Variant report

Variant	esv3435505
Chromosome Location	chr11:60006972-60051885
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	ARID3A	chr11:60033149-60033433	K562	blood:	n/a	n/a
2	ARID3A	chr11:60033093-60033404	HepG2	liver:	n/a	n/a
3	ATF1	chr11:60010430-60010720	K562	blood:	n/a	n/a
4	BCLAF1	chr11:60018899-60019351	GM12878	blood:	n/a	n/a
5	BHLHE40	chr11:60019197-60019217	HepG2	liver:	n/a	n/a
6	BHLHE40	chr11:60033000-60033370	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:60032166-60032451	GM12878	blood:	n/a	n/a
8	CBX3	chr11:60028486-60028851	K562	blood:	n/a	n/a
9	CBX3	chr11:60021655-60021998	K562	blood:	n/a	n/a
10	CBX3	chr11:60018885-60019271	K562	blood:	n/a	n/a
11	CEBPB	chr11:60014452-60014604	HepG2	liver:	n/a	chr11:60014526-60014537
12	CEBPB	chr11:60015424-60015625	K562	blood:	n/a	n/a
13	CEBPB	chr11:60014417-60014654	K562	blood:	n/a	chr11:60014526-60014537
14	CEBPB	chr11:60015508-60015512	A549	lung:	n/a	n/a
15	CTCF	chr11:60019117-60019236	GM12891	blood:	n/a	n/a
16	CTCF	chr11:60033220-60033370	HRE	kidney:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
17	CTCF	chr11:60019025-60019276	A549	lung:	n/a	n/a
18	CTCF	chr11:60033168-60033330	SK-N-SH_RA	brain:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
19	CTCF	chr11:60019020-60019170	GM12868	blood:	n/a	n/a
20	CTCF	chr11:60033107-60033457	T-47D	breast:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
21	CTCF	chr11:60033160-60033310	HAc	cerebellar:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
22	CTCF	chr11:60019060-60019210	HMEC	breast:	n/a	n/a
23	CTCF	chr11:60019117-60019193	NHEK	skin:	n/a	n/a
24	CTCF	chr11:60019072-60019201	GM19239	blood:	n/a	n/a
25	CTCF	chr11:60018915-60019304	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr11:60012920-60013070	Caco-2	colon:	n/a	n/a
27	CTCF	chr11:60033220-60033370	HPAF	blood vessel:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
28	CTCF	chr11:60033159-60033402	K562	blood:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
29	CTCF	chr11:60033200-60033350	HCM	heart:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
30	CTCF	chr11:60019120-60019270	GM12867	blood:	n/a	n/a
31	CTCF	chr11:60033180-60033330	HCPEpiC	choroid plexus:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
32	CTCF	chr11:60018923-60019353	K562	blood:	n/a	n/a
33	CTCF	chr11:60033460-60033610	WI-38	lung:	n/a	n/a
34	CTCF	chr11:60018966-60019236	K562	blood:	n/a	n/a
35	CTCF	chr11:60019080-60019230	Caco-2	colon:	n/a	n/a
36	CTCF	chr11:60033147-60033395	LNCaP	prostate:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
37	CTCF	chr11:60033091-60033464	IMR90	lung:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
38	CTCF	chr11:60033180-60033330	GM12869	blood:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
39	CTCF	chr11:60033220-60033370	HBMEC	blood vessel:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
40	CTCF	chr11:60019060-60019210	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr11:60019040-60019190	NHEK	skin:	n/a	n/a
42	CTCF	chr11:60033220-60033370	RPTEC	kidney:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
43	CTCF	chr11:60033200-60033350	BE2_C	brain:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
44	CTCF	chr11:60033220-60033370	SAEC	small airway:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
45	CTCF	chr11:60033200-60033350	HMEC	breast:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
46	CTCF	chr11:60033160-60033310	AG04450	lung:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
47	CTCF	chr11:60032880-60033030	SAEC	small airway:	n/a	n/a
48	CTCF	chr11:60032460-60032610	GM12865	blood:	n/a	n/a
49	CTCF	chr11:60019080-60019230	GM12874	blood:	n/a	n/a
50	CTCF	chr11:60019100-60019250	GM12869	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:60043430-60043480	AG04449	skin:	fetal
2	chr11:60047483-60047533	GM12891	blood:	n/a
3	chr11:60043430-60043480	AG04449	skin:	fetal
4	chr11:60047483-60047533	GM12891	blood:	n/a
5	chr11:60047483-60047533	NT2-D1	testis:	n/a
6	chr11:60048390-60048440	HCPEpiC	choroid plexus:	n/a
7	chr11:60050143-60050193	HEK293	kidney:	embryo
8	chr11:60050143-60050193	PrEC	prostate:	n/a
9	chr11:60046908-60046958	GM19239	blood:	n/a
10	chr11:60043430-60043480	HRPEpiC	eye:	n/a
11	chr11:60043430-60043480	BJ	skin:	n/a
12	chr11:60043430-60043480	HPAEpiC	pulmonary alveolar:	n/a
13	chr11:60049447-60049497	HEK293	kidney:	embryo
14	chr11:60049475-60049525	HMEC	breast:	n/a
15	chr11:60048004-60048054	BE2_C	brain:	n/a
16	chr11:60046908-60046958	HCF	heart:	n/a
17	chr11:60049447-60049497	U87	brain:	n/a
18	chr11:60043430-60043480	AG09309	skin:	n/a
19	chr11:60043430-60043480	HRE	kidney:	n/a
20	chr11:60048004-60048054	HNPCEpiC	eye:	n/a
21	chr11:60048004-60048054	HRE	kidney:	n/a
22	chr11:60049447-60049497	ProgFib	skin:	n/a
23	chr11:60049097-60049147	HAEpiC	amniotic membrane:	n/a
24	chr11:60050143-60050193	K562	blood:	n/a
25	chr11:60049097-60049147	HCT-116	colon:	n/a
26	chr11:60049097-60049147	MCF10A-Er-Src	breast:	n/a
27	chr11:60050143-60050193	HCM	heart:	n/a
28	chr11:60043430-60043480	HEEpiC	esophagus:	n/a
29	chr11:60048004-60048054	K562	blood:	n/a
30	chr11:60043430-60043480	HUVEC	blood vessel:	n/a
31	chr11:60047483-60047533	HIPEpiC	eye:	n/a
32	chr11:60046908-60046958	H1-hESC	embryonic stem cell:	embryo
33	chr11:60049475-60049525	A549	lung:	n/a
34	chr11:60048004-60048054	MCF-7	breast:	n/a
35	chr11:60043430-60043480	MCF10A-Er-Src	breast:	n/a
36	chr11:60048390-60048440	GM12892	blood:	n/a
37	chr11:60049475-60049525	PANC-1	pancreas:	n/a
38	chr11:60047483-60047533	Hepatocyte	liver:	n/a
39	chr11:60049097-60049147	GM12891	blood:	n/a
40	chr11:60047483-60047533	AoSMC	blood vessel:	n/a
41	chr11:60048221-60048271	SKMC	muscle:	n/a
42	chr11:60047483-60047533	PFSK-1	brain:	n/a
43	chr11:60048221-60048271	K562	blood:	n/a
44	chr11:60048004-60048054	HL-60	blood:	n/a
45	chr11:60048221-60048271	GM12891	blood:	n/a
46	chr11:60049097-60049147	NB4	blood:	n/a
47	chr11:60048004-60048054	ECC-1	luminal epithelium:	n/a
48	chr11:60050143-60050193	HNPCEpiC	eye:	n/a
49	chr11:60049475-60049525	SKMC	muscle:	n/a
50	chr11:60048221-60048271	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:60032800..60033367-chr11:60401726..60402305,2	K562	blood:
2	chr11:60032822..60033979-chr11:60101691..60102332,4	MCF-7	breast:
3	chr11:60006477..60008288-chr11:60011733..60013820,2	K562	blood:
4	chr11:60011050..60013826-chr11:60022902..60024679,2	K562	blood:
5	chr11:60033115..60033927-chr11:60253131..60253845,3	MCF-7	breast:
6	chr11:60033101..60034036-chr11:60236873..60237631,2	MCF-7	breast:
7	chr11:60032789..60033679-chr11:60101235..60102123,2	MCF-7	breast:
8	chr11:60032866..60033678-chr11:60386156..60387030,2	MCF-7	breast:
9	chr11:60033229..60033763-chr11:60252978..60253976,4	K562	blood:
10	chr11:60003942..60006110-chr11:60011944..60013830,2	K562	blood:
11	chr11:59590107..59591267-chr11:60018622..60019728,5	MCF-7	breast:
12	chr11:59590161..59591119-chr11:60018628..60019571,4	K562	blood:
13	chr11:60032810..60033796-chr11:60252992..60253975,8	MCF-7	breast:
14	chr11:60006477..60008288-chr11:60011733..60013820,2	K562	blood:
15	chr11:60011050..60013826-chr11:60022902..60024679,2	K562	blood:

Variant related genes	Relation type
MS4A4E	TF binding region
MS4A4A	TF binding region
MS4A4E	CpG island
MS4A4A	CpG island
ENSG00000166926	chromatin interactions

Extended variants
information (count: 952 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:952 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547572820	chr11:60006999-60007000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553807951	chr11:60007015-60007016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373664780	chr11:60007018-60007019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147692144	chr11:60007019-60007020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542451117	chr11:60007020-60007021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554337368	chr11:60007060-60007061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538047452	chr11:60007104-60007105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575788632	chr11:60007160-60007161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543165658	chr11:60007227-60007228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377257655	chr11:60007303-60007304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564961106	chr11:60007322-60007323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532034418	chr11:60007327-60007328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541000902	chr11:60007328-60007329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556820735	chr11:60007336-60007337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142474731	chr11:60007341-60007342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549645837	chr11:60007355-60007356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191966667	chr11:60007376-60007377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531899665	chr11:60007434-60007435	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs550028017	chr11:60007460-60007461	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs146332969	chr11:60007496-60007497	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs570613412	chr11:60007544-60007545	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs79487981	chr11:60007545-60007546	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs60784752	chr11:60007550-60007551	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs565682433	chr11:60007570-60007571	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs1834554	chr11:60007573-60007574	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542312999	chr11:60007626-60007627	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs147883529	chr11:60007637-60007638	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs80350024	chr11:60007688-60007689	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs190351412	chr11:60007745-60007746	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs558397952	chr11:60007746-60007747	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs576857912	chr11:60007768-60007769	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs657513	chr11:60007822-60007823	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs559387247	chr11:60007869-60007870	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs12271845	chr11:60007876-60007877	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs73485342	chr11:60007893-60007894	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs561536327	chr11:60007913-60007914	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs200027359	chr11:60007921-60007922	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs531838050	chr11:60007927-60007928	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs550331268	chr11:60007942-60007943	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs565273934	chr11:60008000-60008001	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs535340328	chr11:60008009-60008010	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs182596177	chr11:60008067-60008068	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs370981179	chr11:60008086-60008087	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs545355954	chr11:60008095-60008096	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs571934363	chr11:60008124-60008125	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs1019671	chr11:60008151-60008152	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs185872568	chr11:60008167-60008168	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs563986978	chr11:60008184-60008185	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs536214193	chr11:60008257-60008258	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189600237	chr11:60008334-60008335	Flanking Active TSS Enhancers	n/a	n/a	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	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
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Chordoma	18071362	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:60006200-60007400	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr11:60006400-60008000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr11:60007400-60008400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr11:60008000-60008400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
5	chr11:60008200-60008400	Enhancers	Primary B cells from peripheral blood	blood
6	chr11:60008400-60008800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr11:60008400-60009600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr11:60008600-60009800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr11:60008800-60009000	Enhancers	K562	blood
10	chr11:60008800-60011000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr11:60009000-60010200	Weak transcription	K562	blood
12	chr11:60009400-60011000	Enhancers	Primary B cells from cord blood	blood
13	chr11:60009400-60011000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr11:60009400-60011000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr11:60009600-60010600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
16	chr11:60009600-60010800	Enhancers	Primary hematopoietic stem cells	blood
17	chr11:60009800-60010400	Active TSS	Adipose Nuclei	Adipose
18	chr11:60009800-60010600	Enhancers	Primary B cells from peripheral blood	blood
19	chr11:60009800-60010800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:60009800-60011000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr11:60010200-60010600	Enhancers	GM12878-XiMat	blood
22	chr11:60010200-60010800	Enhancers	K562	blood
23	chr11:60010600-60011600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr11:60011000-60011400	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr11:60018200-60022000	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr11:60018400-60018800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr11:60018400-60019000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr11:60018800-60020400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr11:60018800-60021200	Enhancers	HUVEC	blood vessel
30	chr11:60019000-60020000	Enhancers	Ovary	ovary
31	chr11:60019000-60021000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr11:60019000-60021200	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr11:60019200-60020000	Enhancers	GM12878-XiMat	blood
34	chr11:60019200-60021200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr11:60019400-60020800	Enhancers	Primary B cells from cord blood	blood
36	chr11:60019400-60021200	Enhancers	Primary hematopoietic stem cells	blood
37	chr11:60019600-60020200	Enhancers	Liver	Liver
38	chr11:60019600-60021200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr11:60019800-60020000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr11:60019800-60020000	Enhancers	Duodenum Mucosa	Duodenum
41	chr11:60019800-60021000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr11:60020000-60020400	Enhancers	Primary B cells from peripheral blood	blood
43	chr11:60020000-60023400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr11:60020400-60020800	Weak transcription	Primary B cells from peripheral blood	blood
45	chr11:60020400-60021000	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr11:60020800-60021000	Enhancers	Primary B cells from peripheral blood	blood
47	chr11:60020800-60021000	Enhancers	Duodenum Mucosa	Duodenum
48	chr11:60021000-60021200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
49	chr11:60021000-60021400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr11:60021000-60022600	ZNF genes & repeats	Dnd41	blood

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