Variant report

Variant	nsv832173
Chromosome Location	chr11:59788884-59940560
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1029)
CpG islands
(count:1650)
Chromatin interactive
region (count:46)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:59888692-59888945	K562	blood:	n/a	n/a
2	ARID3A	chr11:59884218-59884222	K562	blood:	n/a	n/a
3	ARID3A	chr11:59865771-59866375	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:59892317-59892493	K562	blood:	n/a	n/a
5	ARID3A	chr11:59824079-59824209	K562	blood:	n/a	n/a
6	ARID3A	chr11:59879254-59879456	K562	blood:	n/a	n/a
7	ARID3A	chr11:59893449-59893832	HepG2	liver:	n/a	n/a
8	ATF1	chr11:59894706-59895192	K562	blood:	n/a	n/a
9	ATF1	chr11:59898038-59898339	K562	blood:	n/a	n/a
10	ATF1	chr11:59888743-59889069	K562	blood:	n/a	n/a
11	ATF1	chr11:59823710-59824276	K562	blood:	n/a	n/a
12	ATF1	chr11:59846322-59846529	K562	blood:	n/a	n/a
13	ATF1	chr11:59826690-59826742	K562	blood:	n/a	n/a
14	ATF1	chr11:59853455-59853752	K562	blood:	n/a	n/a
15	ATF3	chr11:59826579-59826826	K562	blood:	n/a	n/a
16	ATF3	chr11:59894590-59895127	K562	blood:	n/a	n/a
17	BACH1	chr11:59894643-59895021	K562	blood:	n/a	n/a
18	BATF	chr11:59826577-59826779	GM12878	blood:	n/a	chr11:59826708-59826719
19	BATF	chr11:59933083-59933319	GM12878	blood:	n/a	chr11:59933195-59933206 chr11:59933200-59933210 chr11:59933196-59933206
20	BATF	chr11:59933032-59933326	GM12878	blood:	n/a	chr11:59933195-59933206 chr11:59933200-59933210 chr11:59933196-59933206
21	BATF	chr11:59935878-59936155	GM12878	blood:	n/a	chr11:59936013-59936024
22	BATF	chr11:59826600-59826779	GM12878	blood:	n/a	chr11:59826708-59826719
23	BATF	chr11:59932241-59932528	GM12878	blood:	n/a	n/a
24	BCL11A	chr11:59917814-59918037	GM12878	blood:	n/a	n/a
25	BHLHE40	chr11:59823862-59824208	K562	blood:	n/a	n/a
26	BHLHE40	chr11:59853433-59853683	K562	blood:	n/a	n/a
27	BHLHE40	chr11:59866021-59866303	HepG2	liver:	n/a	n/a
28	BHLHE40	chr11:59865984-59866313	HepG2	liver:	n/a	n/a
29	BRCA1	chr11:59936747-59937294	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr11:59936531-59937429	K562	blood:	n/a	n/a
31	CBX3	chr11:59901369-59901788	K562	blood:	n/a	n/a
32	CBX3	chr11:59901428-59901731	K562	blood:	n/a	n/a
33	CBX3	chr11:59894599-59895234	K562	blood:	n/a	n/a
34	CBX3	chr11:59847993-59848492	K562	blood:	n/a	n/a
35	CBX3	chr11:59936709-59937256	HCT-116	colon:	n/a	n/a
36	CBX3	chr11:59845690-59846028	K562	blood:	n/a	n/a
37	CBX3	chr11:59844885-59845212	K562	blood:	n/a	n/a
38	CBX3	chr11:59844751-59845266	K562	blood:	n/a	n/a
39	CBX3	chr11:59936750-59937326	K562	blood:	n/a	n/a
40	CBX3	chr11:59932030-59932403	K562	blood:	n/a	n/a
41	CBX3	chr11:59823690-59824234	K562	blood:	n/a	n/a
42	CBX3	chr11:59936668-59937147	HCT-116	colon:	n/a	n/a
43	CBX3	chr11:59888658-59889080	K562	blood:	n/a	n/a
44	CBX3	chr11:59839123-59839432	K562	blood:	n/a	n/a
45	CBX3	chr11:59898047-59898328	HCT-116	colon:	n/a	n/a
46	CCNT2	chr11:59868085-59868279	K562	blood:	n/a	n/a
47	CCNT2	chr11:59823710-59824208	K562	blood:	n/a	n/a
48	CCNT2	chr11:59853478-59853769	K562	blood:	n/a	chr11:59853577-59853597
49	CEBPB	chr11:59792604-59792816	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:59853497-59853883	K562	blood:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59823993-59824043	HEK293	kidney:	embryo
2	chr11:59815177-59815227	PFSK-1	brain:	n/a
3	chr11:59806898-59806948	GM12878	blood:	n/a
4	chr11:59823993-59824043	HEK293	kidney:	embryo
5	chr11:59815177-59815227	PFSK-1	brain:	n/a
6	chr11:59806898-59806948	GM12878	blood:	n/a
7	chr11:59861219-59861269	HCPEpiC	choroid plexus:	n/a
8	chr11:59806898-59806948	NHBE	bronchial:	n/a
9	chr11:59807164-59807214	RPTEC	kidney:	n/a
10	chr11:59824116-59824166	ECC-1	luminal epithelium:	n/a
11	chr11:59807181-59807231	GM12891	blood:	n/a
12	chr11:59824110-59824160	AoSMC	blood vessel:	n/a
13	chr11:59824110-59824160	HCPEpiC	choroid plexus:	n/a
14	chr11:59841011-59841061	NHDF-neo	bronchial:	n/a
15	chr11:59824038-59824088	SK-N-SH_RA	brain:	n/a
16	chr11:59855616-59855666	HL-60	blood:	n/a
17	chr11:59856225-59856275	GM12878	blood:	n/a
18	chr11:59838540-59838590	GM06990	blood:	n/a
19	chr11:59824161-59824211	SK-N-SH_RA	brain:	n/a
20	chr11:59823993-59824043	NHBE	bronchial:	n/a
21	chr11:59855616-59855666	K562	blood:	n/a
22	chr11:59824110-59824160	HAEpiC	amniotic membrane:	n/a
23	chr11:59807594-59807644	HNPCEpiC	eye:	n/a
24	chr11:59940485-59940535	HL-60	blood:	n/a
25	chr11:59823993-59824043	Hela-S3	cervix:	n/a
26	chr11:59824110-59824160	HMEC	breast:	n/a
27	chr11:59807181-59807231	AG04449	skin:	fetal
28	chr11:59807594-59807644	HepG2	liver:	n/a
29	chr11:59824110-59824160	PANC-1	pancreas:	n/a
30	chr11:59823993-59824043	GM19239	blood:	n/a
31	chr11:59808049-59808099	HCPEpiC	choroid plexus:	n/a
32	chr11:59838540-59838590	HUVEC	blood vessel:	n/a
33	chr11:59855616-59855666	RPTEC	kidney:	n/a
34	chr11:59864308-59864358	AG09319	gingival:	n/a
35	chr11:59822727-59822777	PANC-1	pancreas:	n/a
36	chr11:59856358-59856408	AG09309	skin:	n/a
37	chr11:59807830-59807880	AG04450	lung:	fetal
38	chr11:59824038-59824088	A549	lung:	n/a
39	chr11:59824541-59824591	ProgFib	skin:	n/a
40	chr11:59824161-59824211	SK-N-SH	brain:	n/a
41	chr11:59815177-59815227	ECC-1	luminal epithelium:	n/a
42	chr11:59836817-59836867	K562	blood:	n/a
43	chr11:59811802-59811852	CMK	blood:	n/a
44	chr11:59824541-59824591	NT2-D1	testis:	n/a
45	chr11:59823993-59824043	MCF-7	breast:	n/a
46	chr11:59841011-59841061	GM12878	blood:	n/a
47	chr11:59841011-59841061	BE2_C	brain:	n/a
48	chr11:59861219-59861269	HRPEpiC	eye:	n/a
49	chr11:59824541-59824591	HCM	heart:	n/a
50	chr11:59807594-59807644	AG10803	skin:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:59838090..59840392-chr11:59840842..59843824,3	K562	blood:
2	chr11:59886056..59888504-chr11:59892263..59894071,2	K562	blood:
3	chr11:59838090..59840392-chr11:59840842..59843824,3	K562	blood:
4	chr11:59899268..59901225-chr11:59929250..59931810,2	K562	blood:
5	chr11:59857259..59859045-chr11:59866895..59868589,2	K562	blood:
6	chr11:59803531..59806483-chr11:59810026..59812914,2	K562	blood:
7	chr11:59590238..59591135-chr11:59897588..59898633,5	MCF-7	breast:
8	chr11:59878766..59880591-chr11:59882568..59884421,2	K562	blood:
9	chr11:59803708..59805688-chr11:59908661..59910786,2	K562	blood:
10	chr11:59835891..59838239-chr11:59840750..59843127,2	K562	blood:
11	chr11:59855869..59858182-chr11:59858719..59861212,2	K562	blood:
12	chr11:59880513..59883091-chr11:59889484..59891627,2	MCF-7	breast:
13	chr11:59936023..59937006-chr11:59960779..59961684,2	MCF-7	breast:
14	chr11:59929729..59931318-chr11:59936371..59938548,3	K562	blood:
15	chr11:59885540..59886539-chr11:59960885..59961593,3	MCF-7	breast:
16	chr11:59822049..59824288-chr11:59826581..59828945,2	K562	blood:
17	chr11:59929729..59931318-chr11:59936371..59938548,3	K562	blood:
18	chr11:59847145..59850103-chr11:59877853..59879913,2	K562	blood:
19	chr11:59905623..59908151-chr11:59911648..59914024,2	K562	blood:
20	chr11:59524342..59526503-chr11:59895914..59898117,2	K562	blood:
21	chr11:59803531..59806483-chr11:59810026..59812914,2	K562	blood:
22	chr11:59926779..59928855-chr11:59938111..59940679,2	K562	blood:
23	chr11:59857259..59859045-chr11:59866895..59868589,2	K562	blood:
24	chr11:59889345..59891976-chr11:59896394..59897980,2	K562	blood:
25	chr11:59877470..59879979-chr11:59886517..59889179,2	K562	blood:
26	chr11:59926973..59929170-chr11:59934444..59937067,2	K562	blood:
27	chr11:59880513..59883091-chr11:59889484..59891627,2	MCF-7	breast:
28	chr11:59909863..59911734-chr11:59915341..59917142,2	K562	blood:
29	chr11:59589954..59591189-chr11:59897601..59898679,5	K562	blood:
30	chr11:59915996..59916912-chr11:59960707..59961353,2	K562	blood:
31	chr11:59803531..59806711-chr11:59810026..59813268,3	K562	blood:
32	chr11:59877470..59879979-chr11:59886517..59889179,2	K562	blood:
33	chr11:59847145..59850103-chr11:59877853..59879913,2	K562	blood:
34	chr11:59909863..59911734-chr11:59915341..59917142,2	K562	blood:
35	chr11:59886056..59888504-chr11:59892263..59894071,2	K562	blood:
36	chr11:59878766..59880591-chr11:59882568..59884421,2	K562	blood:
37	chr11:59834202..59837077-chr11:59837940..59839542,2	K562	blood:
38	chr11:59899268..59901225-chr11:59929250..59931810,2	K562	blood:
39	chr11:59795306..59797017-chr11:59801858..59803491,2	K562	blood:
40	chr11:59803531..59806711-chr11:59810026..59813268,3	K562	blood:
41	chr11:59521183..59522129-chr11:59897665..59898553,3	K562	blood:
42	chr11:59889345..59891976-chr11:59896394..59897980,2	K562	blood:
43	chr11:59795306..59797017-chr11:59801858..59803491,2	K562	blood:
44	chr11:59822049..59824288-chr11:59826581..59828945,2	K562	blood:
45	chr11:59803708..59805688-chr11:59908661..59910786,2	K562	blood:
46	chr11:59905623..59908151-chr11:59911648..59914024,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLAC1L-1	chr11:59792381-59792478	ENSG00000255393
2	lnc-MS4A3-2	chr11:59860874-59861031	NONHSAT021558
3	lnc-PLAC1L-2	chr11:59828963-59828971	NONHSAT021555
4	lnc-PLAC1L-1	chr11:59798275-59798550	ENSG00000255393
5	lnc-MS4A3-1	chr11:59807933-59807996	NONHSAT021554
6	lnc-MS4A6A-1	chr11:59928198-59928295	ENSG00000254952
7	lnc-MS4A3-2	chr11:59857834-59857943	NONHSAT021558
8	lnc-PLAC1L-1	chr11:59797255-59797402	ENSG00000255393
9	lnc-MS4A3-1	chr11:59810942-59811206	NONHSAT021554
10	lnc-MS4A2-1	chr11:59837004-59837148	NONHSAT021556
11	lnc-PLAC1L-2	chr11:59828405-59828789	NONHSAT021555
12	lnc-MS4A6A-1	chr11:59927160-59927342	ENSG00000254952
13	lnc-MS4A3-2	chr11:59860266-59860321	NONHSAT021558
14	lnc-MS4A3-2	chr11:59863032-59863060	NONHSAT021558
15	lnc-MS4A3-2	chr11:59861438-59861535	NONHSAT021558
16	lnc-MS4A2-1	chr11:59837677-59838454	NONHSAT021556
17	lnc-MS4A6A-1	chr11:59927752-59927855	ENSG00000254952

No data

Variant related genes	Relation type
MS4A2	TF binding region
ENSG00000255393	TF binding region
MS4A3	TF binding region
ENSG00000254952	TF binding region
ENSG00000255331	TF binding region
OOSP2	TF binding region
MS4A2	CpG island
ENSG00000255393	CpG island
MS4A3	CpG island
ENSG00000254952	CpG island
ENSG00000255331	CpG island
OOSP2	CpG island
ENSG00000149534	chromatin interactions
ENSG00000254952	chromatin interactions
ENSG00000149516	chromatin interactions
SENP1	miRNA target sites
PDCD4	miRNA target sites
CCNB1	miRNA target sites
REV3L	miRNA target sites

Extended variants
information (count: 4812 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4812 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181104138	chr11:59789637-59789638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146824117	chr11:59789719-59789720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185890213	chr11:59789731-59789732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559563547	chr11:59789737-59789738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140626219	chr11:59789750-59789751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190569892	chr11:59789756-59789757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75123977	chr11:59789780-59789781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs74662226	chr11:59789795-59789796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142780743	chr11:59789799-59789800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570801955	chr11:59789819-59789820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371279112	chr11:59789820-59789821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528408883	chr11:59789837-59789838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546373684	chr11:59789900-59789901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183131238	chr11:59789906-59789907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569443791	chr11:59789936-59789937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187590737	chr11:59789940-59789941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201414307	chr11:59789944-59789945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148262921	chr11:59789945-59789946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369675058	chr11:59789946-59789947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151047603	chr11:59789964-59789965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530330303	chr11:59789988-59789989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113637952	chr11:59789994-59789995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147981842	chr11:59792396-59792397	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs560285775	chr11:59792445-59792446	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs480569	chr11:59797261-59797262	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs187115145	chr11:59797340-59797341	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs190789865	chr11:59797342-59797343	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs564449220	chr11:59797369-59797370	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs144603206	chr11:59798275-59798276	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs557564327	chr11:59798281-59798282	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs1144744	chr11:59798348-59798349	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs147886812	chr11:59798394-59798395	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs192874894	chr11:59798446-59798447	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs573283534	chr11:59798505-59798506	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs540604688	chr11:59798514-59798515	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs563133008	chr11:59798548-59798549	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs550357356	chr11:59804327-59804328	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs568522472	chr11:59804351-59804352	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs532730948	chr11:59804366-59804367	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs562215351	chr11:59805088-59805089	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs181684445	chr11:59805089-59805090	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs138589053	chr11:59805151-59805152	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs535853665	chr11:59805153-59805154	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs550994432	chr11:59805157-59805158	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs371565353	chr11:59805218-59805219	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs559705957	chr11:59805235-59805236	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs514303	chr11:59805307-59805308	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs547760	chr11:59805328-59805329	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs1299401	chr11:59805377-59805378	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs606767	chr11:59805383-59805384	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Lung adenocarcinoma	17086460	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Chordoma	18071362	CNVD

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59789600-59790000	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr11:59805800-59807000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr11:59807600-59808000	Enhancers	K562	blood
4	chr11:59811400-59812200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr11:59811400-59812200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr11:59811400-59812200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr11:59811400-59812400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr11:59811800-59812000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:59811800-59812200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:59812000-59813400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr11:59812200-59813400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr11:59813400-59813600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
13	chr11:59813400-59813600	Bivalent Enhancer	Brain Angular Gyrus	brain
14	chr11:59813400-59813800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr11:59813400-59813800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:59813400-59813800	Enhancers	Pancreas	Pancrea
17	chr11:59813600-59813800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
18	chr11:59813800-59822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr11:59816000-59816200	Enhancers	Primary hematopoietic stem cells	blood
20	chr11:59821800-59822400	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr11:59822200-59823600	Enhancers	K562	blood
22	chr11:59822400-59822600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr11:59822400-59822800	Enhancers	Primary hematopoietic stem cells	blood
24	chr11:59822400-59822800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr11:59822400-59823200	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr11:59822400-59823400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr11:59822400-59826400	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr11:59822600-59824200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:59822600-59824600	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr11:59822600-59824600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr11:59822800-59823200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr11:59822800-59832000	Weak transcription	Primary hematopoietic stem cells	blood
33	chr11:59823200-59823600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr11:59823200-59824200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:59823400-59823800	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr11:59823400-59824200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr11:59823600-59824000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr11:59823600-59824000	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr11:59823600-59824200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr11:59823600-59824800	Flanking Active TSS	K562	blood
41	chr11:59823800-59824200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr11:59823800-59824200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:59823800-59824200	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr11:59823800-59824200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr11:59823800-59824200	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr11:59823800-59824600	Enhancers	H9 Cell Line	embryonic stem cell
47	chr11:59823800-59824600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr11:59824000-59824400	Enhancers	Primary B cells from cord blood	blood
49	chr11:59824000-59825000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr11:59824200-59824600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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