Variant report

Variant	nsv462956
Chromosome Location	chr6:58272623-58357694
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	ATF2	chr6:58312840-58313086	GM12878	blood:	n/a	n/a
2	ATF2	chr6:58287667-58287899	GM12878	blood:	n/a	n/a
3	ATF2	chr6:58287566-58287962	GM12878	blood:	n/a	n/a
4	BATF	chr6:58326544-58326859	GM12878	blood:	n/a	n/a
5	BATF	chr6:58274807-58275130	GM12878	blood:	n/a	chr6:58274977-58274988
6	BATF	chr6:58287533-58287892	GM12878	blood:	n/a	n/a
7	BATF	chr6:58274740-58275182	GM12878	blood:	n/a	chr6:58274977-58274988
8	BATF	chr6:58312874-58313176	GM12878	blood:	n/a	chr6:58313100-58313108
9	BATF	chr6:58312874-58313181	GM12878	blood:	n/a	chr6:58313100-58313108
10	BCL11A	chr6:58287570-58287800	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:58312858-58313167	GM12878	blood:	n/a	chr6:58313103-58313112
12	BCL11A	chr6:58312939-58313153	GM12878	blood:	n/a	chr6:58313103-58313112
13	BCL11A	chr6:58287319-58287843	GM12878	blood:	n/a	n/a
14	BCLAF1	chr6:58312816-58313161	GM12878	blood:	n/a	chr6:58313103-58313112
15	BCLAF1	chr6:58287452-58288025	GM12878	blood:	n/a	n/a
16	BCLAF1	chr6:58287548-58287910	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:58312965-58313069	GM12878	blood:	n/a	n/a
18	CBX3	chr6:58287493-58287955	K562	blood:	n/a	n/a
19	CBX3	chr6:58287498-58287998	K562	blood:	n/a	n/a
20	CCNT2	chr6:58287622-58287859	K562	blood:	n/a	n/a
21	CEBPB	chr6:58287573-58287962	K562	blood:	n/a	n/a
22	CEBPB	chr6:58302675-58303028	K562	blood:	n/a	n/a
23	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
24	CEBPB	chr6:58287831-58287968	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:58287720-58287958	Hela-S3	cervix:	n/a	n/a
26	CEBPD	chr6:58302568-58303070	K562	blood:	n/a	n/a
27	CEBPD	chr6:58287424-58287881	K562	blood:	n/a	n/a
28	CEBPD	chr6:58300940-58301286	K562	blood:	n/a	n/a
29	CEBPD	chr6:58287449-58287865	HepG2	liver:	n/a	n/a
30	CHD2	chr6:58287615-58287825	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr6:58287662-58287760	GM12878	blood:	n/a	n/a
32	CHD2	chr6:58312973-58313106	GM12878	blood:	n/a	n/a
33	CREB1	chr6:58287533-58287896	A549	lung:	n/a	n/a
34	CTCF	chr6:58287780-58287930	RPTEC	kidney:	n/a	chr6:58287791-58287807 chr6:58287792-58287805 chr6:58287790-58287808 chr6:58287792-58287805
35	CTCF	chr6:58329840-58329990	GM06990	blood:	n/a	n/a
36	CTCF	chr6:58296869-58297200	GM12878	blood:	n/a	n/a
37	CTCF	chr6:58329820-58329970	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr6:58296920-58297070	AG04450	lung:	n/a	n/a
39	CTCF	chr6:58276778-58276946	K562	blood:	n/a	chr6:58276846-58276864 chr6:58276852-58276861 chr6:58276841-58276862
40	CTCF	chr6:58287612-58287947	Lung_OC	lung:	n/a	chr6:58287791-58287807 chr6:58287792-58287805 chr6:58287790-58287808 chr6:58287792-58287805
41	CTCF	chr6:58287676-58288073	HCT-116	colon:	n/a	chr6:58287791-58287807 chr6:58287792-58287805 chr6:58287790-58287808 chr6:58287792-58287805
42	CTCF	chr6:58287760-58287910	HA-sp	spinal cord:	n/a	chr6:58287791-58287807 chr6:58287792-58287805 chr6:58287790-58287808 chr6:58287792-58287805
43	CTCF	chr6:58296939-58297119	HepG2	liver:	n/a	n/a
44	CTCF	chr6:58287740-58287890	GM12869	blood:	n/a	chr6:58287791-58287807 chr6:58287792-58287805 chr6:58287790-58287808 chr6:58287792-58287805
45	CTCF	chr6:58296940-58297090	GM12867	blood:	n/a	n/a
46	CTCF	chr6:58296960-58297110	BE2_C	brain:	n/a	n/a
47	CTCF	chr6:58296960-58297110	NB4	blood:	n/a	n/a
48	CTCF	chr6:58287671-58287924	LNCaP	prostate:	n/a	chr6:58287791-58287807 chr6:58287792-58287805 chr6:58287790-58287808 chr6:58287792-58287805
49	CTCF	chr6:58287650-58287952	GM12878	blood:	n/a	chr6:58287791-58287807 chr6:58287792-58287805 chr6:58287790-58287808 chr6:58287792-58287805
50	CTCF	chr6:58276822-58276938	HepG2	liver:	n/a	chr6:58276846-58276864 chr6:58276852-58276861 chr6:58276841-58276862

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:58287938-58287988	PANC-1	pancreas:	n/a
2	chr6:58287825-58287875	GM12878	blood:	n/a
3	chr6:58287938-58287988	HMEC	breast:	n/a
4	chr6:58287827-58287877	HPAEpiC	pulmonary alveolar:	n/a
5	chr6:58287694-58287744	SK-N-SH	brain:	n/a
6	chr6:58287430-58287480	NB4	blood:	n/a
7	chr6:58289118-58289168	ECC-1	luminal epithelium:	n/a
8	chr6:58289118-58289168	AG09319	gingival:	n/a
9	chr6:58287430-58287480	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:58285006-58285056	SK-N-SH	brain:	n/a
11	chr6:58287827-58287877	GM12878	blood:	n/a
12	chr6:58287758-58287808	GM12892	blood:	n/a
13	chr6:58287694-58287744	MCF10A-Er-Src	breast:	n/a
14	chr6:58285006-58285056	HIPEpiC	eye:	n/a
15	chr6:58287822-58287872	PANC-1	pancreas:	n/a
16	chr6:58285006-58285056	PANC-1	pancreas:	n/a
17	chr6:58287938-58287988	NH-A	brain:	n/a
18	chr6:58285006-58285056	HUVEC	blood vessel:	n/a
19	chr6:58289131-58289181	HAEpiC	amniotic membrane:	n/a
20	chr6:58290947-58290997	BJ	skin:	n/a
21	chr6:58290947-58290997	PrEC	prostate:	n/a
22	chr6:58289131-58289181	U87	brain:	n/a
23	chr6:58287430-58287480	PrEC	prostate:	n/a
24	chr6:58287694-58287744	HCT-116	colon:	n/a
25	chr6:58286735-58286785	AG09309	skin:	n/a
26	chr6:58290947-58290997	K562	blood:	n/a
27	chr6:58287430-58287480	AG09319	gingival:	n/a
28	chr6:58289118-58289168	Caco-2	colon:	n/a
29	chr6:58287822-58287872	HIPEpiC	eye:	n/a
30	chr6:58287827-58287877	GM12892	blood:	n/a
31	chr6:58286735-58286785	BE2_C	brain:	n/a
32	chr6:58287825-58287875	T-47D	breast:	n/a
33	chr6:58287938-58287988	U87	brain:	n/a
34	chr6:58287938-58287988	HRE	kidney:	n/a
35	chr6:58289118-58289168	AG04449	skin:	fetal
36	chr6:58286735-58286785	NHDF-neo	bronchial:	n/a
37	chr6:58287827-58287877	AG04449	skin:	fetal
38	chr6:58287822-58287872	SK-N-SH_RA	brain:	n/a
39	chr6:58287825-58287875	HepG2	liver:	n/a
40	chr6:58286735-58286785	GM19239	blood:	n/a
41	chr6:58290947-58290997	GM19239	blood:	n/a
42	chr6:58287825-58287875	HUVEC	blood vessel:	n/a
43	chr6:58287758-58287808	Caco-2	colon:	n/a
44	chr6:58290947-58290997	AG09319	gingival:	n/a
45	chr6:58285006-58285056	GM12892	blood:	n/a
46	chr6:58287938-58287988	LNCaP	prostate:	n/a
47	chr6:58289118-58289168	HepG2	liver:	n/a
48	chr6:58287694-58287744	CMK	blood:	n/a
49	chr6:58289118-58289168	HL-60	blood:	n/a
50	chr6:58287694-58287744	HPAEpiC	pulmonary alveolar:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB23-3	chr6:58287430-58287502	NONHSAT113319
2	lnc-RAB23-3	chr6:58287430-58287502	NONHSAT113317
3	lnc-RAB23-3	chr6:58275636-58276125	NONHSAT113311
4	lnc-RAB23-3	chr6:58287599-58287654	NONHSAT113319
5	lnc-BAG2-12	chr6:58294832-58295048	l_3195_chr6:58290605-58295048_testes
6	lnc-RAB23-4	chr6:58275151-58276677	ENSG00000215190
7	lnc-RAB23-3	chr6:58275196-58275417	NONHSAT113318
8	lnc-RAB23-3	chr6:58285306-58285389	NONHSAT113317
9	lnc-BAG2-6	chr6:58297873-58297934	ENSG00000225096
10	lnc-BAG2-6	chr6:58298372-58298496	ENSG00000225096
11	lnc-RAB23-3	chr6:58272350-58273455	NONHSAT113311
12	lnc-RAB23-3	chr6:58272400-58273455	NONHSAT113318
13	lnc-RAB23-3	chr6:58276137-58276366	NONHSAT113310
14	lnc-RAB23-3	chr6:58272350-58273455	NONHSAT113310
15	lnc-RAB23-3	chr6:58287599-58287654	NONHSAT113317
16	lnc-RAB23-4	chr6:58272361-58273455	ENSG00000215190
17	lnc-RAB23-3	chr6:58275087-58275346	NONHSAT113319
18	lnc-RAB23-3	chr6:58275196-58275346	NONHSAT113311
19	lnc-RAB23-3	chr6:58275196-58275346	NONHSAT113310
20	lnc-BAG2-6	chr6:58291908-58292021	ENSG00000225096
21	lnc-RAB23-3	chr6:58272393-58273455	NONHSAT113317
22	lnc-RAB23-3	chr6:58285306-58285389	NONHSAT113319
23	lnc-BAG2-12	chr6:58290606-58290988	l_3195_chr6:58290605-58295048_testes

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

Extended variants
information (count: 1931 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1931 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13777	chr6:58272623-58272624	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532752357	chr6:58272624-58272625	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs548052776	chr6:58272640-58272641	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs370939520	chr6:58272641-58272642	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs566276985	chr6:58272652-58272653	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs530388310	chr6:58272706-58272707	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs548614850	chr6:58272726-58272727	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs561435176	chr6:58272755-58272756	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs570015336	chr6:58272768-58272769	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs537076983	chr6:58272804-58272805	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs376902321	chr6:58272820-58272821	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs188782890	chr6:58272825-58272826	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs192496869	chr6:58272830-58272831	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs534802161	chr6:58272838-58272839	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs553505317	chr6:58272870-58272871	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs3749928	chr6:58272913-58272914	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs542874876	chr6:58272973-58272974	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs537804748	chr6:58272980-58272981	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs554604503	chr6:58273001-58273002	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs143030629	chr6:58273035-58273036	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs183387546	chr6:58273064-58273065	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs374283719	chr6:58273078-58273079	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs564965728	chr6:58273087-58273088	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs532196000	chr6:58273123-58273124	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs187481149	chr6:58273127-58273128	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs546959110	chr6:58273168-58273169	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs550913553	chr6:58273176-58273177	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs559950653	chr6:58273184-58273185	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs530262746	chr6:58273189-58273190	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs548840669	chr6:58273205-58273206	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs570298446	chr6:58273225-58273226	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs551346770	chr6:58273238-58273239	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs191580561	chr6:58273265-58273266	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs149591546	chr6:58273268-58273269	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs184064016	chr6:58273323-58273324	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs566720643	chr6:58273335-58273336	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs9500246	chr6:58273398-58273399	Strong transcription Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs553068013	chr6:58273416-58273417	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs565853674	chr6:58273467-58273468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374475741	chr6:58273517-58273518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4928423	chr6:58273526-58273527	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs554846899	chr6:58273541-58273542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201853056	chr6:58273568-58273569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576301840	chr6:58273579-58273580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186531516	chr6:58273612-58273613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569412801	chr6:58273654-58273655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576926735	chr6:58273778-58273779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540075741	chr6:58273824-58273825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541110526	chr6:58273869-58273870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113852176	chr6:58273893-58273894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58243000-58272800	Weak transcription	Fetal Intestine Small	intestine
2	chr6:58244200-58287200	Weak transcription	Right Ventricle	heart
3	chr6:58244800-58273000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr6:58245800-58272800	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr6:58245800-58275000	Weak transcription	Brain Angular Gyrus	brain
6	chr6:58247200-58273200	Weak transcription	Primary B cells from peripheral blood	blood
7	chr6:58250800-58275000	Weak transcription	Gastric	stomach
8	chr6:58250800-58287200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:58261400-58286600	Weak transcription	Brain Germinal Matrix	brain
10	chr6:58267800-58273000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:58268200-58272800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr6:58268600-58274800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr6:58269600-58273000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:58269600-58273000	Weak transcription	Dnd41	blood
15	chr6:58270000-58285800	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr6:58270200-58273000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr6:58270200-58287200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr6:58270600-58272800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr6:58270600-58273000	Weak transcription	Fetal Muscle Trunk	muscle
20	chr6:58270600-58273000	Weak transcription	Stomach Smooth Muscle	stomach
21	chr6:58270600-58274400	Weak transcription	Primary T cells from cord blood	blood
22	chr6:58270600-58287000	Weak transcription	Brain Anterior Caudate	brain
23	chr6:58270800-58273000	Weak transcription	Fetal Thymus	thymus
24	chr6:58270800-58276200	Weak transcription	HSMMtube	muscle
25	chr6:58270800-58286600	Weak transcription	Osteobl	bone
26	chr6:58271000-58272800	Weak transcription	Brain Hippocampus Middle	brain
27	chr6:58271000-58272800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr6:58271000-58272800	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr6:58271000-58273000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:58271000-58273200	Weak transcription	Rectal Smooth Muscle	rectum
31	chr6:58271000-58274800	Weak transcription	Esophagus	oesophagus
32	chr6:58271000-58278600	Weak transcription	NH-A	brain
33	chr6:58271000-58285800	Weak transcription	HepG2	liver
34	chr6:58271000-58286600	Weak transcription	NHDF-Ad	bronchial
35	chr6:58271000-58287000	Weak transcription	NHEK	skin
36	chr6:58271000-58287000	Weak transcription	NHLF	lung
37	chr6:58271000-58287200	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr6:58271200-58272800	Weak transcription	GM12878-XiMat	blood
39	chr6:58271200-58273000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr6:58271200-58273000	Weak transcription	Fetal Lung	lung
41	chr6:58271200-58279000	Weak transcription	Primary hematopoietic stem cells	blood
42	chr6:58271200-58286600	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr6:58271200-58287000	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr6:58271400-58273000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr6:58271400-58273000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:58271400-58274800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr6:58271400-58286600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr6:58271400-58287200	Weak transcription	Pancreas	Pancrea
49	chr6:58271600-58276400	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr6:58271600-58287000	Weak transcription	Colonic Mucosa	Colon

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