Variant report

Variant	nsv428138
Chromosome Location	chr6:29065510-29213176
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:390)
CpG islands
(count:1464)
Chromatin interactive
region (count:17)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr6:29085310-29085494	Hela-S3	cervix:	n/a	n/a
2	CBX3	chr6:29110427-29110694	K562	blood:	n/a	n/a
3	CCNT2	chr6:29201860-29202060	K562	blood:	n/a	n/a
4	CCNT2	chr6:29173754-29173954	K562	blood:	n/a	n/a
5	CEBPB	chr6:29105530-29105876	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr6:29114085-29114404	HepG2	liver:	n/a	chr6:29114234-29114245
7	CEBPB	chr6:29200496-29200846	HepG2	liver:	n/a	chr6:29200693-29200704
8	CEBPB	chr6:29105551-29105846	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:29114019-29114422	Hela-S3	cervix:	n/a	chr6:29114234-29114245
10	CEBPB	chr6:29114877-29115699	Hela-S3	cervix:	n/a	chr6:29115098-29115109
11	CEBPB	chr6:29114947-29115751	IMR90	lung:	n/a	chr6:29115098-29115109
12	CEBPB	chr6:29105506-29105875	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:29105537-29105852	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:29173602-29173813	K562	blood:	n/a	n/a
15	CEBPB	chr6:29200565-29200794	HepG2	liver:	n/a	chr6:29200693-29200704
16	CEBPB	chr6:29114975-29115701	HepG2	liver:	n/a	chr6:29115098-29115109
17	CEBPB	chr6:29114942-29115242	A549	lung:	n/a	chr6:29115098-29115109
18	CEBPB	chr6:29182043-29182319	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:29200508-29200875	HepG2	liver:	n/a	chr6:29200693-29200704
20	CEBPB	chr6:29114969-29115710	K562	blood:	n/a	chr6:29115098-29115109
21	CEBPB	chr6:29157980-29157997	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:29200557-29200875	HepG2	liver:	n/a	chr6:29200693-29200704
23	CEBPB	chr6:29105509-29105880	K562	blood:	n/a	n/a
24	CEBPB	chr6:29115465-29115665	A549	lung:	n/a	n/a
25	CEBPB	chr6:29105558-29105887	MCF-7	breast:	n/a	n/a
26	CEBPB	chr6:29105510-29105876	A549	lung:	n/a	n/a
27	CEBPB	chr6:29109974-29110510	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr6:29072609-29072627	A549	lung:	n/a	n/a
29	CEBPD	chr6:29200568-29200824	HepG2	liver:	n/a	n/a
30	CTCF	chr6:29171800-29171950	RPTEC	kidney:	n/a	n/a
31	CTCF	chr6:29195150-29195296	Gliobla	brain:	n/a	chr6:29195215-29195231 chr6:29195214-29195232 chr6:29195209-29195230
32	CTCF	chr6:29079941-29080353	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:29080020-29080170	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr6:29194891-29195382	HCT-116	colon:	n/a	chr6:29195010-29195018 chr6:29195215-29195231 chr6:29195214-29195232 chr6:29195209-29195230
35	CTCF	chr6:29079945-29080223	K562	blood:	n/a	n/a
36	CTCF	chr6:29113940-29114090	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr6:29195240-29195510	Caco-2	colon:	n/a	n/a
38	CTCF	chr6:29079980-29080130	GM12864	blood:	n/a	n/a
39	CTCF	chr6:29180476-29180547	GM12878	blood:	n/a	n/a
40	CTCF	chr6:29195160-29195310	GM12865	blood:	n/a	chr6:29195215-29195231 chr6:29195214-29195232 chr6:29195209-29195230
41	CTCF	chr6:29080080-29080230	Caco-2	colon:	n/a	n/a
42	CTCF	chr6:29079980-29080130	BE2_C	brain:	n/a	n/a
43	CTCF	chr6:29079985-29080226	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:29079995-29080189	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr6:29080080-29080230	GM12869	blood:	n/a	n/a
46	CTCF	chr6:29079959-29080198	GM12878	blood:	n/a	n/a
47	CTCF	chr6:29080020-29080170	GM12871	blood:	n/a	n/a
48	CTCF	chr6:29080060-29080210	GM12874	blood:	n/a	n/a
49	CTCF	chr6:29149659-29149802	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:29080013-29080188	MCF-7	breast:	n/a	n/a

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29127982-29128032	NH-A	brain:	n/a
2	chr6:29079991-29080041	AG09319	gingival:	n/a
3	chr6:29140126-29140176	K562	blood:	n/a
4	chr6:29141346-29141396	HL-60	blood:	n/a
5	chr6:29141929-29141979	SK-N-SH_RA	brain:	n/a
6	chr6:29141678-29141728	HMEC	breast:	n/a
7	chr6:29141929-29141979	AG04449	skin:	fetal
8	chr6:29127871-29127921	PFSK-1	brain:	n/a
9	chr6:29080040-29080090	HEK293	kidney:	embryo
10	chr6:29127979-29128029	T-47D	breast:	n/a
11	chr6:29080437-29080487	HCF	heart:	n/a
12	chr6:29141565-29141615	HRCEpiC	kidney:	n/a
13	chr6:29080437-29080487	NH-A	brain:	n/a
14	chr6:29140622-29140672	T-47D	breast:	n/a
15	chr6:29127979-29128029	RPTEC	kidney:	n/a
16	chr6:29141346-29141396	GM19239	blood:	n/a
17	chr6:29127979-29128029	NB4	blood:	n/a
18	chr6:29080040-29080090	K562	blood:	n/a
19	chr6:29141346-29141396	GM06990	blood:	n/a
20	chr6:29133972-29134022	GM12891	blood:	n/a
21	chr6:29141565-29141615	HCT-116	colon:	n/a
22	chr6:29080040-29080090	IMR90	lung:	fetal
23	chr6:29079991-29080041	HCF	heart:	n/a
24	chr6:29140622-29140672	CMK	blood:	n/a
25	chr6:29127982-29128032	GM12878	blood:	n/a
26	chr6:29140126-29140176	HEK293	kidney:	embryo
27	chr6:29133961-29134011	AG04450	lung:	fetal
28	chr6:29140622-29140672	HEK293	kidney:	embryo
29	chr6:29203786-29203836	AG09309	skin:	n/a
30	chr6:29133505-29133555	HUVEC	blood vessel:	n/a
31	chr6:29203786-29203836	MCF-7	breast:	n/a
32	chr6:29137756-29137806	HCPEpiC	choroid plexus:	n/a
33	chr6:29140622-29140672	AG09319	gingival:	n/a
34	chr6:29133972-29134022	HEK293	kidney:	embryo
35	chr6:29127979-29128029	NHBE	bronchial:	n/a
36	chr6:29133085-29133135	GM12891	blood:	n/a
37	chr6:29140126-29140176	HCT-116	colon:	n/a
38	chr6:29141678-29141728	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:29141929-29141979	HNPCEpiC	eye:	n/a
40	chr6:29141565-29141615	HUVEC	blood vessel:	n/a
41	chr6:29079939-29079989	AG09319	gingival:	n/a
42	chr6:29125104-29125154	T-47D	breast:	n/a
43	chr6:29079991-29080041	LNCaP	prostate:	n/a
44	chr6:29203786-29203836	ovcar-3	ovarian:	n/a
45	chr6:29125104-29125154	MCF10A-Er-Src	breast:	n/a
46	chr6:29127979-29128029	U87	brain:	n/a
47	chr6:29127982-29128032	ProgFib	skin:	n/a
48	chr6:29133085-29133135	BJ	skin:	n/a
49	chr6:29080437-29080487	GM12878	blood:	n/a
50	chr6:29140126-29140176	HRCEpiC	kidney:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29191595..29194242-chr6:29197251..29198760,2	K562	blood:
2	chr6:29194494..29196563-chr6:29198376..29201189,2	MCF-7	breast:
3	chr6:29153930..29155451-chr6:29159790..29161704,2	K562	blood:
4	chr6:29190205..29192044-chr6:29201799..29204663,2	K562	blood:
5	chr6:29116682..29119190-chr6:29125085..29127105,2	K562	blood:
6	chr6:29040010..29040514-chr6:29194801..29195532,2	K562	blood:
7	chr6:29153930..29155451-chr6:29159790..29161704,2	K562	blood:
8	chr6:29046568..29048555-chr6:29075122..29077377,2	K562	blood:
9	chr6:29056826..29059190-chr6:29178889..29180975,2	K562	blood:
10	chr6:29183742..29186184-chr6:29187800..29190258,2	K562	blood:
11	chr6:29194494..29196563-chr6:29198376..29201189,2	MCF-7	breast:
12	chr6:29059208..29061169-chr6:29175130..29176997,2	K562	blood:
13	chr6:29116682..29119190-chr6:29125085..29127105,2	K562	blood:
14	chr6:29133273..29134852-chr6:29140182..29142699,2	K562	blood:
15	chr6:29016217..29018909-chr6:29120286..29121903,2	K562	blood:
16	chr6:29183742..29186184-chr6:29187800..29190258,2	K562	blood:
17	chr6:29191595..29194242-chr6:29197251..29198760,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR2J2-3	chr6:29204413-29204664	NONHSAT108517
2	lnc-OR2J3-7	chr6:29096487-29096622	NONHSAT108511
3	lnc-OR2J2-2	chr6:29141081-29141412	NONHSAT108513
4	lnc-OR2J2-1	chr6:29163280-29163359	XLOC_005229
5	lnc-OR2J2-1	chr6:29167955-29168401	XLOC_005229
6	lnc-OR14J1-2	chr6:29191651-29191828	NONHSAT108515
7	lnc-OR2J3-7	chr6:29091987-29092123	XLOC_005228
8	lnc-OR2J3-7	chr6:29096434-29096685	XLOC_005228
9	lnc-OR2B3-3	chr6:29111581-29111736	l_3154_chr6:29104220-29111736_testes
10	lnc-OR2J2-3	chr6:29199966-29200102	NONHSAT108517
11	lnc-OR14J1-2	chr6:29191750-29191828	ENSG00000232505
12	lnc-OR14J1-2	chr6:29191777-29191828	ENSG00000232505.2
13	lnc-OR2B3-3	chr6:29104221-29104383	l_3154_chr6:29104220-29111736_testes
14	lnc-OR2J3-7	chr6:29091978-29092123	NONHSAT108511

No data

Variant related genes	Relation type
OR2J4P	TF binding region
ENSG00000227206	TF binding region
OR2H4P	TF binding region
OR2N1P	TF binding region
OR2J3	TF binding region
OR2J2	TF binding region
ENSG00000232505	TF binding region
OR2J1	TF binding region
OR2G1P	TF binding region
OR2J4P	CpG island
ENSG00000227206	CpG island
OR2H4P	CpG island
OR2N1P	CpG island
OR2J3	CpG island
OR2J2	CpG island
ENSG00000232505	CpG island
OR2J1	CpG island
OR2G1P	CpG island
ENSG00000236909	chromatin interactions
ENSG00000204700	chromatin interactions
ENSG00000213911	chromatin interactions
ENSG00000232505	chromatin interactions

Extended variants
information (count: 1577 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1577 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538221824	chr6:29065628-29065629	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs115379280	chr6:29065630-29065631	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs568728669	chr6:29065653-29065654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs534140567	chr6:29065771-29065772	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs533079413	chr6:29065781-29065782	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs576554949	chr6:29065834-29065835	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs145263686	chr6:29065855-29065856	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs555821811	chr6:29065860-29065861	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs386698360	chr6:29068143-29068144	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs111441315	chr6:29068167-29068168	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs534950371	chr6:29075418-29075419	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs555706607	chr6:29075442-29075443	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs558060229	chr6:29075461-29075462	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs191033311	chr6:29075463-29075464	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs532723556	chr6:29076618-29076619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536445324	chr6:29076644-29076645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555483773	chr6:29076649-29076650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572169330	chr6:29076717-29076718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534701138	chr6:29076779-29076780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75320886	chr6:29076835-29076836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117029999	chr6:29076862-29076863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs41317439	chr6:29076883-29076884	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs571546818	chr6:29076955-29076956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557629541	chr6:29076961-29076962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187459905	chr6:29076962-29076963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192838333	chr6:29076971-29076972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376984854	chr6:29077004-29077005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543202172	chr6:29077083-29077084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184927024	chr6:29077120-29077121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371406105	chr6:29077123-29077124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528163450	chr6:29077186-29077187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536745051	chr6:29077187-29077188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539876875	chr6:29077320-29077321	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs545035254	chr6:29077329-29077330	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs564760412	chr6:29077346-29077347	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs3129097	chr6:29077353-29077354	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs377385305	chr6:29077354-29077355	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs189388075	chr6:29077357-29077358	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs56066225	chr6:29077391-29077392	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs529860598	chr6:29077399-29077400	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs375529961	chr6:29077403-29077404	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs181339397	chr6:29077423-29077424	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs375417632	chr6:29077424-29077425	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs184513635	chr6:29077426-29077427	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs534761056	chr6:29077432-29077433	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs186091287	chr6:29089806-29089807	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs556495647	chr6:29089818-29089819	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs568665171	chr6:29089829-29089830	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs576346453	chr6:29089873-29089874	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs144391995	chr6:29089877-29089878	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
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
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29076600-29077400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:29097200-29098800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:29097600-29097800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
4	chr6:29098400-29099000	Enhancers	Fetal Brain Male	brain
5	chr6:29099000-29099200	Weak transcription	Fetal Brain Male	brain
6	chr6:29099600-29099800	Enhancers	Fetal Brain Male	brain
7	chr6:29110000-29112000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:29113800-29115400	Enhancers	Hela-S3	cervix
9	chr6:29114200-29114400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:29114400-29114800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:29115000-29115200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:29154400-29154600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:29168800-29170800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:29170800-29185400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:29179800-29180200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:29180200-29180600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr6:29180600-29180800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr6:29180800-29189600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr6:29183600-29186200	Enhancers	Liver	Liver
20	chr6:29183600-29186200	Enhancers	HepG2	liver
21	chr6:29184000-29184600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr6:29184400-29185000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr6:29184400-29185000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr6:29184400-29185000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr6:29184800-29185000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr6:29185400-29185800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr6:29185800-29212000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:29191600-29191800	Enhancers	Aorta	Aorta
29	chr6:29191800-29195000	Weak transcription	Aorta	Aorta
30	chr6:29192000-29193800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr6:29193600-29194200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr6:29193600-29194600	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr6:29193800-29194200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr6:29193800-29194200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr6:29193800-29194200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:29193800-29194200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr6:29193800-29194200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr6:29193800-29194200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr6:29193800-29194200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:29193800-29194400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr6:29193800-29194400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr6:29194000-29194400	Enhancers	GM12878-XiMat	blood
43	chr6:29194200-29194600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr6:29194200-29203000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:29194400-29195000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr6:29195200-29195400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
47	chr6:29199200-29203600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr6:29199600-29201200	Enhancers	Liver	Liver
49	chr6:29200200-29201200	Enhancers	HepG2	liver
50	chr6:29202600-29205000	Enhancers	HUES64 Cell Line	embryonic stem cell

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