Variant report

Variant	nsv970086
Chromosome Location	chr6:26374877-26378621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:23)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:23 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr6:26378427-26378675	GM12878	blood:	n/a	n/a
2	CTCF	chr6:26375238-26375287	HepG2	liver:	n/a	n/a
3	CTCF	chr6:26375220-26375370	RPTEC	kidney:	n/a	n/a
4	CTCF	chr6:26375208-26375320	MCF-7	breast:	n/a	n/a
5	CTCF	chr6:26375241-26375290	Fibrobl	skin:	n/a	n/a
6	CUX1	chr6:26376629-26376662	GM12878	blood:	n/a	n/a
7	MAFF	chr6:26378400-26378648	HepG2	liver:	n/a	n/a
8	MAFF	chr6:26378477-26378591	K562	blood:	n/a	n/a
9	MAFK	chr6:26378410-26378666	HepG2	liver:	n/a	chr6:26378530-26378545
10	MAFK	chr6:26378461-26378567	K562	blood:	n/a	chr6:26378530-26378545
11	MAFK	chr6:26378397-26378674	IMR90	lung:	n/a	chr6:26378530-26378545
12	MAFK	chr6:26378394-26378674	HepG2	liver:	n/a	chr6:26378530-26378545
13	POLR2A	chr6:26378519-26378561	HepG2	liver:	n/a	n/a
14	POLR2A	chr6:26377390-26377448	HepG2	liver:	n/a	n/a
15	POLR2A	chr6:26377645-26377700	HepG2	liver:	n/a	n/a
16	POLR2A	chr6:26376851-26376954	HepG2	liver:	n/a	n/a
17	POLR2A	chr6:26376973-26377022	HepG2	liver:	n/a	n/a
18	POLR2A	chr6:26378290-26378472	HepG2	liver:	n/a	n/a
19	POLR2A	chr6:26375423-26376057	PFSK-1	brain:	n/a	n/a
20	REST	chr6:26375555-26375832	PFSK-1	brain:	n/a	n/a
21	SPI1	chr6:26376460-26376761	GM12891	blood:	n/a	chr6:26376607-26376616
22	SPI1	chr6:26376502-26376739	GM12891	blood:	n/a	chr6:26376607-26376616
23	SPI1	chr6:26376475-26376762	GM12878	blood:	n/a	chr6:26376607-26376616

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26375990-26376040	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:26375990-26376040	GM19239	blood:	n/a
3	chr6:26375990-26376040	H1-hESC	embryonic stem cell:	embryo
4	chr6:26375990-26376040	HL-60	blood:	n/a
5	chr6:26375990-26376040	PrEC	prostate:	n/a
6	chr6:26375990-26376040	AG09319	gingival:	n/a
7	chr6:26375990-26376040	AG10803	skin:	n/a
8	chr6:26375990-26376040	ProgFib	skin:	n/a
9	chr6:26375990-26376040	HIPEpiC	eye:	n/a
10	chr6:26375990-26376040	SK-N-SH	brain:	n/a
11	chr6:26375990-26376040	U87	brain:	n/a
12	chr6:26375990-26376040	ovcar-3	ovarian:	n/a
13	chr6:26375990-26376040	HAEpiC	amniotic membrane:	n/a
14	chr6:26375990-26376040	HRCEpiC	kidney:	n/a
15	chr6:26375990-26376040	RPTEC	kidney:	n/a
16	chr6:26375990-26376040	HEEpiC	esophagus:	n/a
17	chr6:26375990-26376040	GM12891	blood:	n/a
18	chr6:26375990-26376040	GM12878	blood:	n/a
19	chr6:26375990-26376040	AG09309	skin:	n/a
20	chr6:26375990-26376040	SAEC	small airway:	n/a
21	chr6:26375990-26376040	HCT-116	colon:	n/a
22	chr6:26375990-26376040	Hela-S3	cervix:	n/a
23	chr6:26375990-26376040	SK-N-MC	brain:	n/a
24	chr6:26375990-26376040	IMR90	lung:	fetal
25	chr6:26375990-26376040	ECC-1	luminal epithelium:	n/a
26	chr6:26375990-26376040	CMK	blood:	n/a
27	chr6:26375990-26376040	AG04450	lung:	fetal
28	chr6:26375990-26376040	PANC-1	pancreas:	n/a
29	chr6:26375990-26376040	HRPEpiC	eye:	n/a
30	chr6:26375990-26376040	Hepatocyte	liver:	n/a
31	chr6:26375990-26376040	AG04449	skin:	fetal
32	chr6:26375990-26376040	NH-A	brain:	n/a
33	chr6:26375990-26376040	NT2-D1	testis:	n/a
34	chr6:26375990-26376040	SKMC	muscle:	n/a
35	chr6:26375990-26376040	BE2_C	brain:	n/a
36	chr6:26375990-26376040	Caco-2	colon:	n/a
37	chr6:26375990-26376040	HRE	kidney:	n/a
38	chr6:26375990-26376040	HepG2	liver:	n/a
39	chr6:26375990-26376040	NB4	blood:	n/a
40	chr6:26375990-26376040	NHBE	bronchial:	n/a
41	chr6:26375990-26376040	Jurkat	blood:	n/a
42	chr6:26375990-26376040	T-47D	breast:	n/a
43	chr6:26375990-26376040	MCF-7	breast:	n/a
44	chr6:26375990-26376040	GM12892	blood:	n/a
45	chr6:26375990-26376040	HNPCEpiC	eye:	n/a
46	chr6:26375990-26376040	MCF10A-Er-Src	breast:	n/a
47	chr6:26375990-26376040	SK-N-SH_RA	brain:	n/a
48	chr6:26375990-26376040	K562	blood:	n/a
49	chr6:26375990-26376040	HCM	heart:	n/a
50	chr6:26375990-26376040	A549	lung:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26214943..26217251-chr6:26374280..26376179,2	K562	blood:
2	chr6:26373307..26375855-chr6:26376435..26379484,4	K562	blood:
3	chr6:26373307..26375855-chr6:26376435..26379484,4	K562	blood:
4	chr6:26376258..26380187-chr6:26381333..26383262,3	K562	blood:
5	chr6:26373194..26374949-chr6:26387423..26389905,2	K562	blood:
6	chr6:26370389..26373294-chr6:26375542..26378035,2	K562	blood:
7	chr6:26360109..26361715-chr6:26372989..26375105,2	K562	blood:
8	chr6:26374643..26376462-chr6:26381050..26382858,2	K562	blood:
9	chr6:26370389..26374393-chr6:26375542..26380304,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTN2A2-2	chr6:26374999-26375036	NONHSAT108273
2	lnc-BTN2A2-2	chr6:26372921-26375929	NONHSAT108275

No data

Variant related genes	Relation type
BTN2A2	TF binding region
BTN2A2	CpG island
ENSG00000186470	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000168274	chromatin interactions

Extended variants
information (count: 190 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:190 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377396690	chr6:26374888-26374889	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs733528	chr6:26374903-26374904	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs576426126	chr6:26374909-26374910	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs2073527	chr6:26374978-26374979	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs561730718	chr6:26374992-26374993	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs183684646	chr6:26375023-26375024	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs547513910	chr6:26375036-26375037	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs114264868	chr6:26375056-26375057	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs533385695	chr6:26375058-26375059	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs566001526	chr6:26375065-26375066	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs2073528	chr6:26375143-26375144	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs150175710	chr6:26375156-26375157	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs2073529	chr6:26375159-26375160	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs575958241	chr6:26375214-26375215	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs549372110	chr6:26375230-26375231	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs535632350	chr6:26375236-26375237	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs566107034	chr6:26375241-26375242	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs2073530	chr6:26375243-26375244	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs558265756	chr6:26375246-26375247	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs2073531	chr6:26375256-26375257	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs369750873	chr6:26375286-26375287	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs537513588	chr6:26375618-26375619	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs543060742	chr6:26375641-26375642	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs545900370	chr6:26375642-26375643	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs9393715	chr6:26375645-26375646	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs9348716	chr6:26375658-26375659	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs555367981	chr6:26375709-26375710	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs572031952	chr6:26375744-26375745	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs202070996	chr6:26375797-26375798	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs188300236	chr6:26375810-26375811	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs138643110	chr6:26375821-26375822	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs532887522	chr6:26375844-26375845	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs9379871	chr6:26375854-26375855	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs12206621	chr6:26375881-26375882	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs554252916	chr6:26375941-26375942	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs529438383	chr6:26376015-26376016	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs181807690	chr6:26376026-26376027	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs566221189	chr6:26376041-26376042	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs528748517	chr6:26376054-26376055	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs3757138	chr6:26376103-26376104	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs144525958	chr6:26376106-26376107	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs187160266	chr6:26376126-26376127	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs148632805	chr6:26376149-26376150	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs190829915	chr6:26376153-26376154	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs1985732	chr6:26376161-26376162	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs181656598	chr6:26376210-26376211	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs555666744	chr6:26376265-26376266	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572268902	chr6:26376270-26376271	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs369872392	chr6:26376298-26376299	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375684300	chr6:26376309-26376310	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Autism	22495309	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD

Chromatin state (count:206 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26365800-26375200	Weak transcription	Aorta	Aorta
2	chr6:26366000-26375000	Weak transcription	Brain Anterior Caudate	brain
3	chr6:26366000-26375600	Weak transcription	Gastric	stomach
4	chr6:26366000-26382600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:26366000-26383000	Weak transcription	Brain Hippocampus Middle	brain
6	chr6:26366000-26383200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr6:26366000-26383200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:26366000-26383200	Weak transcription	Pancreas	Pancrea
9	chr6:26366000-26383200	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr6:26366000-26383200	Weak transcription	HSMMtube	muscle
11	chr6:26366000-26383400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr6:26366200-26375000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr6:26366200-26375200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr6:26366200-26375800	Weak transcription	NH-A	brain
15	chr6:26366200-26382400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr6:26366200-26383200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:26366200-26383200	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr6:26367000-26377800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:26367000-26383000	Weak transcription	NHEK	skin
20	chr6:26367000-26383200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:26367400-26375000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr6:26367800-26378600	Weak transcription	Small Intestine	intestine
23	chr6:26368800-26375200	Strong transcription	Primary B cells from cord blood	blood
24	chr6:26368800-26376000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
25	chr6:26369400-26375200	Strong transcription	Fetal Lung	lung
26	chr6:26369400-26377000	Strong transcription	Fetal Muscle Leg	muscle
27	chr6:26369400-26377600	Strong transcription	Primary hematopoietic stem cells	blood
28	chr6:26369400-26378000	Strong transcription	Liver	Liver
29	chr6:26369400-26378200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:26369800-26378200	Strong transcription	Thymus	Thymus
31	chr6:26369800-26383000	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr6:26370200-26375200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:26370200-26375200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr6:26370200-26377800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr6:26370400-26377800	Strong transcription	Duodenum Mucosa	Duodenum
36	chr6:26370400-26378200	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr6:26370400-26383000	Weak transcription	Brain Cingulate Gyrus	brain
38	chr6:26370600-26376000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr6:26370600-26378000	Strong transcription	Fetal Intestine Small	intestine
40	chr6:26370800-26375000	Strong transcription	Primary B cells from peripheral blood	blood
41	chr6:26370800-26375000	Weak transcription	Rectal Smooth Muscle	rectum
42	chr6:26370800-26375200	Strong transcription	Fetal Thymus	thymus
43	chr6:26370800-26376600	Strong transcription	Spleen	Spleen
44	chr6:26370800-26378000	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr6:26370800-26379000	Strong transcription	Primary T cells from cord blood	blood
46	chr6:26370800-26383200	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr6:26371000-26383200	Weak transcription	Right Ventricle	heart
48	chr6:26371400-26377600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:26371800-26378000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr6:26372000-26378000	Strong transcription	Rectal Mucosa Donor 29	rectum

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