Variant report

Variant	nsv1029598
Chromosome Location	chr6:58213416-58358630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1069)
CpG islands
(count:916)
Chromatin interactive
region (count:3)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1069 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:58287667-58287899	GM12878	blood:	n/a	n/a
2	ATF2	chr6:58287566-58287962	GM12878	blood:	n/a	n/a
3	ATF2	chr6:58226933-58227385	GM12878	blood:	n/a	n/a
4	ATF2	chr6:58225246-58225574	GM12878	blood:	n/a	n/a
5	ATF2	chr6:58226948-58227297	GM12878	blood:	n/a	n/a
6	ATF2	chr6:58312840-58313086	GM12878	blood:	n/a	n/a
7	BATF	chr6:58225149-58225723	GM12878	blood:	n/a	n/a
8	BATF	chr6:58241654-58241917	GM12878	blood:	n/a	chr6:58241758-58241769
9	BATF	chr6:58274807-58275130	GM12878	blood:	n/a	chr6:58274977-58274988
10	BATF	chr6:58312874-58313176	GM12878	blood:	n/a	chr6:58313100-58313108
11	BATF	chr6:58225176-58225639	GM12878	blood:	n/a	n/a
12	BATF	chr6:58312874-58313181	GM12878	blood:	n/a	chr6:58313100-58313108
13	BATF	chr6:58326544-58326859	GM12878	blood:	n/a	n/a
14	BATF	chr6:58226989-58227547	GM12878	blood:	n/a	n/a
15	BATF	chr6:58241206-58241440	GM12878	blood:	n/a	chr6:58241313-58241322 chr6:58241337-58241348
16	BATF	chr6:58226995-58227530	GM12878	blood:	n/a	n/a
17	BATF	chr6:58274740-58275182	GM12878	blood:	n/a	chr6:58274977-58274988
18	BATF	chr6:58241686-58241892	GM12878	blood:	n/a	chr6:58241758-58241769
19	BATF	chr6:58287533-58287892	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:58225136-58225637	GM12878	blood:	n/a	n/a
21	BCL11A	chr6:58245996-58246178	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:58287319-58287843	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:58287570-58287800	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:58312939-58313153	GM12878	blood:	n/a	chr6:58313103-58313112
25	BCL11A	chr6:58312858-58313167	GM12878	blood:	n/a	chr6:58313103-58313112
26	BCL11A	chr6:58227066-58227268	GM12878	blood:	n/a	n/a
27	BCL11A	chr6:58226962-58227383	GM12878	blood:	n/a	n/a
28	BCLAF1	chr6:58312816-58313161	GM12878	blood:	n/a	chr6:58313103-58313112
29	BCLAF1	chr6:58287452-58288025	GM12878	blood:	n/a	n/a
30	BCLAF1	chr6:58287548-58287910	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:58312965-58313069	GM12878	blood:	n/a	n/a
32	CBX3	chr6:58287498-58287998	K562	blood:	n/a	n/a
33	CBX3	chr6:58287493-58287955	K562	blood:	n/a	n/a
34	CCNT2	chr6:58287622-58287859	K562	blood:	n/a	n/a
35	CEBPB	chr6:58334093-58334264	HepG2	liver:	n/a	chr6:58334239-58334250 chr6:58334239-58334248 chr6:58334237-58334250 chr6:58334239-58334248 chr6:58334239-58334248 chr6:58334237-58334250 chr6:58334239-58334250 chr6:58334239-58334248 chr6:58334237-58334250 chr6:58334237-58334248
36	CEBPB	chr6:58262027-58262420	K562	blood:	n/a	n/a
37	CEBPB	chr6:58357831-58357857	HepG2	liver:	n/a	chr6:58357833-58357844 chr6:58357834-58357845
38	CEBPB	chr6:58302675-58303028	K562	blood:	n/a	n/a
39	CEBPB	chr6:58287720-58287958	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr6:58287573-58287962	K562	blood:	n/a	n/a
41	CEBPB	chr6:58262093-58262326	K562	blood:	n/a	n/a
42	CEBPB	chr6:58287831-58287968	HepG2	liver:	n/a	n/a
43	CEBPD	chr6:58287449-58287865	HepG2	liver:	n/a	n/a
44	CEBPD	chr6:58302568-58303070	K562	blood:	n/a	n/a
45	CEBPD	chr6:58287424-58287881	K562	blood:	n/a	n/a
46	CEBPD	chr6:58300940-58301286	K562	blood:	n/a	n/a
47	CHD2	chr6:58287662-58287760	GM12878	blood:	n/a	n/a
48	CHD2	chr6:58287615-58287825	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr6:58312973-58313106	GM12878	blood:	n/a	n/a
50	CREB1	chr6:58287533-58287896	A549	lung:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:58263193-58263243	HNPCEpiC	eye:	n/a
2	chr6:58263193-58263243	HNPCEpiC	eye:	n/a
3	chr6:58290947-58290997	HRCEpiC	kidney:	n/a
4	chr6:58287825-58287875	NT2-D1	testis:	n/a
5	chr6:58290947-58290997	HCPEpiC	choroid plexus:	n/a
6	chr6:58263122-58263172	HCM	heart:	n/a
7	chr6:58287822-58287872	NB4	blood:	n/a
8	chr6:58289118-58289168	T-47D	breast:	n/a
9	chr6:58287758-58287808	SK-N-SH	brain:	n/a
10	chr6:58289131-58289181	HRPEpiC	eye:	n/a
11	chr6:58259157-58259207	H1-hESC	embryonic stem cell:	embryo
12	chr6:58285006-58285056	AG04450	lung:	fetal
13	chr6:58287827-58287877	NT2-D1	testis:	n/a
14	chr6:58289118-58289168	HCPEpiC	choroid plexus:	n/a
15	chr6:58263122-58263172	AG04450	lung:	fetal
16	chr6:58287758-58287808	LNCaP	prostate:	n/a
17	chr6:58287938-58287988	HMEC	breast:	n/a
18	chr6:58289131-58289181	HUVEC	blood vessel:	n/a
19	chr6:58263122-58263172	AoSMC	blood vessel:	n/a
20	chr6:58285006-58285056	NH-A	brain:	n/a
21	chr6:58287825-58287875	HEK293	kidney:	embryo
22	chr6:58289118-58289168	Hela-S3	cervix:	n/a
23	chr6:58287758-58287808	HIPEpiC	eye:	n/a
24	chr6:58289118-58289168	SK-N-SH_RA	brain:	n/a
25	chr6:58263193-58263243	HRE	kidney:	n/a
26	chr6:58263122-58263172	T-47D	breast:	n/a
27	chr6:58287938-58287988	HCF	heart:	n/a
28	chr6:58263122-58263172	Caco-2	colon:	n/a
29	chr6:58285006-58285056	HNPCEpiC	eye:	n/a
30	chr6:58287938-58287988	H1-hESC	embryonic stem cell:	embryo
31	chr6:58287758-58287808	GM12891	blood:	n/a
32	chr6:58287758-58287808	HCM	heart:	n/a
33	chr6:58287938-58287988	GM12892	blood:	n/a
34	chr6:58285006-58285056	PANC-1	pancreas:	n/a
35	chr6:58285006-58285056	AG09319	gingival:	n/a
36	chr6:58289131-58289181	AG09319	gingival:	n/a
37	chr6:58263193-58263243	SKMC	muscle:	n/a
38	chr6:58285006-58285056	RPTEC	kidney:	n/a
39	chr6:58287822-58287872	BJ	skin:	n/a
40	chr6:58287430-58287480	CMK	blood:	n/a
41	chr6:58287758-58287808	ProgFib	skin:	n/a
42	chr6:58285006-58285056	NB4	blood:	n/a
43	chr6:58287938-58287988	HEEpiC	esophagus:	n/a
44	chr6:58287430-58287480	T-47D	breast:	n/a
45	chr6:58287758-58287808	K562	blood:	n/a
46	chr6:58286735-58286785	MCF10A-Er-Src	breast:	n/a
47	chr6:58287825-58287875	ProgFib	skin:	n/a
48	chr6:58285006-58285056	K562	blood:	n/a
49	chr6:58289118-58289168	HRE	kidney:	n/a
50	chr6:58263122-58263172	NHDF-neo	bronchial:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:37379216..37379885-chr6:58287233..58287739,2	Hela-S3	cervix:
2	chr6:58293670..58295896-chr6:58296442..58298545,2	K562	blood:
3	chr6:58293670..58295896-chr6:58296442..58300027,3	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB23-3	chr6:58275196-58275417	NONHSAT113318
2	lnc-BAG2-12	chr6:58290606-58290988	l_3195_chr6:58290605-58295048_testes
3	lnc-RAB23-3	chr6:58272350-58273455	NONHSAT113311
4	lnc-RAB23-3	chr6:58275196-58275346	NONHSAT113311
5	lnc-RAB23-3	chr6:58285306-58285389	NONHSAT113317
6	lnc-RAB23-3	chr6:58287599-58287654	NONHSAT113317
7	lnc-RAB23-3	chr6:58239194-58239687	XLOC_005753
8	lnc-RAB23-3	chr6:58275196-58275346	NONHSAT113310
9	lnc-RAB23-3	chr6:58287430-58287502	NONHSAT113317
10	lnc-RAB23-3	chr6:58272400-58273455	NONHSAT113318
11	lnc-BAG2-6	chr6:58291908-58292021	ENSG00000225096
12	lnc-RAB23-3	chr6:58287430-58287502	NONHSAT113319
13	lnc-RAB23-3	chr6:58275636-58276125	NONHSAT113311
14	lnc-RAB23-3	chr6:58234838-58240189	ENSG00000272316.1
15	lnc-BAG2-12	chr6:58294832-58295048	l_3195_chr6:58290605-58295048_testes
16	lnc-RAB23-3	chr6:58276137-58276366	NONHSAT113310
17	lnc-RAB23-3	chr6:58272350-58273455	NONHSAT113310
18	lnc-RAB23-3	chr6:58275087-58275346	NONHSAT113319
19	lnc-RAB23-3	chr6:58234692-58238642	XLOC_005753
20	lnc-BAG2-6	chr6:58297873-58297934	ENSG00000225096
21	lnc-BAG2-5	chr6:58243374-58243434	ENSG00000236143.1
22	lnc-BAG2-6	chr6:58298372-58298496	ENSG00000225096
23	lnc-RAB23-18	chr6:58228887-58229426	ENSG00000271761.1
24	lnc-RAB23-3	chr6:58272393-58273455	NONHSAT113317
25	lnc-RAB23-4	chr6:58275151-58276677	ENSG00000215190
26	lnc-RAB23-4	chr6:58272361-58273455	ENSG00000215190
27	lnc-RAB23-3	chr6:58285306-58285389	NONHSAT113319
28	lnc-BAG2-5	chr6:58243460-58243544	ENSG00000236143.1
29	lnc-RAB23-3	chr6:58287599-58287654	NONHSAT113319

No data

Variant related genes	Relation type
ENSG00000272316	TF binding region
GUSBP4	TF binding region
LINC00680	TF binding region
POM121L14P	TF binding region
GAPDHP15	TF binding region
ENSG00000271761	TF binding region
ENSG00000225096	TF binding region
ENSG00000272316	CpG island
GUSBP4	CpG island
LINC00680	CpG island
POM121L14P	CpG island
GAPDHP15	CpG island
ENSG00000271761	CpG island
ENSG00000225096	CpG island
ENSG00000214563	chromatin interactions
ENSG00000082068	chromatin interactions

Extended variants
information (count: 3348 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3348 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570466791	chr6:58226409-58226410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192445689	chr6:58226440-58226441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552983550	chr6:58226492-58226493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574605464	chr6:58226585-58226586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542405545	chr6:58226604-58226605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184997776	chr6:58226605-58226606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576007669	chr6:58226614-58226615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546518710	chr6:58226618-58226619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564637356	chr6:58226643-58226644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563792240	chr6:58226850-58226851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548419585	chr6:58226901-58226902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577372643	chr6:58226998-58226999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541768695	chr6:58227006-58227007	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540290488	chr6:58227043-58227044	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188926505	chr6:58227048-58227049	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2982029	chr6:58227062-58227063	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529382128	chr6:58227151-58227152	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2475577	chr6:58227216-58227217	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547959592	chr6:58227363-58227364	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559928178	chr6:58227392-58227393	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569559789	chr6:58227429-58227430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6926125	chr6:58227450-58227451	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs552407640	chr6:58227455-58227456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570656566	chr6:58227459-58227460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377143282	chr6:58227517-58227518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552708684	chr6:58227562-58227563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568143685	chr6:58227609-58227610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535594463	chr6:58227673-58227674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557581241	chr6:58227680-58227681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575870299	chr6:58227697-58227698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546087132	chr6:58227703-58227704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2758421	chr6:58227715-58227716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12662930	chr6:58227724-58227725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2472997	chr6:58227747-58227748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2475578	chr6:58227790-58227791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183977765	chr6:58227794-58227795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2758422	chr6:58227809-58227810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs3996679	chr6:58227893-58227894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374820902	chr6:58227913-58227914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs3996680	chr6:58227954-58227955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs3996681	chr6:58227968-58227969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529343082	chr6:58227969-58227970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530777976	chr6:58227970-58227971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544340120	chr6:58228060-58228061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562651654	chr6:58228078-58228079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530681894	chr6:58228089-58228090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs367838057	chr6:58228106-58228107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552105833	chr6:58228114-58228115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs477994	chr6:58228129-58228130	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs189550523	chr6:58228178-58228179	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD

Chromatin state (count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58226400-58228200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:58226800-58227000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:58227000-58227400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:58237800-58245200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr6:58237800-58253400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr6:58238000-58245000	Weak transcription	Fetal Stomach	stomach
7	chr6:58238000-58252600	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr6:58238000-58252800	Weak transcription	Fetal Intestine Large	intestine
9	chr6:58240800-58245800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:58243000-58250200	Weak transcription	Liver	Liver
11	chr6:58243000-58272800	Weak transcription	Fetal Intestine Small	intestine
12	chr6:58243800-58246000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:58243800-58250400	Weak transcription	Primary T cells from cord blood	blood
14	chr6:58243800-58252800	Weak transcription	Rectal Smooth Muscle	rectum
15	chr6:58243800-58254400	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr6:58244000-58248600	Weak transcription	Adipose Nuclei	Adipose
17	chr6:58244000-58248600	Weak transcription	Lung	lung
18	chr6:58244000-58249000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr6:58244000-58250000	Weak transcription	Spleen	Spleen
20	chr6:58244000-58250200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr6:58244000-58250200	Weak transcription	Fetal Muscle Leg	muscle
22	chr6:58244000-58250200	Weak transcription	Ovary	ovary
23	chr6:58244000-58250400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr6:58244000-58250400	Weak transcription	Fetal Lung	lung
25	chr6:58244000-58252600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr6:58244000-58252800	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr6:58244000-58252800	Weak transcription	Thymus	Thymus
28	chr6:58244000-58253000	Weak transcription	Brain Cingulate Gyrus	brain
29	chr6:58244000-58254600	Weak transcription	Brain Anterior Caudate	brain
30	chr6:58244000-58258600	Weak transcription	Pancreas	Pancrea
31	chr6:58244000-58272400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr6:58244200-58252400	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr6:58244200-58287200	Weak transcription	Right Ventricle	heart
34	chr6:58244400-58272600	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr6:58244600-58247000	Weak transcription	Osteobl	bone
36	chr6:58244600-58249800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr6:58244600-58250200	Weak transcription	Colon Smooth Muscle	Colon
38	chr6:58244600-58252600	Weak transcription	Brain Hippocampus Middle	brain
39	chr6:58244600-58253000	Weak transcription	Stomach Smooth Muscle	stomach
40	chr6:58244600-58254400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:58244600-58255400	Weak transcription	Brain Germinal Matrix	brain
42	chr6:58244800-58273000	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr6:58245000-58245800	Strong transcription	Fetal Stomach	stomach
44	chr6:58245200-58245600	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr6:58245600-58253000	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr6:58245800-58246400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr6:58245800-58246600	Weak transcription	Fetal Stomach	stomach
48	chr6:58245800-58247400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:58245800-58248400	Weak transcription	Fetal Muscle Trunk	muscle
50	chr6:58245800-58248800	Weak transcription	HSMMtube	muscle

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