chr2:11916972..11921085,4	K562	blood:
10	chr2:11892034..11894418-chr2:11895630..11897983,2	K562	blood:
11	chr2:11886833..11889158-chr2:11909295..11910808,2	K562	blood:
12	chr2:11864844..11866571-chr2:11873207..11875042,2	K562	blood:
13	chr2:11827642..11829503-chr2:11889193..11891335,2	MCF-7	breast:
14	chr2:11882438..11884776-chr2:11910789..11914613,4	K562	blood:
15	chr2:11870195..11872088-chr2:11885962..11887641,2	MCF-7	breast:
16	chr2:11872902..11874772-chr2:11878776..11881694,2	K562	blood:
17	chr2:11864844..11866571-chr2:11873207..11875042,2	K562	blood:
18	chr2:11892034..11894418-chr2:11895630..11897983,2	K562	blood:
19	chr2:11882508..11884186-chr2:11887506..11889026,2	MCF-7	breast:
20	chr2:11886726..11888240-chr2:11889703..11892013,2	MCF-7	breast:
21	chr2:11867421..11869594-chr2:11885775..11887572,2	MCF-7	breast:
22	chr2:11876175..11878551-chr2:11884561..11886899,2	K562	blood:
23	chr2:11798417..11800277-chr2:11891878..11893871,2	K562	blood:
24	chr2:11872488..11875860-chr2:11884452..11886628,3	K562	blood:
25	chr2:11872902..11874772-chr2:11878776..11881694,2	K562	blood:
26	chr2:10259345..10261058-chr2:11886635..11888299,2	K562	blood:
27	chr2:11882616..11883484-chr2:11891634..11892366,2	K562	blood:
28	chr2:11882411..11885202-chr2:11902345..11904670,2	K562	blood:
29	chr2:11859887..11861729-chr2:11865073..11867523,2	K562	blood:
30	chr2:11886095..11889149-chr2:11892372..11895802,5	MCF-7	breast:
31	chr2:11883702..11885372-chr2:11901343..11903845,2	K562	blood:
32	chr2:11850515..11852161-chr2:11877592..11880491,2	MCF-7	breast:
33	chr2:11878641..11879395-chr2:11919018..11919604,3	K562	blood:
34	chr2:11875528..11877148-chr2:11877418..11878938,2	MCF-7	breast:
35	chr2:11881178..11885762-chr2:11886043..11889477,7	MCF-7	breast:
36	chr2:11869912..11872464-chr2:11874565..11877057,2	K562	blood:
37	chr2:11882508..11884186-chr2:11887506..11889026,2	MCF-7	breast:
38	chr2:11872902..11875689-chr2:11878776..11880592,2	K562	blood:
39	chr2:11878418..11879254-chr2:11919121..11919879,2	MCF-7	breast:
40	chr2:11878332..11879441-chr2:11918884..11919993,17	MCF-7	breast:
41	chr10:32078085..32079585-chr2:11880425..11883011,2	MCF-7	breast:
42	chr2:11678361..11681033-chr2:11884649..11887386,2	MCF-7	breast:
43	chr2:11887777..11889810-chr2:11903193..11905347,2	K562	blood:
44	chr2:11872902..11875689-chr2:11878776..11880592,2	K562	blood:
45	chr2:11890007..11892295-chr2:11917973..11920590,2	K562	blood:
46	chr2:11604255..11606398-chr2:11886112..11888104,2	K562	blood:
47	chr2:11882616..11883484-chr2:11891634..11892366,2	K562	blood:
48	chr2:11879500..11881190-chr2:11886379..11888798,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GREB1-9	chr2:11886087-11886256	NONHSAT069191
2	lnc-GREB1-9	chr2:11881475-11881554	NONHSAT069192
3	lnc-GREB1-9	chr2:11881475-11881554	NONHSAT069191
4	lnc-NTSR2-2	chr2:11882163-11882282	ENSG00000230790.2
5	lnc-NTSR2-2	chr2:11881123-11881428	ENSG00000230790.2
6	lnc-GREB1-9	chr2:11886033-11886256	NONHSAT069192
7	lnc-NTSR2-2	chr2:11885293-11885427	ENSG00000230790.2

No data

Variant related genes	Relation type
ENSG00000203643	TF binding region
ENSG00000230790	TF binding region
LPIN1	TF binding region
ENSG00000203643	CpG island
ENSG00000230790	CpG island
LPIN1	CpG island
ENSG00000272524	chromatin interactions
ENSG00000169016	chromatin interactions
ENSG00000264010	chromatin interactions
ENSG00000196208	chromatin interactions
ENSG00000230790	chromatin interactions
ENSG00000134324	chromatin interactions
ENSG00000203643	chromatin interactions

Extended variants
information (count: 1361 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1361 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13421506	chr2:11864946-11864947	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576457583	chr2:11864949-11864950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143067368	chr2:11864950-11864951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550834958	chr2:11864957-11864958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530284150	chr2:11864958-11864959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181169585	chr2:11865033-11865034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75522670	chr2:11865052-11865053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11895321	chr2:11865066-11865067	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs11889810	chr2:11865074-11865075	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs552864940	chr2:11865102-11865103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546582593	chr2:11865115-11865116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570845450	chr2:11865117-11865118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538260607	chr2:11865121-11865122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116731399	chr2:11865127-11865128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200130784	chr2:11865134-11865135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374948317	chr2:11865135-11865136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368782363	chr2:11865145-11865146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11900114	chr2:11865154-11865155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374325390	chr2:11865159-11865160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148552970	chr2:11865162-11865163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555245127	chr2:11865163-11865164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533822425	chr2:11865169-11865170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10929770	chr2:11865170-11865171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576393740	chr2:11865183-11865184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576543604	chr2:11865184-11865185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs386643238	chr2:11865193-11865194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7580971	chr2:11865194-11865195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532555645	chr2:11865204-11865205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144015240	chr2:11865211-11865212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369473782	chr2:11865215-11865216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111878777	chr2:11865218-11865219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560502315	chr2:11865243-11865244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565187819	chr2:11865247-11865248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552872599	chr2:11865251-11865252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368115738	chr2:11865259-11865260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373491195	chr2:11865260-11865261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564793576	chr2:11865304-11865305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531692862	chr2:11865305-11865306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550209897	chr2:11865307-11865308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139868729	chr2:11865312-11865313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530578289	chr2:11865365-11865366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547898608	chr2:11865366-11865367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550351976	chr2:11865374-11865375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144693584	chr2:11865385-11865386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573696989	chr2:11865386-11865387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550383311	chr2:11865406-11865407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369704064	chr2:11865410-11865411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs59510408	chr2:11865413-11865414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566533769	chr2:11865446-11865447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534120329	chr2:11865506-11865507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Medulloblastoma	20607354	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11861200-11866200	Weak transcription	Right Atrium	heart
2	chr2:11863400-11866800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr2:11863600-11865800	Weak transcription	Liver	Liver
4	chr2:11864400-11867400	Enhancers	Fetal Brain Male	brain
5	chr2:11865600-11867400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr2:11865800-11866200	Bivalent Enhancer	Fetal Stomach	stomach
7	chr2:11865800-11867400	Enhancers	Liver	Liver
8	chr2:11866000-11866600	Enhancers	Placenta	Placenta
9	chr2:11866000-11866800	Enhancers	Fetal Muscle Trunk	muscle
10	chr2:11866000-11867000	Bivalent Enhancer	K562	blood
11	chr2:11866000-11867200	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr2:11866000-11867200	Enhancers	Fetal Brain Female	brain
13	chr2:11866000-11867200	Enhancers	Fetal Lung	lung
14	chr2:11866200-11866600	Enhancers	Right Atrium	heart
15	chr2:11866200-11866800	Enhancers	Fetal Stomach	stomach
16	chr2:11866200-11867200	Enhancers	Fetal Heart	heart
17	chr2:11866400-11866800	Bivalent Enhancer	Fetal Muscle Leg	muscle
18	chr2:11866400-11867200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr2:11866400-11867200	Enhancers	Rectal Smooth Muscle	rectum
20	chr2:11866600-11866800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:11866600-11866800	Weak transcription	Right Atrium	heart
22	chr2:11866800-11867200	Enhancers	Right Atrium	heart
23	chr2:11866800-11867400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr2:11866800-11867400	Enhancers	Colon Smooth Muscle	Colon
25	chr2:11866800-11867600	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr2:11867000-11867200	Enhancers	Right Ventricle	heart
27	chr2:11867000-11867200	Flanking Bivalent TSS/Enh	K562	blood
28	chr2:11867000-11867400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr2:11867000-11867600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:11869600-11869800	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr2:11869600-11870400	Enhancers	Dnd41	blood
32	chr2:11869800-11870400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr2:11870400-11870600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr2:11874000-11874400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:11874200-11874800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr2:11874200-11874800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr2:11874400-11874800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:11874400-11875000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr2:11874400-11876400	Enhancers	Fetal Intestine Large	intestine
40	chr2:11874800-11875200	Enhancers	H1 Cell Line	embryonic stem cell
41	chr2:11874800-11878800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr2:11875000-11878800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr2:11875200-11883000	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr2:11875600-11876000	Enhancers	Fetal Intestine Small	intestine
45	chr2:11875600-11876400	Enhancers	HepG2	liver
46	chr2:11875800-11876000	Enhancers	Colonic Mucosa	Colon
47	chr2:11875800-11876000	Enhancers	Hela-S3	cervix
48	chr2:11875800-11877000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:11876000-11876200	Enhancers	Fetal Thymus	thymus
50	chr2:11876000-11876800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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