Variant report

Variant	nsv898357
Chromosome Location	chr11:105614894-105709856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:105616171-105616181	K562	blood:	n/a	n/a
2	BACH1	chr11:105661657-105661857	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr11:105670024-105670375	HepG2	liver:	n/a	chr11:105670187-105670198
4	CEBPB	chr11:105670033-105670323	K562	blood:	n/a	chr11:105670187-105670198
5	CEBPB	chr11:105616310-105616611	ECC-1	luminal epithelium:	n/a	chr11:105616463-105616476
6	CEBPB	chr11:105670005-105670360	IMR90	lung:	n/a	chr11:105670187-105670198
7	CEBPB	chr11:105675267-105675580	IMR90	lung:	n/a	chr11:105675400-105675411 chr11:105675400-105675409 chr11:105675398-105675411 chr11:105675400-105675409 chr11:105675400-105675409 chr11:105675398-105675411 chr11:105675398-105675411 chr11:105675400-105675409 chr11:105675400-105675411
8	CEBPB	chr11:105616301-105616621	HepG2	liver:	n/a	chr11:105616463-105616476
9	CEBPB	chr11:105623388-105623686	IMR90	lung:	n/a	chr11:105623543-105623552 chr11:105623396-105623407 chr11:105623541-105623552 chr11:105623543-105623552 chr11:105623543-105623552 chr11:105623542-105623553 chr11:105623543-105623552
10	CEBPB	chr11:105647763-105648079	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:105618677-105618941	IMR90	lung:	n/a	chr11:105618768-105618779
12	CEBPB	chr11:105670079-105670283	H1-hESC	embryonic stem cell:	n/a	chr11:105670187-105670198
13	CEBPB	chr11:105670045-105670348	A549	lung:	n/a	chr11:105670187-105670198
14	CEBPB	chr11:105650736-105650858	HepG2	liver:	n/a	chr11:105650765-105650776
15	CEBPB	chr11:105623375-105623705	HepG2	liver:	n/a	chr11:105623543-105623552 chr11:105623396-105623407 chr11:105623541-105623552 chr11:105623543-105623552 chr11:105623543-105623552 chr11:105623542-105623553 chr11:105623543-105623552
16	CEBPB	chr11:105616292-105616652	IMR90	lung:	n/a	chr11:105616463-105616476
17	CEBPB	chr11:105616327-105616581	H1-hESC	embryonic stem cell:	n/a	chr11:105616463-105616476
18	CEBPB	chr11:105625633-105625818	HepG2	liver:	n/a	chr11:105625755-105625766 chr11:105625753-105625764 chr11:105625753-105625766 chr11:105625753-105625766 chr11:105625753-105625766 chr11:105625654-105625665
19	CEBPB	chr11:105618652-105618915	HepG2	liver:	n/a	chr11:105618768-105618779
20	CEBPB	chr11:105670049-105670321	Hela-S3	cervix:	n/a	chr11:105670187-105670198
21	CEBPB	chr11:105623406-105623607	A549	lung:	n/a	chr11:105623543-105623552 chr11:105623541-105623552 chr11:105623543-105623552 chr11:105623543-105623552 chr11:105623542-105623553 chr11:105623543-105623552
22	CEBPB	chr11:105662880-105662968	HepG2	liver:	n/a	chr11:105662936-105662947
23	CEBPB	chr11:105675394-105675477	A549	lung:	n/a	chr11:105675400-105675411 chr11:105675400-105675409 chr11:105675398-105675411 chr11:105675400-105675409 chr11:105675400-105675409 chr11:105675398-105675411 chr11:105675398-105675411 chr11:105675400-105675409 chr11:105675400-105675411
24	CTCF	chr11:105709759-105709850	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr11:105701880-105702030	AG04450	lung:	n/a	n/a
26	CTCF	chr11:105701880-105702150	RPTEC	kidney:	n/a	n/a
27	CTCF	chr11:105698960-105699110	Caco-2	colon:	n/a	n/a
28	CTCF	chr11:105707169-105707234	GM20000	blood:	n/a	n/a
29	CTCF	chr11:105707160-105707200	HepG2	liver:	n/a	n/a
30	CTCF	chr11:105694940-105695090	BE2_C	brain:	n/a	n/a
31	CTCF	chr11:105701860-105702010	NHEK	skin:	n/a	n/a
32	CTCF	chr11:105701880-105702030	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr11:105701880-105702030	HPF	lung:	n/a	n/a
34	CTCF	chr11:105707100-105707250	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr11:105689040-105689190	HL-60	blood:	n/a	n/a
36	CTCF	chr11:105707132-105707234	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr11:105682060-105682210	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr11:105682440-105682590	GM12872	blood:	n/a	n/a
39	CTCF	chr11:105687440-105687590	GM12874	blood:	n/a	n/a
40	CTCF	chr11:105709660-105709810	Caco-2	colon:	n/a	n/a
41	CTCF	chr11:105701960-105702110	BE2_C	brain:	n/a	n/a
42	CTCF	chr11:105667698-105667760	Fibrobl	skin:	n/a	n/a
43	E2F4	chr11:105709507-105709674	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr11:105677067-105677237	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr11:105673754-105674022	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr11:105637560-105637760	MCF10A-Er-Src	breast:	n/a	n/a
47	EBF1	chr11:105699855-105700055	GM12878	blood:	n/a	n/a
48	EP300	chr11:105694455-105694855	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr11:105699980-105699981	GM12878	blood:	n/a	n/a
50	EP300	chr11:105695192-105695636	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:105692831-105692881	GM12891	blood:	n/a
2	chr11:105692831-105692881	HRPEpiC	eye:	n/a
3	chr11:105692831-105692881	HCPEpiC	choroid plexus:	n/a
4	chr11:105692831-105692881	GM12892	blood:	n/a
5	chr11:105692831-105692881	NT2-D1	testis:	n/a
6	chr11:105692831-105692881	IMR90	lung:	fetal
7	chr11:105692831-105692881	Jurkat	blood:	n/a
8	chr11:105692831-105692881	LNCaP	prostate:	n/a
9	chr11:105692831-105692881	HRCEpiC	kidney:	n/a
10	chr11:105692831-105692881	ECC-1	luminal epithelium:	n/a
11	chr11:105692831-105692881	PANC-1	pancreas:	n/a
12	chr11:105692831-105692881	K562	blood:	n/a
13	chr11:105692831-105692881	HIPEpiC	eye:	n/a
14	chr11:105692831-105692881	HRE	kidney:	n/a
15	chr11:105692831-105692881	NHBE	bronchial:	n/a
16	chr11:105692831-105692881	SAEC	small airway:	n/a
17	chr11:105692831-105692881	SKMC	muscle:	n/a
18	chr11:105692831-105692881	HMEC	breast:	n/a
19	chr11:105692831-105692881	Hepatocyte	liver:	n/a
20	chr11:105692831-105692881	A549	lung:	n/a
21	chr11:105692831-105692881	MCF10A-Er-Src	breast:	n/a
22	chr11:105692831-105692881	H1-hESC	embryonic stem cell:	embryo
23	chr11:105692831-105692881	ProgFib	skin:	n/a
24	chr11:105692831-105692881	NH-A	brain:	n/a
25	chr11:105692831-105692881	SK-N-MC	brain:	n/a
26	chr11:105692831-105692881	AG09309	skin:	n/a
27	chr11:105692831-105692881	HEEpiC	esophagus:	n/a
28	chr11:105692831-105692881	CMK	blood:	n/a
29	chr11:105692831-105692881	SK-N-SH	brain:	n/a
30	chr11:105692831-105692881	HPAEpiC	pulmonary alveolar:	n/a
31	chr11:105692831-105692881	HCM	heart:	n/a
32	chr11:105692831-105692881	HCF	heart:	n/a
33	chr11:105692831-105692881	GM06990	blood:	n/a
34	chr11:105692831-105692881	SK-N-SH_RA	brain:	n/a
35	chr11:105692831-105692881	T-47D	breast:	n/a
36	chr11:105692831-105692881	HCT-116	colon:	n/a
37	chr11:105692831-105692881	RPTEC	kidney:	n/a
38	chr11:105692831-105692881	HAEpiC	amniotic membrane:	n/a
39	chr11:105692831-105692881	HEK293	kidney:	embryo
40	chr11:105692831-105692881	PrEC	prostate:	n/a
41	chr11:105692831-105692881	Hela-S3	cervix:	n/a
42	chr11:105692831-105692881	AG04450	lung:	fetal
43	chr11:105692831-105692881	PFSK-1	brain:	n/a
44	chr11:105692831-105692881	Caco-2	colon:	n/a
45	chr11:105692831-105692881	HepG2	liver:	n/a
46	chr11:105692831-105692881	MCF-7	breast:	n/a
47	chr11:105692831-105692881	ovcar-3	ovarian:	n/a
48	chr11:105692831-105692881	HNPCEpiC	eye:	n/a
49	chr11:105692831-105692881	GM12878	blood:	n/a
50	chr11:105692831-105692881	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:105648714..105650582-chr11:105651736..105654609,2	K562	blood:
2	chr11:105655033..105656617-chr11:105660344..105661904,2	K562	blood:
3	chr11:105648714..105650582-chr11:105651736..105654609,2	K562	blood:
4	chr11:105655033..105656617-chr11:105660344..105661904,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AASDHPPT-4	chr11:105625956-105626204	ucscGeneNc_uc001pje_2
2	lnc-AASDHPPT-4	chr11:105628728-105628792	ucscGeneNc_uc001pje_2
3	lnc-AASDHPPT-4	chr11:105630088-105630751	ucscGeneNc_uc001pje_2
4	lnc-AASDHPPT-4	chr11:105632994-105633161	ucscGeneNc_uc001pje_2
5	lnc-AASDHPPT-4	chr11:105636288-105636373	ucscGeneNc_uc001pje_2
6	lnc-AASDHPPT-4	chr11:105638643-105639165	ucscGeneNc_uc001pje_2

Variant related genes	Relation type
GRIA4	TF binding region
RNU4-55P	TF binding region
GRIA4	CpG island
RNU4-55P	CpG island

Extended variants
information (count: 2969 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2969 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2186598	chr11:105614894-105614895	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536065456	chr11:105614908-105614909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554699778	chr11:105614978-105614979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556289001	chr11:105615032-105615033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183110410	chr11:105615086-105615087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558875547	chr11:105615110-105615111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141837824	chr11:105615117-105615118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370462649	chr11:105620428-105620429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555817663	chr11:105620504-105620505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7129691	chr11:105620520-105620521	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs191355842	chr11:105620581-105620582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553826307	chr11:105620615-105620616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12288055	chr11:105620618-105620619	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs542662894	chr11:105620619-105620620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561228441	chr11:105620622-105620623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147532674	chr11:105620729-105620730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563869105	chr11:105620750-105620751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184160223	chr11:105620789-105620790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553476155	chr11:105620825-105620826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138497914	chr11:105620879-105620880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143990178	chr11:105620897-105620898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs578032653	chr11:105620988-105620989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190712262	chr11:105621000-105621001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530384422	chr11:105621040-105621041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74349787	chr11:105621097-105621098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566951729	chr11:105621101-105621102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537431834	chr11:105621126-105621127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181926943	chr11:105621147-105621148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571004802	chr11:105621160-105621161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545030683	chr11:105621167-105621168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538456520	chr11:105621209-105621210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533334979	chr11:105621210-105621211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139098293	chr11:105621218-105621219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536580086	chr11:105621236-105621237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10502062	chr11:105621257-105621258	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs185320301	chr11:105621261-105621262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368530646	chr11:105621262-105621263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188898834	chr11:105621278-105621279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376531533	chr11:105621279-105621280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10502063	chr11:105621281-105621282	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs181348776	chr11:105621295-105621296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541280981	chr11:105621313-105621314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373629942	chr11:105621394-105621395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559869462	chr11:105621437-105621438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377059506	chr11:105621458-105621459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs80044357	chr11:105621471-105621472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548505612	chr11:105621548-105621549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563630157	chr11:105621577-105621578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548006784	chr11:105621578-105621579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528003992	chr11:105621615-105621616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105610800-105615200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr11:105614000-105615200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr11:105620400-105623600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr11:105620800-105624400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr11:105621000-105623600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr11:105623600-105625400	Strong transcription	Cortex derived primary cultured neurospheres	brain
7	chr11:105623600-105626600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr11:105624000-105627400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr11:105624400-105625200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr11:105625200-105625400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr11:105625400-105625600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr11:105625400-105627600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr11:105625600-105627600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr11:105625600-105628000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:105626600-105634200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr11:105627200-105627800	Enhancers	Brain Substantia Nigra	brain
17	chr11:105627200-105628200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr11:105627400-105628000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr11:105627400-105628400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr11:105627600-105628000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr11:105627600-105628200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr11:105627600-105628200	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr11:105627600-105628400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr11:105627600-105628600	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr11:105627600-105629000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr11:105627800-105628200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr11:105628000-105628400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr11:105628000-105629200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:105628000-105629600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:105628200-105629000	Enhancers	Primary hematopoietic stem cells	blood
31	chr11:105628600-105637400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr11:105629000-105637400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr11:105634000-105634600	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr11:105634000-105634600	Enhancers	Brain Substantia Nigra	brain
35	chr11:105634200-105634600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr11:105634600-105638000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr11:105634600-105638400	Weak transcription	Brain Substantia Nigra	brain
38	chr11:105634600-105653800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr11:105637400-105637800	Enhancers	Fetal Brain Female	brain
40	chr11:105637400-105638800	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr11:105637400-105638800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr11:105637400-105639800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr11:105637600-105638200	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr11:105637600-105639400	Enhancers	Brain Germinal Matrix	brain
45	chr11:105637800-105638200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:105637800-105638200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:105637800-105638800	Weak transcription	Fetal Brain Female	brain
48	chr11:105638000-105639000	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr11:105638400-105639200	Enhancers	Brain Substantia Nigra	brain
50	chr11:105638600-105638800	Enhancers	Ovary	ovary

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