Variant report

Variant	nsv1053558
Chromosome Location	chr11:59979460-60061209
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	chr11:60033093-60033404	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:59989275-59989355	K562	blood:	n/a	n/a
3	ARID3A	chr11:60033149-60033433	K562	blood:	n/a	n/a
4	ARID3A	chr11:59996408-59996532	HepG2	liver:	n/a	n/a
5	ATF1	chr11:59989210-59989551	K562	blood:	n/a	n/a
6	ATF1	chr11:60010430-60010720	K562	blood:	n/a	n/a
7	ATF3	chr11:59989167-59989494	K562	blood:	n/a	n/a
8	BCL11A	chr11:60053164-60053501	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr11:60018899-60019351	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:60019197-60019217	HepG2	liver:	n/a	n/a
11	BHLHE40	chr11:60032166-60032451	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:60033000-60033370	GM12878	blood:	n/a	n/a
13	CBX3	chr11:60028486-60028851	K562	blood:	n/a	n/a
14	CBX3	chr11:60018885-60019271	K562	blood:	n/a	n/a
15	CBX3	chr11:60021655-60021998	K562	blood:	n/a	n/a
16	CEBPB	chr11:60002871-60003119	A549	lung:	n/a	chr11:60003007-60003018 chr11:60003006-60003019 chr11:60003034-60003047
17	CEBPB	chr11:59989246-59989558	K562	blood:	n/a	chr11:59989407-59989418
18	CEBPB	chr11:59989294-59989535	K562	blood:	n/a	chr11:59989407-59989418
19	CEBPB	chr11:60015424-60015625	K562	blood:	n/a	n/a
20	CEBPB	chr11:60006700-60006723	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:59989360-59989473	HepG2	liver:	n/a	chr11:59989407-59989418
22	CEBPB	chr11:59989343-59989543	Hela-S3	cervix:	n/a	chr11:59989407-59989418
23	CEBPB	chr11:60015508-60015512	A549	lung:	n/a	n/a
24	CEBPB	chr11:60014452-60014604	HepG2	liver:	n/a	chr11:60014526-60014537
25	CEBPB	chr11:60053281-60053562	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr11:60002943-60003075	K562	blood:	n/a	chr11:60003007-60003018 chr11:60003006-60003019 chr11:60003034-60003047
27	CEBPB	chr11:59989242-59989557	K562	blood:	n/a	chr11:59989407-59989418
28	CEBPB	chr11:59992028-59992228	A549	lung:	n/a	n/a
29	CEBPB	chr11:60002862-60003100	HepG2	liver:	n/a	chr11:60003007-60003018 chr11:60003006-60003019 chr11:60003034-60003047
30	CEBPB	chr11:60014417-60014654	K562	blood:	n/a	chr11:60014526-60014537
31	CTCF	chr11:60033160-60033310	GM12872	blood:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
32	CTCF	chr11:60033160-60033310	WI-38	lung:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
33	CTCF	chr11:60019320-60019470	GM12878	blood:	n/a	n/a
34	CTCF	chr11:60032898-60032899	ProgFib	skin:	n/a	n/a
35	CTCF	chr11:60033220-60033370	GM12868	blood:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
36	CTCF	chr11:60019103-60019205	Fibrobl	skin:	n/a	n/a
37	CTCF	chr11:60033200-60033350	HMF	breast:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
38	CTCF	chr11:60033053-60033513	MCF-7	breast:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
39	CTCF	chr11:60033197-60033362	GM13976	blood:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
40	CTCF	chr11:60033180-60033330	GM12865	blood:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
41	CTCF	chr11:60033200-60033350	AG09319	gingival:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
42	CTCF	chr11:60018920-60019350	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:60033200-60033350	AG10803	skin:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
44	CTCF	chr11:60033091-60033464	IMR90	lung:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
45	CTCF	chr11:60033160-60033310	GM12864	blood:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
46	CTCF	chr11:60019060-60019210	RPTEC	kidney:	n/a	n/a
47	CTCF	chr11:60017896-60017946	GM20000	blood:	n/a	n/a
48	CTCF	chr11:60032820-60032970	GM12864	blood:	n/a	n/a
49	CTCF	chr11:60033240-60033390	BJ	skin:	n/a	chr11:60033272-60033293 chr11:60033270-60033288 chr11:60033273-60033286
50	CTCF	chr11:60019060-60019210	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:60048390-60048440	CMK	blood:	n/a
2	chr11:60049475-60049525	H1-hESC	embryonic stem cell:	embryo
3	chr11:60049097-60049147	SK-N-MC	brain:	n/a
4	chr11:60048390-60048440	MCF-7	breast:	n/a
5	chr11:60043430-60043480	HRE	kidney:	n/a
6	chr11:60048221-60048271	K562	blood:	n/a
7	chr11:60048221-60048271	Hepatocyte	liver:	n/a
8	chr11:60049475-60049525	SK-N-SH	brain:	n/a
9	chr11:60050143-60050193	GM12892	blood:	n/a
10	chr11:60048390-60048440	PFSK-1	brain:	n/a
11	chr11:60050143-60050193	SK-N-SH	brain:	n/a
12	chr11:60046908-60046958	HEK293	kidney:	embryo
13	chr11:60043430-60043480	MCF10A-Er-Src	breast:	n/a
14	chr11:60048004-60048054	NHBE	bronchial:	n/a
15	chr11:60043430-60043480	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:60046908-60046958	HUVEC	blood vessel:	n/a
17	chr11:60046908-60046958	Hepatocyte	liver:	n/a
18	chr11:60047483-60047533	ProgFib	skin:	n/a
19	chr11:60049097-60049147	Caco-2	colon:	n/a
20	chr11:60047483-60047533	CMK	blood:	n/a
21	chr11:60050143-60050193	Hepatocyte	liver:	n/a
22	chr11:60048390-60048440	HCT-116	colon:	n/a
23	chr11:60047483-60047533	HUVEC	blood vessel:	n/a
24	chr11:60049447-60049497	HRE	kidney:	n/a
25	chr11:60048221-60048271	HNPCEpiC	eye:	n/a
26	chr11:60047483-60047533	GM12892	blood:	n/a
27	chr11:60050143-60050193	HEK293	kidney:	embryo
28	chr11:60049097-60049147	ECC-1	luminal epithelium:	n/a
29	chr11:60048221-60048271	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:60050143-60050193	NHDF-neo	bronchial:	n/a
31	chr11:60047483-60047533	ECC-1	luminal epithelium:	n/a
32	chr11:60046908-60046958	Hela-S3	cervix:	n/a
33	chr11:60049097-60049147	PFSK-1	brain:	n/a
34	chr11:60046908-60046958	IMR90	lung:	fetal
35	chr11:60047483-60047533	ovcar-3	ovarian:	n/a
36	chr11:60049447-60049497	HCM	heart:	n/a
37	chr11:60050143-60050193	HL-60	blood:	n/a
38	chr11:60047483-60047533	SK-N-SH	brain:	n/a
39	chr11:60046908-60046958	HL-60	blood:	n/a
40	chr11:60048004-60048054	PANC-1	pancreas:	n/a
41	chr11:60049475-60049525	PrEC	prostate:	n/a
42	chr11:60048004-60048054	AoSMC	blood vessel:	n/a
43	chr11:60047483-60047533	PFSK-1	brain:	n/a
44	chr11:60048390-60048440	AG09309	skin:	n/a
45	chr11:60049475-60049525	RPTEC	kidney:	n/a
46	chr11:60048004-60048054	NHDF-neo	bronchial:	n/a
47	chr11:60049475-60049525	BJ	skin:	n/a
48	chr11:60048004-60048054	T-47D	breast:	n/a
49	chr11:60049097-60049147	HRE	kidney:	n/a
50	chr11:60048390-60048440	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:60011050..60013826-chr11:60022902..60024679,2	K562	blood:
2	chr11:60032822..60033979-chr11:60101691..60102332,4	MCF-7	breast:
3	chr11:60032800..60033367-chr11:60401726..60402305,2	K562	blood:
4	chr11:60003942..60006110-chr11:60011944..60013830,2	K562	blood:
5	chr11:60006477..60008288-chr11:60011733..60013820,2	K562	blood:
6	chr11:60006477..60008288-chr11:60011733..60013820,2	K562	blood:
7	chr11:59590161..59591119-chr11:60018628..60019571,4	K562	blood:
8	chr11:60032789..60033679-chr11:60101235..60102123,2	MCF-7	breast:
9	chr11:59590107..59591267-chr11:60018622..60019728,5	MCF-7	breast:
10	chr11:60003942..60006110-chr11:60011944..60013830,2	K562	blood:
11	chr11:60033101..60034036-chr11:60236873..60237631,2	MCF-7	breast:
12	chr11:60033229..60033763-chr11:60252978..60253976,4	K562	blood:
13	chr11:60033115..60033927-chr11:60253131..60253845,3	MCF-7	breast:
14	chr11:60032866..60033678-chr11:60386156..60387030,2	MCF-7	breast:
15	chr11:60032810..60033796-chr11:60252992..60253975,8	MCF-7	breast:
16	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: 2377 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2377 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541727867	chr11:59979492-59979493	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540715946	chr11:59979495-59979496	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557842080	chr11:59979504-59979505	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574672039	chr11:59979512-59979513	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533820808	chr11:59979520-59979521	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs193052638	chr11:59979543-59979544	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112896529	chr11:59979614-59979615	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75663794	chr11:59979650-59979651	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573868016	chr11:59979680-59979681	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184812853	chr11:59979693-59979694	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189382381	chr11:59979760-59979761	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35160855	chr11:59979783-59979784	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545633387	chr11:59979784-59979785	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74563400	chr11:59979799-59979800	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374801910	chr11:59979822-59979823	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148740368	chr11:59979827-59979828	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs180737906	chr11:59979856-59979857	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559876802	chr11:59979873-59979874	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528809836	chr11:59979892-59979893	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546886549	chr11:59979920-59979921	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561986134	chr11:59979931-59979932	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1151119	chr11:59979932-59979933	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs550716614	chr11:59979970-59979971	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569033358	chr11:59980004-59980005	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs626011	chr11:59980018-59980019	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs386754054	chr11:59980029-59980030	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs626023	chr11:59980030-59980031	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183627417	chr11:59980077-59980078	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534134357	chr11:59980078-59980079	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548890694	chr11:59980115-59980116	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555707630	chr11:59980126-59980127	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375644649	chr11:59980156-59980157	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs636988	chr11:59980164-59980165	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs556367472	chr11:59980169-59980170	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189404084	chr11:59980286-59980287	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181596614	chr11:59980291-59980292	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74321714	chr11:59980293-59980294	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186670933	chr11:59980304-59980305	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571942410	chr11:59980307-59980308	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11230194	chr11:59980315-59980316	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562051566	chr11:59980380-59980381	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112392438	chr11:59980399-59980400	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570889240	chr11:59980433-59980434	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372758649	chr11:59980443-59980444	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539571041	chr11:59980468-59980469	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550781780	chr11:59980512-59980513	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192020637	chr11:59980514-59980515	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533511695	chr11:59980532-59980533	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566912578	chr11:59980550-59980551	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116544689	chr11:59980579-59980580	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Chordoma	18071362	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59973600-59984200	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr11:59973800-59982000	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr11:59981000-59983800	Enhancers	HUVEC	blood vessel
4	chr11:59982000-59983400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr11:59983400-59984000	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr11:59983400-59984000	Enhancers	K562	blood
7	chr11:59984000-59988600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr11:59984000-59988800	Weak transcription	K562	blood
9	chr11:59984200-59986600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr11:59984800-59985000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr11:59986600-59987600	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr11:59986800-59987000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr11:59987600-59988800	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr11:59988600-59989200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr11:59988800-59989200	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr11:59988800-59990000	Enhancers	K562	blood
17	chr11:59989000-59989600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr11:59989200-59989400	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr11:59989200-59989600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr11:59989400-59991200	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr11:59989600-59992200	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr11:59991200-59992400	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr11:59992200-59994200	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr11:59992400-59993000	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr11:59993000-59995200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr11:59994200-59997200	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr11:59995200-59997400	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr11:59996200-59996600	Enhancers	HepG2	liver
29	chr11:59996800-59997800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr11:59997200-59997400	Genic enhancers	Primary monocytes fromperipheralblood	blood
31	chr11:59997200-59997800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:59997400-59997600	Genic enhancers	Monocytes-CD14+_RO01746	blood
33	chr11:59997400-59998600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr11:59997600-59998200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr11:59997800-59998400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr11:59998200-59998600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr11:59998400-60001800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr11:59998600-59999800	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr11:59998600-60000600	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr11:59999800-60003600	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr11:60000600-60002000	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr11:60001800-60002800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr11:60002000-60002400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr11:60002400-60003000	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr11:60002400-60003000	Enhancers	K562	blood
46	chr11:60002400-60003400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr11:60003400-60004000	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr11:60003600-60006400	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr11:60004000-60006200	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr11:60006200-60007400	Enhancers	Monocytes-CD14+_RO01746	blood

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