Variant report

Variant	nsv897019
Chromosome Location	chr11:17475443-17499547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:396)
CpG islands
(count:1222)
Chromatin interactive
region (count:52)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17494927-17495252	HepG2	liver:	n/a	n/a
2	ATF2	chr11:17494857-17495249	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr11:17494961-17495159	K562	blood:	n/a	n/a
4	ATF3	chr11:17494922-17495366	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr11:17498538-17498773	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:17497792-17498055	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr11:17485124-17485418	K562	blood:	n/a	n/a
8	BHLHE40	chr11:17494791-17495186	K562	blood:	n/a	chr11:17494838-17494847 chr11:17494839-17494848 chr11:17494839-17494848 chr11:17494833-17494854
9	BHLHE40	chr11:17484608-17484810	K562	blood:	n/a	n/a
10	BRCA1	chr11:17485135-17485737	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:17484555-17486066	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr11:17498727-17498927	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr11:17488213-17488422	Hela-S3	cervix:	n/a	n/a
14	CHD1	chr11:17498116-17498313	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr11:17484561-17484936	Hela-S3	cervix:	n/a	n/a
16	CREB1	chr11:17489713-17489914	A549	lung:	n/a	n/a
17	CREB1	chr11:17489649-17489992	A549	lung:	n/a	n/a
18	CTBP2	chr11:17497378-17498316	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr11:17493180-17493330	Caco-2	colon:	n/a	n/a
20	CTCF	chr11:17495020-17495170	HRE	kidney:	n/a	n/a
21	CTCF	chr11:17493108-17493352	A549	lung:	n/a	n/a
22	CTCF	chr11:17493180-17493330	HMEC	breast:	n/a	n/a
23	CTCF	chr11:17495020-17495170	HPF	lung:	n/a	n/a
24	CTCF	chr11:17493198-17493324	GM19240	blood:	n/a	n/a
25	CTCF	chr11:17493280-17493430	RPTEC	kidney:	n/a	n/a
26	CTCF	chr11:17495080-17495230	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr11:17495080-17495230	MCF-7	breast:	n/a	n/a
28	CTCF	chr11:17494953-17495237	MCF-7	breast:	n/a	n/a
29	CTCF	chr11:17493190-17493335	GM19239	blood:	n/a	n/a
30	CTCF	chr11:17494951-17495278	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr11:17498100-17498250	HEK293	kidney:	n/a	n/a
32	CTCF	chr11:17493191-17493345	GM12878	blood:	n/a	n/a
33	CTCF	chr11:17482740-17482890	GM12864	blood:	n/a	n/a
34	CTCF	chr11:17498020-17498170	SK-N-SH_RA	brain:	n/a	chr11:17498079-17498097
35	CTCF	chr11:17493200-17493350	GM12873	blood:	n/a	n/a
36	CTCF	chr11:17493237-17493291	Gliobla	brain:	n/a	n/a
37	CTCF	chr11:17494660-17494810	GM12878	blood:	n/a	n/a
38	CTCF	chr11:17494960-17495110	GM12873	blood:	n/a	n/a
39	CTCF	chr11:17495040-17495190	A549	lung:	n/a	n/a
40	CTCF	chr11:17493230-17493303	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr11:17495145-17495217	GM12878	blood:	n/a	n/a
42	CTCF	chr11:17495020-17495170	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr11:17494994-17495203	ECC-1	luminal epithelium:	n/a	n/a
44	CTCF	chr11:17495040-17495190	BE2_C	brain:	n/a	n/a
45	CTCF	chr11:17495300-17495450	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr11:17495020-17495170	HEK293	kidney:	n/a	n/a
47	CTCF	chr11:17494980-17495130	A549	lung:	n/a	n/a
48	CTCF	chr11:17495040-17495190	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr11:17495040-17495190	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr11:17493200-17493350	HepG2	liver:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17496725-17496775	BJ	skin:	n/a
2	chr11:17498329-17498379	NH-A	brain:	n/a
3	chr11:17496725-17496775	BJ	skin:	n/a
4	chr11:17498329-17498379	NH-A	brain:	n/a
5	chr11:17482547-17482597	MCF10A-Er-Src	breast:	n/a
6	chr11:17495097-17495147	GM12892	blood:	n/a
7	chr11:17498329-17498379	AG09309	skin:	n/a
8	chr11:17495097-17495147	HCM	heart:	n/a
9	chr11:17498952-17499002	HRCEpiC	kidney:	n/a
10	chr11:17497967-17498017	BE2_C	brain:	n/a
11	chr11:17498601-17498651	MCF-7	breast:	n/a
12	chr11:17498329-17498379	K562	blood:	n/a
13	chr11:17498329-17498379	LNCaP	prostate:	n/a
14	chr11:17498419-17498469	HRPEpiC	eye:	n/a
15	chr11:17482547-17482597	HRPEpiC	eye:	n/a
16	chr11:17497693-17497743	IMR90	lung:	fetal
17	chr11:17498952-17499002	HIPEpiC	eye:	n/a
18	chr11:17498329-17498379	PFSK-1	brain:	n/a
19	chr11:17498952-17499002	SK-N-MC	brain:	n/a
20	chr11:17498601-17498651	HIPEpiC	eye:	n/a
21	chr11:17496725-17496775	LNCaP	prostate:	n/a
22	chr11:17498514-17498564	ovcar-3	ovarian:	n/a
23	chr11:17498952-17499002	AG09319	gingival:	n/a
24	chr11:17479394-17479444	HCF	heart:	n/a
25	chr11:17496725-17496775	HRE	kidney:	n/a
26	chr11:17498236-17498286	NH-A	brain:	n/a
27	chr11:17495097-17495147	AoSMC	blood vessel:	n/a
28	chr11:17498541-17498591	HRCEpiC	kidney:	n/a
29	chr11:17498541-17498591	ProgFib	skin:	n/a
30	chr11:17498541-17498591	NH-A	brain:	n/a
31	chr11:17498419-17498469	NB4	blood:	n/a
32	chr11:17498952-17499002	AoSMC	blood vessel:	n/a
33	chr11:17498236-17498286	SK-N-SH	brain:	n/a
34	chr11:17479394-17479444	AG09309	skin:	n/a
35	chr11:17498619-17498669	GM12878	blood:	n/a
36	chr11:17497693-17497743	SK-N-SH_RA	brain:	n/a
37	chr11:17498541-17498591	NT2-D1	testis:	n/a
38	chr11:17497808-17497858	GM12891	blood:	n/a
39	chr11:17498329-17498379	HRCEpiC	kidney:	n/a
40	chr11:17498819-17498869	NHBE	bronchial:	n/a
41	chr11:17497693-17497743	K562	blood:	n/a
42	chr11:17496725-17496775	NHBE	bronchial:	n/a
43	chr11:17498329-17498379	RPTEC	kidney:	n/a
44	chr11:17496725-17496775	NB4	blood:	n/a
45	chr11:17497967-17498017	GM19239	blood:	n/a
46	chr11:17482547-17482597	RPTEC	kidney:	n/a
47	chr11:17497808-17497858	HCT-116	colon:	n/a
48	chr11:17496473-17496523	SAEC	small airway:	n/a
49	chr11:17498819-17498869	HIPEpiC	eye:	n/a
50	chr11:17498819-17498869	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:17492351..17494753-chr11:17565764..17567313,2	K562	blood:
2	chr11:17417635..17419450-chr11:17475960..17478290,2	MCF-7	breast:
3	chr11:17405241..17406080-chr11:17492901..17493668,2	MCF-7	breast:
4	chr11:17494629..17496394-chr11:17499346..17501240,2	MCF-7	breast:
5	chr11:17475034..17476631-chr11:17480945..17483490,2	K562	blood:
6	chr11:17405197..17406140-chr11:17492660..17493631,2	K562	blood:
7	chr11:17476148..17478074-chr11:17479961..17481656,2	MCF-7	breast:
8	chr11:17484097..17487260-chr11:17487485..17491025,3	MCF-7	breast:
9	chr11:17490196..17492539-chr11:17495004..17496625,2	K562	blood:
10	chr11:17433853..17435341-chr11:17494678..17495621,7	MCF-7	breast:
11	chr11:17476190..17478862-chr11:17505917..17508222,2	K562	blood:
12	chr11:17471704..17474576-chr11:17475310..17477119,2	MCF-7	breast:
13	chr11:17483603..17486508-chr11:17496196..17498244,2	MCF-7	breast:
14	chr11:17410413..17411265-chr11:17494725..17495652,3	MCF-7	breast:
15	chr11:17407664..17411994-chr11:17495609..17498712,4	MCF-7	breast:
16	chr11:17474460..17476644-chr11:17478483..17480619,2	K562	blood:
17	chr11:17478295..17480154-chr11:17482165..17484728,2	K562	blood:
18	chr11:17408071..17409415-chr11:17493655..17495242,4	MCF-7	breast:
19	chr11:17490196..17492539-chr11:17495004..17496625,2	K562	blood:
20	chr11:17494721..17495546-chr11:17525791..17526792,4	MCF-7	breast:
21	chr11:17478295..17480154-chr11:17482165..17484728,2	K562	blood:
22	chr11:17416000..17416717-chr11:17494745..17495547,2	MCF-7	breast:
23	chr11:17494629..17496394-chr11:17499346..17501240,2	MCF-7	breast:
24	chr11:17408716..17410225-chr11:17496014..17498042,2	MCF-7	breast:
25	chr11:17434007..17434879-chr11:17494696..17495665,4	MCF-7	breast:
26	chr11:17433977..17434919-chr11:17492806..17493693,3	MCF-7	breast:
27	chr11:17494705..17495611-chr11:17525425..17526663,5	MCF-7	breast:
28	chr11:17484097..17487260-chr11:17487485..17491025,3	MCF-7	breast:
29	chr11:17483603..17486508-chr11:17496196..17498244,2	MCF-7	breast:
30	chr11:17376143..17376651-chr11:17494721..17495470,2	MCF-7	breast:
31	chr11:17410437..17411856-chr11:17494552..17495678,7	MCF-7	breast:
32	chr11:17475034..17476631-chr11:17480945..17483490,2	K562	blood:
33	chr11:17499490..17502461-chr11:17527268..17529480,2	MCF-7	breast:
34	chr11:17405274..17406188-chr11:17494608..17495575,4	MCF-7	breast:
35	chr11:17405241..17405887-chr11:17492811..17493698,3	MCF-7	breast:
36	chr11:17411046..17413083-chr11:17494986..17496697,2	K562	blood:
37	chr11:17495130..17495674-chr11:17525856..17526382,2	K562	blood:
38	chr11:17484409..17485269-chr19:13049273..13049928,2	Hela-S3	cervix:
39	chr11:17475103..17476631-chr11:17480945..17482872,2	K562	blood:
40	chr11:17408194..17409948-chr11:17498514..17500744,2	MCF-7	breast:
41	chr11:17407668..17408772-chr11:17492719..17493735,8	MCF-7	breast:
42	chr11:17447052..17448727-chr11:17486518..17488813,2	K562	blood:
43	chr11:17416024..17416970-chr11:17492845..17493349,3	MCF-7	breast:
44	chr11:17462780..17465155-chr11:17480733..17482429,2	K562	blood:
45	chr11:17474460..17476644-chr11:17478483..17480619,2	K562	blood:
46	chr11:17476148..17478074-chr11:17479961..17481656,2	MCF-7	breast:
47	chr11:17407591..17408789-chr11:17492713..17493544,3	MCF-7	breast:
48	chr11:17372929..17375866-chr11:17489485..17491410,2	K562	blood:
49	chr11:17407600..17408460-chr11:17494790..17495622,2	MCF-7	breast:
50	chr11:17475103..17476631-chr11:17480945..17482872,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTOG-1	chr11:17498779-17503911	NONHSAT018236
2	lnc-OTOG-1	chr11:17498451-17498626	NONHSAT018236

No data

Variant related genes	Relation type
ABCC8	TF binding region
ABCC8	CpG island
ENSG00000006071	chromatin interactions
ENSG00000187486	chromatin interactions
ENSG00000188211	chromatin interactions
ENSG00000006611	chromatin interactions
ENSG00000179218	chromatin interactions

Extended variants
information (count: 1005 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1005 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2073585	chr11:17475443-17475444	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565893014	chr11:17475488-17475489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35215529	chr11:17475554-17475555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113519523	chr11:17475595-17475596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113308421	chr11:17475614-17475615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549755089	chr11:17475770-17475771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529298553	chr11:17475786-17475787	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116201946	chr11:17475798-17475799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566072435	chr11:17475823-17475824	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533422288	chr11:17475826-17475827	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539922190	chr11:17475885-17475886	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552071598	chr11:17475934-17475935	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76815168	chr11:17475935-17475936	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537281980	chr11:17475998-17475999	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2057660	chr11:17476017-17476018	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs569803745	chr11:17476027-17476028	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534718709	chr11:17476039-17476040	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs371130066	chr11:17476126-17476127	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs140363973	chr11:17476154-17476155	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577584037	chr11:17476166-17476167	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544948351	chr11:17476214-17476215	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs374239596	chr11:17476273-17476274	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190970928	chr11:17476291-17476292	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2237977	chr11:17476388-17476389	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs561063238	chr11:17476447-17476448	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs4148613	chr11:17476460-17476461	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs541527827	chr11:17476471-17476472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559458131	chr11:17476510-17476511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs2237976	chr11:17476516-17476517	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs533485215	chr11:17476521-17476522	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184009635	chr11:17476523-17476524	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs112271652	chr11:17476551-17476552	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs531012733	chr11:17476647-17476648	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs186362277	chr11:17476679-17476680	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs567510429	chr11:17476690-17476691	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs370457089	chr11:17476724-17476725	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534452878	chr11:17476737-17476738	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546651475	chr11:17476783-17476784	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs73425085	chr11:17476812-17476813	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs78092039	chr11:17476825-17476826	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145683274	chr11:17476828-17476829	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs575659523	chr11:17476829-17476830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536543464	chr11:17476903-17476904	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554841507	chr11:17476911-17476912	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572973917	chr11:17476936-17476937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs541189430	chr11:17476937-17476938	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs190761113	chr11:17476993-17476994	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146586620	chr11:17477018-17477019	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs553739535	chr11:17477019-17477020	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs61880330	chr11:17477035-17477036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Usher syndrome	20538994	CNVD
Usher type I cohort	21436283	CNVD

Chromatin state (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17461200-17497400	Weak transcription	Gastric	stomach
2	chr11:17465800-17481600	Weak transcription	Fetal Brain Female	brain
3	chr11:17465800-17496400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr11:17467400-17478600	Weak transcription	Dnd41	blood
5	chr11:17470200-17482000	Weak transcription	Brain Germinal Matrix	brain
6	chr11:17472400-17489600	Weak transcription	Brain Substantia Nigra	brain
7	chr11:17473600-17478200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr11:17473800-17478800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:17474000-17482200	Weak transcription	Brain Angular Gyrus	brain
10	chr11:17474000-17485000	Weak transcription	Lung	lung
11	chr11:17474400-17479000	Weak transcription	Fetal Muscle Leg	muscle
12	chr11:17474400-17481800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr11:17474600-17476400	Strong transcription	Pancreatic Islets	Pancreatic Islet
14	chr11:17474600-17481800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr11:17474800-17481800	Weak transcription	Brain Anterior Caudate	brain
16	chr11:17474800-17481800	Weak transcription	Brain Cingulate Gyrus	brain
17	chr11:17475800-17476000	Enhancers	Fetal Muscle Trunk	muscle
18	chr11:17476200-17479000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr11:17476400-17480600	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr11:17478400-17480400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr11:17478600-17479200	Bivalent Enhancer	Adipose Nuclei	Adipose
22	chr11:17478600-17479800	Enhancers	Fetal Brain Male	brain
23	chr11:17478600-17480000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:17478600-17480000	Enhancers	Dnd41	blood
25	chr11:17478800-17479600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr11:17478800-17479800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr11:17478800-17480000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr11:17478800-17480200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr11:17478800-17480200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr11:17478800-17480200	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr11:17478800-17480200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr11:17478800-17480400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr11:17479000-17479600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr11:17479000-17479600	Enhancers	Fetal Thymus	thymus
35	chr11:17479000-17479800	Enhancers	Fetal Muscle Leg	muscle
36	chr11:17479000-17480000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr11:17479000-17480200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr11:17479000-17480200	Enhancers	Primary hematopoietic stem cells	blood
39	chr11:17479000-17480200	Enhancers	Fetal Muscle Trunk	muscle
40	chr11:17479000-17481400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr11:17479200-17479600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr11:17479200-17479600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr11:17479200-17479800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr11:17479200-17479800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr11:17479200-17480200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr11:17479200-17482200	Enhancers	Adipose Nuclei	Adipose
47	chr11:17479400-17479600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:17479600-17480000	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr11:17479600-17480000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:17479600-17480000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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