Variant report

Variant	esv1794353
Chromosome Location	chr6:44333489-44350716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:45)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:45 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:44349480-44349832	HepG2	liver:	n/a	n/a
2	CEBPB	chr6:44349594-44349807	A549	lung:	n/a	n/a
3	CEBPB	chr6:44349586-44349853	K562	blood:	n/a	n/a
4	CEBPB	chr6:44349466-44349845	MCF-7	breast:	n/a	n/a
5	CEBPB	chr6:44349517-44349833	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr6:44349472-44349925	HepG2	liver:	n/a	chr6:44349891-44349900
7	CTCF	chr6:44346000-44346150	GM12871	blood:	n/a	n/a
8	CTCF	chr6:44340445-44340496	GM10248	blood:	n/a	n/a
9	E2F4	chr6:44342372-44342572	MCF10A-Er-Src	breast:	n/a	n/a
10	EBF1	chr6:44342915-44343082	GM12878	blood:	n/a	n/a
11	FOS	chr6:44341620-44341748	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr6:44349673-44349765	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr6:44345908-44346071	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr6:44349605-44349800	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr6:44345871-44346076	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr6:44349610-44349789	MCF10A-Er-Src	breast:	n/a	n/a
17	FOXA1	chr6:44334517-44334824	HepG2	liver:	n/a	n/a
18	FOXA1	chr6:44334434-44334774	HepG2	liver:	n/a	n/a
19	FOXA1	chr6:44334511-44334832	HepG2	liver:	n/a	n/a
20	FOXA2	chr6:44349592-44349738	HepG2	liver:	n/a	n/a
21	HDAC2	chr6:44349558-44349825	HepG2	liver:	n/a	n/a
22	HNF4A	chr6:44334526-44334834	HepG2	liver:	n/a	chr6:44334720-44334735
23	HNF4A	chr6:44334600-44334807	HepG2	liver:	n/a	chr6:44334720-44334735
24	HNF4G	chr6:44334527-44334830	HepG2	liver:	n/a	n/a
25	MAX	chr6:44335214-44335483	K562	blood:	n/a	chr6:44335343-44335354 chr6:44335344-44335353
26	MAX	chr6:44349485-44349860	NB4	blood:	n/a	n/a
27	MYC	chr6:44349536-44349871	MCF10A-Er-Src	breast:	n/a	n/a
28	MYC	chr6:44349584-44349810	MCF10A-Er-Src	breast:	n/a	n/a
29	MYC	chr6:44337505-44337589	MCF-7	breast:	n/a	n/a
30	MYC	chr6:44342588-44342730	MCF10A-Er-Src	breast:	n/a	n/a
31	MYC	chr6:44346601-44346652	MCF-7	breast:	n/a	n/a
32	MYC	chr6:44349513-44349835	NB4	blood:	n/a	n/a
33	POLR2A	chr6:44322615-44333993	K562	blood:	n/a	n/a
34	POLR2A	chr6:44336964-44337053	A549	lung:	n/a	n/a
35	POLR2A	chr6:44349401-44349997	HL-60	blood:	n/a	n/a
36	POLR2A	chr6:44349464-44349950	HL-60	blood:	n/a	n/a
37	SETDB1	chr6:44345354-44345663	U2OS	brain:	n/a	n/a
38	SMC3	chr6:44349611-44349768	HepG2	liver:	n/a	n/a
39	SPI1	chr6:44349454-44349934	HL-60	blood:	n/a	n/a
40	STAT3	chr6:44341004-44341153	MCF10A-Er-Src	breast:	n/a	n/a
41	STAT3	chr6:44335590-44335697	MCF10A-Er-Src	breast:	n/a	n/a
42	STAT3	chr6:44349673-44349695	MCF10A-Er-Src	breast:	n/a	n/a
43	STAT3	chr6:44350315-44350322	MCF10A-Er-Src	breast:	n/a	n/a
44	STAT3	chr6:44342427-44342457	MCF10A-Er-Src	breast:	n/a	n/a
45	UBTF	chr6:44335642-44335644	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:44344842-44344892	NHBE	bronchial:	n/a
2	chr6:44344842-44344892	SK-N-MC	brain:	n/a
3	chr6:44344842-44344892	Caco-2	colon:	n/a
4	chr6:44344842-44344892	NH-A	brain:	n/a
5	chr6:44344842-44344892	GM06990	blood:	n/a
6	chr6:44344842-44344892	A549	lung:	n/a
7	chr6:44344842-44344892	Hela-S3	cervix:	n/a
8	chr6:44344842-44344892	PANC-1	pancreas:	n/a
9	chr6:44344842-44344892	GM12878	blood:	n/a
10	chr6:44344842-44344892	HIPEpiC	eye:	n/a
11	chr6:44344842-44344892	HCT-116	colon:	n/a
12	chr6:44344842-44344892	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:44344842-44344892	HEK293	kidney:	embryo
14	chr6:44344842-44344892	HL-60	blood:	n/a
15	chr6:44344842-44344892	AG04450	lung:	fetal
16	chr6:44344842-44344892	ProgFib	skin:	n/a
17	chr6:44344842-44344892	ovcar-3	ovarian:	n/a
18	chr6:44344842-44344892	HCF	heart:	n/a
19	chr6:44344842-44344892	LNCaP	prostate:	n/a
20	chr6:44344842-44344892	AG09319	gingival:	n/a
21	chr6:44344842-44344892	ECC-1	luminal epithelium:	n/a
22	chr6:44344842-44344892	AG04449	skin:	fetal
23	chr6:44344842-44344892	Hepatocyte	liver:	n/a
24	chr6:44344842-44344892	HepG2	liver:	n/a
25	chr6:44344842-44344892	K562	blood:	n/a
26	chr6:44344842-44344892	MCF-7	breast:	n/a
27	chr6:44344842-44344892	BJ	skin:	n/a
28	chr6:44344842-44344892	RPTEC	kidney:	n/a
29	chr6:44344842-44344892	MCF10A-Er-Src	breast:	n/a
30	chr6:44344842-44344892	SKMC	muscle:	n/a
31	chr6:44344842-44344892	AoSMC	blood vessel:	n/a
32	chr6:44344842-44344892	NT2-D1	testis:	n/a
33	chr6:44344842-44344892	HEEpiC	esophagus:	n/a
34	chr6:44344842-44344892	SK-N-SH	brain:	n/a
35	chr6:44344842-44344892	HNPCEpiC	eye:	n/a
36	chr6:44344842-44344892	HUVEC	blood vessel:	n/a
37	chr6:44344842-44344892	HCPEpiC	choroid plexus:	n/a
38	chr6:44344842-44344892	HRCEpiC	kidney:	n/a
39	chr6:44344842-44344892	SK-N-SH_RA	brain:	n/a
40	chr6:44344842-44344892	HRPEpiC	eye:	n/a
41	chr6:44344842-44344892	GM12892	blood:	n/a
42	chr6:44344842-44344892	HAEpiC	amniotic membrane:	n/a
43	chr6:44344842-44344892	CMK	blood:	n/a
44	chr6:44344842-44344892	Jurkat	blood:	n/a
45	chr6:44344842-44344892	NHDF-neo	bronchial:	n/a
46	chr6:44344842-44344892	SAEC	small airway:	n/a
47	chr6:44344842-44344892	HCM	heart:	n/a
48	chr6:44344842-44344892	HRE	kidney:	n/a
49	chr6:44344842-44344892	U87	brain:	n/a
50	chr6:44344842-44344892	H1-hESC	embryonic stem cell:	embryo

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:44350111..44351913-chr6:44352677..44355083,2	MCF-7	breast:
2	chr6:44272651..44274712-chr6:44338316..44340561,2	K562	blood:
3	chr6:44333775..44335329-chr6:44340756..44342946,2	K562	blood:
4	chr6:44343981..44346668-chr6:44351933..44354456,2	MCF-7	breast:
5	chr6:44278856..44282266-chr6:44345336..44347499,3	K562	blood:
6	chr6:44345933..44348931-chr6:44350479..44354332,6	K562	blood:
7	chr6:44326030..44327611-chr6:44332225..44334880,2	MCF-7	breast:
8	chr6:44345933..44348931-chr6:44350479..44354332,6	K562	blood:
9	chr6:44342784..44345720-chr6:44353458..44355449,2	K562	blood:
10	chr6:44333775..44335329-chr6:44340756..44342946,2	K562	blood:
11	chr6:44339222..44342779-chr6:44344698..44347140,3	K562	blood:
12	chr6:44315264..44318217-chr6:44339899..44341797,2	K562	blood:
13	chr6:44340013..44342443-chr6:44347687..44349600,2	K562	blood:
14	chr6:44340013..44342443-chr6:44347687..44349600,2	K562	blood:
15	chr6:44247780..44249654-chr6:44347514..44350331,2	MCF-7	breast:
16	chr6:44339222..44342779-chr6:44344698..44347140,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AARS2-1	chr6:44338508-44338780	expReg_chr6_5009_-

No data

Variant related genes	Relation type
CDC5L	TF binding region
CDC5L	CpG island
ENSG00000096401	chromatin interactions
ENSG00000124608	chromatin interactions

Extended variants
information (count: 606 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529857670	chr6:44334236-44334237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7769100	chr6:44334252-44334253	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs560437783	chr6:44334265-44334266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527767768	chr6:44334268-44334269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552740151	chr6:44334285-44334286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531490260	chr6:44334307-44334308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187520532	chr6:44334344-44334345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192444896	chr6:44334346-44334347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146161526	chr6:44334375-44334376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7769128	chr6:44334388-44334389	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs79557845	chr6:44334399-44334400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148789509	chr6:44334423-44334424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184815497	chr6:44334506-44334507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1909887	chr6:44334650-44334651	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs142409527	chr6:44334716-44334717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1411903	chr6:44334831-44334832	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs150865550	chr6:44334893-44334894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567300239	chr6:44334917-44334918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139358302	chr6:44334928-44334929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145493349	chr6:44334970-44334971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147690051	chr6:44335011-44335012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566727373	chr6:44335051-44335052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560376147	chr6:44335142-44335143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572288608	chr6:44335190-44335191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528091297	chr6:44335220-44335221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546270402	chr6:44335291-44335292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73439581	chr6:44335335-44335336	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs74857992	chr6:44335352-44335353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369457409	chr6:44335384-44335385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142359358	chr6:44335390-44335391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576673755	chr6:44335412-44335413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549901506	chr6:44335422-44335423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539178263	chr6:44335437-44335438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144593713	chr6:44335459-44335460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572495554	chr6:44335473-44335474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555557016	chr6:44335531-44335532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1014528	chr6:44335680-44335681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554664240	chr6:44335696-44335697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192610968	chr6:44335704-44335705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2065361	chr6:44335730-44335731	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs570445004	chr6:44335765-44335766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577429042	chr6:44335807-44335808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537992952	chr6:44335823-44335824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs60347589	chr6:44335854-44335855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574411422	chr6:44335920-44335921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535715783	chr6:44335939-44335940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554132055	chr6:44335957-44335958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111776102	chr6:44335972-44335973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377400346	chr6:44335974-44335975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546009547	chr6:44335985-44335986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
Cancer	20164920	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44334200-44334800	Enhancers	HepG2	liver
2	chr6:44334200-44335400	Enhancers	Liver	Liver
3	chr6:44335200-44335800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr6:44335200-44335800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:44335200-44335800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:44335400-44336000	Enhancers	Primary hematopoietic stem cells	blood
7	chr6:44335400-44340800	Weak transcription	Liver	Liver
8	chr6:44335600-44336200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:44335800-44340600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:44335800-44342400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:44337800-44339200	Enhancers	Brain Germinal Matrix	brain
12	chr6:44338000-44338800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr6:44338400-44339000	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr6:44340400-44341000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:44340400-44341200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr6:44340400-44341200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr6:44340400-44341800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr6:44340400-44342000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:44340400-44342000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr6:44340400-44342400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:44340400-44343000	Enhancers	HMEC	breast
22	chr6:44340400-44343000	Enhancers	NHEK	skin
23	chr6:44340600-44341000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr6:44340600-44341000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr6:44340600-44341000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:44340600-44341800	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr6:44340800-44341000	Enhancers	Liver	Liver
28	chr6:44341000-44341800	Weak transcription	Liver	Liver
29	chr6:44341000-44342600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:44341400-44342000	Enhancers	HSMM	muscle
31	chr6:44341400-44342200	Bivalent Enhancer	HUVEC	blood vessel
32	chr6:44341600-44342000	Enhancers	Muscle Satellite Cultured Cells	--
33	chr6:44341800-44342800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr6:44341800-44343000	Enhancers	Liver	Liver
35	chr6:44341800-44354600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr6:44342000-44342400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:44342400-44342800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:44342400-44343200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr6:44342400-44343200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:44342600-44343200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr6:44342800-44343000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr6:44342800-44343200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:44343000-44343200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:44343200-44351600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr6:44345800-44346600	Enhancers	HepG2	liver
46	chr6:44346400-44346800	Enhancers	Fetal Thymus	thymus
47	chr6:44346600-44354200	Weak transcription	HepG2	liver
48	chr6:44348600-44349400	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr6:44348600-44350400	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr6:44348600-44351000	Enhancers	Primary monocytes fromperipheralblood	blood

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